Positron Annihilation Spectroscopy as a Diagnostic Tool for the Study of LiCoO2 Cathode of Lithium-Ion Batteries

Positron annihilation spectroscopy using lifetime and Doppler broadening allows the characterization of the lithiation state in LiCoO2 thin film used in cathode of lithium-ion batteries. The lifetime results reflect positron spillover because of the presence of graphite in between the oxide grains in real cathode Li-ion batteries. This spillover produces an effect in the measured positron parameters which are sensitive to delocalized electrons from lithium atoms as in Compton scattering results. The first component of the positron lifetime corresponds to a bulk-like state and can be used to characterize the state of charge of the cathode while the second component represents a surface state at the grain-graphite interface

An Interferometric Method for Particle Mass Measurements

We present an interferometric method suitable to measure particle masses and, where applicable to the particle and its corresponding antiparticle, their mass ratio in order to detect possible symmetry violations between matter and antimatter. The method is based on interferometric techniques tunable to the specific mass range of the particle under consideration. The case study of electron and positron is presented, following the recent observation of positron interferometry

Quantum view of Li-ion high mobility at carbon-coated cathode interfaces

Summary: Lithium-ion batteries (LIBs) are among the most promising power sources for electric vehicles, portable electronics and smart grids. In LIBs, the cathode is a major bottleneck, with a particular reference to its low electrical conductivity and Li-ion diffusivity. The coating with carbon layers is generally employed to enhance the electrical conductivity and to protect the active material from degradation during operation. Here, we demonstrate that this layer has a primary role in the lithium diffusivity into the cathode nanoparticles. Positron is a useful quantum probe at the electroactive materials/carbon interface to sense the mobility of Li-ion. Broadband electrical spectroscopy demonstrates that only a small number of Li-ions are moving, and that their diffusion strongly depends on the type of carbon additive. Positron annihilation and broadband electrical spectroscopies are crucial complementary tools to investigate the electronic effect of the carbon phase on the cathode performance and Li-ion dynamics in electroactive materials

Halide Perovskite-Lead Chalcohalide Nanocrystal Heterostructures

We report the synthesis of colloidal CsPbX3-Pb4S3Br2 (X = Cl, Br, I) nanocrystal heterostructures, providing an example of a sharp and atomically resolved epitaxial interface between a metal halide perovskite and a non-perovskite lattice. The CsPbBr3-Pb4S3Br2 nanocrystals are prepared by a two-step direct synthesis using preformed subnanometer CsPbBr3 clusters. Density functional theory calculations indicate the creation of a quasi-type II alignment at the heterointerface as well as the formation of localized trap states, promoting ultrafast separation of photogenerated excitons and carrier trapping, as confirmed by spectroscopic experiments. Postsynthesis reaction with either Cl- or I- ions delivers the corresponding CsPbCl3-Pb4S3Br2 and CsPbI3-Pb4S3Br2 heterostructures, thus enabling anion exchange only in the perovskite domain. An increased structural rigidity is conferred to the perovskite lattice when it is interfaced with the chalcohalide lattice. This is attested by the improved stability of the metastable γphase (or "black"phase) of CsPbI3 in the CsPbI3-Pb4S3Br2 heterostructure

Pulsed production of antihydrogen

Antihydrogen atoms with K or sub-K temperature are a powerful tool to precisely probe the validity of fundamental physics laws and the design of highly sensitive experiments needs antihydrogen with controllable and well defined conditions. We present here experimental results on the production of antihydrogen in a pulsed mode in which the time when 90% of the atoms are produced is known with an uncertainty of ~250 ns. The pulsed source is generated by the charge-exchange reaction between Rydberg positronium atoms\u2014produced via the injection of a pulsed positron beam into a nanochanneled Si target, and excited by laser pulses\u2014and antiprotons, trapped, cooled and manipulated in electromagnetic traps. The pulsed production enables the control of the antihydrogen temperature, the tunability of the Rydberg states, their de-excitation by pulsed lasers and the manipulation through electric field gradients. The production of pulsed antihydrogen is a major landmark in the AEgIS experiment to perform direct measurements of the validity of the Weak Equivalence Principle for antimatter