Separating Geometric and Diffusive Contributions to the Surface Nucleation of Dislocations in Nanoparticles.

While metal nanoparticles are widely used, their small size makes them mechanically unstable. Extensive prior research has demonstrated that nanoparticles with sizes in the range of 10-50 nm fail by the surface nucleation of dislocations, which is a thermally activated process. Two different contributions have been suggested to cause the weakening of smaller particles: first, geometric effects such as increased surface curvature reduce the barrier for dislocation nucleation; second, surface diffusion happens faster on smaller particles, thus accelerating the formation of surface kinks which nucleate dislocations.

Size-Dependent Role of Surfaces in the Deformation of Platinum Nanoparticles.

The mechanical behavior of nanostructures is known to transition from a Hall-Petch-like "smaller-is-stronger" trend, explained by dislocation starvation, to an inverse Hall-Petch "smaller-is-weaker" trend, typically attributed to the effect of surface diffusion. Yet recent work on platinum nanowires demonstrated the persistence of the smaller-is-stronger behavior down to few-nanometer diameters. Here, we used in situ nanomechanical testing inside of a transmission electron microscope (TEM) to study the strength and deformation mechanisms of platinum nanoparticles, revealing the prominent and size-dependent role of surfaces.

Size-dependent shape distributions of platinum nanoparticles.

While it is well established that nanoparticle shape can depend on equilibrium thermodynamics or growth kinetics, recent computational work has suggested the importance of thermal energy in controlling the distribution of shapes in populations of nanoparticles. Here, we used transmission electron microscopy to characterize the shapes of bare platinum nanoparticles and observed a strong dependence of shape distribution on particle size. Specifically, the smallest nanoparticles (<2.

Mechanistic insights into the acetate-accelerated synthesis of crystalline ceria nanoparticles.

Recent increasing uses of ceria in research and industrial applications have fostered continuing developments of efficient routes to synthesize the material. Here we report our investigation of the effects and the mechanistic roles of lithium acetate to accelerate the growth of crystalline ceria nanoparticles in ozone-mediated synthesis. By increasing the mole ratio of the acetate to cerium nitrate in the reactions, the reaction yields of ceria nanoparticles were observed to increase from 10% to up to over 90% by cerium content in 30 min reactions.