Search Results (370)

Newly developed hygrosensitive poly(vinyl alcohol) derivatives comprising grafted poly(N,N-dimethylacrylamide) chains of varied length and graft density are presented. The optical, sensing, and hydration properties of these copolymer thin films prepared by spin-coating were systematically studied. Refractive indices (n), absorption coefficients (k), and thicknesses (d) were calculated via curve fitting of the reflection spectra. Reflectance measurements across a relative humidity range of 5% to 95% were used to evaluate the humidity sensing behavior. Coating swelling exceeding 100% was observed. Hydration levels under high humidity conditions were studied using a quartz crystal microbalance method. This revealed approximately 24% water content in the polymer with the higher grafting density and shorter PDMA chains compared to around 31% in the copolymer with longer PDMA brushes that were loosely grafted The potential application of these copolymers as responsive materials for advanced humidity sensing is discussed. A combined optical and gravimetric approach for characterizing the humidity sensing properties of thin nanosized coatings is demonstrated, providing opportunities for advanced characterization of new functional materials, thus broadly contributing to the state of the art of sensor technologies. Full article

We investigate the role of a statistical complexity measure to assign equilibration in isolated quantum systems. While unitary dynamics preserve global purity, expectation values of observables often exhibit equilibration-like behavior, raising the question of whether a measure of complexity can track this process. In addition to examining observable equilibration, we extend our analysis to study how the complexity of the quantum states evolves, providing insight into the transition from initial coherence to equilibrium. We define a classical statistical complexity measure based on observable entropy and deviation from equilibrium, which captures the dynamical progression towards equilibration and effectively distinguishes between complex and non-complex trajectories. In particular, our measure is sensitive to non-complex dynamics. Such dynamics include the quasi-periodic behavior exhibited by low-dimensional initial states, where the system explores a limited region of Hilbert space while preserving coherence. Numerical simulations of an Ising-like non-integrable Hamiltonian spin-chain model support these findings. Our work provides new insight into the emergence of equilibrium behavior from unitary dynamics and advances complexity as a meaningful tool in the study of the emergence of classicality in microscopic systems. Full article

A novel polyester/graphene nanocomposite fiber was produced using the in situ polymerization protocol with carboxylated graphene and melt spinning technology. The resulting nanocomposite fibers were characterized by X-ray diffraction (XRD), Raman spectroscopy, differential scanning calorimeter (DSC), and scanning electron microscope (SEM). The fibers containing 0.2 wt% graphene fraction showed an excellent dispersity of graphene nanosheets in polymeric matrix. DSC test showed that the efficient polymer-chain grafting depresses the crystallization of PET chains. This graphene-contained PET fabric exhibited attractive antibacterial properties that can be employed in fruit preservation to ensure food safety. Full article

We present a numerical investigation comparing two entanglement generation protocols in finite XX spin chains with varying spin magnitudes ($s=1/2,1,3/2$). Protocol 1 (P1) relies on staggered couplings to steer correlations toward the ends of the chain. At the same time, Protocol 2 (P2) adopts a dual-port architecture that uses optimized boundary fields to mediate virtual excitations between terminal spins. Our results show that P2 consistently outperforms P1 in all spin values, generating higher-fidelity entanglement in shorter timescales when evaluated under the same system parameters. Furthermore, P2 exhibits superior robustness under realistic imperfections, including diagonal and off-diagonal disorder, as well as dephasing noise. To further assess the resilience of both protocols in experimentally relevant settings, we employ the pseudomode formalism to characterize the impact of non-Markovian noise on the entanglement dynamics. Our analysis reveals that the dual-port mechanism (P2) remains effective even when memory effects are present, as it reduces the excitation of bulk modes that would otherwise enhance environment-induced backflow. Together, the scalability, efficiency, and noise resilience of the dual-port approach position it as a promising framework for entanglement distribution in solid-state quantum information platforms. Full article

