4.7 Article

CeO2 modified Fe2O3 for the chemical hydrogen storage and production via cyclic water splitting

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 39, Issue 25, Pages 13381-13388

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2014.04.136

Keywords

Chemical hydrogen storage and production; Fe-Ce mixed oxides; Redox process

Funding

  1. National Natural Science Foundation of China [51204083, 51104074, 51174105, 513744004]
  2. Applied Basic Research Program of Yunnan Province [2012FD016]
  3. candidate talents training fund of Yunnan Province [2012HB009]
  4. Analysis and Testing Foundation of Kunming University of Science and Technology

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The chemical hydrogen storage (hydrogen reduction) and production (water splitting) behaviour of Ce-modified Fe2O3 mixed oxides were investigated. Fe1-xCexO2-delta (x = 0, 0.05, 0.1, 0.2, 0.3, 0.4 and 1) oxides prepared by chemical precipitation were characterized by XRD (X-ray diffraction), H-2-TPR (hydrogen temperature-programmed reduction) and H2O-TPO (steam temperature-programmed oxidation) tests. XRD results showed that two kinds of Fe -Ce-O solid solutions (Ce-based and Fe-based) coexisted in Fe-Ce mixed oxides. H-2-TPR experiment suggested that Ce addition could reduce hydrogen reduction temperature while H2O-TPO experiments over reduced oxides showed that Fe-Ce mixed oxides could split water to produce hydrogen at a lower temperature and complete in a shorter time. Both redox reactions (hydrogen reduction and water splitting) were sensitive to the temperature and active at a high temperature. The successive redox cycles were carried out over the Fe0.7Ce0 3O2-delta mixed oxide at 750 degrees C. It kept a stable production of hydrogen in the successive redox process at the condition of serious agglomeration of the materials. The highest hydrogen storage amount was up to 1.51 wt% for the Fe-Ce sample with a 30% substitution of Ce for Fe. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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