Heating-cooling Cycles Research Articles

Variations in the Thermomechanical and Structural Properties during the Cooling of Shape-Memory R-PETG.

One of the useful features of 3D-printed specimens of recycled polyethylene terephthalate glycol (R-PETG) is the ability to repetitively develop free recovery as well as the work-generating, shape-memory effect. This behavior is enabled by the R-PETG's capacity to stiffen during cooling, thus allowing for a new temporary shape to be induced. Aiming to devise an explanation for the polymer's stiffening, in this study, the variation in some of the R-PETG's parameters during cooling are emphasized and discussed. The evolution of an R-PETG filament's shape was monitored during room-temperature-bending heating-cooling cycles. Straight-shape recovery and the complete loss of stiffness were observed at the start and the end of heating, respectively, followed by the forced straightening of the filament, performed by the operator, around 40 °C, during cooling. The tests performed by dynamic mechanical analysis disclosed the rise of the storage modulus (E') after 100 °C heating followed by either liquid-nitrogen- or air-cooling to room temperature, in such a way that E' was always larger after cooling than initially. Static tests emphasized a peculiar stress variation during a heating-cooling cycle applied in air, within the heating chamber of the tensile testing machine. Tensile-failure tests were performed at -10 °C at a rate of 100 mm/min, with specimens printed at various deposition directions between 10 and 40° to the transversal direction. The specimens printed at 40°, which had the largest ultimate strains, were broken with tensile rates between 100 and 500 mm/min. Deformation rate increase favored the shift from crazing to delamination failure modes. The correlation between the structural changes, the sharp E' increase on heating, and the stiffening induced by cooling represents a novel approach that enables the use of 3D-printed R-PETG for the fabrication of the active parts of low-priced lightweight resettable actuators.

Influence of Sputtering Power on the Properties of Magnetron Sputtered Tin Selenide Films.

The ecofriendly tin selenide (SnSe) is expected to find multiple applications in optoelectronic, photovoltaic, and thermoelectric systems. This work is focused on the thermoelectric properties of thin films. SnSe single crystals exhibit excellent thermoelectric properties, but it is not so in the case of polycrystalline bulk materials. The investigations were motivated by the fact that nanostructuring may lead to an improvement in thermoelectric efficiency, which is evaluated through a dimensionless figure of merit, ZT = S2 σ T/λ, where S is the Seebeck coefficient (V/K), σ is the electrical conductivity (S/m), λ is the thermal conductivity (W/mK), and T is the absolute temperature (K). The main objective of this work was to obtain SnSe films via magnetron sputtering of a single target. Instead of common radiofrequency (RF) magnetron sputtering with a high voltage alternating current (AC) power source, a modified direct current (DC) power supply was employed. This technique in the classical version is not suitable for sputtering targets with relatively low thermal and electrical conductivity, such as SnSe. The proposed solution enabled stable sputtering of this target without detrimental cracking and arcing and resulted in high-quality polycrystalline SnSe films with unprecedented high values of ZT equal to 0.5 at a relatively low temperature of 530 K. All parameters included in ZT were measured in one setup, i.e., Linseis Thin Film Analyzer (TFA). The SnSe films were deposited at sputtering powers of 120, 140, and 170 W. They had the same orthorhombic structure, as determined by X-ray diffraction (XRD), but the thickness and microstructure examined by scanning electron microscopy (SEM) were dependent on the sputtering power. It was demonstrated that thermoelectric efficiency improved with increasing sputtering power and stable values were attained after two heating-cooling cycles. This research additionally provides further insights into the DC sputtering process and opens up new possibilities for magnetron sputtering technology.