The first-principles calculation method was used to study doping elements with atomic numbers in the range of 23–30 (V–Zn) to form a single-atomic-spin nanochannel in a CoTiSb matrix. In a Ni-Sb single-atomic chain with high spin polarization and hole electrical conductivity, V-Sb, Mn-Sb, Fe-Sb, and Co-Sb single-atom chains have 100% spin polarization, indicating that a supercell containing the central atom chain has typical half-metal characteristics, and in the CoTiSb matrix, is centered on very small single-spin nanochannel forms. Using doping elements with atomic numbers between 23 and 27 (V-Co), the total magnetic moment of the supercell is constantly increasing, but the total magnetic moment of the Ni-doped supercell (Ni-Ti supercell) reduces, and a Cr-Ti supercell has an equal total magnetic moment. Doping elements Cu and Zn have atomic numbers higher than the range. Although the material of the nanochannel retains ferromagnetic properties, the spin polarization rate is reduced, and the material no longer has half-metallic properties. Full article

The misfolding and aggregation of proteins into amyloidogenic assemblies are key features of several metabolic and neurodegenerative diseases. Human insulin has long been known to form amyloid fibrils under various conditions, which affects its bioavailability and function. Clinically, insulin aggregation at recurrent injection sites poses a challenge for diabetic patients who rely on insulin therapy. Furthermore, decreased responsiveness to insulin in type 2 diabetic (T2D) patients may lead to its overproduction and accumulation as aggregates. Earlier reports have reported that various factors such as pH, temperature, agitation, and the presence of lipids or other proteins influence insulin aggregation. Our present study aims to elucidate the effects of non–micellar anionic DMPG (1,2–dimyristoyl–sn–glycero–3–phosphoglycerol) lipids on insulin aggregation. Distinct pathways of insulin aggregation and intermediate formation were observed in the presence of DMPG using a ThT fluorescence assay. The formation of soluble intermediates alongside large insulin fibrils was observed in insulin incubated with DMPG via TEM, DLS, and NMR as opposed to insulin aggregates generated without lipids. ¹³C magic angle spinning solid–state NMR and FTIR experiments indicated that lipids do not alter the conformation of insulin fibrils but do alter the time scale of motion of aromatic and aliphatic side chains. Furthermore, the soluble intermediates were found to be more cytotoxic than fibrils generated with or without lipids. Overall, our study elucidates the importance of anionic lipids in dictating the pathways and intermediates associated with insulin aggregation. These findings could be useful in determining various approaches to avoid toxicity and enhance the effectiveness of insulin in therapeutic applications. Full article

It is widely recognized that fine surface structures found in nature contribute to surface functionality, and studies on the design of functional materials based on biomimetics have been actively conducted. In this study, polymer thin films with hierarchically ordered surface structure were prepared by combining both nanoimprinting using anodically oxidized porous alumina (AAO) as a template and surface-initiated atom transfer radical polymerization (SI-ATRP). To prepare such polymer films, we designed a new copolymer (poly{[2-(4-methyl-2-oxo-2H-chromen-7-yloxy)ethyl methacrylate]-co-[2-(2-bromo-2-methylpropionyloxy)ethyl methacrylate]}; poly(MCMA-co-HEMABr)) with coumarin moieties and α-haloester moieties in the pendants. The MCMA repeating units function to fix the pillar structure by photodimerization, and the HEMABr ones act as the polymerization initiation sites for SI-ATRP on the pillar surfaces. Surface structures consisting of vertically oriented multiple pillars were fabricated on the spin-coated poly(MCMA-co-HEMABr) thin films by nanoimprinting using an AAO template. Then, the coumarin moieties inside each pillar were crosslinked by UV light irradiation to fix the pillar structure. SEM observation confirmed that the internally crosslinked pillar structures were maintained even when immersed in organic solvents such as 1,2-dichloroethane and anisole, which are employed as solvents under SI-ATRP conditions. Finally, poly(2,2,2-trifluoroethyl methacrylate) and poly(N-isopropylacrylamide) chains were grafted onto the thin film by SI-ATRP, respectively, to prepare the hierarchically ordered surface structure. Furthermore, in this study, the surface properties as well as the thermoresponsive hydrophilic/hydrophobic switching of the obtained polymer films were investigated. The surface morphology and chemistry of the films with and without pillar structures were compared, especially the interfacial properties expressed as wettability. Grafting poly(TFEMA) increased the static contact angle for both flat and pillar films, and the con-tact angle of the pillar film surface increased from 104° for the flat film sample to 112°, suggesting the contribution of the pillar structure. Meanwhile, the pillar film surface grafted with poly(NIPAM) brought about a significant change in wettability when changing the temperature between 22 °C and 38 °C. Full article

