Single-atom Pt supported on non-metal doped WS2 for photocatalytic CO2 reduction: A first-principles study

被引:17
|
作者
Zhu, Linghao [1 ]
Qin, Cong [1 ]
Wang, Yan [2 ]
Cao, Jianliang [1 ,2 ]
机构
[1] Henan Polytech Univ, Coll Chem & Chem Engn, Jiaozuo 454000, Peoples R China
[2] Henan Polytech Univ, State Collaborat Innovat Ctr Coal Work Safety & Cl, Jiaozuo 454000, Peoples R China
基金
中国国家自然科学基金;
关键词
PhotocatalyticCO(2) reduction; First-principles calculations; Pt; WS2; Single-atom catalysts; TIO2; CH4;
D O I
10.1016/j.apsusc.2023.157252
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Solar conversion of CO2 into energy-rich products a sustainable solution to mitigate the global energy shortage and environmental crisis. Herein, the photocatalytic CO2 reduction of WS2-based single-atom catalysts was investigated using density functional theory. The results indicated that non-metals represented by B, C, and N doped WS2 (X-WS2) could significantly enhance the photocatalytic performance of CO2 reduction. Compare with Pt@WS2, Pt@B-WS2 could reduce the Gibbs free energy from 1.41 to 1.01 eV. The comprehensive results reveal that the introduction of the B atom endowed WS2 with improved metal-support interaction to stabilize the Pt single-atom and effectively promoted charge separation and transfer, leading to higher photocatalytic perfor-mance for converting CO2 to CH4. This study provides a strategy to design superior single-atom catalysts for photocatalytic conversion CO2 to carbon-neutral fuels.
引用
收藏
页数:7
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