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用于固态储氢的镁钛纳米颗粒的气相合成

Gas-phase synthesis of Mg-Ti nanoparticles for solid-state hydrogen storage.

作者信息

Calizzi M, Venturi F, Ponthieu M, Cuevas F, Morandi V, Perkisas T, Bals S, Pasquini L

机构信息

Department of Physics and Astronomy, Alma Mater Studiorum-University of Bologna, via C. Berti-Pichat 6/2, 40127 Bologna, Italy.

出版信息

Phys Chem Chem Phys. 2016 Jan 7;18(1):141-8. doi: 10.1039/c5cp03092g. Epub 2015 Nov 25.

Abstract

Mg-Ti nanostructured samples with different Ti contents were prepared via compaction of nanoparticles grown by inert gas condensation with independent Mg and Ti vapour sources. The growth set-up offered the option to perform in situ hydrogen absorption before compaction. Structural and morphological characterisation was carried out by X-ray diffraction, energy dispersive spectroscopy and electron microscopy. The formation of an extended metastable solid solution of Ti in hcp Mg was detected up to 15 at% Ti in the as-grown nanoparticles, while after in situ hydrogen absorption, phase separation between MgH2 and TiH2 was observed. At a Ti content of 22 at%, a metastable Mg-Ti-H fcc phase was observed after in situ hydrogen absorption. The co-evaporation of Mg and Ti inhibited nanoparticle coalescence and crystallite growth in comparison with the evaporation of Mg only. In situ hydrogen absorption was beneficial to subsequent hydrogen behaviour, studied by high pressure differential scanning calorimetry and isothermal kinetics. A transformed fraction of 90% was reached within 100 s at 300 °C during both hydrogen absorption and desorption. The enthalpy of hydride formation was not observed to differ from bulk MgH2.

摘要

通过使用独立的镁和钛蒸汽源,利用惰性气体冷凝法生长的纳米颗粒压实制备了具有不同钛含量的镁钛纳米结构样品。该生长装置提供了在压实之前进行原位吸氢的选择。通过X射线衍射、能量色散光谱和电子显微镜对结构和形态进行了表征。在生长的纳米颗粒中,检测到钛在六方密堆积镁中形成了扩展的亚稳固溶体,钛含量高达15原子%,而在原位吸氢后,观察到氢化镁和氢化钛之间的相分离。在钛含量为22原子%时,原位吸氢后观察到一种亚稳的镁钛氢面心立方相。与仅蒸发镁相比,镁和钛的共蒸发抑制了纳米颗粒的聚结和微晶生长。原位吸氢有利于随后通过高压差示扫描量热法和等温动力学研究的氢行为。在300℃下,吸氢和解吸过程中在100秒内达到了90%的转变分数。未观察到氢化物形成焓与块状氢化镁有差异。

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