4.6 Article

Interfacial Assemble of Prussian Blue Analog to Access Hierarchical FeNi (oxy)-Hydroxide Nanosheets for Electrocatalytic Water Splitting

期刊

FRONTIERS IN CHEMISTRY
卷 10, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2022.895168

关键词

FeNiOOH nanosheet; Prussian blue analog; oxygen evolution; hydrogen evolution; water splitting

资金

  1. National Natural Science Foundation of China [21972060]
  2. Natural National Science Foundation of Fujian Province [2021J011029, 2020J01931, 2020J01934, 2020J02046]
  3. scientific research project of Fujian Jiangxia University [JXZ2019004]
  4. Middle-aged and Young Teachers' Project of Fujian [JAT200405]
  5. College student innovation and entrepreneurship training program of Fujian [202110395009]
  6. Research Start-up Funds for Introducing Talents of Minjiang University [MJY21029]
  7. Fujian Key Laboratory of Functional Marine Sensing Materials of Minjiang University [MJUKF-FMSM202006]

向作者/读者索取更多资源

Developing facile methods for the synthesis of active and stable electrocatalysts is vital for achieving overall water splitting. In this study, a practical method was demonstrated to obtain FeNiOOH nanosheets on nickel foam as bifunctional electrocatalyst. The FeNiOOH/NF electrode showed low overpotentials and remarkable stability, outperforming the IrO2-Pt/C-based electrolyzer.
Developing facile methods for the synthesis of active and stable electrocatalysts is vitally important to realize overall water splitting. Here, we demonstrate a practical method to obtain FeNiOOH nanosheets on nickel foam (NF) as bifunctional electrocatalyst by growing a FeCo Prussian blue analog with further in situ oxidation under ambient conditions. The binder-free, self-standing FeNiOOH/NF electrode with hierarchical nanostructures requires low overpotentials of 260 mV and 240 mV at a current density of 50 mA cm(-2) for oxygen evolution reaction and hydrogen evolution reaction, respectively, in 1.0 M KOH solution. Therefore, an alkaline water electrolyzer constructed by bifunctional FeNiOOH/NF electrode as both anode and cathode delivers 50 mA cm(-2) under a cell voltage of 1.74 V with remarkable stability, which outperforms the IrO2-Pt/C-based electrolyzer. The excellent performance could be ascribed to the superior FeNiOOH intrinsic activity and the hierarchical structure. This work provides a cost-efficient surface engineering method to obtain binder-free, self-standing bifunctional electrocatalyst on commercial NF, which could be further extended to other energy and environment applications.

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