Understanding the Ag–S interface stability and electrocatalytic activity of CO2 electroreduction in atomically precise Ag25 nanoclusters†

IF 4.2 2区化学 Q2 CHEMISTRY, MULTIDISCIPLINARY

Chemical Communications Pub Date : 2025-01-02 DOI:10.1039/d4cc06185c

Yuting Ye , Xia Zhou , Yuping Chen , Likai Wang , Qing Tang

引用次数: 0

Abstract

Elucidating the catalytic properties of metal nanoclusters (NCs) with essentially the same structure but different core metals is of fundamental interest. Our current studies have demonstrated that the thiolated Ag₂₅(SR)₁₈ NC exhibits SR ligand leaching dynamics and electrocatalytic activity in CO₂ reduction distinct from those of its Au₂₅(SR)₁₈ NC structural analogue.

Abstract Image

查看原文本刊更多论文

原子精密Ag25纳米团簇中Ag-S界面稳定性和CO2电还原活性的研究

阐明具有基本相同结构但核心金属不同的金属纳米团簇（NCs）的催化性能具有重要意义。我们目前的研究表明，硫代Ag25(SR)18 NC具有SR配体浸出动力学和二氧化碳还原电催化活性，与Au25(SR)18 NC结构类似物不同。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

求助全文

约1分钟内获得全文求助全文

来源期刊

Chemical Communications 化学-化学综合

CiteScore

8.60

自引率

4.10%

发文量

2705

审稿时长

1.4 months

期刊介绍： ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.