CN111463410A - Positive electrode material, and preparation method and application thereof - Google Patents
Positive electrode material, and preparation method and application thereof Download PDFInfo
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- H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
- H01M4/505—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
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Abstract
The invention relates to a positive electrode material, which comprises a base material and praseodymium lithium distributed on the surface of the base material and among primary particles of the base material, wherein the chemical general formula of the base material is L izNi1‑x‑yCoxMyO2X is more than or equal to 0 and less than or equal to 0.35, y is more than or equal to 0 and less than or equal to 0.6, z is more than or equal to 0.95 and less than or equal to 1.30, M is any one or combination of at least two of Mn, Al, V, Mg, Mo, Nb and Ti, and the chemical formula of the lithium praseodymium is L iaPrOb2-a-4, wherein the molar weight of praseodymium element in the praseodymium lithium is 0.05-2.00 percent to 1 of the total molar weight of Ni, Co and M elements in the matrix material. According to the invention, the lithium praseodymium oxide is distributed on the surface of the matrix material and among primary particles of the matrix material, so that the positive electrode material is endowed with good electrochemical performance, and the capacity retention rate of 50 cycles is more than or equal to 91.6% under the current density of 1C.
Description
Technical Field
The invention belongs to the field of battery materials, and particularly relates to a positive electrode material, and a preparation method and application thereof.
Background
The intelligent equipment is diversified, and the development of the lithium ion battery is effectively promoted. Meanwhile, the vigorous development of the new energy automobile industry opens up a new blue sea for the application of lithium ion batteries. However, the duration trouble seriously affects the consumption experience. In order to be more market-friendly, the energy density of lithium ion batteries must be continuously increased.
Conventionally, the energy density of lithium ion batteries has been mainly limited by the positive electrode material. Currently, the most mature path to increase the energy density of lithium ion batteries is to accelerate the commercial application of ternary cathode materials, particularly high nickel ternary cathode materials. However, the ternary cathode material has problems in practical applications, and among them, the relatively troublesome problem is that the cycle is poor, and the reasons are mainly as follows: 1. secondary spherical particles are broken due to repeated expansion and contraction changes of the volume of the anode material in charge-discharge cycles; 2. the surface of the anode material with high reactivity has side reaction with the electrolyte, a passivation layer is generated on the surface, and the electrolyte is consumed; 3. the layered structure of the anode material is gradually transformed into a rock salt structure; 4. the reactive metal ions in the positive electrode material are dissolved in the electrolyte.
CN103855384B discloses a rare earth doped and modified lithium ion battery ternary anode material and a preparation method thereof, and the chemical general formula of the material is L iNiaCo1-a-bMnbRxO2/M, wherein 0<a<1,0<b<1,0<1-a-b<1,0.005<x<0.1, R is one or more of rare earth lanthanum, cerium, praseodymium and samarium, and M is a composite coating layer of an oxide of aluminum, titanium or magnesium and carbon. The preparation method comprises the following steps: preparing soluble metal nickel salt, cobalt salt, manganese salt and rare earth compound into mixed salt solution, reacting with mixed alkali solution prepared from NaOH and ammonia water, filtering, washingWashing, drying, ball-milling and uniformly mixing with lithium salt powder, calcining at high temperature to coat a composite coating layer containing aluminum, titanium or magnesium oxide and carbon, and calcining at constant temperature to obtain the lithium ion battery. The method has complex preparation process and cannot meet the requirement of industrial production.
CN107579224A discloses a method for preparing a nickel-cobalt-manganese ternary material doped with rare earth ions, which is characterized in that the rare earth ion-doped compound is an oxide, nitrate, oxalate, chloride or carbonate of lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, yttrium or scandium. Mixing compounds of nickel, cobalt, manganese and rare earth ions, and preparing a dried precursor through the steps of wet grinding, adding ammonia water, adding a lithium compound, aging, drying and the like. And (3) placing the dried precursor in oxygen-enriched air or pure oxygen atmosphere, and preparing the rare earth ion-doped ternary cathode material by adopting a programmed heating method or a temperature-zone-by-temperature-zone heating method, wherein the cycle performance of the material is poor.
CN103872325B discloses a preparation method of a praseodymium-cobalt-phosphorus-doped lithium manganese silicate composite anode material, wherein the chemical formula of the praseodymium-cobalt-phosphorus-doped lithium manganese silicate is L iMn1-x-yCoxPrySi1-zPzO4Wherein: x is 0.2 to 0.25, y is 0.01 to 0.02, and z is 0.22 to 0.34. The preparation method comprises the following steps: (1) preparing a praseodymium-cobalt-phosphorus doped lithium manganese silicate precursor; (2) crushing after heat treatment to obtain precursor powder, dispersing carbon black and active carbon into acetone to form conductive carbon dispersion liquid, mixing the precursor powder with the conductive carbon dispersion liquid, and ball-milling the mixture; (3) drying, and placing in CO/CO at a molar ratio of 1:12And blowing the mixture into an intermittent converter, sintering, grinding and sieving to obtain the product. According to the praseodymium-cobalt-phosphorus-doped manganese lithium silicate composite anode material prepared by the invention, rare earth elements Pr and metal elements Co are doped in the manganese lithium silicate to modify Mn, and P element is used for replacing part of Si element to improve the electronic conductivity and the material activity. The method has complex preparation process and cannot meet the requirement of industrial production.
Therefore, there is a need in the art to develop a cathode material that has good electrochemical properties, is simple in preparation process, and can be industrially produced.
