Search Results (1,091)

Polyaniline (PANI), as a classical conducting polymer, has attracted significant attention in the field of energy storage due to its low cost, facile synthesis, environmental stability, and unique dual electronic/ionic conductivity. Particularly, one-dimensional (1D) nanostructures of PANI, such as nanowires and nanorods, exhibit superior electrochemical performance and cycling stability, attributed to their high surface area and efficient charge transport pathways. This review provides a comprehensive summary of recent advances in 1D PANI-based anode materials for lithium-ion, sodium-ion, and other types of rechargeable batteries. The specific capacity, rate performance, and long-term cycling behavior of these materials are discussed in detail. Moreover, strategies for performance enhancement through combination with carbon materials, metal oxides, and silicon, as well as chemical doping and structural modification, are systematically reviewed. Key challenges including electrochemical stability, structural durability, and large-scale fabrication are analyzed. Finally, the future directions in structural design, composite engineering, and commercialization of 1D PANI anode materials are outlined. This review aims to provide insight and guidance for the further development and practical application of PANI-based energy storage systems. Full article

Photocatalytic pathogen inactivation is gaining increasing importance due to the rising number of microbial species resistant to conventional antibacterial agents. Titanium dioxide (TiO₂)-based photocatalysts have emerged as a promising solution, being not only potent antibacterial agents but also environmentally friendly and capable of simultaneously degrading organic pollutants. This review summarizes recent advances in the antibacterial performance of different TiO₂ modifications, including commercial nanopowders, nanoparticles with various morphologies, thin films, composites, and polymer-supported nanostructures, all primarily activated under UV light. Given the limited ability of pristine TiO₂ to harvest solar radiation, we also highlight the most recent strategies for designing visible-light-responsive TiO₂, such as doping, incorporation of plasmonic metal nanoparticles, formation of heterostructures, and interfacial charge transfer complexes. In addition, we discuss the fundamental structural features of TiO₂, the mechanisms of reactive oxygen species (ROS) generation involved in bacterial inactivation, and kinetic models describing antibacterial efficiency. These insights aim to advance the understanding and development of eco-friendly, cost-effective, and sustainable photocatalytic disinfection technologies. Full article

Flexible upconversion (UC) devices, owing to their unique combination of high–efficiency optical energy conversion and mechanical flexibility, have attracted increasing attention in the fields of optoelectronics, wearable devices, flexible displays, and biomedical applications. However, significant challenges remain in balancing optical performance, mechanical adaptability, long–term stability, and scalable fabrication, which limit their practical deployment. This review systematically introduces five representative upconversion mechanisms—excited–state absorption (ESA), energy transfer upconversion (ETU), energy migration upconversion (EMU), triplet–triplet annihilation upconversion (TTA–UC), and photon avalanche (PA)—highlighting their energy conversion principles, performance characteristics, and applicable scenarios. The article further delves into the flexible transition of upconversion devices, detailing not only the evolution of the luminescent layer from bulk crystals and nanoparticles to polymer composites and hybrid systems, but also the optimization of electrodes from rigid metal films to metal grids, carbon–based materials, and stretchable polymers. These developments significantly enhance the stability and reliability of flexible upconversion devices under bending, stretching, and complex mechanical deformation. Finally, emerging research directions are outlined, including multi–mechanism synergistic design, precise nanostructure engineering, interface optimization, and the construction of high–performance composite systems, emphasizing the broad potential of flexible UC devices in flexible displays, wearable health monitoring, solar energy harvesting, flexible optical communications, and biomedical photonic applications. This work provides critical insights for the design and application of high–performance flexible optoelectronic devices. Full article

