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Start date: 2020 × DDC: 530 × Subject: Polarization × WGL Institute: IPHT ×

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Now showing 1 - 2 of 2
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    Generation of Multiple Vector Optical Bottle Beams
    (Basel : MDPI, 2021) Khonina, Svetlana N.; Porfirev, Alexey P.; Volotovskiy, Sergey G.; Ustinov, Andrey V.; Fomchenkov, Sergey A.; Pavelyev, Vladimir S.; Schröter, Siegmund; Duparré, Michael
    We propose binary diffractive optical elements, combining several axicons of different types (axis-symmetrical and spiral), for the generation of a 3D intensity distribution in the form of multiple vector optical ‘bottle’ beams, which can be tailored by a change in the polarization state of the illumination radiation. The spatial dynamics of the obtained intensity distribution with different polarization states (circular and cylindrical of various orders) were investigated in paraxial mode numerically and experimentally. The designed binary axicons were manufactured using the e-beam lithography technique. The proposed combinations of optical elements can be used for the generation of vector optical traps in the field of laser trapping and manipulation, as well as for performing the spatial transformation of the polarization state of laser radiation, which is crucial in the field of laser-matter interaction for the generation of special morphologies of laser-induced periodic surface structures.
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    Polarization-resolved second-harmonic generation imaging through a multimode fiber
    (Washington, DC : OSA, 2021) Cifuentes, Angel; Pikálek, Tomáš; Ondráčková, Petra; Amezcua-Correa, Rodrigo; Antonio-Lopez, José Enrique; Čižmár, Tomáš; Trägårdh, Johanna
    Multimode fiber-based endoscopes have recently emerged as a tool for minimally invasive endoscopy in tissue, at depths well beyond the reach of multiphoton imaging. Here, we demonstrate label-free second-harmonic generation (SHG) microscopy through such a fiber endoscope. We simultaneously fully control the excitation polarization state and the spatial distribution of the light at the fiber tip, and we use this to implement polarization-resolved SHG imaging, which allows imaging and identification of structural proteins such as collagen and myosin. We image mouse tail tendon and heart tissue, employing the endoscope at depths up to 1 mm, demonstrating that we can differentiate these structural proteins. This method has the potential for enabling instant and in situ diagnosis of tumors and fibrotic conditions in sensitive tissue with minimal damage.