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Mesoporous Carbon Fibers with Tunable Mesoporosity for Electrode Materials in Energy Devices

To improve the properties of mesoporous carbon (MC), used as a catalyst support within electrodes, MC fibers (MCFs) were successfully synthesized by combining organic–organic self-assembly and electrospinning deposition and optimizing heat treatment conditions. The pore structure was controlled by v...

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Autores principales: Huang, Ting-Wei, Nagayama, Mayumi, Matsuda, Junko, Sasaki, Kazunari, Hayashi, Akari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866550/
https://www.ncbi.nlm.nih.gov/pubmed/33573267
http://dx.doi.org/10.3390/molecules26030724
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author Huang, Ting-Wei
Nagayama, Mayumi
Matsuda, Junko
Sasaki, Kazunari
Hayashi, Akari
author_facet Huang, Ting-Wei
Nagayama, Mayumi
Matsuda, Junko
Sasaki, Kazunari
Hayashi, Akari
author_sort Huang, Ting-Wei
collection PubMed
description To improve the properties of mesoporous carbon (MC), used as a catalyst support within electrodes, MC fibers (MCFs) were successfully synthesized by combining organic–organic self-assembly and electrospinning deposition and optimizing heat treatment conditions. The pore structure was controlled by varying the experimental conditions. Among MCFs, MCF-A, which was made in the most acidic condition, resulted in the largest pore diameter (4–5 nm), and the porous structure and carbonization degree were further optimized by adjusting heat treatment conditions. Then, since the fiber structure is expected to have an advantage when MCFs are applied to devices, MCF-A layers were prepared by spray printing. For the resistance to compression, MCF-A layers showed higher resistance (5.5% change in thickness) than the bulk MC layer (12.8% change in thickness). The through-plane resistance was lower when the fiber structure remained more within the thin layer, for example, +8 mΩ for 450 rpm milled MCF-A and +12 mΩ for 800 rpm milled MCF-A against the gas diffusion layer (GDL) 25BC carbon paper without a carbon layer coating. The additional advantages of MCF-A compared with bulk MC demonstrate that MCF-A has the potential to be used as a catalyst support within electrodes in energy devices.
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spelling pubmed-78665502021-02-07 Mesoporous Carbon Fibers with Tunable Mesoporosity for Electrode Materials in Energy Devices Huang, Ting-Wei Nagayama, Mayumi Matsuda, Junko Sasaki, Kazunari Hayashi, Akari Molecules Article To improve the properties of mesoporous carbon (MC), used as a catalyst support within electrodes, MC fibers (MCFs) were successfully synthesized by combining organic–organic self-assembly and electrospinning deposition and optimizing heat treatment conditions. The pore structure was controlled by varying the experimental conditions. Among MCFs, MCF-A, which was made in the most acidic condition, resulted in the largest pore diameter (4–5 nm), and the porous structure and carbonization degree were further optimized by adjusting heat treatment conditions. Then, since the fiber structure is expected to have an advantage when MCFs are applied to devices, MCF-A layers were prepared by spray printing. For the resistance to compression, MCF-A layers showed higher resistance (5.5% change in thickness) than the bulk MC layer (12.8% change in thickness). The through-plane resistance was lower when the fiber structure remained more within the thin layer, for example, +8 mΩ for 450 rpm milled MCF-A and +12 mΩ for 800 rpm milled MCF-A against the gas diffusion layer (GDL) 25BC carbon paper without a carbon layer coating. The additional advantages of MCF-A compared with bulk MC demonstrate that MCF-A has the potential to be used as a catalyst support within electrodes in energy devices. MDPI 2021-01-30 /pmc/articles/PMC7866550/ /pubmed/33573267 http://dx.doi.org/10.3390/molecules26030724 Text en © 2021 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
Huang, Ting-Wei
Nagayama, Mayumi
Matsuda, Junko
Sasaki, Kazunari
Hayashi, Akari
Mesoporous Carbon Fibers with Tunable Mesoporosity for Electrode Materials in Energy Devices
title Mesoporous Carbon Fibers with Tunable Mesoporosity for Electrode Materials in Energy Devices
title_full Mesoporous Carbon Fibers with Tunable Mesoporosity for Electrode Materials in Energy Devices
title_fullStr Mesoporous Carbon Fibers with Tunable Mesoporosity for Electrode Materials in Energy Devices
title_full_unstemmed Mesoporous Carbon Fibers with Tunable Mesoporosity for Electrode Materials in Energy Devices
title_short Mesoporous Carbon Fibers with Tunable Mesoporosity for Electrode Materials in Energy Devices
title_sort mesoporous carbon fibers with tunable mesoporosity for electrode materials in energy devices
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866550/
https://www.ncbi.nlm.nih.gov/pubmed/33573267
http://dx.doi.org/10.3390/molecules26030724
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