Article pubs.acs.org/JACS
Synthesis and Spectroscopy of Silver-Doped PbSe Quantum Dots Daniel M. Kroupa,†,‡,§ Barbara K. Hughes,†,‡,§ Elisa M. Miller,† David T. Moore,† Nicholas C. Anderson,† Boris D. Chernomordik,† Arthur J. Nozik,†,‡ and Matthew C. Beard*,† †
Chemistry & Nanoscience Center, National Renewable Energy Laboratory, Golden, Colorado 80401, United States Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, United States
‡
J. Am. Chem. Soc. 2017.139:10382-10394. Downloaded from pubs.acs.org by UNIV OF LOUISIANA AT LAFAYETTE on 09/29/18. For personal use only.
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ABSTRACT: Electronic impurity doping of bulk semiconductors is an essential component of semiconductor science and technology. Yet there are only a handful of studies demonstrating control of electronic impurities in semiconductor nanocrystals. Here, we studied electronic impurity doping of colloidal PbSe quantum dots (QDs) using a postsynthetic cation exchange reaction in which Pb is exchanged for Ag. We found that varying the concentration of dopants exposed to the as-synthesized PbSe QDs controls the extent of exchange. The electronic impurity doped QDs exhibit the fundamental spectroscopic signatures associated with injecting a free charge carrier into a QD under equilibrium conditions, including a bleach of the first exciton transition and the appearance of a quantumconfined, low-energy intraband absorption feature. Photoelectron spectroscopy confirms that Ag acts as a p-type dopant for PbSe QDs and infrared spectroscopy is consistent with k·p calculations of the size-dependent intraband transition energy. We find that to bleach the first exciton transition by an average of 1 carrier per QD requires that approximately 10% of the Pb be replaced by Ag. We hypothesize that the majority of incorporated Ag remains at the QD surface and does not interact with the core electronic states of the QD. Instead, the excess Ag at the surface promotes the incorporation of
