| Literature DB >> 35417125 |
Elisabeth Hornberger1, Thomas Merzdorf1, Henrike Schmies1, Jessica Hübner1, Malte Klingenhof1, Ulrich Gernert1, Matthias Kroschel1, Björn Anke1, Martin Lerch1, Johannes Schmidt1, Arne Thomas1, Raphaël Chattot2, Isaac Martens2, Jakub Drnec2, Peter Strasser1.
Abstract
Cathode catalyst layers of proton exchange membrane fuel cells (PEMFCs) typically consist of carbon-supported platinum catalysts with varying weight ratios of proton-conducting ionomers. N-Doping of carbon support materials is proposed to enhance the performance and durability of the cathode layer under operating conditions in a PEMFC. However, a detailed understanding of the contributing N-moieties is missing. Here, we report the successful synthesis and fuel cell implementation of Pt electrocatalysts supported on N-doped carbons, with a focus on the analysis of the N-induced effect on catalyst performance and durability. A customized fluidized bed reduction reactor was used to synthesize highly monodisperse Pt nanoparticles deposited on N-doped carbons (N-C), the catalytic oxygen reduction reaction activity and stability of which matched those of state-of-the-art PEMFC catalysts. Operando high-energy X-ray diffraction experiments were conducted using a fourth generation storage ring; the light of extreme brilliance and coherence allows investigating the impact of N-doping on the degradation behavior of the Pt/N-C catalysts. Tests in liquid electrolytes were compared with tests in membrane electrode assemblies in single-cell PEMFCs. Our analysis refines earlier views on the subject of N-doped carbon catalyst supports: it provides evidence that heteroatom doping and thus the incorporation of defects into the carbon backbone do not mitigate the carbon corrosion during high-potential cycling (1-1.5 V) and, however, can promote the cell performance under usual PEMFC operating conditions (0.6-0.9 V).Entities:
Keywords: MEA; N-doped carbon; electrocatalyst; fuel cell; operando HE-XRD; oxygen reduction reaction
Year: 2022 PMID: 35417125 DOI: 10.1021/acsami.2c00762
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229