Details
| Original language | English |
|---|---|
| Pages (from-to) | 4898-4910 |
| Number of pages | 13 |
| Journal | Journal of Materials Chemistry A |
| Volume | 8 |
| Issue number | 9 |
| Publication status | Published - 24 Feb 2020 |
Abstract
In proton exchange membrane water electrolysis (PEMWE) cells the performance and thus the conversion efficiency are influenced by the interface between the porous transport layer (PTL) and the catalyst layer (CL). In the following paper, this interface is modified by the use of femtosecond laser-induced surface structuring, so that the specific surface area of the titanium based fibers of the PTL is increased. The resulting morphology exhibits two roughness levels of (i) a relatively coarse structure featuring tips of a few micrometers in diameter and depth, which are each covered in turn by (ii) a substructure of smaller tips of a few to several hundred nanometers in diameter and depth. PEMWE electrochemical characterization and short-term stress tests reveal that the cell performance is increased due to the laser-structuring of the PTL surface towards the CL. For instance, the cell voltage is reduced by approximately 30 mV after 100 h at 4 A cm-2. These beneficial effects are observed over the entire current density range and thus correspond to a decreased equivalent cell resistance of at least 6 mΩ cm2 for electrical interfacial contact losses and at least 2 mΩ cm2 for mass transport losses. A physical characterization by scanning electron microscopy shows that the CL surface is much rougher and more jagged when using laser-structured fibers. Thus, the gaseous oxygen and the liquid water transport both from and to the active sites of the catalyst seem to be improved.
ASJC Scopus subject areas
- Chemistry(all)
- General Chemistry
- Energy(all)
- Renewable Energy, Sustainability and the Environment
- Materials Science(all)
- General Materials Science
Sustainable Development Goals
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In: Journal of Materials Chemistry A, Vol. 8, No. 9, 24.02.2020, p. 4898-4910.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Femtosecond laser-induced surface structuring of the porous transport layers in proton exchange membrane water electrolysis
AU - Suermann, Michel
AU - Gimpel, Thomas
AU - Bühre, Lena V.
AU - Schade, Wolfgang
AU - Bensmann, Boris
AU - Hanke-Rauschenbach, Richard
N1 - Funding information: The authors gratefully acknowledge the Energy Research Centre of Lower Saxony (EFZN) for the establishment of a discussion platform within the framework of the Competence Network Water Electrolysis of Lower Saxony, from which this cooperation emerged. We also thank Alexander Bomm and Patrick Trinke for their technical and scienti?c support in the preliminary work, as well as Inga Beyers for proofreading. The publication of this article was funded by the Open Access fund of Leibniz Universität Hannover.
PY - 2020/2/24
Y1 - 2020/2/24
N2 - In proton exchange membrane water electrolysis (PEMWE) cells the performance and thus the conversion efficiency are influenced by the interface between the porous transport layer (PTL) and the catalyst layer (CL). In the following paper, this interface is modified by the use of femtosecond laser-induced surface structuring, so that the specific surface area of the titanium based fibers of the PTL is increased. The resulting morphology exhibits two roughness levels of (i) a relatively coarse structure featuring tips of a few micrometers in diameter and depth, which are each covered in turn by (ii) a substructure of smaller tips of a few to several hundred nanometers in diameter and depth. PEMWE electrochemical characterization and short-term stress tests reveal that the cell performance is increased due to the laser-structuring of the PTL surface towards the CL. For instance, the cell voltage is reduced by approximately 30 mV after 100 h at 4 A cm-2. These beneficial effects are observed over the entire current density range and thus correspond to a decreased equivalent cell resistance of at least 6 mΩ cm2 for electrical interfacial contact losses and at least 2 mΩ cm2 for mass transport losses. A physical characterization by scanning electron microscopy shows that the CL surface is much rougher and more jagged when using laser-structured fibers. Thus, the gaseous oxygen and the liquid water transport both from and to the active sites of the catalyst seem to be improved.
AB - In proton exchange membrane water electrolysis (PEMWE) cells the performance and thus the conversion efficiency are influenced by the interface between the porous transport layer (PTL) and the catalyst layer (CL). In the following paper, this interface is modified by the use of femtosecond laser-induced surface structuring, so that the specific surface area of the titanium based fibers of the PTL is increased. The resulting morphology exhibits two roughness levels of (i) a relatively coarse structure featuring tips of a few micrometers in diameter and depth, which are each covered in turn by (ii) a substructure of smaller tips of a few to several hundred nanometers in diameter and depth. PEMWE electrochemical characterization and short-term stress tests reveal that the cell performance is increased due to the laser-structuring of the PTL surface towards the CL. For instance, the cell voltage is reduced by approximately 30 mV after 100 h at 4 A cm-2. These beneficial effects are observed over the entire current density range and thus correspond to a decreased equivalent cell resistance of at least 6 mΩ cm2 for electrical interfacial contact losses and at least 2 mΩ cm2 for mass transport losses. A physical characterization by scanning electron microscopy shows that the CL surface is much rougher and more jagged when using laser-structured fibers. Thus, the gaseous oxygen and the liquid water transport both from and to the active sites of the catalyst seem to be improved.
UR - http://www.scopus.com/inward/record.url?scp=85081226837&partnerID=8YFLogxK
U2 - 10.1039/c9ta12127g
DO - 10.1039/c9ta12127g
M3 - Article
AN - SCOPUS:85081226837
VL - 8
SP - 4898
EP - 4910
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
SN - 2050-7488
IS - 9
ER -