Composite solid electrolyte and preparation method and application thereof

Abstract

The application provides a composite solid electrolyte and a preparation method and application thereof, and relates to the technical field of lithium ion batteries. Specifically, the composite solid electrolyte is prepared from the following components in parts by weight: 10-20 parts of inorganic solid electrolyte, 10-20 parts of polyethylene glycol, 10-20 parts of polyethylene oxide, 1-3 parts of crosslinking agent, 10-20 parts of lithium salt and a certain amount of solvent; wherein the crosslinking agent comprises an isocyanate compound. The application makes the inorganic solid electrolyte and the polyethylene glycol connected through a chemical bond by nucleophilic addition reaction of the crosslinking agent containing an isocyanate group, the inorganic solid electrolyte and the polyethylene glycol, and further optimizes the interface between the organic and inorganic; the organic-inorganic composite solid electrolyte has good ion transmission and a wide electrochemical window, and can effectively improve the cycle performance and rate performance of the lithium battery.

Description

Technical Field

[0001] The present invention relates to the technical field of lithium-ion batteries, and in particular to a composite solid electrolyte and a preparation method and application thereof. Background Art

[0002] With the increasing use of electronic devices and electric vehicles, battery researchers are conducting extensive research on solid-state lithium batteries with high energy density, good flexibility, and high safety to meet consumer demand. Solid-state lithium batteries are considered one of the most promising next-generation lithium battery technologies. With continuous technological breakthroughs and the reduction of large-scale production costs, solid-state lithium batteries have significant advantages in safety, energy density, cycle life, and other aspects, and their industrialization process is expected to accelerate. However, solid-state lithium battery technology still faces many bottlenecks, such as the selection of electrolyte materials, solid-solid interface contact, and fast charging performance.

[0003] Solid-state lithium batteries are categorized as all-solid-state and semi-solid-state batteries, and the solid electrolytes involved primarily include oxide electrolytes, sulfide electrolytes, polymer electrolytes, or composite electrolytes of any combination. Compared to polymer electrolytes or inorganic solid electrolytes, organic-inorganic composite solid electrolytes can effectively balance the electrochemical properties of inorganic electrolytes and the mechanical properties of polymer electrolytes through the synergistic effects between their components, and effectively inhibit the dendrite growth of lithium metal electrodes during charge and discharge.

[0004] However, composite solid electrolytes still have the following problems: First, the weak organic-inorganic interaction in the composite solid electrolyte leads to phase separation and uneven dispersion of inorganic nanoparticles within the composite solid electrolyte, hindering the migration of lithium ions around the interphase and reducing ionic conductivity; Second, lithium ions easily deposit at the organic-inorganic interface and form lithium dendrites, which continue to diffuse within the composite solid electrolyte and eventually cause a short circuit in the battery. Therefore, from the above defects, it can be seen that strengthening the organic-inorganic interaction in the composite solid electrolyte and improving the affinity between the phases are key factors in enhancing the electrochemical performance of the composite solid electrolyte.

[0005] In view of this, the present invention is proposed. Summary of the Invention

[0006] The first purpose of the present invention is to provide a composite solid electrolyte, aiming to optimize the organic-inorganic interface compatibility of the organic-inorganic composite solid electrolyte and solve the defects of conventional composite solid electrolytes such as low conductivity, poor dispersibility, and poor organic-inorganic interface stability.

[0007] The second object of the present invention is to provide a method for preparing the composite solid electrolyte, which is simple, easy to operate, mild in conditions, low in cost, and can meet the needs of achieving mass production.

[0008] A third object of the present invention is to provide a lithium ion battery.

[0009] A fourth object of the present invention is to provide an electrical device.

[0010] In order to achieve the above-mentioned purpose of the present invention, the following technical solutions are adopted:

[0011] A composite solid electrolyte is prepared by including the following components in parts by weight: 10-20 parts of an inorganic solid electrolyte, 10-20 parts of polyethylene glycol, 10-20 parts of polyethylene oxide, 1-3 parts of a cross-linking agent, 10-20 parts of a lithium salt, and a certain amount of solvent;

[0012] Wherein, the cross-linking agent includes isocyanate compounds.

[0013] A method for preparing the composite solid electrolyte comprises the following steps:

[0014] A uniform suspension containing an inorganic solid electrolyte is prepared, and then a cross-linking agent is added to perform a first heat treatment; after the first heat treatment is completed, polyethylene glycol is added to perform a second heat treatment; after the second heat treatment is completed, polyethylene oxide and a lithium salt are added to perform a third heat treatment to obtain a composite slurry;

[0015] The composite slurry is coated on a support plate, and the support plate is peeled off after drying to obtain a composite solid electrolyte.

