Pore-structure-directed CO electroreduction to formate on SnO/C catalysts

• Published in: Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019-08, Vol.7 (31), p.18428-18433
• Main Authors: He, Yeheng, Jiang, Wen-Jie, Zhang, Yun, Huang, Lin-Bo, Hu, Jin-Song
• Format: Article
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/c9ta05937g

Electrochemical reduction of carbon dioxide (CO 2 ) to value-added chemicals and fuels has attracted great interest, although it suffers from low energy efficiency and selectivity. Herein, we discover that the pore structure of a supported catalyst significantly affects the products and efficiency of the electrochemical CO 2 reduction reaction (CO 2 RR). Three-dimensional (3D) porous carbon (PC) sheets with abundant micropores and macropores and mesopore-dominant activated carbon (AC) have been used to construct electrocatalysts with uniformly dispersed SnO 2 nanoparticles. SnO 2 /PC exhibits efficient formate production from the electrochemical CO 2 RR with a high faradaic efficiency of 92% and partial current density of 29 mA cm 2 at 0.86 V, ranking as a top-tier Sn-based catalyst. Importantly, systematic investigation and comparison with SnO 2 /AC show that the space-confinement effect of micropores enhances CO 2 RR selectivity towards formate by inhibiting proton transfer to active sites and thus suppressing the HER process, while the 3D sheet structure with abundant macropores provides mass and charge transport highways, making more active sites accessible for an effective CO 2 RR and thus a larger current density. These findings shed light on the design of efficient electrocatalysts via engineering pore structures for diverse applications. Three-dimensional porous carbon sheets with abundant micropores and macropores are used to uniformly disperse SnO 2 nanoparticles with high loading, and the obtained SnO 2 /PC exhibits efficient formate production from electrochemical CO 2 reduction.