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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.
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页数:7
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