Disclosure of Invention
In view of the shortcomings of the prior art, one of the objectives of the present invention is to provide a positive electrode material, which comprises a matrix material and lithium praseodymium oxide distributed on the surface of the matrix material and among primary particles of the matrix material.
In the prior art, the coating obtained by adopting a coating method is mainly distributed on the surface of the secondary particles of the material, so that the fracture of the secondary particles is not inhibited, and meanwhile, the conductivity of the coating is low, so that the diffusion of lithium ions is hindered, and the discharge specific capacity or the rate capability is reduced.
According to the invention, the lithium praseodymium oxide is distributed on the surface of the base material and among the primary particles of the base material, and has good conductivity, so that the positive electrode material can be endowed with good electrochemical performance, and is filled among the primary particles, and the connection among the primary particles is enhanced, thereby inhibiting the fragmentation of the secondary particles.
In the invention, the lithium praseodymium oxide can physically isolate the positive active material from the electrolyte, so that the surface side reaction and the dissolution of the reaction metal ions are reduced, meanwhile, the lithium praseodymium oxide can also prevent the problem of electrode pulverization caused by repeated expansion and contraction change of the volume of the material in the charge-discharge cycle, and further improve the cycle performance of the positive material, and the capacity retention rate of the positive material after 50 cycles is more than or equal to 91.6 percent under the current density of 1C.
Preferably, the chemical formula of the matrix material is L izNi1-x-yCoxMyO2Preferably 0. ltoreq. x.ltoreq.0.35, 0. ltoreq. y.ltoreq.0.6, 0.95. ltoreq. z.ltoreq.1.30, and M is any one or a combination of at least two of Mn, Al, V, Mg, Mo, Nb, and Ti.
Preferably, 0 ≦ x ≦ 0.35, such as 0.1, 0.15, 0.2, 0.25, 0.3, and so forth.
Preferably, 0. ltoreq. y.ltoreq.0.6, such as 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, etc.
Preferably, said 0.95. ltoreq. z.ltoreq.1.30, such as 1.0, 1.05, 1.10, 1.15, 1.20, 1.25, etc.
Preferably, M is any one or a combination of at least two of Mn, Al, V, Mg, Mo, Nb, and Ti, such as Mn, Al, V, and the like.
Preferably, the chemical formula of the lithium praseodymium oxide is L iaPrObPreferably 2. ltoreq.2 b-a. ltoreq.4, for example 2, 3, 4 etc.
Preferably, the ratio of the molar amount of praseodymium element in the lithium praseodymium to the total molar amount of Ni, Co and M elements in the base material is 0.05-2.00%: 1, such as 0.06%: 1, 0.13%: 1, 0.38%: 1, 0.53%: 1, 1.01%: 1, etc.
It is obvious to those skilled in the art that the total molar amount of the Ni element, the Co element, and the M element in the matrix material of the present invention represents the total molar amount of the Ni element and the M element when x is 0; when y is 0, the total molar amount of Ni element and Co element is represented; when x and y are 0 respectively, the total molar amount of Ni element is represented; when x + y is 1, the total molar amount of the Co element and the M element is represented.
The invention also aims to provide a preparation method of the cathode material, which comprises the following steps:
(1) washing the first electrode material with water, and performing solid-liquid separation to obtain a solid-phase washing product;
(2) mixing the water washing product with a praseodymium source, and drying to obtain a pre-product;
(3) and carrying out heat treatment on the pre-product in a heat treatment atmosphere to obtain the anode material.
In the prior art, L i remains after synthesis of the ternary cathode material, and this part L i is usually expressed as L iOH and L i2CO3Which in turn increases the resistance of the positive electrode active material and also causes gassing problems with the material, L iOH and L i are described herein2CO3L i contained in+Collectively referred to as freeness L i+H consumption measured by chemical titration+Freeness L i can be calculated+And (4) content.
The invention will dissociate L i+Washing the first electrode material with higher content to reduce the content of free L i in the material, and washing the first electrode material with water to obtain residual free L i in the first electrode material+Will be at L iOH and L i2CO3Is mixed with a praseodymium source to prepare the praseodymium lithium distributed on the surface of the matrix material and among primary particles of the matrix material.
Preferably, the first electrode material of step (1) of the present invention has a free L i+The content is 0.2 to 2 wt%, for example, 0.25 wt%, 0.3 wt%, 0.35 wt%, 0.4 wt%, 0.5 wt%, 0.6 wt%, 0.7 wt%, 0.8 wt%, 0.9 wt%, 1.0 wt%, 1.1 wt%, 1.2 wt%, 1.3 wt%, 1.4 wt%, 1.5 wt%, 1.6 wt%, 1.7 wt%, 1.8 wt%, 1.9 wt%, etc.
Preferably, the first electrode material includes any one or a combination of at least two of Ni element, Co element, and M element, and the M element is any one or a combination of at least two of Mn element, Al element, V element, Mg element, Mo element, Nb element, and Ti element.
The first electrode material is washed by water and mixed with a praseodymium source to remove free L i+Drying and heat treatment to obtain a matrix material in the cathode material, wherein the chemical general formula of the matrix material is L izNi1-x- yCoxMyO2Preferably 0. ltoreq. x.ltoreq.0.35, 0. ltoreq. y.ltoreq.0.6, 0.95. ltoreq. z.ltoreq.1.30, and M is any one or a combination of at least two of Mn, Al, V, Mg, Mo, Nb, and Ti.
Preferably, the temperature of the water washing is 10 to 40 ℃, for example, 15 ℃, 20 ℃, 25 ℃, 30 ℃, 35 ℃ and the like.
