Search Results (1,067)

Microwave-assisted polymerization is a transformative technique for synthesizing conductive polymers such as polypyrrole (PPy). Unlike conventional chemical or electrochemical methods that rely on external heating or electrode mediated oxidation, microwave irradiation induces volumetric and selective heating through dipole orientation and ionic conduction, which leads to faster reaction kinetics, improved uniformity and higher yields. This review highlights the fundamental mechanisms governing microwave polymer interactions, compares conventional and microwave-assisted polymerization routes and traces the evolution of pyrrole polymerization. Special emphasis is placed on the microwave-synthesized PPy composites and their superior electrochemical performance in energy storage, sensing and biomedical applications. Case studies of graphene/PPy, PPy–metal oxide (e.g., SnO₂@PPy nanotubes) and magnetic ferrite hybrids (e.g., BaFe₁₂O₁₉/PPy) nanocomposites demonstrate enhanced electrical conductivity, specific capacitance and more uniform nanostructures. Beyond energy storage, microwave polymerization techniques have led to the development of PPy composites that are used for sensing, antimicrobial activity and photothermal cancer therapy, highlighting the technique’s versatility across biomedical sciences. Reactor scale up, temperature and pressure control under sealed conditions, reproducibility and deeper mechanism understanding of how microwave radiation influences nucleation, chain growth, doping and charge transport were identified as the outstanding challenges that must be addressed to transform microwave-assisted synthesis from pilot to industrial scale. Overall, microwave-assisted polymerization is on its way to becoming a mainstream, energy efficient method for manufacturing high performance polymer composite materials. Full article

Programmable peptide hydrogels represent advanced supramolecular biomaterials featured with customizable molecular sequences and tunable self-assembly behaviors, which can biomimetically reconstruct the structural and microenvironmental complexity of native extracellular matrix. This review systematically elaborates the molecular engineering advances of programmable peptide hydrogels following a hierarchical logic from fundamental mechanisms to translational applications. We first interpret the intrinsic self-assembly mechanisms driven by non-covalent interactions and the regulatory effects of typical external microenvironmental stimuli. On this basis, we summarize core rational design principles, covering stimuli-responsive structural optimization, biofunctional modification, and the tunable regulation of physical properties, degradability and immunogenicity. Furthermore, we correlate multi-scale structural features (nanostructures, porous architecture and mechanical properties) with their versatile biomedical functions, and comprehensively discuss their cutting-edge applications in tissue regeneration, targeted drug and gene delivery, cell-mediated therapy, immunomodulation, and anti-infective treatment. Finally, we identify critical translational barriers including batch-to-batch inconsistency, immunogenic risks, and in vivo performance instability, and highlight future directions involving multi-stimuli-responsive systems, artificial intelligence-assisted design, computational modeling, and hybrid material construction. This work systematically clarifies the structure–property–function relationship of peptide hydrogels, and underscores their great potential as next-generation platforms for precision regenerative medicine and targeted disease intervention. Full article

