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Updated: Jun 15, 2025

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Small Interparticle Spacing in Catalyst Layers Forms an Expansive Triple-Phase Interface for Boosting the Current
Asato Inoue1, Sora Nakasone1, Ryotaro Yoshida1
1Research Center for Solar Energy Chemistry, Graduate School of Engineering Science, The University of Osaka, 1-3 Machikaneyama, Toyonaka, Osaka, 560-8531, Japan.
None:
Achieving both high current density and high selectivity for high-value products is crucial for the widespread implementation of CO2 electrolysis. Toward high-current-density electrolysis, it is crucial to design a triple-phase interface, where the catalyst, electrolyte, and gaseous substrate intersect, serving as the active reaction site for CO2 electrolysis. In this study, aims to establish design principles for the triple-phase interface composed of copper nanoparticles (CuNPs) to achieve ultra-high-current-density electrolysis of gaseous CO2 into multicarbon (C2+) products. The C2+ formation activity of electrodes carrying various CuNPs is systematically evaluated under high-current-density (>1 A cm-2) electrolysis conditions. By analyzing the correlations between the electrochemical performances and the physicochemical properties of the catalysts and electrodes, it is identified that the average size of interparticle spacing in the catalyst layer is correlated with the maximum partial current density for C2+ production (jC2+). Smaller interparticle spacings are found to enhance jC2+ by suppressing the excessive electrolyte penetration into the catalyst layer and forming an expansive triple-phase interface. Based on these insights, the optimized electrode, with an average interparticle spacing of 59.4 nm, exhibited a record jC2+ of 2.00 A cm-2 with a faradaic efficiency of 80.1%.
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