Precise Colloidal Plasmonic Photocatalysts Constructed by Multistep Photodepositions

被引:28
作者
Ha, Hyun Dong [1 ,2 ]
Yan, Chang [1 ,2 ]
Katsoukis, Georgios [3 ]
Kamat, Gaurav A. [4 ]
Moreno-Hernandez, Ivan A. [1 ]
Frei, Heinz [3 ]
Alivisatos, A. Paul [1 ,2 ,5 ,6 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
[3] Lawrence Berkeley Natl Lab, Mol Biophys & Integrated Bioimaging Div, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[5] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
[6] Kavli Energy NanoSci Inst, Berkeley, CA 94720 USA
关键词
plasmonic photocatalysis; precise nanostructures; oxygen evolution reaction; photodeposition; Z scheme; Au nanocrystal; WATER-OXIDATION CATALYST; OPTICAL-PROPERTIES; CHARGE SEPARATION; NANOPARTICLES; COCATALYSTS; PHOTOANODES; TUNABILITY; DYNAMICS; NANORODS; CARRIERS;
D O I
10.1021/acs.nanolett.0c03431
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Natural photosynthesis relies on a sophisticated charge transfer pathway among multiple components with precise spatial, energetic, and temporal organizations in the aqueous environment. It continues to inspire and challenge the design and fabrication of artificial multicomponent colloidal nanostructures for solar-to-fuel conversion. Herein, we introduce a plasmonic photocatalyst synthesized with colloidal methods with five integrated components including cocatalysts installed in orthogonal locations. The precise deposition of individual inorganic components on an Au/TiO2 nanodumbell nanostructure is enabled by photoreduction and photooxidation, which selectively occurs at the TiO2 tip sites and Au lateral sites, respectively. Under visible-light irradiation, the photocatalyst exhibited activity of oxygen evolution from water without scavengers. We demonstrate that each component is essential for improving the photocatalytic performance. In addition, mechanistic studies suggest that the photocatalytic reaction requires combining the hot charge carriers derived from exciting both the d-sp interband transition and the localized surface plasmon resonance of Au.
引用
收藏
页码:8661 / 8667
页数:7
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