Publications by authors named "Luka Pavic"

This study examines the influence of ligand design on the structural, optical, and electrical properties of copper-based coordination complexes. Ligands HL and HL were synthesized via the reaction of 5-nitrosalicylaldehyde with 2-hydroxy- or 4-hydroxybenzhydrazide. HL was obtained from the reaction of carbohydrazide and salicylaldehyde, while HL was prepared by condensing 4-methoxysalicylaldehyde with thiocarbohydrazide.

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2,5-Dihydroxyterephthalic acid (H) is well-known for its use in the construction of functional metal-organic frameworks (MOFs). Among them, simple coordination polymers (CPs), such as lithium and sodium coordination polymers with H, have been used successfully to synthesize electrically conductive MOFs and have also demonstrated great potential as positive or negative electrode materials on their own. However, there has been little exploration of the structure and physicochemical properties of these and other alkali complexes of H.

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This study aimed to synthesize molybdenum complexes coordinated with an aroyl hydrazone-type ligand (HL), which was generated through the condensation of 2-hydroxy-5-nitrobenzaldehyde with benzhydrazide. The synthesis yielded two types of mononuclear complexes, specifically [MoO(L)(MeOH)] and [MoO(L)(HO)], as well as a bipyridine-bridged dinuclear complex, [(MoO(L))(4,4'-bpy)]. Those entities were thoroughly characterized using a suite of analytical techniques, including attenuated total reflectance infrared spectroscopy (IR-ATR), elemental analysis (EA), thermogravimetric analysis (TGA), and single-crystal X-ray diffraction (SCXRD).

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Na-V-P-Nb-based materials have gained substantial recognition as cathode materials in high-rate sodium-ion batteries due to their unique properties and compositions, comprising both alkali and transition metal ions, which allow them to exhibit a mixed ionic-polaronic conduction mechanism. In this study, the impact of introducing two transition metal oxides, VO and NbO, on the thermal, (micro)structural, and electrical properties of the 35NaO-25VO-(40 - )PO - NbO system is examined. The starting glass shows the highest values of DC conductivity, , reaching 1.

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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.

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The present study investigates the relationship between the local structure, photocatalytic ability, and cathode performances in sodium-ion batteries (SIBs) and lithium-ion batteries (LIBs) using Ni-substituted goethite nanoparticles (NiFeOOH NPs) with a range of 'x' values from 0 to 0.5. The structural characterization was performed applying various techniques, including X-ray diffractometry (XRD); thermogravimetry differential thermal analysis (TG-DTA); Fourier transform infrared spectroscopy (FT-IR); X-ray absorption spectroscopy (XANES/EXAFS), both measured at room temperature (RT); Fe Mössbauer spectroscopy recorded at RT and low temperatures (LT) from 20 K to 300 K; Brunauer-Emmett-Teller surface area measurement (BET), and diffuse reflectance spectroscopy (DRS).

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Molybdenum coordination complexes are widely applied due to their biological and pharmacological potential, as well as their performance in different catalytic processes. Parent dioxidomolybdenum Schiff base complexes were prepared via the reaction of [MoO(acac)] with a hydrazone Schiff-base tetradentate ligand. A new hydrazone-Schiff base (HL) and its corresponding mononuclear and polynuclear dioxidomolybdenum(VI) complex were synthesized and characterized by spectroscopic methods and elemental analyses, and their thermal behavior was investigated by thermogravimetry.

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Background: The dental ceramic materials are constantly being developed due to their continuous clinical application in the field of esthetic dentistry. Glass ceramics (GC) materials are also of special interest for dental application due to their specific properties; and thus, they can be applied as crowns, veneers and small bridges.

Purpose: However, due to a variety of different GC materials, it is of keen interest to inspect their morphology and ion-diffusion, which also governs aging properties.

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The aim of this study is to investigate the influence of different glass fibers made of commercial silicate, borosilicate, and laboratory-made iron-phosphate compositions, on the preparation of polylactic acid (PLA) composites and their structural and physical properties. The thermal, structural, and electrical properties of prepared PLA-glass fiber composites were studied using differential scanning calorimetry, X-ray diffraction, microscopy, and impedance spectroscopy. The structural as well as morphological, thermal, and electrical properties of all PLA-glass composites were found to be very similar and independent of the composition and aspect ratio of glass fibers.

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Zirconia (ZrO), a widely known material with an extensive range of applications, is especially suitable for dental applications. This kind of dental material is produced in the form of blocks or discs (mostly discs-depending on CAD/CAM machines) by cold isostatic pressing (CIP). Such discs are subsequently milled by CAM/CAD technology into a desirable form.

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In this work, we report the effect of the addition of modifiers and network formers on the polaronic transport in iron phosphate glasses (IPG) in two systems of HfO-BO-FeO-PO, to which up to 8 mol% boron and hafnium are added. The addition of oxides significantly changes the Fe/Fe ratio, thus directly affecting the polaron number density and consequently controlling DC conductivity trends for both series studied by impedance spectroscopy. Moreover, we found that short-range polaron dynamics are also under the influence of structural changes.