[0016] A lithium-ion battery comprises the composite solid electrolyte.

[0017] An electrical device comprises the lithium-ion battery.

[0018] Compared with the prior art, the present invention has the following beneficial effects:

[0019] The present invention provides a composite solid electrolyte that optimizes the organic-inorganic compatibility in a solid electrolyte based on an isocyanate compound, and has outstanding effects such as high conductivity and stable interface contact at room temperature. Specifically, the present invention uses a cross-linking agent containing a specific group (isocyanate group), an inorganic solid electrolyte, and polyethylene glycol to undergo a nucleophilic addition reaction, so that the inorganic solid electrolyte can be cleverly linked to the polyethylene glycol through a chemical bond via the isocyanate group, thereby optimizing the interface between the organic and inorganic; the hydroxyl groups on the surface of the inorganic solid electrolyte will undergo an addition reaction with the isocyanate group to generate a carbamate, thereby constructing an organic-inorganic hybrid cross-linked network between the inorganic solid electrolyte, the isocyanate group, and the polyethylene glycol.

[0020] In the present invention, the inorganic solid electrolyte has good ion transport and a wide electrochemical window, which not only accelerates the transmission speed of lithium ions but also effectively improves the electrochemical window, improves the conductivity of the room temperature electrolyte membrane without reducing the mechanical properties of the membrane, and makes the electrolyte membrane have good interface compatibility with the lithium metal negative electrode, optimizes the impedance of the organic-inorganic interface, thereby improving the cycle performance and rate performance of the battery. BRIEF DESCRIPTION OF THE DRAWINGS

[0021] In order to more clearly illustrate the specific embodiments of the present invention or the technical solutions in the prior art, the following briefly introduces the drawings required for use in the specific embodiments or the description of the prior art. Obviously, the drawings described below are some embodiments of the present invention. For ordinary technicians in this field, other drawings can be obtained based on these drawings without paying any creative work.

[0022] Figure 1 TEM image of LLZTO@TDI, a comparative example of the present invention;

[0023] Figure 2 TEM image of LLZTO@TDI, a comparative example of the present invention;

[0024] Figure 3 The infrared spectra of the composite solid electrolyte (F-30) prepared in Example 1 of the present invention, LLZTO@TDI, paraphenylene diisocyanate (TDI), polyethylene oxide (PEO), and polyethylene glycol (PEG) of the reference example are shown;

[0025] Figure 4 is the XRD diagram of an embodiment of the present invention; wherein, Figure 4 (a) provides the XRD patterns of LLZTO@TDI and LLZTO as control examples. Figure 4 (b) provides XRD patterns of the composite solid electrolytes of Examples 1 to 4 and the comparative example;

[0026] Figure 5 This is a graph showing the change in ionic conductivity of the composite solid electrolyte according to an embodiment of the present invention as a function of temperature;

[0027] Figure 6 This is a graph showing the electrical performance of the button cell produced in Example 1 of the present invention; Figure 6 (a) provides a picture of the room temperature cycle test of a button cell. Figure 6 (b) provides the charge and discharge curves of each cycle number at 0.1C;

[0028] Figure 7 This is a cycle stability test curve of the symmetrical battery prepared in Example 1 of the present invention; Figure 7(a) provides the curves of positive and negative voltage changes during the 2300h cycle of the symmetrical battery. Figure 7 (b) provides the changing curves of positive and negative voltages of the symmetrical battery during the cycle from 2000h to 2010h. DETAILED DESCRIPTION

[0029] The technical solution of the present invention will be clearly and completely described below in conjunction with the accompanying drawings and specific embodiments. However, it will be understood by those skilled in the art that the following embodiments are only some embodiments of the present invention, rather than all embodiments, and are only used to illustrate the present invention and should not be construed as limiting the scope of the present invention. Based on the embodiments in the present invention, all other embodiments obtained by those of ordinary skill in the art without making creative work are within the scope of protection of the present invention. If specific conditions are not specified in the embodiments, they are carried out according to conventional conditions or the conditions recommended by the manufacturer. If the manufacturer is not specified for the reagents or instruments used, they are all conventional products that can be purchased commercially. In addition, the terms "first", "second" and "third" are only used for descriptive purposes and are not to be construed as indicating or implying relative importance.

