4.7 Article

Evolution of the active species and catalytic mechanism of Ti doped NaAlH4 for hydrogen storage

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 42, Issue 9, Pages 6088-6095

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2016.12.105

Keywords

Hydrogen storage; Complex hydrides; NaAlH4; Active species; Catalytic mechanism

Funding

  1. National Natural Science Foundation of China [21406212]
  2. National Magnetic Confinement Fusion Science Program of China [2015GB109004]
  3. Foundation of China Academy of Engineering Physics [PY2014-7-5]
  4. Innovation Team Project of Sichuan Province [2013TD0017]

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The catalytic mechanism of Ti doped NaAlH4 for hydrogen storage remains unconfirmed. Here, we investigated the evolution of active species in Ti doped NaAlH4 system by XRD, XPS and TEM. The results reveal that the evolution of the Ti addition in doped NaAlH4 is Ti3+ -> amorphous Ti-0 -> Al-Ti species -> Al3Ti intermetallic. TEM results show that the average particle size of the Al-Ti species and Al3Ti intermetallic is about 30 nm, and Ti element is uniformly distributed in Al matrix. In further, we discussed the catalytic mechanism and role of active species in Ti doped NaAlH4 system according to experimental and theoretical calculation. The rehydrogenation process of Ti doped NaAlH4 system can be divided into three steps: (1) H-2 dissociation, (2) H atom spillover and alanes (AlxHy) formation and (3) complex hydrides formation. The addition of Ti can catalyze the process of H-2 dissociation, H atom spillover and formation of alanes. More importantly, the current work may provide a general approach to investigate the catalytic mechanism of other doped complex hydrides for hydrogen storage system. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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