Metal Exchange of ZIF-8 and ZIF-67 Nanoparticles with Fe(II) for Enhanced Photocatalytic Performance

双金属片 光催化 催化作用 沸石咪唑盐骨架 X射线光电子能谱 离子交换 纳米颗粒 金属有机骨架 材料科学 无机化学 咪唑酯 金属 化学工程 化学 吸附 纳米技术 离子 有机化学 冶金 工程类
作者
Lehlohonolo E. Mphuthi,Elizabeth Erasmus,Ernst H.G. Langner
出处
期刊:ACS omega [American Chemical Society]
卷期号:6 (47): 31632-31645 被引量:43
标识
DOI:10.1021/acsomega.1c04142
摘要

Zeolitic imidazolate frameworks (ZIFs), such as ZIF-8 and ZIF-67, were found to be efficient catalysts. However, ZIFs are not used much in photocatalysis due to their low photocatalytic activity for most reactions. The photocatalytic activity can be improved by modifying the framework by exchanging the Zn(II) ions (ZIF-8) and Co(II) ions (ZIF-67) with a more photocatalytically active metal(II) ion to form an efficient bimetallic ZIF photocatalyst. Redox-active iron (Fe)-based materials are known to be highly potent photocatalysts. Thus, incorporating iron into ZIFs could significantly enhance their photocatalytic performance. In this study, we modified nanosized ZIF-8(Zn) and ZIF-67(Co) via metal (Fe2+) exchange to produce bimetallic frameworks that are photocatalytically more active than their parent ZIFs. Nanosized ZIF-8 and ZIF-67 were synthesized isothermally in either water or methanol under ambient conditions. From these, Fe-containing bimetallic ZIF-8 and ZIF-67 nanoparticles were synthesized via the metal exchange, and their performance on the photocatalytic degradation of dye was evaluated. The morphology and crystal structures of the pristine ZIF-8 and ZIF-67 nanoparticles were retained to a large extent during the iron exchange. Their Brunauer-Emmett-Teller (BET) surface areas decreased by less than 15% for nZIF-8 and less than 12% for nZIF-67. The binding energy values on X-ray photoelectron spectroscopy (XPS) confirmed the preservation of the oxidation state of Fe(II) during the exchange process. A remarkably higher catalytic activity was observed for the photocatalytic degradation of dye by the Fe-exchanged nZIF-8 and nZIF-67 compared to their parent ZIFs. This proved that the incorporation of Fe(II) centers into the ZIF framework enhanced the photocatalytic activity of the framework dramatically. In addition, these catalysts can be regenerated and reused without an appreciable loss in activity.
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