纳米晶
纳米线
材料科学
纳米技术
还原(数学)
接口(物质)
电化学
电极
化学
复合材料
几何学
毛细管数
数学
物理化学
毛细管作用
作者
Hushui Chen,Taishi Xiao,Yan Xia,Hengyao Song,Xiangyun Xi,Xianwu Huang,Dong Yang,Tongtao Li,Zhengzong Sun,Angang Dong
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-08-29
卷期号:63 (48): e202410039-e202410039
被引量:3
标识
DOI:10.1002/anie.202410039
摘要
Abstract Fine‐tuning the interfacial sites within heterogeneous catalysts is pivotal for unravelling the intricate structure–property relationship and optimizing their catalytic performance. Herein, a simple and versatile mixed‐dimensional assembly approach is proposed to create nanocrystal‐on‐nanowire superstructures with precisely adjustable numbers of biphasic interfaces. This method leverages an efficient self‐assembly process in which colloidal nanocrystals spontaneously organize onto Ag nanowires, driven by the solvophobic effect. Importantly, varying the ratio of the two components during assembly allows for accurate control over both the quantity and contact perimeter of biphasic interfaces. As a proof‐of‐concept demonstration, a series of Au‐on‐Ag superstructures with varying numbers of Au/Ag interfaces are constructed and employed as electrocatalysts for electrochemical CO 2 ‐to‐CO conversion. Experimental results reveal a logarithmic linear relationship between catalytic activity and the number of Au/Ag interfaces per unit mass of Au‐on‐Ag superstructures. This work presents a straightforward approach for precise interface engineering, paving the way for systematic exploration of interface‐dependent catalytic behaviors in heterogeneous catalysts.
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