共 50 条
Hollow spherical biomass derived-carbon dotted with SnS2/g-C3N4 Z-scheme heterojunction for efficient CO2 photoreduction into CO
被引:50
|作者:
Li, Yang
[1
]
Yin, Qiao
[1
]
Zeng, Yingshan
[1
]
Liu, Zhi
[1
]
机构:
[1] Shantou Univ, Coll Sci, Dept Chem, Shantou 515063, Peoples R China
基金:
中国国家自然科学基金;
关键词:
g-C3N4;
SnS2;
Biomass-derived carbon;
CO2;
photoreduction;
Theoretical calculation;
DEGRADATION;
G-C3N4;
REDUCTION;
NITRIDE;
D O I:
10.1016/j.cej.2022.135652
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
The core of realizing the effective CO2 conversion by solar energy is to develop a stable photocatalyst with high CO2 adsorption capacity and high charge separation efficiency. In this work, a hollow spherical Z-scheme SnS2/g-C3N4/C (SCC) photocatalyst is successfully constructed by a morphology-inherited strategy. Biomass mabospores are utilized as both the precursor for formation of hollow spherical structure and carbon source, and the g-C3N4 and SnS2 nanosheets tightly anchor on the surface of mabospores-derived carbon spheres. The Z-scheme SCC heterostructure exhibits 5.5 times activity enhancement on CO2 photoreduction to CO with a high evolution rate up to 40.86 mu mol.g(-1). h(-1). Examined by various photoelectrochemical analysis, the boosted photocatalytic activity originates mainly from the construction of hollow spherical Z-scheme heterojunction, providing the more preferable basic sites for CO2 adsorption, promoting the separation efficiency of electron-hole pairs, as well as increasing the reductionability of electrons in conduction band of g-C3N4. The formed internal electric fields between the g-C3N4 and SnS2 can also further reinforce the spatial separation of photogenerated charge carriers. Theoretical calculations further verify that the SCC Z-scheme heterostructure can effectively decrease the energy barriers of formed intermediates, especially the crucial COOH*, and thus leading to the facile conversion of CO2- to-CO. This work induces a new strategy to construct g-C3N4-based Z-scheme heterojunction assisted by versatile biomasses with optimized structure and enhanced photoelectrochemical merits for efficient CO2 conversion into chemical fuels.
引用
收藏
页数:14
相关论文