The influence of Bi on the structure and physical properties of Ge2Se3-based equichalcogenide glasses and thin films is studied. Thermal analysis shows increased crystallization ability for Bi-modified glasses. Direct current (DC) and alternating current (AC) electrical conductivity for bulk glasses and thin films is investigated in a broad range of temperatures and frequencies, showing a strong dependence on the presence of Bi modifiers. Exposure wavelength dependence of photocurrent is studied at different temperatures for the visible range of spectrum, and correlated with the existence of localized states in the mobility gap of these amorphous semiconductors. Structural peculiarities of the obtained thin films and bulk samples are assessed from X-ray diffraction (XRD) and high-resolution X-ray photoelectron spectroscopy (XPS) measurements. Optical, electrical, and thermal properties are shown to be suitable for various applications in photonics, electronics, and sensor systems.
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Multi-scale chemo-mechanical evolution during crystallization of mixed conducting SrTi 0.65 Fe 0.35 O 3−δ films and correlation to electrical conductivity
Recent work has demonstrated a low-temperature route to fabricating mixed ionic/electronic conducting (MIEC) thin films with enhanced oxygen exchange kinetics by crystallizing amorphous-grown thin films under mild temperatures, eluding conditions for deleterious A-site cation surface segregation. Yet, the complex, multiscale chemical and structural changes during MIEC crystallization and their implications for the electrical properties remain relatively unexplored. In this work, micro-structural and atomic-scale structural and chemical changes in crystallizing SrTi 0.65 Fe 0.35 O 3− δ thin films on insulating (0001)-oriented Al 2 O 3 substrates are observed and correlated to changes in the in-plane electrical conductivity, measured in situ by ac impedance spectroscopy. Synchrotron X-ray absorption spectroscopy at the Fe and Ti K-edges gives direct evidence of oxidation occurring with the onset of crystallization and insight into the atomic-scale structural changes driven by the chemical changes. The observed oxidation, increase in B-site polyhedra symmetry, and alignment of neighboring B-site cation coordination units demonstrate increases in both hole concentration and mobility, thus underpinning the measured increase of in-plane conductivity by over two orders of magnitude during crystallization. High resolution transmission electron microscopy and spectroscopy of films at various degrees of crystallinity reveal compositional uniformity with extensive nano-porosity in the crystallized films, consistent with solid phase contraction expected from both oxidation and crystallization. We suggest that this chemo-mechanically driven dynamic nano-structuring is an additional contributor to the observed electrical behavior. By the point that the films become ∼60% crystalline (according to X-ray diffraction), the conductivity reaches the value of dense, fully crystalline films. Given the resulting high electronic conductivity, this low-temperature processing route leading to semi-crystalline hierarchical films exhibits promise for developing high performance MIECs for low-to-intermediate temperature applications.
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- Award ID(s):
- 1720633
- PAR ID:
- 10330218
- Date Published:
- Journal Name:
- Journal of Materials Chemistry A
- Volume:
- 10
- Issue:
- 5
- ISSN:
- 2050-7488
- Page Range / eLocation ID:
- 2421 to 2433
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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