4.8 Article

Selective Alcohol Dehydrogenation and Hydrogenolysis with Semiconductor-Metal Photocatalysts: Toward Solar-to-Chemical Energy Conversion of Biomass-Relevant Substrates

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 3, Issue 19, Pages 2798-2802

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jz301309d

Keywords

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Funding

  1. Phillips66
  2. U.S. Department of Energy (DOE), Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences through the Ames Laboratory
  3. Iowa State University (ISU) [DE-AC02-07CH11358]
  4. ISU
  5. IPRT
  6. Direct For Mathematical & Physical Scien
  7. Division Of Chemistry [1040098] Funding Source: National Science Foundation

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Photocatalytic conversion of biomass is a potentially transformative concept in renewable energy. Dehydrogenation and hydrogenolysis of biomass-derived alcohols can produce renewable fuels such as H-2 and hydrocarbons, respectively. We have successfully used semiconductor-metal heterostructures for sunlight-driven dehydrogenation and hydrogenolysis of benzyl alcohol. The hetero-structure composition dictates activity, product distribution, and turnovers. A few metal (M = Pt, Pd) islands on the semiconductor (SC) surface significantly enhance activity and selectivity and also greatly stabilize the SC against photoinduced etching and degradation. Under selected conditions, CdS-Pt favors dehydrogenation (H-2) over hydrogenolysis (toluene) 8:1, whereas CdS0.4Se0.6-Pd favors hydrogenolysis over dehydrogenation 3:1. Photochemically generated, surface-adsorbed hydrogen is useful in tandem catalysis, for example, via transfer hydrogenation. We expect this work will lead to new paradigms for sunlight-driven conversions of biomass-relevant substrates.

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