| Literature DB >> 31563060 |
Huiyu Tian1, Xiang Liu1, Zhangqian Liang1, Pengyuan Qiu1, Xiu Qian1, Hongzhi Cui1, Jian Tian2.
Abstract
Recently, broad spectrum (visible and near-infrared (NIR)) light utilization has aroused widespread attention in the research of photocatalysis. While g-C3N4, highly stable, cheap and easily synthesized, shows H2 evolution activity under visible light irradiation, it doesn't perform under NIR light irradiation. Here we report an Au nanorods (NRs)/g-C3N4 heterostructure with Au nanorods on g-C3N4's surface. The most exciting feature of designed Au NRs/g-C3N4 heterostructures is that Au nanorods themselves are excited by visible and NIR light, which produce hot electrons and inject into g-C3N4. The photocatalytic H2 evolution rate of Au NRs/g-C3N4 heterostructures (350.6 μmol g-1 h-1) is nearly 4 times higher than that of g-C3N4 with Pt as cocatalyst (68.9 μmol g-1 h-1) under visible light illumination. The improved photocatalytic activity is ascribed to the increasing visible light-absorbing capacity of transverse surface plasmon resonance (TSPR) of Au nanorods and improved charge separation of Au NRs/g-C3N4 heterostructure. Even more important, Au NRs/g-C3N4 heterostructures achieve NIR photocatalytic H2 evolution performance (63.1 μmol g-1 h-1), owing to the longitudinal SPR (LSPR) effect of Au nanorods induced NIR light harvesting ability.Entities:
Keywords: Au nanorods; Near-infrared; Photocatalytic H(2) production; Visible; g-C(3)N(4)
Year: 2019 PMID: 31563060 DOI: 10.1016/j.jcis.2019.09.075
Source DB: PubMed Journal: J Colloid Interface Sci ISSN: 0021-9797 Impact factor: 8.128