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Interfacial chemical bond and internal electric field modulated Z-scheme Sv-ZnIn2S4/MoSe2 photocatalyst for efficient hydrogen evolution

Xuehua WangCollege of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, P. R. ChinaXianghu WangCollege of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, P. R. ChinaJianfeng HuangSchool of Material Science and Engineering, International S&T Cooperation Foundation of Shaanxi Province, Xi'an Key Laboratory of Green Manufacture of Ceramic Materials, Shaanxi University of Science and Technology, Xi'an, ChinaShaoxiang LiShandong Engineering Technology Research Center for Advanced Coating, Qingdao University of Science and Technology, Qingdao, P. R. ChinaAlan MengKey Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, MOE. College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, P. R. China. [email protected]Zhenjiang LiCollege of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, P. R. China. [email protected]
2021en
ABI

Аннотация

Abstract Construction of Z-scheme heterostructure is of great significance for realizing efficient photocatalytic water splitting. However, the conscious modulation of Z-scheme charge transfer is still a great challenge. Herein, interfacial Mo-S bond and internal electric field modulated Z-scheme heterostructure composed by sulfur vacancies-rich ZnIn 2 S 4 and MoSe 2 was rationally fabricated for efficient photocatalytic hydrogen evolution. Systematic investigations reveal that Mo-S bond and internal electric field induce the Z-scheme charge transfer mechanism as confirmed by the surface photovoltage spectra, DMPO spin-trapping electron paramagnetic resonance spectra and density functional theory calculations. Under the intense synergy among the Mo-S bond, internal electric field and S-vacancies, the optimized photocatalyst exhibits high hydrogen evolution rate of 63.21 mmol∙g −1 ·h −1 with an apparent quantum yield of 76.48% at 420 nm monochromatic light, which is about 18.8-fold of the pristine ZIS. This work affords a useful inspiration on consciously modulating Z-scheme charge transfer by atomic-level interface control and internal electric field to signally promote the photocatalytic performance.

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