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- W4384029642 abstract "The present work gives the hydrogen dissociation energies and electronic structures of Li8−xTixB8FyH32−y (x, y = 0 or/and 1) compounds by first-principles density functional theory calculations, with the aim of providing new insights into the enhanced dehydrogenation of LiBH4 with Ti or/and F additives. The results indicate that substituting more electronegative elements Ti for Li or/and F for H helps to destabilize LiBH4, resulting in decreased hydrogen dissociation energies for favorable H-desorption. This is particularly obvious for LiBH4 sample with Ti + F co-substitution, and associated with the decrease of Li–B, Li–H and B–H bonding interactions, the formation of Ti–B, Ti–H and Li–F bonds, as well as the presence of metallic character. Our work suggests that combined metal cation and nonmetal anion co-doping could effectively modify the properties of LiBH4, which is useful for hydrogen storage applications." @default.
- W4384029642 created "2023-07-13" @default.
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- W4384029642 date "2023-07-01" @default.
- W4384029642 modified "2023-10-16" @default.
- W4384029642 title "Enhanced dehydrogenation of LiBH4 with Ti or/and F additives: Insight from first-principles calculations" @default.
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- W4384029642 doi "https://doi.org/10.1016/j.ijhydene.2023.06.295" @default.
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