4.7 Article

Thermolysis and solid state NMR studies of NaB3H8, NH3B3H7, and NH4B3H8

Journal

DALTON TRANSACTIONS
Volume 42, Issue 3, Pages 701-708

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2dt31365k

Keywords

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Funding

  1. U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy (EERE) [DE-FC3605GO15062]
  2. U.S. Department of Energy, Basic Energy Sciences [DE-FG02-05ER46256]
  3. Australian Research Council [DE120101496]
  4. Australian Research Council [DE120101496] Funding Source: Australian Research Council
  5. U.S. Department of Energy (DOE) [DE-FG02-05ER46256] Funding Source: U.S. Department of Energy (DOE)

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In an effort to broaden the search for high-capacity hydrogen storage materials, three triborane compounds, NaB3H8, NH3B3H7, and NH4B3H8, were studied. In addition to hydrogen, thermal decomposition also releases volatile boranes, and the relative amounts and species depend on the cations (Na+, NH4+) and the Lewis base (NH3). Static-sample hydrogen NMR is used to probe molecular motion in the three solids. In each case, the line width decreases from low temperatures to room temperature in accordance with a model of isotropic or nearly isotropic reorientations. Such motions also explain a deep minimum in the relaxation time T-1. Translational diffusion never appears to be rapid on the 10(-5) s time scale of NMR.

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