Highly stable mesoporous-controlled corncob biochar confined paraffinic material with exceptional latent heat retention performance

Bio-based composites fabricated from bio-sourced waste feedstocks have attracted increasing interest and have shown potential applications in sustainable energy infrastructure development. Thermal management using phase-change materials (PCMs) has appeared as an innovative approach for energy storage and cooling, where pure PCMs that lack thermal stability are encapsulated in solid matrices to ensure the charge/discharge of the latent heat of the composite. However, their energy storage density, thermal stability, and durability are reduced after multiple thermal cycles, besides the complicated and expensive nonrenewable fossil feedstock utilization. Biochar, mostly used for soil remediation, can be redirected and repurposed for the encapsulation of PCMs in renewable energy storage infrastructures. In this study, a “greener” biochar-based composite was fabricated from agricultural corncob-derived biochar (88.9 % mesopore proportion) and a commercially available paraffinic PCM (n-hexadecane) following vacuum impregnation strategies. Corncob biochar combined with hexadecane exhibited an efficient energy per unit mass of 250.6 kJ kg−1 and a latent heat retention of 110.3 % after 500 consecutive thermal cycles. In addition, the corncob biochar/hexadecane composite demonstrated high fractional crystallinity and relative latent heat efficiency (98.9 %). The composite exhibited promising chemical compatibility with composite components, stability, and competitive energy density even compared with a composite made of nonrenewable fossil-based materials, like exfoliated graphene nanoplatelets, which demonstrated reduced latent heat retention after multiple heating-cooling cycles. Intermolecular interactions, such as hydrogen bonding, between the guest molecular chains and host materials played a significant role in the thermal performance of the as-synthesized composite materials. This approach will contribute to overcoming the complexities and costs of composite PCM development in thermal management and thermal energy storage applications and support and advance the UN's sustainable development goal (affordable and clean energy).

X-ray Diffraction Study of Metallized Polyethylene for Creating Heat Storage Systems

The paper analyzes the prospects of using a heat-accumulating material consisting of metallized polyethylene granules. X-ray diffraction analysis has been used to study the influence of the number of heating and cooling cycles of the heat-accumulating material on the change in the degree of crystallinity of polyethylene. It was shown that the proposed heat-accumulating material showed a low resistance and a significant decrease in the degree of crystallinity of polyethylene under the experimental conditions. The crystal structure of polyethylene did not change during cyclic heating and cooling. Grounded on the obtained experimental results, it was determined that a high degree of polyethylene crystallinity is being kept for 200–300 heating-cooling cycles.

Formulation of self-nanoemulsifying drug delivery system (SNEDDS) of combined 70% ethanolic of Begonia medicinalis herbs and Moringa oleifera leaves

Background: Benalu batu (Begonia medicinalis) and kelor leaves (Moringa oleifera) are empirically used as alternative therapies by people in Central Sulawesi to maintain their health. Our previous research showed that the combination of these two plant extracts possessed an immunomodulatory activity. Self-Nanoemulsifying Drug Delivery System (SNEDDS) formulation was performed to improve the extract's bioavailability, solubility and stability. Objective: This study aims to formulate and characterise SNEDDS preparations of combined ethanolic extract of B. medicinalis herbs and M. oleifera leaves and further test its stability. Method: SNEDDS formulation was started by screening for proper oil, surfactant, and co-surfactant. The formula was then optimised using a ternary phase diagram and characterisation. The stability test was performed using centrifugation, heating-cooling, and freeze-thaw cycles. Results: The optimal SNEDDS formula consists of isopropyl myristate (10%), tween 80 (50%) and propylene glycol (40%). The characterisation values obtained were: Transmittance value 83.785 ± 0.275%, particle size 18.666 ± 0.208 nm, polydispersity index 0.664 ± 0.0085, and zeta potential -39.20 ± 0.2 mV. The formula was stable during three stability evaluation tests. Conclusion: The optimal formula met the SNEDDS characteristics requirements and showed good stability.

