Surface Of Nanofibers Research Articles

Surface modification of chitin nanofibers with dopamine as efficient nanosorbents for enhanced removal of dye pollution and metal ions

The development of environmentally friendly and low-cost adsorbents with high adsorption capacity remains a challenge. Herein, chitin nanofiber-polydopamine composite materials (CNDA) have been obtained by surface modification of chitin nanofiber using dopamine. According to the results of transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier Transform Infrared Spectrometer (FTIR), and X-ray photoelectron spectrometer (XPS), polydopamine have been successfully coated on the surface of chitin nanofiber (ChNF). The ability to remove methylene blue (MB) has been analyzed via standard adsorption experiments, indicating that the maximum adsorption capacity (qmax) can reach 196.6 mg/g at MB initial concentration of 50 mg/L. Most importantly, the adsorption kinetics, isotherm, and thermodynamics were used to investigate the MB adsorption mechanism on composites. This indicated that the polydopamine on the surface of chitin nanofiber (ChNF) plays an important role in the MB dye adsorption. Moreover, the removal ability of CNDA to metal ions has also been investigated, indicating high capacities for Fe3+, Mn2+, Cu2+, and Ni2+. Based on their biodegradability and good adsorption capacity, the CNDA composite material can be considered a promising adsorbent for wastewater treatment.

Growth of bimetallic Ni-Co MOFs on a skeleton of electrospun PAN nanofibers and coating on a thin film for SPME of amitriptyline and nortriptyline in urine and plasma samples

In this research, composited bimetallic organic framework-polyacrylonitrile (Ni-Co MOFs-PAN) was applied for thin-film solid phase microextraction (TF-SPME) of tricyclic antidepressant (TCA) drugs from biological samples. The separation and quantification of the analytes were accomplished by HPLC-UV. First, seeded nanofibers with organic ligands were electrospun on a sheet of foil. Then, with the uniform in-situ solvothermal growth of Ni-Co MOFs on the skeletal surface of nanofibers, the nanoparticles were successfully attached to the surfaces without effective bonds and produced a thin layer with a high flexibility, large active surface and abundant functional groups for adsorption. The characteristics of the produced nanocomposite were investigated by Fourier-transform infrared spectroscopy, field emission-scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectroscopy and Brunauer-Emmett-Teller analysis. The stirring rate, pH, ionic strength, adsorption and desorption time along with type and volume of desorption solvents as influential factors on extraction efficiencies of the analytes, were optimized by one variable at a time method. Under optimized conditions, wide linear range for analytes in water and plasma matrices were obtained from 0.2 to 1000.0 μg L−1 and 1.0–1000.0 μg L−1, respectively, with R2 ≥ 0.9925. The limits of detection were in the range of 0.06–0.3 μg L−1 in different media. Good repeatability and reproducibility were attained within intra-day, inter-day and film-to-film RSDs% (n = 3) below 3.3 %, 3.9 % and 4.7 %, respectively. Since desirable relative recoveries were calculated between 91.4 % and 100.4 %. The method can be used for the successful extraction and measurement of amitriptyline and nortriptyline as its metabolite in different sampling time from urine and plasma matrices.

Nano Ag/PPy Biocomposites Based on Graphene Oxide Modified Bacterial Cellulose from the Juice of Xinhui Citrus and Its Antibacterial Activity.

Bacterial cellulose (BC) is a green, natural biopolymer with excellent biocompatibility and a film-forming ability. However, its lack of inherent antibacterial activity restricts its application in medical materials and food preservation. In this study, BC derived from the juice of discarded Xinhui citrus was obtained through fermentation and further modified in situ with graphene oxide (GO) to obtain BC(GO). Subsequently, BC(GO) was loaded with cell-compatible polypyrrole (PPy) and antibacterial agent silver nanoparticles (AgNPs) to prepare Ag-PPy/BC(GO) composite films. Composite films were characterized using Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS) to evaluate their chemical structure and morphology. The results demonstrate effective adsorption of PPy and AgNPs onto the surface of BC nanofibers modified with GO. Antibacterial experiments reveal synergistic antibacterial effects of PPy and AgNPs. The Ag-PPy/BC(GO) membranes exhibit strong antibacterial activity against both Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), with 48-h growth inhibition rates of 75-84% and 82-84%, respectively.

