Issue 25, 2013

Organic photovoltaics based on a crosslinkable PCPDTBT analogue; synthesis, morphological studies, solar cell performance and enhanced lifetime

Abstract

A thermally crosslinkable poly(cyclopentadithiophene-alt-benzothiadiazole) (PCPDTBT) analogue copolymer with 2-ethylhexyl group and 5-hexenyl group on 4,4-positions of cyclopentadithiophene has been synthesised by palladium catalyzed Suzuki coupling reaction. Space-Charge Limited Current (SCLC) devices show hole mobility of up to 3 × 10−4 cm2 V−1 s−1. In addition, organic photovoltaics (OPVs) were fabricated using fullerene derivatives as acceptor materials. The best performing device exhibited Power Conversion Efficiency (PCE) at 2.0%, which could be improved to 3.7% after inclusion of dithiol additives. Most significantly, the lifetime of the OPV was enhanced by the crosslinking; when light soaked at 1 sun of irradiance, a half-life, t1/2 = 419 hours was measured, which is 51% improvement over an OPV using standard PCPDTBT. This higher stability is accounted for the crosslinkable structure of the polymer after annealing. The crosslinking reaction was confirmed by solubility tests, Fourier transform infrared spectroscopy and morphological analysis conducted by Atomic Force Microscopy and simultaneous synchrotron grazing-incidence small-/wide-angle X-ray scattering.

Graphical abstract: Organic photovoltaics based on a crosslinkable PCPDTBT analogue; synthesis, morphological studies, solar cell performance and enhanced lifetime

Supplementary files

Article information

Article type
Paper
Submitted
10 Mar 2013
Accepted
13 May 2013
First published
13 May 2013

J. Mater. Chem. A, 2013,1, 7370-7378

Organic photovoltaics based on a crosslinkable PCPDTBT analogue; synthesis, morphological studies, solar cell performance and enhanced lifetime

H. Waters, J. Kettle, S. Chang, C. Su, W. Wu, U.-Ser Jeng, Y. Tsai and M. Horie, J. Mater. Chem. A, 2013, 1, 7370 DOI: 10.1039/C3TA11002H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements