Explore the vast range of titles available.

Graphitic nanomaterials have emerged as foundational components in nanoscience owing to their exceptional electrical, mechanical, and chemical properties, which can be tuned by controlling dimensionality and structural order. From zero-dimensional (0D) quantum dots, carbon nano-onions, and nanodiamonds to one-dimensional (1D) nanoribbons, two-dimensional (2D) nanowalls, and three-dimensional (3D) graphene foams, these architectures underpin advancements in catalysis, energy storage, sensing, and electronic technologies. Among various synthesis routes, chemical vapor deposition (CVD) provides unmatched versatility, enabling atomic-level control over carbon supply, substrate interactions, and plasma activation to produce well defined graphitic structures directly on functional supports. This review presents a comprehensive, dimension-resolved overview of CVD-derived graphitic nanomaterials, examining how process parameters such as precursor chemistry, temperature, hydrogen etching, and template design govern nucleation, crystallinity, and morphological evolution across 0D to 3D hierarchies. Comparative analyses of Raman, XPS, and XRD data are integrated to relate structural features with growth mechanisms and functional performance. By connecting mechanistic principles across dimensional scales, this review establishes a unified framework for understanding and optimizing CVD synthesis of graphitic nanostructures. It concludes by outlining a path forward for improving how CVD-grown carbon nanomaterials are made, monitored, and integrated into real devices so these can move from lab-scale experiments to practical, scalable technologies.

The discovery of graphene and carbon nanotubes (rolled-up graphene) has excited the world because their extraordinary properties promise tremendous developments in many areas. Like any materials with application potential, it needs to be fabricated in an economically viable manner and at the same time provides the necessary quality for relevant applications. Graphene and carbon nanotubes are no exception to this. In both cases, chemical vapor deposition (CVD) has emerged as the dominant synthesis route since it is already a well-established process both in industry and laboratories. In this work, we review the CVD fabrication of graphene and carbon nanotubes. Initially, we briefly introduce the materials and the CVD process. We then discuss pretreatment steps prior to the CVD reaction. The discussion then switches to the CVD process, provides comparative data for thermal CVD and plasma-enhanced CVD, and includes coverage of kinetics, thermodynamics, catalyst choice, and other aspects of growth as well as post production treatments. Finally, conclusions are drawn and presented.

The polyamide (PA)-12 material used for additive manufacturing was studied in aspects of morphology and their structural properties for basic stages received during 3D laser printing. Samples were real, big-scale production powders. The structure of polymer was evaluated from the crystallinity point of view using XRD, FTIR, and DSC methods and from the surface properties using specific surface evaluation and porosity. Scanning electron microscopy was used to observe morphology of the surface and evaluate the particle size and shape via image analysis. Results were confronted with laser diffraction particles size measurement along with an evaluation of the specific surface area. Fresh PA12 powder was found as inhomogeneous in particle size of material with defective particles, relatively high specific surface, high lamellar crystallite size, and low crystallinity. The scrap PA12 crystallinity was about 2% higher than values for fresh PA12 powder. Particles had a very low, below 1 m2/g, specific surface area; particles sintered as twin particles and often in polyhedral shapes.

Polymethylmethacrylate (PMMA) is commonly used in medical devices for the oral cavity. It is precisely due to its biocompatibility, mechanical strength, wear resistance, and aesthetic qualities that it is so prolific. While widely used in dental and biomedical applications, PMMA has several limitations that necessitate improvement. Due to mechanical limitations, low impact resistance, susceptibility to cracking and wear, low thermal conductivity, and microbial adhesion, various modifications have been introduced. In this study, the PMMA surface was modified with a SiO 2 coating obtained from a TEOS precursor under both acidic and alkaline conditions using the sol-gel method. Additionally, Graphene oxide (GO) and cannabidiol (CBD) were added to the coating, and the mechanical properties of the modified coatings were studied. This study aimed to investigate the effect of surface modification on the physicochemical properties of PMMA. The coatings were subjected to comprehensive physicochemical investigations, including TGA, FTIR, XPS, SEM, surface topography, surface wettability, Shore hardness, and tribological evaluations in artificial saliva. The study confirmed that the modification of PMMA with SiO 2 , GO and CBD has a beneficial effect on their structure, chemical properties, thermal stability, mechanical properties, and potentially the antibacterial of PMMA for used in biomedical applications.

Implant surface properties of Ti6Al4V alloy that is currently used as a biocompatible material because of a variety of unique properties can be improved by a self-organized TiO2 layer. The TiO2 nanotubes forming on the titanium-based materials is a relatively recent technology for the surface properties modification and represents pronounced potential in promoting cell adhesion, proliferation, and differentiation that facilitate an implant osseointegration. This work focuses on the influence of surface treatment quality and anodic oxidation parameters on the structure features and properties of TiO2 nanotube coatings. The nanotubes were formed on Ti6Al4V alloy substrates by simultaneous surface oxidation and controlled dissolving of an oxide film in the presence of fluorine ions. The anodization process on ground or polished samples was performed at experimental condition of 30 V for 1 h. The selected anodized samples were heat treated for 2 h at 500 °C under flowing argon. All samples were characterized by scanning electron microscopy, X-ray diffraction analysis, and Raman spectroscopy. The corrosion rate in physiological solution reached 0.0043, 0.0182, and 0.0998 mm per year for the samples in polished and not-anodized, as-anodized, and anodized-heat treated conditions, respectively.

