Search Results (90)

Biotemplated strategies inspired by natural architecture have emerged as an effective strategy to improve the performance of photocatalytic materials. In this work, TiO₂-based photocatalysts were synthesized using olive leaves as a biological template to reproduce their hierarchical microstructure and enhance photocatalytic hydrogen production. The artificial olive leaf (AOL) support was obtained through a biotemplated ion-exchange process followed by hydrolysis and calcination. It was then modified by photodeposition of Au or Pt nanoparticles. The materials were characterized by SEM, XRD, N₂ adsorption–desorption, UV–Vis spectroscopy, and XPS to evaluate their structural and optical properties. SEM confirmed the successful replication of both the external morphology and internal architecture of the olive leaf, while XRD revealed low crystallinity with anatase as the only TiO₂ phase. Optical characterization showed a reduced band gap (~2.97 eV), and extended absorption toward the visible region, with Au nanoparticles exhibiting a plasmonic band at ~550 nm, whereas Pt enhanced light-harvesting efficiency. XPS indicated the presence of oxygen vacancies and Ti³⁺ species that promote metal–support interactions. Photocatalytic glycerol photoreforming showed a strong enhancement in hydrogen production after noble metal incorporation, reaching up to 14-fold under UV irradiation and 23-fold under simulated solar light for the Pt-modified catalyst, highlighting the synergy between biotemplated structuring and noble metal deposition. Full article

Chronic wounds resulting from bacterial infection remain one of the main challenges in clinical practice. There is a pressing need to develop an injectable hydrogel sealant with multifunctional properties, including remodeling capabilities, self-healing, painless removal, and antibacterial activity, to promote tissue remodeling. In this work, aldehyde carboxymethylated agarose (ACMA) is employed for the first time as a bio-template. Dopamine (DA) is introduced onto the ACMA template via a reversible Schiff-base reaction, endowing it with biomineralization properties to synthesize DA-modified ACMA-Ag nanoparticles (ACMA-DA-Ag). Further, the prepared ACMA-DA-Ag, which possesses both antibacterial activity and injectable behavior, is incorporated into a guar gum hydrogel through the formation of borate/diol bonds, thereby forming a multiple-dynamic-bond crosslinked network. This hydrogel demonstrates adequate mechanical strength, injectability, remodeling capabilities, and self-healing performance. It can reassemble into a new hydrogel within 4 ± 0.6 min upon simple physical contact, and supports tissue adhesion. Furthermore, the hydrogel effectively covers irregular-shaped wound and can be removed without causing secondary injury. More importantly, this multifunctional hydrogel is cost-effective, easy to synthesize, and simple to use, significantly accelerating skin regeneration and promoting the formation of skin appendages, such as hair follicles. The outcome of this research not only serves a tissue sealant for wound healing, but also presents a new strategy for creating novel polysaccharide-based biomaterials. Full article

Magnetic microrobots have emerged as a promising platform for drug delivery in recent years. By enabling remotely controlled motion and precise navigation under external magnetic fields, these systems offer new solutions to overcome the limitations of traditional drug delivery nanocarriers, such as inadequate tissue penetration and heterogeneous biodistribution. Over the past few years, significant advancements have been made in the structural design of magnetic microrobots, as well as in drug loading techniques and stimuli-responsive drug release mechanisms, thereby demonstrating distinct advantages in enhancing therapeutic efficacy and targeting precision. This review provides a comprehensive overview of magnetic drug delivery microrobots, which are categorised into biomimetic structural, bio-templated and advanced material-based types, and introduces their differences in propulsion efficiency and biocompatibility. Additionally, drug loading and release strategies are summarised, including physical adsorption, covalent coupling, encapsulation, and multistimuli-responsive mechanisms such as pH, enzyme activity and thermal triggers. Overall, these advancements highlight the significant potential of magnetic microrobots in targeted drug delivery and emphasise the key challenges in their clinical translation, such as biological safety, large-scale production and precise targeted navigation within complex biological environments. Full article

