106 results about "Lithium ion intercalation" patented technology

The invention relates to the field of batteries, in particular to a long-circulation persistent adhesion type negative electrode composite electrode and a preparation method and application thereof. The long-circulation persistent adhesive type negative electrode composite electrode comprises a current collector, and a first adhesive layer, an active slurry coating and a second adhesive layer which are sequentially coated on two sides of the current collector, according to the invention, through the bonding effect between the second bonding layer and the diaphragm, the pole piece is uniformly stressed during cyclic expansion, the wrinkles of the pole piece are improved, the electrolyte infiltration is better in combination with the oil-absorbing conductive agent, the lithium ion transmission efficiency is improved, and the cycle life is prolonged; an interface structure formed by multi-layer coating can buffer lithium ion intercalation / deintercalation stress, so that the pole piece can still keep good binding power after circulation, and the cycle performance of the lithium ion battery can be effectively improved; the conductive agent contents of the first bonding layer, the active slurry coating and the second bonding layer are distributed in a concave gradient manner, so that the resistance is reduced, and the conductivity is enhanced.

A rechargeable battery is disclosed. The rechargeable battery comprises an anode, a cathode comprising a lithium-ion intercalation host, and an electrolyte comprising a solvent and a halogen-containing compound acting as an active cathode conversion material, wherein the electrolyte is in contact with the anode and the cathode.

The invention belongs to the technical field of battery preparation, and particularly relates to a battery and a device. The battery comprises a negative pole piece and a positive pole piece, the negative pole piece comprises a negative current collector and a negative active material layer arranged on at least one surface of the negative current collector, the negative active material layer comprises a negative active material, and the negative active material comprises a silicon-containing material; the silicon content in the negative electrode active material layer and the elongation at break of the negative electrode current collector meet a specific relational expression, and the positive electrode plate comprises a positive electrode current collector; the silicon content in the negative electrode active material layer and the elongation at break of the positive electrode current collector meet a specific relational expression, so that the risk of negative electrode foil cracking caused by negative electrode expansion can be reduced while the lithium ion embedding capacity of the negative electrode is ensured, the risk of positive and negative electrode short circuit caused by the negative electrode foil breaking process can be avoided, and the service life of the negative electrode is prolonged. And the capacity density, the cycle performance and the safety performance of the battery are improved.

The present invention relates to a disulfonate compound, a preparation method thereof, an electrolyte, and an energy storage device. The disulfonate compound has an #imgabs0# structure and is applied as an additive to an energy storage device, so that a stable SEI film can be formed on the negative electrode surface of the energy storage device, which can inhibit the decomposition of the solvent in the electrolyte. Since a stable SEI film can be formed on the negative electrode surface, the insertion and deintercalation of lithium ions at low temperatures become smooth, thereby improving the low-temperature performance of the energy storage device. On the other hand, the sulfonate group in the disulfonate compound can coordinate with transition metal ions to form a complex, passivating the positive electrode surface, inhibiting the dissolution of positive electrode metal ions, and reducing the decomposition effect of high-oxidation active substances on the solvent, thereby improving the electrochemical performance of the energy storage device under high-temperature conditions. In the energy storage device, the disulfonate compound can inhibit the increase of DC internal resistance, thereby improving the high-temperature performance and low-temperature performance of the energy storage device.

The present application discloses an organic electrolyte and a lithium-ion secondary battery, relating to the field of battery technology. The organic electrolyte comprises: lithium tetrafluorooxalate phosphate and an isocyanate compound; the isocyanate compound is selected from a mixture of one or more of a monoisocyanate compound, a diisocyanate compound, and a polyisocyanate compound; wherein the mass ratio of the lithium tetrafluorooxalate phosphate to the isocyanate compound is 2-5:1. The present application, by applying lithium tetrafluorooxalate phosphate and an isocyanate compound to an organic electrolyte, can form a more stable organic-inorganic composite modified SEI film at the negative electrode interface through binding, thereby effectively reducing direct contact between the organic solvent and the negative electrode interface, improving the reversibility of lithium ion insertion / deinsertion, thereby helping to improve the battery's cycle life characteristics, high temperature storage stability, and low temperature discharge capability.

