Search Results (16)

Efficient thermal management is critical for the performance, safety, and longevity of lithium-ion batteries, particularly in new energy vehicles. This paper presents the development and application of a NiCr/NiSi thin-film thermocouple fabricated via magnetron sputtering on a polyimide substrate, aiming to provide high-precision, fast-response internal temperature measurements for lithium-ion battery systems. The thermocouple demonstrates a Seebeck coefficient of approximately 40.95 μV/°C and a repeatability error of only 0.45%, making it highly suitable for capturing transient thermal events. The main innovation of this work lies in the comprehensive integration of simulation and experimental validation to optimize the thermocouple’s performance for lithium-ion battery applications. This includes static calibration, external short-circuit, and puncture tests, which collectively confirm the thermocouple’s reliability and accuracy. Additionally, the study explores the impact of ambient temperature variations on internal battery temperatures, revealing a nearly linear increase in internal temperature with rising ambient conditions. The findings offer valuable insights for improving battery thermal management systems, establishing early warning thresholds for thermal runaway, and enhancing the overall safety of lithium-ion battery applications. Full article

With the rapid development of electric vehicles, the safety and reliability of lithium-ion batteries (LIBs), as their core energy storage units, have become increasingly prominent. The variation in internal battery pressure is closely related to critical issues such as thermal runaway, mechanical deformation, and lifespan degradation. The non-uniform distribution of internal pressure may trigger localized hot spots or even thermal runaway, posing significant threats to vehicle safety. However, traditional external monitoring methods struggle to accurately reflect internal pressure data, and single-point external pressure measurements fail to capture the true internal state of the battery, particularly within battery modules. This limitation hinders efficient battery management. Addressing the application needs of electric vehicle power batteries, this study integrates thin-film pressure sensors into LIBs through the integrated functional electrode (IFE), enabling distributed in situ monitoring of internal pressure during long-term cycling. Compared to non-implanted benchmark batteries, this design does not compromise electrochemical performance. By analyzing the pressure distribution and evolution data during long-term cycling, the study reveals the dynamic patterns of internal pressure changes in LIBs, offering new solutions for safety warnings and performance optimization of electric vehicle power batteries. This research provides an innovative approach for the internal state monitoring of power batteries, significantly enhancing the safety and reliability of electric vehicle battery systems. Full article

Polyethylene imine (PEI) is a synthetic water-soluble and nitrogen-rich polymer with an ethylene amine repeating unit. It exists in a linear or branched forms and finds applications in various areas. PEI is often chemically modified by crosslinking reactions using molecular and polymeric crosslinkers (e.g., trichlorotriazine, epichlorohydrin, ethylene glycol diglycidyl ether, poly(ethylene glycol) diglycidyl ether, etc.) to increase its stability and reduce its water solubility. PEI (pristine/crosslinked) has a strong affinity for metal cations (e.g., Cu²⁺, Au³⁺, Pb²⁺, etc.), where the nitrogen atoms interact with the metal ions, and hence is suitable to remove metals from water with high efficiency. A thin film of crosslinked PEI on substrates can be prepared and finds diverse applications such as in removing metals and dyes, and biofouling prevention in the marine environment. The copper ion, as an example, can be stored (adsorbed) in a thin film of crosslinked PEI on a carbon cloth substrate, which can be released to water by passing an electric current through the film or with an acid treatment. It has also been reported that crosslinked PEI and composite materials can be used for the adsorption of dyes and gases such as CO₂ and SO₂ from the environment. The performance of pristine/composite/crosslinked PEI in gas, metal ion, and dye adsorption is affected by several factors. The focus of this review is to discuss the different reactions used to crosslink PEI and review the properties of the crosslinked materials and their applications. Studies have shown that the properties of the crosslinked PEI and hence its success in capturing metal ions, dyes, and CO₂ is dependent not only on the type of crosslinker but also on the degree of crosslinking. Full article

