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Fullerene Negative Ions: Formation and Catalysis

We first explore negative-ion formation in fullerenes C(44) to C(136) through low-energy electron elastic scattering total cross sections calculations using our Regge-pole methodology. Then, the formed negative ions C(44)ˉ to C(136)ˉ are used to investigate the catalysis of water oxidation to peroxi...

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Detalles Bibliográficos
Autores principales: Felfli, Zineb, Suggs, Kelvin, Nicholas, Nantambu, Msezane, Alfred Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247440/
https://www.ncbi.nlm.nih.gov/pubmed/32365766
http://dx.doi.org/10.3390/ijms21093159
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author Felfli, Zineb
Suggs, Kelvin
Nicholas, Nantambu
Msezane, Alfred Z.
author_facet Felfli, Zineb
Suggs, Kelvin
Nicholas, Nantambu
Msezane, Alfred Z.
author_sort Felfli, Zineb
collection PubMed
description We first explore negative-ion formation in fullerenes C(44) to C(136) through low-energy electron elastic scattering total cross sections calculations using our Regge-pole methodology. Then, the formed negative ions C(44)ˉ to C(136)ˉ are used to investigate the catalysis of water oxidation to peroxide and water synthesis from H(2) and O(2). The exploited fundamental mechanism underlying negative-ion catalysis involves hydrogen bond strength-weakening/breaking in the transition state. Density Functional Theory transition state calculations found C(60)ˉ optimal for both water and peroxide synthesis, C(100)ˉ increases the energy barrier the most, and C(136)ˉ the most effective catalyst in both water synthesis and oxidation to H(2)O(2).
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spelling pubmed-72474402020-06-10 Fullerene Negative Ions: Formation and Catalysis Felfli, Zineb Suggs, Kelvin Nicholas, Nantambu Msezane, Alfred Z. Int J Mol Sci Article We first explore negative-ion formation in fullerenes C(44) to C(136) through low-energy electron elastic scattering total cross sections calculations using our Regge-pole methodology. Then, the formed negative ions C(44)ˉ to C(136)ˉ are used to investigate the catalysis of water oxidation to peroxide and water synthesis from H(2) and O(2). The exploited fundamental mechanism underlying negative-ion catalysis involves hydrogen bond strength-weakening/breaking in the transition state. Density Functional Theory transition state calculations found C(60)ˉ optimal for both water and peroxide synthesis, C(100)ˉ increases the energy barrier the most, and C(136)ˉ the most effective catalyst in both water synthesis and oxidation to H(2)O(2). MDPI 2020-04-30 /pmc/articles/PMC7247440/ /pubmed/32365766 http://dx.doi.org/10.3390/ijms21093159 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Felfli, Zineb
Suggs, Kelvin
Nicholas, Nantambu
Msezane, Alfred Z.
Fullerene Negative Ions: Formation and Catalysis
title Fullerene Negative Ions: Formation and Catalysis
title_full Fullerene Negative Ions: Formation and Catalysis
title_fullStr Fullerene Negative Ions: Formation and Catalysis
title_full_unstemmed Fullerene Negative Ions: Formation and Catalysis
title_short Fullerene Negative Ions: Formation and Catalysis
title_sort fullerene negative ions: formation and catalysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247440/
https://www.ncbi.nlm.nih.gov/pubmed/32365766
http://dx.doi.org/10.3390/ijms21093159
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