期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 120, 期 6, 页码 3117-3129出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.5b09121
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-
资金
- Office of Science of the U.S. Department of Energy [DE-SC0004993]
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,similar to 0.7 V, with an effective Richardson constant,similar to 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.
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