Fuel Cell Performance of Palladium-Platinum Core-Shell Electrocatalysts Synthesized in Gram-Scale Batches
Author(s) -
Siddique Khateeb,
Sandra Guerreo,
Dong Su,
Robert M. Darling,
Lesia Protsailo,
Minhua Shao
Publication year - 2016
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/2.1301607jes
Subject(s) - platinum , catalysis , palladium , materials science , chemical engineering , electrolyte , shell (structure) , membrane electrode assembly , membrane , fuel cells , proton exchange membrane fuel cell , fabrication , chemistry , nanotechnology , electrode , composite material , organic chemistry , engineering , medicine , biochemistry , alternative medicine , pathology
This article presents the performance of palladium-platinum core-shell catalysts (Pt/Pd/C) for oxygen reduction synthesized in gram-scale batches in both liquid cells and polymer-electrolyte membrane fuel cells. Core-shell catalyst synthesis and characterization, ink fabrication, and cell assembly details are discussed. The Pt mass activity of the Pt/Pd core-shell catalyst was 0.95 A mg–1 at 0.9 V measured in liquid cells (0.1 M HClO4), which was 4.8 times higher than a commercial Pt/C catalyst. The performances of Pt/Pd/C and Pt/C in large single cells (315 cm2) were assessed under various operating conditions. The core-shell catalyst showed consistently higher performance than commercial Pt/C in fuel cell testing. A 20–60 mV improvement across the whole current density range was observed on air. Sensitivities to temperature, humidity, and gas composition were also investigated and the core-shell catalyst showed a consistent benefit over Pt under all conditions. However, the 4.8 times activity enhancement predicated by liquid cell measurements was not fully realized in fuel cells.
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