Organic-inorganic Nanocomposites Research Articles

Research Progress and Application of Layered Rare Earth Hydroxides, a Class of Inorganic Layered Compounds with Photoluminescence.

Inorganic layered compounds are an important part of organic-inorganic functional nanocomposites and offer plentiful opportunities and possibilities for synthesizing new-style multifunctional materials because they could be intercalated, exfoliated, and swollen. In recent years, as inorganic layered materials with photoluminescence, layered rare earth hydroxides (LRHs) have been extensively studied. Due to their rich functionalization ways, they have been applied or shown potential application value in many fields such as pollution detection, biomedicine, photoelectric energy storage, and so on. On account of the basic physical and chemical properties, the basic structures of LRHs may be regulated through exfoliation and intercalation, which provides more possibilities for synthesizing new multifunctional composite materials and broadening and updating their application fields. In this paper, LRHs are extracted from inorganic layered compounds, and the structure, synthesis, research progress, and application of LRHs are summarized in detail, which lays a great theoretical foundation for further exploration and optimization of the application as a composite functional material in industry, medicine, detection, optoelectronics, and other fields.

Anionic polysaccharides mixture control the assembly of nanoscale building blocks of calcium carbonate into hierarchical spherical and rod-shaped mesocrystals.

Biominerals, as complex organic-inorganic nanocomposites synthesized by organisms, exhibit unique properties across various scales. This study investigates the role of soluble organic molecules, specifically acidic polysaccharides such as N-carboxymethyl chitosan (CMC) and chondroitin 6-sulfate (ChS), in regulating the formation of calcium carbonate mesocrystals. Using a precipitation method, the effects of these polymers on the morphology, size, and polymorphism of mesocrystals were evaluated. The findings reveal that the interactions between calcium carbonate and the polymers dictate the morphology of primary nanoparticles, which subsequently assemble into spherical or rod-shaped mesocrystals. Carboxylated polymers were found to stabilize the vaterite phase, while sulfated polymers favored calcite formation. By fine-tuning the polymer quantities, addition rate, and mixing technique, the size and aspect ratio of the mesocrystals can be precisely controlled, enabling targeted morphogenesis. This strategy not only advances the design of tailored mesocrystals but also deepens our understanding of nonclassical crystallization processes mediated by soluble organic biomacromolecules.

Effective remediation of mercury (II) from aqueous solutions using CS-MnFe2O4-CoS-MWCNTs: Box-Behnken design optimization and adsorption isotherm, kinetics, and thermodynamics evaluation.

Mercury (Hg) is a hazardous heavy metal, non-biodegradable and toxic, posing a serious threat to aquatic life and human health. Therefore, the removal of Hg ions from contaminated water using effective and eco-friendly adsorbents is necessary. In the present study, three magnetic chitosan-based organic-inorganic nanocomposites, such as CS-MnFe2O4, CS-MnFe2O4-CoS, and CS-MnFe2O4-CoS-MWCNTs, were designed and constructed to investigate their capacity for adsorbing Hg ions from aqueous solutions. The physicochemical properties of prepared composites were characterized by various analyses. The BET analyses indicated their high surface area and porous structure, and the N2 adsorption-desorption showed that the modification of CS in three stages by MnFe2O4 and crosslinking reaction, CoS preparation, and MWCNT incorporation resulted in increased N2 adsorption. The XRD confirms the synthesis of MnFe2O4 and CoS in the CS matrix and also the distinct peaks of MWCNTs. The CS-MnFe2O4-CoS-MWCNTs showed acceptable thermal stability with 45% char yields and superparamagnetic properties with magnetic saturation (Ms) of 16 emu g-1. The interactive impacts of independent variables (pH, contact time, and adsorbent dosage) on the removal percentage of Hg(II) onto three prepared adsorbents, as well as the process optimization, were assessed by the Box-Behnken design. The optimum conditions were identified, and the data from the analysis of variance showed that the three independent factors (pH, contact time, and adsorbent dosage) significantly influenced the adsorption of Hg(II). The adsorption isotherm and thermodynamics analysis investigation showed that at low concentrations of Hg(II), the adsorption process was both endothermic and spontaneous for the studied adsorbents.

