Enhanced photocatalytic CO2 reduction with suppressing H2 evolution via Pt cocatalyst and surface SiO2 coating

被引:69
作者
Wu, Hua-Kun [1 ,2 ]
Li, Yue-Hua [1 ,2 ]
Qi, Ming-Yu [1 ,2 ]
Lin, Qiong [1 ,2 ]
Xu, Yi-Jun [1 ,2 ]
机构
[1] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350116, Peoples R China
[2] Fuzhou Univ, Coll Chem, New Campus, Fuzhou 350116, Peoples R China
基金
中国国家自然科学基金;
关键词
Core-shell structure; Photocatalytic CO2 reduction; Suppressive H-2 evolution; Photosensitizer; Cocatalyst; METAL-COMPLEXES; PHOTOREDUCTION; TIO2; NANOPARTICLES; GENERATION; OXIDATION; CATALYSTS; BINDING; SIZE; AU;
D O I
10.1016/j.apcatb.2020.119267
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
The photocatalytic CO2 reduction to chemical feedstocks represents a promising route for the utilization of stranded renewable resources, but faces poor activity and selectivity resulting from the fast recombination of photogenerated charge carriers and competing hydrogen (H-2) evolution reaction. Herein, we report the synthesis of core-shell structured Pt/SiO2@SiO2 composites via electrostatic self-assembly and surface SiO2 coating for photocatalytic CO2 reduction with Ru(bpy)(3)(2+) (abbreviated as Ru, bpy = 2'2-bipyridine) as photosensitizer and Pt as cocatalyst under visible light irradiation (lambda > 420 nm). Photoluminescence results illustrate that Pt cocatalyst enhances the transfer of photogenerated electrons from the excited Ru, thereby improving photocatalytic performance. Further surface coating SiO2 prevents Pt from directly contacting with H2O and ameliorates CO2 adsorption ability of catalyst, thus suppressing H-2 evolution and increasing CO selectivity, which also endows the catalyst with enhanced stability. This work would provide an instructive guideline in regulating the selectivity and stability of using transition metal complexes as photosensitizers for photocatalytic CO2 reduction through the cocatalyst loading and surface coating strategy.
引用
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页数:8
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