溶解
电池(电)
电解质
阴极
电极
材料科学
同步加速器
化学工程
化学物理
过渡金属
表征(材料科学)
纳米技术
化学
物理化学
热力学
催化作用
工程类
功率(物理)
核物理学
物理
生物化学
作者
Yuxin Zhang,Anyang Hu,Dawei Xia,Sooyeon Hwang,Sami Sainio,Dennis Nordlund,F. Marc Michel,Robert B. Moore,Luxi Li,Feng Lin
标识
DOI:10.1038/s41565-023-01367-6
摘要
Mn dissolution has been a long-standing, ubiquitous issue that negatively impacts the performance of Mn-based battery materials. Mn dissolution involves complex chemical and structural transformations at the electrode-electrolyte interface. The continuously evolving electrode-electrolyte interface has posed great challenges for characterizing the dynamic interfacial process and quantitatively establishing the correlation with battery performance. In this study, we visualize and quantify the temporally and spatially resolved Mn dissolution/redeposition (D/R) dynamics of electrochemically operating Mn-containing cathodes. The particle-level and electrode-level analyses reveal that the D/R dynamics is associated with distinct interfacial degradation mechanisms at different states of charge. Our results statistically differentiate the contributions of surface reconstruction and Jahn-Teller distortion to the Mn dissolution at different operating voltages. Introducing sulfonated polymers (Nafion) into composite electrodes can modulate the D/R dynamics by trapping the dissolved Mn species and rapidly establishing local Mn D/R equilibrium. This work represents an inaugural effort to pinpoint the chemical and structural transformations responsible for Mn dissolution via an operando synchrotron study and develops an effective method to regulate Mn interfacial dynamics for improving battery performance.
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