Catalyzed alanates for hydrogen storage

被引:217
|
作者
Gross, KJ
Thomas, GJ
Jensen, CM
机构
[1] Sandia Natl Labs, Analyt Mat Sci Dept, Livermore, CA 94551 USA
[2] Univ Hawaii Manoa, Dept Chem, Honolulu, HI 96822 USA
关键词
metal hydride; complex hydride; catalysis; NAlH4; Na3AlH6; hydrogen storage; fuel cell;
D O I
10.1016/S0925-8388(01)01586-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The discovery that hydrogen can be reversibly absorbed and desorbed from complex hydrides (the alanates) by the addition of catalysts has created an entirely new prospect for lightweight hydrogen storage. Unlike the interstitial intermetallic hydrides, these compounds release hydrogen through a series of decomposition /recombination reactions e.g.: NaAlH(4)double left right arrow1/3Na(3)AIH(6) + 2/3Al+H(2)double left right arrowNaH+Al+3/ 2H(2). Initial work resulted in improved catalysts, advanced methods of preparation, and a better understanding of the hydrogen absorption and desorption processes. Recent studies have clarified some of the fundamental material properties, as well as the engineering characteristics of catalyst enhanced sodium alanate. Phase transitions were observed real-time through in situ X-ray powder diffraction. These measurements demonstrate that the decomposition reactions occur through long-range transport of metal species. SEM imaging and EDS analysis verified the segregation of aluminum to the surface of the material during decomposition. The equilibrium thermodynamics of decomposition have now been measured down to room temperature. They show a plateau pressure for the first reaction of I bar at 33degreesC, which suggest that, thermodynamically, this material is ideally suited to on-board hydrogen storage for fuel cell vehicles. Room temperature desorption with slow but measurable kinetics has been recorded for the first time. Studies at temperatures approaching that found in the operation of PEM fuel cells (125-165degreesC) were performed on a scaled-up test bed. The bed demonstrated surprisingly good kinetics and other positive material properties. However, these studies also pointed to the need to develop new non-alkoxide based catalysts and doping methods to increase the capacity and reduce the level of hydrocarbon impurities found in the desorbed hydrogen. For this reason, new Ti-Cl catalysts and doping processes are being developed which show higher capacities and improved kinetics. An overview of the current state-of-the-art will be presented along with our own studies and the implications for the viability of these materials in on-board hydrogen storage applications. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:683 / 690
页数:8
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