Issue 24, 2013

Effects of the morphology of nanostructured ZnO and interface modification on the device configuration and charge transport of ZnO/polymer hybrid solar cells

Abstract

In an organic-based solar cell, the short exciton diffusion length of organic materials requires effective donor–acceptor heterojunction at the nanoscale. In this work, hybrid inorganic/polymer solar cells based on ZnO nanostructures and poly(3-hexylthiophene) (P3HT) are constructed to study the effects of ZnO morphologies and wettability of the surface on the P3HT infiltration ability and charge transport mechanisms. The P3HT infiltrates the ZnO nanorod (NR) more remarkably than ZnO nanoparticle (NP) substrates. Although surface modification with indoline D205 dye molecules improves the wettability (viz. enlarges the contact angle) of NP surface, the P3HT infiltration distance decreases in comparison with the pristine NP case. This leads to relatively low short-circuit current density (Jsc) of the NP devices in comparison with that of the NR devices, even though the surface area of NP layers is larger than that of NR ones. Moreover, surface modification with squaraine dye onto the NR surface shows more significant improvement in Jsc than the NP case. This is due to the well-aligned morphology of the NRs, which facilitates dye modification, P3HT infiltration, and charge transport processes. These indicate that the NRs are more qualified as electron accepting substrates and transport pathway in hybrid solar cells than NPs.

Graphical abstract: Effects of the morphology of nanostructured ZnO and interface modification on the device configuration and charge transport of ZnO/polymer hybrid solar cells

Supplementary files

Article information

Article type
Paper
Submitted
21 Jan 2013
Accepted
28 Jan 2013
First published
29 Jan 2013

Phys. Chem. Chem. Phys., 2013,15, 9516-9522

Effects of the morphology of nanostructured ZnO and interface modification on the device configuration and charge transport of ZnO/polymer hybrid solar cells

P. Ruankham, S. Yoshikawa and T. Sagawa, Phys. Chem. Chem. Phys., 2013, 15, 9516 DOI: 10.1039/C3CP50266J

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