First principles study of enhanced CO2 adsorption on MOF-253 by salt-insertion
First principles study of enhanced CO2 adsorption on MOF-253 by salt-insertion
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MOF-253 盐插入增强 CO2 吸附的第一性原理研究
DOI:
10.1016/j.commatsci.2015.09.006
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发表时间:
2016
期刊:
影响因子:
--
通讯作者:
Qiuju Zhang
中科院分区:
文献类型:
--
作者:
Yang Wu;Lihong Wei;Liang Chen;Qiuju Zhang
We investigated the basic electron variation in salt-chelated MOF-253 and revealed increased CO2adsorption by chelating PdCl2and Cu(BF4)2through the DFT-D2 method. The two N atoms preferentially orient to opposite side of the 2,2′-bipyridine (bpy) in bare MOF-253 to yield a CO2adsorption energy of −0.15 eV, which mainly contributes to the experimentally determined isotopic heat energy of −0.24 eV. Following salt insertion, the two pyridine rings rotate to the same side to hold the salt that binds on NN atoms. While PdCl2insertion does not significantly enhance CO2adsorption, dipole polarization creates multiple adsorption sites by adding a Pdsingle bondCl bond and co-linker site, thereby increasing the adsorption capacity of the resultant material. Cu(BF4)2chelation significantly increases the CO2adsorption energy to −0.49 eV, which is ascribed to the large positive charge of the Cu ion inducing significant electrostatic interactions with the O atom of CO2. Our calculation results demonstrate the effect of inherent electron distribution during salt insertion on CO2adsorption and clearly explain the observed 7 kJ/mol enhancement in CO2absorption upon loading of Cu(BF4)2on MOF-253. This study provides new insights into the selection of an ideal salt for chelation with the open bpy linker to improve gas uptake and illustrates the potential application of catalysis by MOF-253 to gas conversion.
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