Synthesis Of Nanostructures Research Articles

Synthesis of dumbbell-like heteronanostructures encapsulated in ferritin protein: Towards multifunctional protein based opto-magnetic nanomaterials for biomedical theranostic

Dumbbell-like hetero nanostructures based on gold and iron oxides is a promising material for biomedical applications, useful as versatile theranostic agents due the synergistic effect of their optical and magnetic properties. However, achieving precise control on their morphology, size dispersion, colloidal stability, biocompatibility and cell targeting remains as a current challenge. In this study, we address this challenge by employing biomimetic routes, using ferritin protein nanocages as template for these nanoparticles’ synthesis. We present the development of an opto-magnetic nanostructures using the ferritin protein, wherein gold and iron oxide nanostructures were produced within its cavity. Initially, we investigated the synthesis of gold nanostructures within the protein, generating clusters and plasmonic nanoparticles. Subsequently, we optimized the conditions for the superparamagnetic nanoparticles synthesis through controlled iron oxidation, thereby enhancing the magnetic properties of the resulting system. Finally, we produce magnetic nanoparticles in the protein with gold clusters, achieving the coexistence of both nanostructures within a single protein molecule, a novel material unprecedented to date. We observed that factors such as temperature, metal/protein ratios, pH, dialysis, and purification processes all have an impact on protein recovery, loading efficiency, morphology, and nanoparticle size. Our findings highlight the development of ferritin-based nanomaterials as versatile platforms for potential biomedical use as multifunctional theranostic agents.

A novel approach ofdifferentiation of adenoma and carcinoma in lung cancer based on biogenic in situ synthesis of gold nanostructures on various oligonucleotide motifs.

Aunique approach is introducedfor constructing gold nanocrystals (AuNCs) with RNA motif-directed morphologies in a sequence-independent manner and itsapplications in theclinical areaare described. By using this method, a label-free LSPR-based detection method for the SOX2OT transcript, long non-coding RNAs (lncRNAs), which is a prognostic indicator of poor survival in lung cancer patientsis presented. For the first time, we examined how the structural changes of RNA after the heteroduplex formation with a specific DNA probe can change the morphology and LSPR band of AuNCs. Using this method, is was possible to differentiate lung squamous cell carcinoma from adenocarcinoma samples without a need for a prior amplification of the target lncRNA. The approach of using specific DNA probe enables the in situ synthesis of nanocrystals in a different way and expands this method for future translational medicine, particularly detection of specific RNA.

A Family of Twisted Chiral Engineered Inorganic Nanoarchitectures.

Chiral inorganic materials possess unique asymmetric properties that could significantly impact various fields. However, their practical application has been hindered by challenges in creating structurally robust chiral materials. We report the synthesis of well-defined chiral-shaped hollow cobalt oxide nanostructures, extendable to a family of chalcogenides including sulfide, selenide, and telluride through topological transformations. Taking chiral cobalt oxide nanostructures as a representative material, we demonstrate precise control over their chiral architectures, enabling fine-tuning of parameters, such as twist degrees, handedness, and compositions. These chiral nanostructures exhibit high spin selectivity effects that influence the electron transfer processes in catalytic reactions. Leveraging this spin-selective behavior, the chiral cobalt oxide nanoarchitectures demonstrate enhanced electrocatalytic performance in the oxygen evolution reaction compared to their achiral counterparts. Our findings not only expand the library of chiral inorganic materials but also advance the application of chiral effects in fields such as catalysis, spintronics, and beyond.

Integrated One-Step Fabrication of Protonic Sensing Devices for Respiratory Monitoring.

