Sargent, Edward H.
KAUST Grant NumberKUS-11-009-21
Online Publication Date2015-11-19
Print Publication Date2015-12-02
Permanent link to this recordhttp://hdl.handle.net/10754/599577
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Abstract© 2015 American Chemical Society. Inorganic semiconductor nanowires are of interest in nano- and microscale photonic and electronic applications. Here we report the formation of PbSe nanowires based on directional quantum dot alignment and fusion regulated by hybrid organic-inorganic perovskite surface ligands. All material synthesis is carried out at mild temperatures. Passivation of PbSe quantum dots was achieved via a new perovskite ligand exchange. Subsequent in situ ammonium/amine substitution by butylamine enables quantum dots to be capped by butylammonium lead iodide, and this further drives the formation of a PbSe nanowire superlattice in a two-dimensional (2D) perovskite matrix. The average spacing between two adjacent nanowires agrees well with the thickness of single atomic layer of 2D perovskite, consistent with the formation of a new self-assembled semiconductor nanowire:perovskite heterocrystal hybrid.
CitationYang Z, Yassitepe E, Voznyy O, Janmohamed A, Lan X, et al. (2015) Self-Assembled PbSe Nanowire:Perovskite Hybrids. Journal of the American Chemical Society 137: 14869–14872. Available: http://dx.doi.org/10.1021/jacs.5b10641.
SponsorsThis publication is based in part on supported by Award KUS-11-009-21, from King Abdullah University of Science and Technology (KAUST), by the Ontario Research Fund-Research Excellence Program, by the Natural Sciences and Engineering Research Council of Canada (NSERC), and by the International Cooperation of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) grant funded by the Korea government Ministry of Knowledge Economy (2012T100100740). A.J. thanks NSERC for Undergraduate Student Research Award Funding. E.Y. acknowledges support from FAPESP-BEPE fellowship (2014/18327-9). The authors thank E. Palmiano, L. Levina, R. Wolowiec, and D. Kopilovic for helpful discussions.
PublisherAmerican Chemical Society (ACS)
CollectionsPublications Acknowledging KAUST Support
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