Solar thermal decoupled water electrolysis process I: Proof of concept

R. Palumbo, R. B. Diver, C. Larson, E. N. Coker, J. E. Miller, J. Guertin, J. Schoer, M. Meyer, N. P. Siegel

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

A new concept for a solar thermal electrolytic process was developed for the production of H 2 from water. A metal oxide is reduced to a lower oxidation state in air with concentrated solar energy. The reduced oxide is then used either as an anode or solute for the electrolytic production of H 2 in either an aqueous acid or base solution. The presence of the reduced metal oxide as part of the electrolytic cell decreases the potential required for water electrolysis below the ideal 1.23V required when H 2 and O 2 evolve at 1bar and 298K. During electrolysis, H 2 evolves at the cathode at 1bar while the reduced metal oxide is returned to its original oxidation state, thus completing the H 2 production cycle. Ideal sunlight-to-hydrogen thermal efficiencies were established for three oxide systems: Fe 2O 3-Fe 3O 4, Co 3O 4-CoO, and Mn 2O 3-Mn 3O 4. The ideal efficiencies that include radiation heat loss are as high or higher than corresponding ideal values reported in the solar thermal chemistry literature. An exploratory experimental study for the iron oxide system confirmed that the electrolytic and thermal reduction steps occur in a laboratory scale environment.

Original languageEnglish (US)
Pages (from-to)372-380
Number of pages9
JournalChemical Engineering Science
Volume84
DOIs
StatePublished - Dec 24 2012

Bibliographical note

Funding Information:
We thank the Alfred W. Sieving Family for financial support through the Endowed Alfred W. Sieving Chair of Engineering . We are also grateful for financial support from Valparaiso University's College of Engineering .

Keywords

  • Electrochemistry
  • Hydrogen
  • Metal oxides
  • Solar
  • Thermal
  • Thermodynamics

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