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Silane-based hydrogen storage materials for fuel cell application: Hydrogen release via methanolysis and regeneration by hydride reduction from organosilanes

Authors
Han, Won-SikKim, Tae-JinKim, Sung-KwanKim, YongminKim, YeongcheonNam, Suk-WooKang, Sang Ook
Issue Date
Sep-2011
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Hydrosilane; Hydrogen storage material; Regeneration; PEMFC
Citation
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.36, no.19, pp.12305 - 12312
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume
36
Number
19
Start Page
12305
End Page
12312
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/111701
DOI
10.1016/j.ijhydene.2011.06.118
ISSN
0360-3199
Abstract
A series of cyclic- and linear organosilanes, 1-5, was prepared and examined as potential hydrogen storage materials. When a stoichiometric amount of methanol was added to a mixture of cyclic organosilane, (CH2SiH2)(3) (1) or (CH2SiH2CHSiH3)(2) (2), and 5 mol%NaOMe, rapid hydrogen release was observed at room temperature within 10-15 s. The hydrogen storage capacities of compounds 1 and 2 were estimated to be 3.70 and 4.04 wt.-% H-2, respectively. However, to ensure the complete methanolysis from organosilanes including methanol evaporation at exothermic dehydrogenation condition, two equivs of methanol were used. The resulting methoxysilanes, (CH2Si(OMe)(2))(3) (6) and (CH2Si(OMe)(2)CHSi(OMe)(3))(2) (7), were regenerated to the starting organosilanes in high yields by LiAlH4 reduction. Linear organosilanes, SiH3CH2SiH2CH2SiH3 (3), SiH3CH2CH(SiH3)(2) (4), and SiH3CH2CH(SiH3) CH2SiH3 (5) also showed fast hydrogen release kinetics at room temperature with hydrogen storage capacities of 4.26, 4.55, and 4.27 wt.% H-2, respectively; the corresponding methoxysilanes were successfully regenerated by LiAlH4. Compound 1 was further tested as hydrogen source for fuel cell operation. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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