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Thermal Conversion of Unsolvated Mg(B(3)H(8))(2) to BH(4)(–) in the Presence of MgH(2)

[Image: see text] In the search for energy storage materials, metal octahydrotriborates, M(B(3)H(8))(n), n = 1 and 2, are promising candidates for applications such as stationary hydrogen storage and all-solid-state batteries. Therefore, we studied the thermal conversion of unsolvated Mg(B(3)H(8))(2...

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Autores principales: Gigante, Angelina, Leick, Noemi, Lipton, Andrew S., Tran, Ba, Strange, Nicholas A., Bowden, Mark, Martinez, Madison B., Moury, Romain, Gennett, Thomas, Hagemann, Hans, Autrey, Tom S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156084/
https://www.ncbi.nlm.nih.gov/pubmed/37153859
http://dx.doi.org/10.1021/acsaem.1c00159
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author Gigante, Angelina
Leick, Noemi
Lipton, Andrew S.
Tran, Ba
Strange, Nicholas A.
Bowden, Mark
Martinez, Madison B.
Moury, Romain
Gennett, Thomas
Hagemann, Hans
Autrey, Tom S.
author_facet Gigante, Angelina
Leick, Noemi
Lipton, Andrew S.
Tran, Ba
Strange, Nicholas A.
Bowden, Mark
Martinez, Madison B.
Moury, Romain
Gennett, Thomas
Hagemann, Hans
Autrey, Tom S.
author_sort Gigante, Angelina
collection PubMed
description [Image: see text] In the search for energy storage materials, metal octahydrotriborates, M(B(3)H(8))(n), n = 1 and 2, are promising candidates for applications such as stationary hydrogen storage and all-solid-state batteries. Therefore, we studied the thermal conversion of unsolvated Mg(B(3)H(8))(2) to BH(4)(–) as-synthesized and in the presence of MgH(2). The conversion of our unsolvated Mg(B(3)H(8))(2) starts at ∼100 °C and yields ∼22 wt % of BH(4)(–) along with the formation of (closo-hydro)borates and volatile boranes. This loss of boron (B) is a sign of poor cyclability of the system. However, the addition of activated MgH(2) to unsolvated Mg(B(3)H(8))(2) drastically increases the thermal conversion to 85–88 wt % of BH(4)(–) while simultaneously decreasing the amounts of B-losses. Our results strongly indicate that the presence of activated MgH(2) substantially decreases the formation of (closo-hydro)borates and provides the necessary H(2) for the B(3)H(8)-to-BH(4) conversion. This is the first report of a metal octahydrotriborate system to selectively convert to BH(4)(–) under moderate conditions of temperature (200 °C) in less than 1 h, making the MgB(3)H(8)-MgH(2) system very promising for energy storage applications.
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spelling pubmed-101560842023-05-04 Thermal Conversion of Unsolvated Mg(B(3)H(8))(2) to BH(4)(–) in the Presence of MgH(2) Gigante, Angelina Leick, Noemi Lipton, Andrew S. Tran, Ba Strange, Nicholas A. Bowden, Mark Martinez, Madison B. Moury, Romain Gennett, Thomas Hagemann, Hans Autrey, Tom S. ACS Appl Energy Mater [Image: see text] In the search for energy storage materials, metal octahydrotriborates, M(B(3)H(8))(n), n = 1 and 2, are promising candidates for applications such as stationary hydrogen storage and all-solid-state batteries. Therefore, we studied the thermal conversion of unsolvated Mg(B(3)H(8))(2) to BH(4)(–) as-synthesized and in the presence of MgH(2). The conversion of our unsolvated Mg(B(3)H(8))(2) starts at ∼100 °C and yields ∼22 wt % of BH(4)(–) along with the formation of (closo-hydro)borates and volatile boranes. This loss of boron (B) is a sign of poor cyclability of the system. However, the addition of activated MgH(2) to unsolvated Mg(B(3)H(8))(2) drastically increases the thermal conversion to 85–88 wt % of BH(4)(–) while simultaneously decreasing the amounts of B-losses. Our results strongly indicate that the presence of activated MgH(2) substantially decreases the formation of (closo-hydro)borates and provides the necessary H(2) for the B(3)H(8)-to-BH(4) conversion. This is the first report of a metal octahydrotriborate system to selectively convert to BH(4)(–) under moderate conditions of temperature (200 °C) in less than 1 h, making the MgB(3)H(8)-MgH(2) system very promising for energy storage applications. American Chemical Society 2021-04-02 /pmc/articles/PMC10156084/ /pubmed/37153859 http://dx.doi.org/10.1021/acsaem.1c00159 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Gigante, Angelina
Leick, Noemi
Lipton, Andrew S.
Tran, Ba
Strange, Nicholas A.
Bowden, Mark
Martinez, Madison B.
Moury, Romain
Gennett, Thomas
Hagemann, Hans
Autrey, Tom S.
Thermal Conversion of Unsolvated Mg(B(3)H(8))(2) to BH(4)(–) in the Presence of MgH(2)
title Thermal Conversion of Unsolvated Mg(B(3)H(8))(2) to BH(4)(–) in the Presence of MgH(2)
title_full Thermal Conversion of Unsolvated Mg(B(3)H(8))(2) to BH(4)(–) in the Presence of MgH(2)
title_fullStr Thermal Conversion of Unsolvated Mg(B(3)H(8))(2) to BH(4)(–) in the Presence of MgH(2)
title_full_unstemmed Thermal Conversion of Unsolvated Mg(B(3)H(8))(2) to BH(4)(–) in the Presence of MgH(2)
title_short Thermal Conversion of Unsolvated Mg(B(3)H(8))(2) to BH(4)(–) in the Presence of MgH(2)
title_sort thermal conversion of unsolvated mg(b(3)h(8))(2) to bh(4)(–) in the presence of mgh(2)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156084/
https://www.ncbi.nlm.nih.gov/pubmed/37153859
http://dx.doi.org/10.1021/acsaem.1c00159
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