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      Theoretical prediction of nanosizing effects and role of additives in the decomposition of Mg(BH 4) 2

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      RSC Advances
      The Royal Society of Chemistry

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          Abstract

          The energetic transition towards renewable resources is one of the biggest challenges of this century. In this context, the role of H 2 is of paramount importance as a key source of energy that could substitute traditional fossil fuels. This technology, even if available in several manufactures, still needs to be optimized at all levels (production, storage and distribution) to be integrated on a larger scale. Among materials suitable to store H 2, Mg(BH 4) 2 is particularly interesting due to its high content of H 2 in terms of gravimetric density. Nanosizing effects and role of additives in the decomposition of Mg(BH 4) 2 were studied by density functional theory (DFT) modelling. Both effects were analyzed because of their contribution in promoting the decomposition of the material. In particular, to have a quantitative idea of nanosizing effects, we used thin film 2D models corresponding to different crystallographic surfaces and referred to the following reaction: Mg(BH 4) 2 → MgB 2 + 4H 2. When moving from bulk to nanoscale (2D models), a remarkable decrease in the decomposition energy (10–20 kJ mol −1) was predicted depending on the surface and the thin film thickness considered. As regards the role of additives (Ni and Cu), we based our analysis on their effect in perturbing neighboring borohydride groups. We found a clear elongation of some B–H bonds, in particular with the NiF 2 additive (about 0.1 Å). We interpreted this behavior as an indicator of the propensity of borohydride towards dissociation. On the basis of this evidence, we also explored a possible reaction pathway of NiF 2 and CuF 2 on Mg(BH 4) 2 up to H 2 release and pointed out the major catalytic effect of Ni compared to Cu.

          Abstract

          Nanosizing effects and role of additives in the decomposition of Mg(BH 4) 2 were studied by DFT modelling. Decomposition is favoured at the nanoscale with respect to the bulk along with a major catalytic effect of Ni compared to Cu.

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          Most cited references10

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          Nanostructured Metal Hydrides for Hydrogen Storage

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            Is the H 2 economy realizable in the foreseeable future? Part III: H 2 usage technologies, applications, and challenges and opportunities

            Energy enthusiasts in developed countries explore sustainable and efficient pathways for accomplishing zero carbon footprint through the H2 economy. The major objective of the H2 economy review series is to bring out the status, major issues, and opportunities associated with the key components such as H2 production, storage, transportation, distribution, and applications in various energy sectors. Specifically, Part I discussed H2 production methods including the futuristic ones such as photoelectrochemical for small, medium, and large-scale applications, while Part II dealt with the challenges and developments in H2 storage, transportation, and distribution with national and international initiatives. Part III of the H2 economy review discusses the developments and challenges in the areas of H2 application in chemical/metallurgical industries, combustion, and fuel cells. Currently, the majority of H2 is being utilized by a few chemical industries with >60% in the oil refineries sector, by producing grey H2 by steam methane reforming on a large scale. In addition, the review also presents the challenges in various technologies for establishing greener and sustainable H2 society.
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              Nanoconfinement of Molecular Magnesium Borohydride Captured in a Bipyridine-Functionalized Metal-Organic Framework.

              The lower limit of metal hydride nanoconfinement is demonstrated through the coordination of a molecular hydride species to binding sites inside the pores of a metal-organic framework (MOF). Magnesium borohydride, which has a high hydrogen capacity, is incorporated into the pores of UiO-67bpy (Zr6O4(OH)4(bpydc)6 with bpydc2- = 2,2'-bipyridine-5,5'-dicarboxylate) by solvent impregnation. The MOF retained its long-range order, and transmission electron microscopy and elemental mapping confirmed the retention of the crystal morphology and revealed a homogeneous distribution of the hydride within the MOF host. Notably, the B-, N-, and Mg-edge XAS data confirm the coordination of Mg(II) to the N atoms of the chelating bipyridine groups. In situ 11B MAS NMR studies helped elucidate the reaction mechanism and revealed that complete hydrogen release from Mg(BH4)2 occurs as low as 200 °C. Sieverts and thermogravimetric measurements indicate an increase in the rate of hydrogen release, with the onset of hydrogen desorption as low as 120 °C, which is approximately 150 °C lower than that of the bulk material. Furthermore, density functional theory calculations support the improved dehydrogenation properties and confirm the drastically lower activation energy for B-H bond dissociation.
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                Author and article information

                Journal
                RSC Adv
                RSC Adv
                RA
                RSCACL
                RSC Advances
                The Royal Society of Chemistry
                2046-2069
                20 February 2024
                14 February 2024
                20 February 2024
                : 14
                : 9
                : 6398-6409
                Affiliations
                [a ] Dipartimento di Chimica and NIS Interdepartmental Centre, Università degli Studi di Torino via P. Giuria 7 10125 Torino Italy bartolomeo.civalleri@ 123456unito.it
                Author information
                https://orcid.org/0000-0002-2457-1065
                https://orcid.org/0000-0001-7735-3881
                https://orcid.org/0000-0001-7248-2705
                https://orcid.org/0000-0002-2856-9894
                https://orcid.org/0000-0003-3198-3161
                Article
                d3ra08710g
                10.1039/d3ra08710g
                10877581
                38380234
                fc185730-c132-4724-9619-e107ab14f547
                This journal is © The Royal Society of Chemistry
                History
                : 20 December 2023
                : 13 February 2024
                Page count
                Pages: 12
                Funding
                Funded by: Dipartimenti di Eccellenza, doi 10.13039/100017336;
                Award ID: CUP: D13C22003520001
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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