Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783538154530144256 |
---|---|
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). |
format | Online Article Text |
id | pubmed-7247440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT felflizineb fullerenenegativeionsformationandcatalysis AT suggskelvin fullerenenegativeionsformationandcatalysis AT nicholasnantambu fullerenenegativeionsformationandcatalysis AT msezanealfredz fullerenenegativeionsformationandcatalysis |