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Highly Porous Carbon Materials Derived from Silicon Oxycarbides and Effect of the Pyrolysis Temperature on Their Electrochemical Response
The design of a material porous microstructure with interconnected micro-meso-macropores is a key issue for the successful development of carbon-derived materials for supercapacitor applications. Another important issue is the nature of these carbon materials. For those reasons, in this study, novel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530778/ https://www.ncbi.nlm.nih.gov/pubmed/37762172 http://dx.doi.org/10.3390/ijms241813868 |
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author | Merida, Jose Colomer, Maria T. Rubio, Fausto Mazo, M. Alejandra |
author_facet | Merida, Jose Colomer, Maria T. Rubio, Fausto Mazo, M. Alejandra |
author_sort | Merida, Jose |
collection | PubMed |
description | The design of a material porous microstructure with interconnected micro-meso-macropores is a key issue for the successful development of carbon-derived materials for supercapacitor applications. Another important issue is the nature of these carbon materials. For those reasons, in this study, novel hierarchical micro-meso-macroporous silicon oxycarbide-derived carbon (SiOC-DC) was obtained via chlorine etching of carbon-enriched SiOC prepared via pyrolysis (1100–1400 °C) of sol-gel triethoxysilane/dimethyldiphenysiloxane hybrids. In addition, and for the first time, non-conventional Raman parameters combined with the analysis of their microstructural characteristics were considered to establish their relationships with their electrochemical response. The sample pyrolyzed at 1100 °C showed planar and less-defective carbon domains together with the largest specific surface area (SSA) and the highest volume of micro-meso-macropores, which upgraded their electrochemical response. This sample has the highest specific capacitance (C(s) = 101 Fg(−1) (0.2 Ag(−1))), energy (E(d) = 12–7 Wh(−1) kg(−1)), and power densities (P(d) = 0.32–35 kw kg(−1)), showing a good capacitance retention ratio up to 98% after 10,000 charge–discharge cycles at 0.5 Ag(−1). At a pyrolysis temperature ≥ 1200 °C, the carbon domains were highly ordered and tortuous with a high degree of interconnection. However, SSA and pore volumes (micro-meso-macropores) were significantly reduced and downgraded the C(s), E(d), and P(d) values. |
format | Online Article Text |
id | pubmed-10530778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105307782023-09-28 Highly Porous Carbon Materials Derived from Silicon Oxycarbides and Effect of the Pyrolysis Temperature on Their Electrochemical Response Merida, Jose Colomer, Maria T. Rubio, Fausto Mazo, M. Alejandra Int J Mol Sci Article The design of a material porous microstructure with interconnected micro-meso-macropores is a key issue for the successful development of carbon-derived materials for supercapacitor applications. Another important issue is the nature of these carbon materials. For those reasons, in this study, novel hierarchical micro-meso-macroporous silicon oxycarbide-derived carbon (SiOC-DC) was obtained via chlorine etching of carbon-enriched SiOC prepared via pyrolysis (1100–1400 °C) of sol-gel triethoxysilane/dimethyldiphenysiloxane hybrids. In addition, and for the first time, non-conventional Raman parameters combined with the analysis of their microstructural characteristics were considered to establish their relationships with their electrochemical response. The sample pyrolyzed at 1100 °C showed planar and less-defective carbon domains together with the largest specific surface area (SSA) and the highest volume of micro-meso-macropores, which upgraded their electrochemical response. This sample has the highest specific capacitance (C(s) = 101 Fg(−1) (0.2 Ag(−1))), energy (E(d) = 12–7 Wh(−1) kg(−1)), and power densities (P(d) = 0.32–35 kw kg(−1)), showing a good capacitance retention ratio up to 98% after 10,000 charge–discharge cycles at 0.5 Ag(−1). At a pyrolysis temperature ≥ 1200 °C, the carbon domains were highly ordered and tortuous with a high degree of interconnection. However, SSA and pore volumes (micro-meso-macropores) were significantly reduced and downgraded the C(s), E(d), and P(d) values. MDPI 2023-09-08 /pmc/articles/PMC10530778/ /pubmed/37762172 http://dx.doi.org/10.3390/ijms241813868 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Merida, Jose Colomer, Maria T. Rubio, Fausto Mazo, M. Alejandra Highly Porous Carbon Materials Derived from Silicon Oxycarbides and Effect of the Pyrolysis Temperature on Their Electrochemical Response |
title | Highly Porous Carbon Materials Derived from Silicon Oxycarbides and Effect of the Pyrolysis Temperature on Their Electrochemical Response |
title_full | Highly Porous Carbon Materials Derived from Silicon Oxycarbides and Effect of the Pyrolysis Temperature on Their Electrochemical Response |
title_fullStr | Highly Porous Carbon Materials Derived from Silicon Oxycarbides and Effect of the Pyrolysis Temperature on Their Electrochemical Response |
title_full_unstemmed | Highly Porous Carbon Materials Derived from Silicon Oxycarbides and Effect of the Pyrolysis Temperature on Their Electrochemical Response |
title_short | Highly Porous Carbon Materials Derived from Silicon Oxycarbides and Effect of the Pyrolysis Temperature on Their Electrochemical Response |
title_sort | highly porous carbon materials derived from silicon oxycarbides and effect of the pyrolysis temperature on their electrochemical response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530778/ https://www.ncbi.nlm.nih.gov/pubmed/37762172 http://dx.doi.org/10.3390/ijms241813868 |
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