Synergetic benefits of zinc antimony oxide/reduced graphene oxide hybrid anode for enhanced sodium-ion storage

Organic-inorganic hybrid nanocomposites are rapidly evolving as a new generation of materials with attractive properties for electrochemical energy storage. Unfortunately, their practical applications in sodium-ion batteries (SIBs) still require further research due to the unsatisfactory cycling stability and rate performance. This work explores using zinc antimony oxide/reduced graphene oxide (ZSO/rGO) hybrid nanocomposite as an anode material in SIBs. After 150 cycles at 0.05 A g−1, the ZSO/rGO electrode delivers a specific capacity of 357.21 mAh g−1 with a coulombic efficiency of 99.3 %, which is almost 2.5-fold higher than the specific capacity of the pristine ZSO electrode. An in-situ Raman spectroscopy study demonstrates that the sodiation/desodiation mechanism in the ZSO/rGO electrode involves the conversion and alloying reactions in the ZSO nanoparticles. Further electrochemistry analysis reveals that the nanocomposite anode shows synergistic effects by coupling diffusion and surface contribution, in which the latter plays an important role.

Enhancing Power Conversion Efficiency of Organic Solar Cells with Magnetoplasmonic Fe3O4@Au@m-ABS Nanoparticles.

Organic-inorganic nanocomposites have the potential to be used in photovoltaic materials due to their eco-friendliness, suitable band gaps, and high stability. In this work, we integrated gold and Fe3O4 magnetic nanoparticles with poly-m-amino benzene sulfonic (m-ABS) to synthesize Fe3O4@Au@poly-(m-aminobenzenesulfonic acid) (Fe3O4@Au@m-ABS) magneto-plasmonic nanoparticles (MPNPs) to enhance the performance of the organic photovoltaic (OPV). These MPNPs exhibit broad UV-Vis absorption and a low band gap of 2.878 eV, enhancing their suitability for photovoltaic applications. The MPNPs were introduced into the ZnO electron transporting layer (ETL) and active layer to investigate the influence of MPNPs on the power conversion efficiency (PCE) of the OPVs. When 0.1 vol% MPNPs were incorporated in the ETL, the OPVs achieved a PCE of 14.24% and a fill factor (FF) of 69.10%. On the other hand, when 0.1 vol% MPNPs were incorporated in the active layer, the OPVs showed a PCE of 14.11% and an FF of 68.83%. However, the OPVs without MPNPs only possessed a PCE of 13.15% and an FF of 63.69%. The incorporation of MPNPs increased the PCE by 8.3% in the OPV device. These findings suggest that Fe3O4@Au@m-ABS MPNPs are promising nanocomposite materials for enhancing the performance of OPVs.

Biosustainable Multiscale Transparent Nanocomposite Films for Sensitive Pressure and Humidity Sensors.

Light weight, thinness, transparency, flexibility, and insulation are the key indicators for flexible electronic device substrates. The common flexible substrates are usually polymer materials, but their recycling is an overwhelming challenge. Meanwhile, paper substrates are limited in practical applications because of their poor mechanical and thermal stability. However, natural biomaterials have excellent mechanical properties and versatility thanks to their organic-inorganic multiscale structures, which inspired us to design an organic-inorganic nanocomposite film. For this purpose, a bio-inspired multiscale film was developed using cellulose nanofibers with abundant hydrophilic functional groups to assist in dispersing hydroxyapatite nanowires. The thickness of the biosustainable film is only 40 μm, and it incorporates distinctive mechanical properties (strength: 52.8 MPa; toughness: 0.88 MJ m-3) and excellent optical properties (transmittance: 80.0%; haze: 71.2%). Consequently, this film is optimal as a substrate employed for flexible sensors, which can transmit capacitance and resistance signals through wireless Bluetooth, showing an ultrasensitive response to pressure and humidity (for example, responding to finger pressing with 5000% signal change and exhaled water vapor with 4000% signal change). Therefore, the comprehensive performance of the biomimetic multiscale organic-inorganic composite film confers a prominent prospect in flexible electronics devices, food packaging, and plastic substitution.

