Pt/POMs/TiO2 composite nanofibers with an enhanced visible-light photocatalytic performance for environmental remediation

被引:39
|
作者
Shi, Hongfei [1 ,2 ]
Zhao, Tingting [1 ]
Zhang, Yue [3 ]
Tan, Huaqiao [2 ]
Shen, Wenhui [1 ]
Wang, Weidong [1 ]
Li, Yangguang [2 ]
Wang, Enbo [2 ]
机构
[1] Jilin Inst Chem Technol, Inst Petrochem Technol, Jilin 132022, Jilin, Peoples R China
[2] Northeast Normal Univ, Fac Chem, Minist Educ, Key Lab Polyoxometalate Sci, Changchun 130024, Jilin, Peoples R China
[3] PetroChina, Jilin Petrochem Co, Res Inst, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
HYDROGEN EVOLUTION; TIO2; RECOMBINATION; DEGRADATION; WATER; NANOSTRUCTURES; NANOPARTICLES; FABRICATION; CONVERSION; TITANIA;
D O I
10.1039/c9dt02965f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Herein, a novel series of PMo12-TiO2 composites deposited with Pt nanoparticles (NPs), namely X%Pt/PMo12/TiO2 (PMo12 = H3PMo12O40; X stands for wt% of Pt to the PMo12/TiO2 sample and X = 3, 5, 8, and 10), were prepared through a simple electrospinning/calcination method, followed by photoreduction. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images showed that Pt NPs with an average size of 10 +/- 5 nm are well dispersed on the PMo12/TiO2 nanofibers. Photocatalytic tests revealed that the as-prepared Pt/PMo12/TiO2 composite catalysts exhibited excellent and persistent photocatalytic activity for removing methyl orange, tetracycline, Bisphenol A and Cr(vi) under visible-light illumination (lambda > 420 nm). Among the as-prepared composites, the 8%Pt/PMo12/TiO2 sample displayed the best photocatalytic activity with the rate constants of 0.011 min(-1) (MO), 0.043 min(-1) (TC), 0.00615 min(-1) (Bisphenol A) and 0.053 min(-1) (Cr(vi)). The addition of POM PMo12 to the composites enhanced the visible-light adsorption and redox ability of TiO2. Furthermore, Pt NPs exhibited localized surface plasmon resonance (LSPR) absorption, therefore improving the absorption of visible light by PMo12/TiO2. Additionally, intense local electromagnetic fields resulted from LSPR, which greatly facilitated the separation of photo-produced charge carriers in Pt/PMo12/TiO2. The results of free radical- and hole-trapping tests suggested that OH and O-2(-) were responsible for the degradation of MO/TC. Finally, the corresponding photocatalytic mechanism was proposed.
引用
收藏
页码:13353 / 13359
页数:7
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