Search Results (11)

This study employs a multi-technique approach to elucidate how graphene incorporation affects phase formation, microstructure, and thermal behavior in PVA-assisted sol–gel synthesized Ca_2.95Eu_0.05Co₄O_x nanomaterials. XRD confirms the preservation of the primary phases (hexagonal CaCO₃ and cubic CoO) alongside a distinct graphene (002) reflection; a systematic low-angle shift of the calcite (104) peak evidences partial relaxation of residual lattice strain with increasing graphene content, while Scherrer analysis indicates tunable crystallite size. Raman spectroscopy corroborates graphene incorporation through pronounced D (~1300 cm⁻¹) and G (~1580 cm⁻¹) bands and supports the XRD-identified phase coexistence via cobalt-oxide and calcite vibrations in the 200–700 cm⁻¹ region, also indicating increased defect/disorder with graphene loading. SEM shows grain refinement, denser/bridged lamellar textures, and reduced porosity at low–moderate graphene contents (1–3 wt.%), contrasted by agglomeration-driven heterogeneity at higher loadings (5–7 wt.%). EDX reveals increasing carbon with Ca/Co redistribution at accessible surfaces, and TG–DSC corroborates the removal of oxygen-containing groups and oxidative combustion of graphene at mid temperatures. Collectively, Raman–XRD-consistent evidence demonstrates that graphene provides a tunable handle over lattice strain, crystallite size, and grain-boundary architecture, establishing a processing–composition basis for optimizing functional (e.g., electrical/thermoelectric) performance. Full article

The search for new hydrogen evolution reaction (HER) electrocatalysts with lower cost and higher activity and stability than noble metal catalysts is essential. In this regard cobalt phosphide is considered one of the most promising nanomaterials. The present work proposes a simple and efficient method for the synthesis of a nanocomposite of graphene–phosphorene structures decorated with CoP nanoparticles 2–5 nm in size via the electrochemical exfoliation of black phosphorus carried out in the presence of nitrogen-doped few-layer graphene structures and followed by solvothermal synthesis in a Co²⁺-containing solution. The obtained CoP/EEBP/N-FLGS nanocomposite demonstrates high electrocatalytic activity and stability towards HER in an alkaline medium. The nanocomposite is characterized by an overpotential of 190 mV at a current density of 10 mA cm⁻² as well as a small Tafel slope (78 mV dec⁻¹). These characteristics make the CoP/EEBP/N-FLGS nanocomposite superior to most electrocatalysts based on cobalt phosphides. The results of this study could be in demand for the future design and improvement of HER electrocatalysts. Full article

A method for the design and synthesis of a metallopolymer composite (CoNP) based on cobalt nanoparticles using the hyperbranched polyol process was developed. It was shown that hyperbranched polyester polyols in a melted state can be both a reducing agent and a stabilizer of metal nanoparticles at the same time. The mechanism of oxidation of hyperbranched polyol was studied using diffuse reflectance IR spectroscopy. The process of oxidation of OH groups in G4-OH started from 90 °C and finished with the oxidation of aldehyde groups. The composition and properties of nanomaterials were determined with FT-IR and UV-Vis spectroscopy, Nanoparticle Tracking Analysis (NTA), thermogravimetric analysis (TG), powder X-ray diffraction (XRD), NMR relaxation, and in vitro biological tests. The cobalt-containing nanocomposite (CoNP) had a high colloidal stability and contained spheroid polymer aggregates with a diameter of 35–50 nm with immobilized cobalt nanoparticles of 5–7 nm. The values of R₂ and R₁ according to the NMR relaxation method for CoNPs were 6.77 mM·ms⁻¹ × 10⁻⁵ and 4.14 mM·ms⁻¹ × 10⁻⁵ for, respectively. The ratio R₂/R₁ = 0.61 defines the cobalt-containing nanocomposite as a T₁ contrast agent. The synthesized CoNPs were nonhemotoxic (HC₅₀ > 8 g/mL) multifunctional reagents and exhibited the properties of synthetic modulators of the enzymatic activity of chymosin aspartic proteinase and exhibited antimycotic activity against Aspergillus fumigatus. The results of the study show the unique prospects of the developed two-component method of the hyperbranched polyol process for the creation of colloidal multifunctional metal–polymer nanocomposites for theranostics. Full article

