Non-isothermal desorption process of hydrogenated nanocrystalline Pd-capped Mg films investigated by Ion Beam Techniques

被引:21
作者
Ares, J. R. [1 ]
Leardini, F. [2 ]
Diaz-Chao, P. [3 ]
Ferrer, I. J. [1 ]
Fernandez, J. F. [1 ]
Sanchez, C. [1 ]
机构
[1] UAM, Fac Ciencias, Dpto Fis Mat, MIRE Grp,Lab Fis Mat Interes Energet, Madrid 28049, Spain
[2] Univ Roma La Sapienza, Dipartimento Fis, I-00185 Rome, Italy
[3] ENSICAEN, UCBN, CRISMAT, F-14050 Caen, France
关键词
Hydrogen storage; Magnesium hydride; Nanocrystalline film; Ion Beam Techniques; Thermal desorption mechanism; PD/MG THIN-FILMS; MAGNESIUM HYDRIDE; ABSORPTION; KINETICS; STORAGE; GROWTH; NUCLEATION; NANO; H-2;
D O I
10.1016/j.ijhydene.2013.11.130
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanocrystalline Pd-capped Mg films were prepared by e-beam evaporation and hydrided/deuterated in order to investigate the hydride decomposition mechanism. To that aim, different techniques were used (XRD, FEG, TPD-MS, isotope exchange and "in situ" desorption optical measurements). Obtained results show that hydride films decomposed at T = 165 degrees C by a process controlled by the Mg/MgH2 interface reaction with an activation energy E-a = 136 +/- 5 kJ/mol H-2. Interface is located into each MgH2 nanocrystallite according to RBS (Rutherford Backscattering) and ERDA (Elastic Recoil Detection Analysis) measurements performed during hydride decomposition. Moreover, RBS and ERDA spectra also show the formation of a MgxPdy intermixed region. This intermixed region does not modify the type of control mechanism but increases the activation energy of the desorption process and slows down further hydrogenation events. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2587 / 2596
页数:10
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