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The mid‐infrared with a characteristic wavelength of 3–20 μm is important for a wealth of technologies. In particular, mid‐infrared spectroscopy can reveal material composition and structure information by fingerprinting chemical bonds' infrared resonances. Despite these merits, state‐of‐the‐art mid‐infrared techniques are spatially limited above tens of micrometers due to the fundamental diffraction law. Herein, recent progress in the scanning probe nanoscale infrared characterization of biochemical materials and natural specimens beyond this spatial limitation is reviewed. By leveraging the strong tip–sample local interactions, scanning probe nano‐infrared methods probe nanoscale optical and mechanical responses to disclose material composition, heterogeneity, orientation, fine structure, and phase transitions at unprecedented length scales. These advances, therefore, revolutionize the understanding of a broad range of biochemical and natural materials and offer new material manipulation and engineering opportunities close to the ultimate length scales of fundamental physical, chemical, and biological processes. [ABSTRACT FROM AUTHOR]

Achieving subwavelength optical focusing is of great importance in nanophotonics. However, achieving focusing with both a small focal spot size and a large focal length remains elusive so far. Here, a large focal length planar focusing device is presented, utilizing highly oriented Dyakonov polaritons in hyperbolic metamaterial with periodic silver rings as the excitation source. Experimental results show that by controlling the size of the excitation sources, the focal length can reach 6 λ 0 (where λ 0 is the illumination wavelength), and the focal spot size can be reduced to λ 0 /10. This method provides new prospects for planar polariton optical applications. [ABSTRACT FROM AUTHOR]

Guided waves are the perfect carriers of electromagnetic signals in planar miniaturized devices due to their high localization and controlled propagation direction. However, it is still a challenge to control the polarization of propagating guided waves. In this work, the broadband polarization TE‐TM degeneracy of highly localized guided waves propagating along an all‐dielectric metasurface and a subwavelength chain of dielectric high‐index cylinders is discovered, both theoretically and experimentally. Using the discovered near‐field polarization degree of freedom, the polarization transformation for guided waves propagating along a subwavelength chain of dielectric cylinders at any frequency within the finite spectral range is demonstrated experimentally. Namely, the simplest planar near‐field polarization device – the quarter‐wave‐retardation (linear‐to‐circular) polarization transformer of guided waves is implemented. The results obtained discover the polarization degree of freedom for guided waves paving the way toward numerous applications in flat optics and planar photonics. [ABSTRACT FROM AUTHOR]

Multilayer core–shell microparticles with a liquid core and a polycomposite light-absorbing shell (microcapsules) are important components of modern bio- and medical technologies. Opening of the microcapsule shell and payload release can be realized by optical radiation. The photophoretic force is due to the radiation-stimulated thermal gradient and arises from the temperature inhomogeneity of the microparticle. Photophoretic forces, as well as radiation pressure forces, are inherently mechanical forces and can cause microcapsules to move during the opening cycle. We numerically simulate the microcapsule photophoretic motion when illuminated by an intense laser pulse. Numerical calculations of the temperature field in a spherical microcapsule are carried out using the finite element method, taking into account the auxiliary nanoparticles, which are randomly distributed around the capsule and serve to enhance the heating of the capsule under short pulse exposure. The spatial distribution of the absorbed optical power as well as the temporal dynamics of microcapsule heating depending of its size are investigated in detail. We show, for the first time to our knowledge, that under the joint action of light pressure and photophoretic forces, the microcapsule can move along the laser incidence direction both forward and backward at the distance of several tens of nanometers depending on the particle size and conditions of optical absorption. [ABSTRACT FROM AUTHOR]

The mid‐infrared with a characteristic wavelength of 3–20 μm is important for a wealth of technologies. In particular, mid‐infrared spectroscopy can reveal material composition and structure information by fingerprinting chemical bonds’ infrared resonances. Despite these merits, state‐of‐the‐art mid‐infrared techniques are spatially limited above tens of micrometers due to the fundamental diffraction law. Herein, recent progress in the scanning probe nanoscale infrared characterization of biochemical materials and natural specimens beyond this spatial limitation is reviewed. By leveraging the strong tip–sample local interactions, scanning probe nano‐infrared methods probe nanoscale optical and mechanical responses to disclose material composition, heterogeneity, orientation, fine structure, and phase transitions at unprecedented length scales. These advances, therefore, revolutionize the understanding of a broad range of biochemical and natural materials and offer new material manipulation and engineering opportunities close to the ultimate length scales of fundamental physical, chemical, and biological processes.

Two-dimensional (2D) semiconductors, such as transition metal dichalcogenides, have emerged as important candidate materials for next-generation chip-scale optoelectronic devices with the development of large-scale production techniques, such as chemical vapor deposition (CVD). However, 2D materials need to be transferred to other target substrates after growth, during which various micro- and nanoscale defects, such as nanobubbles, are inevitably generated. These nanodefects not only influence the uniformity of 2D semiconductors but also may significantly alter the local optoelectronic properties of the composed devices. Hence, super-resolution discrimination and characterization of nanodefects are highly demanded. Here, we report a near-field nanophotoluminescence (nano-PL) microscope that can quickly screen nanobubbles and investigate their impact on local excitonic properties of 2D semiconductors by directly visualize the PL emission distribution with a very high spatial resolution of ∼10 nm, far below the optical diffraction limit, and a high speed of 10 ms/point under ambient conditions. By using nano-PL microscopy to map the exciton and trion emission intensity distributions in transferred CVD-grown monolayer tungsten disulfide (1L-WS 2 ) flakes, it is found that the PL intensity decreases by 13.4% as the height of the nanobubble increases by every nanometer, which is mainly caused by the suppression of trion emission due to the strong doping effect from the substrate. In addition to the nanobubbles, other types of nanodefects, such as cracks, stacks, and grain boundaries, can also be characterized. The nano-PL method is proven to be a powerful tool for the nondestructive quality inspection of nanodefects as well as the super-resolution exploration of local optoelectronic properties of 2D materials.