Influence of Substrates on the Long-Range Order of Photoelectrodeposited Se-Te Nanostructures
Abstract
The long-range order of anisotropic phototropic Se–Te films grown electrochemically at room temperature under uniform-intensity, polarized, incoherent, near-IR illumination has been investigated using crystalline (111)-oriented Si substrates doped degenerately with either p- or n-type dopants. Fourier-transform (FT) analysis was performed on large-area images obtained with a scanning electron microscope, and peak shapes in the FT spectra were used to determine the pattern fidelity in the deposited Se–Te films. Under nominally identical illumination conditions, phototropic films grown on p^+-Si(111) exhibited a higher degree of anisotropy and a more well-defined pattern period than phototropic films grown on n+-Si(111). Similar differences in the phototropic Se–Te deposit morphology and pattern fidelity on p^+-Si versus n^+-Si were observed when the deposition rate and current densities were controlled for by adjusting the deposition parameters and illumination conditions. The doping-related effects of the Si substrate on the pattern fidelity of the phototropic Se–Te deposits are ascribable to an electrical effect produced by the different interfacial junction energetics between Se–Te and p^+-Si versus n^+-Si that influences the dynamic behavior during phototropic growth at the Se–Te/Si interface.
Additional Information
© 2019 American Chemical Society. Received: December 6, 2018; Revised: January 21, 2019; Published: January 28, 2019. This work is part of the 'Light-Material Interactions in Energy Conversion' Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Award No. DE-SC0001293. XPS and UPS data were collected at the Molecular Materials Research Center of the Beckman Institute of the California Institute of Technology. The authors declare no competing financial interest.Attached Files
Supplemental Material - nl8b04891_si_001.pdf
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Additional details
- Eprint ID
- 92504
- Resolver ID
- CaltechAUTHORS:20190128-155030817
- Department of Energy (DOE)
- DE-SC0001293
- Created
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2019-01-29Created from EPrint's datestamp field
- Updated
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2021-11-16Created from EPrint's last_modified field