Enhancement in the Photorefractive Performance of Organic Composites Photosensitized with Functionalized CdSe Quantum Dots
Abstract
Enhancement in the photorefractive (PR) performance of organic composites photosensitized by CdSe quantum dots (QCdSe) passivated with the charge-transport ligands, sulfonated triphenyldiamine (STPD), is reported. This enhancement is primarily attributed to the ability of the passivating ligand, STPD, to facilitate the charge-transfer process between the QCdSe and the triphenyldiamine (TPD) charge-transport matrix. The PR composites exhibited a maximum photocharge-generation efficiency of 0.9% and two-beam coupling gain coefficient of 110 cm-1. These figures of merit represent a significant improvement over similar composites photosensitized with more conventional trioctylphosphine oxide-passivated QCdSe (TQCdSe). Moreover, composites photosensitized with SQCdSe had a faster response time of Ï" = 128 ms at an electric field of 60 V/µm compared with Ï" = 982 ms for those containing TQCdSe. Because of the molecular similarity between the STPD passivating groups and the TPD-based charge-transport matrix, concentrations of up to 1.4 wt% of SQCdSe are achieved in PR composites without any detectable phase separation, a considerable improvement over the 0.7 wt% for TQCdSe.
Recommended Citation
Y. Liang et al., "Enhancement in the Photorefractive Performance of Organic Composites Photosensitized with Functionalized CdSe Quantum Dots," Optical Materials, vol. 58, pp. 203 - 209, Elsevier B.V., Aug 2016.
The definitive version is available at https://doi.org/10.1016/j.optmat.2016.05.040
Department(s)
Chemistry
Keywords and Phrases
Photorefractive; Quantum dots; Triphenyldiamine
International Standard Serial Number (ISSN)
0925-3467
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2016 Elsevier B.V., All rights reserved.
Publication Date
01 Aug 2016
Comments
The authors wish to acknowledge the Material Research Center at the Missouri University of Science and Technology, the Department of Chemistry at the Missouri University of Science and Technology and the Missouri Research Board.