物理吸附
吸附
金属有机骨架
纳米孔
扩散
材料科学
焓
化学吸附
化学物理
碳纳米管
热力学
化学工程
纳米技术
化学
物理化学
物理
工程类
作者
Yann Magnin,Estelle Dirand,Guillaume Maurin,Philip L. Llewellyn
标识
DOI:10.1021/acsanm.3c03752
摘要
Carbon mitigation is one challenging issue that the world is facing. To tackle the deleterious impacts of CO 2, processes emerged, including chemisorption from amine-based solvents and, more recently, physisorption in nanoporous solids. Physisorption in metal–organic frameworks (MOFs) is currently attracting considerable attention; however, the selection of the optimum sorbent is still challenging. While CO 2 adsorption by MOFs has been widely explored from a thermodynamics standpoint, dynamical aspects remain less explored. CALF-20(Zn) MOF was recently proposed as a promising alternative to the commercially used CO 2 13X zeolite sorbents; however, an in-depth understanding of the nanoscopic mechanisms originating its good performance still has to be achieved. To do so, we deliver some insights into the adsorption and diffusion of CO 2, H 2 O, and mixtures in CALF-20 through atomistic simulations. CALF-20(Zn) was revealed to exhibit unconventional guest–host behaviors that give rise to abnormal guest thermodynamics and dynamics. The hydrophobic nature of the nanoporous solid leads to a low water adsorption enthalpy at low loading, followed by a continuous increase, driven by strong water hydrogen bonds, found to arrange as quasi 1D molecular wires in MOF nanoporosity, recalling water behavior in small-diameter carbon nanotubes. While no superdiffusion was found in the CALF-20(Zn) as compared to carbon nanotubes, this behavior was shown to impact the guest-loading diffusion coefficient profile, with the presence of a minimum that correlates with the inflection point in the adsorption isotherm corresponding to the H 2 O wires formation. Interestingly, the diffusion coefficients of CO 2 and H 2 O were also found to be of the same order of magnitude, with similar nonlinear profiles as a function of the guest loading. We further demonstrated that the diffusion coefficient for CO 2 in the presence of water decreases with increasing water loading.
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