Biosynthesis of Zinc Oxide Nanoparticles on l-Carnosine Biofunctionalized Polyacrylonitrile Nanofibers; a Biomimetic Wound Healing Material.

Multifunctional biohybrid nanofibers (NFs) that can simultaneously drive various cellular activities and confer antibacterial properties are considered desirable in producing advanced wound healing materials. In this study, a bionanohybrid formulation was processed as a NF wound dressing to stimulate the adhesion and proliferation of fibroblast and endothelial cells that play a major role in wound healing. Polyacrylonitrile (PAN) electrospun NFs were hydrolyzed using NaOH and biofunctionalized with l-carnosine (CAR), a dipeptide which could later biosynthesize zinc oxide (ZnO) nanoparticles (NPs) on the NFs surface. The morphological study verified that ZnO NPs are uniformly distributed on the surface of CAR/PAN NFs. Through EDX and XRD analysis, it was validated that the NPs are composed of ZnO and/or ZnO/Zn(OH)2. The presence of CAR and ZnO NPs brought about a superhydrophilicity effect and notably raised the elastic modulus and tensile strength of Zn-CAR/PAN NFs. While CAR ligands were shown to improve the viability of fibroblast (L929) and endothelial (HUVEC) cells, ZnO NPs lowered the positive impact of CAR, most likely due to their repulsive negative surface charge. A scratch assay verified that CAR/PAN NFs and Zn-CAR/PAN NFs aided HUVEC migration more than PAN NFs. Also, an antibacterial assay implied that CAR/PAN NFs and Zn-CAR/PAN NFs are significantly more effective in inhibiting Staphylococcus aureus (S. aureus) than neat PAN NFs are (1000 and 500%, respectively). Taken together, compared to the neat PAN NFs, CAR/PAN NFs with and without the biosynthesized ZnO NPs can support the cellular activities of relevance for wound healing and inactivate bacteria.

A facile route for concurrent fabrication and surface selective functionalization of cellulose nanofibers by lactic acid mediated catalysis

Celulose nanofibers are lightweight, recycable, biodegradable, and renewable. Hence, there is a great interest of using them instead of fossil-based components in new materials and biocomposites. In this study, we disclose an environmentally benign (green) one-step reaction approach to fabricate lactic acid ester functionalized cellulose nanofibrils from wood-derived pulp fibers in high yields. This was accomplished by converting wood-derived pulp fibers to nanofibrillated “cellulose lactate” under mild conditions using lactic acid as both the reaction media and catalyst. Thus, in parallel to the cellulose nanofibril production, concurrent lactic acid-catalyzed esterification of lactic acid to the cellulose nanofibers surface occured. The direct lactic acid esterification, which is a surface selective functionalization and reversible (de-attaching the ester groups by cleavage of the ester bonds), of the cellulose nanofibrils was confirmed by low numbers of degree of substitution, and FT-IR analyses. Thus, autocatalytic esterification and cellulose hydrolysis occurred without the need of metal based or a harsh mineral acid catalysts, which has disadvantages such as acid corrosiveness and high recovery cost of acid. Moreover, adding a mineral acid as a co-catalyst significantly decreased the yield of the nanocellulose. The lactic acid media is successfully recycled in multiple reaction cycles producing the corresponding nanocellulose fibers in high yields. The disclosed green cellulose nanofibril production route is industrial relevant and gives direct access to nanocellulose for use in variety of applications such as sustainable filaments, composites, packaging and strengthening of recycled fibers.

Improved anti-biofilm activity and long-lasting effects of novel serratiopeptidase immobilized on cellulose nanofibers.