[0030] The first aspect of the present invention is to provide a composite solid electrolyte, which is prepared by including the following components in parts by weight: 10 to 20 parts of an inorganic solid electrolyte, 10 to 20 parts of polyethylene glycol, 10 to 20 parts of polyethylene oxide, 1 to 3 parts of a cross-linking agent, 10 to 20 parts of a lithium salt and a certain amount of solvent; wherein the cross-linking agent includes an isocyanate compound.

[0031] As a preferred embodiment, the inorganic solid electrolyte includes LLZO, Li 10 GeP2S 12 , LLZTO and Li3YBr6; in some more preferred embodiments, the inorganic solid electrolyte.

[0032] In the present invention, the inorganic solid electrolyte not only accelerates the transmission of lithium ions but also has a wider electrochemical window. Without reducing the mechanical properties of the electrolyte membrane layer, it improves the conductivity of the electrolyte membrane at room temperature, optimizes the interface of the organic-inorganic solid electrolyte, reduces the impedance of the interface, and thus improves the cycle performance and rate performance of the battery.

[0033] As a preferred embodiment, the molecular weight of the polyethylene glycol is 400 to 4000. As a more preferred embodiment, the molecular weight of the polyethylene glycol is 400 to 2000, including but not limited to any one or a numerical range consisting of any two of 400, 500, 600, 700, 800, 900, 1000, 1200, 1400, 1500, 1600, 1800, and 2000. In the present invention, the polyethylene glycol functions to transport lithium ions and improve the mechanical properties of the composite solid-state electrolyte.

[0034] As a preferred embodiment, the molecular weight of the polyethylene oxide is 10 5 ~2*10 6 , including but not limited to 0.1*10 6 , 0.2*10 6 , 0.5*10 6 , 0.8*10 6 , 1*10 6 , 1.2*10 6 , 1.5*10 6 , 1.8*10 6 、1.9*10 6 , 2*10 6 As a more preferred embodiment, the molecular weight of the polyethylene oxide is 9*10 5 ~1.5*10 6 The role of the polyethylene oxide in the present invention is to transport lithium ions and improve the mechanical properties (mainly toughness) of the composite solid electrolyte. However, it is worth noting that by controlling the amount of the inorganic solid electrolyte, isocyanate group, and polyethylene glycol added in the present invention, the polyethylene oxide basically does not participate in the addition reaction. The polyethylene oxide thus obtained is interspersed in the organic-inorganic hybrid cross-linked network in the composite solid electrolyte in a linear structure.

[0035] In a preferred embodiment, the isocyanate compound includes at least one of 1,3-phenylenediisocyanate, p-phenylenediisocyanate, and 3,5-dinitroisocyanate. The present invention utilizes a specific crosslinking agent, which functions to optimize the organic-inorganic interface through a nucleophilic addition reaction between the hydroxyl groups of polyethylene glycol, LLZTO, and the isocyanate groups of the crosslinking agent.

[0036] As a preferred embodiment, the lithium salt includes at least one of LiPF6, LiClO4, LiTFSI, LiFSI, LiBOB and LiDFOB. In the present invention, the lithium salt provides lithium ions and reduces the glass transition temperature of the polymer electrolyte.

[0037] In the present invention, when the inorganic solid electrolyte, the isocyanate compound, and the lithium salt are selected from two or more of the above-mentioned specific options, the present invention does not have any special restrictions on the ratio of the above-mentioned specific substances, and they can be mixed in any ratio.

[0038] In a preferred embodiment, the solvent includes one or more of N,N-dimethylformamide, benzene, toluene, tetrahydrofuran, acetonitrile, dimethyl sulfoxide, or N-methylpyrrolidone. When the organic solvent is two or more of the above-mentioned specific selections, the present invention does not have any particular restrictions on the ratio of the above-mentioned specific substances, and they can be mixed in any ratio. In some more preferred embodiments, the weight ratio of the solvent is 300-350 parts.

[0039] As a preferred embodiment, the composite solid electrolyte is prepared by including the following components in parts by weight: 12 to 16 parts of inorganic solid electrolyte, 11 to 16 parts of polyethylene glycol, 11 to 16 parts of polyethylene oxide, 1 to 2 parts of cross-linking agent, 10 to 15 parts of lithium salt and 310 to 340 parts of solvent.

