Asymmetric hybrid electrode for capacitor-supported battery

Abstract

Asymmetric hybrid electrode (110) for a capacitor-assisted battery, comprising: a current collector (114) containing an electrically conductive material; a first electroactive portion (118) on a first surface (126) of the current collector (114), the first electroactive portion (118) comprising: a first battery layer (134) with a first electroactive battery material and a first binder; a second electroactive portion (122) on a second surface (130) of the current collector (114) facing away from the first surface (126), the second electroactive portion (122) comprising: a second battery layer (138) with a second electroactive battery material and a second binder; and a capacitive layer (142) comprising: a capacitive electroactive material and a third binder, whereby the first electroactive section (118) and the second electroactive section (122) are asymmetric, the first electroactive battery material and the second electroactive battery material are each positive electroactive materials or each negative electroactive materials, and the asymmetric hybrid electrode (110) has a capacitor hybridization ratio of 0.01 - 1%, wherein the second battery layer (138) is located between the capacitive layer (142) and the current collector (114), the first battery layer (134) is located directly on the first surface (126) of the current collector (114), the second battery layer (138) is located directly on the second surface (130) of the current collector (114), and the capacitive layer (142) is located directly on the second battery layer (138), and wherein the first battery layer (134) has a first thickness (154) of less than 5 mm, the second battery layer (138) has a second thickness (158) of less than 5 mm, and the capacitive layer (142) has a thickness (162) in a range of 1 - 200 µm.

Description

INTRODUCTION

[0001] This section contains background information related to the present disclosure that is not necessarily prior art.

[0002] The present disclosure relates to a hybrid electrode, which may be a positive or negative electrode, with asymmetric coatings. The present disclosure also provides a capacitor-based battery with the asymmetric hybrid electrode and methods for fabricating the asymmetric hybrid electrode.

[0003] High-energy-density electrochemical cells, such as lithium-ion batteries, can be used in a wide variety of consumer products and vehicles, including battery-powered or hybrid electric vehicles. Battery-powered vehicles are a promising transportation option, as technological advances in battery performance and lifetimes continue.

[0004] US 2018 / 0 241 079 A1 discloses an energy storage device comprising a first electrode with an electrochemically active material and a porous carbon material and a second electrode with lithium metal and carbon particles. SUMMARY

[0005] This section contains a general summary of the disclosure and is not a comprehensive disclosure of its full scope or all of its features.

[0006] According to a first aspect, the present disclosure provides an asymmetric hybrid electrode for a capacitor-assisted battery. The asymmetric hybrid electrode comprises a current collector, a first electroactive portion, and a second electroactive portion. The current collector contains an electrically conductive material. The first electroactive portion is located on a first surface of the current collector. The first electroactive portion includes a first battery layer. The first battery layer includes a first electroactive battery material and a first binder. The second electroactive portion is located on a second surface of the current collector, facing away from the first surface. The second electroactive portion includes a second battery layer and a capacitive layer. The second battery layer includes a second electroactive battery material and a second binder.The capacitive layer contains a capacitive electroactive material and a third binder. The first electroactive section and the second electroactive section are asymmetric. The first electroactive material of the battery and the second electroactive material of the battery are each positive electroactive materials or negative electroactive materials. The asymmetric hybrid electrode has a capacitor hybridization ratio of 0.01-1%. The second battery layer is located between the capacitive layer and the current collector. The first battery layer is located directly on the first surface of the current collector. The second battery layer is located directly on the second surface of the current collector. The capacitive layer is located directly on the second battery layer. The first battery layer has a first thickness of less than 5 mm.The second battery layer has a second thickness of less than 5 mm. The capacitive layer has a thickness in the range of 1 - 200 µm.

[0007] In one aspect, the capacitive layer further includes a third electroactive battery material.

[0008] In one aspect, the capacitive layer contains the third electroactive battery material at less than or equal to about 95 wt.% of the capacitive electroactive material.

[0009] In one aspect, the capacitive layer contains the third electroactive battery material at less than or equal to about 20 wt.% of the capacitive electroactive material.

[0010] In one aspect, the first electroactive material of the battery, the second electroactive material of the battery, and the third electroactive material of the battery are the same.

[0011] In one aspect, the first binder, the second binder, and the third binder are identical.

[0012] In one aspect, the first binder, the second binder, and the third binder comprise polyvinylidene fluoride.

[0013] In one case, the hybridization ratio of the capacitor is less than or equal to about 0.7%.

[0014] In one aspect, the first thickness and the second thickness are substantially the same.

[0015] In one aspect, the first electroactive material of the battery and the second electroactive material of the battery are identical.

[0016] In one aspect, the first electroactive material of the battery and the second electroactive material of the battery are positive electroactive materials.

[0017] In one aspect, the positive electroactive materials comprise an olivine compound. The capacitive electroactive material comprises activated carbon. The electrically conductive material comprises aluminum.

[0018] In one aspect, the first electroactive material of the battery and the second electroactive material of the battery are negative electroactive materials.

[0019] In one aspect, the negative electroactive materials comprise a carbon-based electroactive battery material. The capacitive electroactive material comprises a carbon-based capacitive electrode material. The electrically conductive material comprises copper.

[0020] In various aspects, the present disclosure provides an electrochemical cell. The electrochemical cell includes the asymmetric hybrid electrode, a positive battery electrode, and a negative battery electrode.

[0021] In various aspects, the present disclosure provides a method of fabricating an asymmetric hybrid electrode for an electrochemical cell. The method comprises forming a first battery layer on a first surface of a current collector. The first battery layer includes a first electroactive battery material and a first binder. The current collector includes an electrically conductive material. The method further comprises forming a second battery layer on a second surface of the current collector facing away from the first surface. The second battery layer includes a second electroactive battery material and a second binder. The method further comprises forming a capacitive layer on the second battery layer. The capacitive layer includes a capacitive electroactive material and a third binder. The first battery layer defines a first electroactive portion.The second battery layer and the capacitive layer interact to form a second electroactive section. The first electroactive section and the second electroactive section are asymmetric. The first electroactive material of the battery and the second electroactive material of the battery are each positive electroactive materials or are each negative electrode materials. The asymmetric hybrid electrode has a capacitor hybridization ratio of approximately 0.01-1%.

[0022] Further areas of applicability will become apparent from the description provided herein. The description and specific examples in this summary are for illustrative purposes only and are not intended to limit the scope of the present disclosure. BRIEF DESCRIPTION OF THE DRAWINGS

[0023] The drawings described herein are intended to illustrate selected embodiments only and not all possible implementations and are not intended to limit the scope of the present disclosure. Fig. Figure 1 is a schematic diagram of an electrochemical cell for cycling lithium ions; Fig. Figure 2 is a schematic diagram of a capacitive electrode; Fig. Figure 3 is a schematic diagram of a double-sided electrode having a capacitor side and a battery side; Fig. Figure 4 is a schematic diagram of a symmetrical double-sided electrode; Fig. 5 is a schematic representation of an asymmetric hybrid electrode according to various aspects of the present disclosure; Fig. 6 is a schematic representation of a positive asymmetric hybrid electrode according to various aspects of the present disclosure; Fig. 7 is a schematic representation of a negative asymmetric hybrid electrode according to various aspects of the present disclosure; Fig. 8 is a schematic representation of a positive battery electrode according to various aspects of the present disclosure; Fig. 9 is a schematic representation of a negative battery electrode according to various aspects of the present disclosure; Fig. 10 is a schematic diagram of a capacitor-assisted battery ("CAB") according to various aspects of the present disclosure; Fig. 11 is a schematic diagram of another CAB according to various aspects of the present disclosure; Fig. 12 is a schematic representation of another CAB according to various aspects of the present disclosure; Fig. 13 is a flowchart showing a method for manufacturing the asymmetric hybrid electrode of Fig. 5 shows; Fig. Figure 14 is a schematic representation of part of the process of Fig. 13; Fig. Figure 15 is a schematic representation of another part of the process of Fig. 13; Fig. Figure 16 is a schematic representation of another part of the process of Fig. 13; Fig. Figure 17 is a schematic representation of another part of the process of Fig. 13; Fig. Figure 18 is a schematic representation of another part of the process of Fig. 13; and Fig. Figure 19 is a schematic representation of another part of the process of Fig. 13.

