法拉第效率
氧化还原
材料科学
氧气
质子化
质子
电极
化学物理
阴极
八面体
锂(药物)
化学工程
电化学
离子
结晶学
物理化学
化学
晶体结构
有机化学
医学
物理
量子力学
冶金
内分泌学
工程类
作者
Jue Wu,Xiaofeng Zhang,Shiyao Zheng,Haodong Liu,Jinpeng Wu,Riqiang Fu,Yixiao Li,Yuxuan Xiang,Rui Liu,Wenhua Zuo,Zehao Cui,Qi‐Hui Wu,Shunqing Wu,Zonghai Chen,Ping Liu,Wanli Yang,Yong Yang
标识
DOI:10.1021/acsami.9b21738
摘要
As a parent compound of Li-rich electrodes, Li2MnO3 exhibits high capacity during the initial charge; however, it suffers notoriously low Coulombic efficiency due to oxygen and surface activities. Here, we successfully optimize the oxygen activities toward reversible oxygen redox reactions by intentionally introducing protons into lithium octahedral vacancies in the Li2MnO3 system with its original structural integrity maintained. Combining structural probes, theoretical calculations, and resonant inelastic X-ray scattering results, a moderate coupling between the introduced protons and lattice oxygen at the oxidized state is revealed, which stabilizes the oxygen activities during charging. Such a coupling leads to an unprecedented initial Coulombic efficiency (99.2%) with a greatly improved discharge capacity of 302 mAh g–1 in the protonated Li2MnO3 electrodes. These findings directly demonstrate an effective concept for controlling oxygen activities in Li-rich systems, which is critical for developing high-energy cathodes in batteries.
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