Patent Application
20230411607
This application claims the priority to Chinese Application No. 202211611334.3, filed on Dec. 14, 2022, the contents of which are incorporated herein by reference in their entirety.
The present disclosure generally relates to the technical field of lithium-ion battery, and in particular to a modified lithium manganese iron phosphate positive electrode material and a preparation method and an application thereof.
In recent years, the vigorous development of new energy vehicles has driven the rapid growth of demand for lithium-ion power batteries. At present, the positive electrode material of lithium-ion power battery is mainly lithium iron phosphate (LFP) and ternary material. LFP has gradually become a preferred choice of energy storage and power battery companies because of its advantages such as high cost performance, high safety and less limitation by resources. However, the energy density of the LFP is low, which has become a key factor restricting the large-scale application of lithium iron phosphate.
Lithium manganese iron phosphate (LMFP) is a positive electrode material obtained by adding manganese to LFP. The doping of manganese can make LMFP have a higher voltage platform (4.1V vs 3.4V), and the energy density of a battery can increase by 15%. LMFP is therefore a positive electrode material with great application prospects. Currently, the LMFP positive electrode material is still in an early stage of industrialization, mainly because the LMFP has low electron conductivity, a low ion diffusion rate, low initial Coulombic efficiency, and poor cycling performance, which seriously affects the commercial implementation of the LMFP. Therefore, how to improve the electron conductivity, ion transfer rate and cycling stability of the LMFP material is key issues in the current technology. At present, an effective way to solve the technical problem is to carry out an integrated modification of lattice doping and double-coating on the LMFP material.
The following is a summary of the subject matters described in detail herein. The summary is not intended to limit the protection scope of the claims.
According to the present disclosure, a modified lithium manganese iron phosphate positive electrode material includes a doped lithium manganese iron phosphate core and a coating layer disposed on a surface of the doped lithium manganese iron phosphate core, the doped lithium manganese iron phosphate core includes an Nb element, and the coating layer includes LiNbO3 and Nb2O5.
According to the present disclosure, a preparation method for the modified lithium manganese iron phosphate positive electrode material as described above includes: (1) mixing a lithium source, a manganese source, an iron source and a phosphorus source with a solvent to obtain a mixed salt solution, mixing the mixed salt solution, a niobium source and a complexing agent, and drying and sintering the mixture of the mixed salt solution, the niobium source and the complexing agent to obtain a primary sintered material; (2) mixing the primary sintered material obtained in step (1), LiNbO3, Nb2O5 with an organic solvent, and grinding; and (3) baking the material obtained after the grinding in step (2) to obtain the modified lithium manganese iron phosphate positive electrode material.
According to the present disclosure, a positive electrode includes the modified lithium manganese iron phosphate positive electrode material as described above.
According to the present disclosure, a lithium-ion battery includes the positive electrode as described above.
According to an embodiment of the present disclosure, a modified lithium manganese iron phosphate positive electrode material is prepared by a method including step (1), step (2) and step (3).
At step (1), lithium carbonate, manganese sulfate, iron powder, and phosphoric acid were weighed in a molar ratio of Li:Mn:Fe:P=1.08:0.7:0.3:1, added to deionized water, dispersed, stirred and subject to ball milling. Then niobium chloride and sodium alginate were added. The mixture was spray dried after stirring for 3 h at a stirring speed of 1000 rpm, and put into a box furnace protected by a nitrogen atmosphere, heated to 780° C. at a heating rate of 5° C., and held for 10 h to obtain a primary sintered material.
At step (2), LiNbO3 and Nb2O5 were added in a molar ratio of 1:0.25 to a high-speed mixer and mixed at a speed of 800 rpm for a mixing time of 0.5 h to obtain a coating mixture. Then the coating mixture and the primary sintered material obtained in step (1) were dispersed in an ethanol solvent, stirred and ground. The ratio of the mass of the coating mixture to the mass of the primary sintered material is 1%, the ball milling speed was 600 rpm, and the ball milling time was 2 h.
At step (3), the product was sintered in a nitrogen atmosphere at a heating rate of 8° C./min at a sintering temperature of 650° C. for a sintering time of 2 h, and then cooled to room temperature in the nitrogen atmosphere to obtain the modified lithium manganese iron phosphate positive electrode material. The modified lithium manganese iron phosphate positive electrode material has a coating layer with a thickness of 25 nm.