Metal–organic frameworks (MOFs) are also known as porous coordination polymers. This kind of material is constructed with inorganic nodes (metal ions or clusters) with organic linkers and has emerged as a promising class of materials with several unique properties. Well-known applications of MOFs include their use as gas storage and in separation, catalysis, carbon dioxide capture, sensing, slender film gadgets, photodynamic therapy, malignancy biomarkers, treatment, and biomedical imaging. Over the past 15 years, an increasing amount of research has been directed to MOFs due to their advanced applications in fuel cells, supercapacitors, catalytic conversions, and drug delivery systems. Various synthesis methods have been proposed to achieve MOFs with nanometric size and increased surface area, controlled surface topology, and chemical activity for industrial use. In this context, the pharmaceutical industry has been watching the accelerated development of these materials with great attention. Thus, the objective of this work is to study the synthesis, characterization, and toxicity of MOFs as potential technological excipients for the development of drug carriers. This work highlights the use of MOFs not only as delivery systems (DDSs) but also in advanced diagnostics and therapies, such as photodynamic therapy and targeted delivery to tumors. Bibliometric analyses showed a growing interest in the topic, emphasizing its contemporary relevance. Full article

Plasma focus devices represent a class of hot and dense plasma sources that serve a dual role in fundamental plasma research and practical applications. These devices allow the observation of various phenomena, including the z-pinch effect, nuclear fusion reactions, plasma filaments, bursts, shocks, jets, X-rays, neutron pulses, ions, and electron beams. In recent years, considerable efforts have been directed toward miniaturizing plasma focus devices, driven by the pursuit of both basic studies and technological advancements. In this paper, we present the design and construction of a compact, portable pulsed plasma source based on plasma focus technology, operating at the ~2–4 Joule energy range for versatile applications (PF-2J: 120 nF capacitance, 6–9 kV charging voltage, 40 nH inductance, 2.16–4.86 J stored energy, and 10–15 kA maximum current at short circuit). The components of the device, including capacitors, spark gaps, discharge chambers, and power supplies, are transportable within hand luggage. The electrical characteristics of the discharge were thoroughly characterized using voltage and current derivative monitoring techniques. A peak current of 15 kiloamperes was achieved within 110 nanoseconds in a short-circuit configuration at a 9 kV charging voltage. Plasma dynamics were captured through optical refractive diagnostics employing a pulsed Nd-YAG laser with a 170-picosecond pulse duration. Clear evidence of the z-pinch effect was observed during discharges in a deuterium atmosphere at 4 millibars and 6 kilovolts. The measured pinch length and radius were approximately 0.8 mm and less than 100 μm, respectively. Additionally, we explore the potential applications of this compact pulsed plasma source. These include its use as a plasma shock irradiation device for analyzing materials intended for the first wall of nuclear fusion reactors, its capability in material film deposition, and its utility as an educational tool in experimental plasma physics. We also show its potential as a pulsed plasma thruster for nanosatellites, showcasing the advantages of miniaturized plasma focus technology. Full article

The durability of reinforced concrete structures is significantly influenced by the effectiveness of small molecular inhibitors in preventing the corrosion of steel reinforcements. In a concrete environment, the passive film on steel bars serves as a critical protective component. In this study, a molecular dynamics (MD) simulation is used to study the inhibition mechanism of chloride ions by common corrosion inhibitors (2-Amino-2-thiazoline) in concrete in an excess chloride solution. The results reveal that inhibitors adsorb onto the steel surface primarily through van der Waals forces, with more than 90% of the adsorption occurring vertically. Despite this strong adsorption, inhibitors alone do not form a protective film. In the presence of chloride ions, which frequently penetrate concrete, the coverage rate of inhibitors on the steel surface decreases from 74% to 64%. Nevertheless, inhibitor molecules still provide substantial protection in chloride-rich concrete environments. Further analysis indicates that inhibitor molecules inhibit chloride ions in two ways. Corrosion inhibitor molecules actively desorb from the steel surface to capture chloride ions and prevent them from approaching. Additionally, inhibitors form a multi-electron layer on the steel surface to enhance passive film protection and hinder chloride ion diffusion through Coulombic interactions. Full article

