Minimizing Operando Demetallation of Fe-N-C Electrocatalysts in Acidic Medium

催化作用 电解质 铁质 化学 质子交换膜燃料电池 氧化还原 化学工程 无机化学 电极 有机化学 工程类 物理化学
作者
Chang Hyuck Choi,Claudio Baldizzone,George Polymeros,Enrico Pizzutilo,Olga Kasian,Anna K. Schuppert,Nastaran Ranjbar Sahraie,Moulay Tahar Sougrati,Karl J. J. Mayrhofer,Frédéric Jaouen
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:6 (5): 3136-3146 被引量:225
标识
DOI:10.1021/acscatal.6b00643
摘要

For a successful replacement of Pt, tremendous efforts have hitherto been made to develop high-performing Fe-N-C catalysts for the oxygen reduction reaction (ORR) in polymer electrolyte membrane fuel cells (PEMFCs). In comparison to the remarkable progress in activity, the stability of Fe-N-C catalysts still remains critical, however. Fe demetallation in acidic medium is hypothesized to be one critical factor for the overall lifetime. In contrast to the general belief, we herein demonstrate using an operando spectroscopic analysis that catalytically inactive Fe particles exposed to acid electrolytes cannot be fully removed by acid washing due to a relatively high open circuit potential (ca. 0.9 VRHE) leading to the formation of insoluble ferric species, whereas these particles dissolve under PEMFC operating conditions (Ecathode < 0.7 VRHE) due to operando reduction to soluble ferrous cations. To overcome this issue, we demonstrate two approaches: (i) synthesis of Fe-N-C catalysts free of Fe particles and (ii) postsynthesis removal of exposed Fe particles through the control of potential using an external potentiostat or an internal reducing agent (i.e., SnCl2). Operando spectroscopic analyses verified that Fe demetallation during a given voltammetric protocol was dramatically decreased for both synthetically and postsynthetically modified Fe-N-C catalysts, while the initial ORR activity did not significantly change. However, all of these catalysts showed similar performance decay over short-term PEMFC durability tests, demonstrating the lack of a role played by ferrous cations leached from inactive Fe particles on catalyst deactivation. This supports the view that the activity is mainly imparted by FeNxCy moieties. Nevertheless, the presented guidelines are generally applicable to the whole class of Fe-N-C catalysts in order to minimize Fe demetallation in PEMFCs, which provides important advances for the future design of stable electrocatalytic systems for long-term operation.

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