Design and synthesis of LDH nano composite functionalized with trimesic acid and its environmental application in adsorbing organic dyes indigo carmine and methylene blue

This work designed and prepared an organic-inorganic nanocomposite using layered double hydroxide (LDH) inorganic substrate and trimesic acid (TMA) as chelating agent. Subsequently, the synthesized organic-inorganic nanocomposite was assessed using multiple identification methods, including FTIR, EDX, XRD, TGA, and FESEM, and the outcomes demonstrated that the intended structure was successfully prepared. Also, in order to investigate the efficiency of the Mg–Al LDH-TMA nanocomposite as an efficient nano adsorbent, it was used for removal of indigo carmine (IC) and methylene blue (MB) from aqueous solutions. This synthetic nanocomposite showed a high adsorption capacity. The efficiency of the produced nanocomposite in the adsorption of selected dyes was investigated with the help of batch adsorption studies performed in a variety of experimental settings, including dye concentration, adsorbent dose, pH, adsorption temperature and contact time. Furthermore, the produced Mg–Al LDH-TMA nanocomposite exhibits strong stability and can be recycled and reused five times in a row, which is well consistent with the principles of green chemistry.

Fabrication of rGO-decorated hBNNS hybrid nanocomposite via organic-inorganic interfacial chemistry for enhanced electrocatalytic detection of carcinoembryonic antigen.

Organic-inorganic hybrid nanocomposites (OIHN), with tailored surface chemistry, offer ultra-sensitive architecture capable of detecting ultra-low concentrations of target analytes with precision. In the present work, a novel nano-biosensor was fabricated, acquainting dynamic synergy of reduced graphene oxide (rGO) decorated hexagonal boron nitride nanosheets (hBNNS) for detection of carcinoembryonic antigen (CEA). Extensive spectroscopic and microscopic analyses confirmed the successful hydrothermal synthesis of cross-linked rGO-hBNNS nanocomposite. Uniform micro-electrodes of rGO-hBNNS onto pre-hydrolyzed ITO were obtained via electrophoretic deposition (EPD) technique at low DC potential (15V). Optimization of antibody incubation time, pH of supporting electrolyte, and immunoelectrode preparation was thoroughly investigated to enhance nano-biosensing efficacy. rGO-modified hBNNS demonstrated 29% boost in electrochemical performance over bare hBNNS, signifying remarkable electro-catalytic activity of nano-biosensor. The presence of multifunctional groups on the interface facilitated stable crosslinking chemistry, increased immobilization density, and enabled site-specific anchoring of Anti-CEA, resulting in improved binding affinity. The nano-biosensor demonstrated a remarkably low limit of detection of 5.47pg/mL (R2 = 0.99963), indicating exceptional sensitivity and accuracy in detecting CEA concentrations from 0 to 50ng/mL. The clinical evaluation confirmed its exceptional shelf life, minimal cross-reactivity, and robust recovery rates in human serum samples, thereby unraveling the potential for early, highly sensitive, and reliable CEA detection.

Synthesis of organic-inorganic hybrid nanocomposites modified by catalase-like catalytic sites for the controlling of kiwifruit bacterial canker.

Kiwifruit bacterial canker, caused by Pseudomonas syringae pv. Actinidiae (Psa), is one of the most important diseases in kiwifruit, creating huge economic losses to kiwifruit-growing countries around the world. Metal-based nanomaterials offer a promising alternative strategy to combat plant diseases induced by bacterial infection. However, it is still challenging to design highly active nanomaterials for controlling kiwifruit bacterial canker. Here, a novel multifunctional nanocomposite (ZnO@PDA-Mn) is designed that integrates the antibacterial activity of zinc oxide nanoparticles (ZnO NPs) with the plant reactive oxygen species scavenging ability of catalase (CAT) enzyme-like active sites through introducing manganese modified polydopamine (PDA) coating. The results reveal that ZnO@PDA-Mn nanocomposites can efficiently catalyze the conversion of H2O2 to O2 and H2O to achieve excellent CAT-like activity. In vitro experiments demonstrate that ZnO@PDA-Mn nanocomposites maintain the antibacterial activity of ZnO NPs and induce significant damage to bacterial cell membranes. Importantly, ZnO@PDA-Mn nanocomposites display outstanding curative and protective efficiencies of 47.7% and 53.8% at a dose of 200 μg mL-1 against Psa in vivo, which are superior to those of zinc thiozole (20.6% and 8.8%) and ZnO (38.7% and 33.8%). The nanocomposites offer improved in vivo control efficacy through direct bactericidal effects and decreasing oxidative damage in plants induced by bacterial infection. Our research underscores the potential of nanocomposites containing CAT-like active sites in plant protection, offering a promising strategy for sustainable disease management in agriculture.

