Thermal Manipulation of Deactivation Processes in Luminescent Photoelectrochemical Cells Employing Tellurium-Doped Cadmium Sulfide Photoelectrodes.

Abstract

Temperature significantly modifies the efficiencies of luminescence and photocurrent in an n-type, single crystal, CdS:Te-based photoelectrochemical cell (PEC) employing aqueous polyselenide electrolyte. Between 20 and 100 C photocurrent (quantum yield phi sub x) from ultraband gap 501.7 nm excitation increases modestly by less than or = 20%, whereas photocurrent from bandgap edge 514.5 nm excitation increases by about an order of magnitude, reaching 50-100% of the 20 C 501.7 nm photocurrent. Undoped CdS exhibits a similar photocurrent-temperature profile. Higher temperatures thus extend the wavelength response of CdS- and CdS:Te-based PEC's. In contrast to the increase in photocurrent, emissive efficiency (quantum yield phi sub r) of CdS:Te drops by a factor of approximately 10-20 over the same temperature range; this decline is relatively insensitive to potential and excitation wavelength (501.7 or 514.5 nm).

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Document Details

Document Type
Technical Report
Publication Date
Aug 12, 1980
Accession Number
ADA089217

Entities

People

  • Arthur B. Ellis
  • Bradley R. Karas
  • Daniel K. Bilich
  • David J. Morano

Tags

Communities of Interest

  • Energy and Power Technologies
  • Weapons Technologies

DTIC Thesaurus Topics

  • Band Gaps
  • Charge Carriers
  • Chemical Engineering
  • Chemistry
  • Compound Semiconductors
  • Emission Spectra
  • Energy Bands
  • Energy Conversion
  • Materials
  • Materials Science
  • Military Research
  • New York
  • Photoelectrochemical Cells
  • Quantum Efficiency
  • Quantum Yields
  • Semiconductors
  • Spectra

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  • Materials Science and Engineering.
  • Mathematics or Statistics

Technology Areas

  • Quantum Computing