氧合物
选择性
可再生能源
碳氢化合物
电化学
化石燃料
化学
碳纤维
电催化剂
催化作用
纳米技术
材料科学
有机化学
电极
工程类
物理化学
复合材料
电气工程
复合数
作者
Christopher Hahn,Toru Hatsukade,Youn-Geun Kim,Artūras Vailionis,Jack H. Baricuatro,Drew Higgins,Stephanie A. Nitopi,Manuel P. Soriaga,Thomas F. Jaramillo
标识
DOI:10.1073/pnas.1618935114
摘要
Significance Anthropogenic global warming necessitates the development of renewable carbon-free and carbon-neutral technologies for the future. Electrochemical CO 2 reduction is one such technology that has the potential to impact climate change by enabling sustainable routes for the production of fuels and chemicals. Whereas the field of CO 2 reduction has attracted great interest, current state-of-the-art electrocatalysts must be improved in product selectivity and energy efficiency to make this pathway viable for the future. Here, we investigate how controlling the surface structure of copper electrocatalysts can guide CO 2 reduction activity and selectivity. We show how the coordination environment of Cu surfaces influences oxygenate vs. hydrocarbon formation, providing insights on how to improve selectivity and energy efficiency toward more valuable CO 2 reduction products.
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