Controlled Gold Nanorod Reorientation and Hexagonal Order in Micromolded Gold Nanorod@pNIPAM Microgel Chain Arrays.

A one-step soft lithography based pathway to manufacture aligned gold nanorod@poly-(N-isopropylacrylamide) (GNR@pNIPAM) hybrid chains with hexagonal arrangement of the nanorods and with an anisotropic optical response is presented. After demonstration of an efficient synthesis protocol, yielding uniform composite microgels in high concentration, a micromolding procedure using wrinkled polydimethylsiloxane (PDMS) templates to fabricate aligned hybrid chains is introduced. It is found that the self-assembled GNR@pNIPAM microgels inside the PDMS wrinkle grooves can be transferred onto solid substrates, on which they exhibit a hexagonal order, as confirmed by small-angle X-ray scattering.

Diffusive Motion of Linear Microgel Assemblies in Solution.

Due to the ability of microgels to rapidly contract and expand in response to external stimuli, assemblies of interconnected microgels are promising for actuation applications, e.g., as contracting fibers for artificial muscles.

Enhanced upconversion quantum yield near spherical gold nanoparticles - a comprehensive simulation based analysis.

Photon upconversion is promising for many applications. However, the potential of lanthanide doped upconverter materials is typically limited by low absorption coefficients and low upconversion quantum yields (UCQY) under practical irradiance of the excitation. Modifying the photonic environment can strongly enhance the spontaneous emission and therefore also the upconversion luminescence.

Plasmon enhanced upconversion luminescence near gold nanoparticles--simulation and analysis of the interactions: errata.

The procedure used in our previous publication [Opt. Express 20, 271, (2012)] to calculate how coupling to a spherical gold nanoparticle changes the upconversion luminescence of Er(3+) ions contained several errors. The errors are corrected here.

Plasmon enhanced upconversion luminescence near gold nanoparticles-simulation and analysis of the interactions.

We investigate plasmon resonances in gold nanoparticles to enhance the quantum yield of upconverting materials. For this purpose, we use a rate equation model that describes the upconversion of trivalent erbium based upconverters. Changes of the optical field acting on the upconverter and the changes to the transition probabilities of the upconverter in the proximity of a gold nanoparticle are calculated using Mie theory and exact electrodynamic theory respectively.

Radiation damping in metal nanoparticle pairs.

The radiation damping rate of plasmon resonances in pairs of spherical gold nanoparticles is calculated. The radiative line width of the plasmon resonance indicates significant far-field coupling between the nanoparticles over distances many times the particle diameter. The radiation damping of the coupled particle-plasmon mode alternates between superradiant and subradiant behavior when the particle spacing is varied.

Excitation of nanoscale vapor bubbles at the surface of gold nanoparticles in water.

Intense nonequilibrium femtosecond laser excitation of gold nanoparticles in water leads to a transient heating of the nanoparticles, which decays via heat transfer to the water phase. It is shown that the water temperature rises to near the critical temperature and the water undergoes an explosive evaporation in the subnanosecond range. The formation of vapor bubbles shows a threshold dependence on laser fluence.

Drastic reduction of plasmon damping in gold nanorods.

The dephasing of particle plasmons is investigated using light-scattering spectroscopy on individual gold nanoparticles. We find a drastic reduction of the plasmon dephasing rate in nanorods as compared to small nanospheres due to a suppression of interband damping. The rods studied here also show very little radiation damping, due to their small volumes.

Observation of hot-electron pressure in the vibration dynamics of metal nanoparticles.

We investigate the vibration dynamics of ellipsoidal silver nanoparticles, using time-resolved optical pump-probe spectroscopy. When excited with femtosecond laser pulses, the particles execute anisotropic shape oscillations. We show that these vibrations are triggered by the thermal expansion of the optically heated particles.