Pressure/Temperature Phase Diagrams and Superlattices of Organically Functionalized Metal Nanocrystal Monolayers: The Influence of Particle Size, Size Distribution, and Surface Passivant

Abstract

The phase behavior of organically passivated 20−75 Å diameter Ag and Au nanocrystals is investigated by examining surface−area isotherms of Langmuir monolayers and transmission electron micrographs of Langmuir−Blodgett (LB) films. The effects of temperature, organic passivant chain length, and nanocrystal size and composition are studied. Three distinct types of phase behavior are observed and may be classified in terms of the extra (conical) volume (Ve) available to the alkyl capping group as it extends from a nearly spherical metal core. For Ve > 350 Å3, the phase diagram is dominated by extended, low-dimensional structures that, at high pressures, compress into a two-dimensional foamlike phase. This behavior is rationalized as originating from the interpenetration of the ligand shells of adjacent particles. For Ve < 350 Å3, dispersion attractions between the metal cores dominate particle condensation. For 350 Å3 > Ve > 150 Å3, the particles condense to form closest packed structures, which, for sufficiently narrow particle size distributions, are characterized by crystalline phases. For Ve ≈ 30 Å3, the particles irreversibly aggregate into structures similar to those expected from a diffusion-limited-aggregation (DLA) model. Optical properties of certain LB films of the closest packed phases are reported.