Curvature enhanced NH(2)-MIL-53(Al) electrode for boosting ion diffusion and capacitive deionization defluorination

曲率增强的NH(2)-MIL-53(Al)电极可促进离子扩散和电容去离子脱氟

阅读:1

Abstract

Traditional capacitive deionization (CDI) materials typically exhibit low fluorine adsorption capacity (FAC) due to limitations in the optimization of their specific surface area and chemical composition. A prospective strategy for efficient ion storage is modulating the local electric field strength (LEF) by changing the curvature. In this study, we developed a novel modulator-based curvature modulation method to prepare three different morphologies of NH(2)-MIL-53(Al) electrode materials with similar specific surface areas but different curvatures, which were used to investigate the direct constitutive relationship between curvature and CDI performance. The results show that the urchin-like electrode (NCMOF-3) with high surface curvature has an ultra-high fluoride removal capacity (61.29 mg(NaF) g(electrodes) (-1)), a fast fluoride removal rate (mg(NaF) g(electrodes) (-1) min(-1)), and excellent charging/discharging cycle stability (10 000 cycles). CDI performance exceeds all previously reported MOF electrodes. Finally, in combination with the surface curvature/electric field model, we found that higher surface curvature may lead to higher concentration of ion distribution. The mechanism of action may be that high surface curvature enhances the local electric field enhancement (LEFE) effect of the electrode material, which in turn increases the ion storage capacity and diffusion rate during CDI. This study demonstrates firstly the potential effect of curvature on CDI performance by experimental design. More importantly, this study breaks the limitations of material design based on specific surface area and provides new design ideas for next-generation CDI materials based on curvature structure engineering.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。