کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1613438 1005597 2013 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Comparative study of reversible hydrogen storage in alkali-doped fulleranes
موضوعات مرتبط
مهندسی و علوم پایه مهندسی مواد فلزات و آلیاژها
پیش نمایش صفحه اول مقاله
Comparative study of reversible hydrogen storage in alkali-doped fulleranes
چکیده انگلیسی

In this report we describe and compare the hydrogen storage properties of lithium and sodium doped fullerenes prepared via a solvent-assisted mixing process. For the preparation of these samples either NaH or LiH was utilized as the alkali metal source to make material based on either a Na6C60 or Li6C60. Both of the alkali-doped materials can reversibly absorb and desorb hydrogen at much milder conditions than the starting materials used to make them (decomposition temperatures of NaH > 420 °C, LiH > 670 °C, and fullerane > 500 °C). The hydrogen storage properties of the materials were compared by TGA, isothermal desorption, and XRD analysis. It was determined that the sodium-doped material can reversibly store 4.0 wt.% H2 while the lithium doped material can reversibly store 5.0 wt.% H2 through a chemisorption mechanism indicated by the formation and measurement of C–H bonds. XRD analysis of the material demonstrated that a reversible phase transition between fcc and bcc occurs depending on the temperature at which the hydrogenation is performed. In either system the active hydrogen storage material resembles a hydrogenated fullerene (fullerane).


► Catalytic effect of alkali metals of fullerane formation.
► Hydrogen storage properties of alkali metal hydrides and fullerene composites.
► Novel intercalation of Na and Li in the fullerene lattice.
► Reversible phase transformation of C60 from fcc to bcc upon de/rehydrogenation.
► Potential to enable to the formation of other carbon based hydrogen storage systems.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Alloys and Compounds - Volume 580, Supplement 1, 15 December 2013, Pages S364–S367
نویسندگان
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