Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Ergebnis 17 von 2037

Details

Autor(en) / Beteiligte
Titel
Single-Phase Perovskite SrIrO3 Nanofibers as a Highly Efficient Electrocatalyst for a pH-Universal Oxygen Evolution Reaction
Ist Teil von
  • ACS applied energy materials, 2022-05, Vol.5 (5), p.6146-6154
Ort / Verlag
American Chemical Society
Erscheinungsjahr
2022
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • pH-universal electrocatalysts are desirable for high efficiency of water electrolysis. Herein, we report the facile synthesis of single-phase perovskite SrIrO3 nanofibers (NFs) and demonstrate that SrIrO3 NFs are promising electrocatalysts for the oxygen evolution reaction (OER) in a wide range of pH. Single-phase SrIrO3 NFs were synthesized by electrospinning and subsequent calcination processes, and the electrocatalytic performance of SrIrO3 NFs toward the OER was evaluated under acidic, neutral, and alkaline media. A large surface area due to the NF morphology with an average diameter of 105.5 (± 15.5) nm led to enhanced catalytic activity of SrIrO3 NFs, representing smaller overpotentials and Tafel slopes under pH-universal conditions than IrO2/Ir NFs and commercial Ir/C. SrIrO3 NFs also manifested remarkably stable activity for continuous OER operation in all three electrolytes, even though a considerable amount of Sr was leached out of them. The long-lasting high OER activity of SrIrO3 NFs could be ascribed to stable Ir cations taking B sites of the perovskite oxide structure, known as an active site for electrocatalysis. The initial perovskite crystal structure of SrIrO3 was maintained for a certain time even after significant Sr leaching. This work is the first application of SrIrO3 perovskite for pH-universal OER catalysis.
Sprache
Englisch
Identifikatoren
ISSN: 2574-0962
eISSN: 2574-0962
DOI: 10.1021/acsaem.2c00551
Titel-ID: cdi_acs_journals_10_1021_acsaem_2c00551
Format

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX