Published February 18, 2016 | Version Supplemental Material
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Electrical, Photoelectrochemical, and Photoelectron Spectroscopic Investigation of the Interfacial Transport and Energetics of Amorphous TiO₂/Si Heterojunctions

  • 1. ROR icon California Institute of Technology
  • 2. ROR icon Joint Center for Artificial Photosynthesis
  • 3. ROR icon Lawrence Berkeley National Laboratory
  • 4. ROR icon TU Darmstadt

Abstract

Solid-state electrical, photoelectrochemical, and photoelectron spectroscopic techniques have been used to characterize the behavior and electronic structure of interfaces between n-Si, n⁺-Si, or p⁺-Si surfaces and amorphous coatings of TiO₂ formed using atomic-layer deposition. Photoelectrochemical measurements of n-Si/TiO₂/Ni interfaces in contact with a series of one-electron, electrochemically reversible redox systems indicated that the n-Si/TiO₂/Ni structure acted as a buried junction whose photovoltage was independent of the formal potential of the contacting electrolyte. Solid-state current–voltage analysis indicated that the built-in voltage of the n-Si/TiO₂ heterojunction was ∼0.7 V, with an effective Richardson constant ∼1/100th of the value of typical Si/metal Schottky barriers. X-ray photoelectron spectroscopic data allowed formulation of energy band-diagrams for the n-Si/TiO₂, n⁺-Si/TiO₂, and p⁺-Si/TiO₂ interfaces. The XPS data were consistent with the rectifying behavior observed for amorphous TiO₂ interfaces with n-Si and n⁺-Si surfaces and with an ohmic contact at the interface between amorphous TiO₂ and p⁺-Si.

Additional Information

© 2015 American Chemical Society. Received: September 18, 2015. Revised: December 7, 2015. Publication Date (Web): December 15, 2015. This work was supported through the Office of Science of the U.S. Department of Energy under Award DE-SC0004993 to the Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub. The authors thank Dr. Gang Liu and Prof. Chongwu Zhou at the University of Southern California for their support of variable-temperature solid-state transport measurements. The authors also acknowledge Dr. Slobodan Mitrovic and Natalie Becerra for assistance in the collection of XPS data, as well as Dr. Kimberley Papadantonakis for assistance with editing this manuscript. S.H. and M.H.R. contributed equally to this work. The authors declare no competing financial interest.

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Identifiers

Eprint ID
64156
Resolver ID
CaltechAUTHORS:20160202-092151875

Funding

Department of Energy (DOE)
DE-SC0004993
Joint Center for Artificial Photosynthesis (JCAP)

Dates

Created
2016-02-02
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Updated
2023-03-30
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Caltech groups
JCAP