Local intermolecular interactions for selective CO2 capture by zeolitic imidazole frameworks: energy decomposition analysis

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Intermolecular energy decomposition analysis (EDA) is reported for the binding of CO2 with zeolitic imidazole frameworks (ZIF) to provide a molecular level interpretation of the recent capacity and selectivity measurements of several ZIFs and to suggest a theoretical guideline to improve their performance further, using 1 nm size of organic linker fragment of the ZIFs as a target molecule. The EDA suggests that the local electronic interaction of CO2 and the substituent groups, mainly frozen density and polarization interactions with little charge transfer, is the primary binding interaction, but the electron correlation effects can be equally or more important depending on the binding geometry and functional groups. The present correlated calculations identify the preferred ZIF binding sites for various gases including CO2 to be mostly near the benzene substituent groups rather than the plane of imidazole rings. We predict that the NH2-substituted ZIF would have an enhanced capacity of CO2 as compared to the NO2-substituted ZIF that was recently synthesized and reported to be one of the materials with the best capacity results along with high gas selectivity. The present calculations may imply that the local functionality of the linking organics, rather than detailed framework structures, may be of primary importance in designing certain high capacity MOF or ZIF materials.
Publisher
SPRINGER
Issue Date
2012-04
Language
English
Article Type
Article
Keywords

METAL-ORGANIC FRAMEWORK; ELECTRONIC-STRUCTURE METHOD; CARBON-DIOXIDE; MOLECULAR SIMULATION; HYDROGEN ADSORPTION; BASIS-SETS; SPIN; GROUP-11; ELEMENTS; BINDING

Citation

JOURNAL OF NANOPARTICLE RESEARCH, v.14, no.4

ISSN
1388-0764
DOI
10.1007/s11051-012-0793-9
URI
http://hdl.handle.net/10203/97131
Appears in Collection
CH-Journal Papers(저널논문)EEW-Journal Papers(저널논문)
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