Ferroptosis, a form of iron-dependent, lipid peroxidation-driven cell death, has been extensively investigated in recent years, and several studies have suggested that the ferroptosis-inducing properties of iron-containing nanomaterials could be harnessed for cancer treatment. Here we evaluated the potential cytotoxicity of iron oxide nanoparticles, with and without cobalt functionalization (Fe₂O₃ and Fe₂O₃@Co-PEG), using an established, ferroptosis-sensitive fibrosarcoma cell line (HT1080) and a normal fibroblast cell line (BJ). In addition, we evaluated poly (ethylene glycol) (PEG)-poly(lactic-co-glycolic acid) (PLGA)-coated iron oxide nanoparticles (Fe₃O₄-PEG-PLGA). Our results showed that all the nanoparticles tested were essentially non-cytotoxic at concentrations up to 100 μg/mL. However, when the cells were exposed to higher concentrations (200–400 μg/mL), cell death with features of ferroptosis was observed, and this was more pronounced for the Co-functionalized nanoparticles. Furthermore, evidence was provided that the cell death triggered by the nanoparticles was autophagy-dependent. Taken together, the exposure to high concentrations of polymer-coated iron oxide nanoparticles triggers ferroptosis in susceptible human cancer cells. Full article

Nanobiotechnology influences many different areas, including the medical, food, energy, clothing, and cosmetics industries. Considering the wide usage of nanomaterials, it is necessary to investigate the toxicity potentials of specific nanosized molecules. Boron-containing nanoparticles (NPs) are attracting much interest from scientists due to their unique physicochemical properties. However, there is limited information concerning the toxicity of boron-containing NPs, including cobalt boride (Co₂B) NPs. Therefore, in this study, Co₂B NPs were characterized using X-ray crystallography (XRD), transmission electron microscope (TEM), scanning electron microscope (SEM), and energy-dispersive X-ray spectroscopy (EDX) techniques. Then, we performed 3-(4,5-dimethyl-thiazol-2-yl) 2,5-diphenyltetrazolium bromide (MTT), lactate dehydrogenase (LDH) release, and neutral red (NR) assays for assessing cell viability against Co₂B NP exposure on cultured human pulmonary alveolar epithelial cells (HPAEpiC). In addition, whole-genome microarray analysis was carried out to reveal the global gene expression differentiation of HPAEpiC cells after Co₂B NP application. The cell viability tests unveiled an IC50 value for Co₂B NPs of 310.353 mg/L. The results of our microarray analysis displayed 719 gene expression differentiations (FC ≥ 2) among the analyzed 40,000 genes. The performed visualization and integrated discovery (DAVID) analysis revealed that there were interactions between various gene pathways and administration of the NPs. Based on gene ontology biological processes analysis, we found that the P53 signaling pathway, cell cycle, and cancer-affecting genes were mostly affected by the Co₂B NPs. In conclusion, we suggested that Co₂B NPs would be a safe and effective nanomolecule for industrial applications, particularly for medical purposes. Full article

Among many electrode materials, cobalt-based nanomaterials are widely used in supercapacitors because of their high natural abundance, good electrical conductivity, and high specific capacitance. However, there are still some difficulties to overcome, including poor structural stability and low power density. This paper summarizes the research progress of cobalt-based nanomaterials (cobalt oxide, cobalt hydroxide, cobalt-containing ternary metal oxides, etc.) as electrode materials for supercapacitors in recent years and discusses the preparation methods and properties of the materials. Notably, the focus of this paper is on the strategies to improve the electrochemical properties of these materials. We show that the performance of cobalt-based nanomaterials can be improved by designing their morphologies and, among the many morphologies, the mesoporous structure plays a major role. This is because mesoporous structures can mitigate volume changes and improve the performance of pseudo capacitance. This review is dedicated to the study of several cobalt-based nanomaterials in supercapacitors, and we hope that future scholars will make new breakthroughs in morphology design. Full article