Physicochemical and structural characteristics of hybrid nanocomposites based on branched polyimide with a low content of inorganic component

The series of organic-inorganic hybrid nanocomposites based on branched polyimide matrix and with different amounts of tetraethoxysilane (TEOS) (5, 20, and 50 wt.% of the initial polyamic acid mass) were synthesized and studied using nitroxyl paramagnetic probe, measuring dielectric permittivity, X-ray structural analysis and optical microscopy. It was shown that in some cases the introduction of inorganic component is accompanied by a decrease in the segmental mobility of polyimide matrix as a result of the partial immobilization of organic macrochains during the formation of inorganic microregions. In the presence of inorganic component, a weak dependence of the polymer permeability on the content of the organic component in the system is observed, also the specific density changes little with an increase in TEOS content. Extreme changes in the segmental mobility and dielectric permittivity of the branched matrix formed in the presence of 5 wt% TEOS were found compared to systems of other compositions. This can be caused to a large extent by structural changes in the system. At a low content of TEOS occurs significant «loosening» of organic matrix, a sharp decrease in the dielectric constant and a significant increase in the segmental mobility of the polyimide matrix. Small angle X-ray scattering diffractograms demonstrate drastic changes in polyimide composite heterogeneity in the presence of 5 wt.% TEOS content. According to the optical microscopy data, the introduction of TEOS into polyimide is accompanied by the formation of microaggregates of inorganic nanoparticles in the system, the number and average size of which depend on the SiO2 content and looks most homogeneous at a low TEOS content.

Catalytic effect of N-phenylaminopropyl polyheadral oligomeric silsesquioxane in the synthesis of hybrid nanocomposites based on polycyanurate

Organic-inorganic nanocomposites based on heat-resistant crosslinked polycyanurate (PCN) and N-phenylaminopropyl polyhedral oligomeric silsesquioxane (NPAP-POSS), containing eight reactive secondary amino groups, were synthesized using the in situ reactive formation method. Fourier transmission infrared (FTIR) spectroscopy and dynamic differential scanning calorimetry (DSC) methods were used to study the effect of NPAP-POSS on the kinetics of bisphenol E dicyanate ester (DCBE) polycyclotrimerization during the formation of PCN in PCN/NPAP-POSS nanocomposites. The content of the nanofiller was varied from 0.05 to 1.00 wt.%. Based on the results of FTIR spectral studies, the main kinetic peculiarities of PCN formation were found and their changes under the action of NPAP-POSS nanofiller were determined. A significant catalytic effect of NPAP-POSS on the polycyclotrimerization of DCBE was found, which is confirmed by a decrease in the time of the onset of auto-acceleration, an acceleration of the conversion of cyanate groups of DCBE and the formation of triazine cycles of PCN, an increase in the values of the maximum reaction rate, a decrease in the duration of the reaction, etc. The dynamic DSC method also confirmed the catalytic effect of NPAP-POSS on the formation of PCN in the nanocomposites and established the main kinetic characteristics depending on the content of the nanofiller: a significant decrease in the temperature of the exothermic maximum, an increase in the reaction enthalpy, non-monotonic changes in the induction period and reaction rate, etc. From the analysis of the experimental data, it was concluded that the detected changes in the kinetics of the in situ reaction formation of PCN/NPAP-POSS nanocomposites and the recorded catalytic effect of the nanofiller are due to the fact that two chemical processes occur during the synthesis of the nanocomposites: chemical interaction of –O–C≡N groups of DCBE with secondary –NH groups of NPAP-POSS, which led to further embedding of nanoparticles into the resulting polymer matrix and the direct polycyclotrimerization of DCBE with formation of hybrid polycyanurate network. Schemes of the sequential reactions explaining the catalytic effect of the nanofiller in the synthesis of hybrid PCN/NPAP-POSS nanocomposites are proposed. It was concluded that under the selected conditions of the synthesis, the greatest catalytic effect of the nanofiller is manifested at its content of 0.10 wt.%, since for this sample the maximum shift of the reaction exothermic peak towards lower temperatures, the maximum reaction rate, and the minimum induction period and reaction start temperature were recorded. The results of the research make it possible to optimize the synthesis of heat-resistant materials promising for use in special-purpose structures.

