Inelastic Neutron Scattering and Theoretical Studies of H2 Sorption in a Dy(III)-Based Phosphine Coordination Material

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• 作者：Katherine A. Forrest ; Tony Pham ; Peter A. Georgiev ; Jan Peter Embs ; Nolan W. Waggoner ; Adam Hogan ; Simon M. Humphrey ; Juergen Eckert ; Brian Space
• 刊名：Chemistry of Materials
• 出版年：2015
• 出版时间：November 24, 2015
• 年：2015
• 卷：27
• 期：22
• 页码：7619-7626
• 全文大小：480K
• ISSN：1520-5002

文摘

A combined inelastic neutron scattering (INS) and theoretical study of H₂ sorption was performed in PCM-16, a phosphine coordination material (PCM) with the empirical formula [(CH₃)₂NH₂][Dy₂(tctpo)₂(O₂CH)] (tctpo = tris(p-carboxylato)triphenylphosphine oxide). INS measurements at different loadings of H₂ revealed a peak occurring at low rotational tunnelling energies (ca. 5鈥? meV), which corresponds to a high barrier to rotation and, therefore, a strong interaction with the host. Molecular simulations of H₂ sorption in PCM-16 revealed that the H₂ molecules sorbed at two main sites in the material: (1) the (CH₃)₂NH₂⁺ counterions and (2) within the small pores of the framework. Two-dimensional quantum rotation calculations revealed that the peak occurring from approximately 5鈥? meV in the INS spectra for PCM-16 is associated with sorption onto the (CH₃)₂NH₂⁺ ions. These counterions provide for the strongest H₂ sorption sites in the material, which corresponds to an isosteric heat of adsorption (Q_st) value of close to 8 kJ mol^鈥?. The calculated rotational barrier for the (CH₃)₂NH₂⁺鈥揌₂ interaction in PCM-16 (45.60 meV) is higher than those for a number of extant metal鈥搊rganic frameworks (MOFs), especially those that contain open-metal sites. This study provides insights into the H₂ sorption mechanism in a PCM for the first time and shows how the inclusion of counterions in porous materials is a promising method to increase the H₂ sorption energetics in such materials.