We discuss different quench protocols for Ising and XY spin chains in a transverse magnetic field. With a sudden local magnetic field quench as a starting point, we generalize our approach to a large class of local non-sudden quenches. Using finite time path field theory (FTPFT) perturbative methods, we show that the difference between the sudden quench and a class of quenches with non-sudden switching on the perturbation vanishes exponentially with time, apart from non-substantial modifications that are systematically accounted for. As the consequence of causality and analytic properties of functions describing the discussed class of quenches, this is true at any order of perturbation expansion and thus for the resummed perturbation series. The only requirements on functions describing the perturbation strength switched on at a finite time $t=0$ are as follows: (1) their Fourier transform $f\left(p\right)$ is a function that is analytic everywhere in the lower complex semiplane, except at the simple pole at $p=0$ and possibly others with $\Im \left(p\right)<0$; and (2) $f\left(p\right)/p$ converges to zero at infinity in the lower complex semiplane. A prototypical function of this class is $tanh\left(\eta t\right)$, to which the perturbation strength is proportional after the switching at time $t=0$. In the limit of large $\eta$, such a perturbation approaches the case of a sudden quench. It is shown that, because of this new type of universal behavior of Loschmidt echo (LE) that emerges in an exponentially short time scale, our previous results for the sudden local magnetic field quench of Ising and XY chains, obtained by the resummation of the perturbative expansion, extend in the long-time limit to all non-sudden quench protocols in this class, with non-substantial modifications systematically taken into account. We also show that analogous universal behavior exists in disorder quenches, and ultimately global ones. LE is directly connected to the work probability distribution, and the described universal behavior is therefore appropriate in potential concepts of quantum technology related to spin chains. Full article

Nuclear Magnetic Resonance (NMR) and Magnetic Resonance Imaging (MRI) are powerful techniques that have been employed to analyze foodstuffs comprehensively. These techniques offer in-depth information about the chemical composition, structure, and spatial distribution of components in a variety of food products. Quantitative NMR is widely applied for precise quantification of metabolites, authentication of food products, and monitoring of food quality. Low-field ¹H-NMR relaxometry is an important technique for investigating the most abundant components of intact foodstuffs based on relaxation times and amplitude of the NMR signals. In particular, information on water compartments, diffusion, and movement can be obtained by detecting proton signals because of H₂O in foodstuffs. Saffron adulterations with calendula, safflower, turmeric, sandalwood, and tartrazine have been analyzed using benchtop NMR, an alternative to the high-field NMR approach. The fraudulent addition of Robusta to Arabica coffee was investigated by ¹H-NMR Spectroscopy and the marker of Robusta coffee can be detected in the ¹H-NMR spectrum. MRI images can be a reliable tool for appreciating morphological differences in vegetables and fruits. In kiwifruit, the effects of water loss and the states of water were investigated using MRI. It provides informative images regarding the spin density distribution of water molecules and the relationship between water and cellular tissues. ¹H-NMR spectra of aqueous extract of kiwifruits affected by elephantiasis show a higher number of small oligosaccharides than healthy fruits do. One of the frauds that has been detected in the olive oil sector reflects the addition of hazelnut oils to olive oils. However, using the NMR methodology, it is possible to distinguish the two types of oils, since, in hazelnut oils, linolenic fatty chains and squalene are absent, which is also indicated by the ¹H-NMR spectrum. NMR has been applied to detect milk adulterations, such as bovine milk being spiked with known levels of whey, urea, synthetic urine, and synthetic milk. In particular, T2 relaxation time has been found to be significantly affected by adulteration as it increases with adulterant percentage. The ¹H spectrum of honey samples from two botanical species shows the presence of signals due to the specific markers of two botanical species. NMR generates large datasets due to the complexity of food matrices and, to deal with this, chemometrics (multivariate analysis) can be applied to monitor the changes in the constituents of foodstuffs, assess the self-life, and determine the effects of storage conditions. Multivariate analysis could help in managing and interpreting complex NMR data by reducing dimensionality and identifying patterns. NMR spectroscopy followed by multivariate analysis can be channelized for evaluating the nutritional profile of food products by quantifying vitamins, sugars, fatty acids, amino acids, and other nutrients. In this review, we summarize the importance of NMR spectroscopy in chemical profiling and quality assessment of food products employing magnetic resonance technologies and multivariate statistical analysis. Full article

