Electrochemically self-doped WO3/TiO2 nanotubes for photocatalytic degradation of volatile organic compounds

[Display omitted] •Tailoring of the quantity and distribution of OVs in WO3/TNTs matrix by a simple electrochemical step.•Enhancement of charge-transport and reduction of electron-hole recombination by the incorporation of surface OVs.•12 times higher photo-current density and an enhanced photocatal...

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Published inApplied catalysis. B, Environmental Vol. 260; p. 118205
Main Authors Wang, Xiaoguang, Sun, Minghui, Murugananthan, Muthu, Zhang, Yanrong, Zhang, Lizhi
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.01.2020
Elsevier BV
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Abstract [Display omitted] •Tailoring of the quantity and distribution of OVs in WO3/TNTs matrix by a simple electrochemical step.•Enhancement of charge-transport and reduction of electron-hole recombination by the incorporation of surface OVs.•12 times higher photo-current density and an enhanced photocatalytic removal efficiency of VOCs by self-doped R-WO3/TNTs.•Excellent durability during the photodegradation process by the R-WO3/TNTs with open channel structure of the TiO2 nanotubes. In this study, an electrochemically self-doped WO3/TiO2 nanotubes (R-WO3/TNTs) composite film was developed for the photocatalytic degradation of waste gas. The doping of oxygen vacancies (OVs) into the heterojunction of WO3/TNTs was conducted by a simple electrochemical approach, by which the quantity and distribution of OVs on surface as well as bulk were tailored with respect to the applied cathodic potential and the duration of the treatment. With an increase of applied cathodic potential as well as the duration, the quantity of OVs on WO3/TNTs was observed to be consistently raised, while those presented in the surface were raised initially and further showed a plateau trend as the duration extended at a fixed potential. The incorporation of OVs into WO3/TNTs enhanced the charge-transport resistance and reduced the electron-hole recombination, thereby showed an enhanced photocatalytic performance. The R-WO3/TNTs prepared by the electrochemical polarization process at −1.4 V (vs SCE) exhibited a 12 times higher photo-current density and obviously, an enhanced efficiency in the photocatalytic degradation of VOCs with a prolonging photostability compared to that of the pristine WO3/TNTs, under a simulated solar light irradiation. The single-time purification trial demonstrated the effectiveness of the R-WO3/TNTs composite in treating the VOCs for the practical application.
AbstractList [Display omitted] •Tailoring of the quantity and distribution of OVs in WO3/TNTs matrix by a simple electrochemical step.•Enhancement of charge-transport and reduction of electron-hole recombination by the incorporation of surface OVs.•12 times higher photo-current density and an enhanced photocatalytic removal efficiency of VOCs by self-doped R-WO3/TNTs.•Excellent durability during the photodegradation process by the R-WO3/TNTs with open channel structure of the TiO2 nanotubes. In this study, an electrochemically self-doped WO3/TiO2 nanotubes (R-WO3/TNTs) composite film was developed for the photocatalytic degradation of waste gas. The doping of oxygen vacancies (OVs) into the heterojunction of WO3/TNTs was conducted by a simple electrochemical approach, by which the quantity and distribution of OVs on surface as well as bulk were tailored with respect to the applied cathodic potential and the duration of the treatment. With an increase of applied cathodic potential as well as the duration, the quantity of OVs on WO3/TNTs was observed to be consistently raised, while those presented in the surface were raised initially and further showed a plateau trend as the duration extended at a fixed potential. The incorporation of OVs into WO3/TNTs enhanced the charge-transport resistance and reduced the electron-hole recombination, thereby showed an enhanced photocatalytic performance. The R-WO3/TNTs prepared by the electrochemical polarization process at −1.4 V (vs SCE) exhibited a 12 times higher photo-current density and obviously, an enhanced efficiency in the photocatalytic degradation of VOCs with a prolonging photostability compared to that of the pristine WO3/TNTs, under a simulated solar light irradiation. The single-time purification trial demonstrated the effectiveness of the R-WO3/TNTs composite in treating the VOCs for the practical application.
