4.8 Article

Band Edge Engineering of Oxide Photoanodes for Photoelectrochemical Water Splitting: Integration of Subsurface Dipoles with Atomic-Scale Control

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ADVANCED ENERGY MATERIALS
卷 6, 期 7, 页码 -

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.201502154

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资金

  1. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering
  2. Catalysis Science Program within the Chemical Sciences, Geosciences, and Biosciences Division [DE-AC02-76SF00515]
  3. Global Climate and Energy Project at Stanford University
  4. DARE Doctoral Fellowship
  5. NSF [CBET-1433442]
  6. National Science Foundation, Division of Chemical, Bioengineering, Environmental, and Transport Systems (CBET)
  7. U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Fuel Cell Technologies Office

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One of the crucial parameters dictating the efficiency of photoelectrochemical water-splitting is the semiconductor band edge alignment with respect to hydrogen and oxygen redox potentials. Despite the importance of metal oxides in their use as photoelectrodes, studies to control the band edge alignment in aqueous solution have been limited predominantly to compound semiconductors with modulation ranges limited to a few hundred mV. The ability to modulate the flat band potential of oxide photoanodes by as much as 1.3 V, using the insertion of subsurface electrostatic dipoles near a Nb-doped SrTiO3/aqueous electrolyte interface is reported. The tunable range achieved far exceeds previous reports in any semiconductor/aqueous electrolyte system and suggests a general design strategy for highly efficient oxide photoelectrodes.

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