[0024] Corresponding reference numerals indicate corresponding parts in the several views of the drawings. DETAILED DESCRIPTION

[0025] Example embodiments are provided so that this disclosure will be thorough and will fully convey the scope to those skilled in the art. Numerous specific details are set forth, such as examples of specific compositions, components, devices, and methods, in order to provide a thorough understanding of embodiments of the present disclosure. It will be understood by those skilled in the art that specific details need not be used, that example embodiments may be embodied in many different forms, and none should be construed to limit the scope of the disclosure. In some example embodiments, well-known processes, known device structures, and well-known technologies are not described in detail.

[0026] The terminology used herein is for the purpose of describing particular example embodiments only and is not intended to be limiting. As used herein, the singular forms "a," "an," and "the" may also include the plural forms, unless the context clearly indicates otherwise. The terms "comprises," "comprising," "including," and "having" are inclusive and therefore specify the presence of stated features, elements, compositions, steps, integers, acts, and / or components, but do not preclude the presence or addition of one or more other features, integers, steps, acts, elements, components, and / or groups thereof.Although the broad term "comprising" is intended to be a non-limiting term used to describe and claim the various embodiments set forth herein, in certain aspects, the term may alternatively be understood as a more limiting and restrictive term, such as "consisting of" or "consisting essentially of." Therefore, for any given embodiment reciting compositions, materials, components, elements, features, integers, acts, and / or method steps, the present disclosure expressly includes embodiments consisting of, or consisting essentially of, such recited compositions, materials, components, elements, features, integers, acts, and / or method steps.In the case of "consisting of", the alternative embodiment excludes all additional compositions, materials, components, elements, features, integers, acts and / or method steps, while in the case of "consisting essentially of", all additional compositions, materials, components, elements, features, integers, acts and / or method steps that substantially affect the basic and novel features are excluded from such embodiment, but all compositions, materials, components, elements, features, integers, acts and / or method steps that do not substantially affect the basic and novel features may be included in the embodiment.

[0027] All procedures, processes, and operations described herein should not be construed as necessarily being performed in the order discussed or illustrated, unless expressly identified as such. It is also understood that additional or alternative steps may be used unless otherwise noted.

[0028] When a component, element, or layer is described as being "on," "engaging," "connected," or "coupled" to another element or layer, it may be directly on, engaging, connected, or coupled to the other component, element, or layer, or there may be intervening elements or layers. Conversely, when an element is described as being "directly on," "directly engaging," "directly connected," or "directly coupled to" another element or layer, there may be no intervening elements or layers. Other words used to describe the relationship between elements should be interpreted similarly (e.g., "between" versus "directly between," "adjacent" versus "directly next to," etc.).As used herein, the term “and / or” includes all combinations of one or more of the related listed items.

[0029] Although the terms first, second, third, etc. may be used herein to describe various steps, elements, components, regions, layers, and / or sections, those steps, elements, components, regions, layers, and / or sections should not be limited by these terms unless otherwise specified. These terms may only be used to distinguish one step, element, component, region, layer, or section from another step, element, component, region, layer, or section, respectively. Terms such as "first," "second," and other numerical terms, when used herein, do not imply a sequence or order unless clearly indicated by the context.Thus, a first step, element, component, region, layer, or section discussed below could be referred to as a second step, element, component, region, layer, or section without departing from the teachings of the exemplary embodiments.

[0030] Spatially or temporally relative terms such as "before," "after," "inside," "outside," "below," "below," "below," "above," and the like may be used herein for convenience to describe the relationship of one element or feature to one or more other elements or features as illustrated in the figures. Spatially or temporally relative terms may be intended to encompass different orientations of the device or system in use or operation, in addition to the orientation illustrated in the figures.

[0031] Throughout this disclosure, numerical values ​​represent approximate measurements or limits for ranges that include slight deviations from the stated values ​​and embodiments approximately at the stated value, as well as embodiments exactly at the stated value. Other than in the working examples at the end of the detailed description, all numerical values ​​of parameters (e.g., quantities or conditions) in this specification, including the appended claims, are to be understood as being modified in all cases by the term "approximately," regardless of whether "approximately" actually appears before the numerical value or not. "Approximately" means that the stated numerical value allows for slight imprecision (with some approximation to the accuracy of the value; approximately or fairly close to the value; almost).Unless the imprecision implied by "about" is otherwise understood in the art with this ordinary meaning, then "about," as used herein, means at least variations that may result from ordinary methods of measuring and using such parameters. For example, "about" may encompass a variation of less than or equal to 5%, optionally less than or equal to 4%, optionally less than or equal to 3%, optionally less than or equal to 2%, optionally less than or equal to 1%, optionally less than or equal to 0.5%, and in certain aspects, optionally less than or equal to 0.1%.

[0032] In addition, the disclosure of ranges includes the disclosure of all values ​​and further subdivided ranges within the entire range, including the endpoints and subranges specified for the ranges.

[0033] Exemplary embodiments will now be described in more detail with reference to the accompanying drawings.

[0034] The present technology relates to rechargeable lithium-ion batteries that can be used in automotive applications. However, the present technology can also be used in other electrochemical devices that cycle lithium ions, such as handheld electronic devices or energy storage systems (ESS). General function, structure and composition of the electrochemical cell

[0035] An electrochemical cell generally contains a first electrode, e.g., a positive electrode or cathode, a second electrode, e.g., a negative electrode or anode, an electrolyte, and a separator. In a lithium-ion battery pack, electrochemical cells are often electrically connected in a stack to increase overall power. Lithium-ion electrochemical cells work by reversibly shunting lithium ions between the negative electrode and the positive electrode. The separator and electrolyte can be placed between the negative and positive electrodes. The electrolyte is suitable for conducting lithium ions and can be in liquid, gel, or solid form. Lithium ions move from the positive electrode to the negative electrode during battery charging and in the opposite direction during battery discharging.

[0036] Each of the negative and positive electrodes within a stack is typically electrically connected to a current collector (e.g., a metal such as copper for the negative electrode and aluminum for the positive electrode). During battery operation, the current collectors belonging to the two electrodes are connected by an external circuit that allows the electron-generated current to flow between the negative and positive electrodes to compensate for the transport of lithium ions.

[0037] The electrodes can generally be incorporated into various commercially available battery designs, such as prismatic-shaped cells, wound cylindrical cells, button cells, pouch cells, or other suitable cell shapes. The cells can comprise a structure with a single electrode per polarity or a stacked structure with a plurality of positive electrodes and negative electrodes mounted in electrical parallel and / or series circuits. In particular, the battery can comprise a stack of alternating positive and negative electrodes with separators disposed therebetween. While the positive electroactive materials can be used in batteries for primary or single-use, the resulting batteries generally have desirable cycling characteristics for secondary battery use over multiple cycling of the cells.

[0038] An exemplary schematic representation of a lithium-ion battery 20 is shown in Fig. 1. The lithium-ion battery 20 includes a negative electrode 22, a positive electrode 24, and a porous separator 26 (e.g., a microporous or nanoporous polymer separator) disposed between the negative and positive electrodes 22, 24. An electrolyte 30 is disposed between the negative and positive electrodes 22, 24 and in the pores of the porous separator 26. The electrolyte 30 may also be present in the negative electrode 22 and the positive electrode 24, e.g., in pores.