Traditional bulk adsorbents, employed for the removal of dyes and metal ions, often face the drawback of requiring an additional filtration system to separate the filtrate from the adsorbent. In this study, we address this limitation by embedding the adsorbent into the polymer matrix through a process involving dissolution–dispersion, spin-casting, and heat-stretching. Selective dissolution and dispersion facilitate the integration of the adsorbent into the polymer matrix. Meanwhile, spin-casting ensures the formation of a uniform and thin film structure, whereas heat-induced stretching produces a porous matrix with a reduced water contact angle. The adsorbent selectively captures dye molecules, while the porous structure contributes to water permeability. We utilized inexpensive and readily available materials, such as waste polyethylene and calcium carbonate, to fabricate membranes for the removal of methylene blue dye. The effects of various parameters, such as polymer-adsorbent ratio, initial dye concentration, and annealing temperature, were investigated. Equilibrium data were fitted to Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich isotherms. The equilibrium data were best represented by the Langmuir isotherm, with maximum adsorption capacity of 35 mg/g and 43 mg/g at 25 °C and 45 °C, respectively. The membranes can be regenerated and recycled with a 97% dye removal efficiency. The study aims to present a template for adsorbent-embedded polymeric membranes for dye removal, in which adsorbent can be tailored to enhance adsorption capacity and efficiency. Full article

Increasing photon absorption by capturing light is an important way to increase the efficiency of photovoltaic devices. In this regard, the small optical band gap (E_g) and high absorption coefficient of Se-containing thin nanofilms make them ideal for next generation photovoltaic devices based on selenides. Amorphous selenium was introduced into polyamide-6 (PA 6) via a chemical synthesis in a bath and the influence of the products of its reaction with Cd²⁺ and Ag⁺ ions on the film phase composition, topographic and optical properties were evaluated. AFM data have revealed that the surface roughness of the a-Se/PA 6 composite noticeably increases compared to that of unreacted PA 6. However, at later stages of film deposition, the roughness decreases, and the thin film becomes smoother and uniform. The incorporation of solid inorganic nanoparticles into flexible polyamide network causes chain stretching, which has been confirmed by ATR-FTIR spectroscopy data. The data of X-ray diffraction analysis, depending on the stage of synthesis, showed the crystalline composition of the film with peaks of Se₈, CdSe, Ag₂Se and Ag, which may explain the observed optical properties. The optical properties of the composites indicate a shift in the band gap from 4.46 eV for PA 6 to 2.23–1.64 eV upon the stepwise deposition of amorphous Se, CdSe and Ag₂Se. E_g is conveniently located in the visible region of solar energy, making the obtained nanofilms ideal for solar energy harvesting. Full article

In this study, a green chemistry method was used to synthesize polymer composites based on polyethylene oxide (PEO). The method of the remediation of metal complexes used in this study is an environmentally friendly procedure with a low cost. Zinc metal ion (Zn²⁺)-polyphenol (PPHNL) complexes were synthesized for two minutes via the combination of a black tea leaf (BTL) extract solution with dissolved Zn-acetate. Then, UV–Vis and FTIR were carried out for the Zn-PPHNL complexes in a liquid and solid. The FTIR spectra show that BTLs contain sufficient functional groups (O-H, C-H, C=O, C=C, C-O, C-N, and N-H), PPHNL, and conjugated double bonds to produce metal complexes by capturing the cations of Zn-acetate salt. Moreover, FTIR of the BTL and Zn–PPHNL complexes approves the formation of the Zn-PPHNL complex over the wide variation in the intensity of bands. The UV absorption spectra of BTL and Zn-PPHNL indicate complex formation among tea PPHNL and Zn cations, which enhances the absorption spectra of the Zn-PPHNL to 0.1 compared to the figure of 0.01 associated with the extracted tea solution. According to an XRD analysis, an amorphous Zn-PPHNL complex was created when Zn²⁺ ions and PPHNL interacted. Additionally, XRD shows that the structure of the PEO composite becomes a more amorphous structure as the concentration of Zn-PPHNL increases. Furthermore, morphological study via an optical microscope (OM) shows that by increasing the concentration of Zn-PPHNL in a PEO polymer composite the size of the spherulites ascribed to the crystalline phase dramatically decreases. The optical properties of PEO: Zn-PPHNL films, via UV–Vis spectroscopy, were rigorously studied. The E_g is calculated by examining the dielectric loss, which is reduced from 5.5 eV to 0.6 eV by increasing the concentration of Zn-PPHNL in the PEO samples. In addition, Tauc’s form was used to specify the category of electronic transitions in the PEO: Zn-PPHNL films. The impact of crystalline structure and morphology on electronic transition types was discussed. Macroscopic measurable parameters, such as the refractive index and extinction coefficient, were used to determine optical dielectric loss. Fundamental optical dielectric functions were used to determine some key parameters. From the viewpoint of quantum transport, electron transitions were discussed. The merit of this work is that microscopic processes related to electron transition from the VB to the CB can be interpreted interms of measurable macroscopic quantities. Full article