Today, enzymatic treatment is a progressive field in combating biofilm producing pathogens. In this regard, serratiopeptidase, a medicinally important metalloprotease, has been recently highlighted as an enzyme with proved anti-biofilm activity. In the present study, in order to increase the long-lasting effects of the enzyme, serratiopeptidase and the novel engineered forms with enhanced anti-biofilm activity were immobilized on the surface of cellulose nanofibers (CNFs) as a natural polymer with eminent properties. For this, recombinant serratiopeptidases including the native and previously designed enzymes were produced, purified and conjugated to the CNF by chemical and physical methods. Immobilization was confirmed using different scanning and microscopic methods. The enzyme activity was assessed using casein hydrolysis test. Enzyme release analysis was performed using dialysis tube method. Anti-biofilm activity of free and immobilized enzymes has been examined on Staphylococcus aureus and Pseudomonas aeruginosa strains. Finally, cytotoxicity of enzyme-conjugated CNFs was performed by MTT assay. The casein hydrolysis results confirmed fixation of all recombinant enzymes on CNFs by chemical method; however, inadequate fixation of these enzymes was found using cold atmospheric plasma (CAP). The AFM, FTIR, and SEM analysis confirmed appropriate conjugation of enzymes on the surface of CNFs. Immobilization of enzymes on CNFs improved the anti-biofilm activity of serratiopeptidase enzymes. Interestingly, the novel engineered serratiopeptidase (T344 [8-339ss]) exhibited the highest anti-biofilm activity in both conjugated and non-conjugated forms. In conclusion, incorporation of serratiopeptidases into CNFs improves their anti-biofilm activities without baring any cytotoxicity. KEY POINTS: • Enzymes were successfully immobilized on cellulose nanofibers using chemical method. • Immobilization of enzymes on CNFs improved their anti-biofilm activity. • T344 [8-339ss] exhibited the highest anti-biofilm activity in both conjugated and non-conjugated forms.

New plasma-assisted polymerization/activation route leading to a high density primary amine silanization of PCL/PLGA nanofibers for biomedical applications

Surface modification of hydrophobic nanofibers (NFs) to introduce cell-interactive chemical functionalities remains a challenge in biomedical applications. This study presents a novel three-step plasma-based method for synthesizing coatings with improved chemical selectivity compared to conventional plasma polymers. The process involved hexamethyldisiloxane (HMDSO) plasma polymerization followed by helium plasma activation, both performed in a medium-pressure dielectric barrier discharge. Scanning electron microscopy analysis demonstrated that the plasma-based steps did not cause damage to the NFs. X-ray photoelectron spectroscopy (XPS) and water contact angle measurements revealed the formation of a hydrophilic silanol-rich layer after HMDSO plasma polymerization and helium plasma activation. In the third step, (3-aminopropyl)triethoxysilane (APTES) was grafted onto the plasma polymer to introduce primary amine groups onto the surface, as confirmed by XPS. Although the APTES-based layer exhibited partial removal when exposed to aqueous environments, a stable aminated layer remained on the NF surface, which significantly enhanced Schwann cell responses compared to untreated and HMDSO-based coated NFs. This enhancement was confirmed through fluorescent imaging using live-dead staining, immunostaining, and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. These coatings with a high selectivity in their chemical functionality (amines, or other functionalities via silanization agent selection), offer a promising surface functionalization approach for tissue engineering scaffolds.

Multi‐Analyte Sensitive Fluorophore Cross‐Linked Nanofibers Based Antimicrobial Surface Enabling Bacterial Detection and Their Usage as Crystal Growth Template

AbstractIn situ preparation of bifunctional thiazolo[5,4‐d]thiazole (TTz)‐based fluorophore cross‐linked nanofibers is successfully performed. These multifunctional nanofibers are used as both crystal growth template and antibacterial substrate that makes bacterial detection possible simultaneously. These highly fluorescent nanofibers act as optical sensors toward many analytes. The acid, base, and metal cation‐sensitive nature of the 2,5‐bis(4‐hydroxyphenyl)thiazolo[5,4‐d]thiazole (HPhTT) dye makes the prepared PVA nanofibers sensitive against these chemicals. Metal nanoparticles (MNPs) or metal oxide crystal formation occurs on the surface of nanofibers without any reducing agent. The strong interaction between metal cations and fluorophores results in crystal formation on the surface, which is named for the first time as “complexation‐triggered crystalization.” These dye cross‐linked and metal‐interacted nanofibers exhibit antibacterial effect against E. coli (ATCC 25922), S. aureus (ATCC 25923), P. aeruginosa (ATCC 27853), and E. faecalis (ATCC 25922) strains. Also, the emission wavelength change of nanofibers in bacterial contamination makes it possible to use smart nanofiber films for optical bacteria detection. These novel materials pave the way for new applications such as smart wound bands, optical sensors, and one‐step preparation of surface‐enhanced Raman spectroscopy substrate.