The versatility of emulsions as templates for fabricating functional materials has garnered significant attention in recent decades. Emulsions with tailored geometries provide a powerful platform for designing and synthesizing polymeric materials with diverse functionalities. This review summarizes recent advances in emulsion-mediated fabrication of block copolymer (BCP) functional colloids and emulsion-templated construction of gel emulsion and porous hydrogels. Key topics include the generation of high-quality, uniform emulsion droplets, control over the shape and internal nanostructure of BCP colloids, and strategies for constructing polymeric gels and other porous functional materials using gel emulsion as templates. Furthermore, the intrinsic properties of polymers can be pre-engineered with specific stimulus-responsive functionalities prior to the fabrication of polymeric microparticles or porous hydrogels, thus imparting novel and targeted functionalities to the resulting assemblies and porous networks. This study can help in developing crucial strategies and in identifying pathways for the rational design of novel multifunctional materials with applications in drug delivery, sensing, and catalysis. Full article

Single-cell encapsulation, by constructing cell-scale microenvironments, enables precise protection, regulation, and functional enhancement of individual cells, holding significant importance in biomedical fields such as bioanalysis and cell therapy. Although various materials—including polymers, nanoparticles, hydrogels, polyphenols, and inorganic minerals—have been explored for single-cell encapsulation, limitations in controllability, biocompatibility, and multifunctional integration remain. In contrast, DNA nanomaterials offer unique advantages, including programmable architecture, high biocompatibility, precise spatial control, and modular functionality, making them highly suitable for the development of intelligent single-cell encapsulation systems. In this review, a systematic summary of recent advances in DNA nanomaterial-based single-cell encapsulation is presented. The fundamental encoding and assembly principles underlying the engineered encapsulation of cells at the membrane interface using DNA nanostructures are elucidated. Subsequently, the distinctive merits of DNA-based cell encapsulation and its applications in biomedical research are comprehensively summarized. Finally, the prevailing challenges and future directions in this burgeoning field are critically discussed, aiming to provide novel insights and perspectives for the advancement of advanced functional materials in both academic and clinical research pertaining to single-cell encapsulation. Full article

In this work, we investigated the use of a piezoelectric flexible device for energy harvesting. The main goal of the study was to fill the nanostructured pores of anodic aluminum oxide (AAO) films with piezoelectric polymer (PVDF-TrFE) via a modified conventional screen printing technique using blade printing. In this way, it is possible to obtain a composite from nanostructured thin films of polymer nanorods that shows improved charge generation ability compared to other non-nanostructured composites or pure (non-composite) aluminum with similar dimensions. This behavior is due to the effect of the highly developed surface of the material used to fill in the AAO nanopore template and its ability to withstand the application of higher mechanical loads to the structured piezoelectric material during deformation. The contact blade print filling technique can produce nanostructured piezoelectric polymer films with precise geometric parameters in terms of thickness and nanorod diameters, at around 200 nm, and a length of 12 μm. At a low frequency of 17 Hz, the highest root-mean-square (RMS) voltage generated using the nanostructured AAO/PVDF-TrFE sample with aluminum electrodes was around 395 mV. At high frequencies above 1700 Hz, the highest RMS voltage generated using the nanostructured AAO/PVDF-TrFE sample with gold electrodes was around 680 mV. The RMS voltage generated using a uniform (non-nanostructured) layer of PVDF-TrFE was 15% lower across the whole frequency range. Full article

