Title: Enhanced optical absorption and photocatalytic H-2 production activity of g-C3N4/TiO2 heterostructure by interfacial coupling: A DFT plus U study
Authors: Lin, Yanming
Shi, Hailong
Jiang, Zhenyi
Wang, Guanshi
Zhang, Xiaodong
Zhu, Haiyan
Zhang, Ruiqin
Zhu, Chaoyuan
應用化學系分子科學碩博班
Institute of Molecular science
Keywords: g-C3N4/TiO2 heterostructure;Electronic structure;Photocatalytic H-2 production;Density functional theory
Issue Date: 13-Apr-2017
Abstract: The electronic and optical properties of g-C3N4/TiO2 heterostructure are investigated using spin-polarized DFT+U calculations. The equilibrium spacing (1.94 angstrom) and binding energy (24 meV/angstrom(2)) show that g-C3N4/TiO2 is a van der Waals heterostructure. And the calculated band gap of g-C3N4/TiO2 is significantly reduced compared with TiO2. Therefore, the visible light response of g-C3N4/TiO2 heterostructure is remarkably improved. Besides, the predicted type II band alignment would ensure that the electrons can migrate from g-C3N4 monolayer to anatase TiO2 (101) surface, which leads oxidation and redox reactions can occur on g-C3N4 and TiO2, respectively. Finally, a built-in electric field within the interface region will be set. Above processes can benefit the separation of photoexcited carriers and enhance the hydrogen-evolution activity. In addition, compared with TiO2, g-C3N4/TiO2 with higher conduction band minimum energy can effectively produce higher-energy electrons to reduce hydrogen ions. Moreover, the influence of composite distance and the number of g-C3N4 layers are also investigated systematically. The results indicate that the optical absorption is enhanced over the whole spectrum with the increase of the number of g-C3N4 layers. Similar visible light enhancing is also found when the composite distance is decreased. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
URI: http://dx.doi.org/10.1016/j.ijhydene.2017.02.172
http://hdl.handle.net/11536/145589
ISSN: 0360-3199
DOI: 10.1016/j.ijhydene.2017.02.172
Journal: INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume: 42
Begin Page: 9903
End Page: 9913
Appears in Collections:Articles