A MOF platform for incorporation of complementary organic motifs for CO2 binding

被引:48
作者
Deria, Pravas [1 ]
Li, Song [2 ]
Zhang, Hongda [2 ]
Snurr, Randall Q. [2 ]
Hupp, Joseph T. [1 ]
Farha, Omar K. [1 ,3 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[3] King Abdulaziz Univ, Fac Sci, Dept Chem, Jeddah 21413, Saudi Arabia
关键词
CARBON-DIOXIDE CAPTURE; DE-NOVO SYNTHESIS; POROUS MATERIALS; SURFACE-AREA; ADSORPTION; FRAMEWORKS; FUNCTIONALIZATION; STORAGE; GAS; THERMODYNAMICS;
D O I
10.1039/c5cc04808g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CO2 capture is essential for reducing the carbon footprint of coal-fired power plants. Here we show, both experimentally and computationally, a new design strategy for capturing CO2 in nanoporous adsorbents. The approach involves 'complementary organic motifs' (COMs), which have a precise alignment of charge densities that is complementary to the CO2 quadrupole. Two promising COMs were post-synthetically incorporated into a robust metal-organic framework (MOF) material using solvent-assisted ligand incorporation (SALI). We demonstrate that these COM-functionalized MOFs exhibit high capacity and selectivity for CO2 relative to other reported motifs.
引用
收藏
页码:12478 / 12481
页数:4
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