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On the Geometry and Topology of Transformation Optics

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 Added by Yong-Liang Zhang
 Publication date 2013
  fields Physics
and research's language is English




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We generalize the geometrical model of transformation optics to Rieman-Cartan space with torsion by introducing topological defects in physical space. By relaxing the integrable condition, we show explicitly that the generalized equivalent medium are bi-anisotropic where the magnetoelectric coupling parameters emergent as the dislocation density. We also show the generation of orbital angular momentum of light. Our theory may open intriguing venues for controlling the vectorial degree of freedom of light with metamaterials.



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Parallel sorting of orbital angular momentum (OAM) and polarization has recently acquired paramount importance and interest in a wide range of fields ranging from telecommunications to high-dimensional quantum cryptography. Due to their inherently polarization-sensitive optical response, optical elements acting on the geometric phase prove to be useful for processing structured light beams with orthogonal polarization states by means of a single optical platform. In this work, we present the design, fabrication and test of a Pancharatnam-Berry optical element in silicon implementing a log-pol optical transformation at 1310 nm for the realization of an OAM sorter based on the conformal mapping between angular and linear momentum states. The metasurface is realized in the form of continuously-variant subwavelength gratings, providing high-resolution in the definition of the phase pattern. A hybrid device is fabricated assembling the metasurface for the geometric phase control with multi-level diffractive optics for the polarization-independent manipulation of the dynamic phase. The optical characterization confirms the capability to sort orbital angular momentum and circular polarization at the same time.
For many materials, a precise knowledge of their dispersion spectra is insufficient to predict their ordered phases and physical responses. Instead, these materials are classified by the geometrical and topological properties of their wavefunctions. A key challenge is to identify and implement experiments that probe or control these quantum properties. In this review, we describe recent progress in this direction, focusing on nonlinear electromagnetic responses that arise directly from quantum geometry and topology. We give an overview of the field by discussing new theoretical ideas, groundbreaking experiments, and the novel materials that drive them. We conclude by discussing how these techniques can be combined with new device architectures to uncover, probe, and ultimately control novel quantum phases with emergent topological and correlated properties.
We present a method to efficiently multiply or divide the orbital angular momentum (OAM) of light beams using a sequence of two optical elements. The key-element is represented by an optical transformation mapping the azimuthal phase gradient of the input OAM beam onto a circular sector. By combining multiple circular-sector transformations into a single optical element, it is possible to perform the multiplication of the value of the input OAM state by splitting and mapping the phase onto complementary circular sectors. Conversely, by combining multiple inverse transformations, the division of the initial OAM value is achievable, by mapping distinct complementary circular sectors of the input beam into an equal number of circular phase gradients. The optical elements have been fabricated in the form of phase-only diffractive optics with high-resolution electron-beam lithography. Optical tests confirm the capability of the multiplier optics to perform integer multiplication of the input OAM, while the designed dividers are demonstrated to correctly split up the input beam into a complementary set of OAM beams. These elements can find applications for the multiplicative generation of higher-order OAM modes, optical information processing based on OAM-beams transmission, and optical routing/switching in telecom.
The fundamental, or first, band gap is of unmatched importance in the study of photonic crystals. Here, we address precisely where this gap can be opened in the band structure of three-dimensional photonic crystals. Although strongly constrained by symmetry, this problem cannot be addressed directly with conventional band-symmetry analysis due to the existence of a photonic polarization vortex at zero frequency. We develop an approach for overcoming the associated symmetry singularity by incorporating fictitious, auxiliary longitudinal modes. Our strategy also enables us to extend recent developments in symmetry-based topological analysis to the fundamental gap of three-dimensional photonic crystals. Exploiting this, we systematically study the topology of the minimal fundamental gaps. This reveals the existence of topological gap-obstructions that push the fundamental gap higher than what a conventional analysis would suggest. Our work demonstrates that topology can play a crucial role in the opening of the fundamental photonic gap and informs future theoretical and experimental searches for conventional and topological band gaps in three-dimensional photonic crystals.
We consider a hybrid plasmon-exciton system comprised of a resonant molecular subsystem and three Au wires supporting a dipole mode which can be coupled to a dark mode in controllable fashion by variation of a symmetry parameter. The physics of such a system under strong coupling conditions is examined in detail. It is shown that if two wires supporting the dark mode are covered with molecular layers the system exhibits four resonant modes for a strong coupling regime due to asymmetry and lifted degeneracy of the molecular state in this case, while upon having molecular aggregates covering the top wire with dipolar mode, three resonant modes appear. Pump-probe simulations are performed to scrutinize the quantum dynamics and find possible ways to control plasmon-exciton materials. It is demonstrated that one can design hybrid nanomaterials with highly pronounced Fano-type resonances when excited by femtosecond lasers.
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