Enhanced Mobility-Lifetime Products in PbS Colloidal Quantum Dot Photovoltaics
AuthorsJeong, Kwang S.
Schaefer, Andrew W.
Sargent, Edward H.
Asbury, John B.
KAUST Grant NumberKUS-11-009-21
Online Publication Date2011-12-22
Print Publication Date2012-01-24
Permanent link to this recordhttp://hdl.handle.net/10754/598182
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AbstractFigure Persented: Colloidal quantum dot (CQD) photovoltaics offer a promising approach to harvest the near-IR region of the solar spectrum, where half of the sun's power reaching the earth resides. High external quantum efficiencies have been obtained in the visible region in lead chalcogenide CQD photovoltaics. However, the corresponding efficiencies for band gap radiation in the near-infrared lag behind because the thickness of CQD photovoltaic layers from which charge carriers can be extracted is limited by short carrier diffusion lengths. Here, we investigate, using a combination of electrical and optical characterization techniques, ligand passivation strategies aimed at tuning the density and energetic distribution of charge trap states at PbS nanocrystal surfaces. Electrical and optical measurements reveal a more than 7-fold enhancement of the mobility-lifetime product of PbS CQD films treated with 3-mercaptopropionic acid (MPA) in comparison to traditional organic passivation strategies that have been examined in the literature. We show by direct head-to-head comparison that the greater mobility-lifetime products of MPA-treated devices enable markedly greater short-circuit current and higher power conversion efficiency under AM1.5 illumination. Our findings highlight the importance of selecting ligand treatment strategies capable of passivating a diversity of surface states to enable shallower and lower density trap distributions for better transport and more efficient CQD solar cells. © 2011 American Chemical Society.
CitationJeong KS, Tang J, Liu H, Kim J, Schaefer AW, et al. (2012) Enhanced Mobility-Lifetime Products in PbS Colloidal Quantum Dot Photovoltaics. ACS Nano 6: 89–99. Available: http://dx.doi.org/10.1021/nn2039164.
SponsorsThis research was supported in part by the Petroleum Research Fund under Grant No. PRF #49639-ND6, the National Science Foundation under Grant No. 0846241, and the Office of Naval Research under Grant No. N00014-11-1-0239. This publication is also based in part on work supported by Award No. KUS-11-009-21, made by King Abdullah University of Science and Technology (KAUST).
PublisherAmerican Chemical Society (ACS)
CollectionsPublications Acknowledging KAUST Support
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