Vimanshu Chanda, João R. C. Junqueira, Nivedita Sikdar, Ignacio Sanjuán, Michael Braun, Stefan Dieckhöfer, Sabine Seisel, Corina Andronescu
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引用次数: 1
Abstract
Electrochemical conversion of CO2 (CO2RR) has received significant attention since it could provide pathways for renewable energy storage to energy-dense chemicals and synthetic fuels. We developed a novel CuOx/Cu/C type electrocatalyst via pyrolysis, which we used to convert CO2 at industrially relevantly current densities using gas diffusion electrodes. The influence of the pyrolysis conditions on the electrocatalytic CO2RR activity and selectivity was evaluated. Optimization of the electrode structure to mitigate electrowetting was done by mixing the catalyst with polytetrafluoroethylene (PTFE). We found that mixing the most active catalyst with PTFE in a mass ratio of 1 to 0.25 substantially increased the formation of C2H4 displaying 41% Faradaic efficiency (FE) at –240 mA cm–2. Prolonged CO2RR at different current densities shows that the electrode containing 25 wt.% PTFE in the catalyst layer display FEC2H4 > 40% at –280 mA cm–2 for 2 h.
二氧化碳的电化学转化(CO2RR)为可再生能源存储到高能量化学品和合成燃料提供了途径,因此受到了广泛的关注。我们通过热解开发了一种新型的CuOx/Cu/C型电催化剂,我们使用气体扩散电极在工业相关的电流密度下转化二氧化碳。考察了热解条件对电催化CO2RR活性和选择性的影响。通过将催化剂与聚四氟乙烯(PTFE)混合,优化电极结构以减轻电润湿。我们发现,将最活跃的催化剂与聚四氟乙烯以1比0.25的质量比混合,大大增加了C2H4的形成,在-240 mA cm-2时显示出41%的法拉第效率(FE)。在不同电流密度下延长CO2RR表明,在催化剂层中含有25 wt.% PTFE的电极显示FEC2H4 >40%,在-280 mA cm-2下工作2小时。