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Iron-Free Cathode Catalysts for Proton-Exchange-Membrane Fuel Cells: Cobalt Catalysts and the Peroxide Mitigation Approach

机译:用于质子交换膜燃料电池的无铁阴极催化剂:钴催化剂和减少过氧化物的方法

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摘要

High-performance and inexpensive platinum-group-metal (PGM)-free catalysts for the oxygen reduction reaction (ORR) in challenging acidic media are crucial for proton-exchange-membrane fuel cells (PEMFCs). Catalysts based on Fe and N codoped carbon (Fe-N-C) have demonstrated promising activity and stability. However, a serious concern is the Fenton reactions between Fe2+ and H2O2 generating active free radicals, which likely cause degradation of the catalysts, organic ionomers within electrodes, and polymer membranes used in PEMFCs. Alternatively, Co-N-C catalysts with mitigated Fenton reactions have been explored as a promising replacement for Fe and PGM catalysts. Therefore, herein, the focus is on Co-N-C catalysts for the ORR relevant to PEMFC applications. Catalyst synthesis, structure/morphology, activity and stability improvement, and reaction mechanisms are discussed in detail. Combining experimental and theoretical understanding, the aim is to elucidate the structure-property correlations and provide guidance for rational design of advanced Co catalysts with a special emphasis on atomically dispersed single-metal-site catalysts. In the meantime, to reduce H2O2 generation during the ORR on the Co catalysts, potential strategies are outlined to minimize the detrimental effect on fuel cell durability.
机译:在具有挑战性的酸性介质中,用于氧还原反应(ORR)的高性能,廉价的不含铂族金属(PGM)的催化剂对于质子交换膜燃料电池(PEMFC)至关重要。基于Fe和N共掺杂碳(Fe-N-C)的催化剂显示出令人鼓舞的活性和稳定性。但是,一个严重的问题是Fe2 +和H2O2之间的Fenton反应生成活性自由基,这很可能导致PEMFC中使用的催化剂,电极内的有机离聚物和聚合物膜降解。或者,已探索了具有减轻的Fenton反应的Co-N-C催化剂,有望替代Fe和PGM催化剂。因此,在本文中,重点是用于与PEMFC应用有关的ORR的Co-N-C催化剂。详细讨论了催化剂的合成,结构/形态,活性和稳定性的提高以及反应机理。结合实验和理论理解,目的在于阐明结构性质之间的相关性,并为高级Co催化剂的合理设计提供指导,其中特别强调原子分散的单金属中心催化剂。同时,为了减少在Co催化剂上进行ORR时产生的H2O2,概述了可能的策略,以最大程度地减少对燃料电池耐久性的不利影响。

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