4.6 Article

In Situ Synthesis of Superhydrophilic Amorphous NiFe Prussian Blue Analogues for the Oxygen Evolution Reaction at a High Current Density

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 9, 期 16, 页码 5693-5704

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.1c00855

关键词

electrocatalyst; oxygen evolution reaction; Prussian blue analogue; amorphous; superhydrophilic

资金

  1. National Natural Science Foundation of China [11974229]
  2. Science and Technology Innovation Group of Shanxi Province, China [201805D131006]
  3. Key Research and Development Program of Shanxi Province, China [201903D121026]
  4. Natural Science Foundation for Young Scientists of Shanxi Province, China [201901D211397]
  5. Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi [2019L0467]
  6. Innovation project of graduate education in Shanxi Province [2020XSY023]

向作者/读者索取更多资源

In this study, efficient and low-cost NiFe PBA catalysts with remarkable OER performance were synthesized by adjusting the amount of urea and potassium ferricyanide through a facile one-step hydrothermal reaction. The transformed amorphous superhydrophilic NiFe PBA (a-NiHCF) exhibited enhanced structural stability and fast charge transfer, leading to ultralow overpotentials for high current densities, making it a promising candidate for electrocatalytic water splitting applications.
Synthesis of efficient and low-cost catalysts for the oxygen evolution reaction (OER) is a pivotal process for large-scale electrocatalytic water splitting to produce hydrogen. Prussian blue analogues (PBAs) prepared by the conventional co-precipitation method, with a less active site density and a poor electrical transport, are often used as precursors for further preparation of PBA derivatives, such as metal oxides, metal alloys, metal phosphides, and so on, due to their poor OER activity. In this report, controllable synthesis of NiFe PBA with Fe2O3 byproducts on a Ni foam substrate was achieved through a facile one-step hydrothermal reaction by adjusting the amount of urea and potassium ferricyanide. After chemical etching and electrochemical activation, NiFe PBA was entirely transformed into amorphous superhydrophilic NiFe PBA (denoted a-NiHCF), which exhibited a remarkable OER performance at a large current density. To drive high current densities of 400 and 800 mA cm(-2), only ultralow overpotentials of 280 and 309 mV were required, respectively, which far exceed many recently reported OER catalysts. The superior performance can be attributed to the following: (1) in situ growth on a metal foam substrate can improve the structural stability and provide a faster charge transfer as well as oxygen bubble release; (2) chemical etching allows exposing more surface active sites; (3) an electrochemical activation-induced amorphous surface possesses a larger Brunauer-Emmett-Teller surface area, more high-valent oxidation states, and higher intrinsic OER activity; and (4) the superhydrophilic surface structure is conducive to the adsorption of water molecules. These advantages make a-NiHCF a promising candidate for application in the field of electrocatalytic water splitting.

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