材料科学
电化学
离子
氧化还原
过渡金属
阴极
空位缺陷
氧气
分析化学(期刊)
电极
无机化学
结晶学
冶金
物理化学
生物化学
色谱法
催化作用
有机化学
化学
作者
Qinchao Wang,Zulipiya Shadike,Xun‐Lu Li,Jian Bao,Qi‐Qi Qiu,Enyuan Hu,Seong‐Min Bak,Xianghui Xiao,Lu Ma,Xiaojing Wu,Xiao‐Qing Yang,Yong‐Ning Zhou
标识
DOI:10.1002/aenm.202003455
摘要
Abstract Different sodium occupancy sites in P2‐layered cathode materials can reorganize Na‐ion distribution and modify the Na + /vacancy superstructure, which have a vital impact on the Na‐ion transport and Na storage behavior during charge and discharge processes, but have not been investigated specifically and are not yet well understood. Herein, the occupancy ratio of two different Na sites (sites below transition metal ions and sites below oxygen ions along the c direction) in P2‐Na 0.67 [Mn 0.66 Ni 0.33 ]O 2 cathode is tuned successfully by inducing Sb 5+ ions with strong repulsion toward Na sites right below transition metals. It is found that the decrease of Na occupancy right below transition metal ions is beneficial to the electrochemical performance of P2‐layered cathode materials, regarding cycle stability and rate capability. In situ X‐ray absorption spectroscopy reveals that the reversible Mn 3.3+ /Mn 4+ and Ni 2+ /Ni 3+ redox couples provide charge compensation in different voltage regions of 1.8–2.3 and 2.3–4.2 V, respectively. The transmission X‐ray microscopy confirms the uniform redox reaction over the whole electrode particle. In addition, Sb substitution can suppress the “P2‐O2” phase transition in high voltage region by preventing oxygen gliding in a – b planes, thus ensuring robust structure stability during cycling.
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