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

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

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
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