4.6 Article

Soft X-ray characterization of Zn1-xSnxOy electronic structure for thin film photovoltaics

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 14, Issue 29, Pages 10154-10159

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cp41394a

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Funding

  1. Office of Science, Office of Basic Energy Sciences, of the US Department of Energy [DE-AC02-05CH11231]
  2. Swedish research council (VR)
  3. Axel Hultgren's memorial fund
  4. US Department of Energy, Office of Energy Efficiency and Renewable Energy
  5. Swedish Energy Agency

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Zinc tin oxide (Zn1-xSnxOy) has been proposed as an alternative buffer layer material to the toxic, and light narrow-bandgap CdS layer in CuIn1-x,GaxSe2 thin film solar cell modules. In this present study, synchrotron-based soft X-ray absorption and emission spectroscopies have been employed to probe the densities of states of intrinsic ZnO, Zn1-xSnxOy and SnOx thin films grown by atomic layer deposition. A distinct variation in the bandgap is observed with increasing Sn concentration, which has been confirmed independently by combined ellipsometry-reflectometry measurements. These data correlate directly to the open circuit potentials of corresponding solar cells, indicating that the buffer layer composition is associated with a modification of the band discontinuity at the CIGS interface. Resonantly excited emission spectra, which express the admixture of unoccupied O 2p with Zn 3d, 4s, and 4p states, reveal a strong suppression in the hybridization between the O 2p conduction band and the Zn 3d valence band with increasing Sn concentration.

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