Hua Weibo, Zhang Jibin, Zheng Zhuo, Liu Wenyuan, Peng Xihao, Guo Xiao-Dong, Zhong Benhe, Wang Yan-Jie, Wang Xinlong
College of Chemical Engineering, Sichuan University, No. 24 South Section 1, Yihuan Road, Chengdu, 610065, China.
Dalton Trans. 2014 Oct 21;43(39):14824-32. doi: 10.1039/c4dt01611d.
Na-doped Ni-rich LiNi0.5Co0.2Mn0.3O2 cathode material, Li0.97Na0.03Ni0.5Co0.2Mn0.3O2, is synthesized by a hydroxide co-precipitation route. The structural characterization reveals that the substitution of Na for Li results in a more ordered α-NaFeO2 structure, enlarges Li layer spacing, and reduces the degree of cation mixing. The Li0.97Na0.03Ni0.5Co0.2Mn0.3O2 material has a high tap density of 2.17 g cm(-3) that meets the commercial requirement in lithium ion batteries (LIBs). The galvanostatic charge/discharge results show that the electrochemical performance of the Li0.97Na0.03Ni0.5Co0.2Mn0.3O2 is significantly improved. At 0.2, 1, 10, 30 and 50 C, the specific capacities of the Li0.97Na0.03Ni0.5Co0.2Mn0.3O2 are 228.43, 163.12, 121.43, 95.56 and 60.09 mA h g(-1), respectively, which are superior to those of the undoped LiNi0.5Co0.2Mn0.3O2 due to the enlargement of Li layer spacing, the decreased degree of cation mixing, and the rapid diffusion of Li-ion in the bulk lattice after the substitution of Na for Li. Therefore, the Na-doped Ni-rich LiNi0.5Co0.2Mn0.3O2 material is a promising cathode candidate for the next generation of LIBs.
通过氢氧化物共沉淀法合成了钠掺杂的富镍LiNi0.5Co0.2Mn0.3O2正极材料Li0.97Na0.03Ni0.5Co0.2Mn0.3O2。结构表征表明,用钠取代锂会导致形成更有序的α-NaFeO2结构,增大锂层间距,并降低阳离子混合程度。Li0.97Na0.03Ni0.5Co0.2Mn0.3O2材料具有2.17 g cm(-3)的高振实密度,满足锂离子电池(LIBs)的商业要求。恒电流充放电结果表明,Li0.97Na0.03Ni0.5Co0.2Mn0.3O2的电化学性能得到显著改善。在0.2、1、10、30和50 C下,Li0.97Na0.03Ni0.5Co0.2Mn0.3O2的比容量分别为228.43、163.12、121.43、95.56和60.09 mA h g(-1),由于锂层间距增大、阳离子混合程度降低以及用钠取代锂后锂离子在体相晶格中的快速扩散,这些比容量优于未掺杂的LiNi0.5Co0.2Mn0.3O2。因此,钠掺杂的富镍LiNi0.5Co0.2Mn0.3O2材料是下一代LIBs有前景的正极候选材料。