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Unique and facile solvothermal synthesis of mesoporous WO(3) using a solid precursor and a surfactant template as a photoanode for visible-light-driven water oxidation

Mesoporous tungsten trioxide (WO(3)) was prepared from tungstic acid (H(2)WO(4)) as a tungsten precursor with dodecylamine (DDA) as a template to guide porosity of the nanostructure by a solvothermal technique. The WO(3) sample (denoted as WO(3)-DDA) prepared with DDA was moulded on an electrode to...

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Autores principales: Li, Dong, Chandra, Debraj, Saito, Kenji, Yui, Tatsuto, Yagi, Masayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194058/
https://www.ncbi.nlm.nih.gov/pubmed/25313301
http://dx.doi.org/10.1186/1556-276X-9-542
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author Li, Dong
Chandra, Debraj
Saito, Kenji
Yui, Tatsuto
Yagi, Masayuki
author_facet Li, Dong
Chandra, Debraj
Saito, Kenji
Yui, Tatsuto
Yagi, Masayuki
author_sort Li, Dong
collection PubMed
description Mesoporous tungsten trioxide (WO(3)) was prepared from tungstic acid (H(2)WO(4)) as a tungsten precursor with dodecylamine (DDA) as a template to guide porosity of the nanostructure by a solvothermal technique. The WO(3) sample (denoted as WO(3)-DDA) prepared with DDA was moulded on an electrode to yield efficient performance for visible-light-driven photoelectrochemical (PEC) water oxidation. Powder X-ray diffraction (XRD) data of the WO(3)-DDA sample calcined at 400°C indicate a crystalline framework of the mesoporous structure with disordered arrangement of pores. N(2) physisorption studies show a Brunauer-Emmett-Teller (BET) surface area up to 57 m(2) g(-1) together with type IV isotherms and uniform distribution of a nanoscale pore size in the mesopore region. Scanning electron microscopy (SEM) images exhibit well-connected tiny spherical WO(3) particles with a diameter of ca. 5 to 20 nm composing the mesoporous network. The WO(3)-DDA electrode generated photoanodic current density of 1.1 mA cm(-2) at 1.0 V versus Ag/AgCl under visible light irradiation, which is about three times higher than that of the untemplated WO(3). O(2) (1.49 μmol; Faraday efficiency, 65.2%) was evolved during the 1-h photoelectrolysis for the WO(3)-DDA electrode under the conditions employed. The mesoporous electrode turned out to work more efficiently for visible-light-driven water oxidation relative to the untemplated WO(3) electrode.
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spelling pubmed-41940582014-10-13 Unique and facile solvothermal synthesis of mesoporous WO(3) using a solid precursor and a surfactant template as a photoanode for visible-light-driven water oxidation Li, Dong Chandra, Debraj Saito, Kenji Yui, Tatsuto Yagi, Masayuki Nanoscale Res Lett Nano Express Mesoporous tungsten trioxide (WO(3)) was prepared from tungstic acid (H(2)WO(4)) as a tungsten precursor with dodecylamine (DDA) as a template to guide porosity of the nanostructure by a solvothermal technique. The WO(3) sample (denoted as WO(3)-DDA) prepared with DDA was moulded on an electrode to yield efficient performance for visible-light-driven photoelectrochemical (PEC) water oxidation. Powder X-ray diffraction (XRD) data of the WO(3)-DDA sample calcined at 400°C indicate a crystalline framework of the mesoporous structure with disordered arrangement of pores. N(2) physisorption studies show a Brunauer-Emmett-Teller (BET) surface area up to 57 m(2) g(-1) together with type IV isotherms and uniform distribution of a nanoscale pore size in the mesopore region. Scanning electron microscopy (SEM) images exhibit well-connected tiny spherical WO(3) particles with a diameter of ca. 5 to 20 nm composing the mesoporous network. The WO(3)-DDA electrode generated photoanodic current density of 1.1 mA cm(-2) at 1.0 V versus Ag/AgCl under visible light irradiation, which is about three times higher than that of the untemplated WO(3). O(2) (1.49 μmol; Faraday efficiency, 65.2%) was evolved during the 1-h photoelectrolysis for the WO(3)-DDA electrode under the conditions employed. The mesoporous electrode turned out to work more efficiently for visible-light-driven water oxidation relative to the untemplated WO(3) electrode. Springer 2014-10-02 /pmc/articles/PMC4194058/ /pubmed/25313301 http://dx.doi.org/10.1186/1556-276X-9-542 Text en Copyright © 2014 Li et al.; licensee Springer. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Nano Express
Li, Dong
Chandra, Debraj
Saito, Kenji
Yui, Tatsuto
Yagi, Masayuki
Unique and facile solvothermal synthesis of mesoporous WO(3) using a solid precursor and a surfactant template as a photoanode for visible-light-driven water oxidation
title Unique and facile solvothermal synthesis of mesoporous WO(3) using a solid precursor and a surfactant template as a photoanode for visible-light-driven water oxidation
title_full Unique and facile solvothermal synthesis of mesoporous WO(3) using a solid precursor and a surfactant template as a photoanode for visible-light-driven water oxidation
title_fullStr Unique and facile solvothermal synthesis of mesoporous WO(3) using a solid precursor and a surfactant template as a photoanode for visible-light-driven water oxidation
title_full_unstemmed Unique and facile solvothermal synthesis of mesoporous WO(3) using a solid precursor and a surfactant template as a photoanode for visible-light-driven water oxidation
title_short Unique and facile solvothermal synthesis of mesoporous WO(3) using a solid precursor and a surfactant template as a photoanode for visible-light-driven water oxidation
title_sort unique and facile solvothermal synthesis of mesoporous wo(3) using a solid precursor and a surfactant template as a photoanode for visible-light-driven water oxidation
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194058/
https://www.ncbi.nlm.nih.gov/pubmed/25313301
http://dx.doi.org/10.1186/1556-276X-9-542
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