Search Results (86)

Two-dimensional indium selenide (InSe) is a promising material for next-generation electronics, characterized by a small electron effective mass and ultrahigh room-temperature mobility. This review systematically examines the fundamental physics and emerging quantum phenomena intrinsic to InSe. It also addresses the recent discovery of sliding ferroelectricity, which breaks macroscopic spatial inversion symmetry and yields robust polarization states without conventional displacive ionic dynamics. Technological progress from mechanical exfoliation to scalable bottom-up metal–organic chemical vapor deposition is evaluated. The review also covers advanced architecture enabled by InSe, including sub-3 nm-node logic transistors and nonvolatile ferroelectric synaptic devices. Finally, key challenges involving stoichiometric control, back-end-of-line-compatible integration, and environmental instability are discussed in the context of future low-power and neuromorphic computing. Full article

The von Neumann architecture, due to the physical separation between memory and processor, has limited the development of data-intensive applications. Neuromorphic computing technologies inspired by the brain’s parallel and event-driven operation mechanisms have enabled low-power in-memory computing. Memristors with tunable conductance can emulate biological synapses, while flexible memristors further offer mechanical flexibility, making them suitable for wearable electronics and intelligent sensing systems. This review systematically summarizes the switching mechanisms of flexible neuromorphic memristors, including conductive filaments, interface effects, ferroelectricity, phase change, and multiple synergistic mechanisms. It categorically discusses natural and bio-derived materials, synthetic organic/polymer materials, and inorganic functional materials, and introduces strategies for enhancing flexibility. The article also covers device architectures such as sandwich structures, crossbar arrays, and fiber-based textile structures, along with low-temperature fabrication techniques. Finally, it reviews recent advances in neuromorphic computing, in-memory computing, biomimetic sensing, and biomedical wearable systems. Challenges related to mechanical stability and device uniformity are analyzed, and future directions toward self-healing materials and integrated sensing-storage-computing systems are outlined. This comprehensive review bridges the gap between material innovation and system-level integration in flexible neuromorphic memristors, providing a valuable roadmap for accelerating the development of next-generation wearable artificial intelligence, edge computing, and bio-integrated electronic technologies. Full article

Advanced electrical and electronic systems are placing increasingly stringent demands on high-temperature dielectric capacitors. Polyimide (PI) possesses excellent thermal stability, but its low dielectric constant and breakdown strength limit its energy storage performance. To address this, a nanocomposite was designed consisting of the amorphous SiO₂-coated relaxor ferroelectric ceramic 0.6BaTiO₃-0.4Bi(Mg_0.5Ti_0.5)O₃ (BT-BMT@SiO₂) and PI. This core–shell structure improves the organic-inorganic interface and mitigates dielectric mismatch, thereby synergistically enhancing the composite’s dielectric constant, breakdown strength, and energy storage performance. At 150 °C, the breakdown field strength and maximum discharge energy density of the 0.25 vol.% BT-BMT@SiO₂/PI composite reached 381.81 MV/m and 1.14 J/cm³, respectively, representing increases of 32% and 67% compared to pure PI. These results indicate that the synergistic design of relaxor ferroelectric ceramics and core–shell interfaces is an effective strategy for enhancing the high-temperature energy storage performance of PI-based dielectric materials, providing important guidance for the development of high-performance capacitor materials. Full article

Electrical measurements of emerging materials such as thin films, two-dimensional materials, and fragile porous systems are often hindered by damage and contamination caused by conventional contact methods, including metal electrode deposition. In this study, we demonstrate the novelty and advantages of a mechanically compliant “soft probe” over conventional methods and conductive AFM. The non-destructive soft probe achieves stable electrical contact in the repulsive-force regime using a hairpin-shaped spring structure, allowing consistent measurements without active force control nor electrode fabrication. Case studies demonstrate that the soft probe prevents metal penetration and preserves intrinsic properties, as demonstrated in NiO resistive switching devices, and improves interface quality compared to deposited electrodes in ferroelectric measurements. It also enables electrical characterization of fragile materials such as metal–organic frameworks without inducing structural degradation. Furthermore, its mechanical compliance ensures stable operation under vibration and thermal stress, enabling measurements in vacuum and low-temperature environments. These results indicate that the soft probe provides a simple, versatile, and contamination-free platform for reliable electrical measurements, and represents a promising approach for the characterization of a wide range of emerging material systems. Full article

