Singlet state | EPFL Graph Search

In quantum mechanics, a singlet state usually refers to a system in which all electrons are paired. The term 'singlet' originally meant a linked set of particles whose net angular momentum is zero, that is, whose overall spin quantum number s=0. As a result, there is only one spectral line of a singlet state. In contrast, a doublet state contains one unpaired electron and shows splitting of spectral lines into a doublet; and a triplet state has two unpaired electrons and shows threefold splitting of spectral lines. History Singlets and the related spin concepts of doublets and triplets occur frequently in atomic physics and nuclear physics, where one often needs to determine the total spin of a collection of particles. Since the only observed fundamental particle with zero spin is the extremely inaccessible Higgs boson, singlets in everyday physics are necessarily composed of sets of particles whose individual spins are non-zero, e.g. 1/2 or 1. T

Resonant production of the sterile neutrino dark matter and fine-tunings in the neutrino minimal standard model

Ananda Roy

The generation of lepton asymmetry below the electroweak scale has a considerable impact on production of dark matter sterile neutrinos. Oscillations or decays of the heavier sterile neutrinos in the neutrino minimal standard model can give rise to the requisite lepton asymmetry, provided the masses of the heavier neutrinos are sufficiently degenerate. We study the renormalization group evolution of the mass difference of these singlet fermions to understand the degree of necessary fine-tuning. We construct an example of the model that can lead to a technically natural realization of this low-energy degeneracy.

2010

Complexes luminescents de lanthanides avec des dérivés du cyclène comme briques pour l'ingénierie de sondes analytiques biomédicales

This work deals with the engineering of a new luminescent complex of lanthanide, able to be specifically grafted onto biological materials and to emit a characteristic light useful in quantifying the concentration of the target molecules. We have based our molecular design on TbL1, wich possesses a significant quantum yield in water pointing to an efficient intramolecular energy transfer. We have elaborated the synthesis of a ligand derived from L1 and named L3, by functionalizing one of the chromophoric groups into a moiety able to couple the luminescent sensor to biological materials. The synthesis of the complexes was then realized. The thermodynamic study of the ligands L1 and L3, and their terbium complexes in water was made to establish the distribution diagrams and to compare their behaviour, especially at neutral pH. In addition, EuL1 was also investigated and the complexation constants of TbL1, EuL1 and TbL3 in water showed that these molecules are thermodynamically stable in aqueous media. Characterization of EuL3 in the solid state by high resolution luminescence allowed us to determine the geometry of the coordination sphere of the Eu(III) ion, which possesses a distorded C4 symmetry. The detailed study of the Eu(III) ion transitions evidenced two different sites, possibly arising from an equilibrium induced by the competition between a water molecule and the carboxylate function. This interpretation is in line with the measured lifetimes of the Tb(III) and Eu(III) excited states and the calculation of the hydration number of the complexes in aqueous solution. The determination of the energy of the singlet state and triplet states of the ligand, as well as of the emitting levels of the Ln(III) ions in solution showed that their relative values are favorable for a good intramolecular energy transfer. The quantum yields of TbL3 and EuL3, which amount to 2.6 % and 1.4 %, respectively, are lower than those of the complexes with L1, denoting that the presence of the acid function increases losses in the energy transfer. However, these values remain sizeable enough for potential biomedical applications. The study of the intermolecular energy transfer from EuL1, EuL3 and TbL3 to the acceptor Cy5 has proved promising, and the resulting yields were 90 % for EuL1 and 80 % for the complexes with L3.

EPFL2004

Control of spin configuration in half-metallic La0.7Sr0.3MnO3 nano-structures

André Bisig

We investigate the interplay between the governing magnetic energy terms in patterned La0.7Sr0.3MnO3 (LSMO) elements by direct high-resolution x-ray magnetic microscopy as a function of temperature and geometrical parameters. We show that the magnetic configurations evolve from multidomain to flux-closure states (favored by the shape anisotropy) with decreasing element size, with a thickness-dependent crossover at the micrometer scale. The flux-closure states are stable against thermal excitations up to near the Curie temperature. Our results demonstrate control of the spin state in LSMO elements by judicious choice of the geometry, which is key for spintronics applications requiring high spin-polarizations and robust magnetic states. (C) 2011 American Institute of Physics. [doi:10.1063/1.3623480]

2011

Complexes luminescents de lanthanides avec des dérivés du cyclène comme briques pour l'ingénierie de sondes analytiques biomédicales

EPFL2004