铜
电化学
无机化学
氧化铜
氧化物
材料科学
催化作用
二氧化碳电化学还原
化学工程
透射电子显微镜
纳米颗粒
电催化剂
碳纤维
电极
化学
纳米技术
一氧化碳
有机化学
冶金
复合材料
物理化学
工程类
复合数
作者
Rosa M. Arán‐Ais,Rubén Rizo,Philipp Grosse,Gerardo Algara‐Siller,Kassiogé Dembélé,Milivoj Plodinec,Thomas Lunkenbein,See Wee Chee,Beatriz Roldán Cuenya
标识
DOI:10.1038/s41467-020-17220-6
摘要
Abstract Copper is a widely studied catalyst material for the electrochemical conversion of carbon dioxide to valuable hydrocarbons. In particular, copper-based nanostructures expressing predominantly {100} facets have shown high selectivity toward ethylene formation, a desired reaction product. However, the stability of such tailored nanostructures under reaction conditions remains poorly understood. Here, using liquid cell transmission electron microscopy, we show the formation of cubic copper oxide particles from copper sulfate solutions during direct electrochemical synthesis and their subsequent morphological evolution in a carbon dioxide-saturated 0.1 M potassium bicarbonate solution under a reductive potential. Shape-selected synthesis of copper oxide cubes was achieved through: (1) the addition of chloride ions and (2) alternating the potentials within a narrow window where the deposited non-cubic particles dissolve, but cubic ones do not. Our results indicate that copper oxide cubes change their morphology rapidly under carbon dioxide electroreduction-relevant conditions, leading to an extensive re-structuring of the working electrode surface.
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