The utility model relates to a laminated core structure which comprises at least two negative pole pieces, at least one positive pole piece and at least one composite pole piece, the at least two negative pole pieces are sequentially arranged along the first direction; one positive pole piece is arranged between every two adjacent negative pole pieces, or one composite pole piece is arranged between every two adjacent negative pole pieces; the composite pole piece comprises a lithium piece and a polymer, and the high polymer coats the lithium sheet. In the laminated core structure, the lithium sheets can supplement lithium ions consumed by forming a solid electrolyte interface (SEI) film in the formation stage of the battery, so that the loss of active lithium is reduced, the initial coulombic efficiency of the battery is further improved, and the overall performance of the battery is enhanced; meanwhile, the polymer sheet also has a good elastic characteristic and can adapt to volume change caused by lithium ion intercalation and deintercalation in the charging and discharging process of the battery, so that the pressure on the shell is reduced, the deformation of the shell is effectively prevented, and the safety of the battery is improved.

The invention discloses a solid-state battery and a positive electrode material thereof. The solid-state battery consists of a lithium storage positive electrode, a battery electrolyte and a lithium-rich negative electrode. Wherein the lithium-storing positive electrode comprises an embedded lithium-storing transition metal chalcogenide and a composite material of the embedded lithium-storing transition metal chalcogenide. The positive electrode material has ionic conductivity and electronic conductivity at the same time, a three-dimensional ionic and electronic conductive network structure is formed in the positive electrode, and the network structure is beneficial to intercalation and deintercalation of lithium ions. The crystal structure of the transition metal chalcogenide can be a layered structure or a SiFerel phase, and transition metal contained in the transition metal chalcogenide can be at least one of IVB, VB, VIB and VIIB group metal elements. In the lithium ion intercalation and deintercalation process, the transition metal is subjected to valence change reaction. By introducing the positive electrode material, the weight ratio of inactive substances in the battery is effectively reduced, and the energy density of the solid electrolyte is further improved.

The present invention discloses a method for preparing a lithium battery positive electrode material in the field of lithium battery processing technology, comprising: mixing a binder with a liquid solvent to form a glue; mixing a lithium source material, a metal oxide precursor, and a conductive agent to form a premixed material; extracting carbon dioxide for compression and condensation to form supercritical carbon dioxide; mixing the glue and the premixed material, and then introducing the supercritical carbon dioxide and thoroughly mixing to form a mixed slurry; after the mixed slurry is mixed, releasing the carbon dioxide in the mixing container until the pressure in the mixing container returns to atmospheric pressure. The present invention enables the metal oxide precursor to react with the positive electrode raw material in supercritical carbon dioxide to form a stable lithium metal oxide with a layered structure, which can provide a stable lithium ion insertion / deinsertion channel, thereby improving the cycle stability and structural integrity of the material, and further improving the structural stability of the positive electrode material after preparation.

The invention provides a pole piece of a lithium ion battery and a preparation method of the pole piece, the pole piece of the lithium ion battery comprises a current collector and an active material coated on the current collector, and by arranging the active material and an adhesive, the active material can be conveniently and rapidly fixed when being extruded and arranged on the current collector along an angle; the assembly state of the active material on the current collector is stabilized, the active material is placed in the slit die cavity to be extruded, the active material moves and deforms towards the single side direction, so that the structure becomes long and narrow, and the end part of the long and narrow active material is connected with the current collector to be rolled, so that the tortuosity of the lithium ion battery pole piece is reduced, and the service life of the lithium ion battery pole piece is prolonged. And the migration rate of lithium ions in the pole piece and the embedding rate of the lithium ions in the active material are accelerated, meanwhile, the problem that the pole piece is expanded and increased due to lithium ion embedding in the thickness direction of the pole piece is solved, and the probability of deformation of the lithium ion battery is reduced.

The invention provides a carbon-coated titanium-based polyanion composite material for a lithium ion battery and a preparation method of the carbon-coated titanium-based polyanion composite material, and the carbon-coated titanium-based polyanion composite material for the lithium ion battery consists of derivative carbon and a titanium-based polyanion material, the mass percentage of the derived carbon in the carbon-coated titanium-based polyanion composite material for the lithium ion battery is 1.5-24.4%, and the balance is the titanium-based polyanion material. Compared with the prior art, the carbon-coated titanium-based polyanion composite material for the lithium ion battery is obtained by adopting the components, and the titanium-based polyanion material has a stable crystal structure and three-dimensional skeleton characteristics, so that volume deformation caused by lithium ion intercalation / deintercalation in the charging and discharging process can be effectively relieved. After the carbon coating layer is overlaid, a protective layer with excellent conductivity and high mechanical strength is formed on the surface of the material, so that pulverization and falling of active substances in circulation are inhibited, corrosion of electrolyte to the electrode material is blocked, and the cycle life of the battery is remarkably prolonged.

