Increasing durability of Pt-surface-enriched nanosize structure catalysts by multi-step platinum deposition

The sluggish reaction of oxygen reduction in proton-exchange membrane fuel cells (PEMFCs) and the durability of platinum-based catalysts have been major economical and technological barriers to the widespread application of PEMFCs. We report here on two Pt-surface-enriched nanosize structure (Pt-SEN...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of solid state electrochemistry 2020-10, Vol.24 (10), p.2385-2393
Hauptverfasser: Kaplan, Dmitri, Goor, Meital, Burstein, Larisa, Popov, Inna, Shviro, Meital, Peled, Emanuel
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The sluggish reaction of oxygen reduction in proton-exchange membrane fuel cells (PEMFCs) and the durability of platinum-based catalysts have been major economical and technological barriers to the widespread application of PEMFCs. We report here on two Pt-surface-enriched nanosize structure (Pt-SENS) catalysts with iridium core, synthesized with the use of single-step and successive step-by-step electroless deposition of platinum. The synthesized catalysts were studied by energy-dispersive X-ray spectroscopy (SEM-EDS), X-ray photoelectron spectroscopy (XPS), and transmission scanning electron microscopy (STEM). Electrochemical analysis demonstrated improved oxygen reduction reaction (ORR) mass activity of the homemade catalysts by 25–30% compared with commercial 50%Pt/C catalyst and improved durability, by a factor of ~ 3, of the catalyst synthesized by successive step-by-step deposition following accelerated stress test (AST). Higher mass activities are attributed to better platinum utilization as a result of a Pt-surface-enriched structure, while greater durability is attributed to the stabilization of surface platinum by stronger Pt–Ir bonds induced by iridium atoms in the core.
ISSN:1432-8488
1433-0768
DOI:10.1007/s10008-020-04755-3