Cu-Doped Fe2O3 Nanorods for Enhanced Electrocatalytic Nitrogen Fixation to Ammonia

被引:9
|
作者
Takashima, Toshihiro [1 ,2 ,3 ]
Fukasawa, Hikaru [1 ]
Mochida, Takumi [2 ]
Irie, Hiroshi [1 ,2 ,3 ]
机构
[1] Univ Yamanashi, Fac Engn, Dept Appl Chem, Kofu, Yamanashi 4008511, Japan
[2] Univ Yamanashi, Integrated Grad Sch Med Engn & Agr Sci, Kofu, Yamanashi 4008511, Japan
[3] Univ Yamanashi, Clean Energy Res Ctr, Kofu, Yamanashi 4008511, Japan
基金
日本学术振兴会;
关键词
nitrogen reduction; ammonia; electrocatalyst; hematite; doping; oxygen vacancy; OXYGEN VACANCIES; REDUCTION; ALPHA-FE2O3; WATER; CATALYSTS; DOPANT; STATE;
D O I
10.1021/acsanm.3c04712
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The electrochemical nitrogen reduction reaction (NRR) has emerged as a promising approach for synthesizing ammonia (NH3) from nitrogen (N-2) under mild conditions. However, due to the difficulty in activating stable N-2 molecules and the competition with the hydrogen evolution reaction (HER), the development of active NRR electrocatalysts achieving a high NH3 formation rate and a high Faradaic efficiency (FE) is strongly desired. Herein, Cu-doped hematite (Fe2O3) nanorod arrays are synthesized by hydrothermal treatment and annealing under a N-2 atmosphere. At -0.15 V versus reversible hydrogen electrode (RHE), 4.4% Cu-doped Fe2O3 exhibits a NH3 formation rate of 12.5 mu g h(-1) mg(cat.)(-1) and a FE of 16.4%, demonstrating a significant improvement in the NRR performance with Cu doping. The introduction of Cu increases the number of oxygen vacancies on the catalyst surface and induces charge redistribution between the constituent Cu and Fe ions, promoting the adsorption and activation of N-2. Thus, this study not only offers an attractive earth-abundant NRR electrocatalyst but also provides an insight that heteroatom doping is effective to enhance the NRR activity through both defect engineering and electronic modulation.
引用
收藏
页码:23381 / 23389
页数:9
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