Configurations Manipulation of Electrospun Membranes Based on High‐Entropy Alloys–Enabled High‐Performance Solar Water Evaporation

Solar‐driven interfacial steam technology converts photons into heat energy directly and therefore realizes the effective removal of environmental pollutants, which presents huge potential in seawater desalination and freshwater production. To realize efficient and rapid solar‐driven water evaporation, developing and designing efficient photothermal conversion materials is of great significance. Herein, a high‐entropy alloy (HEA) fiber membrane with rapid heating and wide spectral response is synthesized via adjusting high‐entropy metals diffusion on the surface of carbon nanofibers by an electrospinning technology. Benefiting from the low equivalent evaporation enthalpy and high solar spectrum capacity of HEA fibers, the HEA (FeCoNiCuMn)‐carbon nanofiber‐5S2 achieves a rapid steam‐generation rate of 2.74 kg m−2 h−1 with a solar‐to‐vapor conversion efficiency of 99.4% under 1 sun illumination. In addition, the evaporator presented a stable seawater desalination and wastewater purification performance. Therefore, the HEA‐based solar evaporator can be an alternative photothermal material for efficient solar steam generation.

Design and Fabrication of Electrospun PLA-Based Silica-Modified Composite Nanofibers with Antibacterial Properties for Perspective Wound Treatment.

The aim of this study was to develop a novel amikacin (AMI) delivery system with prolonged release based on composite electrospun nanofibers of PLA supplemented with AMI-loaded Si nanoparticles of different morphology. The resultant materials were characterized in terms of their physical properties (scanning electron microscopy, Brunauer-Emmett-Teller analysis, thermogravimetric analysis, water contact angle). High-Performance Liquid Chromatography was used to determine the AMI content in the liquid fractions obtained from the release study. The results show that nanofibers of fumed silica exhibited an aggregated, highly porous structure, whereas nanofibers of mesoporous silica had a spherical morphology. Both silica nanoparticles had a significant effect on the hydrophilic properties of PLA nanofiber surfaces. The liquid fractions were investigated to gauge the encapsulation efficiency (EE) and loading efficiency (LE) of AMI, demonstrating 66% EE and 52% LE for nanofibers of fumed silica compared to nanofibers of mesoporous silica nanoparticles (52% EE and 12.7% LE). The antibacterial activity of the AMI-loaded nanofibers was determined by the Kirby-Bauer Method. These results demonstrated that the PLA-based silica nanofibers effectively enhanced the antibacterial properties against the Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae.

Reduced thermal conductivity and improved ZT of Cu-doped SnS-based bulk thermoelectric materials via compositing SnS nano-fiber strategy

Tin sulfide (SnS), as a low-cost and eco-friendly thermoelectric (TE) material, exhibits relatively poor phonon and charge transport capacities when the long-range ordered layered crystal structure is broken by the grain boundaries of polycrystalline. Nevertheless, doping and compositing are effective strategies for improving the electrical and thermal conductivity. Herein, utilizing the composite powders synthesized via Cu-doped SnS nanosheets grown in-situ on the surface of Cu-doped SnS nanofibers, we design a homogeneous nanofibers composited Cu-doped SnS polycrystalline bulk to boost its TE performance. Comparing with pure phase SnS, Cu doping can effectively increase the carrier concentration and mobility of SnS, realizing an increase of electrical conductivity from 4.11 S·cm−1 to 31.57 S·cm−1. Simultaneously, quite a number of fiber/matrix composite interfaces for phonon scattering are formed due to incorporating of composite nanofibers, which significantly reduce the lattice thermal conductivity of Cu-doped SnS polycrystalline bulk. The results show that thermal conductivity reduced as low as 0.64 W·m−1 K−1 at 324 K when the additive amount of nanofibers was fix at 2 wt%. Ultimately, the power factor and ZT value are markedly enhanced at low and medium temperature ranges (300–500 K) compared with SnS polycrystalline bulk without fiber incorporation. This provides an effective strategy for optimizing the thermoelectric performance of SnS-based polycrystalline.