Mesoscopic precursor anomaly characteristics of red sandstone under uniaxial compression after cyclic high-temperatures

The deformation and failure characteristics of rock caused by periodic changes of temperature are not only significantly different from that under normal temperature, but also significantly different from that produced by a single high-temperature event. Here, using a three-dimensional digital image correlation (3D-DIC) integrated test system, mechanical and micro-damage tests of red sandstone are performed under cycles of high-temperature and natural-cooling with a temperature range of 25°C to 300°C and the number of cycles varying between 0 and 25. Macroscopic, mesoscopic and microscopic characteristics such as rock strength, deformation, strain field and fracture morphology are examined and their evolution with the number of heating-cooling cycles is discussed. Using the time-history evolution of the differentiation rate of the precursor anomaly (En), the characteristic coefficient (K) and the damage variable (DF), three kinds of characteristic time points are put forward to quantify the incubation and development time of precursor abnormal characteristics and are used to divide the whole process of deformation and failure. These time points are the precursor abnormal differentiation time (PADT) tE, the precursor abnormal startup time (PAST) tK, and the precursor abnormal failure time (PAFT) tD. Test results show that: (1) The action of cyclic high-temperature natural-cooling not only shows the strengthening effect of temperature, but also shows the strengthening effect of a certain number of cycles. (2) The evolution sequence of the three precursor abnormal characteristic moments is PADT, PAST and PAFT in turn, and this sequence can intuitively describe the whole complex process of rock deformation and failure, and there are wave peaks in the evolution curve with the number of high-temperature cycle. (3) The effect of high temperature (i.e., 300°C) cyclic heating on rock properties is similar to the threshold effect of a single high-temperature heating event.

Phase Transition and Luminescent Property Change Induced by Different Organic Cations in One-Dimensional Double Perovskites.

Double perovskites (DPs) have attracted attention in the field of luminescence due to their inherent broadband emission of self-trapping excitons. In this work, we choose [(CH3)3NCH2CHCH2]+ and [CH3CHOHCH2NH2]+ as organic cations to synthesize two new organic-inorganic hybrid DPs, [(CH3)3NCH2CHCH2]2KInCl6 (1) and [CH3CHOHCH2NH2]2KInCl6 (2). The [KCl6]3- and [InCl6]3- octahedra are interchangeably connected by sharing two opposite faces, forming a one-dimensional coordination chain. Each K atom coordinates with six chlorine atoms in 1, while it coordinates with two oxygen atoms in addition to the six chlorine atoms in 2. The coordination between ions K and O in compound 2 may have significantly reduced its luminescence. As a result, compound 1 shows bright-yellow light with a quantum yield of more than 90%, while 2 shows weak blue light with a quantum yield of only 0.98%. In addition, different from no phase transition found in 2, 1 undergoes a reversible phase transition at 324/307 K in the heating-cooling cycle. Through structural and spectral analysis and density functional theory calculation, we conclude that the larger degree of [InCl6]3- octahedral distortion and the larger anion distance (In···In) also cause the PLQY of compound 1 to be higher than that of compound 2.

Crack-Resistant and Tissue-Like Artificial Muscles with Low Temperature Activation and High Power Density.

Constructing soft robotics with safe human-machine interactions requires low-modulus, high-power-density artificial muscles that are sensitive to gentle stimuli. In addition, the ability to resist crack propagation during long-term actuation cycles is essential for a long service life. Herein, a material design is proposed to combine all these desirable attributes in a single artificial muscle platform. The design involves the molecular engineering of a liquid crystalline network with crystallizable segments and an ethylene glycol flexible spacer. A high degree of crystallinity can be afforded by utilizing aza-Michael chemistry to produce a low covalent crosslinking density, resulting in crack-insensitivity with a high fracture energy of 33720 J m-2 and a high fatigue threshold of 2250 J m-2. Such crack-resistant artificial muscle with tissue-matched modulus of 0.7MPa can generate a high power density of 450W kg-1 at a low temperature of 40°C. Notably, because of the presence of crystalline domains in the actuated state, no crack propagation is observed after 500 heating-cooling actuation cycles under a static load of 220kPa. This study points to a pathway for the creation of artificial muscles merging seemingly disparate, but desirable properties, broadening their application potential in smart devices.