[0040] As a more preferred embodiment, the composite solid electrolyte is prepared by including the following components in parts by weight: 12 to 13 parts of inorganic solid electrolyte, 12 to 13 parts of polyethylene glycol, 12 to 13 parts of polyethylene oxide, 1 to 1.5 parts of cross-linking agent, 11 to 13 parts of lithium salt and 310 to 330 parts of solvent.

[0041] As a preferred embodiment, the composite solid electrolyte is in a thin film state, and the thickness of the composite solid electrolyte is 100 μm to 150 μm.

[0042] The second aspect of the present invention is to provide a method for preparing the composite solid electrolyte.

[0043] (1) Preparation of organic-inorganic composite reaction slurry: a uniform suspension containing an inorganic solid electrolyte is prepared, and then a cross-linking agent is added and a first heat treatment is performed; after the suspension is completed, polyethylene glycol is added and a second heat treatment is performed; after the suspension is completed, polyethylene oxide and lithium salt are added and a third heat treatment is performed to obtain a composite slurry.

[0044] As a preferred embodiment, during the preparation of the suspension, one or more means including stirring, oscillation, ultrasound, centrifugation, etc. are used to achieve sufficient dispersion of the inorganic solid electrolyte; in some more preferred embodiments, the solution containing the inorganic solid electrolyte is ultrasonically treated at room temperature for 1h to 2h to obtain the suspension.

[0045] As a preferred embodiment, the temperature of the first heat treatment is 40° C. to 80° C., and the time of the first heat treatment is 2 h to 10 h.

[0046] As a preferred embodiment, the temperature of the second heat treatment is 40° C. to 80° C., and the time of the second heat treatment is 2 h to 10 h.

[0047] As a preferred embodiment, the temperature of the third heat treatment is 40° C. to 80° C., and the time of the third heat treatment is 20 h to 40 h.

[0048] As a preferred embodiment, during the addition process of the cross-linking agent, the polyethylene glycol, the polyethylene oxide and the lithium salt and any heat treatment process, the reaction solution is in a stirring state; in some more preferred embodiments, the stirring frequency is 50 rpm to 5000 rpm.

[0049] As a more preferred embodiment, before adding the cross-linking agent, the polyethylene glycol, the polyethylene oxide and the lithium salt, the cross-linking agent solution, the polyethylene glycol solution, the polyethylene oxide and the lithium salt solution are separately prepared in advance to ensure that the raw material components are fully dispersed in the reaction solution.

[0050] (2) Slurry forming treatment: the composite slurry is coated on a support plate, and the support plate is peeled off after drying to obtain a composite solid electrolyte.

[0051] As a preferred embodiment, the coating is performed by one of roller coating, extrusion coating or blade coating; in some more preferred embodiments, a grooved blade or a gravure blade is used to scrape the composite slurry onto the surface of the support plate, and the shape or area of ​​the support plate can be used to control the shape of the composite solid electrolyte, and the support plate is selected from any polymer material plate or film, etc.

[0052] As a preferred embodiment, the drying temperature is 50° C. to 80° C., and the drying time is 20 h to 40 h.

[0053] As a preferred embodiment, the drying is carried out in a vacuum atmosphere.

[0054] The operating method steps and the containers or equipment used in the present invention can be implemented according to conventional processing means of those skilled in the art, except for the above-mentioned limitations and descriptions in the preferred embodiments, and the present invention does not impose any other limitations thereon.

[0055] A third aspect of the present invention is to provide a lithium-ion battery.

[0056] The lithium-ion battery includes the composite solid-state electrolyte. It is understood that the lithium-ion battery is a solid-state lithium battery or a semi-solid-state lithium battery. In addition to the composite solid-state electrolyte, the lithium-ion battery should include electrodes and other necessary or non-essential functional elements or packaging components, etc., which can be arbitrarily selected and combined by those skilled in the art. When the composite solid-state electrolyte described in the present invention is included in the lithium-ion battery, whether or not other electrolyte functional components are also used in the lithium-ion battery, it can be regarded as an embodiment of the present invention.

[0057] As a more preferred embodiment, the electrodes include a positive electrode and a negative electrode; wherein the positive electrode includes a positive electrode active material, a current collector, a conductive agent, and a binder, preferably in a mass ratio of 8:1:1; the positive electrode active material includes at least one of lithium cobalt oxide, lithium manganese oxide, lithium iron phosphate, and lithium iron manganese phosphate; the current collector includes copper foil or aluminum foil; the conductive agent includes at least one of acetylene black, Ketjen black, and carbon nanotubes; and the binder includes at least one of polytetrafluoroethylene, polyurethane, and polyvinylidene fluoride; and the negative electrode is metallic lithium. The present invention has no particular requirements for the assembly method of the lithium-ion battery; assembly methods familiar to those skilled in the art can be used.

