Wu Jue, Zhang Xiaofeng, Zheng Shiyao, Liu Haodong, Wu Jinpeng, Fu Riqiang, Li Yixiao, Xiang Yuxuan, Liu Rui, Zuo Wenhua, Cui Zehao, Wu Qihui, Wu Shunqing, Chen Zonghai, Liu Ping, Yang Wanli, Yang Yong
State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, Department of Chemistry, College of Chemistry and Chemical Engineering, and College of Energy , Xiamen University , Xiamen 361005 , China.
Advanced Light Source , Lawrence Berkeley National Laboratory , One Cyclotron Road , Berkeley , California 94720 , United States.
ACS Appl Mater Interfaces. 2020 Feb 12;12(6):7277-7284. doi: 10.1021/acsami.9b21738. Epub 2020 Jan 29.
As a parent compound of Li-rich electrodes, LiMnO 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 LiMnO 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 in the protonated LiMnO 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.
作为富锂电极的母体化合物,LiMnO在首次充电时表现出高容量;然而,由于氧和表面活性,其库仑效率极低。在此,我们通过有意将质子引入LiMnO体系的锂八面体空位中,成功地优化了氧活性以实现可逆氧氧化还原反应,同时保持其原始结构完整性。结合结构探针、理论计算和共振非弹性X射线散射结果,揭示了引入的质子与氧化态晶格氧之间适度的耦合,这在充电过程中稳定了氧活性。这种耦合使得质子化LiMnO电极具有前所未有的初始库仑效率(99.2%),同时放电容量大幅提高至302 mAh g。这些发现直接证明了一种控制富锂体系中氧活性的有效概念,这对于开发电池中的高能阴极至关重要。