Charge transport in TiO2/MEHPPV polymer photovoltaics

A. J. Breeze, Z. Schlesinger, S. A. Carter, and P. J. Brock
Phys. Rev. B 64, 125205 – Published 10 September 2001
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Abstract

We study the effect of polymer thickness, hole mobility, and morphology on the device properties of polymer-based photovoltaics consisting of MEH-PPV as the optically active layer, TiO2 as the exciton dissociation surface, and ITO and Au electrodes. We demonstrate that the conversion efficiency in these polymer-based photovoltaics is primarily limited by the short exciton diffusion length combined with a low carrier mobility. For MEH-PPV devices with optimal device geometry, we achieve quantum efficiencies of 6% at the maximum absorption of the polymer, open circuit voltages of 1.1 V, current densities of 0.4 mA/cm2 and rectification ratios greater than 105 under 100 mW/cm2 white light illumination. In addition, we achieve fill factors up to 42% at high light intensities and as high as 69% at low light intensities. We conclude by presenting a model that describes charge transport in solidstatepolymer/TiO2-based photovoltaics and suggest methods for improving energy conversion efficiencies in polymer-based photovoltaics.

  • Received 5 June 2000

DOI:https://doi.org/10.1103/PhysRevB.64.125205

©2001 American Physical Society

Authors & Affiliations

A. J. Breeze, Z. Schlesinger, and S. A. Carter*

  • Physics Department, University of California, Santa Cruz, California 95064

P. J. Brock

  • IBM Almaden Research Center, San Jose, California

  • *Author to whom correspondence should be addressed. Email address: sacarter@cats.ucsc.edu

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Vol. 64, Iss. 12 — 15 September 2001

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