Background/Objectives: Titanium alloy Ti₆Al₄V remains the gold standard in dental implantology due to its excellent mechanical properties, corrosion resistance, and biocompatibility. However, implant-associated infections and insufficient osseointegration continue to represent major clinical challenges, mainly related to bacterial biofilm formation and suboptimal surface–tissue interactions. Biofilm formation refers to the adhesion, accumulation, and growth of microbial communities embedded within a self-produced extracellular polymeric matrix on implant surfaces, which contributes to bacterial persistence and resistance to host defense mechanisms. This review aims to critically evaluate recent advances in multifunctional bioceramic coatings for dental implants, with a particular focus on zirconia (ZrO₂)-based systems and their antibacterial mechanisms. Methods: A structured literature analysis was conducted using major scientific databases including PubMed, Scopus, and Web of Science, focusing mainly on studies published between 2015 and 2025 related to CaP, Ag, and ZrO₂-based coatings for dental implants. The review examines their physicochemical properties, antibacterial strategies, ion release behavior, and biological responses, including osteogenic activity and biofilm inhibition. Particular attention is given to hybrid systems integrating multiple functional phases. Results: CaP coatings exhibit excellent osteoconductivity and promote early osseointegration but show limited intrinsic antibacterial activity. Ag-based coatings provide strong broad-spectrum antimicrobial effects through controlled Ag⁺ ion release, although concerns regarding cytotoxicity and dose-dependent responses remain. ZrO₂ coatings significantly enhance corrosion resistance and surface stability, while their antibacterial performance can be improved through nanostructuring, laser surface modification, and ionic doping. Hybrid Ag–CaP–ZrO₂ coatings demonstrate improved antibacterial activity, enhanced corrosion resistance, and better regulation of ion release kinetics and osteogenic response compared with single-component coating systems. Conclusions: Multifunctional bioceramic coatings represent a promising strategy for improving the performance of dental implants and addressing the dual challenge of infection control and tissue integration. However, challenges remain regarding long-term stability, controlled ion release, and limited clinical validation. Future research should focus on the development of smart, stimuli-responsive coatings and standardized evaluation protocols to facilitate clinical translation. Full article

The oxygen reduction reaction (ORR) is a key process in electrochemical energy conversion technologies such as fuel cells and metal–air batteries; however, its sluggish kinetics and reliance on precious metal catalysts limit large-scale application. This review provides a comprehensive overview of recent advances in non-precious nanoscale electrocatalysts for ORR in alkaline media. Particular emphasis is placed on reaction mechanisms, including dominant pathways, kinetics, and key intermediates, as well as the advantages of alkaline electrolytes over acidic systems. The performance of various catalyst classes is systematically discussed, including transition metal-based materials (Fe, Co, Zn, Cu, and bimetallic systems) and metal-free carbon-based electrocatalysts. Special attention is given to heteroatom-doped carbon materials, carbon nanostructures, and emerging hybrid systems such as MXene-based composites. Comparative analysis highlights the relationship between catalyst composition, structure, and electrochemical performance metrics, including half-wave potential, onset potential, Tafel slope, number of electron transfer, and operational stability. Overall, non-precious catalysts demonstrate promising activity and durability, approaching that of noble metals under alkaline conditions. The insights summarized in this review guide the rational design of efficient, cost-effective ORR electrocatalysts and support the development of sustainable energy technologies. Full article

Pesticides are widely used chemical compounds in agriculture, but their presence in water systems represents a significant environmental and health problem. Due to their stability and toxicity, many pesticides are difficult to remove using conventional water treatment methods, which has led to the development of advanced oxidation processes. Photocatalytic processes are based on the activation of semiconductor materials under light irradiation, leading to the formation of reactive species that degrade pesticides into less harmful products. On the other hand, electrocatalytic processes use electrical energy to generate oxidation and reduction reactions on electrode surfaces, enabling efficient degradation of organic pollutants. Both approaches offer high efficiency and the potential for complete mineralization of pesticides. Nanomaterials play a key role in improving these processes, as they provide a large specific surface area, enhanced conductivity, and increased reactivity. In photocatalysis, nanostructured metal oxides such as TiO₂ and ZnO are commonly used, while in electrocatalysis, advanced nanocomposites and modified electrodes are applied to improve electron transfer efficiency and system stability. This review paper provides an overview of recent research in the field of photocatalytic and electrocatalytic systems for pesticide removal from water, with a particular focus on the role of nanomaterials. Special attention is given to current trends, including the development of new nanostructures, hybrid systems, and energy-efficient technologies. The aim of this paper is to present, in a simple and clear way, the potential of these methods and to contribute to a better understanding of their application in environmental protection. Full article

