Proton-Induced Disproportionation of Jahn-Teller-Active Transition-Metal Ions in Oxides Due to Electronically Driven Lattice Instability

被引:65
作者
Asl, Hooman Yaghoobnejad [1 ,2 ]
Manthiram, Arumugam [1 ,2 ]
机构
[1] Univ Texas Austin, Mat Sci & Engn Program, Austin, TX 78712 USA
[2] Univ Texas Austin, Texas Mat Inst, Austin, TX 78712 USA
关键词
MANGANESE-DIOXIDE; CATHODES; LINIO2; WATER; XRD;
D O I
10.1021/jacs.0c10044
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interfacial chemical reactivity of Jahn-Telleractive transition-metal oxides remains an enigmatic area, often leading to uncontrollable phase transformations in the oxide-based technological applications. In particular, the higher tendency of unwanted transition-metal-ion dissolution and side-reactions in Jahn-Teller-active oxides is accompanied by performance degradation in many electrochemical systems, for example, lithium-ion batteries. We show here that the fundamental electronic structure instability that leads to Jahn-Teller (lattice) distortion in an octahedral ligand field is the active chemical driving force for the spontaneous disproportionation, phase transformation, and metal-ion dissolution in transition-metal oxides upon exposure to protons. On the basis of electronic structure analyses and O-18 isotope labeling, we present a mechanism comprising a coupled acid-base/redox reaction that leads to a proton-induced disproportionation of Jahn-Teller-active transition-metal ions, as exemplified by the broad classes of respective oxides.
引用
收藏
页码:21122 / 21130
页数:9
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