According to an embodiment of the present disclosure, a modified lithium manganese iron phosphate positive electrode material is prepared by a method including step (1), step (2) and step (3).
At step (1), lithium carbonate, manganese sulfate, iron powder, and phosphoric acid were weighed in a molar ratio of Li:Mn:Fe:P=1.08:0.7:0.3:1, added to deionized water, dispersed, stirred and subject to ball milling, then niobium chloride and sodium alginate were added. The mixture was spray dried after stirring for 3 h at a stirring speed of 1200 rpm, and put into a box furnace protected by a nitrogen atmosphere, heated to 790° C. at a heating rate of 8° C., and held for 9 h to obtain a primary sintered material.
At step (2), LiNbO3 and Nb2O5 were added in a molar ratio of 1:0.3 to a high-speed mixer and mixed at a speed of 850 rpm for a mixing time of 0.5 h to obtain a coating mixture. Then the coating mixture and the primary sintered material obtained in step (1) were dispersed in an ethanol solvent, stirred and ground. The ratio of the mass of the coating mixture to the mass of the primary sintered material is 1%, the ball milling speed was 600 rpm, and the ball milling time was 2 h.
At step (3), the product was sintered in a nitrogen atmosphere at a heating rate of 8° C./min at a sintering temperature of 680° C. for a sintering time of 2 h, and then cooled to room temperature in the nitrogen atmosphere to obtain the modified lithium manganese iron phosphate positive electrode material.
This example differs from Example 1 only in that the molar ratio of LiNbO3 to Nb2O5 was 1:0.05, and other conditions and parameters were exactly the same as in Example 1.
This example differs from Example 1 only in that the molar ratio of LiNbO3 and Nb2O5 was 1:0.6, and other conditions and parameters were exactly the same as in Example 1.
This comparative example differs from Example 1 only in that Nb was not doped in the core, and other conditions and parameters were exactly the same as in Example 1.
This comparative example differs from Example 1 only in that LiNbO3 was not added, and other conditions and parameters were exactly the same as in Example 1.
This comparative example differs from Example 1 only in that Nb2O5 was not added, and other conditions and parameters were exactly the same as in Example 1.
The lithium manganese iron phosphate positive electrode material prepared in each of Examples 1-4 and Comparative Examples 1-3 was selected as a positive electrode material, a graphite carbon material was selected as a negative electrode material, and a PE/PP polymer material was selected as a separator. The materials were assembled into a jelly roll by winding or laminating, packaged in an aluminum shell or an aluminum plastic film, to which a lithium-ion electrolyte composed of EC/EMC and LiPF6 was injected. Thereby, an aluminum shell or pouch lithium-ion battery was assembled. The battery was tested for its discharge rate at 3 C and the capacity retention rate after 1000 cycles at 1 C at 25° C. The test results were shown in Table 1.
From the comparison between Example 1 and Examples 3-4, it can be seen that in the modified lithium manganese iron phosphate positive electrode material according to the present disclosure, the molar ratio of LiNbO3 and Nb2O5 will affect the performance of the modified lithium manganese iron phosphate positive electrode material. When the molar ratio of LiNbO3 to Nb2O5 is controlled at 1:(0.1-0.4), the performance of the obtained positive electrode material is better. If the molar proportion of LiNbO3 is too great, the material has a poor stability, and a low cycle capacity retention rate. If the molar proportion of Nb2O5 is too great, the rate performance of the material is poor.
From the comparison between Example 1 and Comparative Example 1, it can be seen that the modified lithium manganese iron phosphate core according to the present disclosure has strong interatomic forces after Nb doping, which can stabilize the lattice structure, improve the dissolution of manganese, reduce Li/Ni mixing, and increase the diffusion coefficient of lithium ions.
From the comparison between Example 1 and Comparative Example 2, it can be seen that LiNbO3 can not only act as a physical barrier to enhance interface stability, but also act as a fast ion conductor to promote the rapid conduction of lithium ions.
From the comparison between Example 1 and Comparative Example 3, it can be seen that Nb2O5 has strong stability in a working voltage range, which can effectively inhibit a side reaction between the electrode and an electrolyte and enhance the interface stability, thus improving the cycling stability of the LMFP positive electrode material.
