Sorry, you need to enable JavaScript to visit this website.

H<inf>2</inf> thermal desorption and hydride conversion reactions in Li cells of TiH<inf>2</inf>/C amorphous nanocomposites

TitoloH2 thermal desorption and hydride conversion reactions in Li cells of TiH2/C amorphous nanocomposites
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2015
AutoriVitucci, F.M., Paolone A., Brutti S., Munaò D., Silvestri L., Panero S., and Reale P.
RivistaJournal of Alloys and Compounds
Volume645
PaginazioneS46-S50
ISSN09258388
Parole chiaveConversion reactions, Crystal structure, Dehydrogenation, Electric discharges, Electrochemical process, Electron microscopy, Enthalpy, Galvanostatic cycling, Hydrides, Hydrogen, Hydrogen absorbing material, Lithium, Mass Spectrometry, Mechano-chemical processing, Mechano-chemical routes, Mechanochemical treatment, Nanocomposites, Thermal dehydrogenation, Thermodynamic properties, Thermogravimetric analysis, Transmission electron microscopy, X ray diffraction
Abstract

Abstract Here we investigate the properties of amorphous TiH2/carbon nanocomposites as possible active material in lithium cells. Several TiH2/C mixtures are prepared by a mechanochemical route, by varying the carbon/hydride ratio. Materials are tested in electrochemical cells versus lithium metal in EC:DMC LiPF6 electrolyte by galvanostatic cycling (GC) and are characterized by X-ray diffraction, transmission electron microscopy, thermogravimetry and mass spectrometry. Thermal dehydrogenation processes are altered by the mechanochemical treatment of the sample: milling decreases the hydrogen content of the hydride. On the other hand, the mechanochemical grinding increases the specific capacity delivered during the first GC discharge. We suggest that the electrochemical process is the result of a delicate balance between the absolute quantity of hydrogen and its availability for the hydride conversion reaction. © 2015 Elsevier B.V.

Note

cited By 3

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84938953205&doi=10.1016%2fj.jallcom.2015.01.232&partnerID=40&md5=bb9cc1508adafb3952a0d63bce134f77
DOI10.1016/j.jallcom.2015.01.232
Citation KeyVitucci2015S46