Witnessing pairing correlations in identical-particle systems

Quantum correlations and entanglement in identical-particle systems have been a puzzling question which has attracted vast interest and widely different approaches. Witness formalism developed first for entanglement measurement can be adopted to other kind of correlations. An approach is introduced by Kraus \emph{et al.}, [Phys. Rev. A \textbf{79}, 012306 (2009)] based on pairing correlations in fermionic systems and the use of witness formalism to detect pairing. In this contribution, a two-particle-annihilation operator is used for constructing a two-particle observable as a candidate witness for pairing correlations of both fermionic and bosonic systems. The corresponding separability bounds are also obtained. Two different types of separability definition are introduced for bosonic systems and the separability bounds associated with each type are discussed.

The Role of Mesoscale Plasma Sheet Dynamics in Ring Current Formation

During geomagnetically active periods ions are transported from the magnetotail into the inner magnetosphere and accelerated to energies of tens to hundreds of keV. These energetic ions, of mixed composition with the most important species being H+ and O+, become the dominant source of plasma pressure in the inner magnetosphere. Ion transport and acceleration can occur at different spatial and temporal scales ranging from global quasi-steady convection to localized impulsive injection events and may depend on the ion gyroradius. In this study we ascertain the relative importance of mesoscale flow structures and the effects of ion non-adiabaticity on the produced ring current. For this we use: global magnetohydrodynamic (MHD) simulations to generate self-consistent electromagnetic fields under typical driving conditions which exhibit bursty bulk flows (BBFs); and injected test particles, initialized to match the plasma moments of the MHD simulation, and subsequently evolved according to the kinetic equations of motion. We show that the BBFs produced by our simulation reproduce thermodynamic and magnetic statistics from in situ measurements and are numerically robust. Mining the simulation data we create a data set, over a billion points, connecting particle transport to characteristics of the MHD flow. From this we show that mesoscale bubbles, localized depleted entropy regions, and particle gradient drifts are critical for ion transport. Finally we show, using identical particle ensembles with varying mass, that O+ non-adiabaticity creates qualitative differences in energization and spatial distribution while H+ non-adiabaticity has non-negligible implications for loss timescales.

Entanglement Robustness via Spatial Deformation of Identical Particle Wave Functions

We address the problem of entanglement protection against surrounding noise by a procedure suitably exploiting spatial indistinguishability of identical subsystems. To this purpose, we take two initially separated and entangled identical qubits interacting with two independent noisy environments. Three typical models of environments are considered: amplitude damping channel, phase damping channel and depolarizing channel. After the interaction, we deform the wave functions of the two qubits to make them spatially overlap before performing spatially localized operations and classical communication (sLOCC) and eventually computing the entanglement of the resulting state. This way, we show that spatial indistinguishability of identical qubits can be utilized within the sLOCC operational framework to partially recover the quantum correlations spoiled by the environment. A general behavior emerges: the higher the spatial indistinguishability achieved via deformation, the larger the amount of recovered entanglement.

Highly fluorescent CsPbBr3/TiO2 core/shell perovskite nanocrystals with excellent stability

The poor stability of CsPbX3 (X = Cl, Br, I) perovskite nanocrystals is the most impediment to its application in the field of photoelectrics. In this work, monodisperse CsPbBr3/TiO2 nanocrystals are successfully prepared by coating titanium precursor on the surface of colloidal CsPbBr3 nanocrystals at room temperature. The CsPbBr3/TiO2 nanocomposites exhibit excellent stability, remaining the identical particle size (9.2 nm), crystal structures and optical properties. Time-resolved photoluminescence decay shows that the lifetime of CsPbBr3/TiO2 nanocrystals is about 4.04 ns and keeps great stability after lasting two months in the air. Results show that the coating of TiO2 on CsPbBr3 NCs greatly suppressed the anion exchange and photodegradation, which are the main reasons for dramatically improving their chemical stability and photostability. The results provide an effective method to solve the stability problem of perovskite nanostructures and are expected to have a promising application in optoelectronic fieldsArticle highlights 1. Prepared the all-inorganic CsPbBr3/TiO2 core/shell perovskite nanocrystals by an easy method. 2. Explored its essences of PL and lifetime of the synthesized CsPbBr3/TiO2 perovskite nanocrystals. 3. CsPbBr3/TiO2 nanocrystals show the great thermal stability after the post-annealing. 4. The CsPbBr3/TiO2 nanocrystals have a high PLQY and have a promising application in solar cells.