Magnesium hydride is regarded as one of the most ideal candidates for hydrogen storage, but its relatively high operating temperatures and slow kinetics always hinder its commercial applications. Herein, we first fabricated hard-carbon-sphere-wrapped Ni (Ni/HCS) a mild chemical method; subsequently, the as-prepared additive was introduced to fabricate an Mg-Ni/HCS composite by using hydriding combustion synthesis. Hard carbon spheres (HCS) effectively inhibited the agglomeration of hydride particles during hydrogen storage cycling; they could also provide active sites to promote the nucleation of Mg-based hydrides. During the hydriding combustion synthesis procedure, -formed MgNiH could induce the absorption of MgH, thus triggering its hydrogen properties. Remarkable enhancement in hydrogen absorption properties of the composite was found. The composite absorbed 6.0 wt% H within 5 min at 275 °C; moreover, even at 75 °C, it could still absorb 3.5 wt% H. Furthermore, it delivered a high reversible hydrogen absorption capacity of 6.2 wt% and excellent rate capability at 350 °C. It was also demonstrated that the composite could release 6.2 wt% H at 350 °C within 5 min. A rather low activation energy value (65.9 kJ mol) for the dehydrogenation of MgH was calculated as compared to that for commercial MgH (133.5 kJ mol).
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http://dx.doi.org/10.1039/c8ra05464a | DOI Listing |
Chimia (Aarau)
December 2024
Department of Inorganic Chemistry, Ivan Franko National University of Lviv, Kyryla i Mefodiya St. 6, 79005 Lviv, Ukraine.
In this article, we provide an overview of hydrogen storage materials, taking our previous results as examples. Towards the end of the paper, we present a case study in order to highlight the effects of substitutional alloying, compositional additives, and nanostructuring on the hydrogen sorption properties of magnesium-based intermetallics. Specifically, partial substitution of Mg by Li and d-elements by p-elements leads to structural changes, inducing disorder and the formation of high-entropy alloys.
View Article and Find Full Text PDFMolecules
December 2024
College of Materials Science and Engineering, National Engineering Research Center for Magnesium Alloys, National Innovation Center for Industry-Education Integration of Energy Storage Technology, Chongqing University, Chongqing 400044, China.
Lithium borohydride (LiBH) has emerged as a promising hydrogen storage material due to its exceptional theoretical hydrogen capacity (18.5 wt.%).
View Article and Find Full Text PDFJ Mol Graph Model
November 2024
Department of Optoelectronic Science & Technology, School of Electronic Information and Artificial Intelligence, Shaanxi University of Science & Technology, Xi'an, Shaanxi, 710021, China.
Chemistry
December 2024
Department of Chemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Reactions of a m-terphenylhydridostannylene with β-diketiminato magnesium and calcium hydrides provide bis-μ-hydrido species, the heterobimetallic constitutions of which are maintained after the addition of THF donor solvent. In both cases, reactions with hex-1-ene result in the formation of tetravalent organostannyl alkaline earth derivatives. Whereas the magnesium reagent undergoes facile twofold addition, the calcium-centered process is arrested after a single alkene reduction event.
View Article and Find Full Text PDFChemistry
December 2024
Department of Chemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
The dimeric calcium and magnesium hydrides, [(BDI)AeH] [BDI=HC{(Me)CNDipp}, Dipp=2,6-i-PrCH; Ae=Mg or Ca] do not react with PhGeH in non-coordinating solvent. Addition of THF, however, induces deprotonation and access to monomeric Ae-germanide complexes, [(BDI)Ae{GePh}(THF)], both of which have been structurally characterized. Although this process is facile when Ae=Ca, the analogous magnesium-based reaction requires heating to temperatures >100 °C, under which conditions germanide formation is complicated by THF ring opening and the generation of an alkaline earth germyl-C-terminated n-butoxide, [(BDI)Mg{μ-O(CH)GePh}].
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