Enhancing magnetic dipole emission with magnetic metamaterials

Magnetic dipole（MD） transitions are important for a range of technologies from quantum light sources and displays to lasers and bio-probes. However, the typical MD transitions are much weaker than their electric counterparts and are usually neglected in practical applications. Herein, we experimentally demonstrate that the MD transitions can be significantly enhanced by the well-developed magnetic metamaterials in the visible optical range. The magnetic metamaterials consist of silver nanostrips and a thick silver film, which are separated with an Eu3＋：polymethyl methacrylate（PMMA） film. By controlling the thickness of the Eu3＋：PMMA film, the magnetic resonance has been tuned to match the emission wavelength of MDs. Consequently,the intensity of MD emission has been significantly increased by around 30 times at the magnetic resonance wavelength, whereas the intensity of electric dipole emission is well-preserved. The corresponding numerical calculations reveal that the enhancement is directly generated by the magnetic resonance, which strongly increases the magnetic local density of states around the MD emitter and can efficiently radiate the MD emission into the far field. This is the first demonstration, to the best of our knowledge, that MD transitions can be improved by an additional degree of magnetic freedom, and we believe this research shall pave a new route towards bright magnetic emitters and their potential applications.

Solvent-Induced Symmetry-Breaking Charge Transfer in an Octupolar Triphenylamine Derivative Resolved with Transient Fluorescence Spectroscopy

The excited-state symmetry-breaking charge transfer (SBCT) dynamics in quadrupolar or octupolar molecules without clear infrared markers is usually hard to be tracked directly. In this work, on the basis of the evolution of instantaneous emission dipole moment obtained by femtosecond transient fluorescence spectroscopy, we presented a real-time characterization of the solvent-induced SBCT dynamics in an octupolar triphenylamine derivative. While the emission dipole moment of the octupolar trimer in weakly polar toluene changes little during the excited-state relaxation, it exhibits a fast reduction in a few picoseconds in strongly polar tetrahydrofuran. In comparison with the uorescence dynamics of dipolar monomer, we deduced that the emitting state of the octupolar trimer in strongly polar solvent, which undergoes solvent-induced structural uctuation, changes from exciton-coupled octupolar to excitation localized dipolar symmetry. In weakly polar solvent, the octupolar symmetry of the trimer is largely preserved during the solvation stabilization.

Consequence of shape elongation on emission asymmetry for colloidal CdSe/CdS nanoplatelets

In this paper, we demonstrate that for colloidal CdSe/CdS nanoplatelets, a rectangular shape induces emission asymmetry, in terms of both polarization and emission patterns. Polarimetry and emission pattern analyses are combined to provide information on the orientation of the transition dipoles involved in the nanoplatelet emission. It is shown that for rectangular nanoplatelets, the emission is polarized and the emission patterns are anisotropic, whereas they remain nonpolarized and isotropic for square nanoplatelets. This can be appropriately described by the dielectric antenna effect induced by the elongated shape of the rectangular platelet.