TiO2-NiO p-n nanocomposite with enhanced sonophotocatalytic activity under diffused sunlight

被引:76
作者
Vinoth, R. [1 ]
Karthik, P. [1 ]
Devan, K. [2 ]
Neppolian, B. [1 ]
Ashokkumar, Muthupandian [3 ]
机构
[1] SRM Univ, SRM Res Inst, Madras 603203, Tamil Nadu, India
[2] Madras Christian Coll, Dept Chem, Madras 600059, Tamil Nadu, India
[3] Univ Melbourne, Sch Chem, Melbourne, Vic 3010, Australia
关键词
Sonophotocatalysts; Diffused sunlight; TiO2-NiO; Photocatalysts and synergistic effect; REDUCED GRAPHENE OXIDE; ULTRASOUND ASSISTED SYNTHESIS; WASTE-WATER TREATMENT; PHOTOCATALYTIC DEGRADATION; MESOPOROUS TIO2; METHYL-ORANGE; OXIDATION; NANOPARTICLES; TEMPERATURES; REDUCTION;
D O I
10.1016/j.ultsonch.2016.03.005
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
TiO2-NiO composites with p-n junction were developed by assembling p-type NiO on n-type TiO2 using ultrasound assisted wet impregnation method. The sonophotocatalytic efficiencies of pure TiO2 and TiO2-NiO composites were evaluated under diffused sunlight using methyl orange (MO) as a model pollutant. The impregnation of NiO nanoparticles on TiO2 considerably enhanced the optical absorption in visible region (500-800 nm) due to the formation of p-n junctions at the interface between TiO2 and NiO. The internal electric field induced by the p-n junction led to effective separation of electron-hole pairs and thereby generating a large amount of reactive species for the degradation of MO. The individual effect of ultrasound and diffused sunlight for the degradation of MO was found to be 30% and 6%, respectively. A synergy of 4.8 fold was achieved when ultrasound was combined with photocatalytic degradation process in the presence of diffused sunlight. The sonophotocatalytic activity of TiO2-NiO photocatalysts with different NiO loading was also evaluated and 10 wt% NiO loading was found to be optimal. Moreover, 66% of Total Organic Carbon (TOC) removal was achieved with the optimized TiO2-NiO composite in 140 min. In addition, the TiO2-NiO composite exhibited an enhanced photocurrent response under visible light illumination. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:655 / 663
页数:9
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