Magnesium Hydride Formation within Carbon Aerogel

Magnesium hydride nanoparticles were synthesized within a carbon aerogel (CA) scaffold using a dibutylmagnesium precursor. The synthesis reaction was tracked using small-angle X-ray scattering (SAXS) to analyze the structural evolution during MgH2 formation. The CA/MgH2 composite was also investigat...

Full description

Bibliographic Details
Main Authors: Paskevicius, Mark, Tian, Hu-Yong, Sheppard, Drew, Webb, C., Pitt, Mark, Gray, E., Kirby, N., Buckley, Craig
Format: Journal Article
Published: American Chemical Society 2011
Online Access:http://hdl.handle.net/20.500.11937/6077
_version_ 1848744973123452928
author Paskevicius, Mark
Tian, Hu-Yong
Sheppard, Drew
Webb, C.
Pitt, Mark
Gray, E.
Kirby, N.
Buckley, Craig
author_facet Paskevicius, Mark
Tian, Hu-Yong
Sheppard, Drew
Webb, C.
Pitt, Mark
Gray, E.
Kirby, N.
Buckley, Craig
author_sort Paskevicius, Mark
building Curtin Institutional Repository
collection Online Access
description Magnesium hydride nanoparticles were synthesized within a carbon aerogel (CA) scaffold using a dibutylmagnesium precursor. The synthesis reaction was tracked using small-angle X-ray scattering (SAXS) to analyze the structural evolution during MgH2 formation. The CA/MgH2 composite was also investigated using X-ray diffraction (XRD) and transmission electron microscopy (TEM) to provide a better representation of the physical system. The CA has a large quantity of 2 nm pores as shown by nitrogen adsorption data. Both SAXS and TEM investigations confirm that MgH2 does form within the 2 nm pores but XRD proves that there is also a significant quantity of larger MgH2 particles within the system. Variations between hydrogen desorption isotherms from the CA/MgH2 composite and bulk MgH2 are detected that are indicative of changes in the decomposition properties of the small fraction of 2 nm MgH2 nanoparticles within the CA/MgH2 composite, changes which match theoretical predictions.
first_indexed 2025-11-14T06:09:58Z
format Journal Article
id curtin-20.500.11937-6077
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T06:09:58Z
publishDate 2011
publisher American Chemical Society
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-60772017-09-13T15:54:29Z Magnesium Hydride Formation within Carbon Aerogel Paskevicius, Mark Tian, Hu-Yong Sheppard, Drew Webb, C. Pitt, Mark Gray, E. Kirby, N. Buckley, Craig Magnesium hydride nanoparticles were synthesized within a carbon aerogel (CA) scaffold using a dibutylmagnesium precursor. The synthesis reaction was tracked using small-angle X-ray scattering (SAXS) to analyze the structural evolution during MgH2 formation. The CA/MgH2 composite was also investigated using X-ray diffraction (XRD) and transmission electron microscopy (TEM) to provide a better representation of the physical system. The CA has a large quantity of 2 nm pores as shown by nitrogen adsorption data. Both SAXS and TEM investigations confirm that MgH2 does form within the 2 nm pores but XRD proves that there is also a significant quantity of larger MgH2 particles within the system. Variations between hydrogen desorption isotherms from the CA/MgH2 composite and bulk MgH2 are detected that are indicative of changes in the decomposition properties of the small fraction of 2 nm MgH2 nanoparticles within the CA/MgH2 composite, changes which match theoretical predictions. 2011 Journal Article http://hdl.handle.net/20.500.11937/6077 10.1021/jp1100768 American Chemical Society restricted
spellingShingle Paskevicius, Mark
Tian, Hu-Yong
Sheppard, Drew
Webb, C.
Pitt, Mark
Gray, E.
Kirby, N.
Buckley, Craig
Magnesium Hydride Formation within Carbon Aerogel
title Magnesium Hydride Formation within Carbon Aerogel
title_full Magnesium Hydride Formation within Carbon Aerogel
title_fullStr Magnesium Hydride Formation within Carbon Aerogel
title_full_unstemmed Magnesium Hydride Formation within Carbon Aerogel
title_short Magnesium Hydride Formation within Carbon Aerogel
title_sort magnesium hydride formation within carbon aerogel
url http://hdl.handle.net/20.500.11937/6077