Negative capacitance (NC) has been reported across a wide range of physical systems, yet its interpretation has remained fragmented due to the lack of a unified conceptual framework. Existing explanations—spanning ferroelectric free-energy curvature, tunneling transport, plasmonic resonances, and electronic compressibility—have often been treated as unrelated or even contradictory. This review resolves these inconsistencies by showing that all manifestations of NC arise from non-synchronization between external excitation and internal response. We classify NC into three fundamental categories: temporal mismatch, originating from delays or inertia in charge or polarization dynamics; spatial mismatch, caused by nonuniform field or mode distributions; and quantitative mismatch, resulting from intrinsic parameter reversal such as negative curvature or negative compressibility. Despite their diverse physical origins, these mechanisms share the same mathematical signature (${\mathrm{C}}_{eff}=\partial \mathrm{Q}/\partial \mathrm{V}<0$). Organizing NC within this unified framework clarifies long-standing ambiguities, connects previously isolated research fields, and establishes a systematic foundation for engineering NC in electronic, photonic, and quantum devices. The framework further highlights tunnel-current-induced NC as a representative single-particle mechanism within the temporal mismatch category, expanding the scope of NC beyond ferroelectricity and collective modes. Overall, this work positions NC not as a singular anomaly but as a universal response class emerging from the interplay between excitation and internal dynamics. Full article

Six decades ago, the scientist from Stanford University, W.P. Little, announced a crusade to search for superconductivity, assumed to be heat-resistant in organic materials. Although such an ambitious goal was never realized in practice, this proposal gave rise to the entire ecosystem of studies on “synthetic metals,” creating a diverse community of material, experimental, and theoretical activities in low-dimensional electronic systems. We shall briefly review some key steps in this history, examine its main branches, and recall the consequences that remain on the agenda today. Particularly, we shall focus on a phenomenon of electronic ferroelectricity, whose roots can be found in the suggestion of a would-be superconducting polymer. Full article

In this study, enhancement- and depletion-mode (E- and D-mode) GaN-based 120 nm-wide fin-gated multiple nanochannel metal–oxide–semiconductor high-electron-mobility transistors (MOS-HEMTs) were manufactured on the epitaxial Al_0.83In_0.17N/GaN/Al_0.18Ga_0.82N/GaN two-dimensional electron gas (2DEG) channel layers grown on Si substrates using a metal-organic chemical vapor deposition system. The oxide layer grown directly by the photoelectrochemical oxidation method was used as the gate oxide layer in D-mode MOS-HEMTs. Furthermore, E-mode MOS-HEMTs used ferroelectric stacked LiNbO₃/HfO₂/Al₂O₃ layers as the gate oxide layers. The 120 nm-wide multiple nanochannels and various-length source field plates (SFPs) were fabricated and incorporated into monolithic complementary MOS-HEMTs (CMOS-HEMTs) consisting of D- and E-mode MOS-HEMTs. The resulting monolithic unskewed inverter was achieved by modulating the drain-source current of the D-mode MOS-HEMTs. The noise low margin of 2.03 V and noise high margin of 2.10 V of the unskewed monolithic inverter were obtained. From the dynamic experimental results, the rising time and falling time of the unskewed monolithic inverter were 4.9 μs and 3.2 μs, respectively. The breakdown voltage could be improved by incorporating an SFP. When the SFP edge was located at the center between the gate electrode and the drain electrode, the maximum breakdown voltage of 855 V was obtained. Full article

Fulgides are a class of organic compounds that exhibit photochromic behavior in both the solid state and in solution. These compounds have attracted considerable research interest due to their wide range of potential applications, including photochromic eyewear, smart windows, optical switches, data storage, and chemical and biological sensors. Here, we report the synthesis and crystal structures of fulgides bearing four different para-substituents on the phenyl moiety. All four molecules crystallize in space groups containing an inversion center. The distances between the two carbon atoms that would form the single C–C bond in the cyclized products fall within the range of 3.301–3.475 Å. The observed structural variations are attributed to intermolecular interactions based on Hirshfeld surface analysis. The fulgides exhibit photochromism, but they are not expected to display ferroelectric behavior due to their crystallization in centrosymmetric space groups. Full article