According to an embodiment of the present disclosure, the modified lithium manganese iron phosphate positive electrode material is doped with the Nb element, and double-coated with LiNbO3 and Nb2O5 on the surface. After the Nb doping, the material has strong interatomic forces, which can stabilize the lattice structure, improve the dissolution of manganese, reduce Li/Ni mixing, and increase the diffusion coefficient of lithium ions. Nb2O5 has strong stability in the working voltage range, which can effectively inhibit the side reaction between the electrode and an electrolyte and enhance the interface stability, thus improving the cycling stability of the LMFP positive electrode material. LiNbO3 can not only act as a physical barrier to enhance the interface stability, but also act as a fast ion conductor to promote the rapid conduction of lithium ions.
In an embodiment, the doped lithium manganese iron phosphate core has the chemical formula of LiNbaMnxFe1-xPO4, where 0<a≤0.05, and 0<x<1.
In an embodiment, the coating layer has a thickness of 10-50 nm, for example, 10 nm, 20 nm, 30 nm, 40 nm or 50 nm.
In an embodiment, the molar ratio of LiNbO3 to Nb2O5 in the coating layer is 1:(0.1-0.4) for example, 1:0.1, 1:0.15, 1:0.2, 1:0.25, 1:0.3, 1:0.35, or 1:0.4.
In an embodiment of the present disclosure, an Nb-doped LMFP is first synthesized. Then LiNbO3 and Nb2O5 are mixed in a certain proportion. Then the LMFP is dry-blended with a coating mixture, and then sintered to obtain a doped and double-coated integrated modified LMFP positive electrode material. The obtained coating layer has good uniformity, consistency and conductivity. The preparation process of the method is simple and controllable, and is easy for large-scale industrial production.
In an embodiment, the lithium source in step (1) includes lithium carbonate and/or lithium dihydrogen phosphate.
In an embodiment, the manganese source includes any one of or a combination of at least two of manganese sulfate, manganese carbonate, manganese nitrate, manganese acetate, or manganese oxalate.
In an embodiment, the iron source includes iron phosphate and/or iron powder.
In an embodiment, the phosphorus source includes phosphoric acid and/or ammonium dihydrogen phosphate.
In an embodiment, the molar ratio of elements in the mixed salt solution is Li:Mn:Fe:P=(1-1.6):x:(1-x):1, where 0<x<1.
In an embodiment, the niobium source includes any one of or a combination of at least two of niobium oxide, niobium hydroxide, niobium chloride, niobium sulfate, niobium nitrate or niobium acetate.
In an embodiment, the complexing agent includes sodium alginate.
In an embodiment, the drying in step (1) includes spray drying.
In an embodiment, the temperature of the sintering is 600-900° C., for example, 600° C., 750° C., 800° C., 850° C., or 900° C.
In an embodiment, the time of the sintering is 6-15 h, for example, 6 h, 8 h, 10 h, 12 h, or 15 h.
In an embodiment, the atmosphere for the sintering includes a nitrogen atmosphere.
In an embodiment, the organic solvent in step (2) includes ethanol.
In an embodiment, the speed of the grinding is 500-1000 rpm, for example, 500 rpm, 600 rpm, 700 rpm, 800 rpm, 900 rpm, or 1000 rpm.
In an embodiment, the time of the grinding is 0.3-1 h, for example, 0.3 h, 0.5 h, 0.6 h, 0.8 h, or 1 h.
In an embodiment, the ratio of the total mass of LiNbO3 and Nb2O5 to the mass of the primary sintered material is 0.1-10:100, for example, 0.1:100, 0.5:100, 1:100, 5:100, or 10:100, preferably 0.5-2:100.
In an embodiment, the temperature of the baking in step (3) is 200-650° C., for example, 200° C., 300° C., 400° C., 500° C. or 650° C.
In an embodiment, the time of the baking is 2-15 h, for example, 2 h, 5 h, 8 h, 10 h, or 15 h.
Compared with the related art, the present disclosure has the following beneficial effects:
| Number | Date | Country | Kind |
|---|---|---|---|
| 202211611334.3 | Dec 2022 | CN | national |