Colorimetric detection of Staphylococcus aureus based on self-linkable and hollow organic-inorganic nanocomposites as light-driven oxidase-like nanozyme for cascade signal amplification

Facing increasingly serious bacterial infections and their threat to food safety and human health, exploring specific and sensitive bacterial strategies is indispensable. Nanozyme-based colorimetric biosensors with the superiorities of easy-to-read and catalytic signal amplification have attracted increasing interest. However, few investigations relate to the nanozymes with excellent light-driven oxidase-like activity. In this study, a sensitive colorimetric biosensor for Staphylococcus aureus (S. aureus) detection was constructed based on a light-driven oxidase-like nanozyme (PHCS@CuNcPOPTP) as well as the self-chain linking process. The hollow organic-inorganic nanocomposite (PHCS@CuNcPOPTP) was prepared by a one-step Friedel-Crafts alkylation reaction. The PHCS@CuNcPOPTP exhibited excellent and synergistically enhanced light-driven oxidase-like activity originating from its unique photosensitive properties. Subsequently, PHCS@CuNcPOPTP was served as a scaffold, loading with the rabbit anti-Staphylococcus aureus Rosenbach tropina antibody (bs-4582R, Ab2), DNA1, and DNA2, respectively, to construct signal probes (PHCS@CuNcPOPTP@Au-Ab2/DNA1, PHCS@CuNcPOPTP@Au-DNA1, and PHCS@CuNcPOPTP@Au-DNA2). By the repetitive DNA hybridization among signal probes, a large amount of PHCS@CuNcPOPTP-DNA dendrimers were formed and utilized to trigger the chromogenic reaction without the participation of high-concentration H2O2, resulting in the cascaded catalytic amplification and the lower background signal. As expected, the suggested sensing platform presented ultrasensitive bacterial detection with a remarkably broad linear range (101 to 108 CFU/mL) and a limit of detection (LOD, 3.40 CFU/mL).

Sol-Gel Derived Gelatin-Bioactive Glass Nanocomposite Biomaterials Incorporating Calcium Chloride and Calcium Ethoxide.

Calcium-containing organic-inorganic nanocomposites play an essential role in developing bioactive bone biomaterials. Ideally, bone substitute materials should mimic the organic-inorganic composition of bone. In this study, the roles of calcium chloride (CaCl2) and calcium ethoxide (Ca(OEt)2) were evaluated for the development of sol-gel-derived organic-inorganic biomaterials composed of gelatin, bioactive glass (BG) and multiwall carbon nanotubes (MWCNTs) to create nanocomposites that mimic the elemental composition of bone. Nanocomposites composed of either CaCl2 or Ca(OEt)2 were chemically different but presented uniform elemental distribution. The role of calcium sources in the matrix of the nanocomposites played a major role in the swelling and degradation properties of biomaterials as a function of time, as well as the resulting porous properties of the nanocomposites. Regardless of the calcium source type, biomineralization in simulated body fluid and favorable cell attachment were promoted on the nanocomposites. 10T1/2 cell viability studies using standard media (DMEM with 5% FBS) and conditioned media showed that Ca(OEt)2-based nanocomposites seemed more favorable biomaterials. Collectively, our study demonstrated that CaCl2 and Ca(OEt)2 could be used to prepare sol-gel-derived gelatin-BG-MWCNT nanocomposites, which have the potential to function as bone biomaterials.

Biodistribution and human absorbed dose evaluation of an organic-inorganic nanocomposite containing 198Au (198Au/PG4D)

Biodistribution and human absorbed dose evaluation of an organic-inorganic nanocomposite containing 198Au (198Au/PG4D)

Optimizing magnetic, dielectric, and antimicrobial performance in chitosan-PEG-Fe2O3@NiO nanomagnetic composites

