材料科学
惰性
兴奋剂
亚稳态
化学物理
格子(音乐)
纳米技术
析氧
化学工程
凝聚态物理
电极
光电子学
物理化学
电化学
化学
工程类
有机化学
物理
声学
作者
Ning Qin,Qingmeng Gan,Zhaofeng Zhuang,Yanfang Wang,Yingzhi Li,Zhiqiang Li,Iftikhar Hussain,Chun Zeng,Guiyu Liu,Yunfei Bai,Kaili Zhang,Zhouguang Lu
标识
DOI:10.1002/aenm.202201549
摘要
Abstract It is highly desirable to raise the charge cutoff voltage to realize the potential of LiCoO 2 (LCO) with its ultra‐high theoretical capacity of 275 mAh g ‐1 . However, rapid fading due to structure collapse caused by the formation of the H1‐3 metastable phase and the release of surface lattice oxygen has largely hindered the operation of LCO under voltages of higher than 4.55 V. Here, stable cycling of LCO at 4.6 V through hierarchical doping engineering with inert P‐outside and active Ni‐inside dual doping is achieved. This ingenious outside‐in structure design enables Ni 2+ occupation in the Li layer in the bulk layered phase and P gradient doping at the superficial lattice. Compared with the conventional inert element substitution strategy, the doped active Ni 2+ can not only serve as a “pillar” to restrain the formation of the metastable H1‐3 phase, but also regulate the electronic structure of LCO and trigger the superexchange interaction of Ni 2+ ‐O‐Co 4+ , together with strong P–O coordination to substantially suppress the lattice oxygen escape from the surface. Therefore, it considerably reduces the risk of layer structure collapse and consequently achieves stable and high‐capacity operation over 4.6 V. This hierarchical outside‐in doping strategy may serve as inspiration for stabilizing high energy electrode materials working under high voltages.
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