电催化剂
催化作用
材料科学
电化学
氧气
吸附
密度泛函理论
产量(工程)
选择性
纳米线
工作职能
化学工程
氧还原
纳米技术
无机化学
物理化学
电极
冶金
计算化学
化学
有机化学
图层(电子)
工程类
作者
Zerong Li,Ziyu Ma,Jie Liang,Yuchun Ren,Tingshuai Li,Siran Xu,Qian Liu,Na Li,Bo Tang,Yang Liu,Shuyan Gao,Abdulmohsen Ali Alshehri,Dongwei Ma,Yonglan Luo,Qi Wu,Xuping Sun
标识
DOI:10.1016/j.mtphys.2021.100586
摘要
Electrochemical NO reduction into NH3 addresses the need for harmful NO abatement and offers an attractive alternative to the industrial Haber–Bosch process, but it requires the development of advanced catalysts with high activity and selectivity toward NH3 synthesis. In this work, we report on our recent experimental findings that a MnO2 with oxygen vacancies (VO) nanowire array on Ti mesh (MnO2-x NA/TM) behaves as a high-active and stable electrocatalyst for ambient NO reduction to NH3. In 0.2 M Na2SO4, such catalyst shows a large NH3 yield of 27.51 × 10−10 mol s−1 cm−2 and a high Faradic efficiency of 82.8%, considerably outperforming the pristine MnO2 counterpart (8.83 × 10−10 mol s−1 cm−2, 44.8%). Density function theory calculations indicate that NO adsorption is enhanced on MnO2-x (211) surface due to stronger electronic interaction between NO and Mn atoms as a result of the VO.
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