Glioblastoma remains the most lethal form of brain cancer, where hybrid nanomaterials biofunctionalized with polysaccharide peptides offer disruptive strategies relying on passive/active targeting and multimodal therapy for killing cancer cells. Thus, in this research, we report for the first time the rational design and synthesis of novel hybrid colloidal nanostructures composed of gold nanoparticles stabilized by trisodium citrate (AuNP@TSC) as the oxidase-like nanozyme, coupled with cobalt-doped superparamagnetic iron oxide nanoparticles stabilized by carboxymethylcellulose ligands (Co-MION@CMC) as the peroxidase-like nanozyme. They formed inorganic–inorganic dual-nanozyme systems functionalized by a carboxymethylcellulose biopolymer organic shell, which can trigger a biocatalytic cascade reaction in the cancer tumor microenvironment for the combination of magnetothermal–chemodynamic therapy. These nanoassemblies were produced through a green aqueous process under mild conditions and chemically biofunctionalized with integrin-targeting peptide (iRDG), creating bioengineered nanocarriers. The results demonstrated that the oxidase-like nanozyme (AuNP) was produced with a crystalline face-centered cubic nanostructure, spherical morphology (diameter = 16 ± 3 nm), zeta potential (ZP) of −50 ± 5 mV, and hydrodynamic diameter (D_H) of 15 ± 1 nm. The peroxide-like nanostructure (POD, Co-MION@CMC) contained an inorganic crystalline core of magnetite and had a uniform spherical shape (2R = 7 ± 1 nm) which, summed to the contribution of the CMC shell, rendered a hydrodynamic diameter of 45 ± 4 nm and a negative surface charge (ZP = −41 ± 5 mV). Upon coupling both nanozymes, water-dispersible colloidal supramolecular vesicle-like organic–inorganic nanostructures were produced (AuNP//Co-MION@CMC, ZP = −45 ± 4 mV and D_H = 28 ± 3 nm). They confirmed dual-nanozyme cascade biocatalytic activity targeted by polymer–peptide conjugates (AuNP//Co-MION@CMC_iRGD, ZP = −29 ± 3 mV and D_H = 60 ± 4 nm) to kill brain cancer cells (i.e., bioenergy “starvation” by glucose deprivation and oxidative stress through reactive oxygen species generation), which was boosted by the magneto-hyperthermotherapy effect when submitted to the alternating magnetic field (i.e., induced local thermal stress by “nanoheaters”). This groundwork offers a wide avenue of opportunities to develop innovative theranostic nanoplatforms with multiple integrated functionalities for fighting cancer and reducing the harsh side effects of conventional chemotherapy. Full article

A one-step preparation method for cobalt- and iron-containing nanomaterials based on poly-N-phenylanthranilic acid (P-N-PAA) and magnetic nanoparticles (MNP) was developed for the first time. To synthesize the MNP/P-N-PAA nanocomposites, the precursor is obtained by dissolving a Co (II) salt in a magnetic fluid based on Fe₃O₄/P-N-PAA with a core-shell structure. During IR heating of the precursor in an inert atmosphere at T = 700–800 °C, cobalt interacts with Fe₃O₄ reduction products, which results in the formation of a mixture of spherical Co-Fe, γ-Fe, β-Co and Fe₃C nanoparticles of various sizes in the ranges of 20 < d < 50 nm and 120 < d < 400 nm. The phase composition of the MNP/P-N-PAA nanocomposites depends significantly on the cobalt concentration. The reduction of metals occurs due to the hydrogen released during the dehydrogenation of phenylenamine units of the polymer chain. The introduction of 10–30 wt% cobalt in the composition of nanocomposites leads to a significant increase in the saturation magnetization of MNP/P-N-PAA (M_S = 81.58–149.67 emu/g) compared to neat Fe₃O₄/P-N-PAA (M_S = 18.41–27.58 emu/g). The squareness constant of the hysteresis loop is κ_S = M_R/M_S = 0.040–0.209. The electrical conductivity of the MNP/P-N-PAA nanomaterials does not depend much on frequency and reaches 1.2 × 10⁻¹ S/cm. In the argon flow at 1000 °C, the residue is 77–88%. Full article

