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@PHDTHESIS{Becker:173366,
author = {Becker, Jan Philipp},
title = {{E}lectrochemical {T}exturing and {D}eposition of
{T}ransparent {C}onductive {O}xide {L}ayers for the
{A}pplication in {S}ilicon {T}hin-{F}ilm {S}olar {C}ells},
volume = {247},
school = {RWTH Aachen},
type = {Dr.},
address = {Jülich},
publisher = {Forschungszentrum Jülich GmbH Zentralbibliothek, Verlag},
reportid = {FZJ-2014-06776},
series = {Schriften des Forschungszentrums Jülich Reihe Energie $\&$
Umwelt / Energy $\&$ Environment},
pages = {ix, 156, XXIV S.},
year = {2015},
note = {RWTH Aachen, Diss., 2014},
abstract = {Doped zinc oxide layers are widely used in thin-film solar
cells for several purposes, for instance as transparent
contacts, as a source of light scattering and as part of the
back reflector. Magnetron sputtered, aluminum-doped zinc
oxide thin films provide very high transparency and
conductivity, and are usually flat in the as-deposited
state. To introduce light scattering, a surface texture is
conventionally introduced by post-deposition etching in
diluted hydrochloric acid. However, the ability to obtain
suitable surface morphologies by chemical dissolution is
strongly dependent on the deposition process. Thus,
optimization of zinc oxide thin films requires a careful
trade-off between optical, electric, and morphological
properties. This markedly limits the process window and
excludes layers with excellent optical and electric
properties due to a lack of suitable texturing processes.
Electrochemical methods can help to overcome these
limitations by making novel zinc oxide structures
accessible. Both deposition and dissolution can be achieved
using electrochemical methods. In this context, an advanced
understanding of the stability of polycrystalline zinc oxide
thin films in aqueous solutions is crucial. This work
investigates the zinc oxide/electrolyte interface under
various conditions in order to further the understanding of
the interfacial reactions and the zinc oxide itself.
Cathodic electrochemical deposition was used for the growth
of zinc oxide films and nano-structures from aqueous
solutions. This method utilizes specific manipulation of the
interfacial pH at the substrate surface by reduction of a
suitable precursor such as nitrate or molecular oxygen. The
dependence of the zinc oxide precipitation and
crystallization on several parameters such as the deposition
potential, the bath temperature, the substrate, and the
composition of the electrolyte were investigated.
Temperatures above 50 $^{\circ}$C were found to be necessary
for the crystallization of well defined hexagonal crystals.
The comparison of electrochemical deposition on indium tin
oxide and zinc oxide substrates revealed the fundamental
influence of the substrate on the nucleation. While the
growth on zinc oxide seed layers seemed to proceed
epitaxially, conserving the preferential c-axis orientation
and crystallite size of the substrate, the nucleation on
indium tin oxide substrates depended largely on the applied
potential. With increasing cathodic potential the density of
nucleation sites increased. The crystallite size decreased
simultaneously.},
keywords = {Dissertation (GND)},
cin = {IEK-5},
cid = {I:(DE-Juel1)IEK-5-20101013},
pnm = {121 - Solar cells of the next generation (POF3-121)},
pid = {G:(DE-HGF)POF3-121},
typ = {PUB:(DE-HGF)11 / PUB:(DE-HGF)3},
url = {https://juser.fz-juelich.de/record/173366},
}