The development of direct fabrication routes with seamless integration of both the macro/micropatterning process and nanostructure synthesis is crucial for the commercial realization of cost-effective nanoscale sensor devices. This, if realized, can liberate us from the conventional limitations inherent in nanoscale device manufacturing. Specifically, such fabrication routes can, in principle, address the challenges such as the complexity, multistep nature, and substantial costs associated with existing technologies, which are not suitable for widespread market adoption in everyday-use devices. Herein, we propose a novel yet facile one-step fabrication approach that simultaneously accomplishes both patterning and nanostructure synthesis by employing low-power, cost-effective laser technology with a minimal environmental footprint. Versatile in nature, this approach can enable the incorporation of diverse functionalities spanning a broad spectrum of technologies, encompassing fields such as sensors, catalysts, photonics, energy storage, and biomedical monitoring devices. As a proof of concept, using our approach, we fabricated an ultra responsive, high-speed protonic sensing device for real-time respiratory monitoring. The enhanced temporal characteristics of our as-fabricated device, particularly in the relative humidity levels of interest in breath monitoring (typically over 55%), exhibited a superior response/recovery time in rapid humidity fluctuations. We envisage that the advantages brought by the presented fabrication approach can pave the way to establish a new method for inexpensive large-scale functional-material-based device fabrication.

Snowflake Iron Oxide Architectures: Synthesis and Electrochemical Applications

The synthesis and characterization of iron oxide nanostructures, specifically snowflake architecture, are investigated for their potential applications in electrochemical sensing systems. A Raman spectroscopy analysis reveals phase diversity in the synthesized powders. The pH of the synthesis affects the formation of the hematite (α-Fe2O3) and goethite (α-FeOOH). Scanning electron microscopy (SEM) images confirm the distinct morphologies of the particles, which are selectively obtained through recrystallization during the elongated reaction time. An electrochemical analysis demonstrates the differing behaviors of the particles, with synthesis pH affecting the electrochemical activity and surface area differently for each shape. Cyclic voltammetry measurements reveal reversible dopamine detection processes, with snowflake iron oxide showing lower detection limits than a mixture of snowflakes and cube-like particles. This research contributes to understanding the relationship between iron oxide nanomaterials’ structural, morphological, and electrochemical properties. It offers practical insights into their potential applications in sensor technology, particularly dopamine detection, with implications for biomedical and environmental monitoring.

In Situ Electrochemical Conversion of Biomass-Derived 5-Hydroxymethylfurfural into 2,5-Furandicarboxylic Acid by Time-Controlled Aerosol-Assisted Chemical Vapor Deposited FeNi Catalyst.

The conversion of 5-hydroxymethylfurfural (HMF) into valuable chemicals, such as 2,5-furandicarboxylic acid (FDCA), is pivotal for sustainable chemical production, offering a renewable pathway to biodegradable plastics and high-value organic compounds. This pioneering study explores the synthesis of FeNi nanostructures via aerosol-assisted chemical vapor deposition (AACVD) for the electrochemical oxidation of HMF to FDCA. By adjusting the deposition time, we developed two distinct nanostructures: FeNi-40, which features nanowires with spherical terminations, and FeNi-80, which features aggregated spherical structures. X-ray diffraction (XRD) confirmed that both nanostructures possess a phase-pure face-centered cubic (FCC) crystal structure. Electrochemical tests conducted using FeNi nanocatalysts on Ni foam revealed that FeNi-40 requires a significantly lower onset potential for HMF oxidation (1.32 V vs RHE) compared to FeNi-80 (1.40 V vs RHE). This difference is attributed to the unique nanowire morphology of FeNi-40, which provides a higher density of active sites and a larger electrochemically active surface area, thereby enhancing the efficiency of the electrochemical process. When tested in an H-type electrolyzer with a Nafion membrane, FeNi-40 demonstrated a remarkable Faradaic efficiency of 96.42% and a high product yield, underscoring the potential of morphology-controlled FeNi nanostructures to enhance the efficiency of sustainable electrochemical processes significantly.

Hybrid Silica Cage-Type Nanostructures Made from Triply Hydrophilic Block Copolymers Single Micelles.

