Integrating Plasmonic Nanoparticles with TiO2 Photonic Crystal for Enhancement of Visible-Light-Driven Photocatalysis

被引:223
|
作者
Lu, Ying [1 ]
Yu, Hongtao [1 ]
Chen, Shuo [1 ]
Quan, Xie [1 ]
Zhao, Huimin [1 ]
机构
[1] Dalian Univ Technol, Sch Environm Sci & Technol, Key Lab Ind Ecol & Environm Engn Minist Educ Chin, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
NANOTUBE ARRAY ELECTRODE; GOLD NANOPARTICLES; AMPLIFIED PHOTOCHEMISTRY; HIGHLY EFFICIENT; TITANIA; FILMS; PHOTODEGRADATION; DEGRADATION; FABRICATION; GENERATION;
D O I
10.1021/es202669y
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Aimed at enhancing photocatalysis through intensifying light harvesting, a new photocatalyst was fabricated by infiltrating Au nanopartides into TiO2 photonic crystals (TiO2 PC/Au NPs). Scanning electron microscopy (SEM) and transmission electron microscope (TEM) images showed that the Au NPs with average diameter around 15 nm were dispersed uniformly into the porous TiO2 material. The results of the transmittance spectra demonstrated that the light absorption by Au NPs was amplified after they were infiltrated into TiO2 240, which was fabricated from 240 nm polystyrene spheres. In the photocatalytic experiments of 2,4-dichlorophenol degradation under visible light (lambda > 420 nm) irradiation, the kinetic constant using TiO2 240/Au NPs was 2.3 fold larger than that using TiO2 nanocrystalline/Au NPs (TiO2 NC/Au NPs). The excellent photocatalysis benefited from the cooperatively enhanced light harvesting owing to the localized surface plasmon resonance of Au NPs, which extended the light response spectra and the photonic effect of the TiO2 240 which intensified the plasmonic absorption by Au NPs. The hydroxyl radicals originated from the electroreduction of dissolved oxygen with photogenerated electrons via chain reactions were the main reactive oxygen species responsible for the pollutant degradation.
引用
收藏
页码:1724 / 1730
页数:7
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