Effect of geometry on the coefficient of performance of Ni–Ti elastocaloric parts manufactured via powder bed fusion

This study investigates the greater coefficient of Performance (COP) exhibited by the Ni–Ti lattice geometry (LS) over the solid geometry (SS) for solid-state heating and cooling. The LS's advantageous COP can be attributed to factors including variations in phase transformation behavior, a larger surface area facilitating enhanced heat transfer, and a greater volume of water heated per cycle owing to the cavities. Moreover, the LS demands lower compression forces due to its lower mass and geometry, which contribute to its heightened energy efficiency. Remarkably, the LS achieved a maximum temperature span of 11.2 °C at 40 kN compression force, whereas the SS required 80 kN to attain a similar 12.9 °C span. Both the SS and LS showcased a non-linear correlation with compression force which was attributed to Lauder's transformation and pseudo-elastic behaviors. Additionally, the temperature span of the SS exhibited symmetrical behavior during heating-cooling cycles. Conversely, the LS displayed asymmetry, with a more substantial temperature change during the cooling phase than the heating phase.

Achieving heat storage coatings from ethylene vinyl acetate copolymers and phase change nano-capsules with excellent flame-retardant and thermal comfort performances

The heat-storage coatings from ethylene vinyl acetate (EVA) copolymers were developed by incorporating in-situ synthesized phase change nano-capsules (NEPCMs). The coatings were applied to the interior walls of the building, aimed at enhancing thermal storage and flame-retardant performances. Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) are utilized to evaluate the chemical composition of the NEPCMs. At the same time, the thermal properties and microstructure of NEPCMs and the coatings are analyzed using differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). The enthalpy of NEPCMs is 158.14 J/g, while that of heat-storage coatings is 56.45 J/g. NEPCMs and heat-storage coatings exhibit excellent thermal storage performance even after 200 heating-cooling cycles, demonstrating the excellent thermal stability of NEPCMs and heat-storage coatings. Furthermore, excellent flame-retardant properties are also provided by the heat-storage coating. In dynamic heat transfer experiments, under the same conditions, the heat-storage coatings were capable of maintaining the chamber in the thermal comfort zone (24–28 °C) for 141 min, while the conventional coatings lasted only 34 min. The results show that incorporating heat-storage coatings can effectively enhance the thermal regulation performance of interior walls and improve the thermal comfort of indoor environments. Therefore, heat-storage coatings hold a high potential for application in energy-saving buildings.

Sustainable Thermal Regulation of Electronics via Mitigated Supercooling of Porous Gallium-Based Phase Change Materials.

Gallium liquid metal is one of the promising phase change materials for passive thermal management of electronics due to their high thermal conductivity and latent heat per volume. However, it suffers from severe supercooling, in which molten gallium does not return to solid due to the lack of nucleation. It may require 28.2 °C lower temperature than the original freezing point to address supercooling, leading to unstable thermal regulation performance along fluctuations of cooling condition. Here, gallium is infused into porous copper in an oxide-free environment, forming intermetallic compound impurities at the interfaces to reduce the activation energy for heterogeneous nucleation. The porous-shaped gallium provides ≈63% smaller supercooling than that of the bulk type due to large specific surface area (≈9,070 cm2 per cm3) and high wetting characteristics (≈16° of contact angle) on CuGa2 intermetallic layer. During repetitive heating-cooling cycles, porous-shaped gallium consistently shows propagation of crystallization at even near room temperature (≈25 °C) while maintaining stable performance as thermal buffer, whereas droplet-shaped gallium is gradually degraded due to partial-supercooled state. The findings will improve the responsive thermal regulation performance to relieve a rapid increase in temperature of semiconductors/batteries, and also have a potential for energy storage applications.