Controlling the structure and functionality of porous silica nanoparticles has been a continuous source of innovation with important potential for advanced biomedical applications. Their synthesis, however, usually involves passive surfactants or amphiphilic copolymers that do not add value to the material after synthesis. In contrast, polyion complex (PIC) micelles based on hydrophilic block copolymers allow for the direct synthesis of intrinsically functional hybrid materials. While most previous studies have focused on bulk materials made from double-hydrophilic block copolymers (DHBC), in this work we have synthesized a triple-hydrophilic block copolymer (THBC) and demonstrated both its PIC micellization and its potential for hybrid mesoporous silica nanomaterials. Introducing this THBC has allowed to direct the transition from bulk three-dimensional (3D) materials to zero-dimensional (0D) nanomaterials with cage-type structures. The stabilization and isolation of these nanostructures formed around discrete individual micelles has been made possible by the careful design of the three different blocks that each play a key role. These nanostructures could also be synthesized from hybrid PIC micelles based on THBC-multivalent metal ions complexes, offering a direct route to metal/silica composite nanoparticles. This class of THBC polymers therefore creates significant opportunities for the synthesis of nanostructures with complex and functional architectures.

A Lab Prototype for Rapid Electrochemical Detection of Escherichia coli in Water Using Modified Screen-Printed Electrodes.

Recognizing the need for a hand-held device capable of quantitatively measuring the concentration of bacteria in water, this paper describes a label-free method for rapid detection of Escherichia coli (E. coli) in water via H2O2 decomposition using screen-printed electrodes (SPE) modified with nanostructured metal oxide layers. The study encompasses sensor preparation, bacteria culture, synthesis and characterization of nanostructures, and development of a readout circuitry for lab prototyping. During sensing measurements, the bacteria are first made to interact with H2O2 and subsequently, the H2O2 solution is exposed on the sensing surface. The electrochemical sensors are fabricated by modifying the working electrode of SPE with nanostructured metal oxide layers of MnO2 and TiO2 as these play a crucial role in the detection of E. coli in water. The sensing experiments of MnO2-modified SPE show a significant response to bacteria with a sensitivity of 0.82 mV.mL/log CFU and a limit of detection (LOD) of 1.8 CFU/mL, while the TiO2-modified SPE exhibits a linear response over a wide range of bacterial concentrations with a sensitivity of 1.12 mV·mL/log CFU and a limit of detection of 2.23 CFU/mL. Both sensors demonstrate a rapid response, stability, repeatability, and a recovery time of 70 ms. Additionally, selectivity with respect to other bacteria, wastewater components such as glucose, ammonium sulfate, and sodium carbonate, and testing with RO, DI, and tap water samples are conducted to evaluate the sensors' performance. A detailed sensing mechanism has been developed to comprehend the results, including chemical and biological reactions, metal oxide interfaces, morphology, and other surface studies of the sensing surface. A prototype comprising a sensor chip, an Arduino board, and other necessary circuit components is tested with various bacterial solutions. This enables its use for on-field rapid detection of bacteria in water using smaller volumes and a portable system.

Synthesis and optical properties of SnO2 nanostructure as a novel photosensitizer for deep tumor treatment in photodynamic therapy using UV light and X-ray radiation

Synthesis and optical properties of SnO2 nanostructure as a novel photosensitizer for deep tumor treatment in photodynamic therapy using UV light and X-ray radiation

Synthesis, optical absorption, luminescence, chromaticity, and catalytic properties of undoped CuO and Gd-doped CuO nanostructures for LED devices and waste water treatment applications

The first objective of this present investigation is the co-precipitation synthesized of undoped and various concentrations of Gd-doping in the CuO material as a photocatalyst and methylene blue dye under passing solar light radiation, followed by obtaining their photocatalytic degradation efficiency of 88–96%. Using photoluminescence (PL) data of synthesized undoped and 1%, 3%, and 5 wt% Gd-doped CuO to make a chromaticity diagram for identifying the colour coordinates to scrutinize the applications of light-emitting devices. To trace the diffraction peaks, related crystal system, and vibrational bond of undoped and Gd-doped CuO materials by XRD and FT-IR studies. The morphological structure has been varied in each Gd-dopant concentration when compared to undoped CuO nanostructures through SEM studies. The aforementioned material has a narrow band gap and strong visible emission, as identified by UV–visible and PL spectra.

