4.8 Article

Sr- and Mn-doped LaAlO3-δ for solar thermochemical H2 and CO production

Journal

ENERGY & ENVIRONMENTAL SCIENCE
Volume 6, Issue 8, Pages 2424-2428

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ee41372a

Keywords

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Funding

  1. DOE NNSA [DE-FC52-08NA28752]
  2. Sandia National Laboratories Truman Fellowship in National Security Science and Engineering
  3. National Science Foundation MRSEC program [DMR-0820518]
  4. DOE Fuel Cell Technologies Office as part of the Production technology development area
  5. Laboratory Directed Research and Development at Sandia National Laboratories
  6. United States Department of Energy's National Nuclear Security Administration [DE-AC04-94AL85000]

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The increasing global appetite for energy within the transportation sector will inevitably result in the combustion of more fossil fuel. A renewable-derived approach to carbon-neutral synthetic fuels is therefore needed to offset the negative impacts of this trend, which include climate change. In this communication we report the use of nonstoichiometric perovskite oxides in two-step, solar-thermochemical water or carbon dioxide splitting cycles. We find that LaAlO3 doped with Mn and Sr will efficiently split both gases. Moreover the H-2 yields are 9x greater, and the CO yields 6x greater, than those produced by the current state-of-the-art material, ceria, when reduced at 1350 degrees C and re-oxidized at 1000 degrees C. The temperature at which O-2 begins to evolve from the perovskite is fully 300 degrees C below that of ceria. The materials are also very robust, maintaining their redox activity over at least 80 CO2 splitting cycles. This discovery has profound implications for the development of concentrated solar fuel technologies.

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