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Exploring dopant effects in stannic oxide nanoparticles for CO(2) electro-reduction to formate

The electrosynthesis of formate from CO(2) can mitigate environmental issues while providing an economically valuable product. Although stannic oxide is a good catalytic material for formate production, a metallic phase is formed under high reduction overpotentials, reducing its activity. Here, usin...

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Detalles Bibliográficos
Autores principales: Ko, Young-Jin, Kim, Jun-Yong, Lee, Woong Hee, Kim, Min Gyu, Seong, Tae-Yeon, Park, Jongkil, Jeong, YeonJoo, Min, Byoung Koun, Lee, Wook-Seong, Lee, Dong Ki, Oh, Hyung-Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033853/
https://www.ncbi.nlm.nih.gov/pubmed/35459916
http://dx.doi.org/10.1038/s41467-022-29783-7
Descripción
Sumario:The electrosynthesis of formate from CO(2) can mitigate environmental issues while providing an economically valuable product. Although stannic oxide is a good catalytic material for formate production, a metallic phase is formed under high reduction overpotentials, reducing its activity. Here, using a fluorine-doped tin oxide catalyst, a high Faradaic efficiency for formate (95% at 100 mA cm(−2)) and a maximum partial current density of 330 mA cm(−2) (at 400 mA cm(−2)) is achieved for the electroreduction of CO(2). Furthermore, the formate selectivity (≈90%) is nearly constant over 7 days of operation at a current density of 100 mA cm(−2). In-situ/operando spectroscopies reveal that the fluorine dopant plays a critical role in maintaining the high oxidation state of Sn, leading to enhanced durability at high current densities. First-principle calculation also suggests that the fluorine-doped tin oxide surface could provide a thermodynamically stable environment to form HCOO* intermediate than tin oxide surface. These findings suggest a simple and efficient approach for designing active and durable electrocatalysts for the electrosynthesis of formate from CO(2).