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
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 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
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.