The present application relates to the technical field of battery, in particular to a kind of graphite material and its preparation method and application.The present application provides a kind of graphite material, the graphite material includes graphite body, the graphite body has multiple through-hole structures, the hole diameter R of each through-hole structure is 0.07~1.81 μm;The particle size Dv50 of the graphite material and the hole diameter R of the through-hole structure satisfy:3.9≤Dv50 / R≤107.1.The graphite material of the present application has abundant through-hole structure, provides more channels for lithium ion deintercalation, and shortens the solid-phase diffusion path of lithium ion intercalation, so as to improve the rate performance of graphite negative electrode material, and the through-hole channel structure can improve the wettability and liquid retention of electrolyte, thereby improving the cycle performance of battery.

The utility model provides a battery cell and a battery, the battery cell comprises a roll core structure formed by sequentially laminating and winding a positive pole piece, a diaphragm and a negative pole piece, the negative pole piece further comprises an insulating coating, the insulating coating is coated on a second surface, at least part of the insulating coating is located on the outermost ring of the roll core structure, and the insulating coating is located on the outer ring of the roll core structure in the length direction of the negative pole piece. A first interval exists between the head end of the insulating coating and the tail end of the second negative active material layer; the roll core structure comprises a straight area and bending areas located at the two ends of the straight area, and at least part of the first interval is located in the bending areas. Therefore, the insulating coating can be prevented from covering the negative electrode active material layer and extending between the negative electrode active material layer and the negative electrode current collector, so that the poor conductivity of the region is avoided, the lithium ion embedding speed is reduced in the charging process, and the lithium precipitation of the region is slowed down or even avoided, and the safety performance of the battery in use is further improved; and the reduction of the energy density of the battery formed by the roll core structure due to the increase of the thickness of the region of the roll core structure can be avoided.

The application belongs to the technical field of electrochemical energy storage, and particularly relates to a pre-sodium-embedded hard carbon negative electrode sheet and a preparation method and application thereof. The pre-sodium-embedded hard carbon negative electrode sheet comprises the following raw materials in parts by weight: pre-sodium-embedded hard carbon 70-90 parts, conductive agent 5-15 parts, and binder 5-15 parts; and the pre-embedded amount of sodium in the pre-sodium-embedded hard carbon is 5%-30% of the theoretical sodium storage capacity of the hard carbon. The pre-sodium-embedded hard carbon negative electrode sheet has the following beneficial effects: when assembled into a secondary battery, sodium ions in the negative electrode sheet will preferentially react with an electrolyte to form a stable and dense SEI film mainly composed of sodium-containing compounds on the surface of the hard carbon. When assembled into a full battery for the first time, lithium ions are embedded into the negative electrode from the positive electrode, and a large amount of additional lithium is no longer needed to build the SEI film, thereby effectively improving the first coulomb efficiency of the full battery and improving the initial energy density of the battery.

The application provides high-dispersion iron phosphate, wherein the primary particle size of the iron phosphate is 50-100 nm, the secondary particle size of the iron phosphate is small, the secondary particle size distribution of the iron phosphate is narrow, and the specific surface area of the iron phosphate is 10-12 m 2 / g. When the iron phosphate is used to prepare a positive electrode material, the small secondary particle size and the narrow particle size distribution are beneficial to improving the grinding efficiency, and the iron phosphate cannot be broken, which is beneficial to the batch production of iron lithium and reduces the production cost. In addition, the small primary particle size is beneficial to the subsequent preparation of a positive electrode material with a small primary particle size, the positive electrode material can be more fully contacted with an electrolyte, the lithium ion insertion / desorption is facilitated, the electrochemical activity of the positive electrode material is improved, and the battery capacity and the rate performance are improved. The application also provides a preparation method of the high-dispersion iron phosphate, a positive electrode material and a lithium ion battery.

The present application provides a high-nickel ternary positive electrode active material, which comprises a core Li 1+a [Ni x Co y Mn z M b ]O2, and a first shell layer of fast ion conductor Li α Al X Si Y O4, an oxide of R elements of a second shell layer, and a transition layer Li p R q O w The high-nickel ternary positive electrode active material of the present application has a significantly reduced amount of surface miscellaneous lithium, and creatively converts the surface miscellaneous lithium into an effective component of fast ion conductor Li α Al X Si Y O4, Li p R q O w , which significantly improves the electrolyte decomposition gas caused by the surface miscellaneous lithium, so that the high-nickel ternary lithium ion battery has high energy density, good cycle performance and safety performance.

