Carbon quantum dots (CQDs) were synthesized via a green, one-step hydrothermal method. As CQD precursors, nine amino acids of different structural descriptors (negatively/positively charged in water, polar, hydrophobic, sulfur-containing, and other/complex ones) were surveyed: Asp, Cys, Gly, His, Leu, Lys, Phe, Pro, and Ser. The reactions were performed in an autoclave in the presence of citric acid at 180 °C for 24 h and yielded core–shell CQDs. CQDs were comprehensively characterized by transmission electron microscopy, dynamic light scattering, Raman, UV/Vis, infrared, X-ray photoelectron spectroscopy, and fluorescence spectroscopy. At the excitation wavelength of λex = 350 nm, Cys-, Phe-, Leu-, and Lys-based CQDs displayed the highest quantum yield blue fluorescence90 ± 5, 90 ± 4, 87 ± 5, and 67 ± 3%, respectivelysuperior to the conventional fluorescent dyes. Strikingly, for Lys- and Phe-CQDs, dissimilar trends in the excitation–emission wavelength relationships were identified, that is, constantly strong red shifts versus excitation wavelength-independent emission. Cys- and Lys-CQDs were water-dispersible toward the narrow unimodal distribution of hydrodynamic diameters0.6 and 2.5 nm, respectively. Additionally, Lys- and Cys-CQDs, with high absolute zeta potential values, formed stable aqueous colloids in a broad range of pH (2, 7, and 12). The results constitute important premises for water-based applications of CQDs, such as bioimaging or photocatalysis.

Transfer of the excellent intrinsic properties of individual carbon nanoparticles into real-life applications of the corresponding heat transfer fluids remains challenging. This process requires identification and quantification of the nanoparticle-liquid interface. Here, for the first time, we have determined geometry and properties of this interface by applying transmission electron cryomicroscopy (cryo-TEM). We have systematically investigated how the particle morphology of carbon-based nanomaterials affected the thermal conductivity, specific isobaric heat capacity, thermal diffusivity, density, and viscosity of ionanofluids and/or bucky gels, using a wide range of fillers, especially single-walled carbon nanotubes (SWCNTs) and multi-walled carbon nanotubes (MWCNTs) – both with extreme values of aspect ratio (length to diameter ratio) from 150 to 11,000. Accordingly, hybrid systems composed of various carbon nanomaterials and ionic liquid, namely 1-ethyl-3-methylimidazolium thiocyanate [EMIM][SCN], were prepared and characterized. Most of the analyzed nanodispersions exhibited long-term stability even without any surfactant. Our study revealed that the thermal conductivity could be remarkably improved to the maximum values of 43.9% and 67.8% for ionanofluid and bucky gel (at 1 wt% loadings of MWCNTs and SWCNTs), respectively, compared to the pristine ionic liquid. As a result, the model proposed by Murshed and co-workers has been improved for realistic description of the concentration-dependent thermal conductivity of such hybrid systems. The obtained results undoubtedly indicate the potential of ionanofluids and bucky gels for energy management.

• Multi-wall CNT bundles in ionic liquids are deagglomerated and cut upon sonication. • Prolonged ultrasonication decreases thermal conductivity of ionanofluids. • Extended ultrasonication time reduces viscosity of ionanofluids.

Systematic studies of silver nanoparticle synthesis in a continuous-flow single-mode microwave reactor using polyol process were performed, revealing that the synthesis is exceptionally effective to give very small metal particles at full reaction yield and very high productivity. Inlet concentration of silver nitrate or silver acetate, applied as metal precursors, varied between 10 and 50 mM, and flow rates ranged from 0.635 to 2.5 dm³/h, to give 3–24 s reaction time. Owing to its much higher reactivity, silver acetate was shown to be far superior substrate for the synthesis of small (10–20 nm) spherical silver nanoparticles within a few seconds. Its restricted solubility in ethylene glycol, applied as the solvent and reducing agent, appeared to be vital for effective separation of the stage of particle growth from its nucleation to enable rapid synthesis of small particles in a highly loaded system. This was not possible to obtain using silver nitrate. All the observations could perfectly be explained by a classical LaMer–Dinegar model of NPs’ formation, but taking into account also nonisothermal character of the continuous-flow process and acetate dissolution in the reaction system. The performed studies indicate an optimal strategy for the high-yield fabrication of metal particles using polyol method.