We developed a statistical mechanical theory that describes the adsorption of nanoparticles (NPs) at liquid-vapor surfaces. This theory accounts for the surface to bulk NP thermodynamic equilibrium, as well as the NP mechanical equilibrium, wettability, and line tension at liquid-vapor surfaces. The theory is tested by examining the adsorption of 5 nm diameter dodecanethiol-ligated gold NPs at the liquid-vapor surface of a homologous series of n-alkane solvents, from n-nonane to n-octadecane, where the NP wettability decreases with an increasing n-alkane chain length.

SUMMARY Novel high‐temperature heat transfer fluids (HTFs) with incorporated phase change nanomaterials were synthesized and tested for heat transfer and thermal energy storage. The advanced thermal properties were achieved by preparing a nanofluid consisting of core/shell silica encapsulated tin (Sn/SiO2) nanoparticles dispersed in a synthetic HTF Therminol 66 (TH66) at loadings up to 5 vol%. Tin nanoparticles were synthesized by modified polyole reduction method followed by sol–gel silica encapsulation process. The measured increase in thermal conductivity of the nanofluid (~13% at 5 vol%) was in agreement with Maxwell's effective medium theory. Latent heat of phase change during melting of Sn core added ~11% increase to the volumetric thermal energy storage of the nanofluid when cycled in between 100°C and 270°C. The value could be further improved if thermal cycling is conducted in a narrower temperature range. The experimental results demonstrated dual functionality of the engineered nanofluids as desired for Concentrated Solar Power systems. Viscosity and stability of the nanofluids as well as thermal stability of core/shell nanomaterials) were investigated in a wide temperature range to obtain a perspective on any additional pumping power requirements for the nanofluid over the base fluid. Copyright © 2013 John Wiley & Sons, Ltd.

Here we report the synthesis of monodispersed indium nanoparticles by evaporation/condensation of indium shot using the solvated metal atom dispersion (SMAD) technique, followed by digestive ripening in low boiling point (BP 38 °C) methylene chloride and in a high boiling point (BP 110 °C) toluene solvent. The as-prepared SMAD indium nanoparticles are polydispersed with particle size ranging from 25 to 50 nm, but upon digestive ripening (heating of colloidal material at the boiling point of solvent in presence of excess surface active ligands) in methylene chloride, a remarkable reduction of particle size was achieved. In higher boiling solvent (toluene), where the indium nanoparticles at reflux temperature are probably melted, it does not allow the best result, and less monodispersity is achieved. We employed different surface active ligands (amine, phosphine, and mixed ligands) to passivate these indium nanoparticles. The temporal evolution of the surface plasmon of indium nanoparticles was monitored by in situ UV-vis spectroscopy, and particles were characterized by transmission electron microscopy (TEM) and X-ray diffraction (XRD). The merits of this synthesis procedure are the use of bulk indium as starting material, tuning the particle size in low boiling point solvent, particle size adjustment with the choice of ligand, and a possible scale up.

Here we report synthesis of CdSe quantum dots (QDs) by evaporation of bulk CdSe using the solvated metal atom dispersion method (SMAD), followed by reflux in toluene and in t-butyltoluene (TBT). The as-prepared SMAD product exhibits broad photoluminescence spectra (PL), but upon reflux in toluene or t-butyltoluene, interestingly, the PL spectra become narrow with an increase in fluorescence intensity. The temporal evolution of quantum dots was monitored by in situ UV-vis spectroscopy. The XRD data reveal that the formed CdSe QDs retain the wurtzite structure of the starting bulk CdSe material. The merits of this synthesis procedure are the use of bulk CdSe as starting material, possibility of scale up, elimination of high-temperature injection and size-selective precipitation processes.

Measurements of the solubility curve of a quasi-monodisperse gold nanoparticle solution are given. Temperature quenches from the one-phase to the two-phase regime yielded superclusters of the nanoparticle solid phase with sizes that depended on the quench depth. Classical nucleation theory was used to describe these sizes using a value of the surface tension for the nanoparticle solid phase of 0.042 erg/cm2. This value is consistent with molecule size scaling of the surface tension. In total these results show that suspensions of nanoparticles act like molecular solutions.