Preferably, the time of the water washing is 5-50 min, such as 10min, 20min, 30min, 40min and the like.
Preferably, the mass ratio of the first electrode material to water in the water washing process is 0.5-4: 1, such as 1:1, 1.5:1, 2:1, 2.5:1, 3:1, 3.4:1, and the like.
Preferably, the water content in the water-washed product is 5-15 wt%, such as 7 wt%, 8 wt%, 10 wt%, 12 wt%, 14 wt%, etc.
The water content of the water-washed product is 5-15 wt%, so that a praseodymium source can be better dispersed and infiltrated into the surface of the first electrode material and primary particles after water washing.
Preferably, the water washed product in the step (2) has free L i+The molar ratio of the praseodymium source to the praseodymium element is 1.0-8.0: 1, for example, 2.0:1, 3.0:1, 4.0:1, 5.0:1, 6.0:1, 7.0:1, etc.
Free L i+If the molar ratio of the medium lithium element to the praseodymium element in the praseodymium source is more than 8.0:1, the remaining free L i+More positive active material, and the impedance of the positive active material may increase and aggravate the gas generation problem in the electrochemical reaction process, resulting in poor electrochemical performance of the material, free L i+If the molar ratio of the medium lithium element to the praseodymium element in the praseodymium source is less than 1:1, the praseodymium element will form praseodymium oxide, resulting in poor ion conductivity.
Preferably, the mixing mode of the water washing product and the praseodymium source is ball milling mixing or stirring mixing.
Preferably, the praseodymium source includes any one or a combination of at least two of praseodymium oxide, praseodymium nitrate and praseodymium carbonate.
Preferably, the drying temperature is 60 to 90 ℃, such as 65 ℃, 70 ℃, 75 ℃, 80 ℃, 85 ℃ and the like.
According to the invention, the water evaporation rate of the material is strictly controlled in the drying process, so that the dispersibility of the praseodymium source between the surface of the positive electrode material and primary particles is good, the drying temperature is less than 60 ℃, the water evaporation of the material is too slow, the reaction time is longer, and the industrial production is influenced; the drying temperature is higher than 90 ℃, the water in the material is evaporated too fast, and the dispersibility of the praseodymium source on the surface of the anode material and between primary particles is poor.
Preferably, the drying time is 0.5-5 h, such as 1h, 1.5h, 2h, 2.5h, 3h, 3.5h, 4h, 4.5h and the like.
Preferably, the temperature of the heat treatment in the step (3) is 500 to 700 ℃, for example 550 ℃, 600 ℃, 650 ℃ and the like.
Preferably, the time of the heat treatment is 5-15 h, such as 6h, 7h, 8h, 9h, 10h, 11h, 12h, 13h, 14h and the like.
Preferably, the heat treatment atmosphere includes an oxygen atmosphere or a decarbonated air atmosphere.
The decarbonated air atmosphere in the present invention means an atmosphere obtained by removing carbon dioxide from air.
The invention controls the content of carbon dioxide in the atmosphere during the heat treatment process so as to prevent the carbon dioxide and the electrode material from generating new L i2CO3By-products.
As one of preferable technical solutions, the preparation method of the cathode material of the present invention includes the following steps:
(1) according to the mass ratio of the first electrode material to water of 0.5-4: 1, dissociating L i+Washing the first electrode material with the content of 0.2-2 wt% for 5-50 min at the temperature of 10-40 ℃, and performing solid-liquid separation to obtain a solid-phase washing product with the water content of 5-15 wt%;
(2) ball-milling and mixing the water washing product with a praseodymium source, wherein the water washing product is free L i+The molar ratio of the precursor to praseodymium element in a praseodymium source is 1.0-8.0: 1, and the precursor is dried at the temperature of 60-90 ℃ for 0.5-5 hours to obtain a pre-product;
(3) and carrying out heat treatment on the pre-product for 5-15 h at 500-700 ℃ in an oxygen atmosphere to obtain the anode material.
The invention also aims to provide a preparation method of the cathode material, which comprises the following steps:
(1) dissolving a praseodymium source and a lithium source in water to prepare a mixed solution;
(2) adding the mixed solution into a second electrode material to obtain an electrode material mixed solution, and drying to obtain a pre-product;
(3) and carrying out heat treatment on the pre-product in a heat treatment atmosphere to obtain the anode material.
Free L i in the second electrode material according to the invention+The content is less, so a praseodymium source and a lithium source are added into the second electrode material in a mode of adding the praseodymium source and the lithium source to prepare the cathode material.
According to the invention, the mixed solution containing the praseodymium source and the lithium source is mixed with the second electrode material solution, so that the praseodymium source and the lithium source are better dispersed and infiltrated between the surface of the second electrode material and primary particles.
Preferably, step (2) of the present inventionDissociation L i of the second electrode material+The content is < 0.2 wt%, such as 0.01 wt%, 0.05 wt%, 0.12 wt%, 0.15 wt%, etc.
Preferably, in the step (1), the molar ratio of the lithium element in the lithium source to the praseodymium element in the praseodymium source is 1.0-8.0: 1, such as 2.0:1, 3.0:1, 4.0:1, 5.0:1, 6.0:1, 7.0:1, and the like.
Preferably, the mass ratio of the total mass of the praseodymium source and the lithium source to the water is 0.1-5: 1, such as 0.5:1, 1:1, 1.5:1, 2:1, 2.5:1, 3:1, 3.5:1, 4:1, 4.5:1, and the like.
