In situ dynamic re-structuring and interfacial evolution of SnS2 for high-performance electrochemical CO2 reduction to formate

格式化 纳米团簇 催化作用 材料科学 电化学 纳米片 化学工程 原位 傅里叶变换红外光谱 纳米技术 无机化学 化学 电极 物理化学 有机化学 工程类
作者
Weihua Cheng,Xingyi Xu,Qingliang Liao,Guohua Yao,Chenhao Zhang,Hui Li
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:480: 147922-147922 被引量:3
标识
DOI:10.1016/j.cej.2023.147922
摘要

The conversion of CO2 to value-added fuels and chemicals through electrochemical reduction has garnered substantial traction as an environmentally friendly approach toward a carbon-neutral society. Surface re-structuring of catalysts stands as one of the dynamic behaviors exhibited by electrocatalytic systems, exerting a significant influence on the catalysts' chemical, electronic, and physical characteristics, and thereby impacting their catalytic capabilities. Herein, we have discovered that the re-structured SnS2 nanoflowers with in situ formed Sn nanoclusters exhibit an enhanced Faradic efficiency of up to 93% with long-term stability for selective electroreduction of CO2 to formate with dynamic surface re-structuring. The in situ generated Sn nanoclusters on SnS2 nanoflowers at negative potential were found to play a vital role in facilitating over 90% CO2 electroreduction efficiency to formate. The presence of key intermediate OCHO* was proved through in situ attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. It was also guided by first-principal calculations that the interfacial region between Sn nanoclusters and SnS2 nanosheet acts as the most favorable catalytic site for the formation of OCHO*. This work unveils the significance of surface re-structuring behaviors of electrocatalysts under in situ environment for the pathway and mechanism of CO2 electroreduction, demonstrating the promise of structure-modulated SnS2 as a candidate for formate production.

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