Exploring dopant effects in stannic oxide nanoparticles for CO2 electro-reduction to formateopen access
- Authors
- 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
- Issue Date
- 22-4월-2022
- Publisher
- NATURE PORTFOLIO
- Citation
- NATURE COMMUNICATIONS, v.13, no.1
- Indexed
- SCIE
SCOPUS
- Journal Title
- NATURE COMMUNICATIONS
- Volume
- 13
- Number
- 1
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/141782
- DOI
- 10.1038/s41467-022-29783-7
- ISSN
- 2041-1723
- Abstract
- Though stannic oxides can catalyze CO2 electroreduction to formate, the stability of these catalysts has been limited. Here, the authors demonstrate stable fluorine-doped SnO2 materials toward formate production at current densities of >300 mA/cm(2). The electrosynthesis of formate from CO2 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 CO2. Furthermore, the formate selectivity (approximate to 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 CO2.
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