Preferably, the praseodymium source includes any one or a combination of at least two of praseodymium oxide, praseodymium nitrate and praseodymium carbonate, such as praseodymium nitrate, praseodymium carbonate, and the like.
The praseodymium source does not generate impurities which are difficult to decompose after being introduced.
Preferably, the lithium source includes any one of lithium hydroxide, lithium carbonate, lithium nitrate, lithium acetate and lithium oxalate or a combination of at least two thereof, for example, lithium hydroxide, lithium carbonate, lithium nitrate and the like.
Preferably, the second electrode material includes any one or a combination of at least two of Ni element, Co element, and M element, and the M element is any one or a combination of at least two of Mn element, Al element, V element, Mg element, Mo element, Nb element, and Ti element.
The second electrode material is dried, thermally treated and the like according to the preparation method to obtain a base material in the anode material, wherein the chemical general formula of the base material is L izNi1-x-yCoxMyO2Preferably 0. ltoreq. x.ltoreq.0.35, 0. ltoreq. y.ltoreq.0.6, 0.95. ltoreq. z.ltoreq.1.30, and M is any one or a combination of at least two of Mn, Al, V, Mg, Mo, Nb, and Ti.
Preferably, the ratio of the praseodymium element in the electrode material mixture in step (2) to the total molar amount of the Ni element, Co element and M element in the second electrode material is 0.05% -2% to 1, such as 0.08% to 1, 0.1% to 1, 0.25% to 1, 0.5% to 1, 1% to 1, 1.2% to 1, 1.5% to 1, 1.8% to 1, and so on.
The total molar weight of Ni element, Co element and M element in the second electrode material represents the total molar weight of Ni element and M element when the content of Co element in the second electrode material is 0; when the content of the M element in the second electrode material is 0, the total molar quantity of the Ni and the Co elements is represented; when the contents of Co element and M element in the second electrode material are respectively 0, the Ni element represents the molar weight; when the content of the Ni element is 0, it represents the total molar amount of the Co element and the M element.
Preferably, the mass ratio of the mixed solution to the second electrode material in the step (2) is 0.05-0.15: 1, such as 0.06:1, 0.08:1, 0.1:1, 0.12:1, 0.14:1, etc.
Preferably, the drying temperature is 60 to 90 ℃, such as 65 ℃, 70 ℃, 75 ℃, 80 ℃, 85 ℃ and the like.
The drying temperature is less than 60 ℃, the evaporation of the water in the material is too slow, the reaction time is longer, and the industrial production is influenced; the drying temperature is higher than 90 ℃, the water in the material is evaporated too fast, and the dispersibility of the praseodymium source on the surface of the anode material and between primary particles is poor.
The invention strictly controls the drying rate so as to ensure that the praseodymium source has good dispersibility on the surface of the cathode material and between primary particles.
Preferably, the drying time is 0.5-5 h, such as 1h, 1.5h, 2h, 2.5h, 3h, 3.5h, 4h, 4.5h and the like.
Preferably, the temperature of the heat treatment in the step (4) is 500-700 ℃, such as 550 ℃, 600 ℃, 650 ℃ and the like.
Preferably, the time of the heat treatment is 5-15 h, such as 6h, 7h, 8h, 9h, 10h, 11h, 12h, 13h, 14h and the like.
Preferably, the heat treatment atmosphere includes an oxygen atmosphere or a decarbonated air atmosphere.
The invention strictly controls the content of carbon dioxide in the atmosphere in the heat treatment process and avoids the regeneration of the byproduct L i2CO3。
As a second preferred technical solution, the preparation method of the positive electrode material of the present invention comprises the following steps:
(1) dissolving a praseodymium source and a lithium source in water according to the molar ratio of the lithium element in the lithium source to the praseodymium element in the praseodymium source of 1.0-8.0: 1 to prepare a mixed solution;
(2) according to the mass ratio of the mixed liquid to the second electrode material of 0.05-0.15: 1 and the mass ratio of praseodymium element to the total molar weight of Ni element, Co element and M element in the second electrode material of 0.05-2%: 1, free L i+Adding a second electrode material with the content of less than 0.2 wt% into the mixed solution, and drying at 60-90 ℃ for 0.5-5 h to obtain a pre-product;
(3) and carrying out heat treatment on the pre-product for 5-15 h at 500-700 ℃ in an oxygen atmosphere to obtain the anode material.
The invention also provides the use of the positive electrode material as one of the purposes, and the positive electrode material is applied to the field of batteries, preferably the field of positive electrode materials of lithium ion batteries.
The fifth purpose of the invention is to provide a lithium ion battery, which comprises the cathode material of one purpose.
Preferably, the lithium ion positive electrode material is one of the positive electrode materials described above.
Compared with the prior art, the invention has the following beneficial effects:
(1) according to the invention, the lithium praseodymium oxide is distributed on the surface of the matrix material and among primary particles of the matrix material, so that the positive electrode material is endowed with good electrochemical performance, and the capacity retention rate of the positive electrode material after 50 cycles is more than or equal to 91.6% under the current density of 1C.
(2) The invention will dissociate L i+The first electrode material with higher content is washed by water to reduce the content of free L i in the material and reduce the residual free L i+Mixing with praseodymium source to obtain praseodymium lithium distributed on the surface of the matrix material and among primary particles of the matrix material, wherein the praseodymium lithium is free L i+The second electrode material with low content adopts a mode of adding a praseodymium source and a lithium source, and the praseodymium source and the lithium source are added into the second electrode material, so that the prepared positive electrode material has good electrochemical performance.
