Abstract: The present application provides a positive electrode active material, a positive electrode sheet and a lithium-ion battery. When the battery, which is formed by the positive electrode active material and a lithium metal negative electrode, is discharged to a discharge cut-off voltage of 3.0 V at a rate of less than 1 C after being charged to a SOC of 100% at a rate of less than 1 C with a charge cut-off voltage of 4.55 V to 4.65 V, the number N of discharge peaks in the capacity-voltage differential curve of the battery is not less than 4. Under high-voltage condition, the positive electrode active material not only has excellent specific capacity and cycling performance, but also has more prominent rate performance.

Abstract: The present application provides a positive electrode active material and its use, where the positive electrode active material includes a lithium metal oxide as shown in Formula 1 or Formula 2; in an X-ray diffraction spectrum, the lithium metal oxide has a Cmca space group of a cubic lattice structure, and has a 002 peak with a 2? of 17.9°-18.1°, and a 131 peak with a 2? of 67.0°-67.5°. The positive electrode active material of the present application is beneficial to improving the cycle performance and specific capacity of lithium-ion batteries.

Abstract: A positive electrode active material and the use thereof where the positive electrode active material includes a lithium metal oxide and a lithium-rich material. In an X-ray diffraction pattern, the lithium metal oxide is a space group Cmca of a cubic crystal system, and has a 002 peak at 2? of 17.9°-18.1° and a 131 peak at 2? of 67.0°-67.5°. The lithium-rich material is selected from at least one of Li2NiO2, Li6FeO6, Li2MoO3, Li6CoO4, Li2CuO2, Li2O, Li3N, LiF, LisAlO4, Li5FeO4, and Li2C2O4. The positive electrode active material helps to improve the specific capacity and cycle performance of batteries.

Abstract: Disclosed are a positive electrode material, and a positive electrode plate and a battery including the positive electrode material. The positive electrode material has a special phase structure distinct from that of a conventional lithium cobalt oxide material. The positive electrode material may present a plurality of small charging and discharging platforms in a charging and discharging process. Compared with a conventional high-voltage lithium cobalt oxide material, the positive electrode material exhibits the following advantage in terms of electrochemical performance: under a condition that a charge-discharge cut-off voltage and a charge and discharge rate remain the same, the positive electrode material has higher gram capacity performance and cycling performance. Specifically, compared with an undoped compound that belongs to a P63mc space group and has an O2 phase packed structure, the compound has higher gram capacity and better cycling performance due to an effect of element potassium.

Abstract: Disclosed are a negative electrode plate and a lithium-ion battery including the negative electrode plate. The negative electrode plate of the present disclosure includes a current collector, a negative electrode active layer arranged on at least one functional surface of the current collector, and a lithium source; and the negative electrode active layer includes a negative electrode active material and a polymer, the polymer includes a first structural unit, the first structural unit is selected from an olefin compound containing a substituted or unsubstituted ureido group, and the olefin compound includes at least one cyclic group. The negative electrode plate of the present disclosure can effectively supplement a lithium loss of the lithium-ion battery in an application process, so that initial charge/discharge efficiency and cycling performance of the lithium-ion battery are improved.

Abstract: The present application provides a positive electrode piece, a battery and an electric device. A first aspect of the present disclosure provides a positive electrode piece, the positive electrode piece includes a positive electrode current collector and a positive electrode active layer provided on at least one surface of the positive electrode current collector, and the positive electrode active layer includes a positive electrode active material; in a plane composed of a length direction and a thickness direction of the positive electrode piece, particles of the positive electrode active material have a longest distance a in the length direction of the positive electrode piece, and have a longest distance b in the thickness direction of the positive electrode piece, and in a region not less than 25 ?m*25 ?m, the number of the particles of the positive electrode active material meeting a/b?3 is N, where N?2.

Abstract: The present disclosure provides a positive electrode material, a battery and an electric device. A first aspect of the present disclosure provides a positive electrode material, the positive electrode material is Lin-xNaxCo1-yMeyO2, 0.7?n?1, 0<x?0.15, 0?y?0.15, and Me is selected from one or more of Al, Mg, Ti, Zr, Ni, Mn, Y, La, Sr, W, Sc, Ce, P, Nb, V, Ta, and Te; a X-ray diffraction pattern of the positive electrode material includes a peak 002 corresponding to a crystal plane 002, a peak 004 corresponding to a crystal plane 004, a peak 101 corresponding to a crystal plane 101, a peak 102 corresponding to a crystal plane 102, and a peak 103 corresponding to a crystal plane 103; a peak intensity ratio of the peak 101 to the peak 004 is m, wherein m?1.5.

Abstract: The present application discloses boron-doped lithium rich manganese based materials for cathodes of lithium ion batteries. The disclosed cathode materials can be prepared by co-precipitation and sol-gel methods. The chemical formula of this cathode material is Li[LiaMnbCocNidBx]O2 (a+b+c+d+x=1, a, b, x>0, c?0, d?0, c+d>0). Lithium ion batteries using these cathode materials show impressive improvements in performance and increased tap density at low level of boron doping. The co-precipitation method is particularly suitable for large-scale industrial production. The sol-gel method is simple and can produce fine and uniform particles.

Abstract: The present application discloses boron-doped lithium rich manganese based materials for cathodes of lithium ion batteries. The disclosed cathode materials can be prepared by co-precipitation and sol-gel methods. The chemical formula of this cathode material is Li[LiaMnbCocNidBx]O2 (a+b+c+d+x=1, a, b, x>0, c?0, d?0, c+d>0). Lithium ion batteries using these cathode materials show impressive improvements in performance and increased tap density at low level of boron doping. The co-precipitation method is particularly suitable for large-scale industrial production. The sol-gel method is simple and can produce fine and uniform particles.