2010Journal of Materials ChemistryRequires access

A new family of metal borohydride ammonia borane complexes: Synthesis, structures, and hydrogen storage properties

Hui Wu, Wei Zhou, F. E. Pinkerton, Martin S. Meyer, Srinivas Gadipelli, Taner Yildirim, Terrence J. Udovic, J. J. Rush

Open publisher page 72 citations

Abstract

We report the first two examples of borohydride ammonia borane complexes: Li2(BH4)2NH3BH3 and Ca(BH4)2(NH3BH3)2. Their structures are successfully determined using a combination of X-ray diffraction and first-principles calculations. Both structures are composed of alternating layers of borohydride and ammonia borane. Examination of bond lengths indicates that this arrangement is stabilized via dihydrogen bonding between ammonia borane and their surrounding BH4−, and the interactions between ammonia borane ligands and cations. Our experimental results show that more than 10 wt% and 11 wt% hydrogen can be released from Li2(BH4)2NH3BH3 and Ca(BH4)2(NH3BH3)2, respectively. Negligible ammonia was detected compared to ammonia borane and its ammidoborane derivatives. Further improvements are needed to reduce borazine emission. Cycling studies show that decomposed Li2(BH4)2NH3BH3 and Ca(BH4)2(NH3BH3)2 can be partially hydrogenated under hydrogen pressures at high temperatures.

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We report the first two examples of borohydride ammonia borane complexes: Li2(BH4)2NH3BH3 and Ca(BH4)2(NH3BH3)2. Their structures are successfully determined using a combination of X-ray diffraction and first-principles calculations. Both structures are composed of alternating layers of borohydride and ammonia borane. Examination of bond lengths indicates that this arrangement is stabilized via dihydrogen bonding between ammonia borane and their surrounding BH4−, and the interactions between ammonia borane ligands and cations. Our experimental results show that more than 10 wt% and 11 wt% hydrogen can be released from Li2(BH4)2NH3BH3 and Ca(BH4)2(NH3BH3)2, respectively. Negligible ammonia was detected compared to ammonia borane and its ammidoborane derivatives. Further improvements are needed to reduce borazine emission. Cycling studies show that decomposed Li2(BH4)2NH3BH3 and Ca(BH4)2(NH3BH3)2 can be partially hydrogenated under hydrogen pressures at high temperatures.

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Available abstract

We report the first two examples of borohydride ammonia borane complexes: Li2(BH4)2NH3BH3 and Ca(BH4)2(NH3BH3)2. Their structures are successfully determined using a combination of X-ray diffraction and first-principles calculations. Both structures are composed of alternating layers of borohydride and ammonia borane. Examination of bond lengths indicates that this arrangement is stabilized via dihydrogen bonding between ammonia borane and their surrounding BH4−, and the interactions between ammonia borane ligands and cations. Our experimental results show that more than 10 wt% and 11 wt% hydrogen can be released from Li2(BH4)2NH3BH3 and Ca(BH4)2(NH3BH3)2, respectively. Negligible ammonia was detected compared to ammonia borane and its ammidoborane derivatives. Further improvements are needed to reduce borazine emission. Cycling studies show that decomposed Li2(BH4)2NH3BH3 and Ca(BH4)2(NH3BH3)2 can be partially hydrogenated under hydrogen pressures at high temperatures.

Key concepts: Ammonia borane, Borohydride, Borazine, Borane, Hydrogen storage, Ammonia, Chemistry, Hydrogen

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