Electrochemical Ammonia Synthesis from Nitrite Assisted by In-Situ Generated Hydrogen Atoms on Nickel Phosphide Catalyst

Xiao Yang, Lei Kang, Chuan-Jun Wang, Fulai Liu, Yong Chen
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引用次数: 7

Abstract

Investigating green and effective means for ammonia synthesis is an important but challenging task. Electrochemical ammonia synthesis (EAS) from an indirect route (N2 → NOx → NH3) provides a feasible alternative strategy. The key step in this route is the reduction of NOx to NH3 instead of N2, which requires the investigation of efficient catalysts with high selectivity of NH3. Herein, we initially demonstrate a highly efficient electrochemical reduction of NO2- to NH3 with nickel phosphide (Ni2P) as the catalyst. The system exhibits low onset potential (0.2 V vs. RHE) and high faradaic efficiency (>90%) for EAS. Experimental results and theoretical calculations reveal that the in situ generated hydrogen atoms on the surface of Ni2P greatly promote the reduction of NO2- to NH3.
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在磷化镍催化剂上原位生成氢原子辅助亚硝酸盐电化学合成氨
探索绿色有效的氨合成方法是一项重要而又具有挑战性的任务。间接途径(N2→NOx→NH3)的电化学氨合成(EAS)提供了一种可行的替代策略。这条路线的关键一步是将NOx还原为NH3而不是N2,这就需要研究具有高NH3选择性的高效催化剂。在此,我们初步证明了在磷化镍(Ni2P)作为催化剂的情况下,NO2-的高效电化学还原为NH3。该系统具有低起始电位(相对于RHE为0.2 V)和高法拉第效率(>90%)的EAS。实验结果和理论计算表明,Ni2P表面原位生成的氢原子极大地促进了NO2-还原为NH3。
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