材料科学
阳极
电化学
催化作用
碳纤维
可逆氢电极
氧化还原
化学工程
氢
分析化学(期刊)
电化学能量转换
电极
吸附
无机化学
氢燃料
析氧
电容
电催化剂
化学吸附
分解水
电极电位
标准氢电极
解吸
作者
Yinping Liu,Chao Guo,Fangang Qu,Yida Zhang,Kuo‐Wei Huang,Chunming Xu,Jia Guo,Xu Quan,Yingchun Niu
标识
DOI:10.1002/advs.202512148
摘要
Iron-chromium redox flow batteries (ICRFBs) show promise for large-scale energy storage, but their performance is hindered by the hydrogen evolution reaction (HER) and sluggish anode Cr3⁺/Cr2⁺ redox kinetics. Here, an octahedral In2O3 catalyst with exposed high-activity (222) crystal planes is reported, synthesized via high-temperature solution thermal decomposition and grown in situ on carbon cloth. The catalyst is grown in situ on carbon cloth to form a nanostructured indium-based electrode (In2O3-TCC). Grazing incidence wide-angle X-ray scattering confirms In2O3 phase formation, while XANES reveals abundant oxygen vacancies (Ov) serving as anode reaction active sites. In2O3-TCC exhibits enhanced electrochemical properties, including a tripled double-layer capacitance (8.92 mF cm- 2), a reduced charge transfer resistance (1.042 Ω), and improved Cr3⁺/Cr2⁺ kinetics. Density functional theory (DFT) shows that anode HER suppression arises from favorable H⁺ adsorption energy and a high desorption barrier. Furthermore, an in situ differential electrochemical mass spectrometer (DEMS) confirms effective anode HER suppression. The electrode achieves an energy efficiency of 84.02% at 140 mA cm- 2 and stable performance over 500 cycles. This work offers a new pathway for designing high-efficiency, long-lifetime ICRFB electrodes.
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