| Literature DB >> 32207505 |
Menglei Zhu1, Yuanyuan Wang1, Yan-Hui Deng2, Xiaoniu Peng1, Xina Wang1, Hui Yuan1, Zhong-Jian Yang2, Yalan Wang3, Hao Wang1.
Abstract
Owing to the capacity of efficiently harvesting and converting incident energy, localized surface-plasmon resonance of noble metals was introduced into a metal-semiconductor design for promoting hydrogen evolution. In this study, a plasmonic nanodumbbell structure was employed to strategically modulate the energy transfer in the water reduction reaction. A maximum H2 evolution rate of 80 μmol g-1 h-1 was obtained in the Au-TiO2 nanodumbbells, and further improvement was achieved through surface modification with Pt nanoparticles functioning as active sites, leading to ∼4.3 times enhanced photocatalytic activity. Compared with similar nanostructures reported previously, the present superior photoactivity response is ascribed to the injection process of the energetic hot electrons generated from the excitation and decay of the longitudinal surface-plasmon resonance (LSPR) and transverse surface-plasmon resonance (TSPR) in the Au nanorods, which corresponds to the electric field distribution of the finite-difference-time-domain simulation. These intriguing results, originating from the positive synergistic effect of the plasmon and co-catalyst, demonstrated the mechanism of the plasmon-assisted photochemistry and provided a promising strategy for the rational design of novel plasmonic photocatalysts.Entities:
Year: 2020 PMID: 32207505 DOI: 10.1039/d0nr00441c
Source DB: PubMed Journal: Nanoscale ISSN: 2040-3364 Impact factor: 7.790