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经调制以在衍生泡沫铜上生长的铜铋电催化剂用于高效的一氧化碳到甲酸盐转化。

CuBi electrocatalysts modulated to grow on derived copper foam for efficient CO-to-formate conversion.

作者信息

Lou Wenshuang, Peng Luwei, He Ruinan, Liu Yuyu, Qiao Jinli

机构信息

State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Environmental Science and Engineering, Donghua University, 2999 Ren'min North Road, Shanghai 201620, China.

Institute for Sustainable Energy, College of Sciences, Shanghai University, Shanghai 200444, China.

出版信息

J Colloid Interface Sci. 2022 Jan 15;606(Pt 2):994-1003. doi: 10.1016/j.jcis.2021.08.080. Epub 2021 Aug 18.

Abstract

Electrochemical reduction of CO to fuels and chemicals is an effective way to reduce greenhouse gas emissions and alleviate the energy crisis, but the highly active catalysts necessary for this reaction under mild conditions are still rare. In this work, we grew CuBi bimetallic catalysts on derived copper foam substrates by co-electrodeposition, and then investigated the correlation between co-electrodeposition potential and electrochemical performance in CO-to-formate conversion. Results showed that the bimetallic catalyst formed at a low potential of - 0.6 V vs. AgCl/Ag electrode achieved the highest formate Faradaic efficiency (FE) of 94.4% and a current density of 38.5 mA/cm at a low potential of - 0.97 V vs. reversible hydrogen electrode (RHE). Moreover, a continuous-flow membrane electrode assembly reactor also enabled the catalyst to show better performance (a FE of 98.3% at 56.6 mA/cm) than a traditional H-type reaction cell. This work highlights the vital impact of co-electrodeposition potential on catalyst performance and provides a basis for the modulated growth of bimetallic catalysts on substrates. It also shows the possibility of preparing Bi-based catalysts with no obvious decrease in catalytic activity that have been partially replaced with more economic copper.

摘要

将CO电化学还原为燃料和化学品是减少温室气体排放和缓解能源危机的有效途径,但在温和条件下该反应所需的高活性催化剂仍然很少。在这项工作中,我们通过共电沉积在衍生的泡沫铜基底上生长了CuBi双金属催化剂,然后研究了共电沉积电位与CO转化为甲酸盐的电化学性能之间的相关性。结果表明,相对于AgCl/Ag电极在-0.6 V的低电位下形成的双金属催化剂,在相对于可逆氢电极(RHE)为-0.97 V的低电位下实现了最高的甲酸盐法拉第效率(FE),为94.4%,电流密度为38.5 mA/cm²。此外,连续流膜电极组件反应器也使该催化剂表现出比传统H型反应池更好的性能(在56.6 mA/cm²时FE为98.3%)。这项工作突出了共电沉积电位对催化剂性能的重要影响,并为双金属催化剂在基底上的调控生长提供了依据。它还表明了制备Bi基催化剂的可能性,其催化活性没有明显下降,且已部分被更经济的铜所替代。

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