Title data
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 February 2025)
.
ISSN 1476-4660
DOI: https://doi.org/10.1038/s41563-025-02128-7
Project information
Project title: |
Project's official title Project's id Live-XAS 05K22WC1 HighHy 03SF0689B European Union’s Horizon 2023 No information |
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Project financing: |
Andere Fundamental Research Funds for the Central Universities National Natural Science Foundation of China European Union’s Horizon 2023 |
Abstract in another language
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.
Further data
Item Type: | Article in a journal |
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Refereed: | Yes |
Institutions of the University: | Faculties > Faculty of Engineering Science > Chair Electrochemical Process Engineering > Chair Electrochemical Process Engineering - Univ.-Prof. Dr.-Ing. Christina Roth |
Result of work at the UBT: | Yes |
DDC Subjects: | 500 Science > 540 Chemistry 600 Technology, medicine, applied sciences > 620 Engineering |
Date Deposited: | 10 Mar 2025 07:33 |
Last Modified: | 10 Mar 2025 09:41 |
URI: | https://eref.uni-bayreuth.de/id/eprint/92690 |