The gliding arc plasma technique (glidarc) was used for the precipitation and deposition of Mn or Fe oxides on zirconia fibers. Two types of fibers were used: commercial (Fib Zr(C)) and biomorphic (Fib Zr(B)) ZrO₂ fibers, the latter produced using cotton as a biotemplate. Both series of supported catalysts were characterized physicochemically and morphologically. Scanning Electron Microscopy (SEM) analyses showed that Fib Zr(B) largely retained the morphology of cotton. Fib Zr(B) presented the tetragonal phase (t-ZrO₂), while Fib Zr(C) exhibited the monoclinic phase (m-ZrO₂). Using X-ray Diffraction (XRD), the cryptomelane phase (K_xMn₈O₁₆) was identified only for Mn-Fib Zr(B). In the case of Fe-supported samples, the α-Fe₂O₃ phase appeared clearly in both biomorphic and commercial fibers. SEM and Transmission Electron Microscopy (TEM) images revealed that the precipitated iron oxides appeared to be better distributed than the manganese oxides, covering the outer surface of the fibrous supports more homogeneously. X-ray Photoelectron Spectroscopy (XPS) confirmed that Mn has an average oxidation state between 3+ and 4+, consistent with the cryptomelane phase detected by XRD. The synthesized supported systems were tested as catalysts in soot and CO oxidation, with the Mn-supported fibers proving to be more active than their Fe-containing counterparts in both reactions. Full article

This study presents a sustainable and efficient method for fabricating core–shell structured palladium catalysts using a bacterial template and sol–gel synthesis. This synthesis aligns with green chemistry principles by minimizing waste and enhancing resource efficiency. Our results demonstrate that the bacterial template effectively stabilizes Pd nanoparticles (NPs), preventing significant agglomeration during synthesis and subsequent calcination under different atmospheres and final temperatures. The catalyst samples were characterized by SEM, TEM, XRD, and TGA. The 1 wt% Pd/R@SiO₂ catalyst exhibited high activity in the Suzuki–Miyaura cross-coupling reaction, achieving competitive yields. Furthermore, the catalyst demonstrated a stable performance over five consecutive cycles. This work underscores the potential of biotemplated synthesis as a versatile and eco-friendly platform for producing high-performance, tunable catalysts. Full article

Wood-derived ceramics represent a novel class of bio-based composite materials that integrate the hierarchical porous architecture of natural wood with high-performance ceramic phases such as silicon carbide (SiC). This review systematically summarizes recent advances in the fabrication of SiC woodceramics via two predominant sintering routes—reactive infiltration sintering and hot-press sintering—and elucidates their effects on the resulting microstructure and mechanical properties. This review leverages the intrinsic anisotropic vascular network and multiscale porosity and mechanical strength, achieving ultralightweight yet mechanically robust ceramics with tunable anisotropy and dynamic energy dissipation capabilities. Critical process–structure–property relationships are highlighted, including the role of ceramic reinforcement phases, interfacial engineering, and multiscale toughening mechanisms. The review further explores emerging applications spanning extreme protection (e.g., ballistic armor and aerospace thermal shields), multifunctional devices (such as electromagnetic shielding and tribological components), and architectural innovations including seismic-resistant composites and energy-efficient building materials. Finally, key challenges such as sintering-induced deformation, interfacial bonding limitations, and scalability are discussed alongside future prospects involving low-temperature sintering, nanoscale interface reinforcement, and additive manufacturing. This mini overview provides essential insights into the design and optimization of wood-derived ceramics, advancing their transition from sustainable biomimetic materials to next-generation high-performance structural components. This review synthesizes data from over 50 recent studies (2011–2025) indexed in Scopus and Web of Science, highlighting three key advancements: (1) bio-templated anisotropy breaking the porosity–strength trade-off, (2) reactive vs. hot-press sintering mechanisms, and (3) multifunctional applications in extreme environments. Full article

