4.8 Article

Synthesis of Chemicals Using Solar Energy with Stable Photoelectrochemically Active Heterostructures

期刊

NANO LETTERS
卷 13, 期 5, 页码 2110-2115

出版社

AMER CHEMICAL SOC
DOI: 10.1021/nl400502u

关键词

Artificial photosynthesis; anodic aluminum oxide; H-2 production; solar cell; electrocatalyst

资金

  1. HyperSolar Inc.
  2. UCSB
  3. MRSEC program of the NSF National Science Foundation [DMR-1121053]
  4. ConvEne IGERT Program [NSF-DGE 0801627]
  5. University of California Lab Fees Program [09-LR-08-116809-STUG]

向作者/读者索取更多资源

Efficient and cost-effective conversion of solar energy to useful chemicals and fuels could lead to a significant reduction in fossil hydrocarbon use. Artificial systems that use solar energy to produce chemicals have been reported for more than a century. However the most efficient devices demonstrated, based on traditionally fabricated compound semiconductors, have extremely short working lifetimes due to photocorrosion by the electrolyte. Here we report a stable, scalable design and molecular level fabrication strategy to create photoelectrochemically active heterostructure (PAR) units consisting of an efficient semiconductor light absorber in contact with oxidation and reduction electrocatalysts and otherwise protected by alumina. The functional heterostructures are fabricated by layer-by-layer, template-directed, electrochemical synthesis in porous anodic aluminum oxide membranes to produce high density arrays of electronically autonomous, nanostructured, corrosion resistant, photoactive units (similar to 10(9)-10(10) PAHs per cm(2)). Each PAR unit is isolated from its neighbor by the transparent electrically insulating oxide cellular enclosure that makes the overall assembly fault tolerant. When illuminated with visible light, the free floating devices have been demonstrated to produce hydrogen at a stable rate for over 24 h in corrosive hydroiodic acid electrolyte with light as the only input. The quantum efficiency (averaged over the solar spectrum) for absorbed photons-to-hydrogen conversion was 7.4% and solar-to-hydrogen energy efficiency of incident light was 0.9%. The fabrication approach is scalable for commercial manufacturing and readily adaptable to a variety of earth abundant semiconductors which might otherwise be unstable as photoelectrocatalysts.

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