Nickel-Doped Manganese Dioxide Electrocatalysts with MXene Surface Decoration for Oxygen Evolution Reaction

被引:10
|
作者
Jia, Haowei [1 ]
Guan, Peiyuan [1 ]
Zhou, Yingze [1 ]
Feng, Ziheng [1 ]
Zhu, Renbo [1 ]
Li, Mengyao [1 ]
Wan, Tao [1 ]
Huang, Tianxu [1 ]
Liang, Tianyue [1 ]
Pan, Jun [2 ]
Ma, Zhipeng [3 ]
Xu, Yeqing [4 ]
Wang, Caiyun [4 ]
Chu, Dewei [1 ]
机构
[1] Univ New South Wales, Sch Mat Sci & Engn, Sydney 2052, Australia
[2] Cent South Univ, State Key Lab Powder Met, Changsha 410083, Peoples R China
[3] Univ New South Wales, Sch Chem Engn, Sydney, NSW 2052, Australia
[4] Univ Wollongong, Intelligent Polymer Res Inst, ARC Ctr Excellence Electromat Sci, Wollongong 2500, Australia
关键词
PERFORMANCE; REDUCTION; CARBON; MNO2; DELTA-MNO2; ALPHA-MNO2; GAMMA-MNO2; KINETICS; PHASE;
D O I
10.1021/acs.energyfuels.2c02535
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
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 similar to 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.
引用
收藏
页码:13808 / 13816
页数:9
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