Biomorphic mineralization was employed to synthesize novel Mn–Ce and Mn–Co–Ce oxide fibers using commercial cotton as a biotemplate, aiming to assess their catalytic performance in diesel soot combustion and CO oxidation. Two synthesis protocols—one with and one without citric acid—were investigated. The inclusion of citric acid led to fibers with more uniform morphology, attributed to improved precursor distribution, although synthesis yields decreased for Co-containing systems. In soot combustion tests, Mn–Ce catalysts synthesized with citric acid outperformed their monometallic counterparts. While cobalt incorporation enhanced the mechanical robustness of the fibers, it did not significantly boost catalytic activity. Selected formulations were also evaluated for CO oxidation, with Mn–Co–Ce fibers achieving T₅₀ values in the 240–290 °C range, comparable to Co–Ce nanofibers reported in the literature. These results demonstrate that biomorphic fibers produced through a simple and sustainable route can offer competitive performance in soot and CO oxidation applications. Full article

This study presents a novel, eco-friendly synthesis route for zinc oxide (ZnO) nanoparticles using cladode extracts of Hylocereus undatus acting simultaneously as reducing and improving agents, in alignment with green chemistry principles. The synthesis involved the reaction of zinc sulfate heptahydrate with the plant extract, with the medium pH adjusted using sodium hydroxide (NaOH), followed by calcination at 300 °C, 400 °C, and 500 °C, and then by a washing step to enhance purity. Comprehensive characterization was performed using thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and electrical impedance spectroscopy to investigate the structural, morphological, and dielectric properties of the nanoparticles. The sample calcined at 400 °C, followed by washing (HT400W), exhibits highly crystalline ZnO nanoparticles with a predominant wurtzite structure (93.15 wt% ZnO) and minimal impurities (6.85 wt% Na₂SO₄). SEM analysis indicated a flake-like morphology with nanoscale features (50–100 nm), while Raman spectroscopy confirmed enhanced crystallinity and purity post-washing. Additionally, the HT400W sample exhibited a dielectric constant (ε′) of 16.96 and a low loss tangent (tan δ) of 0.14 at 1 MHz, suggesting superior energy efficiency for high-frequency applications. This green synthesis approach not only eliminates hazardous reagents but also delivers ZnO nanoparticles with good dielectric performance. Furthermore, this work demonstrates the efficacy of a sustainable biotemplate, offering an environmentally friendly approach for synthesizing ZnO nanoparticles with tailored physicochemical properties. Full article

A copper nanoparticles@porous biocarbon substrate was designed for Surface-Enhanced Raman Spectroscopy (SERS) via a simple reduction method. In the detection of three trace antibiotics, the substrate exhibits a very high Raman enhancement efficiency. This is partly because the biocarbon is rich in meso-micropores, which can rapidly trap target molecules. On the other hand, the copper nanoparticles embedded on the surface of the carbon sheets generate a large number of plasmonic hotspots, leading to an increase in Raman signal intensity. These results suggest that this substrate has utility for SERS applications in food safety, medicine, and water pollution detection. Full article

Two-dimensional nanomaterials (2DNMs) exhibit significant potential for the development of functional and specifically targeted biosensors, owing to their unique planar nanosheet structures and distinct physical and chemical properties. Biomodification and biomimetic synthesis offer green and mild approaches for the fabrication of multifunctional nanohybrids with enhanced catalytic, fluorescent, electronic, and optical properties, thereby expanding their utility in constructing high-performance biosensors. In this review, we present recent advances in the synthesis of 2DNM-based nanohybrids via both biomodification and biomimetic strategies for biosensor applications. We discuss covalent and non-covalent biomodification methods involving various biomolecules, including peptides, proteins, DNA/RNA, enzymes, biopolymers, and bioactive polysaccharides. The engineering of biomolecule–nanomaterial interfaces for the creation of biomodified 2DNM-based nanohybrids is also explored. Furthermore, we summarize the biomimetic synthesis of 2DNM-based bio–nanohybrids through pathways such as bio-templating, biomolecule-directed self-assembly, biomineralization, and biomimetic functional integration. The potential applications of these nanohybrids in diverse biosensing platforms—including colorimetric, surface plasmon resonance, electrochemical, fluorescence, photoelectrochemical, and integrated multimodal biosensors—are introduced and discussed. Finally, we analyze the opportunities and challenges associated with this rapidly developing field. We believe this comprehensive review will provide valuable insights into the biofunctionalization of 2DNMs and guide the rational design of advanced biosensors for diagnostic applications. Full article