[0039] A negative electrode current collector 32 may be positioned at or near the negative electrode 22. A positive electrode current collector 34 may be positioned at or near the positive electrode 24. Although not shown, the negative electrode current collector 32 and the positive electrode current collector 34 may be coated on one or both sides. In certain aspects, the current collectors may be coated on both sides with an electroactive material / electrode layer. The negative electrode current collector 32 and the positive electrode current collector 34 each collect free electrons and move them to and from an external circuit 40. The interruptible external circuit 40 includes a load device 42 and connects the negative electrode 22 (via the negative electrode current collector 32) and the positive electrode 24 (via the positive electrode current collector 34).

[0040] The porous separator 26 acts as both an electrical insulator and a mechanical support. Specifically, the porous separator 26 is disposed between the negative electrode 22 and the positive electrode 24 to prevent or reduce physical contact and thus the occurrence of a short circuit. The porous separator 26 not only provides a physical barrier between the two electrodes 22, 24, but can also provide a minimally resistant path for the internal passage of lithium ions (and similar anions) during cycling of the lithium ions to facilitate the function of the lithium-ion battery 20.

[0041] The lithium-ion battery 20 can generate an electric current during discharge through reversible electrochemical reactions that occur when the external circuit 40 is closed (to electrically connect the negative electrode 22 and the positive electrode 24) when the negative electrode 22 contains a relatively larger amount of cyclably movable lithium. The chemical potential difference between the positive electrode 24 and the negative electrode 22 drives the electrons generated by the oxidation of lithium (e.g., intercalated / alloyed / plated lithium) at the negative electrode 22 through the external circuit 40 toward the positive electrode 24. Lithium ions also generated at the negative electrode are simultaneously transported to the positive electrode 24 through the electrolyte 30 and the porous separator 26.The electrons flow through the external circuit 40, and the lithium ions migrate through the porous separator 26 into the electrolyte 30 to intercalate / alloy / plate into a positive electroactive material of the positive electrode 24. The electric current flowing through the external circuit 40 can be harnessed and passed through the load device 42 until the lithium in the negative electrode 22 is consumed and the capacity of the lithium-ion battery 20 has decreased.

[0042] The lithium-ion battery 20 can be charged or recharged at any time by connecting an external power source (e.g., charger) to the lithium-ion battery 20 to reverse the electrochemical reactions that occur during battery discharge. By connecting an external power source to the lithium-ion battery 20, the lithium ions at the positive electrode 24 are forced to move back to the negative electrode 22. The electrons flowing through the external circuit 40 back to the negative electrode 22 and the lithium ions carried by the electrolyte 30 through the separator 26 back to the negative electrode 22 combine at the negative electrode 22, replenishment with stored lithium for consumption during the next battery discharge event.Therefore, each discharge and charge event is considered a cycle in which lithium ions are cyclically moved between the positive electrode 24 and the negative electrode 22.

[0043] The external power source that can be used to charge the lithium-ion battery 20 can vary depending on the size, construction, and particular end application of the lithium-ion battery 20. Some notable and exemplary external power sources include AC power sources, such as an AC outlet or a vehicle alternator. An AC-to-DC converter can be used to charge the battery 20.

[0044] In many lithium-ion battery configurations, the negative electrode current collector 32, the negative electrode 22, the separator 26, the positive electrode 24, and the positive electrode current collector 34 are each fabricated as relatively thin layers (e.g., from a few micrometers to one millimeter or less thick) and assembled in electrically series or parallel layers to achieve a suitable electrical energy and power package. Furthermore, in certain aspects, the lithium-ion battery 20 may include a variety of other components that are not illustrated here but are nevertheless known to those skilled in the art. For example, the lithium-ion battery 20 may include, as non-limiting examples, a housing, seals, terminal caps, tabs, battery terminals, and any other conventional components or materials that may be located within the battery 20, including, but not limited to,between or around the negative electrode 22, the positive electrode 24, and / or the separator 26. As mentioned above, the size and shape of the lithium-ion battery 20 can vary depending on the specific applications for which it is designed. Battery-powered vehicles and portable consumer electronics devices are two examples where the lithium-ion battery 20 is most likely designed to different size, capacity, and power specifications. The lithium-ion battery 20 can also be connected in series or parallel with other similar lithium-ion cells or batteries to produce higher output voltage, energy, and / or power when required by the load device 42.

[0045] Accordingly, the lithium-ion battery 20 can generate an electrical current for the load device 42, which can be operatively connected to the external electrical circuit 40. While the load device 42 can be any number of known electrically powered devices, as non-limiting examples, some specific examples of power-consuming load devices include an electric motor for a hybrid or all-electric vehicle, a laptop computer, a tablet computer, a cell phone, and cordless power tools or appliances. The load device 42 can also be a power-generating device that charges the lithium-ion battery 20 for the purpose of energy storage. In certain other variations, the electrochemical cell can be a supercapacitor, e.g., a lithium-ion-based supercapacitor. electrolyte

[0046] Any suitable electrolyte 30, whether in solid, liquid, or gel form, that can conduct lithium ions between the negative electrode 22 and the positive electrode 24 can be used in the lithium-ion battery 20. In certain aspects, the electrolyte 30 can be a non-aqueous liquid electrolyte solution containing a lithium salt dissolved in an organic solvent or a mixture of organic solvents. Numerous non-aqueous liquid solutions can be used with electrolyte 30 in the lithium-ion battery 20. In certain variations, the electrolyte 30 can contain an aqueous solvent (i.e., a water-based solvent) or a hybrid solvent (e.g., an organic solvent containing at least 1 wt.% water).

[0047] Suitable lithium salts generally have inert anions. Non-limiting examples of lithium salts that can be dissolved in an organic solvent to form the non-aqueous liquid electrolyte solution are lithium hexafluorophosphate (LiPF6); lithium perchlorate (LiClO4); lithium tetrachloroaluminate (LiAlCl4); lithium iodide (LiI1); lithium bromide (LiBr); lithium thiocyanate (LiSCN); lithium tetrafluoroborate (LiBF4); lithium difluorooxalatoborate (LiBF2(C2O4)) (LiODFB), lithium tetraphenylborate (LiB(C6H5)4); lithium bis(oxalate)borate (LiB(C2O4)2) (LiBOB); lithium tetrafluorooxalatophosphate (LiPF4(C2O4)) (LiFOP), lithium nitrate (LiNO3), lithium hexafluoroarsenate (LiAsF6); lithium trifluoromethanesulfonate (LiCF3SO3); Lithium bis(trifluoromethanesulfonimide) (LITFSI) (LiN(CF3SO2)2); lithium fluorosulfonylimide (LIN(FSO2)2) (LiFSI); and combinations thereof. In certain variations, the electrolyte 30 may contain a 1 M concentration of the lithium salts.

[0048] These lithium salts can be dissolved in a variety of organic solvents, e.g., organic ethers or organic carbonates. Organic ethers can include dimethyl ether, glyme (glycol dimethyl ether or dimethoxyethane (DME, e.g., 1,2-dimethoxyethane)), diglyme (diethylene glycol dimethyl ether or bis(2-methoxyethyl) ether), triglyme (tri(ethylene glycol) dimethyl ether), ethers with additional chain structure, such as 1,2-diethoxyethane, ethoxymethoxyethane, 1,3-dimethoxypropane (DMP), cyclic ethers, such as tetrahydrofuran, 2-methyltetrahydrofuran, and combinations thereof. In certain variations, the organic ether compound is selected from the group consisting of: tetrahydrofuran, 2-methyltetrahydrofuran, dioxolane, dimethoxyethane (DME), diglyme (diethylene glycol dimethyl ether), triglyme (tri(ethylene glycol) dimethyl ether), 1,3-dimethoxypropane (DMP), and combinations thereof. Carbonate-based solvents may include various alkyl carbonates, such asCyclic carbonates (e.g., ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate) and acyclic carbonates (e.g., dimethyl carbonate (DMC), diethyl carbonate (DEC), ethyl methyl carbonate (EMC)). Ether-based solvents include cyclic ethers (e.g., tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxolane) and chain-type ethers (e.g., 1,2-dimethoxyethane, 1,2-diethoxyethane, ethoxymethoxyethane).

