Manipulating anion intercalation into layered double hydroxide for alkaline seawater oxidation at high current density

被引:1
|
作者
Wu, Yuewen [1 ]
Chen, Mingpeng [1 ]
Sun, Huachuan [1 ]
Na, Guohao [1 ]
Li, Dequan [1 ]
Wang, Boxue [1 ]
Chen, Yun [1 ]
Zhou, Tong [1 ]
Qiu, Guoyang [1 ]
Zhao, Jianhong [1 ]
Zhang, Yumin [1 ]
Zhang, Jin [1 ]
Liu, Feng [2 ]
Cui, Hao [2 ]
Liu, Qingju [1 ]
机构
[1] Yunnan Univ, Natl Ctr Int Res Photoelect & Energy Mat, Sch Mat & Energy, Yunnan Key Lab Micro Nano Mat & Technol, Kunming 650091, Peoples R China
[2] Yunnan Precious Met Lab Co Ltd, Kunming 650106, Peoples R China
基金
中国国家自然科学基金;
关键词
Alkalinity - Intercalation - Iron alloys - Mendelevium - Potassium hydroxide;
D O I
10.1039/d4cy00842a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 gamma-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. A convenient strategy to manipulate anion intercalation into layered double hydroxide is proposed for efficient alkaline seawater oxidation.
引用
收藏
页码:5206 / 5210
页数:5
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