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Promoted H 2 Generation from NH 3 BH 3 Thermal Dehydrogenation Catalyzed by Metal–Organic Framework Based Catalysts
Author(s) -
Li Yaoqi,
Song Ping,
Zheng Jie,
Li Xingguo
Publication year - 2010
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201000391
Subject(s) - catalysis , dehydrogenation , ammonia borane , kinetics , hydrogen storage , chemistry , hydrogen , metal , metal organic framework , in situ , chemical engineering , chemical kinetics , heterogeneous catalysis , inorganic chemistry , materials science , organic chemistry , physics , adsorption , quantum mechanics , engineering
The application of ammonium borane (AB) as a hydrogen storage material is limited by the sluggish kinetics of H 2 release. Two catalysts based on metal–organic frameworks (MOFs) have been prepared either by applying MOF as precursors or by the in situ reduction method. In the release of H 2 from AB, the high H 2 content of the whole system, the remarkably lower reaction onset temperature, the significantly increased H 2 release rates at ≤90 °C, and the decreased reaction exothermicity have all been achieved with only 1.0 mol % MOF‐based catalyst. Moreover, the clear catalytic diversity of three catalysts has been observed and discussed. The in situ synthesized Ni 0 sites and the MOF supports in the catalysts were proven to show significant and different effects to promote the catalytic activities. With MOF‐based catalysts, both the enhanced kinetics and the high H 2 capacity of the AB system present great advantages for future use.