Search Results (352)

Cobalt-doped iron disulfide (FeS₂) thin films were synthesized via chemical bath deposition (CBD) followed by annealing at 450 °C, yielding phase-pure pyrite structures with multifunctional properties. A deposition temperature of 95 °C is critical for promoting Co incorporation, suppressing sulphur vacancies, and achieving structural stabilization of the film. After annealing, the dendritic morphologies transformed into compact quasi-spherical nanoparticles (~100 nm), which enhanced the crystallinity and optoelectronic performance of the films. The films exhibited strong absorption (>50%) in the visible and near-infrared regions and tunable direct bandgaps (1.14 to 0.96 eV, within the optimal range for single-junction solar cells. Electrical characterization revealed a fourth-order increase in conductivity after annealing (up to 4.78 Ω⁻¹ cm⁻¹) and confirmed stable p-type behavior associated with Co²⁺-induced acceptor states and defect passivation. These results demonstrate that CBD enabled the fabrication of Co-doped FeS₂ thin films with synergistic structural, electrical, and optical properties. The integration of earth-abundant elements and tunable electronic properties makes these films promising absorber materials for the next-generation photovoltaic devices. Full article

In complex electromagnetic environments, traditional static absorbers struggle to meet dynamic control requirements. Tunable absorbers based on metasurfaces have emerged as a research hotspot due to their ability to flexibly control electromagnetic wave properties. This paper provides a systematic review of research progress in tunable absorbers across the microwave, terahertz, and infrared bands, with a focus on analyzing the physical mechanisms, material systems, and performance characteristics of five dynamic control methods: electrical control, magnetic control, optical control, temperature control, and mechanical control. Electrical control achieves rapid response through materials such as graphene and varactor diodes; magnetic control utilizes ferrites and other materials for stable tuning; optical control relies on photosensitive materials for ultrafast switching; temperature control employs phase-change materials for large-range reversible regulation; and mechanical control expands tuning freedom through structural deformation. Research indicates that multi-band compatibility faces challenges due to differences in structural scale and physical mechanisms, necessitating the integration of emerging materials and synergistic control strategies. This paper summarizes the core performance metrics and typical applications of absorbers across various bands and outlines future development directions such as multi-field synergistic control and low-power design, providing theoretical references and technical pathways for the development of intelligent tunable absorber devices. Full article

Intrinsically stretchable polymer ionic conductors (PICs) hold significant application prospects in fields such as flexible sensors, energy storage devices, and wearable electronic devices, serving as promising solutions to prevent mechanical failure in flexible electronics. However, the development of PICs is hindered by an inherent trade-off between mechanical robust and electrical properties. Cellulose, renowned for its high mechanical strength, tunable chemical groups, abundant resources, excellent biocompatibility, and remarkable recyclability and biodegradability, offers a powerful strategy to decouple and enhance mechanical and electrical properties. This review presents recent advances in cellulose-based polymer ionic conductors (CPICs), which exhibit exceptional design versatility for flexible electrodes and strain sensors. We systematically discuss optimization strategies to improve their mechanical properties, electrical conductivity, and environmental stability while analyzing the key factors such as sensitivity, gauge factor, strain range, response time, and cyclic stability, where strain sensing refers to a technique that converts tiny deformations (i.e., strain) of materials or structures under external forces into measurable physical signals (e.g., electrical signals) for real-time monitoring of their deformation degree or stress state. Full article

Neuromorphic computing, inspired by the human brain’s architecture, offers a transformative approach to overcoming the limitations of traditional von Neumann systems by enabling highly parallel, energy-efficient information processing. Among emerging materials, MXenes—a class of two-dimensional transition metal carbides and nitrides—have garnered significant attention due to their exceptional electrical conductivity, tunable surface chemistry, and mechanical flexibility. This review comprehensively examines recent advancements in MXene-based optoelectronic synapses and neurons, focusing on their structural properties, device architectures, and operational mechanisms. We emphasize synergistic electrical–optical modulation in memristive and transistor-based synaptic devices, enabling improved energy efficiency, multilevel plasticity, and fast response times. In parallel, MXene-enabled optoelectronic neurons demonstrate integrate-and-fire dynamics and spatiotemporal information integration crucial for biologically inspired neural computations. Furthermore, this review explores innovative neuromorphic hardware platforms that leverage multifunctional MXene devices to achieve programmable synaptic–neuronal switching, enhancing computational flexibility and scalability. Despite these promising developments, challenges remain in device stability, reproducibility, and large-scale integration. Addressing these gaps through advanced synthesis, defect engineering, and architectural innovation will be pivotal for realizing practical, low-power optoelectronic neuromorphic systems. This review thus provides a critical roadmap for advancing MXene-based materials and devices toward next-generation intelligent computing and adaptive sensory applications. Full article