This study aims to develop sustainable conductive nanocomposites based on poly(lactic acid) (PLA)/poly(ε-caprolactone) (PCL) blends reinforced with multi-walled carbon nanotubes (MWCNT) and graphene nanoplatelets (G), focusing on their multifunctional performance. The novelty lies in the production of hybrid nanocomposites based on PLA/PCL blends with MWCNT/G using conventional industrial processing techniques, enabling the development of eco-friendly nanocomposites with tailored electrical, mechanical, and electromagnetic properties. The nanocomposites were prepared by twin-screw extrusion followed by injection molding. Rheological, scanning electron microscopy (SEM), mechanical, thermal, thermomechanical, electrical conductivity, and electromagnetic shielding properties were systematically evaluated. From a rheological perspective, the PLA/PCL/MWCNT and PLA/PCL/MWCNT/G nanocomposites exhibited a plateau at low frequencies, associated with the formation of a percolated network. This was confirmed by the significant increase in electrical conductivity and electromagnetic shielding response. The morphology observed by SEM showed a refinement of the PCL phase in the PLA matrix with the incorporation of MWCNT. The PLA/PCL/MWCNT/G (4/2 parts per hundred resin, phr) nanocomposite showed a 309% increase in impact strength compared to neat PLA, while maintaining the heat deflection temperature (HDT). The elastic modulus exceeded 2300 MPa and accelerated the crystallization process by more than 15 °C compared to PLA, which makes it important to reduce injection molding time. Additionally, it exhibited the highest electrical conductivity level, around 6.79 × 10⁻⁵ S/cm, which resulted in improved electromagnetic shielding performance in the 8.2–18 GHz range, highlighting the synergistic effect between 1D and 2D fillers. The developed PLA/PCL/MWCNT and PLA/PCL/MWCNT/G nanocomposites demonstrate potential for antistatic applications, combining sustainability with multifunctional performance and industrial scalability. Full article

High-purity copper features excellent electrical conductivity but generally low mechanical properties. Adding a three-dimensional graphene network as reinforcement to make a copper–graphene metal matrix composite is promising for a wide range of applications with better mechanical performance and functional capabilities. However, direct application in a metal matrix is difficult due to unfavorable wetting, which causes poor dispersion and weak interfacial bonding in the graphene–metal system. Here, the powder metallurgy method was used to construct a three-dimensional continuous graphene network in the copper matrix combined with high-pressure torsion. Optimized deformation/thermomechanical treatment enhanced the microstructural development processed by the severe plastic deformation method of high-pressure torsion. The primary advantage of this hybrid process is that it enables us to achieve grains with a size in the ultra-fine or even nanoscale. A homogeneous equiaxed nanostructure without segregation was observed during microstructural characterization, with a grain size of ~300 nm. This study investigated structural development during progressive deformation, and the samples were evaluated from the viewpoint of grain size and grain boundaries. The process significantly increased the microhardness of the copper–graphene composite. The tensile strength reached ~500 MPa at room temperature. The interpenetrating structural feature of graphene promoted interfacial shear stress to a high level, whereas plastic deformation increased the dislocation density and grain boundaries, thus resulting in significantly enhanced load transfer strengthening and crack-bridging toughness simultaneously. Full article

The development of biocompatible functional nanostructures has emerged as a key driver in advancing nanomedicine, environmental remediation, and sustainable energy technologies. However, conventional synthesis methods often rely on toxic reagents, hazardous solvents, and energy-intensive processes, raising significant concerns regarding environmental impact and biological safety. In this context, green synthesis has gained increasing attention as a sustainable alternative, utilizing biological systems, renewable resources, and environmentally benign solvents to produce functional nanomaterials. This mini-review provides an overview of recent advances in the green synthesis of organic, inorganic, and hybrid nanostructures, highlighting their physicochemical properties and functional performance. Particular emphasis is placed on their applications in nanomedicine, including drug delivery, bioimaging, antimicrobial and anticancer therapies, and theranostic platforms. Additionally, their roles in environmental applications, such as pollutant degradation and water treatment, and in energy-related systems, including catalysis, solar energy conversion, and energy storage, are discussed with selected representative examples. Despite significant progress, key challenges remain, including limited mechanistic understanding, reproducibility issues, scalability constraints, and uncertainties related to long-term toxicity and environmental impact. Addressing these limitations will be essential for the safe and large-scale implementation of green nanotechnology. Overall, the integration of green chemistry principles with advanced nanomaterial design offers a promising pathway toward the development of multifunctional, sustainable, and high-performance nanostructures capable of addressing global health, environmental, and energy challenges. Full article

