A composite material in the LiH-LiF-MgB2 system has been synthesized by high-energy ball milling. Some peaks in addition to that of the binary 2LiH-MgB2 and 2LiF-MgB2 systems are observed for the composite material by high-pressure differential scanning calorimetry (HP-DSC), indicating the formation of intermediate phases. In situ synchrotron radiation powder X-ray diffraction (SR-PXD) performed at 60 bar of H-2 and 390 degrees C shows a superposition of both reaction pathways that are typical for 2LiH-MgB2 and 2LiF-MgB2. After hydrogen absorption of the LiH-LiF-MgB2 composite the vibrational modes of LiBH4 were observed by attenuated total reflection infrared (ATR-IR) spectroscopy. The F-19 MAS NMR spectrum of the LiF-LiBH4 sample after heat treatment in hydrogen is strongly dominated by the centerband and spinning sidebands from LiF; in addition, a low-intensity resonance, very similar to that of [BF4](-) ion, is identified.

Hydrogen sorption in the LiH-LiF-MgB2 system

ZAVOROTYNSKA, Olena;SPOTO, Giuseppe;BARICCO, Marcello;
2013-01-01

Abstract

A composite material in the LiH-LiF-MgB2 system has been synthesized by high-energy ball milling. Some peaks in addition to that of the binary 2LiH-MgB2 and 2LiF-MgB2 systems are observed for the composite material by high-pressure differential scanning calorimetry (HP-DSC), indicating the formation of intermediate phases. In situ synchrotron radiation powder X-ray diffraction (SR-PXD) performed at 60 bar of H-2 and 390 degrees C shows a superposition of both reaction pathways that are typical for 2LiH-MgB2 and 2LiF-MgB2. After hydrogen absorption of the LiH-LiF-MgB2 composite the vibrational modes of LiBH4 were observed by attenuated total reflection infrared (ATR-IR) spectroscopy. The F-19 MAS NMR spectrum of the LiF-LiBH4 sample after heat treatment in hydrogen is strongly dominated by the centerband and spinning sidebands from LiF; in addition, a low-intensity resonance, very similar to that of [BF4](-) ion, is identified.
2013
117
17360
17366
http://www.scopus.com/inward/record.url?eid=2-s2.0-84883146695&partnerID=40&md5=f9ed2f2d51e061119026103b901671f0
I. Saldan;M. Schulze;C. Pistidda;R. Gosalawit-Utke;O. Zavorotynska;L. Rude;J. Skibsted;D. Haase;Y. Cerenius;T. Jensen;G. Spoto;M. Baricco;K. Taube;M. Dornheim
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/140608
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