Localized Surface Plasmon Resonance Promotes Metal-Organic Framework-Based Photocatalytic Hydrogen Evolution

被引:102
作者
Li, Zhao [1 ]
Zi, Jiangzhi [1 ]
Luan, Xue [1 ]
Zhong, Yueqi [1 ]
Qu, Minghan [1 ]
Wang, Yuzhe [1 ]
Lian, Zichao [1 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Mat & Chem, Shanghai 200093, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
localized surface plasmon resonance (LSPR); LSPR-induced hot electron transfer; metal-organic framework (MOF); photocatalytic hydrogen evolution; photo-induced carrier dynamics; GOLD NANOPARTICLES; WATER;
D O I
10.1002/adfm.202303069
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Combining metal nanoparticles (NPs) featured with localized surface plasmon resonance (LSPR) with metal-organic framework (MOF)-based photocatalysts is a novel means for achieving efficient separation of electron-hole pairs. Herein, the Au@NH2-UiO-66/CdS composites are successfully synthesized by encapsulating Au NPs with LSPR into the NH2-UiO-66 nanocage, further growing CdS NPs on the surface of the NH2-UiO-66, which exhibits higher photocatalytic activity in hydrogen evolution reaction under visible-light irradiation than that of NH2-UiO-66/CdS and CdS, respectively. Transient absorption measurements reveal that MOF is not only a transit station for electrons generated from CdS to Au, but also a receiver for hot electrons generated from plasmonic Au in Au@MOF/CdS composites. Thus, the LSPR-induced hot electron transfer from Au NPs is an important manifestation to prolong the carrier lifetime and enhance the photocatalytic performance. This work provides insights into investigating the photoinduced carrier dynamics of nanomaterials with LSPR effects for enhancing the MOF-based photocatalytic performance.
引用
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页数:7
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