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ARTICLE
Copyright © 2013 by American Scientific Publishers
All rights reserved.
Printed in the United States of America
Energy and Environment Focus
Vol. 2, pp. 270–276, 2013
(www.aspbs.com/efocus)
Performance of Porous, Nanocolumnar ZnO
Electrodes Obtained at Low Temperature by
Plasma-Enhanced Chemical Vapor Deposition in
Dye-Sensitized Solar Cells
A. G. Vega-Poot
1, 2
, M. Macias-Montero
3
, A. Barranco
3
, A. Borras
3
,
A. R. Gonzalez-Elipe
3
, G. Oskam
2
, and J. A. Anta
1, *
1
Área de Química Física, Departamento de Sistemas Físicos, Químicos y Naturales,
Universidad Pablo de Olavide, 41013 Sevilla, Spain
2
Departamento de Física Aplicada, CINVESTAV-IPN, Mérida, Yucatán, 97310, México
3
Instituto de Ciencia de Materiales de Sevilla (CSIC-Univ. Sevilla), Avda. Américo Vespucio 49, 41092 Sevilla, Spain
ABSTRACT
The photovoltaic performance of dye-sensitized solar cells consisting of mesoporous ZnO nanocolumnar films
prepared at low temperatures by plasma enhanced chemical vapor deposition is studied. The results have been
compared with those of randomly packed nanoparticulate electrodes prepared by doctor-blading a suspension
of two mixed commercial nanopowders and subsequent high temperature annealing. The characterization of the
devices consisted of dye loading and current–voltage curve measurements. The charge collection efficiency was
probed by electrochemical impedance spectroscopy (EIS) under illumination, intensity modulated photovoltage
spectroscopy (IMVS) and intensity modulated photocurrent spectroscopy (IMPS). It has been found that the
nanoparticulate electrodes produce larger photocurrents as a consequence of better dye loading. However,
the combined EIS/IMPS/IMVS study provides self-consistent evidence that transport properties are similar for
both kinds of electrodes, approaching a 100% collection efficiency in both cases. The possibility of using ZnO
nanostructures obtained by low-temperature processing methods for low-cost DSC is discussed.
KEYWORDS: ZnO Nanowires, Dye-Sensitized Solar Cells, Electrochemical Impedance Spectroscopy, Electron
Transport Properties.
1. INTRODUCTION
ZnO is a well-known metal-oxide n-type semiconductor
with interesting applications in photovoltaics, such as in
dye-sensitized solar cells (DSC)
1
extremely thin absorber
solar cells,
2
and hybrid solar cells.
3
ZnO is capable of
yielding different electrode morphologies in a tailored
way by using a large variety of preparation methods.
5
It has good electron transport properties in the bulk and
an adequate band gap for applications in DSC.
5
ZnO-
based photoanodes have reached a record efficiency of a
7.5% under 1-sun illumination by means of hierarchical
nanostructures.
6
However, it has been pointed out
7
that
efficiencies of ZnO-based DSC remain far from their TiO
2
counterparts and that new synthetic routes, rather than
new morphologies, are more interesting to be investigated.
∗
Author to whom correspondence should be addressed.
Email: anta@upo.es
Received: 28 September 2013
Accepted: 14 October 2013
In this regard recombination and/or injection losses for
nanostructures obtained from electrodeposition in aqueous
solution
8
have been detected. Furthermore poor electron
injection from the excited dye to the semiconductor
9 10
has
also been claimed to explain the low performance of ZnO-
based DSCs.
Preparation procedures of ZnO photoanodes for DSC
applications can be divided in wet and dry methods. The
first types are by far the most used, including hydrothermal
synthesis,
11 12
spray pyrolysis,
6
electrodeposition,
13 14
etc.
All these techniques, including dry methods like chemi-
cal vapor deposition
15
require high temperature processing
steps to prepare the photoanodes.
In this work we test the photovoltaic performance
of 1-dimensional ZnO electrodes prepared by plasma-
enhanced chemical vapor deposition (PECVD),
16
a one-
step technique, which, to our knowledge, has not been
previously utilized to prepare ZnO electrodes for DSCs.
The application of this technique in the fabrication
270 Energy Environ. Focus 2013, Vol. 2, No. 4 2326-3040/2013/2/270/007 doi:10.1166/eef.2013.1062