Understanding the Selectivity Differences of NO Electroreduction on Ag and Au Electrodes

Although noble metals Ag and Au have similar chemical reactivities, their catalytic selectivity for NO electroreduction is significantly different. Namely, hydroxylamine is often considerably produced on Ag while not observed on the Au electrode. In this study, first-principles calculations and the electric field controlling constant potential (EFC-CP) method are adopted to unveil the underlying reasons. We first reveal a distinct NO* adsorption configuration, vertical on Ag and inclined on Au, leading to different reduction pathways to NOH* and HNO*, respectively. Via complete electrochemical barrier calculations and detailed kinetic analysis, we find the hydroxylamine selectivity difference between Ag and Au is mainly induced by adsorption strength of NH<sub>2</sub>OH*. On Ag, the obtained NH<sub>2</sub>OH* prefers to desorb and produce hydroxylamine, while NH<sub>2</sub>OH* is bonded strongly to Au and favors further reduction to ammonia. The study advances our understanding of factors regulating product selectivity, providing crucial insights for designing NO electroreduction catalysts toward hydroxylamine production.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2025-03-28
DOI
https://doi.org/10.1021/acs.jpclett.5c00656
Citations
4
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
Field-Weighted Citation Impact
1.56

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article

Understanding the Selectivity Differences of NO Electroreduction on Ag and Au Electrodes

Jianping Xiao, Dong Luan, Jun Long, Lin Li
4 citations
The Journal of Physical Chemistry Letters
Ammonia Synthesis and Nitrogen Reduction
1.56
article

Understanding the Selectivity Differences of NO Electroreduction on Ag and Au Electrodes

Jianping Xiao, Dong Luan, Jun Long, Lin Li
article en
4 citations

Abstract

Although noble metals Ag and Au have similar chemical reactivities, their catalytic selectivity for NO electroreduction is significantly different. Namely, hydroxylamine is often considerably produced on Ag while not observed on the Au electrode. In this study, first-principles calculations and the electric field controlling constant potential (EFC-CP) method are adopted to unveil the underlying reasons. We first reveal a distinct NO* adsorption configuration, vertical on Ag and inclined on Au, leading to different reduction pathways to NOH* and HNO*, respectively. Via complete electrochemical barrier calculations and detailed kinetic analysis, we find the hydroxylamine selectivity difference between Ag and Au is mainly induced by adsorption strength of NH<sub>2</sub>OH*. On Ag, the obtained NH<sub>2</sub>OH* prefers to desorb and produce hydroxylamine, while NH<sub>2</sub>OH* is bonded strongly to Au and favors further reduction to ammonia. The study advances our understanding of factors regulating product selectivity, providing crucial insights for designing NO electroreduction catalysts toward hydroxylamine production.

The Journal of Physical Chemistry LettersVol. 16(14)
Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), Dalian National Laboratory for Clean Energy (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Natural Science Foundation of Liaoning Province, State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, National Key Research and Development Program of China
Openalex Percentile: Top 18%
Ammonia Synthesis and Nitrogen Reduction
1.56
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