[0058] A fourth aspect of the present invention is to provide an electrical device.

[0059] The electrical equipment includes the lithium-ion battery. In some optional embodiments, the electrical equipment can be any device or apparatus that relies on electrical energy to operate or function, including but not limited to new energy vehicles, building electrical equipment, industrial appliances, and household and agricultural appliances. When the lithium-ion battery is included, any electrical equipment equipped with the lithium-ion battery can be an embodiment of the present invention.

[0060] Example 1

[0061] Under nitrogen atmosphere, 0.174 g of LLZTO was dispersed in 3 mL of N,N-dimethylformamide and sonicated at room temperature for 1 h to obtain a homogeneous suspension;

[0062] A solution of N,N-dimethylformamide (1 mL) containing 0.016 g of p-phenylene diisocyanate was added to the above suspension and stirred at 80°C for 5 h;

[0063] Then, a solution of N,N-dimethylformamide (1 mL) containing 0.2 g of polyethylene glycol (molecular weight 2000) was added to the above solution, and heating was continued at 80 °C for 10 h;

[0064] Finally, 0.2 g of polyethylene oxide (molecular weight 100w) and 0.167 g of LiTFSI were added to the above solution, and the temperature was adjusted to 40 °C and heated with stirring for 24 h to obtain a viscous liquid;

[0065] The viscous liquid was spread on a rectangular polytetrafluoroethylene plate of 10×20×2 (cm) using a scraper, dried in a vacuum oven at 60° C. for 24 h, and peeled off to obtain the composite solid electrolyte of this embodiment.

[0066] Example 2

[0067] Under nitrogen atmosphere, 0.044 g of LLZTO was dispersed in 3 mL of N,N-dimethylformamide and sonicated at room temperature for 1 h to obtain a homogeneous suspension;

[0068] A solution of N,N-dimethylformamide (1 mL) containing 0.016 g of p-phenylene diisocyanate was added to the above suspension and stirred at 40°C for 10 h;

[0069] Then, a solution of N,N-dimethylformamide (1 mL) containing 0.2 g of polyethylene glycol was added to the above solution, and heating was continued at 40 °C for 10 h;

[0070] Finally, 0.2 g of polyethylene oxide and 0.167 g of LiTFSI were added to the above solution, and the temperature was adjusted to 40 °C and heated with stirring for 30 h to obtain a viscous liquid;

[0071] The viscous liquid was spread on a rectangular polytetrafluoroethylene plate of 10×20×2 (cm) using a scraper, dried in a vacuum oven at 60° C. for 24 h, and peeled off to obtain the composite solid electrolyte of this embodiment.

[0072] Example 3

[0073] Under nitrogen atmosphere, 0.1 g of LLZTO was dispersed in 3 mL of N,N-dimethylformamide and sonicated at room temperature for 1 h to obtain a homogeneous suspension;

[0074] A solution of N,N-dimethylformamide (1 mL) containing 0.016 g of p-phenylene diisocyanate was added to the above suspension and stirred at 80°C for 5 h;

[0075] Then, a solution of N,N-dimethylformamide (1 mL) containing 0.2 g of polyethylene glycol was added to the above solution, and heating was continued at 80 °C for 5 h;

[0076] Finally, 0.2 g of polyethylene oxide and 0.167 g of LiTFSI were added to the above solution, and the temperature was adjusted to 80 °C and heated with stirring for 20 h to obtain a viscous liquid;

[0077] The viscous liquid was spread on a rectangular polytetrafluoroethylene plate of 10×20×2 (cm) using a scraper, dried in a vacuum oven at 60° C. for 24 h, and peeled off to obtain the composite solid electrolyte of this embodiment.

[0078] Example 4

[0079] Under nitrogen atmosphere, 0.267 g of LLZTO was dispersed in 3 mL of N,N-dimethylformamide and sonicated at room temperature for 1 h to obtain a homogeneous suspension;

[0080] A solution of N,N-dimethylformamide (1 mL) containing 0.016 g of p-phenylene diisocyanate was added to the above suspension and stirred at 80°C for 5 h;

[0081] Then, a solution of N,N-dimethylformamide (1 mL) containing 0.2 g of polyethylene glycol was added to the above solution, and heating was continued at 80 °C for 10 h;

[0082] Finally, 0.2 g of polyethylene oxide and 0.167 g of LiTFSI were added to the above solution, and the temperature was adjusted to 40 °C and heated with stirring for 24 h to obtain a viscous liquid;

[0083] The viscous liquid was spread on a rectangular polytetrafluoroethylene plate of 10×20×2 (cm) using a scraper, dried in a vacuum oven at 80° C. for 20 h, and peeled off to obtain the composite solid electrolyte of this embodiment.