Coagulation–flocculation, historically reliant on simple inorganic salts, has evolved into a technically sophisticated process that is central to the removal of turbidity, suspended solids, organic matter, and an expanding array of micropollutants from complex wastewaters. This review synthesizes six decades of research, charting the transition from classical aluminum and iron salts to high-performance polymeric, biosourced, and hybrid coagulants, and examines their comparative efficiency across multiple performance indicators—turbidity removal (>95%), COD/BOD reduction (up to 90%), and heavy metal abatement (>90%). Emphasis is placed on recent innovations, including magnetic composites, bio–mineral hybrids, and functionalized nanostructures, which integrate multiple mechanisms—charge neutralization, sweep flocculation, polymer bridging, and targeted adsorption—within a single formulation. Beyond performance, the review highlights persistent scientific gaps: incomplete understanding of molecular-scale interactions between coagulants and emerging contaminants such as microplastics, per- and polyfluoroalkyl substances (PFAS), and engineered nanoparticles; limited real-time analysis of flocculation kinetics and floc structural evolution; and the absence of predictive, mechanistically grounded models linking influent chemistry, coagulant properties, and operational parameters. Addressing these knowledge gaps is essential for transitioning from empirical dosing strategies to fully optimized, data-driven control. The integration of advanced coagulation into modular treatment trains, coupled with IoT-enabled sensors, zeta potential monitoring, and AI-based control algorithms, offers the potential to create “Coagulation 4.0” systems—adaptive, efficient, and embedded within circular economy frameworks. In this paradigm, treatment objectives extend beyond regulatory compliance to include resource recovery from coagulation sludge (nutrients, rare metals, construction materials) and substantial reductions in chemical and energy footprints. By uniting advances in material science, process engineering, and real-time control, coagulation–flocculation can retain its central role in water treatment while redefining its contribution to sustainability. In the systems envisioned here, every floc becomes both a vehicle for contaminant removal and a functional carrier in the broader water–energy–resource nexus. Full article

The persistent contamination of water bodies by organic compounds, heavy metals, and pathogenic microorganisms represents a critical environmental and public health concern worldwide. In this context, polymer composite materials have emerged as promising multifunctional platforms for advanced water purification. These materials combine the structural versatility of natural and synthetic polymers with the enhanced physicochemical functionalities of inorganic fillers, such as metal oxides and clay minerals. This review comprehensively analyzes recent developments in polymer composites designed to remove organic, inorganic, and biological pollutants from water systems. Emphasis is placed on key removal mechanisms, adsorption, ion exchange, photocatalysis, and antimicrobial action, alongside relevant synthesis strategies and material properties that influence performance, such as surface area, porosity, functional group availability, and mechanical stability. Representative studies are examined to illustrate contaminant-specific composite designs and removal efficiencies. Despite significant advancements, challenges remain regarding scalability, material regeneration, and the environmental safety of nanostructured components. Future perspectives highlight the potential of bio-based and stimuli-responsive polymers, hybrid systems, and AI-assisted material design in promoting sustainable, efficient, and targeted water purification technologies. Full article

Zinc oxide (ZnO) nanomaterials have emerged as promising candidates for gas sensing applications due to their high sensitivity, fast response–recovery cycles, thermal and chemical stability, and low fabrication cost. However, the performance of pristine ZnO remains limited by high operating temperatures, poor selectivity, and suboptimal detection at low gas concentrations. To address these limitations, significant research efforts have focused on dopant incorporation and polymer hybridization. This review summarizes recent advances in dopant engineering using elements such as Al, Ga, Mg, In, Sn, and transition metals (Co, Ni, Cu), which modulate ZnO’s crystal structure, defect density, carrier concentration, and surface activity—resulting in enhanced gas adsorption and electron transport. Furthermore, ZnO–polymer nanocomposites (e.g., with polyaniline, polypyrrole, PEG, and chitosan) exhibit improved flexibility, surface functionality, and room-temperature responsiveness due to the presence of active functional groups and tunable porosity. The synergistic combination of dopants and polymers facilitates enhanced charge transfer, increased surface area, and stronger gas–molecule interactions. Where applicable, sol–gel-based studies are explicitly highlighted and contrasted with non-sol–gel routes to show how synthesis controls defect chemistry, morphology, and sensing metrics. This review provides a comprehensive understanding of the structure–function relationships in doped ZnO and ZnO–polymer hybrids and offers guidelines for the rational design of next-generation, low-power, and selective gas sensors for environmental and industrial applications. Full article

