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@ARTICLE{Jaegermann:877850,
author = {Jaegermann, Wolfram and Kaiser, Bernhard and Finger,
Friedhelm and Smirnov, Vladimir and Schäfer, Rolf},
title = {{D}esign {C}onsiderations of {E}fficient
{P}hoto-{E}lectrosynthetic {C}ells and its {R}ealization
{U}sing {B}uried {J}unction {S}i {T}hin {F}ilm {M}ulti
{A}bsorber {C}ells},
journal = {Zeitschrift für physikalische Chemie},
volume = {234},
number = {4},
issn = {2196-7156},
address = {Berlin},
publisher = {DeGruyter},
reportid = {FZJ-2020-02474},
pages = {549 - 604},
year = {2020},
abstract = {As is obvious from previous work on semiconductor
photoelectrochemistry, single junction semiconductors do not
provide either the required maximum photovoltage or a high
photocurrent for solar water splitting, which is required
for efficient stand-alone devices. From these experiences we
conclude, that multi-junction devices must be developed for
bias-free water splitting. In this article we present our
design considerations needed for the development of
efficient photo-electro-synthetic cells, which have guided
us during the DFG priority program 1613. At first, we
discuss the fundamental requirements, which must be
fulfilled to lead to effective solar water splitting
devices. Buried junction and photoelectrochemical
arrangements are compared. It will become clear, that the
photovoltaic (PV) and electrochemical (EC) components can be
optimized separately, but that maximized conversion
efficiencies need photovoltages produced in the photovoltaic
part of the device, which are adapted to the electrochemical
performance of the electrolyzer components without energetic
losses in their coupling across the involved interfaces.
Therefore, in part 2 we will present the needs to develop
appropriate interface engineering layers for proper chemical
and electronic surface passivation. In addition, highly
efficient electrocatalysts, either for the hydrogen or
oxygen evolution reaction (HER, OER), must be adjusted in
their energetic coupling to the semiconductor band edges and
to the redox potentials in the electrolyte with minimized
losses in the chemical potentials. The third part of our
paper describes at first the demands and achievements on
developing multijunction thin-film silicon solar cells. With
different arrangements of silicon stacks a wide range of
photovoltages and photocurrents can be provided. These solar
cells are applied as photocathodes in integrated directly
coupled PV-EC devices. For this purpose thin Pt and Ni
catalyst layers are used on top of the solar cells for the
HER and a wire connected RuO2 counter electrode is used for
the OER. Electrochemical stability has been successfully
tested for up to 10,000 s in 0.1 M KOH. Furthermore, we will
illustrate our experimental results on interface engineering
strategies using TiO2 as buffer layer and Pt nanostructures
as HER catalyst. Based on the obtained results the observed
improvements, but also the still given limitations, can be
related to clearly identified non-idealities in surface
engineering either related to recombination losses at the
semiconductor surface reducing photocurrents or due to not
properly-aligned energy states leading to potential losses
across the interfaces.},
cin = {IEK-5},
ddc = {540},
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)16},
UT = {WOS:000528279600002},
doi = {10.1515/zpch-2019-1584},
url = {https://juser.fz-juelich.de/record/877850},
}