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通过金属有机框架中的碱土金属掺杂剂增强氢同位素分离

Enhance Hydrogen Isotopes Separation by Alkali Earth Metal Dopant in Metal-Organic Framework.

作者信息

Dong Wenjun, Yuan Jiamin, Tan Jingyi, Tang Xiaomin, Liu Wentao, Zheng Anmin, Chen Wei

机构信息

School of Materials Science and Engineering, Zhengzhou University, 450001Zhengzhou, Henan, P. R. China.

State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Innovation Academy for Precision Measurement Science and Technology, Chinese Academy of Sciences, 430071Wuhan, P. R. China.

出版信息

J Phys Chem Lett. 2023 Feb 9;14(5):1198-1207. doi: 10.1021/acs.jpclett.2c03657. Epub 2023 Jan 30.

Abstract

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 H/D separation. Based on the zero-point energy and adsorption enthalpy calculated by density functional theory calculations, the Be dopant shows better H/D 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 D/H selectivity. Moreover, the predicted D/H 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 H and D on Be-doped UiO-67 indicate its strong H/D separation performance via KQS.

摘要

基于孔径的动力学量子筛分(KQS)和基于吸附位点的化学亲和量子筛分(CAQS)是多孔材料分离氢同位素混合物的两条途径。将碱土金属(Be、Mg和Ca)掺杂到UiO-67中,以探究这些金属位点是否能促进H/D分离。基于密度泛函理论计算得到的零点能和吸附焓,在基于CAQS的金属有机框架中,Be掺杂剂表现出比其他碱土金属掺杂剂和不饱和金属位点更好的H/D分离性能。轨道相互作用与化学亲和力密切相关,并进一步影响D/H选择性。此外,在77 K时,Be掺杂位点的预测D/H选择性(49.4)甚至大于最佳实验结果(26)。最后,H和D在Be掺杂的UiO-67上的不同动力学行为表明其通过KQS具有很强的H/D分离性能。

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