In recent years, flexible piezoresistive sensors based on polydimethylsiloxane (PDMS) matrix materials have developed rapidly, showing broad application prospects in fields such as human motion monitoring, electronic skin, and intelligent robotics. However, achieving a balance between structural durability and fabrication simplicity remains challenging. Traditional methods for preparing PDMS flexible substrates with high porosity and high stability often require complex, costly processes. Breaking through the constraints of conventional material systems, this study innovatively combines the high elasticity of polydimethylsiloxane (PDMS) with the stochastically distributed porous topology of a sponge-derived biotemplate through biomimetic templating replication technology, fabricating a heterogeneous composite system with an architecturally asymmetric spatial network. After 5000 loading cycles, uncoated samples experienced a thickness reduction of 7.0 mm, while PDMS-coated samples showed minimal thickness changes (2.0–3.0 mm), positively correlated with curing agent content (5:1 to 20:1). The 5:1 ratio sample demonstrated exceptional mechanical stability. As evidenced, the PDMS film-encapsulated architecturally asymmetric spatial network demonstrates superior stress dissipation efficacy, effectively mitigating stress concentration phenomena inherent to symmetric configurations that induce matrix fracture, thereby achieving optimal mechanical stability. Compared to the pre-test resistance distribution of 10–248 Ω, after 5000 cyclic loading cycles, the uncoated samples exhibited a narrowed resistance range of 10–50 Ω, while PDMS-coated samples maintained a broader resistance range (10–240 Ω) as the curing agent ratio increased (from 20:1 to 5:1), demonstrating that increasing the curing agent ratio helps maintain conductive network stability. The 5:1 ratio sample displayed the lowest resistance variation rate attenuation—only 3% after 5000 cycles (vs. 80% for uncoated samples)—and consistently minimal attenuation at all stages, validating superior electrical stability. Under 0–6 kPa pressure, the 5:1 ratio device maintained a linear sensitivity of 0.157 kPa⁻¹, outperforming some existing works. Human motion monitoring experiments further confirmed its reliable signal output. Furthermore, the architecturally asymmetric spatial network of the device enables superior conformability to complex curvilinear geometries, leveraging its structural anisotropy to achieve seamless interfacial adaptation. By synergistically optimizing material composition and structural design, this study provides a novel technical method for developing highly durable flexible electronic devices. Full article

α-Pinene is a very valuable natural raw material for organic syntheses, which is of increasing interest to scientists due to its renewability and relatively low price. This work presents the studies on the oxidation of α-pinene in the presence of two mesoporous titanium-silicate catalysts: standard Ti-SBA-15 and Ti-SBA-15 material, which was obtained by a new and green way using orange peel waste as bio-templates (Ti-SBA-15_orange peels). For the synthesis of the Ti-SBA-15 catalysts, the following raw materials were used: Pluronic P123 as the template (template usually used in the synthesis of SBA-15 materials), tetraethyl orthosilicate as the silicon source, hydrochloric acid, deionized water, and tetraisopropyl orthotitanate as the titanium source. For the synthesis of Ti-SBA-15_orange peels, a catalyst was also properly prepared, and orange peel waste as the co-templates (renewable templates) were used. The two obtained Ti-SBA-15 materials were characterized by the following instrumental methods: XRD, SEM, EDX, UV-Vis, and FTIR. Moreover, the specific surface area and pore size distribution were investigated for these catalysts with help from the nitrogen adsorption–desorption method. Catalytic tests of the obtained catalysts were performed in the oxidation of α-pinene with oxygen and by the method which did not use any solvent (α-pinene was simultaneously the raw material and solvent in this process). During the catalytic tests, the effect of temperature, catalyst content, and reaction time on the selectivities of the appropriate products and the conversion of α-pinene were studied. Depending on the conditions of the oxidation process, the catalyst obtained with the use of orange peels as co-templates showed similar or even higher activity than the standard Ti-SBA-15 catalyst. Full article