This application discloses a method and apparatus for electrochemical extraction to obtain low-impurity lithium ions, relating to the field of capacitive deionization technology. The apparatus includes a positive current collector and a negative current collector with a working surface coated with mesoporous activated carbon material and a chemically de-intercalated lithium ion sieve. A lithium-ion-containing solution circulates between the working surfaces of the positive and negative current collectors. A voltage is applied to insert lithium ions into the chemically de-intercalated lithium ion sieve. After the power is turned off, the cations adsorbed by the mesoporous activated carbon material are re-desorbed. The resulting lithium-ion-intercalated sieve electrode is placed in an electrolyte solution and a voltage is applied to remove lithium. This application uses mesoporous activated carbon material as the negative electrode to adsorb impurity cations in the salt solution. The impurity cations are enriched on the surface of the activated carbon and do not accumulate on the surface of the ion sieve, hindering the absorption of lithium. + By placing the lithium ion extraction device closer to the chemical deintercalation sieve, the content of impurity cations intercalating into the sieve lattice can be reduced, thereby improving the lithium extraction efficiency and purity of the sieve.

This invention discloses a superlattice structure all-solid-state thin-film battery cathode material, its preparation method, and its applications. The cathode material consists of a substrate and a stacked structure deposited on the substrate surface. The stacked structure is formed by alternating deposition of a first transition metal oxide layer and a second transition metal oxide layer from bottom to top. The first and second transition metal oxides of this invention have different work functions and lithium-ion intercalation potentials. An integrated electric field is induced through interface bandgap engineering, synergistically enhancing electron / ion transport dynamics. Simultaneously, lattice pinning and lattice pre-strain are used to suppress structural degradation during cycling. The cathode material provided by this invention exhibits high specific capacity, excellent rate performance, long cycle life, and low preparation temperature, is compatible with semiconductor processes, and is suitable for microelectronic integrated systems.

The invention belongs to the technical field of secondary batteries, and particularly relates to a nickel cobalt manganese oxide precursor and a preparation method and application thereof. According to the nickel cobalt manganese oxide precursor provided by the invention, the specific surface area of the nickel cobalt manganese oxide precursor is 50-150m < 2 > / g, and the pore volume of the nickel cobalt manganese oxide precursor is 0.1-0.5 cm < 3 > / g. Researches find that the specific surface area and the pore volume of the nickel cobalt manganese oxide precursor are limited in a specific range, a more favorable lithium intercalation path can be provided, the reaction activity of a lithium source and the nickel cobalt manganese oxide precursor in the subsequent calcination reaction process is improved, more lithium ions are intercalated into the nickel cobalt lithium manganate material, and the lithium ion battery performance is improved. And the nickel cobalt lithium manganate material with low residual alkali on the surface and excellent electrical performance can be prepared.

The utility model provides a solid-state battery and an electric device. The solid-state battery comprises an electrode assembly, the electrode assembly comprises a positive electrode layer, a negative electrode current collector and a solid-state electrolyte layer, and the solid-state electrolyte layer is located between the positive electrode layer and the negative electrode current collector; at least one surface of the negative current collector is provided with a blind hole, and the opening of the blind hole faces the solid electrolyte layer. According to the solid-state battery, the blind holes are formed in the negative current collector, so that lithium ions can be embedded into the blind holes, the embedding amount of the lithium ions in the surface of the negative current collector is reduced, and the influence of volume expansion caused by lithium ion embedding on a contact interface between the surface of a negative pole piece and a solid-state electrolyte layer is reduced; the improvement of the cycle performance of the solid-state battery is promoted.

The invention belongs to the field of batteries, and particularly discloses a positive pole piece, a preparation method of the positive pole piece, a battery, a battery pack and electric equipment. The positive electrode active material layer is arranged on at least one side of the positive electrode current collector, the positive electrode active material layer comprises ternary positive electrode material particles and a binder, and the binder is located between the different ternary positive electrode material particles and exposes part of the surfaces of the ternary positive electrode material particles; and 0.05 < = ANCM / G < = 0.58. The lithium ion intercalation and deintercalation efficiency is effectively improved, meanwhile, the ion transmission path can be optimized, the stripping force and the electrochemical activity specific surface of the positive pole piece are effectively improved, the resistivity of the positive pole piece is effectively reduced, and the service life of the positive pole piece is prolonged. Therefore, the direct current internal resistance (DCIR) of the battery using the positive pole piece can be effectively reduced, and the mixed material gram volume and the cycle performance of the battery can be effectively improved.

