Gold photosensitized SrTiO3 for visible-light water oxidation induced by Au interband transitions

被引:106
作者
Liu, Lequan [1 ,2 ]
Li, Peng [2 ]
Adisak, Boonchun [2 ,5 ]
Ouyang, Shuxin [2 ,3 ]
Umezawa, Naoto [2 ,3 ]
Ye, Jinhua [1 ,2 ,3 ]
Kodiyath, Rajesh [2 ]
Tanabe, Toyokazu [2 ]
Ramesh, Gubbala V. [2 ]
Ueda, Shigenori [4 ]
Abe, Hideki [2 ,3 ]
机构
[1] Int Ctr Mat Nanoarchitecton WPI MANA, Tsukuba, Ibaraki 3050044, Japan
[2] Natl Inst Mat Sci, Environm Remediat Mat Unit, Tsukuba, Ibaraki 3050044, Japan
[3] Tianjin Univ, Sch Mat Sci & Engn, TU NIMS Joint Res Ctr, Tianjin 300072, Peoples R China
[4] NIMS, SPring8, Synchrotron Xray Stn, Sayo, Hyogo 6795148, Japan
[5] Kasetsart Univ, Dept Phys, Bangkok 10900, Thailand
关键词
SURFACE-PLASMON RESONANCE; METAL NANOPARTICLES; ELECTRON-TRANSFER; TITANIUM-DIOXIDE; TIO2; PHOTOCATALYSTS; ENHANCEMENT; ABSORPTION; REDUCTION; AU-TIO2;
D O I
10.1039/c4ta01988a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Gold nanoparticle (NP) photosensitization over semiconductors with a large band gap has emerged as a promising strategy for developing visible-light responsive photocatalytic materials. However, its application in harsh photocatalytic oxidation still remains a significant challenge. Furthermore, energetic charge carriers created in Au interband transitions under visible light are frequently ignored in this field. In the current work, for the first time, a remarkable visible-light photocatalytic water oxidation activity (14.9 mu mol h(-1): 0.2 g catalyst, 5 mmol AgNO3), even slightly higher than that of commercial WO3, was achieved over Au photosensitized SrTiO3 (1.1 wt%). In an elaborate study, electron transfer from gold to SrTiO3 was confirmed by STEM-EDS characterization on selective Ag deposition over SrTiO3. A combined investigation of apparent quantum efficiency results, theoretical simulation study on Au NPs optical excitation and relative band position analysis in Au/SrTiO3 reveals that these hot electrons transferred from gold to SrTiO3 mainly come from Au interband transitions other than plasmon resonance, while leaving holes on Au with enough oxidative potentials are responsible for water oxidation. The capability of involving Au interband transition in photosensitization for visible light water oxidation opens up new opportunities in designing and preparing visible-light responsive photocatalysts.
引用
收藏
页码:9875 / 9882
页数:8
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