Highly active bifunctional catalyst: Constructing FeWO4-WO3 heterostructure for water and hydrazine oxidation at large current density

被引:28
|
作者
Shen, Fang [1 ]
Wang, Zhenglin [1 ]
Wang, Yamei [1 ]
Qian, Guangfu [1 ]
Pan, Miaojing [1 ]
Luo, Lin [1 ]
Chen, Guoning [2 ]
Wei, Hailang [2 ]
Yin, Shibin [1 ]
机构
[1] Guangxi Univ, Coll Chem & Chem Engn, Key Lab New Proc Technol Nonferrous Met & Mat, State Key Lab Proc Non Ferrous Met & Featured Mat, Nanning 530004, Peoples R China
[2] Guangxi Bossco Environm Protect Technol Co Ltd, 12 Kexing Rd, Nanning 530007, Peoples R China
基金
中国国家自然科学基金;
关键词
catalyst; heterostructure; large current density; oxygen evolution reaction; hydrazine oxidation reaction; EVOLUTION; EFFICIENT; ELECTROCATALYST; NANOSHEETS; PERFORMANCE; ARRAYS; FOAM; CO;
D O I
10.1007/s12274-021-3548-z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Developing high performance anode catalysts for oxygen evolution reaction (OER) and hydrazine oxidation reaction (HzOR) at large current density is an efficient pathway to produce hydrogen. Herein, we synthesize a FeWO4-WO3 heterostructure catalyst growing on nickel foam (FeWO4-WO3/NF) by a combination of hydrothermal and calcination method. It shows good catalytic activity with ultralow potentials for OER (eta(10) = 1.43 V, eta(1.000) = 1.56 V) and HzOR (eta(10) = -0.034 V, eta(1.000) = 0.164 V). Moreover, there is little performance degradation after being tested for 100 h at 1,000 (OER) and 100 (HzOR) mA.cm(-2), indicating good stability. The superior performance could be attributed to the wolframite structure and heterostructure: The former provides a high electrical conductivity to ensure the electronic transfer capability, and the later induces interfacial electron redistribution to enhance the intrinsic activity and stability. The work offers a brand-new way to prepare good performance catalysts for OER and HzOR, especially at large current density.
引用
收藏
页码:4356 / 4361
页数:6
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