[0049] In various embodiments, suitable solvents in addition to those described above may be selected from propylene carbonate, dimethyl carbonate, diethyl carbonate, methyl ethyl carbonate, γ-butyrolactone, dimethyl sulfoxide, acetonitrile, nitromethane, and mixtures thereof.

[0050] If the electrolyte is a solid electrolyte, it may contain a composition selected from the group consisting of: LiTi2(PO4)3, LiGe2(PO4)3, Li7La3Zr2O 12 , Li3xLa 2 / 3 -xTiO3, Li3PO4, Li3N, Li4GeS4, Ref10 GeP2S 12 , Li2S-P2S5, Li6PS5Cl, Li6PS5Br, Li6PS5I, Li3OCl, Li 2,99 Ba 0,005 ClO or any combination thereof. Porous separator

[0051] The separator 26, in certain variations, may comprise a microporous polymeric separator containing a polyolefin, including those made from a homopolymer (derived from a single monomer component) or a heteropolymer (derived from more than one monomer component), which may be either linear or branched. In certain aspects, the polyolefin may be polyethylene (PE), polypropylene (PP), a blend of PE and PP, or multilayer structured porous films of PE and / or PP. Commercially available membranes for the porous polyolefin separator 26 include CELGARD® 2500 (a single-layer polypropylene separator) and CELGARD® 2340 (a three-layer polypropylene / polyethylene / polypropylene separator), available from CELGARD LLC.

[0052] If the porous separator 26 is a microporous polymeric separator, it may be a single layer or a multi-layer laminate. For example, in one embodiment, a single layer of the polyolefin may form the entire microporous polymeric separator 26. In other aspects, the separator 26 may be a fibrous membrane with an abundance of pores extending between the opposing surfaces and may, for example, have a thickness of less than one millimeter. However, as another example, multiple discrete layers of similar or dissimilar polyolefins may be assembled to form the microporous polymeric separator 26. The microporous polymeric separator 26 may alternatively or in addition to the polyolefin also contain other polymers, such as, but not limited to, polyethylene terephthalate (PET), polyvinylidene fluoride (PVdF), polyamide (nylons), polyurethanes, polycarbonates, polyesters, polyetheretherketones (PEEK), polyethersulfones (PES), polyimides (PI), polyamide-imides, polyethers, polyoxymethylene (e.g. acetal), polybutylene terephthalate, polyethylene naphthenate, polybutene, polymethylpentene, polyolefin copolymers, acrylonitrile-butadiene-styrene copolymers (ABS), polystyrene copolymers, polymethyl methacrylate (PMMA), polysiloxane polymers (e.g. polydimethylsiloxane (PDMS)), polybenzimidazole (PBI), polybenzoxazole (PBO), polyphenylenes, polyarylene ether ketones, polyperfluorocyclobutanes, polyvinylidene fluoride copolymers (e.g. PVdF-hexafluoropropylene or (PVdF-HFP)), and Polyvinylidene fluoride terpolymers, polyvinyl fluoride, liquid crystalline polymers (e.g. VECTRAN™ (Hoechst AG, Germany) and ZENITE® (DuPont, Wilmington, DE)), polyaramids, polyphenylene oxide, cellulosic materials, mesoporous silica or a combination thereof.

[0053] Furthermore, the porous separator 26 may be mixed with a ceramic material or its surface may be coated with a ceramic material. For example, a ceramic coating may contain alumina (Al2O3), silicon dioxide (SiO2), or combinations thereof. Various commercially available polymers and commercial products for fabricating the separator 26 are contemplated, as are the many manufacturing processes that may be used to produce such a microporous polymer separator 26. Solid-state electrolyte

[0054] In various aspects, the porous separator 26 and the electrolyte 30 can be replaced with a solid-state electrolyte (SSE) that functions as both an electrolyte and a separator. The SSE can be disposed between a positive electrode and a negative electrode. The SSE facilitates the transfer of lithium ions while mechanically separating and electrically isolating the negative and positive electrodes 22, 24. As a non-limiting example, SSEs can include LiTi2(PO4)3, Li 1,3 Al 0,3 Ti 1,7 (PO4)3 (LATP), LiGe2(PO4)3, Li7La3Zr2O 12 , Li3xLa 2 / 3 -xTiO3, Li3PO4, Li3N, Li4GeS4, Li 10 GeP2S 12 , Li2S-P2S5, Li6PS5Cl, Li6PS5Br, Li6PS5I, Li3OCl, Li 2,99 Ba 0,005 ClO or combinations thereof. current collector

[0055] The negative and positive electrodes 22, 24 are generally connected to the respective negative and positive electrode current collectors 32, 34 to facilitate the flow of electrons between the electrode and the external circuit 40. The current collectors 32, 34 are electrically conductive and may include metal, e.g., a metal foil, a metal mesh or screen, or expanded metal. Expanded metal current collectors refer to metal meshes with a greater thickness so that a larger amount of electroactive material is placed within the metal mesh. Non-limiting examples of electrically conductive materials include copper, nickel, aluminum, stainless steel, titanium, alloys thereof, or combinations thereof.

[0056] The positive electrode current collector 34 may be formed from aluminum or another suitable electrically conductive material known to those skilled in the art. The negative electrode current collector 32 may be formed from copper or another suitable electrically conductive material known to those skilled in the art. Negative electrode current collectors typically do not contain aluminum because aluminum reacts with lithium, causing significant volume expansion and contraction. These drastic volume changes can lead to breakage and / or pulverization of the current collector. Positive & negative electrodes

[0057] The positive electrode 24 may be formed from or include a lithium-based active material capable of undergoing sufficient lithium intercalation and de-intercalation, alloying and de-alloying, or plating and stripping while functioning as the positive terminal of the lithium-ion battery 20. The positive electrode 24 may include a positive electroactive material. Positive electroactive materials may include one or more transition metal cations, such as manganese (Mn), nickel (Ni), cobalt (Co), chromium (Cr), iron (Fe), vanadium (V), and combinations thereof. However, in certain variations, the positive electrode 24 is substantially free of select metal cations, such as nickel (Ni) and cobalt (Co).

[0058] Two exemplary common classes of known electroactive materials that can be used to form the positive electrode 24 are layered lithium transition metal oxides and spinel-phase lithium transition metal oxides. For example, in certain cases, the positive electrode 24 may contain a spinel-type transition metal oxide, such as lithium manganese oxide (Li( 1+x )Mn( 2-x )O4), where x is typically < 0.15, including LiMn2O4 (LMO) and lithium manganese nickel oxide LiMn 1,5 Ni 0,5 O4 (LMNO). In other cases, the positive electrode 24 may contain layered materials such as lithium cobalt oxide (LiCoO2), lithium nickel oxide (LiNiO2), a lithium nickel manganese cobalt oxide (Li(Ni x Mn y Co z )O2), where 0 ≤ x ≤ 1, 0 ≤ y ≤ 1, 0 ≤ z ≤ 1 and x + y + z = 1 (e.g. LiNi 0,6 Mn 0,2 Co 0,2 O2, LiNi 0,7 Mn 0,2 CO 0,1 O2, LiNi 0,8 Mn 0,1Co 0,1 O2 and / or LiMn 0,33 Ni 0,33 CO 0,33 O2), a lithium nickel cobalt metal oxide (LiNi( 1-xy4 )Co x M y O2), where 0 < x < 1, 0 < y < 1 and M can be Al, Mg, Mn or the like. Other known lithium transition metal compounds such as lithium iron phosphate (LiFePO4), lithium iron fluorophosphate (Li2FePO4F) or lithium manganese iron phosphate (LiMnFePO4) can also be used. In certain aspects, the positive electrode 24 can include an electroactive material containing manganese, such as lithium manganese oxide (Li( 1+x )Mn( 2-x )O4), and / or a mixed lithium manganese nickel oxide (LiMn( 2-x )No x O4), where 0 ≤ x ≤ 1. In a lithium-sulfur battery, the positive electrodes can have elemental sulfur as the active material or a sulfur-containing active material.

