Binding energies of hydrogen molecules to isoreticular metal-organic framework materials

Tatsuhiko Sagara, James Klassen, Julia Ortony, Eric D Ganz

Research output: Contribution to journalArticlepeer-review

123 Scopus citations

Abstract

Recently, several novel isoreticular metal-organic framework (IRMOF) structures have been fabricated and tested for hydrogen storage applications. To improve our understanding of these materials, and to promote quantitative calculations and simulations, the binding energies of hydrogen molecules to the MOF have been studied. High-quality second-order Møller-Plesset (MP2) calculations using the resolution of the identity approximation and the quadruple zeta QZVPP basis set were used. These calculations use terminated molecular fragments from the MOF materials. For H2 on the zinc oxide corners, the MP2 binding energy using Zn4 O (HCO2) 6 molecule is 6.28 kJmol. For H2 on the linkers, the binding energy is calculated using lithium-terminated molecular fragments. The MP2 results with coupled-cluster singles and doubles and noniterative triples method corrections and charge-transfer corrections are 4.16 kJmol for IRMOF-1, 4.72 kJmol for IRMOF-3, 4.86 kJmol for IRMOF-6, 4.54 kJmol for IRMOF-8, 5.50 and 4.90 kJmol for IRMOF-12, 4.87 and 4.84 kJmol for IRMOF-14, 5.42 kJmol for IRMOF-18, and 4.97 and 4.66 kJmol for IRMOF-993. The larger linkers are all able to bind multiple hydrogen molecules per side. The linkers of IRMOF-12, IRMOF-993, and IRMOF-14 can bind two to three, three, and four hydrogen molecules per side, respectively. In general, the larger linkers have the largest binding energies, and, together with the enhanced surface area available for binding, will provide increased hydrogen storage. We also find that adding up NH2 or CH3 groups to each linker can provide up to a 33% increase in the binding energy.

Original languageEnglish (US)
Article number014701
JournalJournal of Chemical Physics
Volume123
Issue number1
DOIs
StatePublished - Aug 4 2005

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