A robust visible-light driven BiFeWO6/BiOI nanohybrid with efficient photocatalytic and photoelectrochemical performance

被引:96
作者
Malathi, A. [1 ]
Arunachalam, Prabhakarn [2 ]
Grace, Andrews Nirmala [3 ]
Madhavan, J. [1 ]
Al-Mayouf, Abdullah M. [2 ]
机构
[1] Thiruvalluvar Univ, Dept Chem, Solar Energy Lab, Vellore 632115, Tamil Nadu, India
[2] King Saud Univ, Coll Sci, Chem Dept, Electrochem Res Grp, Riyadh 11451, Saudi Arabia
[3] VIT Univ, Ctr Nanotechnol Res, Vellore 632014, Tamil Nadu, India
关键词
BiFeWO6/BiOI; Rhodamine B; Photocatalysis; Visible light; Reusability; HYDROTHERMAL SYNTHESIS; ASSISTED SYNTHESIS; HIGHLY EFFICIENT; FACILE SYNTHESIS; BIOI; NANOCOMPOSITES; IRRADIATION; DYE; HETEROJUNCTIONS; PHOTOACTIVITY;
D O I
10.1016/j.apsusc.2017.03.199
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 work, an efficient visible-light active BiFeWO6/BiOI nanocomposite was fabricated by mixing various weight percentages (1%, 2% and 3%) of BiFeWO6 on BiOI via facile one-step wet impregnation method. The synthesized BiFeWO6/BiOI nanocomposite were investigated by XRD, FT-IR, FE-SEM, HR-TEM, EDAX, UV-vis DRS and BET. The photocatalytic activity of synthesized BiFeWO6/BiOI nanocomposite photocatalysts were assessed for the photodegradation of Rhodamine B (RhB) under visible-light illumination. The optimum 1% BiFeWO6/BiOI nanocomposite showed 92% efficiency of RhB after 90 min. The photoluminescence (PL) and photoelectrochemical measurements revealed that the 1% BiFeWO6/BiOI nanocomposite greatly enhanced the charge carrier separation and thus by slowing down the recombination rate of the photoinduced charge carriers. The radical trapping experiment inferred the h(+) and 02(center dot-) as the important active species responsible for the photodegradation of RhB. The higher photocatalytic activity and recyclability revealed that the BiFeWO6/BiOI nanocomposite could be a promising material in wastewater treatment and other environmental remediation applications. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:85 / 95
页数:11
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