In this study, an electrochemically self-doped WO3/TiO2 nanotubes (R-WO3/TNTs) composite film was developed for the photocatalytic degradation of waste gas. The doping of oxygen vacancies (OVs) into the heterojunction of WO3/TNTs was conducted by a simple electrochemical approach, by which the quantity and distribution of OVs on surface as well as bulk were tailored with respect to the applied cathodic potential and the duration of the treatment. With an increase of applied cathodic potential as well as the duration, the quantity of OVs on WO3/TNTs was observed to be consistently raised, while those presented in the surface were raised initially and further showed a plateau trend as the duration extended at a fixed potential. The incorporation of OVs into WO3/TNTs enhanced the charge-transport resistance and reduced the electron-hole recombination, thereby showed an enhanced photocatalytic performance. The R-WO3/TNTs prepared by the electrochemical polarization process at −1.4 V (vs SCE) exhibited a 12 times higher photo-current density and obviously, an enhanced efficiency in the photocatalytic degradation of VOCs with a prolonging photostability compared to that of the pristine WO3/TNTs, under a simulated solar light irradiation. The single-time purification trial demonstrated the effectiveness of the R-WO3/TNTs composite in treating the VOCs for the practical application.
ArticleNumber 118205
Author Wang, Xiaoguang
Zhang, Lizhi
Murugananthan, Muthu
Zhang, Yanrong
Sun, Minghui
Author_xml – sequence: 1
  givenname: Xiaoguang
  surname: Wang
  fullname: Wang, Xiaoguang
  organization: School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan, 430074, PR China
– sequence: 2
  givenname: Minghui
  surname: Sun
  fullname: Sun, Minghui
  organization: School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan, 430074, PR China
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  givenname: Muthu
  orcidid: 0000-0003-0575-5018
  surname: Murugananthan
  fullname: Murugananthan, Muthu
  organization: Department of Chemistry, PSG College of Technology, Peelamedu, Coimbatore, 641004, India
– sequence: 4
  givenname: Yanrong
  orcidid: 0000-0002-8793-090X
  surname: Zhang
  fullname: Zhang, Yanrong
  email: yanrong_zhang@hust.edu.cn
  organization: School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan, 430074, PR China
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  givenname: Lizhi
  orcidid: 0000-0002-6842-9167
  surname: Zhang
  fullname: Zhang, Lizhi
  email: zhanglz@mail.ccnu.edu.cn
  organization: Institute of Environmental Chemistry, Central China Normal University, Wuhan, 430079, PR China
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Keywords VOC degradation
Electrochemical self-doping
Photocatalysis
WO3/TiO2 nanotubes
Oxygen vacancy
Language English
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SSID ssj0002328
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Snippet [Display omitted] •Tailoring of the quantity and distribution of OVs in WO3/TNTs matrix by a simple electrochemical step.•Enhancement of charge-transport and...
In this study, an electrochemically self-doped WO3/TiO2 nanotubes (R-WO3/TNTs) composite film was developed for the photocatalytic degradation of waste gas....
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SubjectTerms Charge transport
Electrochemical self-doping
Electrochemistry
Electrode polarization
Exhaust gases
Heterojunctions
Holes (electron deficiencies)
Irradiation
Light irradiation
Nanotechnology
Nanotubes
Organic compounds
Oxygen vacancy
Photocatalysis
Photodegradation
Purification
Recombination
Titanium dioxide
Tungsten oxides
VOC degradation
VOCs
Volatile organic compounds
WO3/TiO2 nanotubes
Title Electrochemically self-doped WO3/TiO2 nanotubes for photocatalytic degradation of volatile organic compounds
URI https://dx.doi.org/10.1016/j.apcatb.2019.118205
https://www.proquest.com/docview/2315501659
Volume 260
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