(3) In a further preferable technical scheme, the invention controls the free L i in the first electrode material after water washing by controlling the temperature and time of water washing+Content, eliminationExcess free L i+Thereby reducing the impedance of the anode material; according to the invention, the water content in the water-washed product is 5-15 wt%, so that a praseodymium source can be better dispersed and infiltrated into the surface of the first electrode material after water washing and between primary particles, and the cycle performance of the material is improved; the invention strictly controls the water evaporation rate of the material in the drying process, thereby ensuring that the praseodymium source has good dispersibility between the surface of the anode material and primary particles, and further improving the cycle performance of the material.
Drawings
Fig. 1 is an SEM image of the positive electrode material obtained in example 1 of the present invention.
Fig. 2 is an SEM image of the positive electrode material obtained in comparative example 1 of the present invention.
Detailed Description
For the purpose of facilitating an understanding of the present invention, the present invention will now be described by way of examples. It should be understood by those skilled in the art that the examples are only for the understanding of the present invention and should not be construed as the specific limitations of the present invention.
Example 1
The preparation method of the cathode material comprises the following steps:
(1) press L iNi0.8Co0.1Mn0.1O2The mass ratio of the active component to the water is 3.4:1, and the content of free L i is 0.5 wt% of L iNi0.8Co0.1Mn0.1O2Washing with water at 30 deg.C for 30min, and performing solid-liquid separation to obtain solid-phase washing product with water content of 10 wt%;
(2) mixing the water-washed product with Pr2O3Ball milling and mixing, and separating L i in the water washing product+And Pr2O3The molar ratio of the medium praseodymium element is 4.0:1, and a pre-product is obtained after drying for 4 hours at 70 ℃;
(3) and (2) carrying out heat treatment on the pre-product in an oxygen atmosphere at 600 ℃ for 10h to obtain an SEM image of the cathode material as shown in figure 1, wherein the ratio of the molar weight of praseodymium to the total molar weight of Ni, Co and Mn in the matrix material is 0.13%: 1, and the cathode material has uniform particle size distribution, the particle size is 10-20 mu m and a coating layer is arranged on the surface.
Example 2
The difference from example 1 is that the product of step (2) water washing is free L i+And Pr2O3The molar ratio of the praseodymium element in the positive electrode material is 1.0:1, and the molar ratio of the molar amount of the praseodymium element in the positive electrode material to the total molar amount of the Ni, Co and Mn elements in the matrix material is 0.52 percent to 1.
Example 3
The difference from example 1 is that the product of step (2) water washing is free L i+And Pr2O3The molar ratio of the praseodymium element in the positive electrode material is 8.0:1, and the molar ratio of the molar amount of the praseodymium element in the positive electrode material to the total molar amount of the Ni, Co and Mn elements in the matrix material is 0.06: 1.
Example 4
The difference from example 1 is that the product of step (2) water washing is free L i+And Pr2O3The molar ratio of the praseodymium element in the positive electrode material is 0.5:1, and the molar ratio of the molar amount of the praseodymium element in the positive electrode material to the total molar amount of the Ni, Co and Mn elements in the matrix material is 1.01: 1.
Example 5
The difference from example 1 is that the product of step (2) water washing is free L i+And Pr2O3The molar ratio of the medium praseodymium element is 9.0:1, and the molar ratio of the molar amount of the praseodymium element in the positive electrode material to the total molar amount of the Ni, Co and Mn elements in the matrix material is 0.06: 1.
Example 6
The preparation method of the cathode material comprises the following steps:
(1) press L iNi0.8Co0.1Al0.1O2The mass ratio of the free L i to the water is 4:1+L iNi in an amount of 0.35 wt%0.8Co0.1Al0.1O2Washing with water at 10 deg.C for 50min, and performing solid-liquid separation to obtain solid phase washing product with water content of 5 wt%;
(2) ball-milling and mixing the water washing product with praseodymium nitrate, wherein the water washing product contains free L i+The molar ratio of the precursor to praseodymium element in praseodymium nitrate is 4.0:1, and a pre-product is obtained after drying for 5 hours at 60 ℃;
(3) and (3) carrying out heat treatment on the pre-product for 15h at 500 ℃ in an oxygen atmosphere to obtain a positive electrode material, wherein the molar weight ratio of praseodymium to the total molar weight of Ni, Co and Al elements in the matrix material is 0.09%: 1.
Example 7
The preparation method of the cathode material comprises the following steps:
(1) press L iNi0.8Co0.1Al0.1O2The mass ratio of the free L i to the water is 4:1+L iNi in an amount of 0.35 wt%0.8Co0.1Al0.1O2Washing with water at 10 deg.C for 50min, and performing solid-liquid separation to obtain solid phase washing product with water content of 5 wt%;
(2) ball-milling and mixing the water washing product with praseodymium nitrate, wherein the water washing product contains free L i+The molar ratio of the precursor to praseodymium element in praseodymium nitrate is 1:1, and the precursor is obtained after drying for 5 hours at 60 ℃;
(3) and (3) carrying out heat treatment on the pre-product for 15h at 500 ℃ in an oxygen atmosphere to obtain a positive electrode material with the molar weight of praseodymium element and the total molar weight of Ni, Co and Al elements in the matrix material being 0.38% to 1.
