Photocatalytic reduction of Cr(VI) by iron tungstosilicate under visible light

被引:16
|
作者
Cen, Qing [1 ]
Gao, Qiaoyuan [1 ]
Zhang, Chenlu [1 ]
Liu, Yingqi [1 ]
Wang, Qi [1 ,2 ]
Wang, Qi [1 ,2 ]
机构
[1] Zhejiang Gongshang Univ, Sch Environm Sci & Engn, Hangzhou 310018, Peoples R China
[2] Chinese Acad Sci, Inst Plasma Phys, Key Lab Photovolta & Energy Conversat Mat, 350 Shushanhu Rd, Hefei 230031, Peoples R China
基金
中国国家自然科学基金;
关键词
H4SiW12O40; Photocatalysis; Polyoxometalates; Cr(VI) reduction; FeSiW; ENVIRONMENTAL REMEDIATION; AQUEOUS-SOLUTION; POLYOXOMETALATE; HYBRID; COMPOSITE; SOLAR; DYE; DEGRADATION; CONVERSION; OXIDATION;
D O I
10.1016/j.jcis.2019.11.098
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
In this study, visible-light-active iron tungstosilicate (FeSiW) was fabricated via solvothermal method. Fe3+ was applied as counter ion to precipitate with silicotungstic acid (H4SiW12O40) in methanol solution. It can be observed from FT-IR spectra that the Keggin structure of SiW12O404- was well maintained in FeSiW. Besides, the effect of different initial molar ratios of Fe3+ to H4SiW12O40 was investigated (from 4:1 to 4:4). By photoelectrochemical characterizations, such as photocurrent response and Mott-Schottky (M-S) plots, easiest generation of electron-hole pairs and lowest charge transfer resistance can be observed on FeSiW with initial molar ratio of 4:3. Moreover, FeSiW with 4:3 ratio also displayed highest activity for photocatalytic reduction of Cr(VI), despite of the largest band gap (ca. 2.71 eV). The lowest unoccupied molecular orbital (LUMO) and highest occupied molecular orbital (HOMO) of the optimized FeSiW were estimated to be +0.03 V and 2.74 V vs NHE, respectively, which were thermodynamically feasible for Cr(VI) reduction and H2O oxidation. Even under acidic condition (pH 3), the optimized photocatalyst displayed good stability in cyclic runs. Therefore, the present study opens a new way for heterogeneous polyoxometalates as efficient photocatalyst for environmental application. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:12 / 20
页数:9
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