Self-assembled infinite silver cluster with atomic precision as a scalable catalyst for CO2-electroreduction under industry-relevant reaction rates†

EES catalysis Pub Date : 2024-10-18 DOI:10.1039/D4EY00160E
Leonard Curet, William Lafargue dit-Hauret, Jordi Benet-Buchholz, Marta Martínez-Belmonte, Dominique Foix, Emilio Palomares, Laurent Billon, Didier Begué and Aurelien Viterisi
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Abstract

The multi-gram synthesis of a phenylacetylide silver cluster catalyst and its application to the electroreduction of CO2 to carbon monoxide is described. The procedure involves one synthetic step from commercially available precursors and yields highly crystalline silver acetylide clusters in quantitative yields with no required purification. The crystal structure of the cluster was resolved from the native powder using cutting-edge electron diffraction techniques (3D-ED), and showed to consist of an infinite silver tubular core with radially disposed phenylacetylene ligands. Its catalytic properties were investigated at industry-relevant rates in a flow cell electrolyser. Faradaic efficiencies for CO above 95% were achieved at current densities reaching 350 mA cm−2. The catalyst's selectivity and stability were shown to be the result of the unique polymeric structure, a result supported by electrochemical characterisation and DFT modelling.

Abstract Image

具有原子精度的自组装无限银簇作为工业相关反应速率下二氧化碳电还原的可扩展催化剂
介绍了多克苯乙基银簇催化剂的合成及其在CO2电还原制一氧化碳中的应用。该过程涉及一个合成步骤,从商业上可用的前体,并产生高结晶的乙酰化银簇在定量产量,不需要纯化。利用尖端的电子衍射技术(3D-ED)从天然粉末中分辨出簇的晶体结构,并显示由无限银管核心组成,径向分布的苯乙炔配体。在流动电池电解槽中以工业相关的速率研究了其催化性能。当电流密度达到350 mA cm−2时,CO的法拉第效率达到95%以上。催化剂的选择性和稳定性被证明是独特的聚合物结构的结果,这一结果得到了电化学表征和DFT模型的支持。
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