Ni3N as an Active Hydrogen Oxidation Reaction Catalyst in Alkaline Medium

被引:238
|
作者
Ni, Weiyan [1 ]
Krammer, Anna [2 ]
Hsu, Chia-Shuo [3 ]
Chen, Hao Ming [3 ]
Schuler, Andreas [2 ]
Hu, Xile [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn ISIC, Lab Inorgan Synth & Catalysis LSCI, BCH 3305, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Inst Civil Engn IIC, Solar Energy & Bldg Phys Lab LESO PB, GC AO 391 Batiment GC, CH-1015 Lausanne, Switzerland
[3] Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan
关键词
alkaline fuel cells; electrocatalysis; hydrogen evolution; hydrogen oxidation reaction; nickel; RANEY-NICKEL CATALYST; FUEL-CELLS; METAL; NANOSHEETS; ELECTROCATALYSTS; ELECTRODES; MECHANISM; SHELL;
D O I
10.1002/anie.201902751
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydroxide-exchange membrane fuel cells can potentially utilize platinum-group-metal (PGM)-free electrocatalysts, offering cost and scalability advantages over more developed proton-exchange membrane fuel cells. However, there is a lack of non-precious electrocatalysts that are active and stable for the hydrogen oxidation reaction (HOR) relevant to hydroxide-exchange membrane fuel cells. Here we report the discovery and development of Ni3N as an active and robust HOR catalyst in alkaline medium. A supported version of the catalyst, Ni3N/C, exhibits by far the highest mass activity and break-down potential for a PGM-free catalyst. The catalyst also exhibits Pt-like activity for hydrogen evolution reaction (HER) in alkaline medium. Spectroscopy data reveal a downshift of the Ni d band going from Ni to Ni3N and interfacial charge transfer from Ni3N to the carbon support. These properties weaken the binding energy of hydrogen and oxygen species, resulting in remarkable HOR activity and stability.
引用
收藏
页码:7445 / 7449
页数:5
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