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Boron-doped Nanodiamond as an Electrode Material for Aqueous Electric Double-layer Capacitors

Herein, a conductive boron-doped nanodiamond (BDND) particle is prepared as an electrode material for an aqueous electric double-layer capacitor with high power and energy densities. The BDND is obtained by depositing a boron-doped diamond (BDD) on a nanodiamond particle substrate with a primary par...

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Autores principales: Miyashita, Kenjo, Kondo, Takeshi, Sugai, Seiya, Tei, Takahiro, Nishikawa, Masahiro, Tojo, Toshifumi, Yuasa, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882838/
https://www.ncbi.nlm.nih.gov/pubmed/31780797
http://dx.doi.org/10.1038/s41598-019-54197-9
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author Miyashita, Kenjo
Kondo, Takeshi
Sugai, Seiya
Tei, Takahiro
Nishikawa, Masahiro
Tojo, Toshifumi
Yuasa, Makoto
author_facet Miyashita, Kenjo
Kondo, Takeshi
Sugai, Seiya
Tei, Takahiro
Nishikawa, Masahiro
Tojo, Toshifumi
Yuasa, Makoto
author_sort Miyashita, Kenjo
collection PubMed
description Herein, a conductive boron-doped nanodiamond (BDND) particle is prepared as an electrode material for an aqueous electric double-layer capacitor with high power and energy densities. The BDND is obtained by depositing a boron-doped diamond (BDD) on a nanodiamond particle substrate with a primary particle size of 4.7 nm via microwave plasma-assisted chemical vapor deposition, followed by heat treatment in air. The BDND comprises BDD and sp(2) carbon components, and exhibits a conductivity above 10(−2) S cm(−1) and a specific surface area of 650 m(2) g(−1). Cyclic voltammetry measurements recorded in 1 M H(2)SO(4) at a BDND electrode in a two-electrode system shows a capacitance of 15.1 F g(−1) and a wide potential window (cell voltage) of 1.8 V, which is much larger than that obtained at an activated carbon electrode, i.e., 0.8 V. Furthermore, the cell voltage of the BDND electrode reaches 2.8 V when using saturated NaClO(4) as electrolyte. The energy and power densities per unit weight of the BDND for charging–discharging in 1 M H(2)SO(4) at the BDND electrode cell are 10 Wh kg(−1) and 10(4) W kg(−1), respectively, and the energy and power densities per unit volume of the BDND layer are 3–4 mWh cm(−3) and 10 W cm(−3), respectively. Therefore, the BDND is a promising candidate for the development of a compact aqueous EDLC device with high energy and power densities.
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spelling pubmed-68828382019-12-06 Boron-doped Nanodiamond as an Electrode Material for Aqueous Electric Double-layer Capacitors Miyashita, Kenjo Kondo, Takeshi Sugai, Seiya Tei, Takahiro Nishikawa, Masahiro Tojo, Toshifumi Yuasa, Makoto Sci Rep Article Herein, a conductive boron-doped nanodiamond (BDND) particle is prepared as an electrode material for an aqueous electric double-layer capacitor with high power and energy densities. The BDND is obtained by depositing a boron-doped diamond (BDD) on a nanodiamond particle substrate with a primary particle size of 4.7 nm via microwave plasma-assisted chemical vapor deposition, followed by heat treatment in air. The BDND comprises BDD and sp(2) carbon components, and exhibits a conductivity above 10(−2) S cm(−1) and a specific surface area of 650 m(2) g(−1). Cyclic voltammetry measurements recorded in 1 M H(2)SO(4) at a BDND electrode in a two-electrode system shows a capacitance of 15.1 F g(−1) and a wide potential window (cell voltage) of 1.8 V, which is much larger than that obtained at an activated carbon electrode, i.e., 0.8 V. Furthermore, the cell voltage of the BDND electrode reaches 2.8 V when using saturated NaClO(4) as electrolyte. The energy and power densities per unit weight of the BDND for charging–discharging in 1 M H(2)SO(4) at the BDND electrode cell are 10 Wh kg(−1) and 10(4) W kg(−1), respectively, and the energy and power densities per unit volume of the BDND layer are 3–4 mWh cm(−3) and 10 W cm(−3), respectively. Therefore, the BDND is a promising candidate for the development of a compact aqueous EDLC device with high energy and power densities. Nature Publishing Group UK 2019-11-28 /pmc/articles/PMC6882838/ /pubmed/31780797 http://dx.doi.org/10.1038/s41598-019-54197-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Miyashita, Kenjo
Kondo, Takeshi
Sugai, Seiya
Tei, Takahiro
Nishikawa, Masahiro
Tojo, Toshifumi
Yuasa, Makoto
Boron-doped Nanodiamond as an Electrode Material for Aqueous Electric Double-layer Capacitors
title Boron-doped Nanodiamond as an Electrode Material for Aqueous Electric Double-layer Capacitors
title_full Boron-doped Nanodiamond as an Electrode Material for Aqueous Electric Double-layer Capacitors
title_fullStr Boron-doped Nanodiamond as an Electrode Material for Aqueous Electric Double-layer Capacitors
title_full_unstemmed Boron-doped Nanodiamond as an Electrode Material for Aqueous Electric Double-layer Capacitors
title_short Boron-doped Nanodiamond as an Electrode Material for Aqueous Electric Double-layer Capacitors
title_sort boron-doped nanodiamond as an electrode material for aqueous electric double-layer capacitors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882838/
https://www.ncbi.nlm.nih.gov/pubmed/31780797
http://dx.doi.org/10.1038/s41598-019-54197-9
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