Hydrogen cycling in γ-Mg(BH4)2 with cobalt-based additives

Magnesium borohydride (Mg(BH4)2) is an attractive candidate as a hydrogen storage material due to its high hydrogen content and predicted favorable thermodynamics. In this work we demonstrate reversible hydrogen desorption in partially decomposed Mg(BH4)2 which was ball milled together with 2 mol% C...

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Main Authors: Zavorotynska, O., Saldan, I., Hino, S., Humphries, Terry, Deledda, S., Hauback, B.
Format: Journal Article
Published: Royal Society of Chemistry 2015
Online Access:http://hdl.handle.net/20.500.11937/13418
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author Zavorotynska, O.
Saldan, I.
Hino, S.
Humphries, Terry
Deledda, S.
Hauback, B.
author_facet Zavorotynska, O.
Saldan, I.
Hino, S.
Humphries, Terry
Deledda, S.
Hauback, B.
author_sort Zavorotynska, O.
building Curtin Institutional Repository
collection Online Access
description Magnesium borohydride (Mg(BH4)2) is an attractive candidate as a hydrogen storage material due to its high hydrogen content and predicted favorable thermodynamics. In this work we demonstrate reversible hydrogen desorption in partially decomposed Mg(BH4)2 which was ball milled together with 2 mol% Co-based additives. Powder X-ray diffraction and infrared spectroscopy showed that after partial decomposition at 285 °C, amorphous boron-hydride compounds were formed. Rehydrogenation at equivalent temperatures and hydrogen pressures of 120 bar yielded the formation of crystalline Mg(BH4)2 in the first cycle, and amorphous Mg(BH4)2 with other boron–hydrogen compounds upon the third H2 absorption. Reversibility was observed in the samples with and without Co-based additives, although the additives enhanced hydrogen desorption kinetics in the first cycle. X-ray absorption spectroscopy at Co K-edge revealed that all the additives, apart from Co2B, reacted during the first desorption to form new stable species.
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institution Curtin University Malaysia
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publishDate 2015
publisher Royal Society of Chemistry
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spelling curtin-20.500.11937-134182023-08-02T06:55:50Z Hydrogen cycling in γ-Mg(BH4)2 with cobalt-based additives Zavorotynska, O. Saldan, I. Hino, S. Humphries, Terry Deledda, S. Hauback, B. Magnesium borohydride (Mg(BH4)2) is an attractive candidate as a hydrogen storage material due to its high hydrogen content and predicted favorable thermodynamics. In this work we demonstrate reversible hydrogen desorption in partially decomposed Mg(BH4)2 which was ball milled together with 2 mol% Co-based additives. Powder X-ray diffraction and infrared spectroscopy showed that after partial decomposition at 285 °C, amorphous boron-hydride compounds were formed. Rehydrogenation at equivalent temperatures and hydrogen pressures of 120 bar yielded the formation of crystalline Mg(BH4)2 in the first cycle, and amorphous Mg(BH4)2 with other boron–hydrogen compounds upon the third H2 absorption. Reversibility was observed in the samples with and without Co-based additives, although the additives enhanced hydrogen desorption kinetics in the first cycle. X-ray absorption spectroscopy at Co K-edge revealed that all the additives, apart from Co2B, reacted during the first desorption to form new stable species. 2015 Journal Article http://hdl.handle.net/20.500.11937/13418 10.1039/c5ta00511f Royal Society of Chemistry unknown
spellingShingle Zavorotynska, O.
Saldan, I.
Hino, S.
Humphries, Terry
Deledda, S.
Hauback, B.
Hydrogen cycling in γ-Mg(BH4)2 with cobalt-based additives
title Hydrogen cycling in γ-Mg(BH4)2 with cobalt-based additives
title_full Hydrogen cycling in γ-Mg(BH4)2 with cobalt-based additives
title_fullStr Hydrogen cycling in γ-Mg(BH4)2 with cobalt-based additives
title_full_unstemmed Hydrogen cycling in γ-Mg(BH4)2 with cobalt-based additives
title_short Hydrogen cycling in γ-Mg(BH4)2 with cobalt-based additives
title_sort hydrogen cycling in γ-mg(bh4)2 with cobalt-based additives
url http://hdl.handle.net/20.500.11937/13418