Multi-Channel Hollow Carbon Nanofibers with Graphene-Like Shell-Structure and Ultrahigh Surface Area for High-Performance Zn-Ion Hybrid Capacitors.

Porous carbon is the most promising cathode material for Zn-ion hybrid capacitors (ZIHCs), but is limited by insufficient active adsorption sites and slow ion diffusion kinetics during charge storage. Herein, a pore construction-pore expansion strategy for synthesizing multi-channel hollow carbon nanofibers (MCHCNF) is proposed, in which the sacrificial template-induced multi-channel structure eliminates the diffusion barrier for enhancing ion diffusion kinetics, and the generated ultrahigh surface area and high-density defective structures effectively increase the quantity of active sites for charge storage. Additionally, a graphene-like shell structure formed on the carbon nanofiber surface facilitates fast electron transport, and the highly matchable pore size of MCHCNF with electrolyte-ions favors the accommodation of charge carriers. These advantages lead to the optimized ZIHCs exhibit high capacity (191.4mAhg-1 ), high energy (133.1Whkg-1 ), along with outstanding cycling stability (93.0% capacity retention over 15000 cycles). Systematic ex situ characterizations reveal that the dual-adsorption of anions and cations synergistically ensures the outstanding electrochemical performance, highlighting the importance of the highly-developed porous structure of MCHCNF. This work not only provides a promising strategy for improving the capacitive capability of porous materials but also sheds light on charge storage mechanisms and rational design for advanced energy storage devices.

Electrospun core-sheath PCL nanofibers loaded with nHA and simvastatin and their potential bone regeneration applications.

Introduction: Drugs and biocompatible nanoparticles have raised significant potential in advancing the bone regeneration. Electrospinning technology enables the full realization of the value of drugs and nanoparticles. Methods: In this study, we have successfully fabricated core-sheath nanofibers solely composed of polycaprolactone (PCL) polymer. Simvastatin (SIM) was confined to the core of the nanofibers while nanohydroxyapatite (nHA) was loaded on the nanofiber surface. Results: All the prepared nanofibers exhibited a cylindrical micromorphology, and the core-sheath structure was exploited using a Transmission Electron Microscope. X-ray pattern results indicated that SIM was in an amorphous state within nanofibers, while Fourier Transform InfraRed spectroscopy showed excellent chemical compatibility among SIM, nHA, and PCL. The actual loading of nHA within the nanofiber was determined by a thermogravimetric test due to the high melting point of nHA. Core-sheath nanofibers could release SIM for 672h, which was attributed to the core-sheath structure. Furthermore, nanofibers loaded with SIM or nHA had a positive impact on cell proliferation, with the core-sheath nanofibers displaying the most favorable cell proliferation behavior. Discussion: Such a synergistic facilitation strategy based on materials and nanostructure may encourage researchers to exploit new biomedical materials in future.

Preparation, characterization, and bioactivity of reinforced monetite with chitosan-gelatin electrospun composite scaffold for bone tissue engineering

