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Disordered photonic structures are promising for the realization of physical unclonable functions-physical objects that can overcome the limitations of conventional digital security and can enable cryptographic protocols immune against attacks by future quantum computers. The physical configuration of traditional physical unclonable functions is either fixed or can only be permanently modified, allowing one token per device and limiting their practicality. Here we overcome this limitation by creating reconfigurable structures made by light-transformable polymers in which the physical structure of the unclonable function can be reconfigured reversibly. Our approach allows the simultaneous coexistence of multiple physical unclonable functions within one device. The physical transformation is done all-optically in a reversible and spatially controlled fashion, allowing the generation of more complex keys. At the same time, as a set of switchable individual physical unclonable functions, it enables the authentication of multiple clients and allows for the practical implementations of quantum secure authentication and nonlinear generators of cryptographic keys., (© 2024. The Author(s), under exclusive licence to Springer Nature Limited.)

Disordered photonic materials can diffuse and localize light through random multiple scattering, offering opportunities to study mesoscopic phenomena, control light-matter interactions, and provide new strategies for photonic applications. Light transport in such media is governed by photonic modes characterized by resonances with finite spectral width and spatial extent. Considerable steps have been made recently towards control over the transport using wavefront shaping techniques. The selective engineering of individual modes, however, has been addressed only theoretically. Here, we experimentally demonstrate the possibility to engineer the confinement and the mutual interaction of modes in a two-dimensional disordered photonic structure. The strong light confinement is achieved at the fabrication stage by an optimization of the structure, and an accurate and local tuning of the mode resonance frequencies is achieved via post-fabrication processes. To show the versatility of our technique, we selectively control the detuning between overlapping localized modes and observe both frequency crossing and anti-crossing behaviours, thereby paving the way for the creation of open transmission channels in strongly scattering media.

Elaborating reliable and versatile strategies for efficient light coupling between free space and thin films is of crucial importance for new technologies in energy efficiency. Nanostructured materials have opened unprecedented opportunities for light management, notably in thin-film solar cells. Efficient coherent light trapping has been accomplished through the careful design of plasmonic nanoparticles and gratings, resonant dielectric particles and photonic crystals. Alternative approaches have used randomly textured surfaces as strong light diffusers to benefit from their broadband and wide-angle properties. Here, we propose a new strategy for photon management in thin films that combines both advantages of an efficient trapping due to coherent optical effects and broadband/wide-angle properties due to disorder. Our approach consists of the excitation of electromagnetic modes formed by multiple light scattering and wave interference in two-dimensional random media. We show, by numerical calculations, that the spectral and angular responses of thin films containing disordered photonic patterns are intimately related to the in-plane light transport process and can be tuned through structural correlations. Our findings, which are applicable to all waves, are particularly suited for improving the absorption efficiency of thin-film solar cells and can provide a new approach for high-extraction-efficiency light-emitting diodes.