Thermally stable Ni foam-supported inverse CeAlOx/Ni ensemble as an active structured catalyst for CO2 hydrogenation to methane

Nickel is the most widely used inexpensive active metal center of the heterogeneous catalysts for CO2 hydrogenation to methane. However, Ni-based catalysts suffer from severe deactivation in CO2 methanation reaction due to the irreversible sintering and coke deposition caused by the inevitable localized hotspots generated during the vigorously exothermic reaction. Herein, we demonstrate the inverse CeAlOx/Ni composite constructed on the Ni-foam structure support realizes remarkable CO2 methanation catalytic activity and stability in a wide operation temperature range from 240 to 600 °C. Significantly, CeAlOx/Ni/Ni-foam catalyst maintains its initial activity after seven drastic heating-cooling cycles from RT to 240 to 600 °C. Meanwhile, the structure catalyst also shows water resistance and long-term stability under reaction condition. The promising thermal stability and water-resistance of CeAlOx/Ni/Ni-foam originate from the excellent heat and mass transport efficiency which eliminates local hotspots and the formation of Ni-foam stabilized CeAlOx/Ni inverse composites which effectively anchored the active species and prevents carbon deposition from CH4 decomposition.

Effect of waterproofing materials on resistivity and pore properties of concrete under insolation and rain

The poor resistance of concrete to insolation and rain remains a major contributor to waterproofing system failures. This study investigated the effect of waterproofing materials on the resistivity and pore properties of concrete when exposed to heating-cooling cycles. Three types of concrete and four different waterproofing conditions were prepared under heating-cooling cycles. Resistivity and pore properties such as air content and roundness were measured. The effects of heating-cooling cycles, waterproofing conditions, and concrete type were analyzed. The resistivity-air content model was established. The resistance of concrete to heating-cooling cycles (Crhc) was quantified. The results showed that heating-cooling cycles increased the air content and decreased the resistivity. The resistivity had a high correlation with the air content, and the coefficient of determination R2 exceeded 0.95. Specimens with the rigid-flexible composite waterproofing material (RFCW) had the highest Crhc. The penetrating crystallization of rigid waterproofing material and the high ductility of flexible waterproofing material worked together on concrete, making it the most effective in improving the resistance of concrete to heating-cooling cycles. This study contributes to the solution of waterproofing system failures and presents methods for calculating the resistivity of concrete and quantifying the resistance of concrete to heating-cooling cycles.

Evolution of phase composition of cordierite-sapphirine ceramics in terms of the temperature dependence of Young’s modulus and damping determined via the impulse excitation technique (IET)

Ceramics from the magnesia-alumina-silica (MAS) system are common products of the ceramic industry. The phase composition of these systems can be rather complex, especially when feldspar is added as a flux, and thus attempts to correlate the composition and structure of these ceramics to their properties are quite rare, especially when considerable amounts of glass phase and sapphirine appear after firing. In this paper an attempt is made to correlate, for a talc-kaolin-alumina-feldspar mixture resulting in cordierite-sapphirine ceramics after firing to 1250 °C, the resulting elastic properties (Young’s modulus), as determined via the impulse excitation technique (IET), with the phase composition, determined via X-ray diffraction (XRD). Moreover, it is shown how the evolution of the phase composition and microstructure is reflected in the temperature dependence of Young’s modulus and damping during heating-cooling cycles with maximum temperatures ranging from 1000 to 1250 °C.

Young’s modulus and damping of partially sintered potassium sodium niobate (KNN) ceramics and its temperature dependence determined via the impulse excitation technique (IET)

Potassium sodium niobate (KNN) is suitable for the preparation of lead-free piezoelectric ceramics, and thus the elastic properties and damping behavior should be reliably known for practical applications. In this work we compare partially sintered KNN ceramics prepared by uniaxial and conventional sintering from three different KNN powders and show that the impulse excitation technique (IET) is perfectly suited to determine Young’s modulus at room temperature as well as the temperature dependence of Young’s modulus and damping (heating-cooling cycles with maximum temperature 800 °C). Room temperature values of the effective Young’s modulus of partially sintered KNN ceramics are below the predictions for convex pores and above a recently published numerical benchmark relation for concave pores. The phase transition temperatures determined by the IET are 160–190 °C for the low-temperature orthorhombic-tetragonal / tetragonal-orthorhombic transition and 388–412 °C for the high-temperature tetragonal-cubic / cubic-tetragonal transition, with hysteresis 12–25 K.