In this study, chitosan-gelatin-monetite (CGM)-based electrospun scaffolds have been developed that closely mimicked the microstructure and chemical composition of the extracellular matrix of natural bone. CGM-based nanofibrous composite scaffolds were prepared with the help of the electrospinning technique, post-cross-linked using ethyl(dimethylaminopropyl)carbodiimide and N-hydroxysuccinimide solution to improve their stability in an aqueous environment. The prepared chitosan/gelatin (CG) scaffold showed an average fiber diameter of 308 ± 17 nm, whereas 5 and 7 wt% monetite containing CGM5 and CGM7 scaffolds, exhibited an average fiber diameter of 287 ± 13 and 265 ± 9 nm, respectively, revealing the fine distribution of monetite particles on the fibrous surface. The distribution of monetite nanoparticles onto the CG nanofibrous surface was confirmed using x-ray diffraction, Fourier transform infrared, and EDAX. Moreover, the addition of 7 wt% monetite into the CG electrospun matrix increased their ultimate tensile strength from 7.62 ± 0.13 MPa in the CG scaffold to 14.34 ± 0.39 MPa in the CGM7 scaffold. Simulated body fluid study and staining with alizarin red S (ARS) confirmed the higher mineralization ability of monetite-containing scaffolds compared to that revealed by the CG scaffold. The monetite incorporation into the CG matrix improved its osteogenic properties, including pre-osteoblast MG-63 cell adhesion, proliferation, and differentiation, when seeded with the cells. A higher degree of cellular adhesion, spreading, and migration was observed on the monetite-incorporated CG scaffold than that on the CG scaffold. From 3-(4, 5-dimethylthiazol-2-yl-2, 5-diphenyltetrazolium bromide) MTT assay, alkaline phosphatase activity, ARS staining, and immunocytochemistry study, the cultured cells discovered a more conducive microenvironment to proliferate and subsequently differentiate into osteoblast lineage in contact with CGM7 nanofibers rather than that in CGM0 and CGM5. In-vitro results indicated that electrospun CGM-based composite scaffolds could be used as a potential candidate to repair and regenerate new bone tissues.

Iridium incorporated cobalt-based hydroxide on nickel-contained carbon nanofibers renders highly efficient oxygen evolution reaction

The construction of high-performance oxygen evolution reaction (OER) electrocatalysts is crucial for energy applications. Here, we demonstrate a reliable route to incorporate iridium (Ir) into cobalt (Co)-based hydroxide derived from ZIF-67 on the surface of Ni-contained carbon nanofibers (denoted as Ni-CNFs/Ir-Co(OH)2) as an electrocatalyst to boost its alkaline OER property. The optimized Ni-CNFs/Ir-Co(OH)2 sample exhibits an extraordinary OER activity with an overpotential of only 240 mV to reach 10 mA cm−2, much lower than that of commercial IrO2 electrocatalyst (331 mV). The theoretical results illustrate the highly active Co sites of Iredge-Co(OH)2 for OER. Furthermore, the distinct nanofibrous architecture of Ni-CNFs endows with a desirable electrical conductivity of the catalyst, thus the Ni-CNFs/Ir-Co(OH)2 sample presents a desirable durability for OER testing. In addition, a total water electrolyzer is built by using the prepared Ni-CNFs/Ir-Co(OH)2 and Pt/C as electrodes, which requires only 1.50 V at 10 mA cm−2, superior to the value of Pt/C||IrO2 cell (1.62 V). This study puts forward an effective route to explore superior OER electrocatalysts by engineering the electronic structure of metal hydroxide for energy applications.

All-in-one coupling of 3D hybridized nanocarbon microelectrode for portable monitoring of doxycycline hyclate

The simultaneous balance of electrode materials and electrode structures can energize the development of innovative electrochemical sensors. In this work, a 3D nanocarbon layer of hybrid heteroatoms and metal atoms (CN/Fe) with excellent electrical properties and abundant active sites was self-constructed on the surface of a quartz-based nanofiber by high-temperature pyrolysis. Further, the nanofiber tip was selected as the sensing region to develop an electrochemical sensing platform with high sensitivity, miniaturization, and portability. A common broad-spectrum antibiotic (Doxycycline hyclate, DOX) was used as a model to evaluate the designed miniaturized sensing platform, and the stability, reproducibility, and applicability of the microsensor were verified in a variety of real samples, including algal solution, milk, human serum, and cell culture media. The results show that the proposed sensing platform has a detection limit as low as 82 nM in aqueous environments. Furthermore, it is further shown that coupling the design of electrode materials and electrode structures facilitates the development of electrochemical sensors with more practical applications. This concept will open up new avenues for the development of electrochemical sensors that meet many application scenarios.

