共 57 条
S-scheme CuWO4@g-C3N4 core-shell microsphere for CO2 photoreduction
被引:25
作者:

Lu, Zhao
论文数: 0 引用数: 0
h-index: 0
机构:
HKUST Shenzhen Hong Kong Collaborat Innovat Res In, Shenzhen, Peoples R China
Hong Kong Polytech Univ, Dept Civil & Environm Engn, Hong Kong, Peoples R China HKUST Shenzhen Hong Kong Collaborat Innovat Res In, Shenzhen, Peoples R China

Wang, Zhongliao
论文数: 0 引用数: 0
h-index: 0
机构:
Huaibei Normal Univ, Key Lab Green & Precise Synthet Chem & Applicat, Anhui Prov Key Lab Pollutant Sensit Mat & Environm, Sch Phys & Elect Informat,Minist Educ, Huaibei 235000, Peoples R China HKUST Shenzhen Hong Kong Collaborat Innovat Res In, Shenzhen, Peoples R China
机构:
[1] HKUST Shenzhen Hong Kong Collaborat Innovat Res In, Shenzhen, Peoples R China
[2] Hong Kong Polytech Univ, Dept Civil & Environm Engn, Hong Kong, Peoples R China
[3] Huaibei Normal Univ, Key Lab Green & Precise Synthet Chem & Applicat, Anhui Prov Key Lab Pollutant Sensit Mat & Environm, Sch Phys & Elect Informat,Minist Educ, Huaibei 235000, Peoples R China
关键词:
S-scheme;
CuWO4;
Microspheres;
CO2;
photoreduction;
PHOTOCATALYST;
CUWO4;
HETEROJUNCTION;
DEGRADATION;
FABRICATION;
COMPOSITES;
CHEMISTRY;
D O I:
10.1016/j.mssp.2022.107177
中图分类号:
TM [电工技术];
TN [电子技术、通信技术];
学科分类号:
0808 ;
0809 ;
摘要:
Utilizing solar energy to achieve artificial photosynthesis of chemical fuel is prevalent in tackling CO2 excessive emissions and energy deficiency. Engineering tailored morphology and constructing matched heterostructure are two significant schemes to elevate the CO2 photoconversion efficiency of g-C3N4-based composite. Herein, a novel S-scheme CuWO4@g-C3N4 core-shell microspheres were designed by a template-free hydrothermal and annealing approach. The CuWO4@g-C3N4 composite exhibits improved visible light harvesting, increased BET specific area, and enhanced CO2 adsorption ability. Further, S-scheme CuWO4@g-C3N4 heterojunction facilitates charge separation and realizes strong redox capability, contributing to elevated CO2 photoreduction perfor-mance. The CO yield rate for CuWO4@g-C3N4 composite reaches about 4.15 mu mol g-1 h-1, which is 2.7 folds that of bare g-C3N4 (1.56 mu mol g-1 h-1). Theoretical calculations unveil that the hydrogenation and reduction of *OCHO to *HCOOH are involved in a higher Eb of 0.39 eV than CO (0.24 eV), contributing to a high selectivity for CO yield. This work can be employed to fabricate more various g-C3N4-based composites for artificial photosynthesis.
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