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Unraveling a Graphene Exfoliation Technique Analogy in the Making of Ultrathin Nickel–Iron Oxyhydroxides@Nickel Foam to Promote the OER

过电位 电催化剂 材料科学 析氧 剥脱关节 石墨烯 催化作用 化学工程 氢氧化物 层状双氢氧化物 氧化剂 纳米技术 无机化学 电化学 冶金 电极 化学 有机化学 物理化学 工程类 生物化学
作者
Zubair Ahmed,Krishankant,Ritu Rai,Rajinder Kumar,Takahiro Maruyama,Chandan Bera,Vivek Bagchi
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (46): 55281-55291 被引量:36
标识
DOI:10.1021/acsami.1c19536
摘要

One of the major objectives of using the improved Hummers' method was to exfoliate the graphene layers by oxidizing and thereafter reducing them to obtain highly conductive reduced graphene layers, which can be used in the construction of electronic devices or as a part of catalyst composites in energy conversion reactions. Herein, we have employed a similar idea to exfoliate the layered double hydroxide (LDH), which is proposed as a promising material for the oxygen evolution reaction (OER) electrocatalysis. Usually, the efficiency of these materials is largely restricted due to their sheetlike morphology, which is susceptible to stacking. In this work, NiFe-LDH sheets were fabricated on nickel foam in a one-step co-precipitation technique and their ultrathin nanosheets (∼2 nm) are obtained by in situ oxygen-plasma-controlled exfoliation. In addition, the oxygen vacancies in exfoliated sheets were generated by a chemical reduction method that further improved the electronic conductivity and overall electrocatalytic performance of the catalyst. This approach can address the limitations of NiFe-LDH, such as poor conductivity and low stability, making it more efficient for electrocatalysis. It is also observed that the catalyst having 60 s O-plasma exposure after chemical reduction, i.e., NiFe-OOHOV, outperformed remaining electrocatalysts and exhibited superior OER activity with a low overpotential of 330 mV to achieve a high current density of 50 mA cm-2. The catalyst also displayed an ECSA-normalized OER overpotential of 288 mV at a current density of 10 mA cm-2 and exhibited excellent long-term stability (120 h) in an alkaline electrolyte. Remarkably, ultrathin defect-rich catalyst continuously produced O2, resulting in a high faradaic efficiency of 98.1% for the OER.
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