A study of thermal stability and electrical switching behaviour of Ge–Te–In chalcogenide glass system
Autor: | D. Sushamma, S. Asokan, Achamma George, P. Predeep |
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Rok vydání: | 2017 |
Předmět: |
Materials science
Coordination number Analytical chemistry General Physics and Astronomy Chalcogenide glass 02 engineering and technology Activation energy 021001 nanoscience & nanotechnology 01 natural sciences law.invention Differential scanning calorimetry law 0103 physical sciences Thermal stability Crystallization 010306 general physics 0210 nano-technology Glass transition Voltage |
Zdroj: | Indian Journal of Physics. 91:1013-1020 |
ISSN: | 0974-9845 0973-1458 |
DOI: | 10.1007/s12648-017-0985-3 |
Popis: | Bulk Ge20Te80−xInx(x = 0, 6, 10 and 16) glasses are prepared by the conventional melt quenching technique. The crystallization mechanism is studied using differential scanning calorimetry performed at different heating rates under non-isothermal conditions. Also the electrical switching behavior of the given glass system has been investigated. The glass transition temperature (Tg), the peak crystallization temperature (Tp), the thermal stability (Tc–Tg), the average value of the activation energy for the glass transition (Eg), and the average value of the activation energy for crystallization (Ec), are calculated for the given glass system. The glasses studied are found to exhibit a current controlled negative-resistance behaviour and memory switching. Further, the switching voltage (Vt) is found to increase linearly with sample thickness in the range of 0.2–0.45 mm. It is observed that the variation of switching voltage (Vt) of Ge–Te–In glasses show a maximum value at an average coordination number = 2.52 (at x = 6, onset of rigidity percolation), there after decreases and a minimum is seen in the switching voltage at an average coordination number = 2.68 (at x = 14), which is likely to be the chemical threshold of the system. Beyond x = 14, switching voltage is found to increase again with composition. |
Databáze: | OpenAIRE |
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