RADON-222 DETECTION USING BETA-DECAY PRODUCTS

The paper shows the possibility of determining of the radon by the radiometer on a base of multi-channel time analyzer of beta – decay products of radon. The radiometer consist of an electrostatic aerosol collector combined with the air intake, Geiger-Muller counter for detection of beta particles and multi-channel time analyzer. Accumulation time of aerosol sample takes up to 20 min, the time data processing is done by the radiometer about 5 hours. The data processing is at off-line mode using the computer decomposition process of decay spectrum

Ultrafast manipulation of the NiO antiferromagnetic order via sub gap optical excitation

Wide band gap insulators such as NiO offer the exciting prospect of coherently manipulating electronic correlations with strong optical fields. Contrary to metals where rapid dephasing of optical excitation via electronic processes occurs, the sub gap excitation in charge transfer insulators has been shown to couple to low energy bosonic excitations. However, it is currently unknown if the bosonic dressing field is composed of phonons or magnons. Here we use the prototypical charge transfer insulator NiO to demonstrate that 1.5 eV sub gap optical excitation leads to a renormalised NiO band gap in combination with a significant reduction of the antiferromagnetic order. We employ element specific X ray reflectivity at the FLASH free electron laser to demonstrate the reduction of the upper band edge at the O 1s 2p core valence resonance K edge whereas the antiferromagnetic order is probed via X ray magnetic linear dichroism XMLD at the Ni 2p 3d resonance L2 edge . Comparing the transient XMLD spectral line shape to ground state measurements allows us to extract a spin temperature rise of 65 5 K for time delays longer than 400 fs while at earlier times a non equilibrium spin state is formed. We identify transient mid gap states being formed during the first 200 fs accompanied by a band gap reduction lasting at least up to the maximum measured time delay of 2.4 ps. Electronic structure calculations indicate that magnon excitations significantly contribute to the reduction of the NiO band ga

Ultrafast modification of the electronic structure of a correlated insulator

A nontrivial balance between Coulomb repulsion and kinematic effects determines the electronic structure of correlated electron materials. The use of electromagnetic fields strong enough to rival these native microscopic interactions allows us to study the electronic response as well as the time scales and energies involved in using quantum effects for possible applications. We use element specific transient x ray absorption spectroscopy and high harmonic generation to measure the response to ultrashort off resonant optical fields in the prototypical correlated electron insulator NiO. Surprisingly, fields of up to 0.22 V lead to no detectable changes in the correlated Ni 3d orbitals contrary to previous predictions. A transient directional charge transfer is uncovered, a behavior that is captured by first principles theory. Our results highlight the importance of retardation effects in electronic screening and pinpoints a key challenge in functionalizing correlated materials for ultrafast device operatio

Ultrafast modification of the electronic structure of a correlated insulator

A nontrivial balance between Coulomb repulsion and kinematic effects determines the electronic structure of correlated electron materials. The use of electromagnetic fields strong enough to rival these native microscopic interactions allows us to study the electronic response as well as the time scales and energies involved in using quantum effects for possible applications. We use element-specific transient x-ray absorption spectroscopy and high-harmonic generation to measure the response to ultrashort off-resonant optical fields in the prototypical correlated electron insulator NiO. Surprisingly, fields of up to 0.22 V/Å lead to no detectable changes in the correlated Ni $3d$ orbitals contrary to previous predictions. A transient directional charge transfer is uncovered, a behavior that is captured by first-principles theory. Our results highlight the importance of retardation effects in electronic screening and pinpoints a key challenge in functionalizing correlated materials for ultrafast device operation

Ultrafast modification of the electronic structure of a correlated insulator

A nontrivial balance between Coulomb repulsion and kinematic effects determines the electronic structure of correlated electron materials. The use of electromagnetic fields strong enough to rival these native microscopic interactions allows us to study the electronic response as well as the time scales and energies involved in using quantum effects for possible applications. We use element-specific transient x-ray absorption spectroscopy and high-harmonic generation to measure the response to ultrashort off-resonant optical fields in the prototypical correlated electron insulator NiO. Surprisingly, fields of up to 0.22 V/angstrom lead to no detectable changes in the correlated Ni 3d orbitals contrary to previous predictions. A transient directional charge transfer is uncovered, a behavior that is captured by first-principles theory. Our results highlight the importance of retardation effects in electronic screening and pinpoints a key challenge in functionalizing correlated materials for ultrafast device operation