کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
7744235 | 1498221 | 2018 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Observation of the metal-insulator transition of VO2 in glasses and nanomaterials of MV2O5-P2O5 system (M Li, Na, Mg)
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
الکتروشیمی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
In this research, special attention has been paid to an observation of a metal-insulator transition (MIT) in lithium/sodium/magnesium-vanadate-phosphate glasses and nanomaterials. Two series (A & B) of glassy 90MV2O5 â
10P2O5 (M Li, Na, Mg) samples were prepared by melt-quenching technique at 1300â¯Â°C using double-crucible technique. Series B was synthesized in more reducing conditions. DSC traces of the synthesized samples were typical for glassy materials. Glass transition and crystallization occurred in series A at significantly higher temperatures than in series B. In addition, an endothermic peak was observed at low temperature (67â¯Â°C). XRD patterns of the samples contained amorphous halo, but also some diffraction reflexes corresponding to monoclinic VO2. In series A, the reflexes had low intensity, whereas in series B the intensity of the peaks at the same positions was significantly higher. Dependences of electrical conductivity were typical for nanocrystallized glasses in case of series A, whereas in series B a reversible change of the conductivity was observed at 67â¯Â°C. Samples of series A exhibited positive and constant Seebeck coefficient S within wide temperature range, whereas in series B a change in thermoelectric power was observed above 67â¯Â°C. All these phenomena around 67â¯Â°C are due to metal-insulator transition in VO2 impurities in the samples.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Solid State Ionics - Volume 322, September 2018, Pages 11-17
Journal: Solid State Ionics - Volume 322, September 2018, Pages 11-17
نویسندگان
Tomasz K. Pietrzak, Wiktoria K. Zajkowska, Marek Wasiucionek, Jerzy E. Garbarczyk,