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@PHDTHESIS{Ramler:1052712,
author = {Ramler, Denise},
title = {{D}evelopment of an oxygen ion conducting solid oxide
electrolysis cell based on gadolinium-doped cerium oxide as
fuel electrode and electrolyte material},
volume = {689},
school = {RWTH Aachen University},
type = {Dissertation},
address = {Jülich},
publisher = {Forschungszentrum Jülich GmbH Zentralbibliothek, Verlag},
reportid = {FZJ-2026-01069},
isbn = {978-3-95806-879-7},
series = {Schriften des Forschungszentrums Jülich Reihe Energie $\&$
Umwelt / Energy $\&$ Environment},
pages = {ix, 162},
year = {2026},
note = {Dissertation, RWTH Aachen University, 2025},
abstract = {The global transition toward CO2-neutral energy systems
requires a significant expansion of hydrogen technologies,
with solid oxide electrolysis cells (SOECs) offering a
highly efficient route for hydrogen production via
high-temperature electrolysis. However, despite their
superior efficiency, SOECs remain technologically less
mature than low-temperature alternatives such as alkaline or
proton exchange membrane electrolyzers. Advancing SOEC
development therefore demands innovation in both cell design
and manufacturing strategies to achieve high performance,
mechanical stability, and costefficiency. This dissertation
focuses on the development and investigation of fully
screen-printed, fuel electrodesupported solid oxide cells
featuring a co-sintered tri-layer electrolyte architecture.
The work was conducted within the framework of the ElChFest
project, which aims to model the electro-chemomechanical
behavior of gadolinium-doped ceria based solid oxide cells
and understand crack formation phenomena in the electrolyte
during operation. A key objective was to fabricate
mechanically robust and electrochemically efficient cells by
optimizing the interplay between powder properties, paste
formulation, sintering behavior, and final microstructure.
Particular attention was paid to residual stresses induced
during manufacturing. The fabrication strategy centered
around screen printing as a scalable and cost-effective
deposition method. The project included the transition of
previously sputtered barrier layers to screen-printed
alternatives. A comprehensive study of powder processing
(encompassing pre-calcination and milling) was carried out
to tailor the sintering behavior and enable co-sintering of
the multi-layer cell. Rheological characterization of
screen-printing pastes revealed strong correlations between
print quality and parameters such as damping factor, yield
point, and particle distribution asymmetry. These findings
highlighted the critical role of paste rheology in achieving
defect-free and reproducible ceramic layers. The sintering
behavior of gadolinium-doped ceria (GDC) and
yttria-stabilized zirconia (YSZ) powders was evaluated using
both bulk pellets and screen-printed layers.
Gadolinium-doped ceria exhibited an earlier onset of
sintering and higher shrinkage than yttria-stabilized
zirconia. While co-doping and precalcination effectively
modified sintering kinetics, translating these findings to
printed layers required further adaptation due to the
mechanical constraints induced by the support. Co-sintering
trials showed that substrate shrinkage behavior had a
significant influence on electrolyte densification.
Pre-calcined NiO-8YSZ substrates often inhibited proper
densification, leading to increased porosity and cell
warping. The development of the tri-layer electrolyte
revealed additional microstructural challenges. Interfacial
porosity driven by interdiffusion and Kirkendall effects was
observed at the GDC/YSZ interfaces, when screen printing was
used. This porosity was not present in cells with sputtered
barrier layers. Consequently, optimizing the sintering
temperature became a balancing act between achieving
sufficient densification and suppressing
interdiffusion-related degradation. Electrochemical
characterization confirmed that cells with Ni-GDC fuel
electrodes outperformed conventional Ni-YSZ cells in terms
of stability, validating the choice of doped ceria. While
the best electrochemical performance was achieved in cells
with sputtered barrier layers, the fully screen-printed
cells showed competitive initial current densities and
area-specific resistances comparable to the stateof- the-art
Jülich Type III reference design. These results underscore
the viability of screen printing for fabricating
high-performance SOECs, provided that careful attention is
paid to interfacial engineering and sintering conditions. In
summary, this work demonstrates that fully screen-printed,
fuel electrode-supported SOECs with trilayer electrolytes
can be fabricated with high quality and performance but
require tightly controlled processing conditions. The
findings emphasize the need for compatible sintering
behaviors, advanced paste rheology control, and substrate
design tailored for co-sintering. Future work should focus
on developing novel, shrinkage-matched substrates to reduce
sintering temperatures without compromising densification.
Additional research into long-term stability under realistic
electrolysis conditions, reversible operation, and varying
steam concentrations is also essential to enable the broader
deployment of this technology in hydrogen production and
energy conversion.},
cin = {IMD-2},
cid = {I:(DE-Juel1)IMD-2-20101013},
pnm = {1231 - Electrochemistry for Hydrogen (POF4-123)},
pid = {G:(DE-HGF)POF4-1231},
typ = {PUB:(DE-HGF)3 / PUB:(DE-HGF)11},
doi = {10.34734/FZJ-2026-01069},
url = {https://juser.fz-juelich.de/record/1052712},
}