AI Article Synopsis

  • The study demonstrates efficient transfer of spin-triplet excitons from organic semiconductors to inorganic semiconductors, specifically through pentacene and lead selenide (PbSe) nanocrystals.
  • Using ultrafast optical absorption spectroscopy, researchers found that triplet excitons transfer to PbSe in less than 1 picosecond and at a rate of 1.9 triplets for each absorbed photon, dependent on the bandgap being close to resonant energy.
  • Post-transfer, the excitations can lead to either charge separation for photovoltaic applications or glowing emissions for light-emitting technologies.

Article Abstract

The efficient transfer of energy between organic and inorganic semiconductors is a widely sought after property, but has so far been limited to the transfer of spin-singlet excitons. Here we report efficient resonant-energy transfer of molecular spin-triplet excitons from organic semiconductors to inorganic semiconductors. We use ultrafast optical absorption spectroscopy to track the dynamics of triplets, generated in pentacene through singlet exciton fission, at the interface with lead selenide (PbSe) nanocrystals. We show that triplets transfer to PbSe rapidly (<1 ps) and efficiently, with 1.9 triplets transferred for every photon absorbed in pentacene, but only when the bandgap of the nanocrystals is close to resonance (±0.2 eV) with the triplet energy. Following triplet transfer, the excitation can undergo either charge separation, allowing photovoltaic operation, or radiative recombination in the nanocrystal, enabling luminescent harvesting of triplet exciton energy in light-emitting structures.

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Source
http://dx.doi.org/10.1038/nmat4093DOI Listing

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