材料科学
兴奋剂
阴极
结构稳定性
氧化物
电极
相变
离子
电压
降级(电信)
锂(药物)
化学工程
过渡金属
格子(音乐)
光电子学
电气工程
化学
凝聚态物理
冶金
物理化学
催化作用
结构工程
工程类
内分泌学
有机化学
物理
医学
生物化学
声学
作者
Yan Mo,Lingjun Guo,Baodong Du,Hongfei Jin,Bokai Cao,Yang Lu,De Li,Yong Chen
标识
DOI:10.1016/j.jpowsour.2020.228699
摘要
Ni-based layered oxide LiNi0.8Co0.1Mn0.1O2 shows great promise for high-energy lithium-ion batteries. But the realization of its high capacity is often at the expanse of chemical and structural stability because deeply delithiation upon charge can leave the structure more vulnerable. Herein, we demonstrate that this problem can be alleviated by concurrently introducing some of Na+ and Ti4+ to obtained Li0.98Na0.01Ni0.78Co0.1Mn0.1Ti0.02O2 (NT-NCM). The co-doping successfully accelerates the phase transition process (H1 to H2 and to H3), and the enhanced reversible capacity and capacity retention at a high cut-off voltage of 4.5 V are achieved with the NT-NCM electrode. This is possible due to the less lattice stress and mechanical degradation after co-doping during prolonged cycling; the enlarged c axis distance and reduced Li+/Ni2+ mixing for doped one assist in enhancing the Li-ion transportation.
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