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介孔α-FeO@g-CN-NCs的简便合成用于高效双功能电催化活性(析氧反应/氧还原反应)

Facile Synthesis of Mesoporous α-FeO@g-CN-NCs for Efficient Bifunctional Electro-catalytic Activity (OER/ORR).

作者信息

Alduhaish Osamah, Ubaidullah Mohd, Al-Enizi Abdullah M, Alhokbany Norah, Alshehri Saad M, Ahmed Jahangeer

机构信息

Department of Chemistry, College of Science, King Saud University, Riyadh, 11451, Saudi Arabia.

出版信息

Sci Rep. 2019 Oct 2;9(1):14139. doi: 10.1038/s41598-019-50780-2.

Abstract

Mesoporous α-iron oxide@graphitized-carbon nitride nanocomposites (α-FeO@g-CN-NCs) were synthesized using urea-formaldehyde (UF) resins at 400 °C/2 h. The mesoporous nature of the prepared nanocomposites was observed from electron microscopy and surface area measurements. The electrochemical measurements show the bifunctional nature of mesoporous α-FeO@g-CN-NCs in electrolysis of water for oxygen evolution and oxygen reduction reactions (OER/ORR) using 0.5 M KOH. Higher current density of mesoporous α-FeO@g-CN-NCs reveals the enhanced electrochemical performance compared to pure FeO nanoparticles (NPs). The onset potential, over-potential and Tafel slopes of mesoporous α-FeO@g-CN-NCs were found lower than that of pure α-FeO-NPs. Rotating disc electrode experiments followed by the K-L equation were used to investigate 4e redox system. Therefore, the mesoporous α-FeO@g-CN-NCs bifunctional electro-catalysts can be considered as potential future low-cost alternatives for Pt/C catalysts, which are currently used in fuel cells.

摘要

介孔α-氧化铁@石墨化氮化碳纳米复合材料(α-FeO@g-CN-NCs)是在400 °C/2 h条件下使用脲醛(UF)树脂合成的。通过电子显微镜和表面积测量观察到所制备纳米复合材料的介孔性质。电化学测量表明,介孔α-FeO@g-CN-NCs在使用0.5 M KOH进行水电解析氧和氧还原反应(OER/ORR)中具有双功能性质。与纯FeO纳米颗粒(NPs)相比,介孔α-FeO@g-CN-NCs更高的电流密度表明其电化学性能得到了增强。发现介孔α-FeO@g-CN-NCs的起始电位、过电位和塔菲尔斜率低于纯α-FeO-NPs。采用旋转圆盘电极实验并结合K-L方程来研究4e氧化还原体系。因此,介孔α-FeO@g-CN-NCs双功能电催化剂可被视为目前用于燃料电池的Pt/C催化剂未来潜在的低成本替代品。

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