[0059] The positive electroactive materials can be powder compositions. The positive electroactive materials can be mixed with an optional electrically conductive material (e.g., electrically conductive particles) and a polymeric binder. The binder can both hold the positive electroactive material together and impart ionic conductivity to the positive electrode 24.

[0060] The negative electrode 22 may contain a negative electroactive material as a lithium host material, which may function as the negative terminal of the lithium-ion battery 20. Common negative electroactive materials include lithium insert materials or alloy host materials. Such materials may include carbon-based materials such as lithium-graphite intercalation compounds, lithium-silicon compounds, lithium-tin alloys, or lithium titanate Li. 4+x Ti5O 12, where 0 ≤ x ≤ 3, such as Li4Ti5O 12 (LTO).

[0061] In certain aspects, the negative electrode 22 may contain lithium, and in certain variations, metallic lithium, and the lithium-ion battery 20. The negative electrode 22 may be a lithium metal electrode (LME). The lithium-ion battery 20 may be a lithium metal battery or cell. Metallic lithium for use in the negative electrode of a rechargeable battery has several potential advantages, including the highest theoretical capacity and the lowest electrochemical potential. For example, batteries with lithium metal anodes can have a higher energy density, which can potentially double the storage capacity, so the battery may be half the size but still last the same amount of time as other lithium-ion batteries.

[0062] In certain variations, the negative electrode 22 may optionally include an electrically conductive material as well as one or more polymeric binder materials to structurally hold the lithium material together.

[0063] Advanced energy storage and systems are in demand to meet the energy and / or power requirements for a wide variety of products, including automotive products such as start-stop systems (e.g., 12V start-stop systems), mild hybrid systems (e.g., 48V hybrid systems), battery-assisted systems, hybrid electric vehicles (“HEVs”), and electric vehicles (“EVs”). Capacitors can deliver high power density (e.g., approximately 10 kW / kg) in power-based applications, and lithium-ion batteries can deliver high energy densities (e.g., approximately 50–300 Wh / kg). In various cases, capacitor-assisted batteries (“CABs”) (e.g., a lithium-ion capacitor hybridized with a lithium-ion battery in a single-cell core) can offer several advantages over lithium-ion batteries, such as improved capability for pulsed power delivery in both warm and cold temperatures.For example, integrated capacitor materials or supercapacitor materials can be used to provide current during engine start, thus limiting the current draw from the lithium-ion battery during start-up, especially in cold weather applications such as cold start.

[0064] Capacitor materials can be integrated into electrochemical cells in various ways. In one example, as shown in Fig. 2, an electrochemical cell comprises at least one capacitive electrode 60 having capacitive electroactive coatings 62 on both sides of a current collector 64. In another example, as shown in Fig. 3, a double-sided electrode 70 includes a capacitive electroactive coating 72 on one side of a current collector 74 and an electroactive battery coating 76 on the other side of the current collector 78. In another example, as shown in Fig. 4, a double-sided electrode 80 is symmetrical, with each side of a current collector 82 having a capacitive electrode coating 84 and an electroactive battery coating 86. Asymmetric hybrid electrodes

[0065] In various aspects, the present disclosure provides an asymmetric hybrid electrode for an electrochemical cell, such as a CAB. The electrode contains both an electroactive battery material and a capacitive electroactive material. The electrode comprises a current collector, a first electroactive portion on a first surface of the current collector, and a second electroactive portion on a second surface of the current collector. The first and second electroactive portions are asymmetric. The first electroactive portion includes a first battery layer having a first electroactive battery material and a first binder. The second electroactive portion includes a second battery layer and a capacitive layer. The second battery layer includes a second electroactive battery material and a second binder.The capacitive layer contains a capacitive electroactive material and a third binder. In certain aspects, the capacitive layer also contains a third electroactive battery material. The first, second, and third electroactive materials of the battery are both positive electroactive materials or both negative electroactive materials. Accordingly, the electrode is a positive asymmetric hybrid electrode or a negative asymmetric hybrid electrode.

[0066] The asymmetric hybrid electrode has, compared to the electrodes made of Fig. 2 - 4 a low capacitor hybridization ratio (CHR). The CHR is defined as follows: CHR=CCMCCM+CBM×100%, where C CM the capacitance of the capacitive material and C BMthe capacity of the battery material. In certain aspects, the asymmetric hybrid electrode according to various aspects of the present disclosure has a CHR of less than or equal to about 1% (e.g., less than or equal to about 0.9%, less than or equal to about 0.8%, less than or equal to about 0.7%, less than or equal to about 0.6%, less than or equal to about 0.5%, less than or equal to about 0.4%, less than or equal to about 0.3%, less than or equal to about 0.2%, less than or equal to about 0.1%, less than or equal to about 0.09%, less than or equal to about 0.08%, less than or equal to about 0.07%, less than or equal to about 0.06%, less than or equal to about 0.05%, less than or equal to about 0.04%, less than or equal to about 0.03%, less than or equal to about 0.02%, or less than or equal to about 0.01%). In certain aspects, the CHR is greater than or equal to 0% (e.g.greater than or equal to 0.01%, greater than or equal to 0.02%, greater than or equal to 0.03%, greater than or equal to 0.04%, greater than or equal to 0.05%, greater than or equal to 0.06%, greater than or equal to 0.07%, greater than or equal to 0.08%, greater than or equal to 0.09%, greater than or equal to 0.1%, greater than or equal to 0.2%, greater than or equal to 0.5%). In one example, the CHR is in a range of 0.01 - 1%. Furthermore, the CHR can be adjusted by changing the layer thicknesses and / or the composition of the capacitive layer. In one example, the capacitive layer is free of battery electrode material, and the CHR is 0. The asymmetric hybrid electrode can therefore be adjusted compared to the electrodes of the . Fig. 2 - 4 have improved mass and volumetric energy densities.

[0067] In Fig. 5 illustrates an asymmetric hybrid electrode 110 according to various aspects of the present disclosure. The electrode 110 includes a current collector 114, a first electroactive portion 118, and a second electroactive portion 122. The first electroactive portion 118 is disposed on a first surface 126 of the current collector 114. The second electroactive portion 122 is disposed on a second surface 130 of the current collector 114, facing away from the first surface 126.

[0068] The first electroactive portion 118 includes a first battery layer 134. The second electroactive portion 122 includes a second battery layer 138 and a capacitive layer 142. In certain aspects, the second battery layer 138 is disposed between the current collector 114 and the capacitive layer 142, as shown. However, in certain other aspects, a capacitive layer is disposed between a current collector and a second electroactive layer of the battery, for example, directly on the current collector.

[0069] The first and second electroactive sections 118, 122 are arranged asymmetrically around the current collector 114. Accordingly, the first and second sections 118, 122 differ in the number of layers, the type of layers (i.e., battery, full-capacitive, hybrid), the composition of the layers, and / or the thickness of the layers. In one example, the first and second battery layers 134, 138 are substantially identical, and the first electroactive section 118 is free of a capacitive or hybrid electroactive layer.