Bioactive Compounds and Potential Health Benefits through Cosmetic Applications of Cherry Stem Extract.

Cherry stems, prized in traditional medicine for their potent antioxidant and anti-inflammatory properties, derive their efficacy from abundant polyphenols and anthocyanins. This makes them an ideal option for addressing skin aging and diseases. This study aimed to assess the antioxidant and anti-inflammatory effects of cherry stem extract for potential skincare use. To this end, the extract was first comprehensively characterized by HPLC-ESI-qTOF-MS. The extract's total phenolic content (TPC), antioxidant capacity, radical scavenging efficiency, and its ability to inhibit enzymes related to skin aging were determined. A total of 146 compounds were annotated in the cherry stem extract. The extract effectively fought against NO· and HOCl radicals with IC50 values of 2.32 and 5.4 mg/L. Additionally, it inhibited HYALase, collagenase, and XOD enzymes with IC50 values of 7.39, 111.92, and 10 mg/L, respectively. Based on the promising results that were obtained, the extract was subsequently gently integrated into a cosmetic gel at different concentrations and subjected to further stability evaluations. The accelerated stability was assessed through temperature ramping, heating-cooling cycles, and centrifugation, while the long-term stability was evaluated by storing the formulations under light and dark conditions for three months. The gel formulation enriched with cherry stem extract exhibited good stability and compatibility for topical application. Cherry stem extract may be a valuable ingredient for creating beneficial skincare cosmeceuticals.

Green, recyclable and high latent heat form-stable phase change composites supported by cellulose nanofibers for thermal energy management

Efficiently addressing the challenge of leakage is crucial in the advancement of solid-liquid phase change thermal storage composite materials; however, numerous existing preparation methods often entail complexity and high energy consumption. Herein, a straightforward blending approach was adopted to fabricate stable phase change nanocomposites capitalizing on the interaction between TEMPO-oxidized cellulose nanofibers (TOCNF) and polyethylene glycol (PEG) molecules. By adjusting the ratio of TOCNF to PEG and the molecular weights of PEG, TOCNF/PEG phase change composites (TPCC) with customizable phase transition temperature (40.3–59.1 °C) and high phase transition latent heat (126.3–172.1 J/g) were obtained. The TPCC of high-loaded PEG (80–95 wt%) ensured a leakage rate of less than 1.7 wt% after 100 heating-cooling cycles. Moreover, TPCC exhibits excellent optical properties with a transmittance of over 90 % at room temperature and up to 96 % after heating. The thermal response analysis of TPCC demonstrates exceptional thermal-induced flexibility and good thermal stability, as well as recyclability and reshaping ability. This study may inspire others to design bio-based phase change composites with potential applications in thermal energy storage and management of smart-energy buildings, photothermal response devices, and waste heat-generating electronics.