There is a growing interest in eco-friendly and cost-effective organic-inorganic nanocomposites due to their alignment with the principles of “green” chemistry, as well as their biocompatibility and non-toxicity. This study focused on producing Chitosan-PEG-Fe2O3@NiO nanomagnetic composites to improve the stability, dielectric properties, and antimicrobial effectiveness of these nanocomposite materials. The process involved synthesizing Fe2O3@NiO via sol-gel and polymerizing chitosan-PEG. The nanocomposites were characterized by XRD, TEM, FTIR, optical, dielectric, and VSM. Incorporating Fe2O3@NiO significantly improved stability, and the interaction with Fe2O3 during the sol-gel process facilitated the formation of NiFe2O4 with an increase in the crystallinity within the chitosan-PEG matrix. The study examined optical and dielectric properties, highlighting that the 3 NiO-doped chitosan-PEG-Fe2O3 composites had high electrical conductivity (1.8 ∗ 10−3 S/cm) and a significant dielectric constant (106 at low frequencies). As the ratio of NiO NPs within the chitosan-PEG-Fe2O3 increases, the energy band gap of chitosan-PEG-Fe2O3 films decreases up to 3.7 eV. This decrease is owing to the quantum confinement effect. These composites also demonstrated improved antimicrobial activity against E. coli and S. aureus and higher activity in the presence of nanomagnetic particles. The minimum inhibitory concentrations of CS-PEG-Fe2O3/NiO NPs against (Bacillus cereus, M. luteus, S. aureus and (S. enterica, H. pylori, E. coli) were (22–35 mm) and (21–34 mm), respectively.

Efficient pre-concentration of trace levels of the synthetic food dye in foodstuff samples through an adsorption extraction technique using a novel inorganic–organic nanocomposite

In the present study, a maleic acid-functionalized exfoliated graphite/calcium hydroxide (MA-EG/Ca(OH)2) was constructed and employed as a novel inorganic–organic nanocomposite for an efficient dispersive solid-phase microextraction (DSPME) of trace levels of sunset yellow (SY), a synthetic food dye in foodstuff samples before UV–Vis determination. To identify and characterize of the sorbent, various analytical techniques were utilized, including, Fourier transform-infrared spectroscopy (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX), and Brunauer-Emmett-Teller (BET) analyses. The MA-EG/Ca(OH)2 exhibited a specific surface area of 40.35 m2 g−1 and adsorption capacity of 46.72 mg g−1 towards SY. Central composite design (CCD) in conjunction with a response surface methodology (RSM)-based ANOVA analysis was applied for evaluation and optimization of effective factors including pH (X1), sorbent mass (X2), contact time (X3), and elution volume (X4). According to the results, the optimum values were pH: 6.0, sorbent mass: 12 mg, contact time: 12 min, and elution volume: 0.18 µL. Under theses optimized conditions, DSPME/UV–Vis determination demonstrated a linear range of 50–4800 ng mL−1, a limit of detection (LOD) of 12.45 ng mL−1, and a limit of quantification (LOQ) of 41.49 ng mL−1 (n = 3). The relative standard deviation (RSD) at low concentration level (50–500 ng mL−1) of SY was 4.58 %. Recovery values in different concentration levels were in the range of 96.4–102.9 %. Overall, the proposed method showed the superior features, including ease of synthesizing the sorbent, acceptable LOD and LOQ values, remarkable sensitivity, a wide operational range, good reusability (up to five cycles), environmentally friendly as well as cost-effectiveness, that make it a promising candidate for the analysis of SY in foodstuff samples.

Protein-guided biomimetic nanomaterials: a versatile theranostic nanoplatform for biomedical applications.

Over the years, bioinspired mineralization-based approaches have been applied to synthesize multifunctional organic-inorganic nanocomposites. These nanocomposites can address the growing demands of modern biomedical applications. Proteins, serving as vital biological templates, play a pivotal role in the nucleation and growth processes of various organic-inorganic nanocomposites. Protein-mineralized nanomaterials (PMNMs) have attracted significant interest from researchers due to their facile and convenient preparation, strong physiological activity, stability, impressive biocompatibility, and biodegradability. Nevertheless, few comprehensive reviews have expounded on the progress of these nanomaterials in biomedicine. This article systematically reviews the principles and strategies for constructing nanomaterials using protein-directed biomineralization and biomimetic mineralization techniques. Subsequently, we focus on their recent applications in the biomedical field, encompassing areas such as bioimaging, as well as anti-tumor, anti-bacterial, and anti-inflammatory therapies. Furthermore, we discuss the challenges encountered in practical applications of these materials and explore their potential in future applications. This review aspired to catalyze the continued development of these bioinspired nanomaterials in drug development and clinical diagnosis, ultimately contributing to the fields of precision medicine and translational medicine.

