可逆氢电极
电催化剂
纳米棒
电化学
无机化学
氨生产
法拉第效率
催化作用
氧化还原
材料科学
杂原子
氨
析氧
兴奋剂
电极
化学
纳米技术
工作电极
物理化学
戒指(化学)
生物化学
光电子学
有机化学
作者
Toshihiro Takashima,Hikaru Fukasawa,Takumi MOCHIDA,Hiroshi Irie
标识
DOI:10.1021/acsanm.3c04712
摘要
The electrochemical nitrogen reduction reaction (NRR) has emerged as a promising approach for synthesizing ammonia (NH3) from nitrogen (N2) under mild conditions. However, due to the difficulty in activating stable N2 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 N2 atmosphere. At −0.15 V versus reversible hydrogen electrode (RHE), 4.4% Cu-doped Fe2O3 exhibits a NH3 formation rate of 12.5 μg h–1 mgcat.–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 N2. 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.
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