This study investigates the hydrothermal modification of commercial titanium dioxide (TiO₂) in the presence of a natural licorice root extract (Glycyrrhiza glabra L.), serving as a stabilizing and growth-modulating agent. The experimental framework combines hydrothermal treatment in a Teflon-lined autoclave with subsequent thermal calcination to elucidate the structural, morphological, and chemical evolution of the material. The plant-based extract significantly influences particle assembly during synthesis, fostering the formation of an initial organic–inorganic hybrid system that results in enhanced morphological homogeneity compared to pristine TiO₂. Thermal analyses (TGA and DSC) demonstrated the progressive decomposition of the organic components with increasing temperature, yielding a thermally stable, predominantly inorganic material at 600 °C. Scanning Electron Microscopy (SEM) observations confirmed a more uniform particle distribution in the modified samples. X-ray diffraction (XRD) patterns corroborated that the primary crystalline phase of TiO₂ remains intact across all conditions, with structural variations limited to peak definition and long-range organization. Furthermore, FTIR spectroscopy supported the preservation of characteristic TiO₂ vibrational features while indicating a gradual depletion of weakly bound surface species following thermal treatment. In conclusion, these findings demonstrate that natural extracts can effectively function as growth-modulating agents, steering material organization without altering its intrinsic chemical properties. This approach aligns with the principles of Green Chemistry and the circular economy, highlighting the potential of renewable plant-based resources as functional additives for the sustainable processing of inorganic materials. Rather than seeking to outperform commercial benchmarks, this work establishes a viable and low-environmental-impact strategy for morphological and structural modulation. Full article

Micro- and nanoplastic (MNP) pollution has emerged as a global environmental and health concern, driving the rapid development of sensor technologies for faster, more sensitive, and field-deployable detection. This review synthesizes recent advances in optical, electrochemical, and biosensor platforms for MNP analysis and compares their analytical performance and practical feasibility. Optical sensors, including plasmonic, spectroscopic, and colorimetric systems, enable label-free and often rapid detection with material discrimination capability, and are well-suited for screening applications, though they commonly exhibit higher detection limits and matrix interference. Electrochemical sensors demonstrate the highest analytical sensitivity overall, frequently reaching low µg L⁻¹ to ng mL⁻¹ levels, with strong potential for miniaturization and on-site deployment; performance is further enhanced by nanostructured electrodes, photoelectrochemical designs, and signal amplification strategies. Biosensors incorporating peptides, aptamers, enzymes, or engineered proteins provide improved polymer selectivity and enable targeted detection, but face challenges related to stability, cross-reactivity, and reproducibility in complex samples. Practically, portable electrochemical and simple optical colorimetric platforms are currently the most feasible for field use, while hybrid bio-electrochemical systems show the highest performance potential. Future research should prioritize robust selective recognition elements, antifouling interfaces, standardized validation protocols, mixed-polymer quantification models, and integration with machine learning to enable reliable, real-world MNP monitoring. Full article