Example 8
The preparation method of the cathode material comprises the following steps:
(1) according to the lithium element and Pr in the lithium hydroxide2O3The mole ratio of the medium praseodymium element is 4.0:1, and the medium praseodymium element is formed by adding Pr2O3And lithium hydroxide are dissolved in water to prepare a mixed solution;
(2) according to the mixture ratio of L iNi0.6Co0.2Mn0.2O2Has a mass ratio of 0.1:1, Pr2O3Praseodymium (III) element and L iNi0.6Co0.2Mn0.2O2The total molar weight of Ni element, Co element and Mn element is 0.1%: 1, free L i+L iNi in an amount of 0.1 wt%0.6Co0.2Mn0.2O2Adding the mixture into the mixed solution, and drying the mixture for 3 hours at 70 ℃ to obtain a pre-product;
(3) and carrying out heat treatment on the pre-product for 10h at 600 ℃ in an oxygen atmosphere to obtain the anode material.
Example 9
The difference from example 8 is that lithium element and Pr in the lithium hydroxide of step (1)2O3The molar ratio of the medium praseodymium element is 1.0: 1.
Example 10
The difference from example 8 is that lithium element and Pr in the lithium hydroxide of step (1)2O3The molar ratio of the medium praseodymium element is 8.0: 1.
Example 11
The difference from example 8 is that lithium element and Pr in the lithium hydroxide of step (1)2O3The molar ratio of the medium praseodymium element is 0.5: 1.
Example 12
The difference from example 8 is that lithium element and Pr in the lithium hydroxide of step (1)2O3The molar ratio of the medium praseodymium element is 9.0: 1.
Example 13
Differs from example 8 in the step (2) Pr2O3Praseodymium (III) element and L iNi0.6Co0.2Mn0.2O2The total molar weight ratio of Ni element, Co element and Mn element is 0.05%: 1.
Example 14
Differs from example 8 in the step (2) Pr2O3Praseodymium (III) element and L iNi0.6Co0.2Mn0.2O2The total molar weight ratio of Ni element, Co element and Mn element is 0.5% to 1.
Example 15
Differs from example 8 in the step (2) Pr2O3Praseodymium (III) element and L iNi0.6Co0.2Mn0.2O2The total molar weight ratio of Ni element, Co element and Mn element is 1% to 1.
Example 16
Differs from example 8 in the step (2) Pr2O3Praseodymium (III) element and L iNi0.6Co0.2Mn0.2O2The total molar weight ratio of Ni element, Co element and Mn element is 2% to 1.
Comparative example 1
Zone of example 1Except that no Pr is added in the step (2)2O3The SEM image of the prepared cathode material is shown in FIG. 2, and it can be seen that the cathode material is easy to agglomerate to generate large particles with the particle size of 10-40 μm, and the surface of the cathode material is free of a coating layer.
Comparative example 2
The difference from example 8 is that no Pr was added in step (1)2O3。
Comparative example 3
The preparation method of the cathode material comprises the following steps:
(1) mixing nickel salt, cobalt salt, manganese salt and praseodymium salt according to the metal molar ratio of 0.75:0.1:0.1:0.05, dissolving the mixture in deionized water to prepare a mixed salt solution with the concentration of 1 mol/L, and mixing the mixed salt solution, a 2 mol/L precipitator NaOH solution and a complexing agent NH 323·H2The O solution is cocurrent flowed with the three, added into a reactor which takes NaOH solution with pH of 11.25 as base solution, the pH is controlled to be kept at 11.25 plus or minus 0.05 all the time, stirred and reacted for 24 hours at 50 ℃, overflowed to obtain product slurry, the product slurry is aged for 20 hours, and filtered to obtain Ni0.75Co0.1Mn0.1Pr0.05(OH)2A multi-element precursor;
(2) mixing the multi-element precursor with L iOH according to the metal molar ratio of 1:1.05, putting the mixture into a sintering furnace for sintering, pretreating at 580 ℃ for 5 hours, grinding for 0.5 hour, then roasting at 930 ℃ for 16 hours, controlling the oxygen content to be more than 40 vol%, and controlling the furnace pressure to be 2.0MPa to obtain a sintered crude product;
(4) grinding and screening the crude product to obtain a finished product of the monocrystal-like multi-component material with a chemical formula of L i1.02Ni0.75Co0.1Mn0.1Pr0.05O2。
And (3) performance testing:
the prepared positive electrode material is subjected to the following performance tests:
(1) the battery assembly is that the anode material prepared by the invention is made into an anode plate, the cathode is a metal lithium plate, the diaphragm is Celgard2400, and the electrolyte is L iPF of 1 mol/L6and/DMC + DEC, assembling to obtain CR2025 button cell. The preparation process of the positive pole piece comprises the following steps:mixing the prepared positive electrode material, conductive agent acetylene black and binder PVDF (polyvinylidene fluoride) according to the mass ratio of 90:5:5, using N-methylpyrrolidone NMP as a solvent to prepare slurry, coating the slurry on an aluminum foil, drying the aluminum foil at 120 ℃ for 12 hours, and rolling and punching the aluminum foil into a wafer with the diameter of 8.4mm to be used as a positive electrode piece.
