Dynamic recombination of triplet excitons in polymer heterojunctions*

Abstract

The dynamic recombination of two triplet excitons with opposite spins in the heterojunction structure has been investigated using a nonadiabatic evolution method. We demonstrate that luminous composite states including the excited polaron and the biexciton can be formed efficiently via the triplet exciton–triplet exciton reaction in the heterojunction and therefore this reaction can enhance the electroluminescence efficiency considerably, which is consistent qualitatively with experimental observations. Meanwhile, we find that, although the heterojunctions are beneficial to the generation of luminescent particles, large band offset caused by the heterojunction structure is not helpful to improve the electroluminescence efficiency. In addition, the mechanism of the triplet exciton–triplet exciton reaction in heterojunction is different from that of two similar coupling chains. Our results may deepen the understanding of the electroluminescence mechanism in polymer light-emitting devices.

Inducing Shifted Edge Modes by the Spin‐Dependent Time‐Periodical Driving and the Corresponding Topological Phase Transitions

“…[ 10 ] Time‐periodic systems with both Floquet zero and $$\pm \frac{\omega }{2}$$ edge modes can be of anomalous bulk‐edge correspondence. [ 11,12 ]…”