阴极
电化学
氧气
化学物理
离子
组态熵
固溶体
格子(音乐)
材料科学
晶体结构
化学
热力学
电极
物理化学
结晶学
物理
声学
有机化学
冶金
作者
Shuyu Zhou,Yuxuan Sun,Tong Gao,Junhong Liao,Shi‐Xi Zhao,Guozhong Cao
标识
DOI:10.1002/anie.202311930
摘要
Cation-disordered Rocksalt oxides (DRXs) are a promising new class of cathode materials for Li-ion batteries due to their natural abundance, low cost and great electrochemical performance. High entropy strategy in Mn-based DRXs appears to be an effective strategy for improving the rate capability, but it suffers from challenges including capacity degradation. The present paper reports a new group of high entropy DRXs (HE DRX) based on Ni2+ -Nb5+ pair; the structural and chemical evolution upon cycling of DRXs with an increasing transition metal (TM) species are systematically investigated. An explanation is proposed for how the crystal field stability energy determines that HE DRX could exist in single Rocksalt solid solution structures. We further reveal that the charge compensation mechanism in HE DRX is the result of various TM synergistic effect. More importantly, through various in situ and ex situ techniques and theoretical calculation, the effective integration of more TM cation species within the HE DRX framework promotes better Li+ diffusion and improves lattice oxygen stability, consequently increasing capacity upon cycling.
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