NH 4+-mediated interfacial chemistry for collaborative dual-pathway high-mass-loading energy storage
NH 4+-mediated interfacial chemistry for collaborative dual-pathway high-mass-loading energy storage
研究概述
调控NH4+介导的MnO2界面化学及部分羟基化程度,协同实现MnO2/Mn2+可逆转化和NH4+储存。在27.1 mg/cm²高负载下获得13.8 F/cm²面电容,并稳定循环6000次;计算表明界面电荷重分布降低转化限速步骤的能垒。
谱图与表征信息
Fig. 5 Fine structure characterization and theoretical calculations for understanding the integrated storage mechanism. (a) Mn K-edge XANES spectra of the Rec-NM-MnO2 electrode in NH4
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