Structural and Size Effects on the Spectroscopic and Redox Properties of CdSe Nanocrystals in Solution: The Role of Defect States

Authors

  • Dr. Matteo Amelia,

    1. Dipartimento di Chimica “G. Ciamician”, Università di Bologna via Selmi 2, 40126 Bologna (Italy), Fax: (+39) 051 2099456
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  • Stefania Impellizzeri,

    1. Department of Chemistry, University of Miami, 1301 Memorial Drive, Coral Gables, FL 33146-0431 (USA), Fax: (+1) 305 284 4571
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  • Simone Monaco,

    1. Dipartimento di Chimica “G. Ciamician”, Università di Bologna via Selmi 2, 40126 Bologna (Italy), Fax: (+39) 051 2099456
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  • Dr. Ibrahim Yildiz,

    1. Department of Chemistry, University of Miami, 1301 Memorial Drive, Coral Gables, FL 33146-0431 (USA), Fax: (+1) 305 284 4571
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  • Dr. Serena Silvi,

    1. Dipartimento di Chimica “G. Ciamician”, Università di Bologna via Selmi 2, 40126 Bologna (Italy), Fax: (+39) 051 2099456
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  • Prof. Françisco M. Raymo,

    Corresponding author
    1. Department of Chemistry, University of Miami, 1301 Memorial Drive, Coral Gables, FL 33146-0431 (USA), Fax: (+1) 305 284 4571
    • Department of Chemistry, University of Miami, 1301 Memorial Drive, Coral Gables, FL 33146-0431 (USA), Fax: (+1) 305 284 4571
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  • Prof. Alberto Credi

    Corresponding author
    1. Dipartimento di Chimica “G. Ciamician”, Università di Bologna via Selmi 2, 40126 Bologna (Italy), Fax: (+39) 051 2099456
    • Dipartimento di Chimica “G. Ciamician”, Università di Bologna via Selmi 2, 40126 Bologna (Italy), Fax: (+39) 051 2099456
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Abstract

Two series of CdSe quantum dots (QDs) with different diameters are prepared, according to frequently used protocols of the same synthetic procedure. For each sample the photophysical properties and the potentials for the first reduction and oxidation processes in organic solution are determined. The band gap obtained from electrochemical experiments is compared with that determined from the absorption and luminescence spectra. While the optical band gap decreases upon increasing the nanocrystal diameter, as expected on the basis of quantum confinement, the redox potentials and the electrochemical band gap are not monotonously related to the QD size. For both series, the smallest and largest QDs are both easier to oxidize and reduce than mid-sized QDs. In fact, the latter samples exhibit very broad voltammetric profiles, which suggests that the heterogeneous electron-transfer processes from/to the electrode are kinetically hindered. Conversely, the electrochemical band gap for the smallest and largest particles of each series is somewhat smaller than the optical band gap. These results indicate that, while the optical band gap depends on the actual electron–hole recombination within the nanocrystal, and therefore follows the size dependence expected from the particle-in-a-box model, the electrochemical processes of these QDs are strongly affected by other factors, such as the presence of surface defects. The investigations suggest that the influence of these defects on the potential values is more important for the smallest and largest QDs of each series, as confirmed by the respective luminescence bands and quantum yields. An interpretation for the size-dependent evolution of the surface defects in these nanocrystals is proposed based on the mechanism of their formation and growth.

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