Yuewen Wu, Mingpeng Chen, Huachuan Sun, Guohao Na, Dequan Li, Boxue Wang, Yun Chen, Tong Zhou, Guoyang Qiu, Jianhong Zhao, Yumin Zhang, Jin Zhang, Feng Liu, Hao Cui and Qingju Liu
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引用次数: 0
摘要
在这项工作中,我们提出了一种将阴离子插层到层状双氢氧化物中的便捷策略。所获得的镍铁合金 LDH-Cl- 电极在高电流密度的碱性海水中表现出卓越的 OER 性能,既具有低过电位,又具有高稳定性。在电流密度为 200 mA cm-2 的 1 M KOH 和碱性海水中,过电位分别为 255 mV 和 350 mV。此外,NiFe LDH-Cl- 可在 200 mA cm-2 下稳定运行 100 小时。原位拉曼研究表明,活性 γ-NiOOH 是在低电位下通过表面重构在 NiFe LDH-Cl- 上生成的,Cl- 插层有助于优化 Eg 和 A1g 的峰面积比,这对碱性海水 OER 是有利的。
Manipulating anion intercalation into layered double hydroxide for alkaline seawater oxidation at high current density†
In this work, we propose a convenient strategy to manipulate anion intercalation into layered double hydroxide. The obtained NiFe LDH-Cl− electrode shows outstanding OER performance with both low overpotentials and high stability in alkaline seawater at high current density. Ultra-low overpotentials of 255 mV and 350 mV are required in 1 M KOH and alkaline seawater at a current density of 200 mA cm−2. In addition, NiFe LDH-Cl− can stably operate at 200 mA cm−2 for 100 h. In situ Raman studies reveal that the active γ-NiOOH is generated on NiFe LDH-Cl− at a low potential by surface reconstruction, and Cl− intercalation helps optimize the peak area ratio of Eg and A1g, which can be favorable for the alkaline seawater OER.
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
Impact factor: 5.0
Time to first decision (peer reviewed only): 31 days