Seed-Mediated Growth and Advanced Characterization of Chiral Gold Nanorods.

The controlled growth of gold nanostructures with complex shapes and reduced symmetry, exemplified by chiral gold nanorods and nanoparticles, is one of the most dynamic fields of nanochemistry. A timely summary of underlying concepts, including growth mechanisms and redefined chirality measures, would further promote this research area. In this perspective, we aim to establish qualitative connections between the chiral shapes and growth conditions, specifically for the seed-mediated synthesis of chiral gold nanorods as a convenient case of chiral morphogenesis. The crystallographic and morphological features of achiral nanorods used as seeds, the experimental conditions during chiral growth, and the symmetry of the chiral inducers, can all be exploited to obtain nanorods with intricate chiral shapes. Chirality characterization (such as electron tomography techniques) and quantification (including chirality measures) emerge as critical aspects to comprehensively explore and understand such structures, enabling optimization of their geometric and optical features. We conclude by discussing relevant challenges to be addressed toward a better controlled synthesis of chiral plasmonic nanostructures.

Synthesis and Antibacterial Properties of Manganese Dioxide Nanostructures: A Review

Synthesis and Antibacterial Properties of Manganese Dioxide Nanostructures: A Review

Synthesis of ZnO nanostructure via CBD and solvothermal method using seed technique

Synthesis of ZnO nanostructure via CBD and solvothermal method using seed technique

Carboxymethyl cellulose assisted morphology controlled synthesis of Mn3O4 nanostructures for adsorptive removal of malachite green from water

The physicochemical properties of manganese oxides and their different applications mainly depend upon their crystallite size, morphology, phase structure, and surface properties, which are again dependent on the preparation methods. So, a simple, cost-effective, and versatile synthesis method for such materials is highly desirable. Intending to accomplish this, herein we report the synthesis of Mn3O4 nanostructures by alkaline hydrolysis of the corresponding metal ions in an aqueous medium. The addition of a biodegradable polymer, sodium salt of carboxymethyl cellulose (Na-CMC) assisted the development of specific morphology, which is tunable by varying the concentration of the biopolymer. The spectroscopic, microscopic, and diffractometric analyses of the synthesized Mn3O4 nanostructures confirm that this particular simple technique is very effective in controlling the morphology of the formed nanostructures. These Mn3O4 nanostructures exhibit excellent adsorption capacity in the removal of malachite green (MG) from its aqueous solution under ambient conditions. The adsorption process is exothermic following pseudo-second-order kinetics with a maximum dye adsorption capacity of 489.68 mg g−1 according to the Sips isotherm model. The Mn3O4 nanostructures can be reused for up to five cycles of dye adsorption without significant loss of their adsorption performance.

Nanostructured codoped neodymium orthoferrite synthesized via the hydrothermal route for photocatalytic annihilation of crystal violet dye

Current research demonstrates the synergistic effects of gadolinium (Gd)/copper (Cu) codoping and nanotechnology on various physicochemical and photocatalytic features of neodymium iron oxide (NIO) perovskites. X-ray diffraction (XRD) and Fourier transform infrared (FTIR) studies the synthesis of pure neodymium oxide (NIO-I) and its codoped counterpart (NIO-II) with a perovskite-type crystal structure via simple hydrothermal techniques. Through codoping and nanostructural synthesis, the surface characteristics, as well as the optical, electrical, and optoelectronic properties of the neodymium iron oxide perovskite, were enhanced, as confirmed by Brunner−Emmett−Teller (BET), UV/Vis, current−voltage (I−V), and photoluminescence (PL) studies. In terms of photocatalytic activity, the NIO-II perovskite outperforms its undoped NIO-I counterpart, eliminating 91.8 % of crystal violet (CV) dye in less than 50 min with a rate constant value (k) of 0.019 min−1. However, the undoped counterpart removed 63.8 % of the CV dye, with a comparatively lower rate constant of 0.013 min−1 under the same conditions. Under alkaline conditions, the NIO-II catalyst demonstrates superior efficiency in degrading CV dye; moreover, it maintains an efficiency of 96.8 %, even after undergoing five cycles of reuse. Through the use of rare earth and transition metal codoping, this study reveals a new way to fine-tune the structural and other pertinent properties of semiconductor perovskites, ensuring their practical use for the treatment of polluted water.

