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Natalia Lindner

Publications and source records attributed to Natalia Lindner.

2 recordsLinked to original sources

Emergence of ferromagnetic state due to structural disorder in pseudo-binary Ce(Fe0.9Co0.1)2 compound

The changes in magnetic properties of Ce(Fe0.9Co0.1)2 compound with increasing disorder are discussed in the paper. Homogeneous alloys are known to undergo the phase transition from ferromagnetic to antiferromagnetic state accompanied by the structural distortion of the cubic Laves C15 phase into the rhombohedral one. Various stimuli, like the structural disorder, or applied magnetic field, can force the emergence of ferromagnetism at low temperatures. We initially introduced the structural disorder using rapid quenching. Further changes were made by severe plastic deformation. The presence of a ferromagnetic phase in a low-temperature region is reported here and accompanies the deterioration of a first-order phase transition. We show, based on electronic calculations, that the structural motifs arising from various distortions of the initial MgCu2-type structure, caused by the partial replacement of Fe with Co atoms, are characterized by stable antiferromagnetic order. This neglects simple structural distortions as the source of ferromagnetism. The presence of a strongly defective structure understood as a topologically disordered volume, reduced the fraction transformed from a ferromagnetic to an antiferromagnetic state. Therefore, a strong reduction of isothermal entropy changes was also observed, as it decreased from 1.94 Jkg-1K-1 and -1.43 Jkg-1K-1 ({\Delta}{\mu}0H = 4 T) to 0.30 Jkg-1K-1 and -0.96 Jkg-1K-1 for antiferromagnetic-ferromagnetic and ferromagnetic-paramagnetic transition, respectively.

cond-mat.mtrl-sci

Ultrafast two-colour X-ray emission spectroscopy reveals excited state landscape in a base metal dyad

Effective photoinduced charge transfer makes molecular bimetallic assemblies attractive for applications as active light induced proton reduction systems. For a more sustainable future, development of competitive base metal dyads is mandatory. However, the electron transfer mechanisms from the photosensitizer to the proton reduction catalyst in base metal dyads remain so far unexplored. We study a Fe-Co dyad that exhibits photocatalytic H2 production activity using femtosecond X-ray emission spectroscopy, complemented by ultrafast optical spectroscopy and theoretical time-dependent DFT calculations, to understand the electronic and structural dynamics after photoexcitation and during the subsequent charge transfer process from the FeII photosensitizer to the cobaloxime catalyst. Using this novel approach, the simultaneous measurement of the transient Kalpha X-ray emission at the iron and cobalt K-edges in a two-colour experiment is enabled making it possible to correlate the excited state dynamics to the electron transfer processes. The methodology, therefore, provides a clear and direct spectroscopic evidence of the Fe->Co electron transfer responsible for the proton reduction activity.

physics.chem-ph