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 |