High-pressure/low-temperature neutron scattering of gas inclusion compounds: Progress and prospects

  1. Yusheng Zhao*,,
  2. Hongwu Xu*,,
  3. Luke L. Daemen*,
  4. Konstantin Lokshin*,§,
  5. Kimberly T. Tait*,
  6. Wendy L. Mao*,
  7. Junhua Luo*,
  8. Robert P. Currier, and
  9. Donald D. Hickmott
  1. *Los Alamos Neutron Science Center,
  2. Earth and Environmental Sciences Division, and
  3. Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545; and
  4. §Department of Materials Science and Engineering, University of Tennessee, Knoxville, TN 37996
  1. Communicated by Ho-kwang Mao, Carnegie Institution of Washington, Washington, DC, and approved January 5, 2007 (received for review September 14, 2006)

Abstract

Alternative energy resources such as hydrogen and methane gases are becoming increasingly important for the future economy. A major challenge for using hydrogen is to develop suitable materials to store it under a variety of conditions, which requires systematic studies of the structures, stability, and kinetics of various hydrogen-storing compounds. Neutron scattering is particularly useful for these studies. We have developed high-pressure/low-temperature gas/fluid cells in conjunction with neutron diffraction and inelastic neutron scattering instruments allowing in situ and real-time examination of gas uptake/release processes. We studied the formation of methane and hydrogen clathrates, a group of inclusion compounds consisting of frameworks of hydrogen-bonded H2O molecules with gas molecules trapped inside the cages. Our results reveal that clathrate can store up to four hydrogen molecules in each of its large cages with an intermolecular H2–H2 distance of only 2.93 Å. This distance is much shorter than that in the solid/metallic hydrogen (3.78 Å), suggesting a strong densification effect of the clathrate framework on the enclosed hydrogen molecules. The framework-pressurizing effect is striking and may exist in other inclusion compounds such as metal-organic frameworks (MOFs). Owing to the enormous variety and flexibility of their frameworks, inclusion compounds may offer superior properties for storage of hydrogen and/or hydrogen-rich molecules, relative to other types of compounds. We have investigated the hydrogen storage properties of two MOFs, Cu3[Co(CN)6]2 and Cu3(BTC)2 (BTC = benzenetricarboxylate), and our preliminary results demonstrate that the developed neutron-scattering techniques are equally well suited for studying MOFs and other inclusion compounds.

Footnotes

  • To whom correspondence should be addressed. E-mail: yzhao{at}lanl.gov
  • Author contributions: Y.Z., L.L.D., K.L., W.L.M., and R.P.C. designed research; Y.Z., H.X., L.L.D., K.L., K.T.T., W.L.M., J.L., and D.D.H. performed research; Y.Z., H.X., L.L.D., K.L., K.T.T., W.L.M., and J.L. analyzed data; and Y.Z., H.X., L.L.D., K.L., K.T.T., W.L.M., R.P.C., and D.D.H. wrote the paper.

  • The authors declare no conflict of interest.

  • Abbreviations:
    BTC,
    benzenetricarboxylate;
    MOF,
    metal-organic framework;
    HIPPO,
    high-pressure preferred-orientation.
  • Freely available online through the PNAS open access option.

« Previous | Next Article »Table of Contents
OPEN ACCESS ARTICLE