[0084] Example 5

[0085] Under nitrogen atmosphere, 0.174 g of LLZTO was dispersed in 3 mL of N,N-dimethylformamide and sonicated at room temperature for 1 h to obtain a homogeneous suspension;

[0086] A solution of N,N-dimethylformamide (1 mL) containing 0.016 g of p-phenylene diisocyanate was added to the above suspension and stirred at 80°C for 5 h;

[0087] Then, a solution of N,N-dimethylformamide (1 mL) containing 0.3 g of polyethylene glycol was added to the above solution, and heating was continued at 80 °C for 10 h;

[0088] Finally, 0.1 g of polyethylene oxide and 0.167 g of LiTFSI were added to the above solution, and the temperature was adjusted to 40 °C and heated with stirring for 24 h to obtain a viscous liquid;

[0089] The viscous liquid was spread on a rectangular polytetrafluoroethylene plate of 10×20×2 (cm) using a scraper, dried in a vacuum oven at 60° C. for 24 h, and peeled off to obtain the composite solid electrolyte of this embodiment.

[0090] Example 6

[0091] 0.174 g of LLZO was dispersed in 3 mL of N,N-dimethylformamide under a nitrogen atmosphere, and a uniform suspension was obtained by ultrasonic treatment at room temperature for 1 h;

[0092] A solution containing 0.016 g of 1,3-phenylene diisocyanate in N,N-dimethylformamide (1 mL) was added to the above suspension, and stirring was performed at 80°C for 5 h under heating;

[0093] Thereafter, a solution containing 0.2 g of polyethylene glycol in N,N-dimethylformamide (1 mL) was added to the above solution, and heating was continued at 80°C for 10 h;

[0094] Finally, 0.2 g of polyethylene oxide and 0.167 g of a lithium salt (LiPF6 and LiFSI, mass ratio 1:1) were added to the above solution, and heating was performed at 40°C for 24 h with stirring to obtain a viscous liquid;

[0095] The viscous liquid was doctor-bladed onto a rectangular polytetrafluoroethylene plate of 10 x 20 x 2 (cm) using a doctor blade, and the composite solid-state electrolyte of the present example was obtained by drying in a vacuum oven at 60°C for 24 h, peeling off the film, and the like.

[0096] Example 7

[0097] 0.174 g of Li3YBr6 was dispersed in 3 mL of N,N-dimethylformamide under a nitrogen atmosphere, and a uniform suspension was obtained by ultrasonic treatment at room temperature for 1 h;

[0098] A solution containing 0.016 g of 3,5-dinitroisocyanate in N,N-dimethylformamide (1 mL) was added to the above suspension, and stirring was performed at 80°C for 5 h under heating;

[0099] Thereafter, a solution containing 0.2 g of polyethylene glycol in N,N-dimethylformamide (1 mL) was added to the above solution, and heating was continued at 80°C for 10 h;

[0100] Finally, 0.2 g of polyethylene oxide and 0.167 g of a lithium salt (LiTFSI and LiDFOB, mass ratio 1:1) were added to the above solution, and heating was performed at 40°C for 24 h with stirring to obtain a viscous liquid;

[0101] The viscous liquid was doctor-bladed onto a rectangular polytetrafluoroethylene plate of 10 x 20 x 2 (cm) using a doctor blade, and the composite solid-state electrolyte of the present example was obtained by drying in a vacuum oven at 60°C for 24 h, peeling off the film, and the like.

[0102] Comparative Example

[0103] Under nitrogen atmosphere, 0.174 g of LLZTO was dispersed in 3 mL of N,N-dimethylformamide and sonicated at room temperature for 1 h to obtain a homogeneous suspension;

[0104] A solution of N,N-dimethylformamide (1 mL) containing 0.016 g of p-phenylene diisocyanate was added to the above suspension and stirred at 80°C for 5 h;

[0105] The obtained product was washed with N,N-dimethylformamide and centrifuged several times, dried in a vacuum oven at 60°C for 24 hours, and the film was removed to obtain the solid product LLZTO@TDI of this reference example.