The application relates to the technical field of batteries and discloses a formation method of a battery and the battery. The application controls the voltage and the current of each formation process in a segmented formation mode, reduces the intensity of side reactions under high potential, effectively discharges reaction gas, avoids continuous gas production of residual active substances in a high-temperature aging stage, eliminates swelling and black spot lithium precipitation defects, and improves long-term stability of the battery; the voltage is further increased to 35%-50% of the nominal capacity, which is beneficial to battery exhaust and can control polarization of the battery to prevent capacity loss and super-thickness risk of the battery under high temperature. In addition, the application controls the current rate of the third charging to be less than the current rate of the second charging, the current rate of the second charging is less than or equal to 0.2C, increases the reaction time of the lithium supplement agent, promotes complete reaction of the lithium supplement agent, simultaneously, lithium ions are embedded into the negative electrode more slowly and uniformly in small-current charging, the risk of lithium precipitation is greatly reduced, swelling and black spot lithium precipitation defects are eliminated, and the long-term stability of the lithium ion battery is improved.

The invention provides an embedded lithium / tungsten carbide nanowire composite material as well as a preparation method and application thereof. The structure of the intercalated lithium / tungsten carbide nanowire composite material is as follows: lithium ions are intercalated into internal crystal lattices of tungsten carbide nanowires. The preparation method comprises the following steps: firstly, growing a tungsten oxide nanowire precursor on the surface of the substrate through a hydrothermal reaction; then, ethidene diamine is adopted as a carbonizer, and the tungsten oxide nanowire is converted into a tungsten carbide nanowire structure; and finally, placing the obtained tungsten carbide nanowire in an electrolyte containing lithium hexafluorophosphate, and realizing embedding of lithium ions by using an electrochemical lithium tuning technology, thereby obtaining the intercalated lithium / tungsten carbide nanowire composite structure material. The preparation method is simple in technological process, high in safety, convenient to operate and low in cost; the prepared composite structure is excellent in electro-catalytic performance and has potential wide application value.

The invention discloses a negative plate, a secondary battery and electric equipment. The negative plate comprises a current collector layer which is arranged in sequence, the first active material layer comprises a first graphite material, and the OI1 value of the first graphite material is 8-15; and the second active substance layer comprises a second graphite material and a silicon-based material, and the OI2 value is 0-8. The included angle between the first active material layer and the current collector is small, and the contact area with the current collector is increased, so that the bonding force between the active material and the current collector is enhanced, extension is reduced, and the problems of pole piece demolding and breakage are solved. Meanwhile, the included angle between the second active material layer and the current collector is increased, and the active material is approximately vertically arranged, so that a lithium ion channel is optimized, lithium deintercalation and lithium intercalation are easier, the charge-discharge performance is enhanced, and the overall expansion of lithium ion intercalation is converted into the direction parallel to the current collector from the direction perpendicular to the current collector; and meanwhile, the transverse expansion is limited by the arrangement of the graphite at the bottom layer, so that a synergistic effect is generated.

The present disclosure relates to a negative active material for a lithium secondary battery, a lithium secondary battery comprising the same, and a method of preparing the same. The negative active material comprises a coating layer self-bound to the surface of a carbonaceous material and containing porous carbon particles, thereby exhibiting reduced electrical resistance during intercalation of lithium ions on the surface of the carbonaceous material and providing improved surface reactivity and structural stability, thereby providing improved high-rate charge characteristics without causing deterioration of charge / discharge efficiency and life characteristics when used as a negative active material for a lithium secondary battery. The negative active material comprises a carbonaceous material and a carbon coating layer self-bound to the surface of the carbonaceous material. Here, the self-bound amorphous carbon coating layer can optionally have a controlled pore structure by chemical etching.

A graphite material, a preparation method therefor, a negative electrode material, and a secondary battery. The graphite material has a plurality of pores. Some of the plurality of pores have a pore size range of 2-120 nm. The total pore volume of some pores is in a range of 0.015 cm3 / g to 0.035 cm3 / g. Pores having a pore size of 2 nm or more and d1 or less account for 50% by volume of the total pore volume, wherein d1 is 75-96 nm. The pore structure of the graphite material has an appropriate pore size and pore volume. This pore structure can provide sufficient transmission channels having an appropriate width for lithium ions without remarkably affecting the capacity of a material and increase the number of sites at which lithium ions are intercalated or deintercalated and the intercalation or deintercalation rate of lithium ions. By further defining the pore size range of pores accounting for 50% by volume with respect to the total pore volume and by means of the cooperation of the pore volume and the pore size, side reactions of the negative electrode material during an electrochemical reaction can be reduced, thereby greatly improving the rate performance of the negative electrode material, thus achieving charging and discharging at a large current.

