Improving Hydrogen Adsorption Enthalpy Through Coordinatively Unsaturated Cobalt in Porous Polymers

被引:16
|
作者
Yuan, Shengwen [2 ]
White, Desiree [2 ]
Mason, Alex [2 ]
Reprogle, Briana [2 ]
Ferrandon, Magali S. [2 ]
Yu, Luping [1 ]
Liu, Di-Jia [2 ]
机构
[1] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
[2] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA
关键词
adsorption; hydrogen; microporosity; porous organic polymer; INTRINSIC MICROPOROSITY PIMS; HIGH-SURFACE-AREA; COVALENT ORGANIC FRAMEWORKS; GAS-ADSORPTION; POTENTIAL ADSORBENTS; NANOPOROUS POLYMERS; CONJUGATED POLYMERS; PORE-SIZE; STORAGE; NETWORKS;
D O I
10.1002/marc.201100797
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The design and synthesis of a new porous organic polymer (POP) incorporated with cobalt carbonyl complexes through built-in bipyridinic coordination sites for hydrogen storage are described. A thermal activation process was developed to remove the ligated carbonyl and carbon dioxide in order to expose the cobalt atomically inside of porous structure. Various spectroscopic and physical characterization techniques were used to study the coordinated Co sites and the POP's surface property. Upon thermal activation, this new cobalt-containing POP showed improved hydrogen uptake capacity and isosteric heat of adsorption.
引用
收藏
页码:407 / 413
页数:7
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