Evidence of orbital reconstruction at interfaces in ultrathin La0.67Sr0.33MnO3 films

Linear dichroism (LD) in x-ray absorption, diffraction, transport, and magnetization measurements on thin La(0.7)Sr(0.3)MnO(3) films grown on different substrates, allow identification of a peculiar interface effect, related just to the presence of the interface. We report the LD signature of preferential 3d-e(g)(3z(2)-r(2)) occupation at the interface, suppressing the double exchange mechanism. This surface orbital reconstruction is opposite to that favored by residual strain and is independent of dipolar fields, the chemical nature of the substrate and the presence of capping layers.     

Isomer spectroscopy in (216)(90)Th(126) and the magicity of (218)(92)U(126)

Excited states in (216)Th were investigated via prompt and delayed gamma decays and the recoil-decay tagging method. The decay schemes of the I(pi) = (8+), t(1/2) = 128(8) micros, the I(pi) = (11-), t(1/2) = 615(55) ns, and the I(pi) = (14+), t(1/2) > or = 130 ns isomers were established. The configuration pi h(9/2)f(7/2) is assigned to the I(pi) = (8+) isomer, which implies that the h(9/2) and f(7/2) states are nearly degenerate. This is ascribed to increased binding of the f(7/2) orbital by its coupling to a low-lying I(pi) = (3-) state at E(x) = 1687 keV. The role of octupole and pairing correlations for a Z = 92 shell closure prediction is discussed on the basis of shell model calculations.     

Isomeric states in proton-unbound 187, 189Bi isotopes

Prompt and delayed gamma-ray spectroscopy of very neutron-deficient bismuth isotopes ^{187, 189}Bi has been performed using the Recoil Decay Tagging (RTD) method. The isomeric i _13/2 states have been identified and their lifetimes have been measured. The systematics of these long-lived M2 isomers has been extended to the proton-unbound isotopes. The general behaviour of single-proton states is discussed within the systematics and interpreted within the shell-model framework. Received: 2 May 2002 / Accepted: 3 June 2002 / Published online: 19 November 2002 RID="a" ID="a"e-mail: wkorten@cea.fr RID="b" ID="b"Present address: GANIL, Caen, France. RID="c" ID="c"Present address: Radiation and Nuclear Safety Authority, P.O. Box 14, FIN-00881 Helsinki. Communicated by D. Schwalm     

In-beam studies of very neutron-deficient heavy nuclei

The JYFL gas-filled recoil separator RITU, combined with Ge detector arrays and a SACRED magnetic solenoid spectrometer, has been successfully employed in recoil-decay-tagging (RDT) experiments in order to probe structures of very neutron-deficient heavy nuclei. The present contribution focuses on the light Pb region where the new data extend the systematics of shape-coexisting yrast states towards the proton dripline. Similarities between band structures and their relation to possible multi-particle multi-hole intruder excitations will be discussed. Received: 21 March 2002 / Accepted: 16 May 2002 / Published online: 31 October 2002 RID="a" ID="a"e-mail: rauno.julin@phys.jyu.fi     

Spectroscopy of the neutron-deficient nuclide 171Pt

The decay out of the πh _11/2νh _11/2 band to the known low-energy levels in ¹³²La was studied using the reaction ¹⁰⁰Mo + ³⁶S at 160 MeV beam energy. The low-energy level scheme has been further developed and unambiguous spin and parity values have been assigned to the levels connecting the band to the 6^- isomeric state. According to the new level scheme the spins in the πh _11/2νh _11/2 band are shifted up by one unit compared to the earlier tentative experimental values. The obtained new spins prove the existence of signature inversion in ¹³²La and give further support to the spin assignments made for the πh _11/2νh _11/2 bands in the neighbouring odd-odd La isotopes from level energy systematics. Received: 7 May 2002 / Accepted: 31 October 2002 / Published online: 17 January 2003 RID="a" ID="a"e-mail: timar@atomki.hu RID="b" ID="b"Present address: Dipartimento di Matematica e Fisica, Università di Camerino, via Madonna delle Carceri, I-62032 Camerino, Italy. Communicated by J. ?yst?     

