Infrared (IR) spectroscopy has evolved into a powerful analytical technique to probe molecular and lattice vibrations, low-energy electronic excitations and correlations, and related collective surface plasmon, phonon, or other polaritonic resonances. In combination with scanning probe microscopy, near-field infrared nano-spectroscopy and -imaging techniques have recently emerged as a frontier in imaging science, enabling the study of complex heterogeneous materials with simultaneous nanoscale spatial resolution and chemical and quantum state spectroscopic specificity. Here, we describe synchrotron infrared nano-spectroscopy (SINS), which takes advantage of the low-noise, broadband, high spectral irradiance, and coherence of synchrotron infrared radiation for near-field infrared measurements across the mid-to far-infrared with nanometer spatial resolution. This powerful combination provides a qualitatively new form of broadband spatio-spectral analysis of nanoscale, mesoscale, and surface phenomena that were previously difficult to study with IR techniques, or even any form of microspectroscopy in general. We review the development of SINS, describe its technical implementations, and highlight selected examples representative of the rapidly growing range of 2 applications in physics, chemistry, biology, materials science, geology, and atmospheric and space sciences.
Highly nonlinear optical materials with fast third-order nonlinear optical response are crucial for the operation of all-optical photonic devices, such as switches for signal processing and computation, power limiters, and saturable absorbers. The nonlinear response of traditional optical materials is weak, thus requiring large light intensities to induce significant changes in their properties. Here we show that optical control of the coupling rate in subwavelength patch antennas coupled to intersubband transitions in multi-quantum-well semiconductor heterostructures can provide a giant third-order nonlinear response, on the order of
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ContentsS1: Optical characterization of Au-silica Janus particles S2: Tethering efficiency of single DNA molecules to Au-silica Janus particles S3: Forces acting on a free optically trapped Au-silica Janus particle S4: Axial displacement of optically trapped DNA-tethered Au-silica Janus particles S5: Axial optical forces in the limit of small radial displacements S6: Thermophoretic force on free Au-silica Janus particles. S7: Thermophoretic force S8: Free to DNA-tethered thermophoretic force conversion S9: Force-extension curve of a partially de-hybridized DNA molecule S10: Temperature distribution around an optically trapped Janus particle S11: Melting curve of the 9-kb-long dsDNA S12: Lifetime of DIG-antiDIG bond.
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