Waste nanomaterials pose environmental and human health concerns and they need to be urgently and efficiently managed. In this study, a fungal biotemplate was used to accumulate and recover nano-Fe₂O₃ materials from an aqueous solution. Then, recovered nano-Fe₂O₃ materials were activated to form a high-performance magnetic porous carbon composite (FePC) for energy storage and organic pollutant removal. The results indicate that high concentrations (500 mg/L) of 50 nm Fe₂O₃ particles can be completely recovered using a cross-linked Neurospora crassa fungus (NC), primarily because of its encapsulation function. In addition, the surface area, degree of graphitization, and heteroatom content of the FePC materials can be boosted by the catalytic effects of the incorporated Fe atoms. The developed FePC materials exhibit potential as high electrical double-layer capacitors as well as strong retention capabilities, excellent stability, and efficient adsorption of triclosan (TCS, ~526 mg/g). Additionally, these FePC materials exhibit superior capacities for energy storage and pollutant reduction compared to commercial and reported carbon materials. These results reveal a sustainable route for the recovery and reutilization of nanomaterials. Full article

Titanium dioxide demonstrates promising potential in the energy storage field due to its high theoretical specific capacity and economic viability. However, its practical application is hindered by intrinsic limitations including low electronic conductivity and slow lithium-ion transport. In general, nature inspires the biotemplating synthesis of artificially functional materials with hierarchical structures. Learning from the bioinspired synthesis process, we adopt a facile biomimetic approach to synthesize graphene-based anatase TiO₂ nanoparticle/nanorod hierarchical structure. The rod-shaped anatase is assembled nanoparticles with a diameter of 20 to 50 nm, and the surface of graphene is deposited by nanoparticles of 5 to 10 nm. The composite also possesses a high surface area and a mesoporous structure. This unique structure not only reduces the transportation pathway of lithium ions and electrons but also enhances the electric conductivity and tolerates the volume change. As an anode electrode, the bioinspired hierarchical structure exhibits a high reversible capacity of 160 mA h g⁻¹ after 180 cycles at a current rate of 1C, highlighting the effectiveness of bioinspired design. Full article

This study presents an efficient and environmentally sustainable synthesis of ZnO nanoparticles using a starch-mediated sol-gel approach. This method yields crystalline mesoporous ZnO NPs with a hexagonal wurtzite structure. The synthesized nanoparticles demonstrated remarkable multifunctionality across three critical applications. In photocatalysis, the ZnO NPs exhibited exceptional efficiency, achieving complete degradation of methylene blue within 15 min at pH 11, significantly surpassing the performance of commercial ZnO. Under neutral pH conditions, the nanoparticles effectively degraded various organic dyes, including methylene blue, rhodamine B, and methyl orange, following pseudo-first-order kinetics. The methylene blue degradation process was aligned with the Langmuir–Hinshelwood model, emphasizing their advanced catalytic properties. For supercapacitor applications, the ZnO NPs attained a high specific capacitance of 550 F/g at 1 A/g, underscoring their potential as energy storage solutions. Additionally, the nanoparticles demonstrated strong UV-induced antiradical activity, with an EC₅₀ of 32.2 μg/mL in DPPH assays. Notably, the cytotoxicity evaluation revealed an LC₅₀ of 1648 μg/mL, indicating excellent biocompatibility. This study highlights a sustainable approach for the synthesis of multifunctional ZnO NPs that offers effective solutions for environmental remediation, energy storage, and biomedical applications. Full article