Complementary Operando Spectroscopy identification of in-situ generated metastable charge-asymmetry Cu 2 -CuN 3 clusters for CO 2 reduction to ethanol
NATURE COMMUNICATIONS(2022)
Abstract
Copper-based materials can reliably convert carbon dioxide into multi-carbon products but they suffer from poor activity and product selectivity. The atomic structure-activity relationship of electrocatalysts for the selectivity is controversial due to the lacking of systemic multiple dimensions for operando condition study. Herein, we synthesized high-performance CO 2 RR catalyst comprising of CuO clusters supported on N-doped carbon nanosheets, which exhibited high C 2+ products Faradaic efficiency of 73% including decent ethanol selectivity of 51% with a partial current density of 14.4 mA/cm −2 at −1.1 V vs. RHE. We evidenced catalyst restructuring and tracked the variation of the active states under reaction conditions, presenting the atomic structure-activity relationship of this catalyst. Operando XAS, XANES simulations and Quasi-in-situ XPS analyses identified a reversible potential-dependent transformation from dispersed CuO clusters to Cu 2 -CuN 3 clusters which are the optimal sites. This cluster can’t exist without the applied potential. The N-doping dispersed the reduced Cu n clusters uniformly and maintained excellent stability and high activity with adjusting the charge distribution between the Cu atoms and N-doped carbon interface. By combining Operando FTIR and DFT calculations, it was recognized that the Cu 2 -CuN 3 clusters displayed charge-asymmetric sites which were intensified by CH 3 * adsorbing, beneficial to the formation of the high-efficiency asymmetric ethanol.
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Key words
Electrocatalysis,Energy,Science,Humanities and Social Sciences,multidisciplinary
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