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dc.contributor.authorTang, Jiang
dc.contributor.authorBrzozowski, Lukasz
dc.contributor.authorBarkhouse, D. Aaron R.
dc.contributor.authorWang, Xihua
dc.contributor.authorDebnath, Ratan
dc.contributor.authorWolowiec, Remigiusz
dc.contributor.authorPalmiano, Elenita
dc.contributor.authorLevina, Larissa
dc.contributor.authorPattantyus-Abraham, Andras G.
dc.contributor.authorJamakosmanovic, Damir
dc.contributor.authorSargent, Edward H.
dc.date.accessioned2016-02-28T05:50:56Z
dc.date.available2016-02-28T05:50:56Z
dc.date.issued2010-01-27
dc.identifier.citationTang J, Brzozowski L, Barkhouse DAR, Wang X, Debnath R, et al. (2010) Quantum Dot Photovoltaics in the Extreme Quantum Confinement Regime: The Surface-Chemical Origins of Exceptional Air- and Light-Stability. ACS Nano 4: 869–878. Available: http://dx.doi.org/10.1021/nn901564q.
dc.identifier.issn1936-0851
dc.identifier.issn1936-086X
dc.identifier.pmid20104859
dc.identifier.doi10.1021/nn901564q
dc.identifier.urihttp://hdl.handle.net/10754/599428
dc.description.abstractWe report colloidal quantum dot (CQDs) photovoltaics having a ∼930 nm bandgap. The devices exhibit AM1.5G power conversion efficiencies in excess of 2%. Remarkably, the devices are stable in air under many tens of hours of solar illumination without the need for encapsulation. We explore herein the origins of this ordersof-magnitude improvement in air stability compared to larger PbS dots. We find that small and large dots form dramatically different oxidation products, with small dots forming lead sulfite primarily and large dots, lead sulfate. The lead sulfite produced on small dots results in shallow electron traps that are compatible with excellent device performance; whereas the sulfates formed on large dots lead to deep traps, midgap recombination, and consequent catastrophic loss of performance. We propose and offer evidence in support of an explanation based on the high rate of oxidation of sulfur-rich surfaces preponderant in highly faceted large-diameter PbS colloidal quantum dots. © 2010 American Chemical Society.
dc.description.sponsorshipWe thank Vlad Sukhovatkin, Kyle Kemp, Ghada Koleilat, Illan Kramer, and Steven Huang for their assistance and insights. J. Tang thanks Dr. Dan Grozea, Dr. Srebri Petrov and Dr. Haizheng Zhong for material characterization and fruitful discussion. R. Debnath acknowledges the financial support of an e8 scholarship. This publication was supported in part by Award No. KUS-11-009-21 made by King Abdullah University of Science and Technology (KAUST).
dc.publisherAmerican Chemical Society (ACS)
dc.subjectColloidal quantum dot photovoltaics
dc.subjectOptoelectronic device stability
dc.subjectOxidation products
dc.subjectRecombination
dc.subjectSurface spectroscopy
dc.subjectTransport in colloidal quantum dot solids
dc.subjectTraps
dc.titleQuantum Dot Photovoltaics in the Extreme Quantum Confinement Regime: The Surface-Chemical Origins of Exceptional Air- and Light-Stability
dc.typeArticle
dc.identifier.journalACS Nano
dc.contributor.institutionUniversity of Toronto, Toronto, Canada
kaust.grant.numberKUS-11-009-21
dc.date.published-online2010-01-27
dc.date.published-print2010-02-23


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