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Seeing sharper or becoming invisible are visions strongly driving the development of THz metamaterials. Strings are a preferred architecture of metamaterials as they extend continuously along one dimension. Here, we demonstrate that laterally interconnecting strings by structural elements that are placed in oscillation nodes such as to not quench electromagnetic resonances enables manufacturing of self-supported free-standing all-metal metamaterials. Upright S-strings, interconnected by rods, form a space-grid which we call meta-foil. In this way, we introduce binding between the atoms of the metamaterial, thus doing away with conventional frozen-in solutions like matrix embedding or thin films on substrates. Meta-foils are locally stiff, yet globally flexible. Even bent to cylinders of 1 cm radius, they maintain their spectral response, thus becoming true metamaterials on curved surfaces. Exploiting UV/X-ray lithography and ultimately plastic moulding, meta-foils can be cost-effectively manufactured in large areas and quantities to serve as optical elements.
Acquiring precise information about the mode content of a laser is critical for multiplexed optical communications, optical imaging with active wave-front control, and quantum-limited interferometric measurements. Hologram-based mode decomposition de
Stacked layers of metal meshes embedded in a dielectric substrate are routinely used for providing spectral selection at THz frequencies. Recent work has shown that particular geometries allow the refractive index to be tuned to produce practical art
Femtosecond-scale ultrafast imaging is an essential tool for visualizing ultrafast dynamics in molecular biology, physical chemistry, atomic physics, and fluid dynamics. Pump-probe imaging and a streak camera are the most widely used techniques, but
Laser-frequency stabilization with on-chip photonic integrated circuits will provide compact, low cost solutions to realize spectrally pure laser sources. Developing high-performance and scalable lasers is critical for applications including quantum
We describe an ultrafast time resolved pump-probe spectroscopy setup aimed at studying the switching of nanophotonic structures. Both fs pump and probe pulses can be independently tuned over broad frequency range between 3850 and 21050 cm$^{-1}$. A b