Electro-oxidation of a cobalt based steel in LiOH: a non-noble metal based electro-catalyst suitable for durable water-splitting in an acidic milieu

Autor(en): Schaefer, Helmut
Kuepper, Karsten 
Mueller-Buschbaum, Klaus
Daum, Diemo
Steinhart, Martin 
Wollschlaeger, Joachim 
Krupp, Ulrich
Schmidt, Mercedes
Han, Weijia
Stangl, Johannes
Stichwörter: ARTIFICIAL PHOTOSYNTHESIS; Chemistry; Chemistry, Multidisciplinary; EFFICIENT; ELECTROCATALYSTS; HYDROGEN; Materials Science; Materials Science, Multidisciplinary; MEDIA; Nanoscience & Nanotechnology; OXIDATION; OXIDE; OXYGEN EVOLUTION REACTION; Physics; Physics, Applied; Science & Technology - Other Topics; STABILITY; STAINLESS-STEEL
Erscheinungsdatum: 2017
Herausgeber: ROYAL SOC CHEMISTRY
Journal: NANOSCALE
Volumen: 9
Ausgabe: 45
Startseite: 17829
Seitenende: 17838
Zusammenfassung: 
The use of proton exchange membrane (PEM) electrolyzers is the method of choice for the conversion of solar energy when frequently occurring changes of the current load are an issue. However, this technique requires electrolytes with low pH. All oxygen evolving electrodes working durably and actively in acids contain IrOx. Due to their scarcity and high acquisition costs, noble elements like Pt, Ru and Ir need to be replaced by earth abundant elements. We have evaluated a cobalt containing steel for use as an oxygen-forming electrode in H2SO4. We found that the dissolving of ingredients out of the steel electrode at oxidative potential in sulfuric acid, which is a well-known, serious issue, can be substantially reduced when the steel is electro-oxidized in LiOH prior to electrocatalysis. Under optimized synthesis conditions a cobalt-containing tool steel was rendered into a durable oxygen evolution reaction (OER) electrocatalyst (weight loss: 39 mu g mm(-2) after 50 000 s of chronopotentiometry at pH 1) that exhibits overpotentials down to 574 mV at 10 mA cm(-2) current density at pH 1. Focused ion beam SEM (FIB-SEM) was successfully used to create a structure-stability relationship.
ISSN: 20403364
DOI: 10.1039/c7nr06527b

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