ABSTRACT
In recent years, considerable effort has been devoted to the synthesis and characterization of two-dimensional materials. Liquid phase exfoliation (LPE) represents a simple, large-scale method to exfoliate layered materials down to mono- and few-layer flakes. In this context, the contactless trapping, characterization, and manipulation of individual nanosheets hold perspectives for increased accuracy in flake metrology and the assembly of novel functional materials. Here, we use optical forces for high-resolution structural characterization and precise mechanical positioning of nanosheets of hexagonal boron nitride, molybdenum disulfide, and tungsten disulfide obtained by LPE. Weakly optically absorbing nanosheets of boron nitride are trapped in optical tweezers. The analysis of the thermal fluctuations allows a direct measurement of optical forces and the mean flake size in a liquid environment. Measured optical trapping constants are compared with T-matrix light scattering calculations to show a quadratic size scaling for small size, as expected for a bidimensional system. In contrast, strongly absorbing nanosheets of molybdenum disulfide and tungsten disulfide are not stably trapped due to the dominance of radiation pressure over the optical trapping force. Thus, optical forces are used to pattern a substrate by selectively depositing nanosheets in short times (minutes) and without any preparation of the surface. This study will be useful for improving ink-jet printing and for a better engineering of optoelectronic devices based on two-dimensional materials.
ABSTRACT
Optical trapping of silver nanoplatelets obtained with a simple room temperature chemical synthesis technique is reported. Trap spring constants are measured for platelets with different diameters to investigate the size-scaling behaviour. Experimental data are compared with models of optical forces based on the dipole approximation and on electromagnetic scattering within a T-matrix framework. Finally, we discuss applications of these nanoplatelets for surface-enhanced Raman spectroscopy.
ABSTRACT
Chirality is one of the most prominent and intriguing aspects of nature, from spiral galaxies down to aminoacids. Despite the wide range of living and non-living, natural and artificial chiral systems at different scales, the origin of chirality-induced phenomena is often puzzling. Here we assess the onset of chiral optomechanics, exploiting the control of the interaction between chiral entities. We perform an experimental and theoretical investigation of the simultaneous optical trapping and rotation of spherulite-like chiral microparticles. Due to their shell structure (Bragg dielectric resonator), the microparticles function as omnidirectional chiral mirrors yielding highly polarization-dependent optomechanical effects. The coupling of linear and angular momentum, mediated by the optical polarization and the microparticles chiral reflectance, allows for fine tuning of chirality-induced optical forces and torques. This offers tools for optomechanics, optical sorting and sensing and optofluidics.
ABSTRACT
We present the result of an investigation into the optical trapping of spherical microparticles using laser beams with a spatially inhomogeneous polarization direction [cylindrical vector beams (CVBs)]. We perform three-dimensional tracking of the Brownian fluctuations in the position of a trapped particle and extract the trap spring constants. We characterize the trap geometry by the aspect ratio of spring constants in the directions transverse and parallel to the beam propagation direction and evaluate this figure of merit as a function of polarization angle. We show that the additional degree of freedom present in CVBs allows us to control the optical trap strength and geometry by adjusting only the polarization of the trapping beam. Experimental results are compared with a theoretical model of optical trapping using CVBs derived from electromagnetic scattering theory in the T-matrix framework.
ABSTRACT
We study theoretically the quantum optical properties of hybrid molecules composed of an individual quantum dot and a metallic nanoparticle. We calculate the resonance fluorescence of this composite system. Its incoherent part, arising from nonlinear quantum processes, is enhanced by more than 2 orders of magnitude as compared to that of the dot alone. The coupling between the two systems gives rise to a Fano interference effect which strongly influences the quantum statistical properties of the scattered photons: a small frequency shift of the incident light field may cause changes in the intensity correlation function of the scattered field of orders of magnitude. The system opens a good perspective for applications in active metamaterials and ultracompact single-photon devices.
ABSTRACT
We study the optical trapping of highly elongated linear nanostructures in the focal region of a high-numerical aperture lens (optical tweezers). The radiation torque and trapping force on these nanostructures that are modeled as chains of identical spherical scatterers are calculated by means of multipole field expansions in the framework of the transition matrix approach. We investigate both orientational and trapping stability and calculate force constants and trap parameters in order to clarify the role of the linear geometry in the optical trapping mechanism. Furthermore, we calculate optical trapping of nanowires of different materials and compare our theoretical findings with available experimental results.
Subject(s)
Models, Theoretical , Nanostructures/chemistry , Optical Tweezers , TorqueABSTRACT
The effectiveness of modeling atmospheric ice crystals of varying aspect ratios as clusters of spheres is investigated by calculation of the backscattered intensity in the millimeter-wave range by the transition matrix approach. Both single crystals and dispersions with a few choices of the orientational distribution are considered. Our calculations reproduce the features of the backscattered intensity that are due to the overall symmetry of the crystals and yield results in agreement with analogous calculations performed by other authors within the framework of the discrete dipole approximation.
ABSTRACT
Our previous theory for calculating the scattering pattern from a single aggregate of spheres deposited on a dielectric substrate is extended to deal with a dispersion of identical aggregates onto the substrate with a random distribution of their orientations. To this end the definition of the transition matrix of an aggregate is generalized to take account of the presence of the substrate; then the transformation properties under rotation of the newly defined transition matrix are used to perform analytically the required orientational averages. When the patterns calculated with this theory are compared with the calculations for a single aggregate, it can easily be seen that the features that reveal the anisotropy of the scatterers are not canceled by the averaging procedure.
ABSTRACT
The extinction spectrum from single and aggregated hemispheres whose flat faces lie on a reflecting surface is calculated, and some of the expected resonances are found to disappear for specific choices of the direction and the polarization of the incident wave. This resonance-suppressing effect is fully explained for the case of single hemispheres, whereas for the case of aggregated hemispheres the guidelines for its explanation are given.
ABSTRACT
The optical properties of a cloud of anisotropic dielectric particles when the orientational distribution is made nonrandom by interaction with an electrostatic field are studied. Since the interaction energy is determined by the polarizability of the particles, a general expression for the polarizability of nonspherical particles is worked out. In particular, we investigated the response to the electrostatic field of two different dispersions whose component particles are built as clusters of four identical spheres. Although in one cloud the clusters were shaped as linear chains, and in the other cloud the clusters were shaped as squares, the optical properties of both dispersions as a function of the static field are rather similar. There are, however, noticeable ranges of size within which the optical response of the two kinds of particles is substantially different.
ABSTRACT
The formalism that was previously devised [J. Opt. Soc. Am. A 9, 1327 (1992)] to deal with the optical properties of homogeneous spheres containing an eccentric spherical inclusion is extended to the case of several inclusions. The extinction efficiency of dielectric spheres containing two identical metallic inclusions is calculated for a few significant geometries. Extinction by a low-density dispersion of the anisotropic scatterers mentioned above is also evaluated. Our results show that the subdivision of the included material has quite visible effects that strongly depend on both the polarization of the incident light and the geometric arrangement of the inclusions.
