Hydrogen production and simultaneous photoelectrocatalytic pollutant oxidation using a TiO2/WO3 nanostructured photoanode under visible light irradiation

被引:39
作者
Guaraldo, T. T. [1 ]
Goncales, V. R. [2 ]
Silva, B. F. [1 ]
de Torresi, S. I. C. [2 ]
Zanoni, M. V. B. [1 ]
机构
[1] Sao Paulo State Univ UNESP, Inst Chem, Rua Prof Francisco Degni 55, BR-14800900 Araraquara, SP, Brazil
[2] Sao Paulo Univ USP, Inst Chem, Ave Prof Lineu Prestes 748,Cidade Univ, BR-05599970 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Bicomponent electrodes; TiO2/WO3; templates; Photoelectrochemical hydrogen production; Dye degradation; DIOXIDE BILAYER COATINGS; REACTIVE BLACK 5; PULSED ELECTRODEPOSITION; THIN-FILMS; DEGRADATION; WATER; TEMPLATE;
D O I
10.1016/j.jelechem.2015.07.034
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Photoelectrochemical (PEC) hydrogen production and simultaneous organic waste degradation is a re-emerging field. The main challenge of this technique has been the synthesis of new photoanode materials that are active towards visible light. Coupling close band gap energy oxides can be used to obtain materials with new optical and electronic properties. For this purpose, Ti/TiO2/WO3 electrodes were prepared by electrochemical. anodization followed by templating and cathodic electrodeposition. The nanostructured bicomponent material was used as a photoanode for simultaneous hydrogen generation and organic dye degradation. A good photoactivity response (11 mA cm-(2)) was obtained under UV and visible light irradiation, when compared to pure TiO2 (8 mA cm-(2)). Optimization of photoelectrochemical conditions revealed that pH optimization had a major impact on H-2 production, resulting in satisfactory hydrogen generation efficiency (46%) and dye removal (100% discoloration and 85% reduction in TOC). A dye oxidation mechanism is proposed, based on LC-MS/MS analyses. The TiO2/WO3 photoanode could potentially be used for environmental remediation and hydrogen generation under solar irradiation. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:188 / 196
页数:9
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