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Exciton Bimolecular Annihilation Dynamics in Push-Pull Semiconductor Polymers.


ABSTRACT: Exciton-exciton annihilation is a ubiquitous nonlinear dynamic phenomenon in materials hosting Frenkel excitons. In this work, we investigate the nonlinear exciton dynamics of an electron push-pull conjugated polymer by fluence-dependent transient absorption and excitation-correlation photoluminescence spectroscopy, where we can quantitatively show the latter to be a more selective probe of the nonlinear dynamics. Simulations based on a time-independent exciton annihilation model show a decreasing trend for the extracted annihilation rates with excitation fluence. Further investigation of the fluence-dependent transients suggests that the exciton-exciton annihilation bimolecular rates are not constant in time, displaying a t-1/2 time dependence, which we rationalize as reflective of one-dimensional exciton diffusion, with a diffusion length estimated to be 9 ± 2 nm. In addition, exciton annihilation gives rise to a long-lived species that recombines on a nanosecond time scale. Our conclusions shed broad light onto nonlinear exciton dynamics in push-pull conjugated polymers.

SUBMITTER: Zheng Y 

PROVIDER: S-EPMC10788955 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature

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Exciton Bimolecular Annihilation Dynamics in Push-Pull Semiconductor Polymers.

Zheng Yulong Y   Venkatesh Rahul R   Rojas-Gatjens Esteban E   Reichmanis Elsa E   Silva-Acuña Carlos C  

The journal of physical chemistry letters 20240102 1


Exciton-exciton annihilation is a ubiquitous nonlinear dynamic phenomenon in materials hosting Frenkel excitons. In this work, we investigate the nonlinear exciton dynamics of an electron push-pull conjugated polymer by fluence-dependent transient absorption and excitation-correlation photoluminescence spectroscopy, where we can quantitatively show the latter to be a more selective probe of the nonlinear dynamics. Simulations based on a time-independent exciton annihilation model show a decreasi  ...[more]

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