The range of lubricant applications has broadened to include multiple sectors, aiming to optimize the operational efficiency of mechanical systems. Given their adaptable friction-reducing properties, lubricants have recently been incorporated into energy harvesting technologies such as triboelectric nanogenerators (TENGs). In such devices, lubricants are essential for mitigating wear, facilitating heat dissipation, eliminating contaminants, and prolonging the service life of mechanically actuated energy harvesters. Notably, emerging developments in sliding and rotational-mode TENGs leverage lubricants to improve electrical output while reducing interface degradation. However, despite significant potential, TENGs still face inherent challenges, including interface friction and energy losses from air breakdown. Recent research indicates that these drawbacks can be effectively addressed by the intentional use of polymer-based lubricants, which contribute to maintaining micro/nanostructured surfaces and minimizing air breakdown, thereby enhancing charge storage capability and increasing device robustness. This review systematically examines the categories, physicochemical attributes, and operational roles of polymeric lubricants used in TENG technology. It underscores their combined function is both primary and support materials to augment triboelectric efficiency. In addition, the article assesses how different lubricants impact device performance and durability, providing a critical analysis of their suitability based on the operational benchmarks of lubricant-embedded TENG configurations. Full article

Owing to the inherent safety, environmental friendliness, and high theoretical capacity (820 mAh g⁻¹) of zinc metal, aqueous zinc-ion batteries (AZIBs) have emerged as up-and-coming alternatives to organic lithium-ion batteries. However, the insufficient electrochemically active sites, poor structural stability, and severe interfacial side reactions of cathode materials have always been key challenges, restricting battery gravimetric energy density and cycling stability. This article systematically reviews current mainstream AZIB cathode material systems, encompassing layered manganese- and vanadium-based metal oxides, Prussian blue analogs, and emerging organic polymers. It focuses on analyzing the energy storage mechanisms of different material systems and their structural evolution during Zn²⁺ (de)intercalation. Furthermore, mechanisms of innovative strategies for improving cathodes are thoroughly examined here, such as nanostructure engineering, lattice doping control, and surface coating modification, to address common issues like structural degradation, manganese/vanadium dissolution, and interface passivation. Finally, this article proposes future research directions: utilizing multi-scale in situ characterization to elucidate actual reaction pathways, constructing artificial interface layers to suppress side reactions, and optimizing full-cell design. This review provides a new perspective for developing practical AZIBs with high specific energy and long lifespans. Full article

Polymer materials have become promising candidates for next-generation energy storage, with structural tunability, multifunctionality, and compatibility with a variety of device platforms. They have a molecular design capable of customizing ion and electron transport routes, integrating redox-active species, and enhancing interfacial stability, surpassing the drawbacks of traditional inorganic systems. New developments have been made in multifunctional polymers that have the ability to combine conductivity, mechanical properties, thermal stability, and self-healing into a single scaffold system, which is useful in battery, supercapacitor, and solid-state applications. By incorporating polymers with carbon nanostructures, ceramics, or two-dimensional materials, hybrid polymer nanocomposites improve electrochemical performance, durability, and mechanical compliance, and the solid polymer electrolytes, as well as artificial solid electrolyte interphases, resolve dendrite growth and safety issues. The multifunctionality also extends to flexibility, stretchability, and miniaturization, which implies that polymers are suitable for use in wearable devices and biomedical devices. At the same time, sustainable polymer innovation focuses on bio-based feedstocks, which can be recycled, and green synthesis pathways. Polymer discovery using artificial intelligence and machine learning is faster than standard methods, predicts structure–property–performance relationships, and can be rationally engineered. Although there are difficulties in stability during long periods, scalability, and trade-offs between indeedness and mechanical endurance, polymers are a promising avenue with regard to dependable, safe, and sustainable power storage. This review presents the molecular strategies, multifunctional uses, and prospects, where polymers are at the center of the next-generation energy technologies. Full article