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Lowering the constitutive domains of semiconducting oxides to the nano-range has recently opened up the possibility of added benefit in the research area of sensing materials, in terms both of greater specific surface area and pore volume. Among such nanomaterials, ceria has attracted much attention; therefore, we chemically derived homogeneous ceria nanoparticle slurries. One set of samples was tape-casted onto a conducting glass substrate to form thin-films of various thicknesses, thereby avoiding demanding reaction conditions typical of physical depositions, while the other was pressed into pellets.

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In this paper, we studied the influence of polyvinylpyrrolidone (PVP) as a stabilization additive on optical and electrical properties of perovskite formamidinium lead iodide (FAPI) polycrystalline thin films on ZnO nanorods (ZNR). FAPI (as an active layer) was deposited from a single solution on ZNR (low temperature processed electron transport layer) using a one-step method with the inclusion of an anti-solvent. The role of PVP in the formation of the active layer was investigated by scanning electron microscopy and contact angle measurements to observe the effect on morphology, while X-ray diffraction was used as a method to study the stability of the film in an ambient environment.

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Over the last decade, zirconia (ZrO)-based ceramic materials have become more applicable to modern dental medicine due to the sustained development of diverse computer-aided design/computer-aided manufacturing (CAD/CAM) systems. However, before the cementation and clinical application, the freshly prepared zirconia material (e.g.

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Ion conducting oxide glasses are attractive materials for application in various electrochemical devices and an understanding of the structure-transport properties relationship is crucial for their development. An interesting effect of glass structure on the dynamics of mobile ions is the mixed glass-former effect which causes a non-linear change of ionic conductivity when glass-forming oxides get gradually substituted. Here, we report a strong, positive effect of structural changes on the conductivity of sodium ions in two glass systems 40Na2O-xMoO3-(60-x)P2O5 and 40Na2O-xWO3-(60-x)P2O5; x = 0-50 mol% where a conventional glass-forming oxide (P2O5) is gradually replaced by WO3/MoO3 which are conditional ones.

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In this study, two different dental ceramics, based on zirconia-reinforced lithium-silicate (LS1) glass-ceramics (Celtra Duo, Dentsply Sirona, Bensheim, Germany) and lithium disilicate (LS2) ceramics (IPS e.max CAD, Ivoclar, Vivadent, Schaan, Liechtenstein) were examined. They were tested prior to and after the crystallization by sintering in the dental furnace.

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One-dimensional (1D) oxalate-bridged homometallic {[Mn(bpy)(CO)]·1.5HO} () (bpy = 2,2'-bipyridine) and heterodimetallic {[CrCu(bpy)(CHOH)(HO)(CO)][Cu(bpy)Cr(CO)]·CHCl·CHOH·HO} () coordination polymers, as well as the three-dimensional (3D) heterotrimetallic {[CaCrCu(phen)(CO)]·4CHCN·2HO} () (1,10-phenanthroline) network, have been synthesized by a building block approach using a layering technique, and characterized by single-crystal X-ray diffraction, infrared (IR) and impedance spectroscopies and magnetization measurements. During the crystallization process partial decomposition of the tris(oxalate)chromate(III) happened and 1D polymers and were formed.

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Transparent conducting oxides (TCO) with high electrical conductivity and at the same time high transparency in the visible spectrum are an important class of materials widely used in many devices requiring a transparent contact such as light-emitting diodes, solar cells and display screens. Since the improvement of electrical conductivity usually leads to degradation of optical transparency, a fine-tuning sample preparation process and a better understanding of the correlation between structural and transport properties is necessary for optimizing the properties of TCO for use in such devices. Here we report a structural and magnetotransport study of tin oxide (SnO), a well-known and commonly used TCO, prepared by a simple and relatively cheap Atmospheric Pressure Chemical Vapour Deposition (APCVD) method in the form of thin films deposited on soda-lime glass substrates.

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We report on the electrical properties of glasses with nominal composition BO-(100-)[40FeO-60PO], = 2-20, mol.%. The conduction transport in these glasses is polaronic and shows a strong dependence on FeO content and polaron number density.

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This work focuses on the in-situ characterization of multi-walled carbon nanotube (CNT) motions in thin random networks under strain. Many fine-grain models have been devised to account for CNT motions in carbon nanotube networks (CNN). However, the validation of these models relies on mesoscopic or macroscopic data with very little experimental validation of the physical mechanisms actually arising at the CNT scale.

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Ground coat enamels for low carbon steel that contain silica as a mill addition have been developed to study the changes of their properties. Acid-resistant commercial enamel where silica addition was varied from 0 to 10.0 wt % was used for this investigation.

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The electrical and dielectric properties of three series of glasses, xHfO-(40 - x)FeO-60PO, 0 ≤ x ≤ 8 mol%, xCeO-(40 - x)FeO-60PO, 0 ≤ x ≤ 8 mol%, and xHfO-(38 - x)FeO-2BO-60PO 2 ≤ x ≤ 6 mol%, have been investigated by impedance spectroscopy over a wide frequency and temperature range. As expected, these glasses exhibit polaronic conductivity which strongly depends on the fraction of ferrous ions, Fe/Fe. Following a detailed discussion on the DC conductivity, we use the MIGRATION concept to model their conductivity spectra.

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