Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-27T00:24:24.119Z Has data issue: false hasContentIssue false
  • English
  • Français

Synthesis and Characterization of Nanoscale Transition Metal Complex for Hydrogen Storage

Published online by Cambridge University Press:  15 February 2011

Sesha S. Srinivasan ,
Matthew T. Smith ,
Deepak Deshpande ,
Eias K. Stefanakos ,
Yogi Goswami ,
Michael Jurczyk ,
Arun Kumar  and
Ashok Kumar
Sesha S. Srinivasan
Affiliation:
Clean Energy Research Center, College of Engineering, University of South Florida, Tampa, FL- 33620
Matthew T. Smith
Affiliation:
Clean Energy Research Center, College of Engineering, University of South Florida, Tampa, FL- 33620
Deepak Deshpande
Affiliation:
Solar Energy and Energy Conversion Laboratory, College of Engineering, University of Florida, Gainesville, FL 32611
Eias K. Stefanakos
Affiliation:
Clean Energy Research Center, College of Engineering, University of South Florida, Tampa, FL- 33620
Yogi Goswami
Affiliation:
Solar Energy and Energy Conversion Laboratory, College of Engineering, University of Florida, Gainesville, FL 32611
Michael Jurczyk
Affiliation:
Clean Energy Research Center, College of Engineering, University of South Florida, Tampa, FL- 33620
Arun Kumar
Affiliation:
Clean Energy Research Center, College of Engineering, University of South Florida, Tampa, FL- 33620
Ashok Kumar
Affiliation:
Clean Energy Research Center, College of Engineering, University of South Florida, Tampa, FL- 33620
Get access

Abstract

The development of light weight hydrogen storage systems with high volumetric and gravimetric hydrogen densities is indeed essential for the on-board fuel cell vehicular applications [1]. Among the different hydrogen storage systems designed and developed so far, Ti- doped sodium aluminum hydrides exhibit potential promise of reversible hydrogen storage capacity (4-5 wt.%) at moderate temperatures [2,3]. However, the poor cyclic stability of these hydrides due to the partial reversibility of the two step reactions necessitates the development of exotic materials or tailoring the known hydride systems. On the other hand, transition metal complex hydrides, TMHx (T = Mg; M = Fe, Co, Ni) have also been identified as potential candidates for hydrogen storage [4-6] and/or analogous to alanates [7]. These hydrides especially Mg2FeH6, have shown excellent cyclic capacities (more than 500 cycles) even without a catalyst [8]. Besides, Mg2FeH6 possesses the highest volumetric and gravimetric hydrogen densities of 150 kg/m3 and 5.6 wt.% respectively [9]. However, at low temperatures, the rate of release of hydrogen and the effective reversible hydrogen capacity seems poor. Recent reports declared that the enhancement in the cycling kinetics and reduction in the operating temperature is very much possible by using a distorted nano-scale Mg structure [10, 11], doping the host lattice with Ti- species and/or lattice substitution [12]. Keeping these facts in view, the present investigation aims to improve the sorption kinetics and thermodynamics of Mg2FeH6, by 1) preparing nano-scale Mg-Fe-H system using mechano-chemical synthesis process, 2) surface localized catalyst (Ti- species) doping and 3) cationic substitution of Na+/Li+ for Mg2+ by incorporating NaH/LiH. The synergistic behavior of the tailored nano-scale transition metal complex for hydrogen storage is outlined.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 884: Symposium GG – Materials and Technology for Hydrogen Storage and Generation , 2005 , GG4.2
Copyright
Copyright © Materials Research Society 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

[1] Report of the Basic Energy Science Workshop on Hydrogen Production, Storage and use prepared by Argonne National Laboratory, May 13-15 (2003).Google Scholar
[2] Bogdanovic, B., Schwickardi, M., International Patent WO97/03919 (1997)Google Scholar
[3] Jensen, C.M., Zidan, R., US Patent 6,471,935 B2 (2002)Google Scholar
[4] Selvam, P., Yvon, K., Int. J. Hydrogen Energy, 16, 9 (1991) 615Google Scholar
[5] Huot, J., S, Boily, Akiba, E., Schulz, R., J. Alloys Comp., 280 (1998) 306 Google Scholar
[6] Vegge, T., Jensen, Lise S.H, Bonde, J., Munter, T.R., Norskov, J.K., J. Alloys Comp., 386 (2005) 1–7 Google Scholar
[7] Bogdanovic, B. et al, Phys. Chem. Chem. Phys., 6 (2004) 4369–4374 Google Scholar
[8] Bogdanovic, B., Reiser, A., Schlichte, K., Spliethoff, B., Tesche, B., J. Alloys Comp., 345 (2002) 77–89 Google Scholar
[9] Zuttel, A., Materialstoday, September (2003) 24–33 Google Scholar
[10] http://europa.eu.int/comm/research/energy/pdf/efchp hydrogen4.pdfGoogle Scholar
[11] Herrich, M., Ismail, N., Lyubina, J., Handstein, A., Pratt, A., Gutfleisch, O., Mat. Sci. Engg. B108 (2004) 28–32 Google Scholar
[12] http://eere.energy.gov/hydrogenandfuelcells/pdfs/iiib2_gross.pdfGoogle Scholar