Investigation of interparticle interactions of larger (4.63 nm) monolayer protected gold clusters during quantized double layer charging

In this article, the effect of interparticle interactions of 4.63 nm sized monolayer protected gold clusters (Au MPCs) during quantized double layer (QDL) charging has been investigated using electrochemical techniques. Voltammetry and scanning tunneling microscopy have been used to compare their electron transfer behavior. Furthermore, since the QDL process is diffusion controlled, the diffusion coefficient values have been estimated at various charge steps using two independent electroanalytical techniques, viz. chronoamperometry and impedance. These results show that higher core charge facilitates higher diffusion coefficient values, and indicate that repulsive interactions dominate for charged MPCs compared to those of its neutral analogue, which are mainly attractive in nature. Additionally, the electron transfer rate constants at various charge steps have been estimated from the impedance results, showing comparatively faster electron transfer rate at higher charge states

Phase transitions in octanethiol-capped Ag nanocluster microfilm assemblies

We describe phase transitions in microfilm assemblies of octanethiol (OT)-capped 2-4 nm-diameter Ag nanoclusters prepared from solutions with OT/Ag+ ratios of ∼50. Using DSC we observe two melting/crystallization-type reversible phase transitions: one at ∼61 °C due to interdigiated unattached octanethiol, and the other at ∼125 °C due to the phase comprised of the assembly of OT-capped nanoclusters. Increased thermal fluctuations weaken the inter-chain hydrophobic interactions between interdigitated OT molecules, leading to both phase transitions. The thiolate bond of OT-molecules bound to Ag nanoclusters are more rigid, thereby requiring a higher temperature to increase the flexibility of the alkyl chain of OT, and to melt the nanocluster assembly. The mobility of the nanoclusters in the melt is limited, and morphological features of the original assemblies are retained during recrystallization. No observable mass loss is detected up to ∼180 °C, above which OT molecules desorb from the Ag nanoclusters

Hydrophobic anchoring of monolayer-protected gold nanoclusters to carbon nanotubes

Creating hybrid nanostructures consisting of disparate nanoscale blocks is of interest for exploring new types of quantum device architectures. Here, we demonstrate the novel anchoring of monolayer-protected gold nanoclusters of 1-3 nm diameter to sidewalls of carbon nanotubes (CNTs) via hydrophobic interactions between octanethiols capping the nanoclusters and acetone-activated CNT surfaces. Such molecularly interlinked hybrid nanoblocks are attractive for building biocompatible nanodevices

Templateless room-temperature assembly of nanowire networks from nanoparticles

We demonstrate a new, room-temperature approach to assemble two-dimensional and three-dimensional networks of gold nanowires by agitating nanoparticles in a toluene-aqueous mixture, without the use of templates. The nanowires have a uniform diameter of about 5 nm and consist of coalesced face-centered cubic nanocrystals. Toluene molecules passivate the gold surfaces during nanoparticle coalescence, rendering the nanowires hydrophobic and enabling their transfer into the toluene layer. Such templateless low-temperature assembly of mesostructures from nanoscale building blocks open up new possibilities for creating porous self-supporting nanocatalysts, nanowires for device interconnection, and low-density high-strength nanofillers for composites