Abstract
The marriage of colloidal semiconductor nanocrystals and functional organic molecules has brought unique opportunities in emerging photonic and optoelectronic applications. Traditional semiconductor nanocrystals have been widely demonstrated to initiate efficient triplet energy transfer at the nanocrystal-acene interface. Herein, we report that unlike conventional semiconductor nanocrystals, lead halide perovskite nanocrystals promote an efficient Dexter-like singlet energy transfer to surface-anchored pentacene molecules rather than triplet energy transfer. Subsequently, molecular pentacene triplets are efficiently generated via singlet fission on the nanocrystal surface. Our demonstrated strategy not only unveils the obscure energy dynamics between perovskite nanocrystal and acenes, but also brings important perspectives of utilizing singlet fission throughout the solar spectrum.
Original language | English |
---|---|
Pages (from-to) | 4919-4927 |
Number of pages | 9 |
Journal | Journal of the American Chemical Society |
Volume | 141 |
Issue number | 12 |
DOIs | |
State | Published - Mar 27 2019 |
Bibliographical note
Funding Information:We gratefully acknowledge support for nanocrystal synthesis, ligand exchange, and characterization of energy transfer from the Center for Hybrid Organic Inorganic Semiconductors for Energy (CHOISE) an Energy Frontier Research Center funded by the Office of Basic Energy Sciences, Office of Science within the U.S. Department of Energy through contract number DE-AC36-08G028308. Work on spectroscopy and mechanisms of singlet fission was supported by the Solar Photochemistry Program funded by the Office of Basic Energy Sciences, Office of Science, Division of Chemical Sciences, Geosciences, and Biosciences. Organic Synthesis was supported by NSF (DMREF-1627428). The views expressed in the article do not necessarily represent the views of the DOE or the U.S. Government. The U.S. Government retains and the publisher, by accepting the article for publication, acknowledges that the U.S. Government retains a nonexclusive, paidup, irrevocable, worldwide license to publish or reproduce the published form of this work, or allow others to do so, for U.S. Government purposes.
Funding Information:
We gratefully acknowledge support for nanocrystal synthesis, ligand exchange, and characterization of energy transfer from the Center for Hybrid Organic Inorganic Semiconductors for Energy (CHOISE) an Energy Frontier Research Center funded by the Office of Basic Energy Sciences, Office of Science within the U.S. Department of Energy through contract number DE-AC36-08G028308. Work on spectroscopy and mechanisms of singlet fission was supported by the Solar Photochemistry Program funded by the Office of Basic Energy Sciences, Office of Science, Division of Chemical Sciences, Geosciences, and Biosciences. Organic Synthesis was supported by NSF (DMREF-1627428). The views expressed in the article do not necessarily represent the views of the DOE or the U.S. Government. The U.S. Government retains and the publisher, by accepting the article for publication, acknowledges that the U.S. Government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this work, or allow others to do so, for U.S. Government purposes.
Publisher Copyright:
© 2019 American Chemical Society.
ASJC Scopus subject areas
- Catalysis
- Chemistry (all)
- Biochemistry
- Colloid and Surface Chemistry