Tomer Drori

Ultrafast intersystem-crossing in platinum containing π-conjugated polymers with tunable spin-orbit coupling

The development of efficient organic light-emitting diodes (OLED) and organic photovoltaic cells requires control over the dynamics of spin sensitive excitations. Embedding heavy metal atoms in π-conjugated polymer chains enhances the spin-orbit coupling (SOC), and thus facilitates intersystem crossing (ISC) from the singlet to triplet manifolds. Here we use various nonlinear optical spectroscopies such as two-photon absorption and electroabsorption in conjunction with electronic structure calculations, for studying the energies, emission bands and ultrafast dynamics of spin photoexcitations in two newly synthesized π-conjugated polymers that contain intrachain platinum (Pt) atoms separated by one (Pt-1) or three (Pt-3) organic spacer units. The controllable SOC in these polymers leads to a record ISC time of <~1 ps in Pt-1 and ~6 ps in Pt-3. The tunable ultrafast ISC rate modulates the intensity ratio of the phosphorescence and fluorescence emission bands, with potential applications for white OLEDs.

Illumination-induced metastable polaron-supporting state in poly( p -phenylene vinylene) films

We discovered a new metastable polaron-supporting phase in pristine films of a soluble derivative of poly-p-phenylene vinylene (MEH-PPV) that is induced by UV illumination. In the initial un-illuminated phase A, the films do not show long-lived photogenerated polarons. However, prolonged UV illumination for several hours induces a reversible, me-tastable phase B that shows abundant long-lived photogenerated polarons. Phase B films transform back to the original phase A within 1/2 hour in the dark at room temperature. We propose a reversible mechanism in which UV illumination creates metastable deep defects that substantially increase the photogenerated polaron lifetime.