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Increasing Polymer Solar Cell Active Layer Efficiency and Organization by Adding Gold-Functionalized Reduced Graphene Oxide

Published online by Cambridge University Press:  21 February 2013

Rebecca Isseroff
Affiliation:
Dept of Materials Science and Engineering, SBU, Stony Brook, NY 11794-2275 Lawrence High School, Cedarhurst, NY 11516
Andrew Chen
Affiliation:
Lawrence High School, Cedarhurst, NY 11516
Sneha Chittabathini
Affiliation:
Lawrence High School, Cedarhurst, NY 11516
Alexandra Tse
Affiliation:
Lawrence High School, Cedarhurst, NY 11516
Cheng Pan
Affiliation:
Dept of Materials Science and Engineering, SBU, Stony Brook, NY 11794-2275
Benjamin Goldman
Affiliation:
Yeshiva University, NY, NY 10033
Hongfei Li
Affiliation:
Dept of Materials Science and Engineering, SBU, Stony Brook, NY 11794-2275
Benjamin Akhavan
Affiliation:
Rambam High School, Lawrence, NY 11559
Jonathan Sokolov
Affiliation:
Dept of Materials Science and Engineering, SBU, Stony Brook, NY 11794-2275
Miriam Rafailovich
Affiliation:
Dept of Materials Science and Engineering, SBU, Stony Brook, NY 11794-2275
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Abstract

Relatively low efficiency is one of the main obstacles to overcome in the engineering of organic bulk heterojunction (BHJ) solar cells. Reduced graphene oxide (RGO), which has high conductivity, has been proposed to enhance the function of PCBM in the interfacial dissociation of excitons, but incorporating it into the hydrophobic photoactive polymers has proved challenging. Here we describe a novel technique for incorporating Au nanoparticles (AuNp) into the structure of the RGO. The AuNps then interact with the sulfur groups on the photoactive polymer component, while the RGO interacts via π – π stacking with the chemically similar PCBM, thereby anchoring the complex to the polymer interface. Graphene oxide was synthesized and then reduced in the presence of a gold salt. The resulting gold-functionalized RGO (AuRGO) sheets were characterized using TGA, FTIR, and TEM. The AuRGO was not soluble in chlorobenzene; however, in the presence of P3HT, the AuRGO dissolved, suggesting a reaction between the gold and the sulfur of the P3HT via a metal-thiolate bond. At 2 mg/ml, AuRGO increased the solar cell efficiency approximately 50% over the control, but higher concentrations produced large, columnar structures which blocked the electrode from having a uniform contact with the active layer.

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Articles
Copyright
Copyright © Materials Research Society 2013

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