Biopolymers have emerged as a transformative class of materials that reconcile high-performance functionality with environmental stewardship. Their inherent capacity for controlled degradation and biocompatibility has driven rapid advancements across electronics, sensing, actuation, and healthcare. In flexible electronics, these polymers serve as substrates, dielectrics, and conductive composites that enable transient devices, reducing electronic waste without compromising electrical performance. Within sensing and actuation, biodegradable polymer matrices facilitate the development of fully resorbable biosensors and soft actuators. These systems harness tailored degradation kinetics to achieve temporal control over signal transduction and mechanical response, unlocking applications in in vivo monitoring and on-demand drug delivery. In healthcare, biodegradable polymers underpin novel approaches in tissue engineering, wound healing, and bioresorbable implants. Their tunable chemical architectures and processing versatility allow for precise regulation of mechanical properties, degradation rates, and therapeutic payloads, fostering seamless integration with biological environments. The convergence of these emerging applications underscores the pivotal role of biodegradable polymers in advancing sustainable technology and personalized medicine. Continued interdisciplinary research into polymer design, processing strategies, and integration techniques will accelerate commercialization and broaden the impact of these lower eCO₂ value materials across diverse sectors. This perspective article comments on the innovation in these sectors that go beyond the applications of biodegradable materials in packaging applications. Full article

Polybenzoxazines (PBZs) have garnered significant attention as a versatile class of precursors for the development of advanced carbon-based materials, particularly in the field of electrochemical energy storage. This review comprehensively examines recent progress in the synthesis, structural design, and application of polybenzoxazine-derived materials for supercapacitor electrodes. Owing to their intrinsic nitrogen content, tunable functionality, and excellent thermal and mechanical stability, polybenzoxazines serve as ideal precursors for producing nitrogen-doped porous carbons with high surface areas and desirable electrochemical properties. This review discusses the influence of molecular design, polymerization conditions, and carbonization parameters on the resulting microstructure and performance of the materials. Furthermore, the electrochemical behavior of these materials in both electric double-layer capacitors (EDLCs) and pseudocapacitors is analyzed in detail. Challenges such as optimizing pore architecture, improving conductivity, and achieving scalable synthesis are also addressed. This article highlights emerging trends and offers perspectives on the future development of polybenzoxazine-derived materials for next-generation high-performance supercapacitors. Full article

The convergence of carbon nanomaterials and functional polymers has led to the emergence of smart carbon–polymer nanocomposites (CPNCs), which possess exceptional potential for next-generation sensing and actuation systems. These hybrid materials exhibit unique combinations of electrical, thermal, and mechanical properties, along with tunable responsiveness to external stimuli such as strain, pressure, temperature, light, and chemical environments. This review provides a comprehensive overview of recent advances in the design and synthesis of CPNCs, focusing on their application in multifunctional sensors and actuator technologies. Key carbon nanomaterials including graphene, carbon nanotubes (CNTs), and MXenes were examined in the context of their integration into polymer matrices to enhance performance parameters such as sensitivity, flexibility, response time, and durability. The review also highlights novel fabrication techniques, such as 3D printing, self-assembly, and in situ polymerization, that are driving innovation in device architectures. Applications in wearable electronics, soft robotics, biomedical diagnostics, and environmental monitoring are discussed to illustrate the transformative impact of CPNCs. Finally, this review addresses current challenges and outlines future research directions toward scalable manufacturing, environmental stability, and multifunctional integration for the real-world deployment of smart sensing and actuation systems. Full article

Bacterial cellulose (BC) is a high-purity biopolymer with excellent physicochemical and mechanical properties, including high crystallinity, water absorption, biocompatibility, and structural tunability. However, its large-scale production is hindered by high substrate costs and limited sustainability. In this study, spent black tea waste was utilized as a low-cost and eco-friendly carbon source for BC synthesis by Komagataeibacter xylinus ATCC 53524 under varying initial pH conditions (4–9). Six different BC membranes were produced and systematically characterized in terms of mechanical strength, water absorption capacity, electrical conductivity, antimicrobial performance, and polyvinyl alcohol (PVA) attachment efficiency. Morphological and chemical analyses were conducted using SEM and FTIR techniques to investigate pH-induced structural variations. The results revealed that the BC6 sample (pH 6) exhibited the highest tensile strength (2.4 MPa), elongation (13%), PVA incorporation (12%), and electrical conductivity, confirming the positive impact of near-neutral conditions on nanofiber assembly and functional integration. In contrast, the BC4 sample (pH 4) demonstrated strong antimicrobial activity (log reduction = 3.5) against E. coli, suggesting that acidic pH conditions enhance bioactivity. SEM images confirmed the most cohesive and uniform fiber morphology at pH 6, while FTIR spectra indicated the preservation of characteristic cellulose functional groups across all samples. Overall, this study presents a sustainable and efficient strategy for BC production using food waste and demonstrates that synthesis pH is a key parameter in tuning its functional performance. The optimized BC membranes show potential for biomedical, flexible electronic, and antibacterial material applications, particularly in wearable electrode technologies. Full article

