Femtosecond laser-induced surface structuring of porous nickel substituting anodic catalyst layers for alkaline oxygen evolution reaction

• Femtosecond lasered generated surface structures act as efficient AEMWE electrode without the need of additional catalyst. • The LIPPS achieved a 17 % increase in situ cell performance (1.32 A cm⁻² @ 2.0 V) compared to the initial felt (1.10 A cm⁻² @ 2.0 V). • Overpotentials were reduced by up to 6.9 % at 10 mA cm⁻² and 9.6 % at 100 mA cm⁻² compared to unprocessed felt. • Tafel slopes of the structures varied between 66 mV dec −1 and 76 mV dec −1 . Femtosecond laser-induced nano structuring offers a novel approach to enhance the performance of porous transport layers (PTLs) in anion-exchange membrane water electrolysis. By applying ultrashort laser pulses to nickel felts, distinct surface morphologies were generated, including high-spatial-frequency laser-induced periodic surface structures (HSFL-LIPSS), irregular ablated surfaces, and hybrid structures. Surface area analysis revealed increases of up to 4-fold for LIPSS, 6-fold for hybrid structures (LIPSS+Ablation), and 9-fold for ablated surfaces compared to untreated fibers. Electrochemical testing showed reduced overpotentials for laser-treated samples, comparable to state-of-the-art electrodes despite the absence of catalyst layers. Overpotentials could be reduced by up to 6.5 % at 10 mA cm −2 and by up to 9.6 % at 100 mA cm −2 compared to the unprocessed felt. Notably, ablated structures, with the highest surface areas, exhibited microcavities that may entrap oxygen bubbles, limiting active site and reaction rates. The LIPSS structures demonstrated the lowest activation losses and highest current density (1.32 A cm⁻² at 2.0 V) due to their periodic morphology and enhanced electrolyte flow, representing a 17 % improvement at 2.0 V compared to the untreated felts. Moreover, Tafel slopes down to 66 mV dec −1 denote a performant kinetic while oxidation charge measurements revealed pronounced peaks for laser-treated samples, with ablated surfaces achieving the highest charge of 16.76 ± 1.64 C cm⁻². Chronopotentiometry revealed the LIPSS structures showing the highest resistance to degradation among the structured samples. These findings suggest femtosecond laser nano structuring as a promising method to improve PTL performance. Further application of catalyst layers could amplify the electrochemical efficiency of these advanced materials.

Authors

Institutions

Publication Details

Journal
Applied Surface Science Advances
Published
2025-05-09
DOI
https://doi.org/10.1016/j.apsadv.2025.100756
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Femtosecond laser-induced surface structuring of porous nickel substituting anodic catalyst layers for alkaline oxygen evolution reaction

Florian J. Wirkert, Ulrich Rost, Michael Brodmann, Cemal Esen et al.
Applied Surface Science Advances
Electrocatalysts for Energy Conversion
article

Femtosecond laser-induced surface structuring of porous nickel substituting anodic catalyst layers for alkaline oxygen evolution reaction

Florian J. Wirkert, Ulrich Rost, Michael Brodmann, Cemal Esen, Maximilian Cieluch, Philipp Maack, Norbert Kazamer, Haujin Salih
article en

Abstract

• Femtosecond lasered generated surface structures act as efficient AEMWE electrode without the need of additional catalyst. • The LIPPS achieved a 17 % increase in situ cell performance (1.32 A cm⁻² @ 2.0 V) compared to the initial felt (1.10 A cm⁻² @ 2.0 V). • Overpotentials were reduced by up to 6.9 % at 10 mA cm⁻² and 9.6 % at 100 mA cm⁻² compared to unprocessed felt. • Tafel slopes of the structures varied between 66 mV dec −1 and 76 mV dec −1 . Femtosecond laser-induced nano structuring offers a novel approach to enhance the performance of porous transport layers (PTLs) in anion-exchange membrane water electrolysis. By applying ultrashort laser pulses to nickel felts, distinct surface morphologies were generated, including high-spatial-frequency laser-induced periodic surface structures (HSFL-LIPSS), irregular ablated surfaces, and hybrid structures. Surface area analysis revealed increases of up to 4-fold for LIPSS, 6-fold for hybrid structures (LIPSS+Ablation), and 9-fold for ablated surfaces compared to untreated fibers. Electrochemical testing showed reduced overpotentials for laser-treated samples, comparable to state-of-the-art electrodes despite the absence of catalyst layers. Overpotentials could be reduced by up to 6.5 % at 10 mA cm −2 and by up to 9.6 % at 100 mA cm −2 compared to the unprocessed felt. Notably, ablated structures, with the highest surface areas, exhibited microcavities that may entrap oxygen bubbles, limiting active site and reaction rates. The LIPSS structures demonstrated the lowest activation losses and highest current density (1.32 A cm⁻² at 2.0 V) due to their periodic morphology and enhanced electrolyte flow, representing a 17 % improvement at 2.0 V compared to the untreated felts. Moreover, Tafel slopes down to 66 mV dec −1 denote a performant kinetic while oxidation charge measurements revealed pronounced peaks for laser-treated samples, with ablated surfaces achieving the highest charge of 16.76 ± 1.64 C cm⁻². Chronopotentiometry revealed the LIPSS structures showing the highest resistance to degradation among the structured samples. These findings suggest femtosecond laser nano structuring as a promising method to improve PTL performance. Further application of catalyst layers could amplify the electrochemical efficiency of these advanced materials.

Applied Surface Science AdvancesVol. 27
Westfälische Hochschule (DE), BG Klinikum Bergmannstrost Halle (DE), Ruhr University Bochum (DE)
Openalex Percentile: Top 94%
Electrocatalysts for Energy Conversion
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.