Hydrogenation of Magnesium Nickel Boride for Reversible Hydrogen Storage
Abstract
We report that a ternary magnesium nickel boride (MgNi_(2.5)B_2) mixed with LiH and MgH_2 can be hydrogenated reversibly forming LiBH_4 and Mg_2NiH_4 at temperatures below 300 °C. The ternary boride was prepared by sintering a mechanically milled mixture of MgB_2 and Ni precursors at 975 °C under inert atmosphere. Hydrogenation of the ternary, milled with LiH and MgH_2, was performed under 100 to 160 bar H_2 at temperatures up to 350 °C. Analysis using X-ray diffraction, Fourier transform infrared, and ^(11)B magic angle spinning NMR confirmed that the ternary boride was hydrogenated forming borohydride anions. The reaction was reversible with hydrogenation kinetics that improved over three cycles. This work suggests that there may be other ternary or higher order boride phases useful for reversible hydrogen storage.
Additional Information
© 2009 American Chemical Society. Received Date: October 7, 2009. Accepted Date: October 27, 2009. Published on Web Date: November 06, 2009. We thank the US Department of Energy (DOE contract DE-FC36-05GO15067) and DE-AI-01-05EE11105 for support of this work. We also thank Dr. Jason Zan and Joseph Reiter at the Jet Propulsion Laboratory for assisting with sample handlings. The NMR facility at Caltech was supported by the National Science Foundation (NSF) under Grant Number 9724240 and partially supported by the MRSEC Program of the NSF under Award Number DMR-0520565.Attached Files
Supplemental Material - jz900102y_si_001.pdf
Files
Name | Size | Download all |
---|---|---|
md5:b2c57d64f9a4e6cc441505bbaf90ef6b
|
1.3 MB | Preview Download |
Additional details
- Eprint ID
- 18568
- Resolver ID
- CaltechAUTHORS:20100604-134329483
- Department of Energy (DOE)
- DE-FC36-05GO15067
- NSF
- DMR-9724240
- NSF
- DMR-0520565
- Department of Energy (DOE)
- DE-Al-01-05EE11105
- Created
-
2010-06-23Created from EPrint's datestamp field
- Updated
-
2021-11-08Created from EPrint's last_modified field