Activation of coherent lattice phonon following ultrafast molecular spin-state photo-switching: A molecule-to-lattice energy transfer.

We combine ultrafast optical spectroscopy with femtosecond X-ray absorption to study the photo-switching dynamics of the [Fe(PM-AzA)2(NCS)2] spin-crossover molecular solid. The light-induced excited spin-state trapping process switches the molecules from low spin to high spin (HS) states on the sub-picosecond timescale. The change of the electronic state (<50 fs) induces a structural reorganization of the molecule within 160 fs. This transformation is accompanied by coherent molecular vibrations in the HS potential and especially a rapidly damped Fe-ligand breathing mode. The time-resolved studies evidence a delayed activation of coherent optical phonons of the lattice surrounding the photoexcited molecules.

Influence of pressure on the magnetic ordering of CeNiSnH and CeNiSnH(1.8) hydrides.

The magnetic properties of the antiferromagnet CeNiSnH and of the ferromagnet CeNiSnH(1.8) on hydrostatic pressure (0≤P≤10.8 bar) have been determined using a miniature piston-cylinder CuBe pressure cell. With increasing P, the Néel temperature of CeNiSnH increases weakly from 4.77 to 5.01 K whereas the Curie temperature of CeNiSnH(1.8) decreases rapidly from 7.16 to 5.30 K. Similar pressure dependence is also observed in the critical field of the metamagnetic transition of CeNiSnH and in the coercive field of CeNiSnH(1.8). Electronic structure calculations for these hydrides within the density functional theory show agreement with the experimental findings. Detailed examination of the chemical bonding features point to the conclusion that the antibonding Ce-Ni states below the Fermi level for CeNiSnH(1.8) could be responsible for the decrease of its Curie temperature under applied pressure.

Influence of Ce-H bonding on the physical properties of the hydrides CeCoSiH(1.0) and CeCoGeH(1.0).

The hydrides CeCoSiH(1.0) and CeCoGeH(1.0) which crystallize like the parent antiferromagnetic compounds CeCoSi and CeCoGe in the tetragonal CeFeSi-type structure, have been investigated by specific heat and thermoelectric power measurements and (1)H nuclear magnetic resonance (NMR). CeCoSiH(1.0) is an intermediate valence compound whereas CeCoGeH(1.0) can be considered as a nearly trivalent cerium compound. This behaviour is corroborated by the occurrence of a slight broadening of the (1)H NMR signal in the sequence [Formula: see text]. The band structure calculations performed on these hydrides reveal the existence of strong bonding Ce-H interaction, found to be larger in CeCoSiH(1.0) than in CeCoGeH(1.0).