Metal-Organic Framework Materials with Ultrahigh Surface Areas: Is the Sky the Limit?

被引:1530
作者
Farha, Omar K. [1 ,2 ]
Eryazici, Ibrahim [1 ,2 ]
Jeong, Nak Cheon [1 ,2 ,5 ]
Hauser, Brad G. [1 ,2 ]
Wilmer, Christopher E. [3 ]
Sarjeant, Amy A. [1 ,2 ]
Snurr, Randall Q. [3 ]
Nguyen, SonBinh T. [1 ,2 ]
Yazaydin, A. Oezguer [4 ]
Hupp, Joseph T. [1 ,2 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[4] Univ Surrey, Dept Chem Engn, Guildford GU2 7XH, Surrey, England
[5] Daegu Gyeongbuk Inst Sci & Technol, Dept Emerging Mat Sci, Taegu 711873, South Korea
关键词
HYDROGEN STORAGE; COORDINATION COPOLYMER; ENERGY-TRANSFER; ADSORPTION; DESIGN; ACTIVATION; POROSITY; ROUTE;
D O I
10.1021/ja3055639
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have synthesized, characterized, and computationally simulated/validated the behavior of two new metal organic framework (MOF) materials displaying the highest experimental Brunauer-Emmett-Teller (BET) surface areas of any porous materials reported to date (similar to 7000 m(2)/g). Key to evacuating the initially solvent-filled materials without pore collapse, and thereby accessing the ultrahigh areas, is the use of a supercritical CO2 activation technique. Additionally, we demonstrate computationally that by shifting from phenyl groups to "space efficient" acetylene moieties as linker expansion units, the hypothetical maximum surface area for a MOF material is substantially greater than previously envisioned (similar to 14600 m(2)/g (or greater) versus similar to 10500 m(2)/g).
引用
收藏
页码:15016 / 15021
页数:6
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