Abstract

Recently, synthetic optical materials represented via non-Hermitian Hamiltonians have attracted significant attention because of their nonorthogonal eigensystems, enabling unidirectionality, nonreciprocity and unconventional beam dynamics. Such systems demand carefully configured complex optical potentials to create skewed vector spaces with a desired metric distortion. In this paper, we report optically generated non-Hermitian photonic lattices with versatile control of real and imaginary sub-lattices. In the proposed method, such lattices are generated by vector-field holographic interference of two elliptically polarized pump beams on azobenzene-doped polymer thin films. We experimentally observe violation of Friedel's law of diffraction, indicating the onset of complex lattice formation. We further create an exact parity-time symmetric lattice to demonstrate totally asymmetric diffraction at the spontaneous symmetry-breaking threshold, referred to as an exceptional point. On this basis, we provide the experimental demonstration of reconfigurable non-Hermitian photonic lattices in the optical domain and observe the purest exceptional point ever reported to date.

Highlights

  • Synthetic optical materials represented via non-Hermitian Hamiltonians have attracted significant attention because of their nonorthogonal eigensystems, enabling unidirectionality, nonreciprocity and unconventional beam dynamics

  • Engineered optical materials have been extensively studied in the pursuit of new materials with exotic properties unavailable from natural substances, especially within the context of photonic crystals[1] and metamaterials[2]

  • In seminal papers on PT-symmetric Hamiltonians[3,4,5], Bender and coworkers showed that such Hamiltonians display completely real-valued energy spectra below certain phase-transition thresholds, referred to as exceptional points

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Summary

Introduction

Synthetic optical materials represented via non-Hermitian Hamiltonians have attracted significant attention because of their nonorthogonal eigensystems, enabling unidirectionality, nonreciprocity and unconventional beam dynamics. These two sub-grating components originate from distinct mechanisms: the former is generated by optical gradient forces and consequent migration of azobenzene–polymer complexes[22], while the latter is formed by polarization-induced reorientation of azo-dye molecules[23].

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