(2) Electrochemical test, namely testing the prepared button cell on a test system L AND battery of Wuhanjinnuo electronics Limited under a normal temperature condition, wherein a charging AND discharging voltage interval is 3.0-4.3V, a 1C current density is defined as 200 mA/g.50-cycle retention ratio which is the specific discharge capacity/the specific discharge capacity of 50 cycles, in the table, 0.1C/0.1C represents that the button cell is charged to a charging cut-off voltage under the current density of 0.1C AND is discharged to the discharge cut-off voltage under the current density of 0.1C, 0.5C/0.5C represents that the button cell is charged to the charging cut-off voltage under the current density of 0.5C, the button cell is discharged to the discharge cut-off voltage under the current density of 0.5C AND is discharged to the discharge cut-off voltage under the current density of 0.5C, AND 0.5C/1C represents that the button cell is charged to the discharge cut-off voltage under the current density of 0.5C AND is discharged to the specific discharge voltage under the charge cut-off voltage under the current density of 0.5C AND is discharged to the discharge specific discharge voltage under the charge cut-off voltage under the charge density of 0.5C.
TABLE 1
As can be seen from Table 1, in the embodiments 1 to 16, lithium praseodymium oxide is distributed on the surface of the matrix material and among primary particles of the matrix material, so that the prepared material has excellent cycle performance, the 50-week capacity retention rate is more than or equal to 91.6% under the condition of 0.5C/1C, the comprehensive electrochemical performance of the embodiment 1 is the best, and the 50-week capacity retention rate is more than 96% under the condition of 0.5C/1C.
As can be seen from Table 1, example 4 was compared with example 1 at 0.1C/0.1C, 0.5C/0.5C, 0.5C/1C and 0.5C/2The lower first discharge specific capacity under C probably due to the addition of Pr in example 42O3The content is too high, so that the active capacity of electrochemical reaction is low, and the first discharge specific capacity of the prepared material is low.
As can be seen from Table 1, the capacity retention rate at 50 weeks is lower in example 5 than in example 1 under the condition of 0.5C/1C, probably because Pr in example 52O3The content is too low, and the content of the praseodymium lithium generated by the reaction is too low, so that the isolation between the positive active material and the electrolyte is poor, the cycle performance of the material is poor, and the capacity retention rate is low.
As can be seen from Table 1, in example 11, the specific first discharge capacity was lower under the conditions of 0.1C/0.1C, 0.5C/0.5C, 0.5C/1C and 0.5C/2C than that of example 8, probably because of the free L i in example 11+The content is too low, so that the active capacity of electrochemical reaction is low, and the first discharge specific capacity of the prepared material is low.
As can be seen from Table 1, in example 12, the 50-week capacity retention was lower than that in example 8 under the 0.5C/1C condition, probably because Pr in example 52O3The content is too low, and the content of the lithium praseodymium generated by the reaction is too low, so that the isolation between the positive active material and the electrolyte is poor, side reactions and metal ions are dissolved out more, the cycle performance of the material is poor, and the capacity retention rate is low.
As can be seen from Table 1, in comparative example 1, the 50-week capacity retention ratio was too low at 0.5C/1C compared to that of example 1, probably because no Pr was added in comparative example 12O3On the contrary, the water washing exposes more active surfaces, which causes the side reaction to be intensified during the electrochemical reaction, and further the impedance of the anode active material is increased faster, so the cycle performance of the anode material is poor, and the specific discharge capacity is lower.
As can be seen from Table 1, comparative example 2 has a lower specific discharge capacity at 0.1C/0.1C, 0.5C/0.5C, 0.5C/1C and 0.5C/2C than example 8, and a lower capacity retention at 50 weeks at 0.5C/1C, probably because no Pr was added in comparative example 22O3The side reactions are more during the electrochemical reaction, and the impedance of the positive active material is increased faster, so the cycle performance of the positive material is poor, and the specific discharge capacity is lower.
As can be seen from Table 1, in comparative example 3, the first discharge specific capacity was lower under the conditions of 0.1C/0.1C, 0.5C/0.5C, 0.5C/1C and 0.5C/2C and the 50-cycle capacity retention was lower under the condition of 0.5C/1C, compared with those of example 1 and example 8, probably because the praseodymium element existed in the form of element doping in the positive electrode material L i in comparative example 31.02Ni0.75Co0.1Mn0.1Pr0.05O2In the method, the occurrence of side reactions on the surface of the positive electrode cannot be reduced, and meanwhile, praseodymium element cannot play a role in improving the capacity, so that the comparative example 3 has poor cycle performance and lower specific discharge capacity compared with the examples 1 and 8.
The applicant states that the present invention is illustrated by the above examples to show the detailed process equipment and process flow of the present invention, but the present invention is not limited to the above detailed process equipment and process flow, i.e. it does not mean that the present invention must rely on the above detailed process equipment and process flow to be implemented. It should be understood by those skilled in the art that any modification of the present invention, equivalent substitutions of the raw materials of the product of the present invention, addition of auxiliary components, selection of specific modes, etc., are within the scope and disclosure of the present invention.
Claims (10)
1. A positive electrode material is characterized by comprising a base material and lithium praseodymium oxide distributed on the surface of the base material and among primary particles of the base material.
2. The positive electrode material according to claim 1, wherein the base material has a chemical formula of L izNi1-x- yCoxMyO2Preferably, x is more than or equal to 0 and less than or equal to 0.35, y is more than or equal to 0 and less than or equal to 0.6, z is more than or equal to 0.95 and less than or equal to 1.30, and M is any one or the combination of at least two of Mn, Al, V, Mg, Mo, Nb and Ti;
preferably, the chemical formula of the lithium praseodymium oxide is L iaPrObPreferably 2. ltoreq. 2 b-a. ltoreq.4;
preferably, the ratio of the molar weight of the praseodymium element in the praseodymium lithium to the total molar weight of the Ni element, the Co element and the M element in the base material is 0.05-2.00%: 1.
