Early-stage dynamics of metallic droplets embedded in the nanotextured Mott insulating phase of V2 O3

Unveiling the physics that governs the intertwining between the nanoscale self-organization and the dynamics of insulator-to-metal transitions (IMTs) is key for controlling on demand the ultrafast switching in strongly correlated materials and nanodevices. A paradigmatic case is the IMT in V2O3, for which the mechanism that leads to the nucleation and growth of metallic nanodroplets out of the supposedly homogeneous Mott insulating phase is still a mystery. Here, we combine x-ray photoemission electron microscopy and ultrafast nonequilibrium optical spectroscopy to investigate the early-stage dynamics of isolated metallic nanodroplets across the IMT in V2O3 thin films. Our experiments show that the low-temperature monoclinic antiferromagnetic insulating phase is characterized by the spontaneous formation of striped polydomains, with different lattice distortions. The insulating domain boundaries accommodate the birth of metallic nanodroplets, whose nonequilibrium expansion can be triggered by the photoinduced change of the 3d-orbital occupation. We address the relation between the spontaneous nanotexture of the Mott insulating phase in V2O3 and the timescale of the metallic seeds growth. We speculate that the photoinduced metallic growth can proceed along a nonthermal pathway in which the monoclinic lattice symmetry of the insulating phase is partially retained

Nanoscale self-organization and metastable non-thermal metallicity in Mott insulators

Mott transitions in real materials are first order and almost always associated with lattice distortions, both features promoting the emergence of nanotextured phases. This nanoscale self-organization creates spatially inhomogeneous regions, which can host and protect transient non-thermal electronic and lattice states triggered by light excitation. Here, we combine time-resolved X-ray microscopy with a Landau-Ginzburg functional approach for calculating the strain and electronic real-space configurations. We investigate V2O3, the archetypal Mott insulator in which nanoscale self-organization already exists in the low-temperature monoclinic phase and strongly affects the transition towards the high-temperature corundum metallic phase. Our joint experimental-theoretical approach uncovers a remarkable out-of-equilibrium phenomenon: the photo-induced stabilisation of the long sought monoclinic metal phase, which is absent at equilibrium and in homogeneous materials, but emerges as a metastable state solely when light excitation is combined with the underlying nanotexture of the monoclinic lattice.status: publishe

Evolution of deformation in neutron-rich Ba isotopes up to A=150

The occurrence of octupolar shapes in the Ba isotopic chain was recently established experimentally up to N = 90. To further extend the systematics, the evolution of shapes in the most neutron-rich members of the Z = 56 isotopic chain accessible at present, Ba-148,Ba-150, has been studied via beta decay at the ISOLDE Decay Station. This paper reports on the first measurement of the positive-and negative-parity low-spin excited states of 150Ba and presents an extension of the beta-decay scheme of Cs-148. Employing the fast timing technique, half-lives for the 2(1)(+) level in both nuclei have been determined, resulting in T-1/2 = 1.51(1) ns for Ba-148 and T-1/2 = 3.4(2) ns for Ba-150. The systematics of low-spin states, together with the experimental determination of the B(E2 : 2(+) -> 0(+)) transition probabilities, indicate an increasing collectivity in Ba148-150, towards prolate deformed shapes. The experimental data are compared to symmetry conserving configuration mixing (SCCM) calculations, confirming an evolution of increasingly quadrupole deformed shapes with a definite octupolar character.Peer reviewe

Lifetime measurements of the low-lying excited states of ²⁰⁸Po

In this study we present the preliminary results about the lifetimes of the 2₂⁺, 4₁⁺ states of ²⁰⁸Po and the upper limit of the lifetime of the 2₁⁺ state. For measuring the lifetimes of the 2₁⁺ and 4₁⁺ states the Recoil Distance Doppler Shift (RDDS) method and for the lifetime of the 2₂⁺ state the Doppler Shift Attenuation method (DSAM) were used. The resulting absolute transition strength B(M1 ; 2₂⁺ → 2₁⁺) ≥ 0.122(20) μN² reveals the predominant isovector nature of the 2₂⁺ state of ²⁰⁸Po

Coulomb dissociation of O-16 into He-4 and C-12

We measured the Coulomb dissociation of O-16 into He-4 and C-12 within the FAIR Phase-0 program at GSI Helmholtzzentrum fur Schwerionenforschung Darmstadt, Germany. From this we will extract the photon dissociation cross section O-16(alpha,gamma)C-12, which is the time reversed reaction to C-12(alpha,gamma)O-16. With this indirect method, we aim to improve on the accuracy of the experimental data at lower energies than measured so far. The expected low cross section for the Coulomb dissociation reaction and close magnetic rigidity of beam and fragments demand a high precision measurement. Hence, new detector systems were built and radical changes to the (RB)-B-3 setup were necessary to cope with the high-intensity O-16 beam. All tracking detectors were designed to let the unreacted O-16 ions pass, while detecting the C-12 and He-4