[0106] like Figure 1 、 Figure 2 The transmission electron microscope (TEM) image of LLZTO@TDI in the control example is provided as shown; Figure 1 、 Figure 2 It can be seen that a nucleophilic addition reaction occurs between p-phenylene diisocyanate and the hydroxyl group of LLZTO, indicating that LLZTO and polyethylene glycol can be cleverly linked together through a chemical bond via the isocyanate group.

[0107] like Figure 3 The figure shows the infrared spectra of the composite solid electrolyte (F-30) prepared in Example 1, LLZTO@TDI, paraphenylene diisocyanate (TDI), polyethylene oxide (PEO) and polyethylene glycol (PEG) of the control example; Figure 3 It can be seen that in the infrared spectrum of p-phenylene diisocyanate, at 2270 cm -1 The characteristic absorption peak of isocyanate group (-NCO) is at 1521cm, while the characteristic peak of -NCO disappears in the infrared spectrum of LLZTO@TDI, and a new -NH (1521cm -1 )、-C=O(1657cm -1 ) absorption band appears; indicating that esterification reaction occurs between hydroxyl group and isocyanate; further, in the infrared spectrum of composite solid electrolyte F-30, at 3433cm -1 The stretching vibration peak of -OH is at 1099cm -1 is the stretching vibration peak of COC, indicating that polyethylene glycol was successfully grafted onto the LLZTO surface through p-phenylene diisocyanate.

[0108] like Figure 4 As shown, Figure 4 (a) Provides X-ray diffraction (XRD) spectra of LLZTO@TDI and LLZTO as control examples, where the “80-0457” curve corresponds to the XRD data standard card curve of LLZTO; Figure 4(b) provided the X-ray diffraction (XRD) spectrum of the composite solid-state electrolyte corresponding to Example 1 (F-30), the composite solid-state electrolyte corresponding to Example 2 (F-10), the composite solid-state electrolyte corresponding to Example 3 (F-20), the composite solid-state electrolyte corresponding to Example 4 (F-40), and the LLZTO@TDI corresponding to the control (F-0); from Figure 4 It can be seen that there is no obvious difference between LLZTO@TDI and LLZTO in XRD, which indicates that LLZTO can still maintain the original crystal structure in the surface modification process; further through Figure 4 (b) It can be seen that, compared with the pure organic polymer, the embedding of LLZTO reduces the crystallinity of the polymer electrolyte, indicating that the amorphous phase region in the polymer electrolyte increases, thereby improving the ionic conductivity.

[0109] As Figure 5 shown, the ion conductivity-temperature curve of the composite solid-state electrolyte is provided, wherein 0%, 20%, 30%, and 40% correspond to the composite solid-state electrolyte obtained in the control, Example 3, Example 1, and Example 4, respectively; from Figure 5 It can be seen that, under the premise that the film thickness is about 140 μm, the ion conductivity of the examples is obviously improved compared with the control at any temperature, because the Lewis acid-base reaction between LLZTO and the polymer chain segment reduces the crystallinity of the polymer and enhances the migration of Li + in the polymer chain; with the increase of temperature, the ion conductivity of the examples is further increased.

[0110] Test Example

[0111] (1) The composite solid-state electrolyte prepared in each example is used as the electrolyte to assemble a button cell, the positive active material is lithium iron phosphate, the current collector is aluminum foil, the conductive agent is acetylene black, and the binder is polytetrafluoroethylene (the mass ratio of the positive active material, the conductive agent, and the binder is 8:1:1); the negative electrode is metal lithium. The initial discharge capacity of each button cell at 0.1C rate is tested, and then the discharge capacity after 120 cycles of charge and discharge at 0.1C is tested, and the coulombic efficiency is calculated. As shown in Table 1, the coulombic efficiency values of each example are provided.

[0112] Further, Figure 6 The electrical performance test diagram of the button cell prepared in Example 1 is provided, wherein Figure 6 (a) is the room temperature cycle test diagram of the button cell corresponding to Example 1, Figure 6 (b) is the charge-discharge curve diagram of the button cell corresponding to Example 1 at different cycle numbers at 0.1C, further, Figure 6(b) provides the discharge characteristic curves at the 1st, 30th, 60th, 90th, and 120th cycles, which correspond to the 1st, 30th, 60th, 90th, and 120th curves in the figure respectively; Figure 6 (a) and (b) show that at a rate of 0.1C, the initial discharge capacity of the composite solid electrolyte is 153.7 mAh g -1 , and maintained 154.9 mAh g after 120 cycles -1 , and the Coulombic efficiency is 99.7%, indicating that the Li / F-30 / LFP battery assembled with the modified electrolyte membrane has excellent long cycle performance.