[0070] In certain aspects, the first battery layer 134 is disposed directly on the first surface 126 of the current collector 114 without another electroactive layer therebetween. The first battery layer 134 may be the only electroactive layer on a first side 146 of the current collector 114, such that the first battery layer 134 forms an outermost layer on the first side 146. The second battery layer 138 is disposed directly on the second surface 130 of the current collector 114 without another electroactive layer therebetween. The capacitive layer 142 is disposed directly on the second battery layer 138 without another electroactive layer therebetween. The second battery layer 138 and the capacitive layer 142 may be the only electroactive layers on a second side 150 of the electrode 110, such that the capacitive layer 142 forms an outermost layer on the second side 150.Therefore, the electrode 110 can contain exactly three electroactive layers.

[0071] The first battery layer 134 has a first thickness 154. In certain aspects, the first thickness 154 is less than about 5 mm (e.g., 10-500 µm, 10-250 µm, 10-100 µm, 10-20 µm, 20-50 µm, 50-100 µm, 100-250 µm, 250-500 µm, 500 µm-1 mm, 1-2 mm, about 2-3 mm, 3-4 mm, or 4-5 mm). In one example, the first thickness 154 is about 10-100 µm. The second battery layer 138 has a second thickness 158. In certain aspects, the second thickness 158 is less than about 5 mm (e.g., 10-500 µm, 10-250 µm, 10-100 µm, 10-20 µm, 20-50 µm, 50-100 µm, 100-250 µm, 250-500 µm, 500 µm-1 mm, 1-2 mm, about 2-3 mm, 3-4 mm, or 4-5 mm). In one example, the second thickness 158 is about 10-100 µm. The first and second thicknesses 154, 158 may be the same or different.

[0072] The capacitive layer 142 has a third thickness 162. In certain aspects, the third thickness 162 is 1-200 µm (e.g., 1-10 µm, 1-5 µm, 5-10 µm, 10-25 µm, 25-50 µm, 50-100 µm, 100-150 µm, 150-200 µm).

[0073] The current collector 114 contains an electrically conductive material as described above in the discussion on Fig. 1 are described.

[0074] The first battery layer 134 contains a first electroactive battery material and a first binder. The second battery layer 138 contains a second electroactive battery material and a second binder. The capacitive layer 142 contains a capacitive electroactive material and a third binder. In certain aspects, the capacitive layer 142 also contains a third electroactive battery material. When the capacitive layer 142 contains the third electroactive material of the battery, it may also be referred to as a "hybrid layer." The first battery layer 134, the second battery layer 138, and / or the capacitive layer 142 may also contain a conductive additive.

[0075] The first and second battery layers 134, 138 may have the same or a different composition. In certain aspects, each of the first and second battery layers 134, 138 contains 80-98 wt.% of the respective first or second electroactive battery material, 0.5-10 wt.% of the respective first or second binder, and 0.5-10 wt.% of the conductive additive.

[0076] The capacitive layer 142 generally contains electroactive material (capacitive electroactive material plus optional electroactive battery material) at 70-98 wt.%, the third binder at 1-15 wt.%, and the conductive additive at 1-15 wt.%. The third electroactive battery material is present at about 0-95 wt.% of the capacitive electroactive material (e.g., 0-20%, 0-5%, 5-10%, 10-15%, 15-20%, 15-25%, 25-35%, 35-45%, 45-55%, 55-65%, 65-75%, 75-85%, or 85-95%). In one example, the proportion of the third electroactive material of the battery is less than 20 wt% of the capacitive electroactive material.

[0077] The first, second and third electroactive materials of the battery are either positive electroactive materials of the battery (see discussion on Fig. 6) or negative electroactive materials of the battery (see discussion on Fig. 7). The first, second, and third electroactive materials of the battery may be the same or different. In certain aspects, the first, second, and third electroactive materials of the battery are identical.

[0078] The first, second, and third electroactive materials of the battery may be in the form of particles. The first, second, and third particles of the electroactive battery material each have a first, second, and third average particle size. The first, second, and third average particle sizes may be the same or different. In certain aspects, each of the first, second, and third average particle sizes is in a range of 0.5-50 µm (e.g., 0.5-30 µm, 0.5-15 µm, 0.5-10 µm, 0.5-5 µm, 0.5-2 µm, 0.5-1 µm, 5-50 µm, 5-30 µm, 5-15 µm, 15-30 µm, or 30-50 µm). In one example, the first, second and third average particle sizes are in a range of 5 - 15 µm.

[0079] The capacitive electroactive material may contain a metal oxide (e.g. MO x, where M is Co, Ru, Nb, Pb, Ge, Ni, Cu, Fe, Mn, Rh, Pd, Cr, Mo, and / or W); a metal sulfide (e.g., TiS2, CuS, and / or FeS); a carbon (e.g., activated carbon, graphene, carbon nanotubes, graphite, carbon aerogel, carbide-derived carbon, and / or graphene oxide); a polymer (e.g., polyaniline, polyacetylene, poly(3-methylthiophene), polypyrrole, poly(paraphenylene), polyacene, and / or polythiophene), or a combination thereof. In certain aspects, the capacitive electroactive material comprises activated carbon. In certain aspects, the capacitive electroactive material includes graphene. The above capacitive electroactive materials can be used in a positive hybrid electrode or in a negative hybrid electrode.

[0080] The capacitive electroactive material can be in the form of particles. The particles can have an average size of 50 nm - 20 µm (e.g., 1 - 8 µm, 2 - 4 µm). Smaller capacitive electroactive materials can facilitate the formation of thinner capacitive layers.

[0081] The first, second, and third binders can be independently selected from polyvinylidene difluoride (PVDF), polytetrafluoroethylene (PTFE), ethylene propylene diene monomer (EPDM) rubber or carboxymethylcellulose (CMC), a nitrile butadiene rubber (NBR), styrene butadiene rubber (SBR), polyacrylate (PAA), lithium polyacrylate (LiPAA), sodium polyacrylate (NaPAA), sodium alginate, lithium alginate, or any combination thereof. In certain aspects, the first, second, and third binders are identical. In one example, the first, second, and third binders all contain PVDF.

[0082] With reference to Fig. 6, a positive asymmetric hybrid electrode 210 is shown according to various aspects of the present disclosure. The electrode 210 is similar to the electrode 110 in Fig. 5. The electrode 210 generally includes a positive electrode current collector 214, a first electroactive portion 218 on a first side 220 of the current collector 214, and a second electroactive portion 222 on a second side 224 of the current collector 214.

[0083] The first electroactive section 218 contains a first battery layer 226. The second electroactive section 222 includes a second battery layer 230 and a capacitive layer 234. The first battery layer 226 contains a first positive electroactive battery material and a first binder. The second battery layer 230 contains a second positive electroactive battery material and a second binder. The capacitive layer 234 contains a capacitive electroactive material as described with respect to the capacitive layer 142 in Fig. 5, and a third binder. The capacitive layer 234 may optionally also contain a third positive electroactive battery material.

[0084] The first, second and third positive electroactive materials of the battery may include all positive electroactive materials discussed in Fig. 1. Additionally or alternatively, in certain aspects, the positive electroactive battery materials are independently selected from an olivine compound, a rock salt layered oxide, a spinel, a tavorite, a borate, a silicate, an organic compound, other types of positive electrode materials, or any combination thereof. The olivine compound may include, for example, LiV2(PO4)3, LiFePO4 (LFP), LiCoPO4, and / or a lithium manganese iron phosphate (LMFP), to name a few examples. LMFPs may include, for example, LiMnFePO4 and / or LiMn x Fe 1-x PO4, where 0 ≤ x ≤ 1, to name a few examples. Examples of LiMn x Fe 1-x PO4, where 0 ≤ x ≤ 1, include LiMn 0,7 Fe 0,3 PO4, LiMn 0,6 Fe 0,4 PO4, LiMn 0,8 Fe 0,2 PO4 and LiMn 0,75 Fe 0,25 PO4, to name a few examples. The rock salt layered oxide can include LiNi x Mny Co 1-x-y O2, LiNi x Mn 1-x O2, Li 1+x MO2, (e.g. LiCoO2, LiNiO2, LiMnO2 and / or LiNi 0,5 Mn 0,5 O2), a lithium nickel manganese cobalt oxide (NMC) (e.g. NMC 111, NMC 523, NMC 622, NMC 721 and / or NMC 811), and / or a lithium nickel cobalt aluminum oxide (NCA)), to name a few examples. The spinel can be, for example, LiMn2O4 and / or LiNi 0,5 Mn 1,5O4. The tavorite compound may, for example, comprise LiVPO4F. The borate compound may, for example, comprise LiFeBO3, LiCoBO3, and / or LiMnBO3. The silicate compound may, for example, comprise Li2FeSiO4, Li2MnSiO4, and / or LiMnSiO4F. The organic compound may, for example, comprise dilithium (2,5-dilithiooxy) terephthalate and / or polyimide. An example of another type of positive electroactive material is a sulfur-containing material, such as sulfur. In one example, the positive electroactive material contains one or more olivine compounds and has a tap density of less than about 2 g / cm 3 , optionally less than about 1.3 g / cm 3 or optionally less than about 1 g / cm 3 .

