The rotational dynamics of H2 adsorbed in covalent organic frameworks

Abstract

A combined inelastic neutron scattering (INS) and theoretical study was carried out on H₂ adsorbed in two covalent organic framework (COF) materials: COF-1 and COF-102. These COFs are synthesized from self-condensation reactions of 1,4-benzenediboronic acid (BDBA) and tetra(4-(dihydroxy)borylphenyl)methane (TBPM) molecules, respectively. Molecular simulations of H₂ adsorption in COF-1 revealed that the H₂ molecules occupy the region between two eclipsed layers of the COF. The most favorable H₂ binding site in COF-1 is located between two B₃O₃ clusters of the eclipsed layers. Two distinct H₂ binding sites were identified in COF-102 from the simulations: the B₃O₃ clusters and the phenyl rings of the tetraphenylmethyl units. Two-dimensional quantum rotation calculations for H₂ adsorbed at the considered sites in both COFs resulted in rotational transitions that are in good agreement with those that appear in the corresponding INS spectra. Such calculations were important for interpreting the INS spectra in these materials. Calculation of the rotational potential energy surface for H₂ bound at the most favorable adsorption site in COF-1 and COF-102 revealed unusually high rotational barriers that are attributed to the nature of the B₃O₃ rings. The values for these barriers to rotation are greater than or comparable to those observed in some metal–organic frameworks (MOFs) that possess open-metal sites. This study demonstrates the power of using INS experiments in conjunction with theoretical calculations to gain valuable insights into the nature of the binding sites and, for the first time, the rotational dynamics of H₂ adsorbed in COFs.