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Oxygen-Cluster-Modified Anatase with Graphene Leads to Efficient and Recyclable Photo-Catalytic Conversion of CO(2) to CH(4) Supported by the Positron Annihilation Study

Anatase TiO(2) hollow nanoboxes were synthesized and combined with the graphene oxide to get nanocomposite of TiO(2)/rGO (TG). Graphene oxide was used to modify the Oxygen-Clusters and bulk to surface defects. Anatase and TG composite were characterized with the positron annihilation, XPS, EPR, EIS...

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Autores principales: Ahmed, Gulzar, Raziq, Fazal, Hanif, Muddasir, Khan, Javid, Munawar, Khurram Shahzad, Wu, Mingmei, Cao, Xingzhong, Liu, Zhongwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739302/
https://www.ncbi.nlm.nih.gov/pubmed/31511596
http://dx.doi.org/10.1038/s41598-019-49694-w
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author Ahmed, Gulzar
Raziq, Fazal
Hanif, Muddasir
Khan, Javid
Munawar, Khurram Shahzad
Wu, Mingmei
Cao, Xingzhong
Liu, Zhongwu
author_facet Ahmed, Gulzar
Raziq, Fazal
Hanif, Muddasir
Khan, Javid
Munawar, Khurram Shahzad
Wu, Mingmei
Cao, Xingzhong
Liu, Zhongwu
author_sort Ahmed, Gulzar
collection PubMed
description Anatase TiO(2) hollow nanoboxes were synthesized and combined with the graphene oxide to get nanocomposite of TiO(2)/rGO (TG). Graphene oxide was used to modify the Oxygen-Clusters and bulk to surface defects. Anatase and TG composite were characterized with the positron annihilation, XPS, EPR, EIS and photocurrent response analysis. The relative affects of defects on the photocatalytic reduction (CO(2) to CH(4)) were studied. The TG composites showed highest photo-catalytic activity after GO coupling (49 µmol g(−1) h(−1)), 28.6 times higher photocurrent yields much higher quantum efficiency (3.17%@400 nm) when compared to the TiO(2) nanoboxes. The mechanism of enhanced photo-catalytic CO(2) conversion to CH(4) elucidated through electrochemical and photo-catalytic experiments with traceable isotope containing carbon dioxide ((13)CO(2)). For the first time we discovered that diminishing the comparative concentration ratio of anatase from the bulk to surface defects could significantly increase the conversion of CO(2) to CH(4).
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spelling pubmed-67393022019-09-22 Oxygen-Cluster-Modified Anatase with Graphene Leads to Efficient and Recyclable Photo-Catalytic Conversion of CO(2) to CH(4) Supported by the Positron Annihilation Study Ahmed, Gulzar Raziq, Fazal Hanif, Muddasir Khan, Javid Munawar, Khurram Shahzad Wu, Mingmei Cao, Xingzhong Liu, Zhongwu Sci Rep Article Anatase TiO(2) hollow nanoboxes were synthesized and combined with the graphene oxide to get nanocomposite of TiO(2)/rGO (TG). Graphene oxide was used to modify the Oxygen-Clusters and bulk to surface defects. Anatase and TG composite were characterized with the positron annihilation, XPS, EPR, EIS and photocurrent response analysis. The relative affects of defects on the photocatalytic reduction (CO(2) to CH(4)) were studied. The TG composites showed highest photo-catalytic activity after GO coupling (49 µmol g(−1) h(−1)), 28.6 times higher photocurrent yields much higher quantum efficiency (3.17%@400 nm) when compared to the TiO(2) nanoboxes. The mechanism of enhanced photo-catalytic CO(2) conversion to CH(4) elucidated through electrochemical and photo-catalytic experiments with traceable isotope containing carbon dioxide ((13)CO(2)). For the first time we discovered that diminishing the comparative concentration ratio of anatase from the bulk to surface defects could significantly increase the conversion of CO(2) to CH(4). Nature Publishing Group UK 2019-09-11 /pmc/articles/PMC6739302/ /pubmed/31511596 http://dx.doi.org/10.1038/s41598-019-49694-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ahmed, Gulzar
Raziq, Fazal
Hanif, Muddasir
Khan, Javid
Munawar, Khurram Shahzad
Wu, Mingmei
Cao, Xingzhong
Liu, Zhongwu
Oxygen-Cluster-Modified Anatase with Graphene Leads to Efficient and Recyclable Photo-Catalytic Conversion of CO(2) to CH(4) Supported by the Positron Annihilation Study
title Oxygen-Cluster-Modified Anatase with Graphene Leads to Efficient and Recyclable Photo-Catalytic Conversion of CO(2) to CH(4) Supported by the Positron Annihilation Study
title_full Oxygen-Cluster-Modified Anatase with Graphene Leads to Efficient and Recyclable Photo-Catalytic Conversion of CO(2) to CH(4) Supported by the Positron Annihilation Study
title_fullStr Oxygen-Cluster-Modified Anatase with Graphene Leads to Efficient and Recyclable Photo-Catalytic Conversion of CO(2) to CH(4) Supported by the Positron Annihilation Study
title_full_unstemmed Oxygen-Cluster-Modified Anatase with Graphene Leads to Efficient and Recyclable Photo-Catalytic Conversion of CO(2) to CH(4) Supported by the Positron Annihilation Study
title_short Oxygen-Cluster-Modified Anatase with Graphene Leads to Efficient and Recyclable Photo-Catalytic Conversion of CO(2) to CH(4) Supported by the Positron Annihilation Study
title_sort oxygen-cluster-modified anatase with graphene leads to efficient and recyclable photo-catalytic conversion of co(2) to ch(4) supported by the positron annihilation study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739302/
https://www.ncbi.nlm.nih.gov/pubmed/31511596
http://dx.doi.org/10.1038/s41598-019-49694-w
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