A micro-mechanical insight into the thermo-mechanical behaviour of clays

The response of fine-grained soils to the combined effects of stress and temperature is a problem of growing concern in geoenvironmental engineering. Unlike most materials, fine-grained soils subjected to heating under drained conditions can exhibit either reversible expansion or irreversible contraction, depending on their loading history. This clay complex thermo-mechanical behaviour is widely reported in the literature, but its origin is still unknown. This paper explores the particle-scale origin of clay thermo-mechanical behaviour and helps to inform constitutive thermo-mechanical models. Clay particle interactions include non-contact forces, which are electrochemical in nature and prevail in face-to-face configuration and contact forces, which are mechanical forces transferred from one particle to another through a contact surface, typical of edge-to-face configuration. Non-contact forces include electrostatic Coulombic forces and van der Waals attractive forces. This paper proposes a combined numerical and analytical approach to quantify the elementary interactions between clay particles. The results are used to interpret typical stress-thermal paths, such as compression tests at different temperatures and heating-cooling cycles at constant mechanical stress. It is concluded that the electrochemical interactions governing the face-to-face particle configuration can only explain the elastic volumetric response of over-consolidated clays subjected to heating. The thermo-plastic behaviour associated with the reduction of the pre-consolidation pressure with temperature and the volumetric plastic compressive strain in response to heating in normally-consolidated clays is attributed to the edge-to-face particle configurations.

Comparative gelation characteristics of carrageenan via rheological and optical techniques: Glazing gels with different sweeteners

Glazing gels used as decorative gels are most often applied by hot spraying of solutions based on fast-setting hydrocolloids. The formation of a non-sticky gel at room conditions is crucial for their use. Gel formation and gel melting of carrageenan-based glazing gels (CGGs) with various sweeteners (trehalose, erythritol with stevia, maltitol, oligofructose, and nutriose with sucralose and acesulfame) were monitored during cooling-heating cycles using both the oscillatory rheology and the multispeckle diffusing wave spectroscopy (MS-DWS). In addition, rheological properties (shear viscosity of sols, the viscoelastic properties of gels, gel breaking strain) and texture properties (gel strength, elasticity and rupture force) were evaluated. The 12% addition of sweeteners resulted in a significant increase in gelling and melting temperatures by 2–6 °C compared to the sugar-free control sample (42 °C and 57 °C, resp.). MS-DWS, as opposed to oscillatory rheology, allowed determining of the characteristic temperatures at the beginning, middle and end of the phase transitions. The rheology gelling temperatures correlated best with the end of the gelation process, while the melting temperatures corresponded to the middle point temperature of the MS-DWS. Mechanical properties showed CGGs create a continuous gel structure characterized by a viscoelastic solid with comparable hardness and strength at small deformation, and greater elasticity compared to the sugar-free control sample. CGGs containing small molecule sweeteners formed stronger gels against rupture at large deformation than those ones with macromolecular structure. Sols of all CGGs were clear dispersions at 70 °C with Newtonian fluids characteristics and low viscosity (in the range of 9.3–10.9 mPas). These findings prove CGGs with various sugar-replaced sweeteners could be applied by hot spraying method and indicate how MS-DWS can be used to monitor gelation processes.

Temperature dependent resistivity switching in CuxO thin films chemically synthesized from high pressure plasma-deposited copper iodide

A facile chemical synthetic method was used to synthesize CuxO thin films on glass substrate via in-situ chemical reaction of CuI thin films in NaOH solution at ambient temperature. CuI thin films were produced by a low-cost plasma-assisted dissociation of the chemical vapor of CuI in acetonitrile (CH3CN) at a pressure of 60 Torr. The prepared CuxO thin films were annealed at various temperatures. The XRD studies unveiled the amorphous character of the CuxO thin films. The SEM images indicated that the surfaces of the films were smooth and smoothness depended on annealing temperature. The EDS studies revealed the presence of huge amounts of C and O with a little amount of Cu in the films which resulted due to the deposition of C produced through dissociation of CH3CN in plasma and O produced from chemical reaction in solution. The optical studies showed that transmittance of the CuxO thin films decreased from that of the CuI thin films and depended on the annealing temperatures. The bandgap of the CuxO thin films decreased with annealing temperature and was in the range of 2.30–2.98 eV. The CuxO thin films exhibited resistivity switching behavior in the first heating-cooling cycle and then the resistivity increased with temperature indicating the metallic behavior. These results are propitious for the application CuxO thin films in solar cells and memristor devices.