The Crystallization Behavior of a Na2O-GeO2-P2O5 Glass System: A (Micro)Structural, Electrical, and Dielectric Study
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Published:2024-01-07
Issue:2
Volume:17
Page:306
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ISSN:1996-1944
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Container-title:Materials
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language:en
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Short-container-title:Materials
Author:
Marijan Sara1, Razum Marta1, Sklepić Kerhač Kristina1, Mošner Petr2, Koudelka Ladislav2, Pisk Jana3ORCID, Moguš-Milanković Andrea1ORCID, Skoko Željko4ORCID, Pavić Luka1ORCID
Affiliation:
1. Division of Materials Chemistry, Ruđer Bošković Institute, Bijenička 54, 10000 Zagreb, Croatia 2. Department of General and Inorganic Chemistry, Faculty of Chemical Technology, University of Pardubice, 53210 Pardubice, Czech Republic 3. Department of Chemistry, Faculty of Science, University of Zagreb, Horvatovac 102a, 10000 Zagreb, Croatia 4. Department of Physics, Faculty of Science, University of Zagreb, Bijenička 32, 10000 Zagreb, Croatia
Abstract
Sodium-phosphate-based glass-ceramics (GCs) are promising materials for a wide range of applications, including solid-state sodium-ion batteries, microelectronic packaging substrates, and humidity sensors. This study investigated the impact of 24 h heat-treatments (HT) at varying temperatures on Na-Ge-P glass, with a focus on (micro)structural, electrical, and dielectric properties of prepared GCs. Various techniques such as powder X-ray diffraction (PXRD), infrared spectroscopy-attenuated total reflection (IR-ATR), and scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) were employed. With the elevation of HT temperature, crystallinity progressively rose; at 450 °C, the microstructure retained amorphous traits featuring nanometric grains, whereas at 550 °C, HT resulted in fully crystallized structures characterized by square-shaped micron-scale grains of NaPO3. The insight into the evaluation of electrical and dielectric properties was provided by Solid-State Impedance Spectroscopy (SS-IS), revealing a strong correlation with the conditions of controlled crystallization and observed (micro)structure. Compared to the initial glass, which showed DC conductivity (σDC) on the order of magnitude 10−7 Ω−1 cm−1 at 393 K, the obtained GCs exhibited a lower σDC ranging from 10−8 to 10−10 Ω−1 cm−1. With the rise in HT temperature, σDC further decreased due to the crystallization of the NaPO3 phase, depleting the glass matrix of mobile Na+ ions. The prepared GCs showed improved dielectric parameters in comparison to the initial glass, with a noticeable increase in dielectric constant values (~20) followed by a decline in dielectric loss (~10−3) values as the HT temperatures rise. Particularly, the GC obtained at @450 stood out as the optimal sample, showcasing an elevated dielectric constant and low dielectric loss value, along with moderate ionic conductivity. This research uncovers the intricate relationship between heat-treatment conditions and material properties, emphasizing that controlled crystallization allows for precise modifications to microstructure and phase composition within the remaining glassy phase, ultimately facilitating the fine-tuning of material properties.
Funder
Croatian Science Foundation Croatian Academy of Science and Arts (HAZU) 2019
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