[0085] Some positive electroactive materials, such as olivine compounds, rock salt layered oxides, and / or spinels, can be coated and / or doped. Dopants can include magnesium (Mg), aluminum (Al), yttrium (Y), scandium (Sc), and the like. For example, the positive electroactive material can contain one or more of the following materials: LiMn 0,7 Mg 0,05 Fe 0,25 PO4, LiMn 0,75 Al 0,05 Fe 0,2 PO4, LiMn 0,75 Al 0,03 Fe 0,22 PO4, LiMn 0,75 Al 0,03 Fe 0,22 PO4, LiMn 0,7 Al 0,02 Fe 0,28 PO4, LiMn 0,7 Mg 0,02 Al 0,03 Fe 0,25 PO4, and the like. In certain aspects, a positive electroactive material containing an LMFP compound may be doped with about 10 wt.% of one or more dopants.

[0086] In certain aspects, the capacitive layer 234 is a hybrid electroactive layer containing the third positive electroactive battery material. The positive electrode current collector 214 contains aluminum. The first, second, and third positive electroactive materials of the battery contain LFP. The capacitive electroactive material comprises activated carbon.

[0087] In Fig. 7, a negative asymmetric hybrid electrode 260 is shown according to various aspects of the present disclosure. The electrode 260 is similar to the electrode 110 in Fig. 5. The electrode 260 generally includes a negative electrode current collector 264, a first electroactive portion 266 on a first side 268 of the current collector 264, and a second electroactive portion 270 on a second side 274 of the current collector 264.

[0088] The first electroactive section 266 contains a first battery layer 278. The second electroactive section 270 includes a second battery layer 282 and a capacitive layer 286. The first battery layer 278 contains a first negative electroactive battery material and a first binder. The second battery layer 282 contains a second negative electroactive battery material and a second binder. The capacitive layer 286 contains a capacitive electroactive material as described with respect to the capacitive layer 142 in Fig. 5, and a third binder. The capacitive layer 286 may optionally also contain a third negative electroactive battery material.

[0089] The first, second and third negative electroactive materials of the battery may include any of the negative electroactive materials discussed in the discussion on Fig. 1. Additionally or alternatively, in certain aspects, the negative electroactive materials of the battery are independently selected from a carbon-containing material (e.g., carbon nanotubes, graphite, graphene), a lithium-containing material (e.g., lithium, a lithium alloy), a tin-containing material (e.g., tin, a tin alloy), a lithium titanium oxide (e.g., Li4Ti5O 12 ), a metal oxide (e.g., V2O5, SnO2, Co3O4), a metal sulfide (e.g., FeS), a silicon-containing material (e.g., silicon, silicon oxide, a silicon alloy, silicon-graphite, silicon oxide-graphite, silicon alloy-graphite, each of which may optionally be lithiated), or any combination thereof. In one example, the negative electroactive material of the battery comprises silicon-graphite with a mixture of about 95 wt.% graphite and about 5 wt.% silicon.

[0090] In certain aspects, the capacitive layer 286 is a hybrid electroactive layer containing the third negative electroactive battery material. The current collector 264 contains copper. The first, second, and third negative electroactive materials of the battery contain graphite. The capacitive electroactive material contains graphene. Hybrid electrochemical cells

[0091] In various aspects, the present disclosure provides a hybrid electrochemical cell, such as a CAB. The hybrid electrochemical cell includes at least one positive asymmetric hybrid electrode (e.g., electrode 210 of Fig. 5) and / or at least one negative asymmetric hybrid electrode (e.g. the electrode 260 of Fig. 6). The electrochemical cell also includes at least one positive battery electrode (e.g., electrode 310 in Fig. 8, see below) and at least one negative battery electrode (e.g. electrode 330 in Fig. 9, see below). In certain aspects, the electrochemical cell may include one more negative electrode (i.e., negative battery electrode and / or negative asymmetric hybrid electrode) than positive electrodes (i.e., positive battery electrodes and / or positive asymmetric hybrid electrodes). The electrochemical hybrid cell may have a stacked or wound structure.

[0092] Fig. Figure 8 shows a positive battery electrode 310 according to various aspects of the present disclosure. The positive battery electrode 310 includes a positive electrode current collector 314 (e.g., an aluminum foil) and two battery layers 318. Each battery layer 318 contains a positive electroactive battery material, as discussed in the discussion of Fig. 6. In one example, the positive electroactive material of the battery includes LFP. The positive battery electrode 310 may be free of capacitive electroactive material. In certain aspects, the battery layers 318 are substantially identical in composition and thickness.

[0093] Fig. Figure 9 shows a negative battery electrode 330 according to various aspects of the present disclosure. The negative battery electrode 330 includes a negative electrode current collector 334 (e.g., a copper foil) and two battery layers 338. Each battery layer 338 contains a negative electroactive battery material, as discussed in the discussion of Fig. 7. In one example, the negative electroactive material of the battery includes graphite. The negative battery electrode 330 may be free of capacitive electroactive material. In certain aspects, the battery layers 338 are substantially identical in composition and thickness.

[0094] In certain aspects, all positive battery electrodes and positive asymmetric hybrid electrodes contain the same positive electroactive battery material. However, in other aspects, the electrodes contain different positive electroactive materials. In certain aspects, all negative battery electrodes and negative asymmetric hybrid electrodes contain the same negative electroactive battery material. However, in other aspects, the electrodes contain different negative electroactive materials.

[0095] The electrochemical cell also contains a porous separator between each electrode. The porous separator may be similar to the porous separators described above in the discussion on Fig. 1 were described.

[0096] The electrochemical cell also contains an electrolyte, e.g., in the pores of the electrodes and porous separators. The electrolyte may be a liquid or a semi-solid electrolyte. In certain aspects, the electrolyte contains a lithium salt. The lithium salt may include lithium bis(oxalato)borate (LiBOB), lithium oxalyldifluoroborate (LiODFB), lithium fluoroalkyl phosphate (LiFAP), LiPF6, LiAsF6, LiBF4, LiClO4, LiCF3SO3, LiTFSI, lithium bis(fluorosulfonyl)imide (LiFSI), lithium bis-trifluoromethanesulfonimide (LITFSI), or any combination thereof. In certain aspects, the electrochemical cell alternatively contains a solid-state electrolyte that serves as both an electrolyte and a separator.

[0097] Examples of hybrid electrochemical cells or CABs are in Fig. 10 - 12 and are described below. The electrochemical cells comprise the electrodes of Fig. 6 - 9. However, the electrochemical cells may additionally or alternatively contain other electrodes according to various aspects of the present disclosure.