Electron spectroscopy study in the NbN growth for NbN/AlN interfaces

NbN superconductor and wide band gap AlN thin films were deposited using sputtering at room temperature. Study of the nitride interfaces are forerunner to the growth Josephson junctions that are considered able to work in the terahertz frequency. We find that to be compatible with lithography technology and to have a high critical transition temperature, the substrate should not be overheated, and this means working in low power regime to limit the induced heating of the plasma. X-ray photoelectron spectroscopy and X-ray diffraction analysis were performed on samples deposited on crystalline, amorphous, flexible, and nanostructured substrates. The experimental results suggest us how to improve the deposition process in order to obtain the best nitride films as well as NbN/AlN/NbN trilayers for Josephson junction applications.     

Nanoscopic coexistence of magnetism and superconductivity in YBa2Cu3O6+x detected by muon spin rotation

We performed zero and transverse field muon spin rotation experiments on a large number of YBa2Cu3O6+x samples. We detect the coexistence of antiferromagnetic (AF) short range magnetism with superconductivity below T(f) < or = 10 K in compositions 0.37 < or = x < or = 0.39. Most muons experience local AF fields, even when a SQUID detects a full superconducting volume fraction, which points to a local minimal interference organization of short AF stripes embedded in the superconductor. A detailed phase diagram is produced and the consequences of the minimal interference are discussed.     

Antiviral properties from plants of the Mediterranean flora

Natural products are a successful source in drug discovery, playing a significant role in maintaining human health. We investigated the in vitro cytotoxicity and antiviral activity of extracts from 18 traditionally used Mediterranean plants. Noteworthy antiviral activity was found in the extract obtained from the branches of Daphne gnidium L. against human immunodeficiency virus type-1 (EC₅₀ = 0.08 μg/mL) and coxsackievirus B5 (EC₅₀ = 0.10 μg/mL). Other relevant activities were found against BVDV, YFV, Sb-1, RSV and HSV-1. Interestingly, extracts from Artemisia arborescens L. and Rubus ulmifolius Schott, as well as those from D. gnidium L., showed activities against two different viruses. This extensive antiviral screening allowed us to identify attractive activities, offering opportunities to develop lead compounds with a great pharmaceutical potential.     

Observation of a rotational band in the odd-Z transfermium nucleus 101251Md

A rotational band has been unambiguously observed in an odd-proton transfermium nucleus for the first time. An in-beam gamma-ray spectroscopic study of 101/251Md has been performed using the gamma-ray array JUROGAM combined with the gas-filled separator RITU and the focal plane device GREAT. The experimental results, compared to Hartree-Fock-Bogolyubov calculations, lead to the interpretation that the rotational band is built on the [521]1/2(-) Nilsson state.     

Atomic XAFS as a tool to probe the reactivity of metal oxide catalysts: quantifying metal oxide support effects

The potential of atomic XAFS (AXAFS) to directly probe the catalytic performances of a set of supported metal oxide catalysts has been explored for the first time. For this purpose, a series of 1 wt % supported vanadium oxide catalysts have been prepared differing in their oxidic support material (SiO2, Al2O3, Nb2O5, and ZrO2). Previous characterization results have shown that these catalysts contain the same molecular structure on all supports, i.e., a monomeric VO4 species. It was found that the catalytic activity for the selective oxidation of methanol to formaldehyde and the oxidative dehydrogenation of propane to propene increases in the order SiO2 < Al2O3 < Nb2O5 < ZrO2. The opposite trend was observed for the dehydrogenation of propane to propene in the absence of oxygen. Interestingly, the intensity of the Fourier transform AXAFS peak decreases in the same order. This can be interpreted by an increase in the binding energy of the vanadium valence orbitals when the ionicity of the support (increasing electron charge on the support oxygen atoms) increases. Moreover, detailed EXAFS analysis shows a systematic decrease of the V-Ob(-M(support)) and an increase of a the V-O(H) bond length, when going from SiO2 to ZrO2. This implies a more reactive OH group for ZrO2, in line with the catalytic data. These results show that the electronic structure and consequently the catalytic behavior of the VO4 cluster depend on the ionicity of the support oxide. These results demonstrate that AXAFS spectroscopy can be used to understand and predict the catalytic performances of supported metal oxide catalysts. Furthermore, it enables the user to gather quantitative insight in metal oxide support interactions.