4 research outputs found
Monitoring the orientation of rare-earth-doped nanorods for flow shear tomography
Rare-earth phosphors exhibit unique luminescence polarization features
originating from the anisotropic symmetry of the emitter ion's chemical
environment. However, to take advantage of this peculiar property, it is
necessary to control and measure the ensemble orientation of the host particles
with a high degree of precision. Here, we show a methodology to obtain the
photoluminescence polarization of Eu-doped LaPO4 nano rods assembled in an
electrically modulated liquid-crystalline phase. We measure Eu3+ emission
spectra for the three main optimal configurations ({\sigma}, {\pi} and
{\alpha}, depending on the direction of observation and the polarization axes)
and use them as a reference for the nano rod orientation analysis. Based on the
fact that flowing nano rods tend to orient along the shear strain profile, we
use this orientation analysis to measure the local shear rate in a flowing
liquid. The potential of this approach is then demonstrated through tomographic
imaging of the shear rate distribution in a microfluidic system.Comment: 8 pages, 3 figures + supplementary files for experimental and
numerical method
Rare-earth complexes of mesomorphic Schiff's base ligands
Rare-earth complexes of mesomorphicSchiff's bases, 4-[(alkylimino)methyl]-3-hydroxyphenyl-4- alkyloxybenzoates, were synthesized. Whereas the ligands LH display a nematic and/or a smectic C phase, the metal complexes show a viscous smectic A phase and decompose at the clearing point. The mesophase was investigated by hot-stage polarizing optical microscopy, by differential scanning calorimetry and by high temperature X-ray diffraction. Two types of complex were found, [Ln(LH)(3)(NO3)(3)] and [Ln(LH)(2)L(NO3)(2)], depending on the ligand or the central metal ion. The first coordination sphere of the rare-earth ion in these metallomesogens is comparable to that in the structure of complexes with 4- alkoxy-N-alkyl-2-hydroxybenzaldimine ligands