Activated reduced graphene oxide materials (a-rGO) with variation of N₂ BET surface area 1000–3000 m² g⁻¹ were tested in supercapacitors. Correlations between electrode performance and pore size, pore volume, N₂ and H₂O BET surface area were evaluated.

Detonation nanodiamond (ND) is a suitable source material to produce unique samples consisting of almost uniform diamond nanocrystals (d = 3–5 nm). Such samples exist in the form of long stable aqueous dispersions with narrow size distribution of diamond particles. The material is finding ever increasing application in biomedicine. The major problem in producing monodispersed diamond colloids lies in the necessity of deagglomeration of detonation soot and/or removing of clusters formed by already isolated core particles in dry powders. To do this one must have an effective method to monitor the aggregation state or dispersity of powders and gels prior to the preparation of aqueous dispersions. In the absence of dispersity control at various stages of preparation the reproducibility of properties of existing ND materials is poor. In this paper we introduce differential scanning calorimetry (DSC) as a new tool capable to distinguish the state of aggregation in dry and wetted ND materials and to follow changes in this state under different types of treatment. Samples with identical X-ray diffraction patterns (XRD) and high resolution transmission electron microscopy (HRTEM) images gave visibly different DSC traces. Strong correlation was found between dynamic light scattering (DLS) data for colloids and DSC parameters for gels and powders of the same material. Based on DSC data we improved dispersity of existing ND materials and isolated samples with the best possible DSC parameters. These were true monodispersed easily dispersible fractions of ND particles with diameters of ca. 3 nm.

Swelling of Hummers graphene oxide (HGO) membranes in a set of progressively longer liquid alcohols (methanol to 1-nonanol) was studied using synchrotron radiation XRD after air ageing over prolonged periods of time.

In recent years, the demand for more efficient cooling circuits has resulted in active studies of nanofluids, two-component liquids consisting of a base fluid, and dispersed nanoparticles with high thermal conductivity. From the viewpoint of both physics and chemistry, nanofluids are systems that require the characterization of many interconnected thermal and chemical properties. This perspective article sums up the state of the art and recent trends in the development and applications of nanofluids and especially carbon nanofluids. A focus of the paper is the possibilities of photothermal and photoacoustic methods—as techniques combining molecular spectroscopy and thermal characterization—for the assessment of thermal conductivity and thermal diffusivity of nanofluids. The possibilities of photothermal spectroscopy for wider characterization of nanofluids and related materials are discussed and compared with other techniques. As nanofluids are one of the examples of complex objects dedicated to photothermal spectroscopy, more general outlooks of phototermics are also discussed.

Multilayered intercalation of 1-octanol into the structure of Brodie graphite oxide (B-GO) was studied as a function of temperature and pressure.