[0098] In Fig. 10, an exemplary electrochemical cell 410 is illustrated in accordance with various aspects of the present disclosure. The electrochemical cell 410 includes the positive battery electrode 310 (see also Fig. 8 and the related discussion), the negative battery electrode 330 (see also Fig. 9 and the associated discussion) and the positive asymmetric hybrid electrode 210 (see Fig. 6 and the related discussion). Specifically, the electrochemical cell 410 includes a positive battery electrode 310, three negative battery electrodes 330, and a positive asymmetric hybrid electrode 210. The positive asymmetric hybrid electrode 210 is disposed between two of the negative battery electrodes 330. In certain aspects, the positive asymmetric hybrid electrode 210 is oriented such that the capacitive layer 234 is closer to the center of the electrochemical cell 410. A porous separator 414 is disposed between each of the electrodes 310, 330, and 410.

[0099] In Fig. 11, another hybrid electrochemical cell 430 is illustrated according to various aspects of the present disclosure. The electrochemical cell 430 includes the positive battery electrode 310 (see also Fig. 8 and the related discussion), the negative battery electrode 330 (see also Fig. 9 and the associated discussion) and the negative asymmetric hybrid electrode 260 (see Fig. 7 and the related discussion). In particular, the electrochemical cell 430 includes two positive battery electrodes 310, two negative battery electrodes 330, and a negative asymmetric hybrid electrode 260. The negative asymmetric hybrid electrode 260 is disposed between two positive battery electrodes 310. A porous separator 434 is disposed between each of the electrodes 310, 330, and 260.

[0100] In Fig. 12, another hybrid electrochemical cell 450 is illustrated according to various aspects of the present disclosure. The electrochemical cell 450 includes the positive battery electrode 310 (see also Fig. 8 and the related discussion), the negative battery electrode 330 (see also Fig. 9 and the associated discussion), the positive asymmetric hybrid electrode 210 (see Fig. 6 and the associated discussion) and the negative asymmetric hybrid electrode 260 (see Fig. 7 and the related discussion). In particular, the electrochemical cell 450 includes two positive battery electrodes 310, three negative battery electrodes 330, a positive asymmetric hybrid electrode 210, and a negative asymmetric hybrid electrode 260. The positive asymmetric hybrid electrode 210 is disposed between two negative battery electrodes 330. The negative asymmetric hybrid electrode 260 is disposed between the two positive battery electrodes 310. A porous separator 454 is disposed between each of the electrodes 310, 330, and 210. Method for producing a hybrid electrode

[0101] In various aspects, the present disclosure provides a method for fabricating an asymmetric hybrid electrode. With respect to Fig. 13, the method generally comprises forming a pair of battery layers at 510, forming a capacitive electrode layer at 514, and optionally assembling an electrochemical cell at 518. The method is illustrated using the asymmetric hybrid electrode 110 as an example from Fig. 5; however, the method is also suitable for producing other asymmetric hybrid electrodes within the meaning of the present disclosure. For example, step 514 may be performed before step 510 to form a capacitive layer disposed directly on a current collector, with a pair of battery layers disposed on the capacitive layer and on the other side of the current collector, respectively.

[0102] At 510, the method includes forming a pair of battery layers.

[0103] In Fig. Figure 14 illustrates a method for coating the current collector 114 according to various aspects of the present disclosure. Specifically, a first mold 610 applies first slurries 614 to the first and second surfaces 126, 130 of the current collector 114. Each slurry 614 includes the respective first or second electroactive battery material, the respective first or second binder, the optional conductive filler, and a first solvent.

[0104] With reference to Fig. 15 the first slurry 614 ( Fig. 14) to form electrode precursor layers 626 according to various aspects of the present disclosure. Drying comprises removing at least a portion of the first solvent from the slurry 614, e.g., substantially all of the first solvent.

[0105] As in Fig. 16, the electrode precursor layers 626 ( Fig. 15) by a first pressing machine 638 to form the first and second battery layers 134, 138 according to various aspects of the present disclosure. After calendering, the third and fourth surfaces 642, 644 of the first and second battery layers 134, 138, respectively, may be substantially smooth.

[0106] Back to Fig. 13: At 514, the method includes forming a capacitive layer.

[0107] With reference to Fig. 17 illustrates a method for coating the second battery layer 138 according to various aspects of the present disclosure. Specifically, a second mold 654 applies a second slurry 658 to the fourth surface 644 of the second battery layer 138. In certain other aspects, the second slurry 658 may be applied using a vertical coating machine configured to form thin layers. The slurry 658 may include the capacitive electroactive material, the third binder, the optional third electroactive battery material, the optional conductive filler, and a second solvent.

[0108] As in Fig. 18, the second slurry 658 ( Fig. 18) to form a capacitive precursor layer 670 according to various aspects of the present disclosure. During drying, at least a portion of the second solvent is removed, for example, substantially all of the second solvent.

[0109] With reference to Fig. 19, the capacitive precursor layer 670 ( Fig. 18) is calendered by a second pressing machine 682 to form the capacitive layer 142 according to various aspects of the present disclosure. After calendering, a fifth surface 686 of the capacitive layer 142 may be substantially smooth.

[0110] In certain aspects, the method also includes notching to form the asymmetric capacitive hybrid electrode 110.

[0111] Back to Fig. 13: The method may further comprise assembling an electrochemical cell with the asymmetric hybrid electrode according to known methods. The electrochemical cell may be similar to the electrochemical cells 410, 430, and 450 of the Fig. 10, Fig. 11 or 12.

[0112] The foregoing description of the embodiments is for purposes of illustration and description. It is not intended to be exhaustive or limiting of the disclosure. Individual elements or features of a particular embodiment are generally not limited to that particular embodiment, but are optionally interchangeable and may be used in a selected embodiment even if not specifically shown or described. The same may also be varied in many respects. Such variations are not to be considered as departing from the disclosure, and all such changes are intended to be included within the scope of the disclosure.

Claims

[1] Asymmetric hybrid electrode (110) for a capacitor-assisted battery, comprising: a current collector (114) containing an electrically conductive material; a first electroactive portion (118) on a first surface (126) of the current collector (114), the first electroactive portion (118) comprising: a first battery layer (134) with a first electroactive battery material and a first binder; a second electroactive portion (122) on a second surface (130) of the current collector (114) facing away from the first surface (126), the second electroactive portion (122) comprising: a second battery layer (138) with a second electroactive battery material and a second binder; and a capacitive layer (142) comprising: a capacitive electroactive material and a third binder, whereby the first electroactive section (118) and the second electroactive section (122) are asymmetric, the first electroactive battery material and the second electroactive battery material are each positive electroactive materials or each negative electroactive materials, and the asymmetric hybrid electrode (110) has a capacitor hybridization ratio of 0.01 - 1%, wherein the second battery layer (138) is located between the capacitive layer (142) and the current collector (114), the first battery layer (134) is located directly on the first surface (126) of the current collector (114), the second battery layer (138) is located directly on the second surface (130) of the current collector (114), and the capacitive layer (142) is located directly on the second battery layer (138), and wherein the first battery layer (134) has a first thickness (154) of less than 5 mm, the second battery layer (138) has a second thickness (158) of less than 5 mm, and the capacitive layer (142) has a thickness (162) in a range of 1 - 200 µm. [2] The asymmetric hybrid electrode (110) of claim 1, wherein the capacitive layer (142) further includes a third electroactive battery material. [3] The asymmetric hybrid electrode (110) of claim 2, wherein the capacitive layer (142) contains the third electroactive battery material at less than or equal to about 95% by weight of the capacitive electroactive material. [4] The asymmetric hybrid electrode (110) of claim 2 or 3, wherein the first electroactive battery material, the second electroactive battery material, and the third electroactive battery material are the same. [5] Asymmetric hybrid electrode (110) according to any one of the preceding claims, wherein the first binder, the second binder and the third binder are the same. [6] The asymmetric hybrid electrode (110) of any preceding claim, wherein the capacitor hybridization ratio is less than or equal to about 0.7%.

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