Polytetrafluoroethylene (PTFE) has been widely used as a high-frequency dielectric substrate due to its excellent dielectric properties and thermal stability. However, with its low intrinsic thermal conductivity, PTFE falls short in meeting the escalating heat dissipation demands of high-power density, high-frequency communication systems. Although the thermal conductivity of PTFE composites can be effectively improved by the high thermal conductivity fillers, it is always accompanied by a decline in dielectric properties. Molecular chain ordering is regarded as an effective strategy to improve the intrinsic thermal conductivity of polymers while maintaining dielectric properties. Unfortunately, the conventional preparation methods for ordered molecular chains, such as electrostatic spinning and uniaxial stretching, are not applicable to the preparation of PTFE substrates. In this work, fluorinated graphite (FGi) is employed to induce the in-plane orientation of PTFE molecular chains. As a result, the PTFE composite with 0.5 wt% FGi loading exhibits an in-plane thermal conductivity of 1.21 W·m⁻¹·K⁻¹, six times higher than the in-plane thermal conductivity of pure PTFE. In addition, this composite exhibits a superior dielectric constant of 2.06 and dielectric loss of 0.0021 at 40 GHz. This work introduces a facile method to achieve improved thermal conductivity of PTFE while maintaining its excellent dielectric properties. Full article

Ionic liquids (ILs) can ideally reduce defects and improve the film stability of emissive metal halide perovskite films. In this work, we measure how the structure and emission of methylammonium lead tribromide (MAPbBr₃) perovskite films is modulated by long alkyl chain-containing pyridinium, imidazolium, or pyrrolidinium ILs. Two different film deposition methods are compared, with the resultant films characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and photoluminescence (PL) spectroscopy. For the latter, the differences in PL intensity of the perovskite are quantified using photoluminescence quantum efficiency (PLQE) measurements. It is found that a spin coating method in conjunction with the use of an imidazolium-containing IL (for a given precursor concentration) produces the strongest emissive perovskite. This optimal enhancement is attributed to a function of accessible surface charges associated with the heterocyclic cation of a given IL and perovskite defect passivation by bromide, the latter elucidated with the help of density functional theory. Proof-of-concept device fabrication is demonstrated for the case of a light emitting diode (LED) with the IL present in the emissive perovskite layer. Full article

