掺杂剂
选择性
吸附
碱金属
氢
无机化学
金属
化学
密度泛函理论
金属有机骨架
兴奋剂
焓
物理化学
材料科学
催化作用
计算化学
热力学
有机化学
物理
光电子学
作者
Wenjun Dong,Jiamin Yuan,Jingyi Tan,Xiaomin Tang,Wen Tao Liu,Anmin Zheng,Wei Chen
标识
DOI:10.1021/acs.jpclett.2c03657
摘要
Kinetic quantum sieving (KQS) based on pore size and chemical affinity quantum sieving (CAQS) based on adsorption site are two routes of porous materials to separate hydrogen isotope mixtures. Alkali earth metals (Be, Mg, and Ca) were doped into UiO-67 to explore whether these metal sites can promote H2/D2 separation. Based on the zero-point energy and adsorption enthalpy calculated by density functional theory calculations, the Be dopant shows better H2/D2 separation performance than other alkali earth metal dopants and unsaturated metal sites in metal-organic frameworks based on CAQS. Orbital interaction strongly relates to the chemical affinity and further influences the D2/H2 selectivity. Moreover, the predicted D2/H2 selectivity of Be-doped sites (49.4) at 77 K is even larger than the best experimental result (26). Finally, the different dynamic behaviors of H2 and D2 on Be-doped UiO-67 indicate its strong H2/D2 separation performance via KQS.
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