Efficient and stable noble-metal-free catalyst for acidic water oxidation

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作者
Sanjiang Pan
Hao Li
Dan Liu
Rui Huang
Xuelei Pan
Dan Ren
Jun Li
Mohsen Shakouri
Qixing Zhang
Manjing Wang
Changchun Wei
Liqiang Mai
Bo Zhang
Ying Zhao
Zhenbin Wang
Michael Graetzel
Xiaodan Zhang
机构
[1] Solar Energy Research Center,Institute of Photoelectronic Thin Film Devices and Technology, Renewable Energy Conversion and Storage Center
[2] Nankai University,Advanced Institute for Materials Research (WPI
[3] Key Laboratory of Photoelectronic Thin Film Devices and Technology of Tianjin,AIMR)
[4] Haihe Laboratory of Sustainable Chemical Transformations,Institute of Flexible Electronics (IFE)
[5] Engineering Research Center of Thin Film Photoelectronic Technology of Ministry of Education,State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science
[6] Collaborative Innovation Center of Chemical Science and Engineering (Tianjin),State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, International School of Materials Science and Engineering
[7] Tohoku University,Laboratory of Photonics and Interfaces
[8] Northwestern Polytechnical University (NPU),State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, School of Materials Science and Engineering
[9] Fudan University,Catalysis Theory Center, Department of Physics
[10] Wuhan University of Technology,undefined
[11] Ecole Polytechnique Federale de Lausanne,undefined
[12] Canadian Light Source,undefined
[13] Inc. (CLSI),undefined
[14] Wuhan University of Technology,undefined
[15] Technical University of Denmark,undefined
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摘要
Developing non-noble catalysts with superior activity and durability for oxygen evolution reaction (OER) in acidic media is paramount for hydrogen production from water. Still, challenges remain due to the inadequate activity and stability of the OER catalyst. Here, we report a cost-effective and stable manganese oxybromide (Mn7.5O10Br3) catalyst exhibiting an excellent OER activity in acidic electrolytes, with an overpotential of as low as 295 ± 5 mV at a current density of 10 mA cm−2. Mn7.5O10Br3 maintains good stability under operating conditions for at least 500 h. In situ Raman spectroscopy, X ray absorption near edge spectroscopy, and density functional theory calculations confirm that a self-oxidized surface with enhanced electronic transmission capacity forms on Mn7.5O10Br3 and is responsible for both the high catalytic activity and long-term stability during catalysis. The development of Mn7.5O10Br3 as an OER catalyst provides crucial insights into the design of non-noble metal electrocatalysts for water oxidation.
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