Organic light-emitting diodes (OLEDs) have emerged as a critical battleground in display technology due to their self-emissive and foldable properties. However, the adoption of polyimide (PI) as a flexible substrate material introduces technical challenges, particularly image sticking. This study proposes an interfacial polarization mechanism to explain this phenomenon, confirmed through dielectric and ferroelectric spectroscopy. The results show that introducing an amorphous silicon (α-Si) interlayer significantly improves interface compatibility, increasing the polarization response frequency from 74 Hz to 116 Hz and reducing residual polarization strength from 2.81 nC/cm² to 1.00 nC/cm². Practical tests on OLED devices demonstrate that the optimized structure (PI/α-Si/SiO₂) lowers the image sticking score from 3.46 to 1.67, validating the proposed mechanism. This research provides both theoretical insights and practical solutions for mitigating image sticking in flexible OLED displays. Full article

Dielectric crystals with switchable electric polarizations represent the key functional materials utilized for a broad range of practical applications. They allow for academically intriguing platforms, where the use of a strong external electric field can potentially unveil hidden crystal phases. Proton–π-electron correlated bistable systems turn out to be promising for exploring such electrically induced crystal polymorphisms, mainly because strong π-electronic polarization can be sensitively switched depending on mobile hydrogen locations. Pseudo-symmetry and hydrogen disorder are utilized as clues for the data mining of the Cambridge Structural Database in the search for molecular candidates with novel switchable dielectrics. The polarization hysteresis, electrostriction, and second harmonic generation of the candidates were experimentally evaluated, together with the re-inspection of crystal structure. This feature article highlights the rich variation and competition of some candidate polarization configurations and switching modes in close relation to high and efficient electrical energy storage/discharge, large electrostriction effects, polarization rotations, and multistage switching phenomena. The experimental findings are well-reproduced by the computational optimization of crystal structure and the simulation of the switchable polarization, piezoelectric coefficients, and relative stability for each of the real or hypothetical hydrogen-ordered crystal phases. Effective prediction and strategic design are thereby guaranteed by systematically understanding the appropriate integration of experimental, computational, and data sciences. Full article

BaTiO₃ (BT) is an essential material for many applications due to its dielectric, ferroelectric, and piezoelectric properties; nevertheless, it has been reported to possess a “critical size” in the nanoscale below which its outstanding properties are lost and the paraelectric cubic phase is stabilized at room temperature instead of the tetragonal phase. This value depends on multiple factors, mostly resulting from the synthesis route and conditions. Especially, internal stresses are known to promote the loss of tetragonality. Stresses are commonly present in water-containing synthesis routes because of the incorporation of hydroxyl groups into the oxygen sublattice of BaTiO₃. On the other hand, the use of an organic solvent instead of water as a reaction medium overcomes the mentioned problem. This work presents a one-pot water-free solvothermal treatment of a Ti(O-iPr)₄-Ba(OH)₂·8H₂O sol in methanol in the presence of small amounts of oleic acid, which allows the synthesis of spherical crystalline BT nanoparticles (from ~12 nm to ~30 nm in diameter) at temperatures as low as 100 °C with a cubic/tetragonal crystal structure confirmed by powder XRD, but predominantly tetragonal according to the Raman spectra. The retention of the tetragonal crystal structure is attributed to the lack of lattice hydroxyls (confirmed by FTIR spectroscopy) resulting from the use of an organic solvent (methanol) as reaction medium. To the best of the author’s knowledge, this synthesis approach is the first report of tetragonal BT nanoparticles synthesized in methanol without the addition of extra water and without the need for a post-synthetic calcination step. Full article