With the increasing demand for sustainable and green energy, electric energy storage technologies have received enough attention and extensive research. Among them, Li-ion batteries (LIBs) are widely used because of their excellent performance, but in practical applications, the electrochemical performance of electrode materials is not satisfactory. Carbon-based materials with high chemical stability, strong conductivity, high specific surface area, and good capacity retention are traditional anode materials in electrochemical energy storage devices, while cobalt-based nano-materials have been widely used in LIBs anodes because of their high theoretical specific capacity. This paper gives a systematic summary of the state of research of cobalt-containing nanomaterials, carbon nanomaterials, and their composites in LIBs anodes. Moreover, the preparation methods of electrode materials and measures to improve electrochemical performance are also summarized. The electrochemical performance of anode materials can be significantly improved by compounding carbon nanomaterials with cobalt nanomaterials. Composite materials have better electrical conductivity, as well as higher cycle ability and reversibility than single materials, and the synergistic effect between them can explain this phenomenon. In addition, the electrochemical performance of materials can be significantly improved by adjusting the microstructure of materials (especially preparing them into porous structures). Among the different microscopic morphologies of materials, porous structure can provide more positions for chimerism of lithium ions, shorten the diffusion distance between electrons and ions, and thus promote the transfer of lithium ions and the diffusion of electrolytes. Full article

Nanostructuration is one of the most promising strategies to develop performant electrode materials for energy storage devices, such as hybrid supercapacitors. In this work, we studied the influence of precipitation medium and the use of a series of 1-alkyl-3-methylimidazolium bromide ionic liquids for the nanostructuration of β(III) cobalt oxyhydroxides. Then, the effect of the nanostructuration and the impact of the different ionic liquids used during synthesis were investigated in terms of energy storage performances. First, we demonstrated that forward precipitation, in a cobalt-rich medium, leads to smaller particles with higher specific surface areas (SSA) and an enhanced mesoporosity. Introduction of ionic liquids (ILs) in the precipitation medium further strongly increased the specific surface area and the mesoporosity to achieve well-nanostructured materials with a very high SSA of 265 m²/g and porosity of 0.43 cm³/g. Additionally, we showed that ILs used as surfactant and template also functionalize the nanomaterial surface, leading to a beneficial synergy between the highly ionic conductive IL and the cobalt oxyhydroxide, which lowers the resistance charge transfer and improves the specific capacity. The nature of the ionic liquid had an important influence on the final electrochemical properties and the best performances were reached with the ionic liquid containing the longest alkyl chain. Full article

In this work, stable hydrophobic nanocomposites are made from electrospun fibers of polystyrene (PS) containing a hybrid filler combination of (i) hexagonal boron nitride (hBN) and (ii) cobalt oxide (Co₃O₄) nanomaterials. Good synergistic interaction is observed between the nanomaterials, since the growth of Co₃O₄ was carried out in presence of white graphene nanosheets. Filler synergy modifies the PS surfaces, by enhancing the filler-polymer interfacial interactions and provides good tensile strength. The hydrophobic films are gamma irradiated to improve crosslinking within the polymer nanocomposites. Since gamma irradiation enhances the surface roughness, its hydrophobicity/oleophilicity increases much and the final nanofibers show good oil-water separation efficiency. The nanofibers act as sponge clothing to skim the oil from a mixture of oil and water. Durability of the fibers in hot water and in presence of ultrasonic waves is also tested and good response is achieved. Contact angle studies are performed to investigate the surface properties and to check the influence of gamma irradiation on the surface wettability. The gamma-irradiated PS nanocomposite fiber shows a contact angle of 152° ± 2° compared to the 140° ± 1° of the neat PS fiber, evidencing the superhydrophobicity. Both the effects of crosslink density enhancement and hybrid filler distribution make the composite fibers stronger in oil absorption application even at higher operation temperatures. The fibers are reported to be robust and durable, in addition. Full article