Abstract
Fluorescence resonance energy transfer (FRET) enables photosynthetic light harvesting1, wavelength downconversion in light-emitting diodes2 (LEDs), and optical biosensing schemes3. The rate and efficiency of this donor to acceptor transfer of excitation between chromophores dictates the utility of FRET and can unlock new device operation motifs including quantum-funnel solar cells4, non-contact chromophore pumping from a proximal LED5, and markedly reduced gain thresholds6. However, the fastest reported FRET time constants involving spherical quantum dots (0.12–1 ns; refs 7, 8, 9) do not outpace biexciton Auger recombination (0.01–0.1 ns; ref. 10), which impedes multiexciton-driven applications including electrically pumped lasers11 and carrier-multiplication-enhanced photovoltaics12,13. Few-monolayer-thick semiconductor nanoplatelets (NPLs) with tens-of-nanometre lateral dimensions14 exhibit intense optical transitions14 and hundreds-of-picosecond Auger recombination15,16, but heretofore lack FRET characterizations. We examine binary CdSe NPL solids and show that interplate FRET (∼6–23 ps, presumably for co-facial arrangements) can occur 15–50 times faster than Auger recombination15,16 and demonstrate multiexcitonic FRET, making such materials ideal candidates for advanced technologies.
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Acknowledgements
This work was performed, in part, at the Center for Nanoscale Materials, a US Department of Energy, Office of Science, Office of Basic Energy Sciences User Facility under Contract No. DE-AC02-06CH11357. C.E.R. acknowledges support by a National Science Foundation Graduate Research Fellowship under Grant No. DGE-0824162. D.V.T. acknowledges support by the NSF MRSEC Program under Award Number DMR 14-20709 and thanks the II-VI Foundation and Keck Foundation. H.Z. and A.O.G. acknowledge support by the US Army Research Office under grant number W911NF-12-1-0407 and the Volkswagen Foundation (Germany).
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Sample synthesis and electron microscopy were performed by I.F. and D.V.T. Optical measurements and data analysis were performed by C.E.R. and R.D.S. Computational work was performed by H.Z., A.O.G. and S.K.G. All authors contributed to the writing of the manuscript.
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Rowland, C., Fedin, I., Zhang, H. et al. Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary CdSe nanoplatelet solids. Nature Mater 14, 484–489 (2015). https://doi.org/10.1038/nmat4231
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DOI: https://doi.org/10.1038/nmat4231
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