Identical carbonization and KOH activation procedures result in very similar activated carbons with ultra-high BET surface area (up to ∼3500 m² g⁻¹) when applied to several types of precursors: pine, spruce, and larch cones, and bark/wood chips.

The commonly used electrode Pt supported on a carbon (Pt/C) catalyst has demonstrated underperforming electrochemical durability in proton exchange membrane fuel cell (PEMFC) harsh operation conditions, especially in terms of Pt electrochemical instability and carbon corrosion. Gold nanoparticles (AuNPs) are considered one of the best alternative catalysts of PtNPs due to their remarkable selectivity for oxygen reduction reaction (ORR) and electrochemical stability in strong acid conditions, attributes which are ideal for practical PEMFC applications. In this work, we propose a new, facile and low-cost approach to prepare AuNPs supported on reduced graphene oxide nanocompounds (AuNPs/rGO). The morphological and structural properties of the as-prepared AuNPs/rGO were studied using various microscopic and spectroscopic techniques, namely, Raman Spectroscopy, Scanning Electron Microscopy (SEM), Scanning Transmission Electron Microscopy (STEM), X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), specific surface area (Brunauer–Emmett–Teller, BET). A mesoporous structure with narrow pore size distribution centered at 2 nm approximately, where the pores are regular and interconnected was successfully fabricated. The prepared catalyst was exposed to an accelerated stress test (potential cycles between −0.8 and +0.2 in KOH 1 M solution). The voltammetric stability test indicated a slight degradation after 1500 cycles. The electrochemical stability was assigned to the combined effect of AuNPs formed during chemical synthesis and to graphene oxide support.

Reduced graphene oxide (rGO) is a promising graphene-based material, with transversal applicability to a wide range of technological fields. Nevertheless, the common use of efficient—but hazardous to environment and toxic—reducing agents prevents its application in biological and other fields. Consequently, the development of green reducing strategies is a requirement to overcome this issue. Herein, a green, simple, and cost-effective one-step reduction methodology is presented. Graphene oxide (GO) was hydrothermally reduced in the presence of caffeic acid (CA), a natural occurring phenolic compound. The improvement of the hydrothermal reduction through the presence of CA is confirmed by XRD, Raman, XPS and TGA analysis. Moreover, CA polymerizes under hydrothermal conditions with the formation of spherical and non-spherical carbon particles, which can be useful for further rGO functionalization. FTIR and XPS confirm the oxygen removal in the reduced samples. The high-resolution scanning transmission electron microscopy (HRSTEM) images also support the reduction, showing rGO samples with an ordered graphitic layered structure. The promising rGO synthesized by this eco-friendly methodology can be explored for many applications.

Our work presents, for the first time, a comprehensive study of the synthesis of fully metallic platinum nanoparticles (Pt-NPs) involving the ablation process in double distilled water using a KrF excimer laser. To obtain detailed information on Pt-NP morphology and optical properties, prepared colloids were characterized using High Resolution Scanning Transmission Electron Microscopy (HR-STEM) with advanced capabilities for Energy Dispersive X-ray Analysis (EDX), UV/Vis optical spectroscopy, and Direct Analysis in Real Time—Mass Spectrometry (DART-MS). The influence of the applied laser fluence and laser repetition rate (RR) values on the characteristics of the obtained Pt-NPs and the ablation process, respectively, were also analyzed. Spherical and spherical-like nanoparticles exhibiting aggregation were produced. The Pt-NP mean size values were between 2.2 ± 1.2 nm and 4.0 ± 1.0 nm, while their interplanar distance measurements showed a face-centered cubic (FFC) Pt lattice (111), as revealed by HR–STEM measurements, for all investigated samples. The smallest mean size of 2.2 nm of the Pt-NPs was obtained using a 2.3 J cm⁻² laser fluence at a 10 Hz RR, and the narrowest size distribution of the NPs was obtained with a 2.3 J cm⁻² laser fluence at a 40 Hz RR. A linear dependence of the Pt-NP diameters versus the laser repetition rate was found at a constant fluence of 2.3 J cm⁻². The proposed eco-friendly synthesis route of Pt-NPs, because of its relative simplicity, has the potential for use in industrial production.

Despite the fact that the electrochemical biosensors based on glucose oxidase represent the golden standard for the management of diabetes, the elaboration of nonenzymatic sensors became extensively studied as an out-of-the-box concept that aims to simplify the existing approach. An important point of view is represented by the low price of the sensing device that has positive effects for both end-users and healthcare systems. The enzyme-free sensors based on low-cost materials such as transition metals have similar analytical properties to the commercial ones while eliminating the issues associated with the presence of the enzyme, such as the stability issues and limited shelf-life. The development of nanoporous nanomaterials for biomedical applications and electrocatalysis was referred to as an alternative to the conventional methods due to their enlarged area, electrical properties, ease of functionalization and not least to their low cost. Herein, we report the development of an electrochemical nonenzymatic sensor for glucose based on 3D copper nanostructures with Ni foams as promotor of the enhanced nanoporous morphology. The sensors were successfully tested in the presence of the designated target, even in the presence of common interference agents found in biological samples.

Nano carbons, such as graphene and carbon nanotubes, show very interesting electrochemical properties and are becoming a focus of interest in many areas, including electrodeposition of carbon–metal composites for battery application. The aim of this study was to incorporate carbon materials (namely oxidized multi-walled carbon nanotubes (ox-MWCNT), pristine multi-walled carbon nanotubes (P-MWCNT), and reduced graphene oxide (rGO)) into a metallic tin matrix. Formation of the carbon–tin composite materials was achieved by electrodeposition from a choline chloride-based ionic solvent. The different structures and treatments of the carbon materials will create metallic composites with different characteristics. The electrochemical characterization of Sn and Sn composites was performed using chronoamperometry, potentiometry, electrochemical impedance, and cyclic voltammetry. The initial growth stages of Sn and Sn composites were characterized by a glassy-carbon (GC) electrode surface. Nucleation studies were carried out, and the effect of the carbon materials was characterized using the Scharifker and Hills (SH) and Scharifker and Mostany (SM) models. Through a non-linear fitting method, it was shown that the nucleation of Sn and Sn composites on a GC surface occurred through a 3D instantaneous process with growth controlled by diffusion. According to Raman and XRD analysis, carbon materials were successfully incorporated at the Sn matrix. AFM and SEM images showed that the carbon incorporation influences the coverage of the surface as well as the size and shape of the agglomerate. From the analysis of the corrosion tests, it is possible to say that Sn-composite films exhibit a comparable or slightly better corrosion performance as compared to pure Sn films.