Dynamic Hydrogen Production from Methanol/Water Photo-Splitting Using Core@Shell-Structured CuS@TiO2 Catalyst Wrapped by High Concentrated TiO2 Particles

This study focused on the dynamic hydrogen production ability of a core@shell-structured CuS@TiO2 photocatalyst coated with a high concentration of TiO2 particles. The rectangular-shaped CuS particles, 100 nm in length and 60 nm in width, were surrounded by a high concentration of anatase TiO2 parti...

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Main Authors: Younghwan Im, Sora Kang, Kang Min Kim, Taeil Ju, Gi Bo Han, No-Kuk Park, Tae Jin Lee, Misook Kang
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:International Journal of Photoenergy
Online Access:http://dx.doi.org/10.1155/2013/452542
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author Younghwan Im
Sora Kang
Kang Min Kim
Taeil Ju
Gi Bo Han
No-Kuk Park
Tae Jin Lee
Misook Kang
author_facet Younghwan Im
Sora Kang
Kang Min Kim
Taeil Ju
Gi Bo Han
No-Kuk Park
Tae Jin Lee
Misook Kang
author_sort Younghwan Im
collection DOAJ
description This study focused on the dynamic hydrogen production ability of a core@shell-structured CuS@TiO2 photocatalyst coated with a high concentration of TiO2 particles. The rectangular-shaped CuS particles, 100 nm in length and 60 nm in width, were surrounded by a high concentration of anatase TiO2 particles (>4~5 mol). The synthesized core@shell-structured CuS@TiO2 particles absorbed a long wavelength (a short band gap) above 700 nm compared to that pure TiO2, which at approximately 300 nm, leading to easier electronic transitions, even at low energy. Hydrogen evolution from methanol/water photo-splitting over the core@shell-structured CuS@TiO2 photocatalyst increased approximately 10-fold compared to that over pure CuS. In particular, 1.9 mmol of hydrogen gas was produced after 10 hours when 0.5 g of 1CuS@4TiO2 was used at pH = 7. This level of production was increased to more than 4-fold at higher pH. Cyclic voltammetry and UV-visible absorption spectroscopy confirmed that the CuS in CuS@TiO2 strongly withdraws the excited electrons from the valence band in TiO2 because of the higher reduction potential than TiO2, resulting in a slower recombination rate between the electrons and holes and higher photoactivity.
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institution Kabale University
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publishDate 2013-01-01
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series International Journal of Photoenergy
spelling doaj-art-1ad7ef72a7974a8d91d7f10e306f4af42025-02-03T06:12:02ZengWileyInternational Journal of Photoenergy1110-662X1687-529X2013-01-01201310.1155/2013/452542452542Dynamic Hydrogen Production from Methanol/Water Photo-Splitting Using Core@Shell-Structured CuS@TiO2 Catalyst Wrapped by High Concentrated TiO2 ParticlesYounghwan Im0Sora Kang1Kang Min Kim2Taeil Ju3Gi Bo Han4No-Kuk Park5Tae Jin Lee6Misook Kang7Department of Chemistry, College of Science, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Republic of KoreaDepartment of Chemistry, College of Science, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Republic of KoreaDepartment of Chemistry, College of Science, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Republic of KoreaDepartment of Chemistry, College of Science, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Republic of KoreaPlant Engineering Division, Institute for Advanced Engineering, 633-2 Goan-ri, Baegam-myeon, Cheoin-gu, Yongin-si, Gyeonggi 449-863, Republic of KoreaSchool of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Republic of KoreaSchool of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Republic of KoreaDepartment of Chemistry, College of Science, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Republic of KoreaThis study focused on the dynamic hydrogen production ability of a core@shell-structured CuS@TiO2 photocatalyst coated with a high concentration of TiO2 particles. The rectangular-shaped CuS particles, 100 nm in length and 60 nm in width, were surrounded by a high concentration of anatase TiO2 particles (>4~5 mol). The synthesized core@shell-structured CuS@TiO2 particles absorbed a long wavelength (a short band gap) above 700 nm compared to that pure TiO2, which at approximately 300 nm, leading to easier electronic transitions, even at low energy. Hydrogen evolution from methanol/water photo-splitting over the core@shell-structured CuS@TiO2 photocatalyst increased approximately 10-fold compared to that over pure CuS. In particular, 1.9 mmol of hydrogen gas was produced after 10 hours when 0.5 g of 1CuS@4TiO2 was used at pH = 7. This level of production was increased to more than 4-fold at higher pH. Cyclic voltammetry and UV-visible absorption spectroscopy confirmed that the CuS in CuS@TiO2 strongly withdraws the excited electrons from the valence band in TiO2 because of the higher reduction potential than TiO2, resulting in a slower recombination rate between the electrons and holes and higher photoactivity.http://dx.doi.org/10.1155/2013/452542
spellingShingle Younghwan Im
Sora Kang
Kang Min Kim
Taeil Ju
Gi Bo Han
No-Kuk Park
Tae Jin Lee
Misook Kang
Dynamic Hydrogen Production from Methanol/Water Photo-Splitting Using Core@Shell-Structured CuS@TiO2 Catalyst Wrapped by High Concentrated TiO2 Particles
International Journal of Photoenergy
title Dynamic Hydrogen Production from Methanol/Water Photo-Splitting Using Core@Shell-Structured CuS@TiO2 Catalyst Wrapped by High Concentrated TiO2 Particles
title_full Dynamic Hydrogen Production from Methanol/Water Photo-Splitting Using Core@Shell-Structured CuS@TiO2 Catalyst Wrapped by High Concentrated TiO2 Particles
title_fullStr Dynamic Hydrogen Production from Methanol/Water Photo-Splitting Using Core@Shell-Structured CuS@TiO2 Catalyst Wrapped by High Concentrated TiO2 Particles
title_full_unstemmed Dynamic Hydrogen Production from Methanol/Water Photo-Splitting Using Core@Shell-Structured CuS@TiO2 Catalyst Wrapped by High Concentrated TiO2 Particles
title_short Dynamic Hydrogen Production from Methanol/Water Photo-Splitting Using Core@Shell-Structured CuS@TiO2 Catalyst Wrapped by High Concentrated TiO2 Particles
title_sort dynamic hydrogen production from methanol water photo splitting using core shell structured cus tio2 catalyst wrapped by high concentrated tio2 particles
url http://dx.doi.org/10.1155/2013/452542
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