4.7 Article

Developing zeolitic imidazolate frameworks 67-derived fluorides using 2-methylimidazole and ammonia fluoride for energy storage and electrocatalysis

期刊

ENERGY
卷 239, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.energy.2021.122129

关键词

Ammonia fluoride; Electrocatalysis; Fluoride; Supercapacitor; ZIF67; 2-Methylimidazole

向作者/读者索取更多资源

In this study, bimetallic ZIF-67-derived fluoride was successfully synthesized for supercapacitors and electrocatalytic water splitting. Through optimization, the highest capacitance and electrical conductivity, as well as excellent energy storage and catalytic performance, were achieved.
Zeolitic imidazolate framework 67 (ZIF67) with large surface area and tunable structure is one of the promising electroactive materials of electrochemical devices. In this study, NH4F and nickel salt are applied to synthesize bimetallic ZIF67-derived fluoride for supercapacitor (SC) and electrocatalytic water splitting at the first time. Nickel with multiple redox states enhances energy storage and catalytic ability. NH4F can confine crystalline growth and induce fluoride formation. Ratio of 2-methylimidazole to NH4F for synthesis is optimized regarding to surface area and electrical conductivity. The highest specific capacitance (CF) of 735.7 F/g at 20 mV/s is obtained for ZIF67-derived fluoride prepared using 2methylimidazole to NH4F ratio of 2 to 1, due to smaller particle size and high electrical conductivity. The symmetric SC shows the maximum energy density of 24.6 Wh/kg at 0.6 kW/kg. The CF retention of 100 % and Coulombic efficiency higher than 96 % are obtained in 6000 times charge/discharge process. The ZIF67-derived fluoride and IrO2 composite is fabricated as electrocatalyst for water splitting. This composite shows a high current density of 0.11 A/cm(2) at 1.6 VRHE and a small overpotential of 1.58 VRHE at 0.10 A/cm(2). Current density retention of 100 % after continuous illumination for 600 min is also achieved. (c) 2021 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据