SearcharxivSearch

arXiv subjects

Zhaoxin Wu

Publications and source records attributed to Zhaoxin Wu.

5 recordsLinked to original sources

Fractality-induced photonic topological insulators

Fractal lattices have recently emerged as a promising setting for topological wave physics, but in most realizations the topological character is inherited from externally engineered couplings, gauge fields, or temporal modulation rather than from the fractal geometry itself. Here, we experimentally realize a photonic higher-order topological insulator in which the topology is induced solely by the self-similar geometry of a Sierpi\'nski-gasket lattice. Following the isospectral reduction method recently proposed by Eek \textit{et al.}~\cite{Eek2025}, we show that the fractal waveguide array with uniform nearest-neighbor couplings can be mapped onto an effective breathing Kagome model that supports corner states. We selectively excite these modes with a weakly coupled detuned auxiliary waveguide and directly observe robust corner localization in real space, whereas an otherwise equivalent uniform triangular lattice exhibits only bulk diffraction under the same protocol. Spectral analysis and open-boundary calculations associate the observed states with nontrivial $C_3$ rotational topology, and disorder measurements further show that the corner localization persists over a finite range of random and symmetry-preserving disorder. Our results establish fractal geometry itself as a mechanism for generating topological boundary states in photonic lattices.

physics.optics

Nonlinear Photonic Tripartite Phase

Anderson localization is usually understood as a transition between extended and localized phases, with criticality confined to a single mobility edge. Recent advances predict that quasiperiodic systems can instead host a finite critical window bounded by mobility edges, in which localized, critical and extended states coexist. Yet both the experimental realization of this regime and whether interactions can provide controlled access to it remain unknown. Here, we realize such a tripartite phase in a nonlinear quasiperiodic photonic lattice and show that Kerr nonlinearity, acting as an effective interaction, enables state-selective access to the critical window. By tracking wavepacket dynamics, we distinguish localized, critical and extended transport regimes and uncover a state-selective response: rather than simply reinforcing localization through self-trapping, weak nonlinearity drives low-energy localized states into the critical window, whereas stronger nonlinearity restores localization. By contrast, critical, extended and high-energy localized states evolve monotonically towards self-trapped behaviour. Our results reveal a state-selective mechanism by which interactions provide controlled access to a pre-existing critical window in quasiperiodic systems.

cond-mat.mes-hall

Quantum boomerang effect of light

The quantum boomerang effect is a counterintuitive phenomenon where a wave packet, despite having an initial momentum, returns to its starting position in a disordered medium. However, up to now, the experimental exploration of this effect remains largely unexplored. Here, we report the experimental observation of the quantum boomerang effect of light. Our experiment is based on a one-dimensional disordered photonic lattice, which is composed of on-chip optical waveguides with engineered on-site random potential. We first characterize this optical disordered system by demonstrating the static Anderson localization of light beams. Next, through launching a kinetic light beam into the system, we observe that the light beam first moves away from its starting point, arrives at a maximum value, reverses its direction, and returns to its original position over time, confirming the observation of the quantum boomerang effect of light. Surprisingly, we find that optical loss, usually considered to be detrimental to optical experiments, can enhance the quantum boomerang effect by accelerating the light back to its original position. Our work provides new insights into the light-matter interactions in disordered medium and opens an avenue for future study of this phenomenon in nonlinear and many-photon contexts.

physics.optics

Harvesting the triplet excitons of quasi-two-dimensional perovskite toward highly efficient white light-emitting diodes

Utilization of triplet excitons, which generally emit poorly, is always fundamental to realize highly efficient organic light-emitting diodes (LEDs). While triplet harvest and energy transfer via electron exchange between triplet donor and acceptor are fully understood in doped organic phosphorescence and delayed fluorescence systems, the utilization and energy transfer of triplet excitons in quasi-two-dimensional (quasi-2D) perovskite are still ambiguous. Here, we use an orange-phosphorescence-emitting ultrathin organic layer to probe triplet behavior in the sky-blue-emitting quasi-2D perovskite. The delicate white LEDs architecture enables a carefully tailored Dexter-like energy-transfer mode that largely rescues the triplet excitons in quasi-2D perovskite. Our white organic-inorganic LEDs achieve maximum forward-viewing external quantum efficiency of 8.6% and luminance over 15000 cd m-2, exhibiting a significant efficiency enhancement versus the corresponding sky-blue perovskite LED (4.6%). The efficient management of energy transfer between excitons in quasi-2D perovskite and Frenkel excitons in organic layer opens the door to fully utilizing excitons for white organic-inorganic LEDs.

physics.optics

Impermeable Inorganic Walls Sandwiching Photoactive Layer toward Inverted Perovskite Solar and Indoor-Photovoltaic Devices

Interfaces between the perovskite active layer and the charge-transport layers (CTLs) play a critical role in both efficiency and stability of halide-perovskite photovoltaics. One of the major concerns is that surface defects of perovskite could cause detrimental nonradiative recombination and material degradation. In this work, we addressed this challenging problem by inserting ultrathin alkali-fluoride (AF) films between the tri-cation lead-iodide perovskite layer and both CTLs. This bilateral inorganic walls strategy makes use of both physical-blocking and chemical-anchoring functionalities of the continuous, uniform and compact AF framework: on the one hand, the uniformly distributed alkali-iodine coordination at the perovskite-AF interfaces effectively suppresses the formation of iodine-vacancy defects at the surfaces and grain boundaries of the whole perovskite film, thus reducing the trap-assisted recombination at the perovskite-CTL interfaces and therewith the open-voltage loss; on the other hand, the impermeable AF buffer layers effectively prevent the bidirectional ion migration at the perovskite-CTLs interfaces even under harsh working conditions. As a result, a power-conversion efficiency (PCE) of 22.02% (certified efficiency 20.4%) with low open-voltage deficit (< 0.4V) was achieved for the low-temperature processed inverted planar perovskite solar cells. Exceptional operational stability (500 h, ISOS-L-2) and thermal stability (1000 h, ISOS-D-2) were obtained. Meanwhile, a 35.7% PCE was obtained under dim-light source (1000 lux white LED light) with the optimized device, which is among the best records in perovskite indoor photovoltaics.

cond-mat.mtrl-sci