Bismuth-based oxyfluorides (BiO_xF_3−2x) have recently emerged as promising photocatalysts due to their unique electronic structures and tunable physicochemical properties. This review provides a comprehensive overview of these materials, focusing on their crystal structures, band gap characteristics, and photocatalytic performance. Particular attention is given to BiOF, Bi₇O₅F₁₁, and β-BiO_xF_3−2x, highlighting the influence of fluorine’s high electronegativity and internal electric fields on charge separation and light absorption. The potential of Aurivillius-type oxyfluorides is also discussed. Structural modifications, such as the introduction of oxygen vacancies, morphology control, and metal/non-metal doping, are examined for their effects on photocatalytic efficiency. Furthermore, various synthesis techniques and heterojunction engineering strategies involving semiconductors, carbon-based materials, and metal nanoparticles are explored to improve light harvesting and reduce charge recombination. Applications in pollutant degradation and CO₂ photoconversion are reviewed, demonstrating the versatility of these materials. Despite their promise, the challenges associated with phase identification and composition control are also emphasized, underlining the need for rigorous structural characterization. Future directions for optimizing the photocatalytic activity of bismuth-based oxyfluorides are outlined, focusing on strategies to enhance their performance. Full article

This work focuses on the synthesis and the comprehensive characterization of polydianiline (PDANI) polymer, obtained via oxidative polymerization of dianiline, a low-toxicity and more environmentally friendly starting monomer for polyaniline (PANI) formation. Despite the structural similarity to PANI, PDANI remains underexplored, especially regarding the effect of different synthesis conditions. Here, we investigate how chloride, sulfate, and camphor sulfonate dopants, combined with green solvents such as water and DMSO, modulate the final properties of PDANI in the emeraldine salt configuration. The produced materials were extensively characterized using a multi-technique approach. FTIR, Raman, EPR, and UV-Vis spectroscopies provided insights into chemical structure, molecular order, and polaron population. Electrical conductivity was disclosed via current-voltage (I-V) measurements, while cyclic voltammetry (CV) and coulovoltammetry (QV) were employed to evaluate redox activity and charge reversibility. The resulting PDANI displays structural and functional features comparable to those of PANI synthesized under similar conditions. Notably, the nature of the dopant and acidic medium was found to crucially govern the oxidation level, molecular organization, and electrochemical performance, boosting PDANI as a tunable and sustainable alternative for applications ranging from electronics to energy storage. Full article

Colloidal quantum dots (CQDs) have attracted significant attention in optoelectronics due to their size-tunable bandgap, high photoluminescence quantum yield, and solution processability, which enable integration into compact and energy-efficient systems. This review consolidates recent progress in multifunctional CQD-based light-emitting devices and on-chip integration strategies. This review systematically examines fundamental CQD properties (quantum confinement, carrier dynamics, and core–shell heterostructures), key synthesis methods including hot injection, ligand-assisted reprecipitation, and microfluidic flow synthesis, and device innovations such as light-emitting field-effect transistors, light-emitting solar cells, and light-emitting memristors, alongside on-chip components including ongoing electrically pumped lasers and photodetectors. This review concludes that synergies in material engineering, device design, and system innovation are pivotal for next-generation optoelectronics, though challenges such as environmental instability, Auger recombination, and CMOS compatibility require future breakthroughs in atomic-layer deposition, 3D heterostructures, and data-driven optimization. Full article

Electrospun nanofibers have emerged as a versatile platform for developing advanced materials with diverse applications, owing to their high surface-area-to-volume ratio and tunable properties. The incorporation of metal oxide nanoparticles, such as titanium dioxide (TiO₂), has proven effective in further enhancing the functional performance of these materials, particularly in optoelectrical, antibacterial, and antioxidant domains. This study presents the first report of electrospun multifunctional nanofibers from a ternary blend of polyvinyl alcohol (PVA), polyvinylpyrrolidone (PVP), and polyacrylamide (PAAm) blended with TiO₂ nanoparticles at 0, 1, 3, and 5 wt.%. The objective was to develop nanocomposites with enhanced structural, optical, electrical, antibacterial, and antioxidant properties for applications in environmental, biomedical, and industrial fields. The nanofibers were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Fourier-transform infrared spectroscopy (FTIR), UV–visible spectrophotometry, and DC electrical conductivity tests. Antibacterial efficacy was assessed against Escherichia coli and Staphylococcus aureus via the Kirby–Bauer disk diffusion method, while antioxidant activity was evaluated using the DPPH radical scavenging assay. Results demonstrated that TiO₂ incorporation increased nanofiber diameters (21.5–35.1 nm), enhanced crystallinity, and introduced Ti–O bonding, confirming successful nanoparticle integration. Optically, the nanocomposites exhibited reduced band gaps (from 3.575 eV to 3.320 eV) and increased refractive indices with higher TiO₂ nanoparticle content, highlighting their potential for advanced optoelectronic devices such as UV sensors and transparent electrodes. Electrically, conductivity improved due to increased charge carrier mobility and conductive pathways, making them suitable for flexible electronics and sensing applications. The 5 wt.% TiO₂-doped nanofibers demonstrated superior antibacterial activity, particularly against E. coli (18.2 mm inhibition zone), and antioxidant performance comparable to ascorbic acid (95.32% DPPH inhibition), showcasing their relevance for biomedical applications like wound dressings and food packaging. These findings highlight the potential of PVA-PVP-PAAm/TiO₂ nanofibers as useful materials for moisture sensors, antibacterial agents, and antioxidants, advancing applications in medical devices and environmental technologies. Full article