3. A method for producing the positive electrode material according to claim 1 or 2, characterized by comprising the steps of:
(1) washing the first electrode material with water, and performing solid-liquid separation to obtain a solid-phase washing product;
(2) mixing the water washing product with a praseodymium source, and drying to obtain a pre-product;
(3) and carrying out heat treatment on the pre-product in a heat treatment atmosphere to obtain the anode material.
4. The method of claim 3, wherein the first electrode material of step (1) has free L i radicals+The content is 0.2-2 wt%;
preferably, the first electrode material includes any one or a combination of at least two of Ni element, Co element, and M element, the M element being any one or a combination of at least two of Mn element, Al element, V element, Mg element, Mo element, Nb element, and Ti element;
preferably, the temperature of the water washing is 10-40 ℃;
preferably, the time of water washing is 5-50 min;
preferably, the mass ratio of the first electrode material to water in the water washing process is 0.5-4: 1;
preferably, the water content of the water washing product is 5-15 wt%;
preferably, the water washed product in the step (2) has free L i+The molar ratio of the praseodymium source to praseodymium element in the praseodymium source is 1.0-8.0: 1;
preferably, the mixing mode of the water washing product and the praseodymium source is ball milling mixing or stirring mixing;
preferably, the praseodymium source comprises any one or a combination of at least two of praseodymium oxide, praseodymium nitrate and praseodymium carbonate;
preferably, the drying temperature is 60-90 ℃;
preferably, the drying time is 0.5-5 h;
preferably, the temperature of the heat treatment in the step (3) is 500-700 ℃;
preferably, the heat treatment time is 5-15 h;
preferably, the heat treatment atmosphere includes an oxygen atmosphere or a decarbonated air atmosphere.
5. The method for producing a positive electrode material according to claim 3 or 4, comprising the steps of:
(1) according to the mass ratio of the first electrode material to water of 0.5-4: 1, dissociating L i+Washing the first electrode material with the content of 0.2-2 wt% for 5-50 min at the temperature of 10-40 ℃, and performing solid-liquid separation to obtain a solid-phase washing product with the water content of 5-15 wt%;
(2) ball-milling and mixing the water washing product with a praseodymium source, wherein the water washing product is free L i+The molar ratio of the precursor to praseodymium element in a praseodymium source is 1.0-8.0: 1, and the precursor is dried at the temperature of 60-90 ℃ for 0.5-5 hours to obtain a pre-product;
(3) and carrying out heat treatment on the pre-product for 5-15 h at 500-700 ℃ in an oxygen atmosphere to obtain the anode material.
6. A method for producing a positive electrode material according to claim 1 or 2, comprising the steps of:
(1) dissolving a praseodymium source and a lithium source in water to prepare a mixed solution;
(2) adding the mixed solution into a second electrode material to obtain an electrode material mixed solution, and drying to obtain a pre-product;
(3) and carrying out heat treatment on the pre-product in a heat treatment atmosphere to obtain the anode material.
7. The method of claim 6, wherein the second electrode material of step (2) is free L i+The content is less than 0.2 wt%;
preferably, the molar ratio of the lithium element in the lithium source to the praseodymium element in the praseodymium source in the step (1) is 1.0-8.0: 1;
preferably, the mass ratio of the total mass of the praseodymium source and the lithium source to the water is 0.1-5: 1;
preferably, the praseodymium source comprises any one or a combination of at least two of praseodymium oxide, praseodymium nitrate and praseodymium carbonate;
preferably, the lithium source comprises any one of lithium hydroxide, lithium carbonate, lithium nitrate, lithium acetate and lithium oxalate or a combination of at least two thereof;
preferably, the second electrode material includes any one or a combination of at least two of Ni element, Co element, and M element, the M element being any one or a combination of at least two of Mn element, Al element, V element, Mg element, Mo element, Nb element, and Ti element;
preferably, the ratio of praseodymium element in the electrode material mixed solution in the step (2) to the total molar weight of Ni element, Co element and M element in the second electrode material is 0.05% -2%: 1;
preferably, the mass ratio of the mixed solution to the second electrode material in the step (2) is 0.05-0.15: 1;
preferably, the drying temperature is 60-90 ℃;
preferably, the drying time is 0.5-5 h;
preferably, the temperature of the heat treatment in the step (4) is 500-700 ℃;
preferably, the heat treatment time is 5-15 h;
preferably, the heat treatment atmosphere includes an oxygen atmosphere or a decarbonated air atmosphere.
8. The method for producing a positive electrode material according to claim 6 or 7, comprising the steps of:
(1) dissolving a praseodymium source and a lithium source in water according to the molar ratio of the lithium element in the lithium source to the praseodymium element in the praseodymium source of 1.0-8.0: 1 to prepare a mixed solution;
(2) according to the mixed liquidThe mass ratio of the praseodymium element to the total molar amount of the Ni element, the Co element and the M element in the second electrode material is 0.05-2%: 1, and L i is dissociated+Adding a second electrode material with the content of less than 0.2 wt% into the mixed solution, and drying at 60-90 ℃ for 0.5-5 h to obtain a pre-product;
(3) and carrying out heat treatment on the pre-product for 5-15 h at 500-700 ℃ in an oxygen atmosphere to obtain the anode material.
9. Use of a positive electrode material according to claim 1 or 2, in the field of batteries, preferably in the field of positive electrode materials for lithium ion batteries.
10. A lithium ion battery, characterized in that the lithium ion battery comprises the positive electrode material according to claim 1 or 2;
preferably, the lithium ion battery cathode material is the cathode material of claim 1 or 2.
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