[0113] (2) The composite solid electrolyte prepared in each example was used as the electrolyte to assemble a Li / / Li symmetrical button cell, with both the positive and negative electrodes being metallic lithium. By using a lithium foil with a diameter of 16 mm, the -2 At a current density of 1h Li + Electroplating and 1h Li + The stripping cycle was run, and the negative voltage and positive voltage represented the electroplating lithium ions and the stripping lithium ions, respectively. After 2300 h of continuous cycling, the values ​​of the positive and negative voltages at the last cycle were recorded and reported in Table 1.

[0114] Further, Figure 7 This is the cycle stability test curve of the symmetrical battery prepared in Example 1 of the present invention. Figure 7 (a) Figure 7 (b) is the cycle stability curve of the symmetrical battery obtained in Example 1; Figure 7 (a) Corresponding to the change curve of positive and negative voltage during the cycle of 2300 hours (due to the high point density, it appears shaded), Figure 7 (b) Corresponding curves of positive and negative voltage changes during the cycle of 2000 to 2010 hours; the upper and lower limits of the curve indicate that the electrolyte membrane has excellent interface stability with the lithium negative electrode.

[0115] Table 1

[0116]

[0117]

[0118] Although the present invention has been illustrated and described using specific embodiments, it should be appreciated that the above embodiments are merely intended to illustrate the technical solutions of the present invention rather than to limit them. Those skilled in the art should understand that the technical solutions described in the above embodiments may be modified, or some or all of the technical features thereof may be replaced by equivalents, without departing from the spirit and scope of the present invention. However, these modifications or replacements do not deviate from the essence of the corresponding technical solutions within the scope of the technical solutions of the embodiments of the present invention. Therefore, this means that all such replacements and modifications within the scope of the present invention are included in the appended claims.

Claims

1. A composite solid electrolyte, characterized in that: The composite solid electrolyte is prepared by including the following components in parts by weight: 10-20 parts of inorganic solid electrolyte, 10-20 parts of polyethylene glycol, 10-20 parts of polyethylene oxide, 1-3 parts of cross-linking agent, 10-20 parts of lithium salt and some solvent; Wherein, the cross-linking agent includes isocyanate compounds.

2. The composite solid electrolyte according to claim 1, characterized in that The inorganic solid electrolyte includes LLZO, Li 10 GeP2S 12 , LLZTO and Li3YBr6.

3. The composite solid electrolyte according to claim 1, characterized in that The molecular weight of the polyethylene glycol is 400 to 4000; And / or, the molecular weight of the polyethylene oxide is 10 5 ~2*10 6 .

4. The composite solid electrolyte according to claim 1, characterized in that The isocyanate compound includes at least one of 1,3-phenylene diisocyanate, p-phenylene diisocyanate and 3,5-dinitroisocyanate.

5. The composite solid electrolyte according to claim 1, characterized in that The lithium salt includes at least one of LiPF6, LiClO4, LiTFSI, LiFSI, LiBOB and LiDFOB.

6. The method for preparing a composite solid electrolyte according to any one of claims 1 to 5, wherein: The preparation method comprises the following steps: A uniform suspension containing an inorganic solid electrolyte is prepared, and then a cross-linking agent is added to perform a first heat treatment; after the first heat treatment is completed, polyethylene glycol is added to perform a second heat treatment; after the second heat treatment is completed, polyethylene oxide and a lithium salt are added to perform a third heat treatment to obtain a composite slurry; The composite slurry is coated on a support plate, and the support plate is peeled off after drying to obtain a composite solid electrolyte.

7. The method for preparing a composite solid electrolyte according to claim 6, characterized in that: The temperatures of the first heat treatment, the second heat treatment and the third heat treatment are independently 40° C. to 80° C.; The time for the first heat treatment and / or the second heat treatment is 2 hours to 10 hours, and the time for the third heat treatment is 20 hours to 40 hours.

8. The method for preparing a composite solid electrolyte according to claim 6, wherein: The drying temperature is 50° C. to 80° C., and the drying time is 20 hours to 40 hours.

9. A lithium-ion battery, characterized in that: The lithium-ion battery comprises the composite solid electrolyte according to any one of claims 1 to 5.

10. An electrical device, characterized in that: The electric device comprises the lithium-ion battery as claimed in claim 9.

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