Advanced nanomaterials are becoming increasingly critical for improving the efficiency, durability, and sustainability of bioenergy systems, with applications spanning biomass conversion, catalysis, and bioelectrochemical energy generation. This systematic bibliometric and thematic review analyses Scopus-indexed literature from 2020 to 2025 to elucidate global research trends in nanomaterial characterisation and performance evaluation for bioenergy applications. Bibliometric mapping using VOSviewer version 1.6.18 reveals a rapidly growing research landscape structured around three dominant themes: nanocatalysts for biodiesel and bioethanol production, nanostructured enhancements in bioelectrochemical and anaerobic digestion systems, and surface-engineered materials for energy conversion and storage. The review highlights the pivotal role of structural and morphological characterisation techniques including SEM, TEM, AFM, and XRD in establishing structure–property–performance relationships that underpin catalytic activity, electron transfer efficiency, and system stability. Beyond short-term catalytic and electrochemical metrics, increasing attention is given to mechanical stability, durability, and long-term operational reliability, which are shown to be critical determinants of scalability. Emerging strategies such as additive manufacturing and hybrid material systems enable the integration of nanomaterials into architected, mechanically robust structures, mitigating degradation and enhancing sustained performance. A concise conceptual framework is presented to link nanomaterial classes, characterisation challenges, targeted bioenergy applications, and scalability constraints. Despite significant progress, gaps remain in standardised characterisation protocols, durability-focused testing, and life-cycle assessment. Addressing these challenges is essential for translating laboratory-scale advances into scalable, sustainable bioenergy technologies. Full article

(1) Background: The development of advanced dental biomaterials has significantly improved restorative dentistry, shifting the focus from purely mechanical restoration toward materials capable of interacting biologically with oral tissues. Modern restorative materials are expected to demonstrate high biocompatibility, adequate mechanical properties, and potential bioactivity that may support tissue preservation and long-term clinical performance. This review aims to analyze recent advances in next-generation dental restorative materials and to evaluate their biological compatibility and potential clinical relevance. (2) Methods: A narrative literature review was conducted using major scientific databases, including PubMed, Scopus, and Web of Science, focusing on studies addressing advanced polymer-based composites, bioactive restorative materials, dental ceramics, computer-aided design and computer-aided manufacturing (CAD–CAM) restorative systems, and nanostructured biomaterials used in restorative dentistry. Relevant studies published in recent years were analyzed with respect to material composition, biological response, and reported clinical performance. (3) Results: The reviewed literature indicates that modern dental biomaterials, including nanocomposites, bioactive glass-containing materials, calcium silicate–based systems, and hybrid ceramic materials, show improved mechanical stability, enhanced remineralization potential, and reduced bacterial adhesion compared with traditional restorative materials. Advances in nanotechnology and material engineering have also contributed to the development of antimicrobial and bioactive restorative systems. (4) Conclusions: Next-generation dental restorative materials demonstrate promising characteristics that may improve clinical outcomes and biological integration in restorative dentistry; however, further long-term clinical investigations are required to fully confirm their safety, durability, and long-term effectiveness. Full article

