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024 7 _ |a 10.1016/j.ijhydene.2015.12.185
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024 7 _ |a 1879-3487
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100 1 _ |a Paskevicius, Mark
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245 _ _ |a Cyclic stability and structure of nanoconfined Ti-doped $\mathrm{NaAlH_{4}}$
260 _ _ |a New York, NY [u.a.]
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500 _ _ |a (c) Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. Post referee full text in progress (embargo 1 year from 1 February 2016).
520 _ _ |a NaAlH4 was melt infiltrated within a CO$_2$ activated carbon aerogel, which had been preloaded with TiCl$_3$. Nanoconfinement was verified by Small Angle X-Ray Scattering (SAXS) and the nature of the Ti was investigated with Anomalous SAXS (ASAXS) and X-Ray Absorption Near Edge Structure (XANES) to determine its size and chemical state. The Ti is found to be in a similar state to that found in the bulk Ti-doped NaAlH$_4$ system where it exists as Al$_{1−x}$Ti$_x$ nanoalloys. Crystalline phases exist within the carbon aerogel pores, which are analysed by in-situ Powder X-Ray Diffraction (PXD) during hydrogen cycling. The in-situ data reveals that the hydrogen release from NaAlH$_4$ and its hydrogen uptake occurs through the Na$_3$AlH$_6$ intermediate when confined at this size scale. The hydrogen capacity from the nanoconfined NaAlH$_4$ is found to initially be much higher in this CO$_2$ activated aerogel compared with previous studies into unactivated aerogels.
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773 _ _ |a 10.1016/j.ijhydene.2015.12.185
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