Polypyrrole fabricated Laponite RD conductive nanocomposites: influence of grafting efficiency on structural and conductive properties.

In the present work novel conductive organic-inorganic nanocomposites were produced by grafting of pyrrole monomer onto silanized Laponite RD utilizing emulsion graft polymerization. Influence of some important factors like concentration of monomer, initiator and surfactant were investigated on grafting efficiency. Grafting of polypyrrole chains onto modified Laponite RD was verified by Fourier transform infrared spectroscopy (FT-IR). Scanning electron microscope (SEM) revealed the spherical particles of nanocomposite with average diameter of 271.5 nm. XRD pattern showed that molecular framework of pure polypyrrole almost remains same in nanocomposite. Surface area and pore volume of Laponite RD, measured by Brunauer-Emmett-Teller (BET) analysis, was also altered indicating effective grafting of polypyrrole chains onto modified substrate. Maximum grafting efficiency (%), determined gravimetrically, was 87.3% at monomer, initiator, and surfactant concentrations of 1.50, 1.00, and 0.50% respectively. Prepared nanocomposites with grafting efficiency of 87.3% have displayed maximum electrical conductivity of 0.23 × 10-2 Scm-1. These nanocomposites can be used for manifold applications like biomedical and energy storage devices.

Advances in organic–inorganic nanocomposites for cancer imaging and therapy

Abstract “All in one” organic–inorganic nanocomposites with high biocompatibility and excellent physicochemical properties have recently attracted special attention in cancer imaging and therapy. Combination of organic and inorganic materials confers the nanocomposites with superior biocompatibility and biodegradability of organic materials, as well as magnetic, mechanical, and optical properties of inorganic materials. Increased endeavors have been made to produce diverse organic–inorganic nanocomposites and investigate their potential applications in cancer treatment. Thus, a systematic review of research progresses of diverse organic–inorganic nanocomposites in cancer imaging and therapy is indispensable. Following a brief overview of nanocomposites synthesis, classification, and functionalization, the current review is focused on comprehensively summarizing representatives of both organic–inorganic nanoscale nanocomposites (including organic-silica, organic-carbon, organic-quantum dots, organic-platinum family metals, organic-gold, organic metal oxides, and other nanocomposites) and organic–inorganic molecular nanocomposites (including metal-organic frameworks, organosilica nanoparticles, and amorphous metal coordination polymer particles), and further analyzing their working mechanism in cancer imaging and therapy. Finally, the challenges and future perspectives of organic–inorganic nanocomposites are addressed for promoting their developments and clinical application in cancer treatment.

Interfacial Tension-Impelled Self-Assembly and Morphology Tuning of Poly(3,4-ethylene dioxythiophene)/Tellurium Nanocomposites at Various Liquid/Liquid Interfaces.

Compared to the enormous number of nanostructures that have been documented, the variety of nanostructures produced by organic polymerization is rather limited. We devised an unconventional route and a sustainable approach to distribute tellurium nanoparticles (Te NPs) in a poly(3,4-ethylene dioxythiophene) (PEDOT) matrix to form semiconducting organic-inorganic nanocomposites for potential applications in electrochemical sensing. The adopted strategy of in situ liquid/liquid interface-assisted polymerization aids in the formation of intimately tethered Te NPs on the PEDOT polymer chains, thereby preventing the aggregation of Te NPs. The untapped versatility inherent to using biphasic systems for interfacial polymerization is explored at three interface systems of immiscible solvents: chloroform/water, dichloromethane/water, and hexane/water, giving rise to PEDOT/Te nanocomposite (PTeNC) of distinct morphology. Chemical nature, crystallinity, and morphology investigations proved the successful formation of PTeNC in different interface systems. Consequently, the temporal evolution of interfacial tension in the preferential adsorption of nanoparticles and final product morphology was monitored by pendant drop tensiometry. Owing to the role of morphology, PTeNC synthesized at the hexane/water interface showcased the best electrocatalytic behavior toward nonenzymatic detection of l-ascorbic acid, an essential nutritional factor, and a neuromodulator with a limit of detection of 0.66 μM and excellent sensitivity, selectivity, and reproducibility. Hence, we envision that interface-assisted polymerization offers a nascent and robust strategy for encapsulating unusual electrode materials in polymeric matrices.