Pinus koraiensis nut-coated film is a kind of by-product of nut processing, which has been shown to contain flavonoids, polyphenols, and other substances that can be used to produce natural antioxidant extracts. In this study, response surface methodology (RSM) was used to optimize the extraction process of flavonoids of P. koraiensis nut-coated film (PNF), and macroporous resin HPD600 was used to purify PNF (P-PNF). Its antioxidant activity was examined by DPPH (1,1-diphenyl-2-picrylhydrazyl) radical scavenging capacity, oxygen free radical absorption capacity (ORAC), total oxygen radical capture (TRAP), and iron ion reduction capacity. Under the ideal extraction conditions comprising a cellulase dosage of 90 U/g, a material/liquid ratio of 1:20 (g/mL), and an extraction time of 2 h, the PNF yield was 3.37%. Purification conditions were sample concentration of 2.0 mg/mL, pH of 5, water washing volume of 3 bed volume (BV), eluent ethanol concentration of 50%, and volume of 2 BV. The P-PNF recovery was 84.32%, and purity increased from 33.80% to 61.70%. Additionally, P-PNF showed increased antioxidant activity compared to PNF. Cumulatively, this study obtained the optimal values for the process parameters in order to achieve the maximum rates of extraction of PNF for economically optimal production at an industrial scale. Full article

We studied the micropattern fidelity of a Norland Optical Adhesive 81 (NOA81) microsieve made by soft-lithography and laser micromachining. Ablation opens replicated cavities, resulting in three-dimensional (3D) micropores. We previously demonstrated that microsieves can capture cells by passive pumping. Flow, capture yield, and cell survival depend on the control of the micropore geometry and must yield high reproducibility within the device and from device to device. We investigated the NOA81 film thickness, the laser pulse repetition rate, the number of pulses, and the beam focusing distance. For NOA81 films spin-coated between 600 and 1200 rpm, the pulse number controls the breaching of films to form the pore’s aperture and dominates the process. Pulse repetition rates between 50 and 200 Hz had no observable influence. We also explored laser focal plane to substrate distance to find the most effective ablation conditions. Scanning electron micrographs (SEM) of focused ion beam (FIB)-cut cross sections of the NOA81 micropores and inverted micropore copies in polydimethylsiloxane (PDMS) show a smooth surface topology with minimal debris. Our studies reveal that the combined process allows for a 3D micropore quality from device to device with a large enough process window for biological studies. Full article

We report high refractive-index (RI) films composed of polyhedral oligomeric silsesquioxane (SSQ) matrices and various lanthanoid cations. The SSQ matrices were constructed from octaammonium SSQ by connecting with bipyridine dicarboxylic acid, which is expected to capture cations. By modulating the feed ratio between SSQ and dicarboxylic acid, the series of the SSQ matrices were obtained with variable cross-linking ratios among the SSQ units. Thin transparent films were able to be prepared through the drop-casting method with the aqueous mixtures containing SSQ matrices and various kinds of lanthanoid salts up to 40 wt %. From RI measurements, it was revealed that the increase of the amount of the metal ion can significantly lift up the RI values. In particular, critical losses of Abbe numbers, which theoretically have the trade-off relationship toward increases in RI values, were hardly detected. This effect could be obtained by cation assembly in local spots that are assisted by SSQ. Full article

