X射线光电子能谱
锰
材料科学
价(化学)
傅里叶变换红外光谱
电化学
水溶液
氧化物
无机化学
分析化学(期刊)
化学工程
化学
电极
物理化学
有机化学
工程类
冶金
作者
Tzu‐Hao Lu,Chenghui Zeng,Haozhe Zhang,Xin Shi,Yanxia Yu,Xihong Lu
出处
期刊:Small
[Wiley]
日期:2023-01-02
卷期号:19 (14)
被引量:19
标识
DOI:10.1002/smll.202206727
摘要
Ammonium ions (NH4+ ), as non-metallic charge carriers, are attracting attention in aqueous batteries due to its low molar mass, element sufficiency, and non-toxicity. However, the host materials for NH4+ storage are still limited. Herein, an oxygen defects-rich manganese oxide (MnO2-x ) for NH4+ storage are reported. The oxygen defects can endow the MnO2-x sample with improved electric conductivity and low interface activation energy. The electrochemical reaction mechanism is also verified by using ex situ X-ray photoelectron spectroscopy (XPS) and fourier transform infrared spectroscopy (FT-IR), demonstrating the insertion and extraction of NH4+ in the MnO2-x by formation/breaking of a hydrogen bond. As a result, MnO2-x delivers a high capacity of 109.9 mAh g-1 at the current density of 0.5 A g-1 and retention of 24 mAh g-1 after 1000 cycles at the current density of 4 A g-1 , outperforming the pristine MnO2 sample.
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