Phase transformations induced by short optical pulses are mainstream in studies on the dynamics of cooperative electronic states. We present a semiphenomenological modeling of spatiotemporal effects expected when optical excitons are intricate with the order parameter such as in, e.g., organic compounds with neutral-ionic ferroelectric phase transitions. A conceptual complication appears here, where both the excitation and the ground state ordering are built from the intermolecular electronic transfer. To describe both thermodynamic and dynamic effects on the same root, we adopt, for the phase transition, a view of the excitonic insulator—a hypothetical phase of a semiconductor that appears if the exciton energy becomes negative. After the initial pumping pulse, a quasi-condensate of excitons can appear as a macroscopic quantum state that then evolves, while interacting with other degrees of freedom which are prone to an instability. The self-trapping of excitons enhances their density, which can locally surpass a critical value to trigger the phase transformation. The system is stratified in domains that evolve through dynamical phase transitions and may persist even after the initiating excitons have recombined. Full article

Dielectric capacitors offer immense application potential in advanced electrical and electronic systems with their unique ultrahigh power density. Polymer-based dielectric composites with high energy density are urgently needed to meet the ever-growing demand for the integration and miniaturization of electronic devices. However, the universal contradictory relationship between permittivity and breakdown strength in traditional ceramic/polymer nanocomposite still poses a huge challenge for a breakthrough in energy density. In this work, all-organic carbon quantum dot CDs were synthesized and introduced into a poly(vinylidene fluoride) PVDF polymer matrix to achieve significantly boosted energy storage performance. The ultrasmall and surface functionalized CDs facilitate the polar β-phase transition and crystallinity of PVDF polymer and modulate the energy level and traps of the nanocomposite. Surprisingly, a synergistic dielectric enhancement and loss reduction were achieved in CD/PVDF nanocomposite. For one thing, the improvement in ε_r and high-field D_m originates from the CD-induced polar transition and interface polarization. For another thing, the suppressed dielectric loss and high-field D_r are attributed to the conductive loss depression via the introduction of deep trap levels to capture charges. More importantly, E_b was largely strengthened from 521.9 kV mm⁻¹ to 627.2 kV mm⁻¹ by utilizing the coulomb-blockade effect of CDs to construct energy barriers and impede carrier migration. As a result, compared to the 9.9 J cm⁻³ for pristine PVDF, the highest discharge energy density of 18.3 J cm⁻³ was obtained in a 0.5 wt% CD/PVDF nanocomposite, which is competitive with most analogous PVDF-based nanocomposites. This study demonstrates a new paradigm of organic quantum dot-enhanced ferroelectric polymer-based dielectric energy storage performance and will promote its application for electrostatic film capacitors. Full article

Polymer composites of P(VDF-TrFE) and Tris(hydroxymethyl) nitromethane as filler material with different concentrations have been prepared. Tris(hydroxymethyl) nitromethane is an organic ferroelectric material with low preparation cost and easy processing, and it is also lightweight. Its properties enable it to be a potential candidate for use as filler material in polymers to improve their ferroelectric, dielectric, and piezoelectric properties. We investigated the effect of filler content on the ferroelectric and dielectric properties of the polymer. Our results show that Tris(hydroxymethyl) nitromethane retains its crystallinity after embedding it in the polymer matrix. It does not alter the crystalline ferroelectric β-phase of the polymer. All composites possess higher polarization compared to pure P(VDF-TrFE). Up to 11.4 µC/cm² remnant polarization and a dielectric constant of 14 at 1000 Hz have been obtained with the free-standing 10 wt% composite film. Full article

Recently, two new polymorphs have been added to the nematic class: the polar-twisted nematic (N_PT) in 2016 and the ferroelectric nematic (N_F) in 2020. Comprised of achiral molecules, both exhibit local polar ordering and adopt modulated structures, right- and left-handed helical organizations—form chirality—albeit on vastly different dimensional scales; modulations have a ~10 nanometer pitch in the N_PT and ~500 nm in the N_F. Here, we focus on the structure and symmetries of the N_PT phase and the ensuing physical properties. Based on an array of order parameters that fully describe the molecular ordering and the nano-modulations thereof, we present a consistent formulation of the dielectric, optical, surface anchoring, and elasticity properties of the N_PT materials. We show that these properties are distinctly different from those associated with an elastically modulated, locally uniaxial, nematic. Full article