The objective of this work is to study the delamination of bismuth ferrite prepared by atomic layer deposition on highly oriented pyrolytic graphite (HOPG) substrate. The samples’ structures and compositions are provided by XPS, secondary ion mass spectrometry (SIMS) and Raman spectroscopy. The resulting films demonstrate buckling and delamination from the substrates. The composition inside the resulting bubbles is in a gaseous state. It contains the reaction products captured on the surface during the deposition of the film. The topography of Bi-Fe-O thin films was studied in vacuum and under atmospheric conditions using simultaneous SEM and atomic force microscopy (AFM). Besides complementary advanced imaging, a correlative SEM-AFM analysis provides the possibility of testing the mechanical properties by using a variation of pressure. In this work, the possibility of studying the surface tension of the thin films using a joint SEM-AFM analysis is shown. Full article

We have investigated the effect of electron effective mass (m_e*) and tail acceptor-like edge traps density (N_TA) on the electrical characteristics of amorphous-InGaZnO (a-IGZO) thin-film transistors (TFTs) through numerical simulation. To examine the credibility of our simulation, we found that by adjusting m_e* to 0.34 of the free electron mass (m_o), we can preferentially derive the experimentally obtained electrical properties of conventional a-IGZO TFTs through our simulation. Our initial simulation considered the effect of m_e* on the electrical characteristics independent of N_TA. We varied the m_e* value while not changing the other variables related to traps density not dependent on it. As m_e* was incremented to 0.44 m_o, the field-effect mobility (µ_fe) and the on-state current (I_on) decreased due to the higher sub-gap scattering based on electron capture behavior. However, the threshold voltage (V_th) was not significantly changed due to fixed effective acceptor-like traps (N_TA). In reality, since the magnitude of N_TA was affected by the magnitude of m_e*, we controlled m_e* together with N_TA value as a secondary simulation. As the magnitude of both m_e* and N_TA increased, µ_fe and Ion deceased showing the same phenomena as the first simulation. The magnitude of V_th was higher when compared to the first simulation due to the lower conductivity in the channel. In this regard, our simulation methods showed that controlling m_e* and N_TA simultaneously would be expected to predict and optimize the electrical characteristics of a-IGZO TFTs more precisely. Full article

An efficient process was developed allowing the removal of metal ions from polycontaminated aqueous solutions by combining modified colloids and membranes. Firstly, filtration experiments were performed using polyethersulfone membranes modified by a self-assembled multilayer film of polyelectrolytes. These polymer-modified membranes allowed the uptake of more than 90% of the metal ions initially present in the contaminated solutions (for solutions concentrated at 50 mg L⁻¹). Secondly, adsorption experiments were carried out with colloidal silica encapsulated with carboxymethyl chitosan (SiO₂-CMCS) or with mesoporous silica functionalized by grafting of 1,4,8,11-tetraazacyclotetradecane, i.e., cyclam (SiO₂-cyclam). The adsorption capacity of these compounds was shown to be higher than numerous other literature-known adsorbents, reaching 68 and 61 mg g⁻¹ towards Cu(II) for SiO₂-CMCS and SiO₂-cyclam, respectively. Finally, by coupling adsorption with ultrafiltration in the tangential mode, the removal of Cu(II), Ni(II) and Zn(II) ions was found to be improved, allowing to reach a removal efficiency of 99% towards Cu(II), Ni(II) and Zn(II) ions at a metal concentration of 50 mg L⁻¹, and a promising removal efficiency around 70% at a very high metal concentration of 1200 mg L⁻¹. The mechanisms involved in the capture of the metal ions by modified membranes and colloids are also discussed. Full article