This study aims to point out the main drawback with respect to the design of simulated body environments. Three media commonly used for the simulation of the identical body environment were selected, i.e., Kokubo’s simulated body fluid that simulates the inorganic component of human blood plasma, human blood plasma, and phosphate buffer saline. A comparison was performed of the effects of the media on collagen scaffolds. The mechanical and structural effects of the media were determined via the application of compression mechanical tests, the determination of mass loss, and image and micro-CT analyses. The adsorption of various components from the media was characterized employing energy-dispersive spectrometry. The phase composition of the materials before and after exposure was determined using X-ray diffraction. Infrared spectroscopy was employed for the interpretation of changes in the collagen secondary structure. Major differences in terms of the mechanical properties and mass loss were observed between the three media. Conversely, only minor structural changes were detected. Since no general recommendation exists for selecting the simulated body environment, it is necessary to avoid the simplification of the results and, ideally, to utilize alternative methods to describe the various aspects of degradation processes that occur in the media.

Novel biomedical composites, based on organically modified vermiculite and montmorillonite with deposited Ca-deficient hydroxyapatite (CDH), were prepared. The monoionic sodium forms of vermiculite and montmorillonite were intercalated with chlorhexidine diacetate (CA). The surfaces of organoclays were used for the precipitation of Ca-deficient hydroxyapatite. The composites with Ca-deficient hydroxyapatite showed very good antibacterial effects, similar to the antimicrobial activity of pure organoclay samples. Better antibacterial activity was shown in the organically modified montmorillonite sample with Ca-deficient hydroxyapatite compared with the vermiculite composite, but, in the case of Staphylococcus aureus, both composites showed the same minimum inhibitory concentration (MIC) value. The antimicrobial effect of composites against bacteria and fungi increased with the time of exposure. The structural characterization of all the prepared materials, performed using X-ray diffraction and FT infrared spectroscopy analysis, detected no changes in the original clay or CDH during the intercalation or precipitation process, therefore we expect the strength of the compounds to be in the original power.

Hollow graphitic nanoshells (HGSs) are widely investigated as battery materials because their conductive shells and internal voids can simultaneously influence ion transport, electron percolation, and mechanical stress accommodation. Yet, the field remains largely morphology-driven, with performance often attributed generically to “hollowness” rather than to structural parameters. This review examines HGSs from a parameter-oriented perspective. It highlights key structural features, including graphitization degree, shell thickness, cavity size, pore architecture, and defect or dopant chemistry. These features collectively shape electrochemical behavior. We discuss how these features influence transport kinetics, interphase stability, volumetric efficiency, and mechanical resilience across insertion, metal anode, multivalent, solid-state, and halogen chemistries. Major synthesis approaches, including hard-templated, soft-templated, self-templated, and biomass-derived routes, are evaluated based on the structural control they provide and the influence of synthesis conditions on shell architecture, graphitic ordering, and pore structure. Special attention is given to how these structural features develop during processing and how they affect ion accessibility, conductivity, and stability. Finally, we outline a shift toward quantitative, parameter-driven engineering supported by operando diagnostics, electrode-level modeling, and standardized reporting. HGSs will only achieve practical relevance when structural optimization extends beyond particle morphology to transport uniformity, interfacial stability, network connectivity, and life-cycle responsibility.

The main goal of this research is to investigate the effectiveness of graphitic carbon nitride (g-C 3 N 4 , g-CN) in both bulk and nanosheet forms, which have been surface-modified with silver nanoparticles (Ag NPs), as photocatalysts for the degradation of acid orange 7 (AO7), a model dye. The photodegradation of AO7 dye molecules in water was used to test the potential photocatalytic properties of these powder materials under two different lamps with wavelengths of 368 nm (UV light) and 420 nm (VIS light). To produce Ag NPs (Ag content 0.5, 1.5, and 3 wt%) on the g-CN materials, a new synthesis route based on a wet and low-temperature method was proposed, eliminating the need for reducing agents. The photodegradation activity of the samples increased with increasing silver content, with the best photocatalytic performances achieved for bulk g-CN samples and nanosheet silver-modified samples (with the highest content of 3 wt% Ag) under UV light, i.e., more than 75% and 78%, respectively. The VIS-induced photocatalytic activity of both examined series was higher than that of UV. The highest activities of 92% and 98% were achieved for the 1.5% Ag-modified g-CN bulk and nanosheet materials. This research presents an innovative, affordable, and environmentally friendly chemical approach to synthesizing photocatalysts that can be used for degrading organic pollutants in wastewater treatment.

Low-density polyethylene is one of the basic polymers used in medicine for a variety of purposes; so, the relevant improvements in functional properties are discussed here, making it safer to use as devices or implants during surgery or injury. The objective of the laboratory-prepared material was to study the antimicrobial and biocompatible properties of low-density polyethylene composites with 3 wt. % hybrid nanoclay filler. We found that the antimicrobial activity was mainly related to the filler, i.e., the hybrid type, where inorganic clay minerals, vermiculite or montmorillonite, were intercalated with organic chlorhexidine diacetate and subsequently decorated with Ca-deficient hydroxyapatite. After fusion of the hybrid nanofiller with polyethylene, intense exfoliation of the clay layers occurred. This phenomenon was confirmed by the analysis of the X-ray diffraction patterns of the composite, where the original basal peak of the clays decreased or completely disappeared, and the optimal distribution of the filler was observed using the transmission mode of light microscopy. Functional property testing showed that the composites have good antibacterial activity against Staphylococcus aureus, and the biocompatibility prediction demonstrated the formation of Ca- and P-containing particles through an in vitro experiment, thus applicable for medical use.