Electrochemically Robust Ferberite (FeWO4) Nanostructure as an Anode Material for Alkaline Water- and Alcohol-Oxidation Reaction

被引:27
作者
Adak, Mrinal Kanti [1 ]
Rajput, Anubha [1 ]
Mallick, Laxmikanta [1 ]
Chakraborty, Biswarup [1 ]
机构
[1] Indian Inst Technol Delhi, Dept Chem, New Delhi 110016, India
关键词
ferberite FeWO4; robust iron material; electrocatalysis; oxygen-evolution reaction; alcohol electro-oxidation; OXYGEN EVOLUTION REACTION; HIGHLY EFFICIENT; ADVANCED ELECTROCATALYST; HYDROTHERMAL SYNTHESIS; IRON SULFIDE; NANORODS; NANOPARTICLES; CATALYST; OXIDE; COMPLEXES;
D O I
10.1021/acsaem.1c03995
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
Due to the inferior conductivity and lability to dissolution during electrocatalysis, iron catalysts lack superior electrochemical performance. However, recent studies on transition-metal oxyhydroxides depict that iron is the active site for water oxidation. Herein, a heterobimetallic ferberite iron-tungstate nanostructure has been employed as an efficient anode material not only for alkaline oxygen evolution reaction (OER) involving water and ethanol oxidation but also as a non-noble metal-based anode for overall water splitting (OWS). The presence of tungstate in the nanostructure improves the efficiency of OER, as reflected in the overpotential value of 282 (+/- 3) mV at 10 mA cm(-2) and the Tafel slope of 54 mV dec(-1), which is far better compared to that of pure iron-oxyhydroxides as well as some noble metal-based catalysts. A fair activity of the FeWO4 anode further helped to construct a water electrolyzer coupled with a commercial Pt cathode, giving a cell potential of only 1.66 V to reach 10 mA cm(-2) current density. The strong binding of [FeO6] with the corner- and edge-shared [WO6] presumably provides facile electron conduction as well as robustness in the structure, which results in long durability during OER and OWS. This study showcases a facile approach to design a stable anode relying on earth-abundant metal precursors, which has remained a perdurable challenge so far.
引用
收藏
页码:5652 / 5665
页数:14
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