Two-dimensional (2D) materials are promising candidates for neuromorphic computing owing to their atomically thin structure and tunable optoelectronic properties. However, achieving controllable synaptic behavior via defect engineering remains challenging. In this work, we introduce X-ray irradiation as a facile strategy to modulate defect states and enhance synaptic plasticity in WSe₂-based optoelectronic synapses. The introduction of selenium vacancies via irradiation significantly improved both electrical and optical responses. Under electrical stimulation, short-term potentiation (STP) exhibited enhanced excitatory postsynaptic current (EPSC) retention exceeding 10%, measured 20 s after the stimulation peak. In addition, the nonlinearity of long-term potentiation (LTP) and long-term depression (LTD) was reduced, and the signal decay time was extended. Under optical stimulation, STP showed more than 4% improvement in EPSC retention at 16 s with similar relaxation enhancement. These effects are attributed to irradiation-induced defect states that facilitate charge carrier trapping and extend signal persistence. Moreover, the reduced nonlinearity in synaptic weight modulation improved the recognition accuracy of handwritten digits in a CrossSim-simulated MNIST task, increasing from 88.5% to 93.75%. This study demonstrates that X-ray irradiation is an effective method for modulating synaptic weights in 2D materials, offering a universal strategy for defect engineering in neuromorphic device applications. Full article

The regeneration of large segmental bone defects remains a significant challenge. While electrical stimulation has demonstrated the potential to accelerate bone healing, clinical translation has been hindered by the lack of safe, localized delivery methods. In this study, we present a novel strategy combining piezoelectric and electrically conductive polymers with allograft demineralized bones to create stimuli-responsive, biologically relevant scaffolds via pneumatic 3D printing. These scaffolds exhibit enhanced piezoelectric potential and tunable electrical properties, enabling both electrical and mechanical stimulation of cells (without external stimulators). Under dynamic culturing conditions (i.e., ultrasound stimulation), human bone marrow-derived mesenchymal stromal cells cultured on these scaffolds displayed significantly elevated osteogenic protein expression (i.e., alkaline phosphatase and osteocalcin) and mineralization (confirmed via xylenol orange mineral staining) after two weeks. This work introduces a bioinspired, printable ink in conjunction with a simple fabrication approach for creating dual-responsive scaffolds with high potential for functional bone tissue regeneration. Full article

Graphene, a two-dimensional carbon material with a hexagonal lattice structure, possesses remarkable properties. Exceptional electrical conductivity, mechanical strength, and high surface area that make it a powerful platform for biosensing applications. Its sp²-hybridised network facilitates efficient electron mobility and enables diverse surface functionalisation through bio-interfacing. This review highlights the core detection mechanisms in graphene-based biosensors. Optical sensing techniques, such as surface plasmon resonance (SPR) and surface-enhanced Raman scattering (SERS), benefit significantly from graphene’s strong light–matter interaction, which enhances signal sensitivity. Although graphene itself lacks intrinsic piezoelectricity, its integration with piezoelectric substrates can augment the performance of piezoelectric biosensors. In electrochemical sensing, graphene-based electrodes support rapid electron transfer, enabling fast response times across a range of techniques, including impedance spectroscopy, amperometry, and voltammetry. Graphene field-effect transistors (GFETs), which leverage graphene’s high carrier mobility, offer real-time, label-free, and highly sensitive detection of biomolecules. In addition, the review also explores multiplexed detection strategies vital for point-of-care diagnostics. Graphene’s nanoscale dimensions and tunable surface chemistry facilitate both array-based configurations and the simultaneous detection of multiple biomarkers. This adaptability makes graphene an ideal material for compact, scalable, and accurate biosensor platforms. Continued advancements in graphene biofunctionalisation, sensing modalities, and integrated multiplexing are driving the development of next-generation biosensors with superior sensitivity, selectivity, and diagnostic reliability. Full article