A negative electrode material, including graphite, where the negative electrode material has an I-order lithium intercalation plateau potential P1 of 30 mV to 75 mV and an II-order lithium intercalation plateau potential P2 of 90 mV to 110 mV. The use of the negative electrode material of this application can significantly improve the cycling performance of the electrochemical apparatus using the negative electrode material under high voltage and high temperature, enhance the gram capacity of the negative electrode material, while maintaining the initial efficiency of the negative electrode material.

The application belongs to the technical field of battery preparation, and particularly relates to a battery and a device. The battery comprises a negative electrode sheet, the negative electrode sheet comprises a current collector and a negative electrode active material layer arranged on at least one surface of the current collector, the negative electrode active material layer comprises a negative electrode active material, and the negative electrode active material comprises a silicon-containing material. The silicon content in the negative electrode active material layer and the elongation at break of the negative electrode current collector satisfy a specific relationship, which not only can ensure the lithium ion embedding capacity of the negative electrode while reducing the risk of negative electrode foil cracking caused by negative electrode expansion, but also can avoid the risk of positive and negative electrode short circuit caused by the negative electrode foil cracking process, thereby improving the capacity density, cycle performance and safety performance of the battery.

The invention provides a battery cell and a battery, and the battery cell comprises a positive plate which comprises a positive current collector and positive active material layers respectively arranged on at least one side of the positive current collector; the negative plate comprises a negative current collector and negative active material layers arranged on two opposite sides of the negative current collector; the diaphragms are positioned between the adjacent positive plates and negative plates; at least one groove group is formed in the side surface, deviating from the negative electrode current collector, of the negative electrode active material layer, the groove group at least comprises a first groove and a second groove, the width of the first groove is greater than that of the second groove, and / or the depth of the first groove is greater than that of the second groove. The lithium ion intercalation and deintercalation rate is improved, and the capacity and the energy density of the battery are further improved.

This invention discloses a continuous electrochemical lithium extraction device and process from salt lakes, belonging to the field of lithium extraction technology. The device employs a two-chamber structure, separated into a brine chamber and a recovery chamber by a membrane electrode assembly (MEA). By applying voltage to both the brine chamber and the recovery chamber on either side of the MEA, lithium ions are inserted into the MEA in the brine chamber and extracted from the MEA in the recovery chamber. Simultaneously, an oxygen evolution reaction occurs at the electrode in the brine chamber, and a hydrogen evolution reaction occurs at the electrode in the recovery chamber. The MEA, the two-chamber structure, and the liquid path remain fixed throughout the process, eliminating the need to move electrodes, switch chambers, or change liquid paths, thus achieving continuous operation. Furthermore, OH- is generated at the hydrogen evolution electrode in the recovery chamber. ‑ Li released from the membrane electrode + This combination forms a high-value-added lithium hydroxide solution. The device of this invention has a simple structure, is easy to operate, has a recyclable membrane electrode, high lithium-ion selectivity, no acid or alkali consumption, and is environmentally friendly. It is suitable for lithium extraction from high magnesium-to-lithium ratio salt lake brines.

The invention discloses a graphite negative electrode material and a preparation method and application thereof, and belongs to the technical field of negative electrode materials. The graphite negative electrode material comprises a plurality of composite particles, and each composite particle comprises graphite and a barium titanate coating layer located on the surface of the graphite; the relative distribution ratio average value gt of the barium titanate coating layer on the end surface of the graphite; and 50%. In the lithium ion charging and discharging process, graphite can generate volume change and generate stress, barium titanate is used as a piezoelectric material and can generate electric charges and change a lithium intercalation electric field when being stressed, so that intercalation of lithium ions is promoted, the fast charging performance of a graphite negative electrode is improved, and meanwhile, lithium deposition and lithium loss can be reduced. The barium titanate coating layer is mainly formed on the end surface of the graphite, so that the barium titanate can play a role, and unnecessary coating is reduced, thereby avoiding reduction of specific capacity and hindering of lithium ion embedding caused by excessive barium titanate. The graphite negative electrode material provided by the invention is beneficial to improving the rate capability and cycling stability of the battery.