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锚定在缺陷MoS上的非金属单原子:一种用于将NO还原为NH的新型电催化剂。

Non-metal single atoms anchored on defective MoS: a novel electrocatalyst for NO reduction to NH.

作者信息

Liu Yifan, Tursun Mamutjan, Hu Guangzhi, Abdukayum Abdukader, Wu Chao

机构信息

Xinjiang Key Laboratory of Novel Functional Materials Chemistry, College of Chemistry and Environmental Sciences, Kashi University Kashi 844000 PR China

Qilu Lake Field Scientific Observation and Research Station for Plateau Shallow Lake in Yunnan Province, Institute for Ecological Research and Pollution Control of Plateau Lakes, School of Ecology and Environmental Science, Yunnan University Kunming 650504 China.

出版信息

RSC Adv. 2025 Aug 19;15(36):29323-29334. doi: 10.1039/d5ra04718h. eCollection 2025 Aug 18.

Abstract

The electrocatalytic nitric oxide reduction reaction (eNORR) is a highly significant because it provides a sustainable and cost-effective way to combine the elimination of nitric oxide (NO) with synthesis of ammonia (NH). This study comprehensively investigates the performance of single non-metal atom catalysts (NM@MoS), which are composed of single non-metal atoms that are embedded in vacancy defects in MoS. Our results demonstrate that eight NM@MoS catalysts (NM = B, C, N, O, P, Si, Se, and Te) exhibit remarkable thermodynamic stability. The Si, C, N, B and P@MoS catalysts in particular effectively adsorb and activate NO molecules, displaying high catalytic activity during the subsequent protonation process. Their values are 0, 0, -0.36, -0.62, and -0.70 V, respectively. Furthermore, a detailed selectivity analysis revealed that the N, P, C, and Si@MoS catalysts exhibit high NH selectivity. This theoretical study has effectively identified and evaluated NM@MoS catalysts based on stability, selectivity and high catalytic activity with a focus on NO removal and NH synthesis.

摘要

电催化一氧化氮还原反应(eNORR)非常重要,因为它提供了一种可持续且具有成本效益的方法,将一氧化氮(NO)的消除与氨(NH₃)的合成结合起来。本研究全面考察了单非金属原子催化剂(NM@MoS₂)的性能,这些催化剂由嵌入MoS₂空位缺陷中的单非金属原子组成。我们的结果表明,八种NM@MoS₂催化剂(NM = B、C、N、O、P、Si、Se和Te)表现出显著的热力学稳定性。特别是Si、C、N、B和P@MoS₂催化剂能有效吸附并活化NO分子,在随后的质子化过程中显示出高催化活性。它们的起始过电位分别为0、0、-0.36、-0.62和-0.70 V。此外,详细的选择性分析表明,N、P、C和Si@MoS₂催化剂表现出高NH₃选择性。这项理论研究基于稳定性、选择性和高催化活性,有效地识别和评估了以NO去除和NH₃合成为重点的NM@MoS₂催化剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36f2/12377346/c6d5c2833ef7/d5ra04718h-f1.jpg

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