Silver shelled gold nanorods for sensitive detection of cholesterol and triglycerides

We report the synthesis of bimetallic plasmonic nanostructure of silver shelled gold nanorods (Ag–Au NRs), subsequently employed for the selective detection of cholesterol (Cho) and triglycerides (TGl) utilizing Surface Enhanced Raman Spectroscopy (SERS). In this direction, the gold nanorods (Au NRs) were synthesized via seed mediated growth method followed by forming a silver shell with reduction of AgNO3 onto Au NRs. Ag–Au NRs showed significantly augmented SERS property owing to hybridization of Localized Surface Plasmon Resonances (LSPR) of silver and gold. The enhanced plasmonic property was thus employed for biosensing. For this, two different Raman reporter molecules, 5,5′–dithiobis–(2–nitrobenzoic acid) (DTNB) and 4–aminothiophenol (4ATP) were immobilized separately on Ag–Au NRs to synthesize SERS active nanoprobes, before the attachment of the bioreceptors – cholesterol oxidase (ChOx) and lipase (Lp) to form ChOx–DTNB–Ag–Au NRs and Lp–4ATP–Ag–Au NRs. These nanoprobes were then utilized for the quantification of Cho and TGl via liquid mode Raman spectroscopic study. The change in SERS spectral intensity of DTNB and 4ATP were systematically recorded in reference to the baseline sample to mark the calibration for both Cho and TGl. Additionally, interference studies considering effects of ascorbic acid, glucose, sodium and potassium ion were performed to unveil excellent selectivity of the proposed method.

Composite hydroxide mediated synthesis of barium-doped strontium oxide nanostructures for energy storage applications

Composite hydroxide mediated synthesis of barium-doped strontium oxide nanostructures for energy storage applications

A density functional benchmark for dehydrogenation and dehalogenation reactions on coinage metal surfaces.

The on-surface synthesis of low-dimensional organic nanostructures has been extensively investigated through both experimental and theoretical methods, particularly by density functional theory (DFT). However, the complex mixture of interactions often poses challenges within the DFT framework, and there is a knowledge-gap regarding how the choice of DFT approach affects the computed results. Here, five different approaches including vdW interactions, i.e., PBE+D3, PBE+vdWsurf, rev-vdW-DF2, r2SCAN+rVV10 and BEEF-vdW, are employed to describe three prototypical on-surface reactions; dehydrogenation of benzene, debromination of bromobenzene, and deiodination of iodobenzene on the (111) facets of the coinage metals. Overall, rev-vdW-DF2 outperforms the other methods in describing benzene adsorption, whereas BEEF-vdW falls short. For dehydrogenation and debromination on Cu(111), all functionals except BEEF-vdW give reasonable activation energies compared to experiments. A similar trend is observed for Ag(111) and Au(111), with BEEF-vdW yielding significantly higher activation and reaction energies. For dehalogenation, all the five vdW approaches correctly capture the reactivity trend - Cu(111) > Ag(111) > Au(111) - and the expected hierarchy between bromobenzene desorption and carbon- bromine activation. Only BEEF-vdW fails to predict the faster kinetics of deiodination than the iodobenzene desorption.Our work forms a basis for evaluating density functionals in describing chemical reactions on surfaces.