The present research article deals with the thermal degradation study of epoxy resins filled with hybrid nanostructured forms of carbon under oxidative conditions. In particular, the formulated polymer composites (denoted as HYB_0.1%_CNTs:GNs and HYB_0.5%_CNTs:GNs, respectively) consist of two kinds of fillers, namely multi-walled carbon nanotubes (CNTs) and graphene nanosheets (GNs), mixed together with two different total mass amounts: 0.1 and 0.5%. In both kinds of nanocomposites, three different CNT:GN mixing ratios were considered (5:1, 1:1, and 1:5, respectively), thus providing a total of six hybrid samples. The thermal behavior of these samples was studied by simultaneous thermogravimetry and differential thermal analysis (TG/DTA) under flowing air, and two processes took place in distinct temperature ranges. In each step, about 50% of mass loss is detected with an exothermic effect in the corresponding DTA curve, with the second one accompanied by an intense heat release. The kinetic analysis of the two-stage oxidative thermal degradation was investigated using a model-free isoconversional approach. A non-Arrhenian behavior of the temperature function k(T) was assumed, and lifetime prediction was estimated at temperatures close to those of the possible applications. Isoconversional analysis shows nearly constant activation energies for all composites except HYB_0.1%_5:1 (from 142 to 96 kJ·mol⁻¹), while lifetime predictions indicate that thermal stability increases with graphene content at 0.1% loading (HYB_0.1%_1:5) and with CNT content at 0.5% loading (HYB_0.5%_5:1), with uncertainties below 7%. Finally, because of the π–π bond interactions between the CNTs and the GNs dispersed in the epoxy resin matrix, an effective and remarkable electrical performance was found and a correlation with both electrical and morphological properties was established. In this regard, Tunneling Atomic Force Microscopy (TUNA) proved to be particularly powerful in allowing the simultaneous mapping of topography and localized conductive networks with exceptional sensitivity to nanofiller dispersion, such as CNTs and GNs. DC conductivity increased by up to nine orders of magnitude at 0.1 wt% hybrid loading (up to 3.73 × 10⁻⁴ S/m vs. 1.06 × 10⁻¹³ S/m for CNT-only), with nanoscale TUNA currents (−1.9 to 4.5 pA) mirroring macroscopic trends, while at 0.5 wt% all hybrids reached 10⁻² S/m, indicating reduced synergy once a fully developed conductive network is established. Full article

The rapid global transition toward electric vehicles (EVs) demands lithium-ion battery (LIB) systems that ensure both extreme performance and uncompromising safety. However, the inherent thermal asymmetry within battery packs—driven by non-uniform heat generation and localized hotspots—remains a critical bottleneck, accelerating degradation and triggering thermal runaway. Phase change materials (PCMs) have emerged as pivotal thermal buffers due to their high latent heat capacity and ability to maintain passive thermal symmetry. This review provides a comprehensive analysis of recent advancements in PCM-based battery thermal management systems (BTMSs), transitioning from material-level nanostructural enhancements to system-level hybrid architectures. Unlike traditional reviews, we critically evaluate how the integration of multidimensional conductive fillers and advanced encapsulation technologies resolves the trade-offs between energy density and thermal response rates. Furthermore, the synergistic coordination between PCMs and active cooling strategies (liquid, air, and heat pipes) is synthesized to provide a roadmap for achieving global thermal equilibrium under extreme fast-charging (XFC) conditions. Full article

The Fenton reaction remains one of the most widely investigated advanced oxidation processes for wastewater treatment due to its ability to generate highly reactive oxygen species capable of degrading persistent organic pollutants. However, classical homogeneous Fenton systems suffer from significant limitations, including narrow pH applicability, iron sludge generation, and poor catalyst reusability. In response, extensive research has focused on the development of heterogeneous and advanced Fenton-like catalysts aimed at overcoming these challenges while enhancing catalytic efficiency and operational stability. This review provides a comprehensive and critical analysis of the evolution of Fenton catalysis, from classical homogeneous systems to advanced materials, including nanostructured catalysts, carbon-based Fe–N–C systems, metal–organic frameworks, and single-atom catalysts. A unified evaluation framework is proposed, integrating key performance parameters such as catalytic activity, manufacturability, stability, and catalyst lifespan. Comparative analysis reveals that improvements in activity are often accompanied by trade-offs in cost and scalability, indicating that the most advanced materials do not necessarily provide the best practical performance. A life cycle-oriented perspective is incorporated, emphasizing catalyst reuse, lifespan, and iron leaching, and providing quantitative insight into cumulative catalytic performance. The results demonstrate that long-term efficiency is governed not only by intrinsic activity but also by durability and operational stability under realistic conditions. Finally, current challenges and future directions are discussed, including scalable synthesis, improved mechanistic understanding, and integration into hybrid treatment systems. This review bridges the gap between fundamental research and practical application by highlighting the importance of balancing performance, stability, and sustainability in the design of next-generation Fenton catalysts. Full article