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Surface Oxygen Injection in Tin Disulfide Nanosheets for Efficient CO(2) Electroreduction to Formate and Syngas

Surface chemistry modification represents a promising strategy to tailor the adsorption and activation of reaction intermediates for enhancing activity. Herein, we designed a surface oxygen-injection strategy to tune the electronic structure of SnS(2) nanosheets, which showed effectively enhanced el...

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Detalles Bibliográficos
Autores principales: Chen, Tao, Liu, Tong, Ding, Tao, Pang, Beibei, Wang, Lan, Liu, Xiaokang, Shen, Xinyi, Wang, Sicong, Wu, Dan, Liu, Dong, Cao, Linlin, Luo, Qiquan, Zhang, Wei, Zhu, Wenkun, Yao, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421506/
https://www.ncbi.nlm.nih.gov/pubmed/34490543
http://dx.doi.org/10.1007/s40820-021-00703-6
Descripción
Sumario:Surface chemistry modification represents a promising strategy to tailor the adsorption and activation of reaction intermediates for enhancing activity. Herein, we designed a surface oxygen-injection strategy to tune the electronic structure of SnS(2) nanosheets, which showed effectively enhanced electrocatalytic activity and selectivity of CO(2) reduction to formate and syngas (CO and H(2)). The oxygen-injection SnS(2) nanosheets exhibit a remarkable Faradaic efficiency of 91.6% for carbonaceous products with a current density of 24.1 mA cm(−2) at −0.9 V vs RHE, including 83.2% for formate production and 16.5% for syngas with the CO/H(2) ratio of 1:1. By operando X-ray absorption spectroscopy, we unravel the in situ surface oxygen doping into the matrix during reaction, thereby optimizing the Sn local electronic states. Operando synchrotron radiation infrared spectroscopy along with theoretical calculations further reveals that the surface oxygen doping facilitated the CO(2) activation and enhanced the affinity for HCOO* species. This result demonstrates the potential strategy of surface oxygen injection for the rational design of advanced catalysts for CO(2) electroreduction. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-021-00703-6.