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Operando-informed precatalyst programming towards reliable high-current-density electrolysis

Titelangaben

Xia, Lu ; Ferreira Gomes Lobo, Bruna ; Jiang, Wulyu ; Escalera-López, Daniel ; Wang, Yang ; Hu, Yang ; Faid, Alaa Y. ; Wang, Kaiwen ; Chen, Tengyu ; Zhao, Kaiqi ; Zhang, Xu ; Zhou, Yingtang ; Ram, Ranit ; Polesso, Barbara ; Guha, Anku ; Su, Jiaqi ; Lobo, Carlos M. S. ; Haumann, Michael ; Spatschek, Robert ; Sunde, Svein ; Gan, Lin ; Huang, Ming ; Zhou, Xiaoyuan ; Roth, Christina ; Lehnert, Werner ; Cherevko, Serhiy ; Gan, Liyong ; García de Arquer, F. Pelayo ; Shviro, Meital:
Operando-informed precatalyst programming towards reliable high-current-density electrolysis.
In: Nature Materials. (28 Februar 2025) .
ISSN 1476-4660
DOI: https://doi.org/10.1038/s41563-025-02128-7

Angaben zu Projekten

Projekttitel:
Offizieller Projekttitel
Projekt-ID
Live-XAS
05K22WC1
HighHy
03SF0689B
European Union’s Horizon 2023
Ohne Angabe

Projektfinanzierung: Andere
Fundamental Research Funds for the Central Universities
National Natural Science Foundation of China
European Union’s Horizon 2023

Abstract

Electrocatalysts support crucial industrial processes and emerging decarbonization technologies, but their design is hindered by structural and compositional changes during operation, especially at application-relevant current densities. Here we use operando X-ray spectroscopy and modelling to track, and eventually direct, the reconstruction of iron sulfides and oxides for the oxygen evolution reaction. We show that inappropriate activation protocols lead to uncontrollable Fe oxidation and irreversible catalyst degradation, compromising stability and reliability and precluding predictive design. Based on these, we develop activation programming strategies that, considering the thermodynamics and kinetics of surface reconstruction, offer control over precatalyst oxidation. This enables reliable predictions and the design of active and stable electrocatalysts. In a NixFe1−xS2 model system, this leads to a threefold improvement in durability after programmed activation, with a cell degradation rate of 0.12 mV h−1 over 550 h (standard operation: 0.29 mV h−1, constrained to 200 h), in an anion exchange membrane water electrolyser operating at 1 A cm−2. This work bridges predictive modelling and experimental design, improving the electrocatalyst reliability for industrial water electrolysis and beyond at high current densities.

Weitere Angaben

Publikationsform: Artikel in einer Zeitschrift
Begutachteter Beitrag: Ja
Institutionen der Universität: Fakultäten > Fakultät für Ingenieurwissenschaften > Lehrstuhl Werkstoffverfahrenstechnik > Lehrstuhl Werkstoffverfahrenstechnik - Univ.-Prof. Dr.-Ing. Christina Roth
Titel an der UBT entstanden: Ja
Themengebiete aus DDC: 500 Naturwissenschaften und Mathematik > 540 Chemie
600 Technik, Medizin, angewandte Wissenschaften > 620 Ingenieurwissenschaften
Eingestellt am: 10 Mär 2025 07:33
Letzte Änderung: 10 Mär 2025 09:41
URI: https://eref.uni-bayreuth.de/id/eprint/92690