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Hydrogen storage in metal -organic f...

Rowsell, Jesse.

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Hydrogen storage in metal -organic frameworks: An investigation of structure -property relationships.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Hydrogen storage in metal -organic frameworks: An investigation of structure -property relationships./
作者:	Rowsell, Jesse.
面頁冊數:	349 p.
附註:	Source: Dissertation Abstracts International, Volume: 66-10, Section: B, page: 5398.
Contained By:	Dissertation Abstracts International66-10B.
標題:	Chemistry, Inorganic. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3192766
ISBN:	9780542365805

Hydrogen storage in metal -organic frameworks: An investigation of structure -property relationships.
Rowsell, Jesse.

Hydrogen storage in metal -organic frameworks: An investigation of structure -property relationships. - 349 p.

Source: Dissertation Abstracts International, Volume: 66-10, Section: B, page: 5398.

Thesis (Ph.D.)--University of Michigan, 2005.

Metal-organic frameworks (MOFs) have been identified as candidate hydrogen storage materials due to their ability to physisorb large quantities of small molecules. Thirteen compounds (IRMOF-1, -2, -3, -6, -8, -9, -11, -13, -18, -20, MOF-74, MOF-177 and HKUST-1) have been prepared and fully characterized for the evaluation of their dihydrogen (H2) adsorption properties. All compounds display approximately type I isotherms with no hysteresis at 77 K up to 1 atm. The amount adsorbed ranges from 0.89 to 2.54 wt%; however, saturation is not achieved under these conditions. The influences of link functionalization, catenation and topology are examined for the eleven MOFs composed of Zn4O(O2C-)6 clusters. Enhanced H2 uptake by catenated compounds is rationalized by increased overlap of the surface potentials within their narrower pores. This is corroborated by the larger isosteric heat of adsorption of IRMOF-11 compared to IRMOF-1. Inelastic neutron scattering spectroscopic analysis of four Zn4O-based materials (IRMOF-1, -8, -11, and MOF-74) under a range of H2 loading suggests the presence of multiple localized adsorption sites on both the inorganic and organic moieties. To determine the structural details of the adsorption sites, variable temperature single crystal X-ray diffraction was used to analyze adsorbed argon and dinitrogen molecules in IRMOF-1. The principle binding site was found to be the same for both adsorbates and is located on faces of the octahedral Zn4O(O2C-)6 clusters with close contacts to three carboxylate groups. A total of eight symmetry-independent adsorption sites were identified for argon at 30 K. Similar sites were observed for dinitrogen, suggesting that they are good model adsorbates for the behaviour of dihydrogen. Two additional materials composed of inorganic clusters with coordinatively unsaturated metal sites (MOF-74, HKUST-1) were examined and their increased capacities and isosteric heats of adsorption provide further evidence that the interaction is strongest at the inorganic clusters. This enhancement becomes less important at high pressure, where large pore volume proves to be the greater contributor to capacity.

ISBN: 9780542365805Subjects--Topical Terms:

517253
Chemistry, Inorganic.

Hydrogen storage in metal -organic frameworks: An investigation of structure -property relationships.
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245 1 0 $a Hydrogen storage in metal -organic frameworks: An investigation of structure -property relationships.
300 $a 349 p.
500 $a Source: Dissertation Abstracts International, Volume: 66-10, Section: B, page: 5398.
500 $a Chair: Omar M. Yaghi.
502 $a Thesis (Ph.D.)--University of Michigan, 2005.
520 $a Metal-organic frameworks (MOFs) have been identified as candidate hydrogen storage materials due to their ability to physisorb large quantities of small molecules. Thirteen compounds (IRMOF-1, -2, -3, -6, -8, -9, -11, -13, -18, -20, MOF-74, MOF-177 and HKUST-1) have been prepared and fully characterized for the evaluation of their dihydrogen (H2) adsorption properties. All compounds display approximately type I isotherms with no hysteresis at 77 K up to 1 atm. The amount adsorbed ranges from 0.89 to 2.54 wt%; however, saturation is not achieved under these conditions. The influences of link functionalization, catenation and topology are examined for the eleven MOFs composed of Zn4O(O2C-)6 clusters. Enhanced H2 uptake by catenated compounds is rationalized by increased overlap of the surface potentials within their narrower pores. This is corroborated by the larger isosteric heat of adsorption of IRMOF-11 compared to IRMOF-1. Inelastic neutron scattering spectroscopic analysis of four Zn4O-based materials (IRMOF-1, -8, -11, and MOF-74) under a range of H2 loading suggests the presence of multiple localized adsorption sites on both the inorganic and organic moieties. To determine the structural details of the adsorption sites, variable temperature single crystal X-ray diffraction was used to analyze adsorbed argon and dinitrogen molecules in IRMOF-1. The principle binding site was found to be the same for both adsorbates and is located on faces of the octahedral Zn4O(O2C-)6 clusters with close contacts to three carboxylate groups. A total of eight symmetry-independent adsorption sites were identified for argon at 30 K. Similar sites were observed for dinitrogen, suggesting that they are good model adsorbates for the behaviour of dihydrogen. Two additional materials composed of inorganic clusters with coordinatively unsaturated metal sites (MOF-74, HKUST-1) were examined and their increased capacities and isosteric heats of adsorption provide further evidence that the interaction is strongest at the inorganic clusters. This enhancement becomes less important at high pressure, where large pore volume proves to be the greater contributor to capacity.
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