Dynamic Bubbling Balanced Proactive CO2 Capture and Reduction on a Triple-Phase Interface Nanoporous Electrocatalyst

• Published in: Journal of the American Chemical Society 2024-08, Vol.146 (31), p.21335-21347
• Main Authors: Zhang, Wei, Yu, Ao, Mao, Haiyan, Feng, Guangxia, Li, Cheng, Wang, Guanzhi, Chang, Jinfa, Halat, David, Li, Zhao, Yu, Weilai, Shi, Yaping, Liu, Shengwen, Fox, David W., Zhuang, Hao, Cai, Angela, Wu, Bing, Joshua, Fnu, Martinez, John R., Zhai, Lei, Gu, M. Danny, Shan, Xiaonan, Reimer, Jeffrey A., Cui, Yi, Yang, Yang
• Format: Article
• Language: English
• Subjects: electrodes; interfaces; oxides; phase transitions; porosity
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.4c02786

The formation and preservation of the active phase of the catalysts at the triple-phase interface during CO2 capture and reduction is essential for improving the conversion efficiency of CO2 electroreduction toward value-added chemicals and fuels under operational conditions. Designing such ideal catalysts that can mitigate parasitic hydrogen generation and prevent active phase degradation during the CO2 reduction reaction (CO2RR), however, remains a significant challenge. Herein, we developed an interfacial engineering strategy to build a new SnO x catalyst by invoking multiscale approaches. This catalyst features a hierarchically nanoporous structure coated with an organic F-monolayer that modifies the triple-phase interface in aqueous electrolytes, substantially reducing competing hydrogen generation (less than 5%) and enhancing CO2RR selectivity (∼90%). This rationally designed triple-phase interface overcomes the issue of limited CO2 solubility in aqueous electrolytes via proactive CO2 capture and reduction. Concurrently, we utilized pulsed square-wave potentials to dynamically recover the active phase for the CO2RR to regulate the production of C1 products such as formate and carbon monoxide (CO). This protocol ensures profoundly enhanced CO2RR selectivity (∼90%) compared with constant potential (∼70%) applied at −0.8 V (V vs RHE). We further achieved a mechanistic understanding of the CO2 capture and reduction processes under pulsed square-wave potentials via in situ Raman spectroscopy, thereby observing the potential-dependent intensity of Raman vibrational modes of the active phase and CO2RR intermediates. This work will inspire material design strategies by leveraging triple-phase interface engineering for emerging electrochemical processes, as technology moves toward electrification and decarbonization.