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The wave function of two identical bosons remains invariant under particle exchange—a fundamental quantum symmetry that underlies Bose-Einstein statistics. We report the experimental observation of bosonic exchange symmetry in the temporal wave function of photon pairs generated via spontaneous four-wave mixing in a three-level cold atomic ensemble. The measured two-photon temporal correlations show excellent agreement with theoretical predictions based on symmetrized bosonic wave functions. In addition, we perform time-resolved two-photon interference to reconstruct the complex temporal wave function. Both the amplitude and phase profiles exhibit clear symmetry under photon exchange, providing a confirmation of bosonic exchange symmetry in the time domain. 

In a recent article [X. Lai et al., Phys. Rev. Lett. 133, 033601 (2024)], the coherence time of degenerate entangled photon pairs (biphotons) generated via backward spontaneous four-wave mixing in a cold atomic ensemble was shown to be immune to optical loss and dephasing. This finding is crucial for practical applications in quantum information processing, quantum communication, and networking, where loss is inevitable. However, in studying the underlying mechanism for this loss- and dephasing-insensitive biphoton coherence time, the previous article did not take quantum noise into account. In this work, we employ the Heisenberg-Langevin approach to study this effect and provide a rigorous theoretical proof of the symmetry-protected biphoton coherence by taking quantum noise into consideration, as compared to the perturbation theory in the interaction picture. 

We report an experimental demonstration of anti-parity-time symmetric optical four-wave mixing in thermal rubidium vapor, where the propagation of probe and stokes fields in a double-Λ scheme is governed by a non-Hermitian Hamiltonian. We are particularly interested in studying quantum intensity correlations between the two fields near the exceptional point, taking into account loss and accompanied Langevin noise. Our experimental measurements of classical four-wave mixing gain and the associated two-mode relative-intensity squeezing are in reasonable agreement with the theoretical predictions. 

The electrical characterization and ammonia vapor (NH₃) response of a p‐Si/n‐poly[benzimidazobenzophenanthroline] (n‐BBL) thin‐film junction diode are reported. The presence of a depletion layer at the n‐BBL/p‐Si interface is verifiedviacapacitance–voltage measurements, and the built‐in potential is ≈1.8 V. Using the standard diode equation for data analysis, the turn‐on voltage, rectification ratio, and ideality parameter are found to be 2 V, 16, and 6, respectively. The diode is also tested in the presence of NH₃vapor where it retained its asymmetricJ–Vbehavior with increased currents and an insignificant change in device parameters. NH₃is believed to interact with the adsorbed O₂⁻species on the n‐BBL surface liberating electrons that enhance the diode current. The response time, recovery time, and sensitivity of the diode are 65 s, 121 s, and 52%, respectively. The removal of the gas restores the diode characteristics to their near original shape making it reusable. The diode is also electrically characterized as a function of temperature and is found to retain its rectifying behavior down to 150 K. The rectifying and gas‐sensing features make the diode multifunctional, which expands the range of applications of this ladder‐type conducting polymer. 

Abstract Developing stable and efficient electrocatalysts is vital for boosting oxygen evolution reaction (OER) rates in sustainable hydrogen production. High-entropy oxides (HEOs) consist of five or more metal cations, providing opportunities to tune their catalytic properties toward high OER efficiency. This work combines theoretical and experimental studies to scrutinize the OER activity and stability for spinel-type HEOs. Density functional theory confirms that randomly mixed metal sites show thermodynamic stability, with intermediate adsorption energies displaying wider distributions due to mixing-induced equatorial strain in active metal-oxygen bonds. The rapid sol-flame method is employed to synthesize HEO, comprising five 3d-transition metal cations, which exhibits superior OER activity and durability under alkaline conditions, outperforming lower-entropy oxides, even with partial surface oxidations. The study highlights that the enhanced activity of HEO is primarily attributed to the mixing of multiple elements, leading to strain effects near the active site, as well as surface composition and coverage. 

Abstract Phonon polaritons, the hybrid quasiparticles resulting from the coupling of photons and lattice vibrations, have gained significant attention in the field of layered van der Waals heterostructures. Particular interest has been paid to hetero‐bicrystals composed of molybdenum oxide (MoO₃) and hexagonal boron nitride (hBN), which feature polariton dispersion tailorable via avoided polariton mode crossings. In this work, the polariton eigenmodes in MoO₃‐hBN hetero‐bicrystals self‐assembled on ultrasmooth gold are systematically studied using synchrotron infrared nanospectroscopy. It is experimentally demonstrated that the spectral gap in bicrystal dispersion and corresponding regimes of negative refraction can be tuned by material layer thickness, and these results are quantitatively matched with a simple analytic model. Polaritonic cavity modes and polariton propagation along “forbidden” directions are also investigated in microscale bicrystals, which arise from the finite in‐plane dimension of the synthesized MoO₃micro‐ribbons. The findings shed light on the unique dispersion properties of polaritons in van der Waals heterostructures and pave the way for applications leveraging deeply sub‐wavelength mid‐infrared light‐matter interactions.