A DFT study of volatile organic compounds adsorption on transition metal deposited graphene

© 2016 Elsevier B.V. Recently, elevated global emission of volatile organic compounds (VOCs) was associated to the acceleration and increasing severity of climate change worldwide. In this work, we investigated the performance of VOCs removal via modified carbon-based adsorbent using density functio...

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Main Authors: Manaschai Kunaseth, Preeyaporn Poldorn, Anchalee Junkeaw, Jittima Meeprasert, Chompoonut Rungnim, Supawadee Namuangruk, Nawee Kungwan, Chan Inntam, Siriporn Jungsuttiwong
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Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/46980
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spelling th-cmuir.6653943832-469802018-04-25T07:27:22Z A DFT study of volatile organic compounds adsorption on transition metal deposited graphene Manaschai Kunaseth Preeyaporn Poldorn Anchalee Junkeaw Jittima Meeprasert Chompoonut Rungnim Supawadee Namuangruk Nawee Kungwan Chan Inntam Siriporn Jungsuttiwong Agricultural and Biological Sciences © 2016 Elsevier B.V. Recently, elevated global emission of volatile organic compounds (VOCs) was associated to the acceleration and increasing severity of climate change worldwide. In this work, we investigated the performance of VOCs removal via modified carbon-based adsorbent using density functional theory. Here, four transition metals (TMs) including Pd, Pt, Ag, and Au were deposited onto single-vacancy defective graphene (SDG) surface to increase the adsorption efficiency. Five prototypical VOCs including benzene, furan, pyrrole, pyridine, and thiophene were used to study the adsorption capability of metal-deposited graphene adsorbent. Calculation results revealed that Pd, Pt, Au, and Ag atoms and nanoclusters bind strongly onto the SDG surface. In this study, benzene, furan and pyrrole bind in the π-interaction mode using delocalized π-electron in aromatic ring, while pyridine and thiophene favor X- interaction mode, donating lone pair electron from heteroatom. In terms of adsorption, pyridine VOC adsorption strengths to the TM-cluster doped SDG surfaces are Pt 4 (−2.11 eV)  >  Pd 4 (−2.05 eV)  >  Ag 4 (−1.53 eV)  >  Au 4 (−1.87 eV). Our findings indicate that TM-doped SDG is a suitable adsorbent material for VOC removal. In addition, partial density of states analysis suggests that benzene, furan, and pyrrole interactions with TM cluster are based on p-orbitals of carbon atoms, while pyridine and thiophene interactions are facilitated by hybridized sp 2 -orbitals of heteroatoms. This work provides a key insight into the fundamentals of VOCs adsorption on carbon-based adsorbent. 2018-04-25T07:07:25Z 2018-04-25T07:07:25Z 2017-02-28 Journal 01694332 2-s2.0-85006810513 10.1016/j.apsusc.2016.11.238 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85006810513&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/46980
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Agricultural and Biological Sciences
spellingShingle Agricultural and Biological Sciences
Manaschai Kunaseth
Preeyaporn Poldorn
Anchalee Junkeaw
Jittima Meeprasert
Chompoonut Rungnim
Supawadee Namuangruk
Nawee Kungwan
Chan Inntam
Siriporn Jungsuttiwong
A DFT study of volatile organic compounds adsorption on transition metal deposited graphene
description © 2016 Elsevier B.V. Recently, elevated global emission of volatile organic compounds (VOCs) was associated to the acceleration and increasing severity of climate change worldwide. In this work, we investigated the performance of VOCs removal via modified carbon-based adsorbent using density functional theory. Here, four transition metals (TMs) including Pd, Pt, Ag, and Au were deposited onto single-vacancy defective graphene (SDG) surface to increase the adsorption efficiency. Five prototypical VOCs including benzene, furan, pyrrole, pyridine, and thiophene were used to study the adsorption capability of metal-deposited graphene adsorbent. Calculation results revealed that Pd, Pt, Au, and Ag atoms and nanoclusters bind strongly onto the SDG surface. In this study, benzene, furan and pyrrole bind in the π-interaction mode using delocalized π-electron in aromatic ring, while pyridine and thiophene favor X- interaction mode, donating lone pair electron from heteroatom. In terms of adsorption, pyridine VOC adsorption strengths to the TM-cluster doped SDG surfaces are Pt 4 (−2.11 eV)  >  Pd 4 (−2.05 eV)  >  Ag 4 (−1.53 eV)  >  Au 4 (−1.87 eV). Our findings indicate that TM-doped SDG is a suitable adsorbent material for VOC removal. In addition, partial density of states analysis suggests that benzene, furan, and pyrrole interactions with TM cluster are based on p-orbitals of carbon atoms, while pyridine and thiophene interactions are facilitated by hybridized sp 2 -orbitals of heteroatoms. This work provides a key insight into the fundamentals of VOCs adsorption on carbon-based adsorbent.
format Journal
author Manaschai Kunaseth
Preeyaporn Poldorn
Anchalee Junkeaw
Jittima Meeprasert
Chompoonut Rungnim
Supawadee Namuangruk
Nawee Kungwan
Chan Inntam
Siriporn Jungsuttiwong
author_facet Manaschai Kunaseth
Preeyaporn Poldorn
Anchalee Junkeaw
Jittima Meeprasert
Chompoonut Rungnim
Supawadee Namuangruk
Nawee Kungwan
Chan Inntam
Siriporn Jungsuttiwong
author_sort Manaschai Kunaseth
title A DFT study of volatile organic compounds adsorption on transition metal deposited graphene
title_short A DFT study of volatile organic compounds adsorption on transition metal deposited graphene
title_full A DFT study of volatile organic compounds adsorption on transition metal deposited graphene
title_fullStr A DFT study of volatile organic compounds adsorption on transition metal deposited graphene
title_full_unstemmed A DFT study of volatile organic compounds adsorption on transition metal deposited graphene
title_sort dft study of volatile organic compounds adsorption on transition metal deposited graphene
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85006810513&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/46980
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