As atoms and molecules condense to form solids, a crystalline state can emerge with its highly ordered geometry and subnanometric lattice constant. In some physical systems, such as ferroelectric perovskites, a perfect crystalline structure forms even when the condensing substances are non-stoichiometric. The resulting solids have compositional disorder and complex macroscopic properties, such as giant susceptibilities and non-ergodicity. Here, we observe the spontaneous formation of a cubic structure in composite ferroelectric potassium-lithium-tantalate-niobate with micrometric lattice constant, 10(4) times larger than that of the underlying perovskite lattice. The 3D effect is observed in specifically designed samples in which the substitutional mixture varies periodically along one specific crystal axis. Laser propagation indicates a coherent polarization super-crystal that produces an optical X-ray diffractometry, an ordered mesoscopic state of matter with important implications for critical phenomena and applications in miniaturized 3D optical technologies.

We demonstrate an electro-optic response that is linear in the amplitude but independent of the sign of the applied electric field. The symmetry-preserving linear electro-optic effect emerges at low applied electric fields in freezing nanodisordered KNTN above the dielectric peak temperature, deep into the nominal paraelectric phase. Strong temperature dependence allows us to attribute the phenomenon to an anomalously reduced thermal agitation in the reorientational response of the underlying polar-nanoregions.

We propose and provide experimental evidence of a mechanism able to support negative intrinsic effective mass. The idea is to use a shape-sensitive nonlinearity to change the sign of the mass in the leading linear propagation equation. Intrinsic negative-mass dynamics is reported for light beams in a ferroelectric crystal substrate, where the diffusive photorefractive nonlinearity leads to a negative-mass Schrödinger equation. The signature of inverted dynamics is the observation of beams repelled from strongly guiding integrated waveguides irrespective of wavelength and intensity and suggests shape-sensitive nonlinearity as a basic mechanism leading to intrinsic negative mass.

We study the formation of 2D self-trapped beams in nanodisordered potassium-sodium-tantalate-niobate (KNTN) cooled below the dynamic glass transition. Supercooling is shown to accelerate the photorefractive response and enhance steady-state anisotropy. Effects in the excited state are attributed to the anomalous slim-loop polarization curve typical of relaxors dominated by non-interacting polar-nano-regions.

We demonstrate rejuvenation in scale-free optical propagation. The phenomenon is caused by the non-ergodic relaxation of the dipolar glass that mediates the photorefractive nonlinearity in compositionally-disordered lithium-enriched potassium-tantalate-niobate (KTN:Li). We implement rejuvenation to halt aging in the dipolar glass and extend the duration of beam diffraction cancellation.

The observation of initial time dynamics of self-trapping in photorefractive media indicates that optical spatial solitons supported by intense cumulative nonlinearities manifest temporally nonlocal signatures in the form of stretched exponential behavior. This general result, supported also by numerical predictions, is triggered by wave shaping in a time-constant buildup map, a consequence of the spatially resolved inertial response intrinsic to the geometrical transition from a diffracting to a self-focused beam, inherent to soliton appearance.