Liquid crystals exhibit unique properties that can be tailored in response to external stimuli. Significant research is directed toward the development of luminescent materials exhibiting liquid crystallinity for various applications. The present work reports Au(I) complexes featuring N-heterocyclic carbene and phenyl acetylide ligands. Metal complexes enable the utilization of the triplet excitons through their inherent spin–orbit coupling, promoting intersystem crossing from singlet (S_n) to triplet (T_n) states to observe room-temperature phosphorescence (RTP). The strong bonds between carbene and Au enhance the thermal stability, and the substituted benzimidazole ring alters the thermodynamic and photophysical properties of the complexes. Incorporating the acetylide ligands with long alkoxy chains led to the formation of liquid crystalline (LC) phases, which exhibited stability over a wide temperature range. Additionally, the luminescence behavior was affected by the ethynyl ligands, and high quantum yields of RTP were observed. This study establishes the development of LC Au(I) complexes with a thermodynamically stable LC mesophase over a wide temperature range for applications in the field of light-emitting functional materials. Full article

We present a model of classical binary time series derived from a matrix product state (MPS) Ansatz widely used in one-dimensional quantum systems. We discuss how this quantum Ansatz allows us to generate classical time series in a sequential manner. Our time series are built in two steps: First, a lower-level series (the driving noise or the increments) is created directly from the MPS representation, which is then integrated to create our ultimate higher-level series. The lower- and higher-level series have clear interpretations in the quantum context, and we elaborate on this correspondence with specific examples such as the spin-1/2 Ising model in a transverse field (ITF model), where spin configurations correspond to the increments of discrete-time, discrete-level stochastic processes with finite or infinite autocorrelation lengths, Gaussian or non-Gaussian limit distributions, nontrivial Hurst exponents, multifractality, asymptotic self-similarity, etc. Our time series model is a parametric model, and we investigate how flexible the model is in some synthetic and real-life calibration problems. Full article

Quantum batteries represent a new and promising technological application of quantum mechanics, offering the potential for enhanced energy storage and fast charging. In this work, we study a quantum battery composed of three two-level systems with XXZ coupling operating under open boundary conditions. We investigate the role played by ferromagnetic and antiferromagnetic initial configurations on the charging dynamics of the battery. Two charging mechanisms are explored: static charging, where the battery interacts with a constant classical external field, and harmonic charging, where the field oscillates periodically over time. Our results demonstrate that static charging can be more efficient in the ferromagnetic case, achieving maximum energy due to complete population inversion between the ground and excited states. In contrast, harmonic charging excels in the antiferromagnetic case. By analyzing the stored energy and the average charging power in these two regimes, we highlight the impact of anisotropy on the performance of quantum batteries. Our findings provide valuable insights for optimizing quantum battery performance based on the system’s initial state and coupling configuration, paving the way for the study of more efficient quantum devices for energy storage. Full article

We study the topological defects and spin structures of rotating SU(3) spin–orbit-coupled spin F$=1$ Bose–Einstein condensates (BECs) in an in-plane quadrupole field with ferromagnetic spin interaction, and the BECs is confined by a harmonic trap. Without rotation, as the quadrupole field strength is increased, the spin F$=1$ BECs with SU(3) spin–orbit coupling (SOC) evolves from the initial Thomas–Fermi phase into the stripe phase; then, it enters a vortex–antivortex cluster state and eventually a polar-core vortex state. In the absence of rotation with the given quadrupole field, the enhancing SU(3) SOC strength can cause a phase transition from a central Mermin–Ho vortex to a vortex–antivortex cluster, subsequently converting to a bending vortex–antivortex chain. In addition, when considering rotation, it is found that this system generates the following five typical quantum phases: a three-vortex-chain cluster structure with mutual angles of approximately ${\displaystyle \frac{2\pi }{3}}$, a tree-fork-like vortex chain cluster, a rotationally symmetric vortex necklace, a diagonal vortex chain cluster, and a density hole vortex cluster. Particularly, the system exhibits unusual topological structures and spin textures, such as a bending half-skyrmion–half-antiskyrmion (meron–antimeron) chain, three half-skyrmion (meron) chains with mutual angles of an approximately ${\displaystyle \frac{2\pi }{3}}$, slightly curved diagonal half-skyrmion (meron) cluster lattice, a skyrmion–half-skyrmion (skyrmion-meron) necklace, and a tree-fork-like half-skyrmion (meron) chain cluster lattice. Full article