Abstract
Construction of semiconductor heterojunctions is an efficient strategy to improve photo-induced charges separation and thus enhance photocatalytic activities. Herein, g-C3N4/TiO2 heterostructures were prepared via a facile thermal procedure, with TiO2 nanorods as matrix and g-C3N4 as visible-light sensitizer. Heterojunctions formed while precursors cyanamide polymerized to g-C3N4 and protonated titanate nanotube (H-TNTs) dehydrated and shrinked to TiO2 nanorods. Notably, confined polymerization of g-C3N4 occurred at both external surface and internal space of H-TNTs with the assistant of vacuum treatment, while NH3 released from cyanamide decomposition yielded abundant oxygen vacancies (VO) in TiO2 nanorods. Compared with pristine TiO2 nanorods, the heterostructured g-C3N4/TiO2 nanorods possess 1.7 times more active in photocatalytic removal of organic dye Orange II. A mechanism was proposed for heterostructured g-C3N4/TiO2 nanorods, being attributed to synergistic increasing light harvesting by VO and charges separation by heterojunctions.
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This work was financially supported by A Project of Shandong Province Higher Educational Science and Technology Program (No. J18KA011) and Doctoral Found of QUST (No. 010022803).
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Jiang, D., Sun, X., Zhang, H. et al. Nanotube confinement-induced g-C3N4/TiO2 nanorods with rich oxygen vacancies for enhanced photocatalytic water decontamination. Appl. Phys. A 126, 246 (2020). https://doi.org/10.1007/s00339-020-3430-y
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DOI: https://doi.org/10.1007/s00339-020-3430-y