Structural, optical, and thermal investigation of SnO2 nanoparticles incorporated PANI nanofibers as an emissive layer material

Nowadays, polyaniline (PANI) based nanocomposites have emerged as a boon that has opened a new door for researchers working in a wide range of applications, including optoelectronic devices, electrochromic devices, batteries, medicinal materials, and imaging devices. Pure PANI and PANI/SnO2 nanocomposites were synthesized via chemical oxidative polymerization using FeCl3 as an oxidative agent. FESEM analysis reveals a spherical aggregated structure of SnO2 nanoparticles on the surface of PANI nanofibers. Particle sizes of 15% PS nanocomposite are estimated to be 12–23 nm through HR-TEM. XPS has been employed to find out the chemical oxidation states of the optimized nanocomposites. Direct optical band gaps and optical conductivities of nanocomposites were calculated via Tauc's plot method through UV–Visible spectroscopy. Thermogravimetric study shows the thermal stability is enhanced for the 15% PS nanocomposite. The PL intensity of the PANI can be tuned by varying the concentrations of SnO2 nanoparticles. The highest PL intensity is observed for 15% PS nanocomposite. Color purity is estimated at ∼91.6% for blue emission color. Enhanced PL intensity and thermal stability are insisted that 15% PS nanocomposite might be used as an emissive material in polymer-based blue light-emitting diodes application.

Electrospun PA6 Nanofibers Bearing the CeO2 Dephosphorylation Catalyst.

Two types of CeO2 nanoparticles (CeNPs) prepared by low-temperature (<100 °C) precipitation methods in water were successfully immobilized in a matrix of electrospun PA6 nanofibers. The colloidal solutions of CeNPs in AcOH were directly mixed with the polymer solution before the needle electrospinning process, thereby achieving their good dispersion in the nanofibers. CeNPs embedded in the structure and on the surface of nanofibers exposing their reactive surfaces showed robust dephosphorylation catalytic activity, as demonstrated by monitoring the hydrolytic cleavage of three phosphodiester molecules (p-NP-TMP, p-NPPC, BNPP) in water by the HPLC method. This procedure allowed us to study the kinetics and mechanism of the hydrolytic cleavage and the ability of immobilized CeNPs to cleave different types of P-O bonds. One of the main hydrolysis products, p-nitrophenol, was effectively adsorbed on PA6 nanofibers, which may allow the selective separation of the degradation products after hydrolysis.

Enhanced stability of methylammonium lead bromide perovskite interlaced on cellulose nanofiber

The interest in highly luminescent organic-inorganic hybrid perovskite, methylammonium lead bromide (MLB) nanocrystals (NCs) has grown significantly due to their many applications in optoelectronics. However, the biggest hurdle has been the effective use of the materials in large optoelectronic applications and their poor stability in various environmental conditions. To address the problem of the poor stability of highly luminescent MLB nanostructures, we synthesized MLB NCs on the surface of cellulose nanofibers (CNF) for the first time. The synthesized (MLB@CNF) composite shows green emission peak at 529 nm. The scanning electron microscopy images confirm that perovskite NCs are well attached to the surface of cellulose nanofiber. These composite materials offer improved stability and luminescent features in moist environments for over six months. The developed interfacial interaction strategy will provide a novel approach to obtain durable nanocrystals using cellulose-based materials.

Fabrication of Visible Light Sensitive Electrospun TiO2 Nanofibers Using Squaric Acid for Photocatalytic Application

Degradation of organic pollutants using photocatalysts has gained utmost importance, due to the increasing environmental pollution. Despite various attempts to improve the photocatalytic efficiency of well-known photocatalysts such as titanium dioxide (TiO2), by making them visible light active, various issues need to be resolved. In this work, attempts have been made to improve the visible light absorption capacities of the electrospun TiO2 nanofibers by modification using squaric acid (SqA). An interfacial charge transfer complex is formed by the condensation reaction between the hydroxyl groups on the surface of the TiO2 nanofibers and the SqA ligand. Various characterizations confirmed that the modification using SqA had led to the formation of the interfacial charge transfer layer, without affecting the crystallinity or morphology of the TiO2 nanofibers. The modified TiO2 nanofibers showed sensitivity to visible light with red shift in the optical absorption. It exhibited an improved photocatalytic efficiency of 85% against the degradation of tetracycline, compared with 60% for unmodified TiO2 nanofibers. It also showed an increased rate of degradation of 0.21 mg/L/min, when compared with the 0.13 mg/L/min of unmodified TiO2 nanofibers.