光催化
表面等离子共振
材料科学
光化学
可见光谱
纳米颗粒
石墨氮化碳
等离子体子
三乙醇胺
纳米技术
催化作用
化学
光电子学
分析化学(期刊)
有机化学
作者
Zhiying Guo,Fangxu Dai,Huixiang Yin,Mingming Zhang,Jun Xing,Lei Wang
标识
DOI:10.1016/j.colcom.2022.100615
摘要
Gold nanoparticles (Au NPs) are widely utilized to broaden the light absorption of the photocatalysts due to their localized surface plasmon resonance (LSPR). However, the photocatalytic mechanism of Au/photocatalyst heterostructure involving charges transfer and reactive sites is still in dispute. Here, we synthesized a typical system Au/graphite carbon nitride (g-C3N4) and demonstrate that the role of Au NPs in the LSPR enhanced photocatalysis. Under visible light, the photoexcited electrons of g-C3N4 would transfer to Au NPs and reduce protons into hydrogen together with hot electrons of Au NPs. The hot holes of Au NPs would flow to g-C3N4 and oxidize triethanolamine. Therefore, the Au NPs play a dual role, plasma, and cocatalyst, in the LSPR enhanced photocatalyst. When λ > 420 nm, Au /g-C3N4 has hydrogen production of 159.9 μmol g−1 h−1. Our findings confirm the significance of metal plasma in photocatalytic reaction and benefit designing photocatalysts with boosting performance.
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