Conjugation-Length Dependence of Spin-Dependent Exciton Formation Rates inΠ-Conjugated Oligomers and Polymers

Abstract
We have measured the ratio, r=σS/σT of the formation cross section, σ of singlet and triplet excitons from polarons in π-conjugated oligomer and polymer films, using a spectroscopic technique we developed recently. We discovered a universal relation between r and the conjugation length (CL): r1 depends linearly on CL1, irrespective of the chain structure. Since r is directly related to the maximum possible electroluminescence quantum efficiency in organic light emitting diodes (OLED), our results indicate that polymers have an advantage over small molecules in OLED applications.