Hochdruckuntersuchungen zum Magnetismus in Eu(II)-Chalcogeniden und metallischen Fe-Systemen mit nuklearer Vorwärtsstreuung von Synchrotronstrahlung und Mössbauerspektroskopie

von Kirsten RupprechtPaderborn, Univ., Diss., 200

Magnetic behaviour of Eu_2CuSi_3: Large negative magnetoresistance above Curie temperature

We report here the results of magnetic susceptibility, electrical-resistivity, magnetoresistance (MR), heat-capacity and ^{151}Eu Mossbauer effect measurements on the compound, Eu_2CuSi_3, crystallizing in an AlB_2-derived hexagonal structure. The results establish that Eu ions are divalent, undergoing long-range ferromagnetic-ordering below (T_C=) 37 K. An interesting observation is that the sign of MR is negative even at temperatures close to 3T_C, with increasing magnitude with decreasing temperature exhibiting a peak at T_C. This observation, being made for a Cu containing magnetic rare-earth compound for the first time, is of relevance to the field of collosal magnetoresistance.Comment: To appear in PRB, RevTex, 4 pages text + 6 psFigs. Related to our earlier work on Gd systems (see cond-mat/9811382, cond-mat/9811387, cond-mat/9812069, cond-mat/9812365

All-XUV Pump-Probe Transient Absorption Spectroscopy of the Structural Molecular Dynamics of Di-iodomethane

In this work, we use an extreme-ultraviolet (XUV) free-electron laser (FEL) to resonantly excite the I: 4$d_{5/2}–σ^∗$ transition of a gas-phase di-iodomethane (CH$_2$I$_2$) target. This site-specific excitation generates a 4$d$ core hole located at an iodine site, which leaves the molecule in a well-defined excited state. We subsequently measure the time-dependent absorption change of the molecule with the FEL probe spectrum centered on the same I: 4$_d$ resonance. Using ab initio calculations of absorption spectra of a transient isomerization pathway observed in earlier studies, our time-resolved measurements allow us to assign the timescales of the previously reported direct and indirect dissociation pathways. The presented method is thus sensitive to excited-state molecular geometries in a time-resolved manner, following a core-resonant site-specific trigger