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首页> 外文期刊>ChemSusChem >Facile Formation of Nanostructured Manganese Oxide Films as High-Performance Catalysts for the Oxygen Evolution Reaction
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Facile Formation of Nanostructured Manganese Oxide Films as High-Performance Catalysts for the Oxygen Evolution Reaction

机译:纳米结构锰氧化物膜的体面形成为氧气进化反应的高性能催化剂

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摘要

The development of inexpensive, earth abundant, and bioinspired oxygen evolution electrocatalysts that are easily accessible and scalable is a principal requirement with regard to the feasibility of water splitting for large-scale chemical energy storage. A unique, versatile, and scalable approach has been developed to fabricate manganese oxide films from single layers to multilayers with a controlled thickness and high reproducibility. The produced MnOx films are composed of small nanostructures that are assembled closely in the form of porous sponge-like layers. The films were investigated for the electrochemical oxygen evolution reaction in alkaline media and demonstrate a remarkable activity as well as a superior stability of over 60 h. To elucidate the catalytically active species, as well as the striking structural characteristics, the films were further examined in depth by using SEM, TEM, and X-ray photoelectron spectroscopy, as well as quasi insitu extended X-ray absorption fine structure and X-ray absorption near edge structure analysis. The MnOx catalyst films excel because of a favorably high fraction of Mn3+ ions that are retained even after operation at oxidizing potentials. Upon exposure to oxidizing potentials in strongly alkaline aqueous electrolyte, the catalyst material maintains its structural integrity at the nanostructural, morphological, and atomic level.
机译:易于访问和可扩展的廉价,地球丰富和生物悬浮的氧气进化电催化剂的开发是关于大规模化学能量储存的水分裂的可行性的主要要求。已经开发了一种独特的通用和可扩展的方法,以制造从单层的氧化锰膜,以控制厚度和高再现性的多层。所生产的MNOX膜由小纳米结构组成,该纳米结构紧密地组装在多孔海绵状层的形式上。研究了薄膜以在碱性培养基中进行电化学氧进化反应,并表现出显着的活性以及超过60小时的优异稳定性。为了阐明催化活性物质,以及引人注目的结构特征,通过使用SEM,TEM和X射线光电子能谱进一步深入地进一步检查薄膜,以及准Insitu延伸X射线吸收细结构和X-边缘结构分析附近的光线吸收。 MNOX催化剂薄膜胶片由于甚至在氧化电位的操作之后均未保留的MN3 +离子的有利高分。在暴露于强碱性电解质中氧化电位后,催化剂材料在纳米结构,形态学和原子水平处保持其结构完整性。

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