过电位
锰
催化作用
镍
析氧
分解水
化学
兴奋剂
材料科学
纳米技术
化学工程
电化学
冶金
电极
有机化学
光催化
物理化学
工程类
光电子学
作者
Haowei Jia,Peiyuan Guan,Yingze Zhou,Ziheng Feng,Renbo Zhu,Mengyao Li,Tao Wan,Tianxu Huang,Tianyue Liang,Jun Pan,Zhipeng Ma,Yeqing Xu,Caiyun Wang,Dewei Chu
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2022-11-02
卷期号:36 (22): 13808-13816
被引量:4
标识
DOI:10.1021/acs.energyfuels.2c02535
摘要
Electrochemical water splitting (EWS) has been considered as an ideal strategy to produce renewable hydrogen energy. However, the application of EWS is hindered by its sluggish kinetics of oxygen evolution half-reaction. In this work, we successfully prepared an efficient MXene-Ni0.075Mn0.925O2/CC catalyst for oxygen evolution reaction (OER) enhanced by a novel electrodeposition process. By corroborating from characterization results, the Ni element has been successfully doped into the MnO2 crystal. In addition, electron microscopy images visualized that MXene firmly cooperated with the Ni-doped MnO2. With the proper amount of Ni doping in the pristine MnO2, more defects were induced. In addition, the two-dimensional (2D) MXene cooperation collaboratively provided more mass transport channels for OER. Therefore, the prepared MXene-Ni0.075Mn0.925O2/CC catalyst exhibited an outstanding catalytic performance with an overpotential of ∼410 mV at a constant current density of 50 mA cm–2, about 105 mV smaller than that of the pristine MnO2/CC catalyst. The proposed electrodeposition method may pave the way for future designing of binder-free electrocatalytic materials for EWS.
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