To enhance the scope of therapeutic interventions using star polymeric nanoparticles of desired concentrations, an understanding of the effect of converting aqueous formulations into stable redispersible dry powders by freeze drying on their physicochemical and biological properties is essential. We demonstrate that parameters such as the choice of the cryoprotectant, its molecular weight, and concentration play an important role during lyophilization and reconstitution processes. We hypothesized that utilizing cryoprotectants akin to shell-forming polymers may be ideal in protection against aggregation and keeping the nanostructures intact during lyophilization and reconstitution, as well as retaining the overall biological efficacy of their cargo. Through an evaluation of miktoarm polymer-based nanoparticles, we demonstrate that PEG_2k at 1% w/v concentration provides the optimized cryoprotection, and the resulting solid formulations upon redispersion in an aqueous medium preserve the desired nanoparticle and curcumin properties. PEG_2k at 1% w/v is more efficient than PEG_5k and saccharides including glucose, sucrose, trehalose, and mannitol in enhancing the integrity of micelles during lyophilization and reconstitution. Addition of PEG_2k 1% w/v (with or without lyophilization and redispersion) enhances drug release in PBS buffer, while it has no impact in the cell culture media. Nanoformulations protect endothelial cells from cytotoxicity of curcumin, and addition of cryoprotectant or the lyophilization/redispersion processes did not impair anti-inflammatory efficacy of curcumin. Full article

This study describes the approach to develop hybrid nanostructures made of four varieties of ceramic nanotubes and three types of conductive polymers embedded with gold nanoparticles through a novel technique, which can exhibit distinct sensory properties not documented in the existing literature. Atomic force microscopy (AFM) analysis highlighted the characteristics of their surface roughness, identifying which could be the best choice for electrochemical electrodes depending on their surface structure. The incorporation of gold nanoparticles modifies the surface structure and forces the original grains to create voids that allow the gold particles to penetrate deeper and gather in small clusters, which in turn leads to a minor increase in grain size and localized sharpening of the peaks. The analysis mainly identified the peaks that were higher in relation to the valleys to identify a Gaussian distribution. It turned out that the configuration of ZnO nanotubes in the composites leads to the highest Ra values, with Al₂O₃ nanotubes coming in second place. Regarding the contribution of conducting polymers, PANI:EB presented the highest importance for all composites, while P3HT was relevant in several other cases. The evaluation of the electrode roughness, as described in this paper, is essential for the evaluation of its potential electrochemical activity and acts as a reliable measure that goes beyond the role of the evaluation of the active surface area (EASA). In our opinion, the evaluation of the EASA by traditional approaches described in the literature is not relevant for sensor applications, since the evaluation of the electrode surface structure must be performed before electrochemical tests, because the general electrochemical tests designed for sensor applications do not evaluate the EASA. Consequently, a thorough assessment of the electrode surface structure is advised, choosing the optimal electrodes according to this design, and additional data obtained from cyclic voltammetry will finally ascertain the true EASA and the actual performance of the respective electrode for identifying the target molecules. Full article

Poly(3-hexylthiophene-2,5-diyl) (P3HT) is a semiconducting, electron donor polymer which, in addition to its intensive use in optoelectronic devices, is increasingly investigated in biological systems. However, there are conflicting reports about the biocompatibility of P3HT, and no direct comparison between P3HT films and P3HT nanoparticles has been conducted. In this context, we investigated the viability of bEnd.3 endothelial cells when such cells are grown onto P3HT films or incubated with P3HT nanoparticles and subjected to trains of moderate power density, relatively long light pulses. We observed that, while P3HT films do not decrease the viability of bEnd.3 cells at all, P3HT nanoparticles lower the viability of bEND.3 cells by ~20%, when the nanoparticles also contain [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) as electron acceptor, and by ~30%, when the nanoparticles do not contain PCBM. Interestingly, the used photoexcitation protocol did not impact the biocompatibility of the P3HT-based materials. The obtained results reveal that (i). nanostructuring has a detrimental impact on the compatibility of P3HT with bEND.3 endothelial cells, and (ii). P3HT-based materials can be safely combined with light when used in biological systems because light, as used in the present study, does not alter the biocompatibility of such materials. Full article