4.7 Article

Engineering of SnO2/TiO2 heterojunction compact interface with efficient charge transfer pathway for photocatalytic hydrogen evolution

期刊

CHINESE CHEMICAL LETTERS
卷 34, 期 1, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2022.01.018

关键词

Photocatalysis; SnO2-TiO2 heterojunction; Solvent thermal; Charge transfer; Hydrogen evolution

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In this work, a compact and stable photocatalyst (SnO2/TiO2 heterostructure) with abundant oxygen vacancies was prepared. The heterojunction system provides active sites for catalytic reactions and promotes the separation and migration of photogenerated carriers. The hydrogen production rate of SnO2/TiO2 is significantly higher than that of TiO2 due to its good dynamical properties.
Fabricating an efficient charge transfer pathway at the compact interface between two kinds of semiconductors is an important strategy for designing hydrogen production heterojunction photocatalysts. In this work, we prepared a compact, stable and oxygen vacancy-rich photocatalyst (SnO2/TiO2 heterostructure) via a simple and reasonable in-situ synthesis method. Briefly, SnCl2-2H(2)O is hydrolyzed on the TiO2 precursor. After the pyrolysis process, SnO2 nanoparticles (5 nm) were dispersed on the surface of ultra-thin TiO2 nanosheets uniformly. Herein, the heterojunction system can offer abundant oxygen vacancies, which can act as active sites for catalytic reactions. Meanwhile, the interfacial contact of SnO2/TiO2 grading semiconductor oxide is uniform and tight, which can promote the separation and migration of photogenerated carriers. As shown in the experimental results, the hydrogen production rate of SnO2/TiO2 is 16.7 mmol h(-1) g(-1) (4.4 times higher than that of TiO2), which is owing to its good dynamical properties. This work demonstrates an efficient strategy of tight combining SnO2/TiO2 with abundant oxygen vacancies to improve catalytic efficiency. (c) 2022 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.

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