Hyperthermia and biological investigation of a novel magnetic nanobiocomposite based on acacia gum-silk fibroin hydrogel embedded with poly vinyl alcohol

The design and synthesis of biocompatible nanostructures for biomedical applications are considered vital challenges. Herein, a nanobiocomposite based on acacia hydrogel, natural silk fibroin protein, and synthetic protein fibers of polyvinyl alcohol was fabricated and magnetized with iron oxide nanoparticles (Fe3O4 MNPs). The structural properties of the hybrid nanobiocomposite were investigated by essential analyses such as Fourier Transform Infrared Spectrometer (FTIR), Field emission scanning electron microscopy (FE-SEM), and X-ray powder diffraction)XRD(analyses, Thermogravimetric and Differential thermogravimetric analysis (TGA-DTG), Vibrating-sample magnetometry (VSM), and Energy Dispersive X-Ray Analysis (EDX). The biological activities and functional properties of the prepared magnetic nanobiocomposite were studied. Results proved that this nanobiocomposite is non-toxic to the healthy HEK293T cell line. In addition, the synthesized nanobiocomposite showed an approximately 22 % reduction in cell viability of BT549 cells after 72 h. All results confirmed the anti-cancer properties of nanobiocomposite against breast cancer cell lines. Therefore, the prepared nanobiocomposite is an excellent material that can use for in-vivo application. Finally, the hyperthermia application was evaluated for this nanobiocomposite. The SAR was measured 93.08 (W/g) at 100 kHz.

Synthesis of Starfish-Shaped ZnS Nanostructures by Hydrothermal Method and Their Electrochemical Sensing of Dopamine.

Introduction Dopamine serves an essential function as a neurotransmitter, influencing the regulation of movement, cognitive processes, and emotional states. The identification of abnormal dopamine levels is critical for clinical diagnoses and scientific research, given its links to various disorders, including depression, schizophrenia, and Parkinson's disease. The distinctive electrochemical characteristics, stability, and broad bandgap of zinc sulfide (ZnS) nanostructures render them particularly fascinating. The hydrothermal method is recognized as an effective and economical approach for the fabrication of ZnS nanostructures, exhibiting a range of morphologies. Utilizing this method to create ZnS nanostructures leads to the formation of structures characterized by extensive surface areas, hierarchical designs, and improved electrochemical properties. Aim The objective is to examine the electrochemical characteristics of ZnS starfish-shaped nanostructures produced through the hydrothermal technique and to assess their viability as a sensing platform for dopamine detection. Materials and methods To synthesize ZnS nanoflowers, stoichiometric amounts of transition metal salts were prepared: 10 mM of Zn(NO3)2•3H2O and 30 mM of sodium thiosulfate (Na2S2O3•5H2O) were dissolved in 30 mL of deionized water and stirred for 20 minutes. The solutions were then combined and transferred into a 100 mL Teflon autoclave reactor, which was heated at 200 °C for 12 hours in a furnace. This process utilized the hydrothermal technique to produce the desired ZnS nanoflowers. Result The crystalline arrangement of ZnS was validated by X-ray diffraction (XRD) analysis, aligning with the Joint Committee on Powder Diffraction Standards (JCPDS). Moreover, field emission scanning electron microscopy (FE-SEM) illustrated the particle morphology of ZnS, showing a range between 200 and 500 nm size. Additionally, the cyclic voltammetry results indicated that the modified electrode produced a greater current response than the bare electrode, highlighting its improved sensitivity to dopamine molecules. Conclusion ZnSnanoparticles were synthesized via a hydrothermal method and characterized using XRDand FE-SEM. These nanoparticles were used for electrochemical dopamine detection, showing potential for advanced sensing platforms. Integrating ZnS into microfluidic devices enables real-time dopamine monitoring, opening new possibilities for healthcare and neurochemical research. Exploring surface engineering techniques could further enhance the electrochemical performance of ZnS-based sensors.