Electrochemistry-Induced Direct Deposition of Nanoscale Thin Zeolitic Imidazolate Framework-8 Films on Insulator Substrates

IF 3.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Takashi Ito*, Samantha G. Jenkins, Soenke Seifert and Ahmet Uysal, 
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Abstract

Electrochemical approaches have been explored as controlled means to prepare thin films of metal–organic frameworks (MOFs) on electrodes but have rarely been used to form insulator films on insulator surfaces. Herein, we report an electrochemistry-based approach to direct deposition of a thin film of zeolitic imidazolate framework-8 (ZIF-8) onto an insulator surface. The film deposition was induced by a cathodic reaction at an electrode that was placed above the insulator with a separation of ≈100 μm in a methanol solution containing ZnCl2 and 2-methylimidizole. The effects of the electrode and insulator material, applied potential, electrode–substrate distance, deposition time, and the number of deposition cycles were systematically investigated to gain insight into the deposition mechanism. The results of these measurements were consistent with a hypothesized mechanism involving cathodic base generation at the working electrode for ligand deprotonation, formation of intermediate species, their diffusion toward the substrate, and the formation of ZIF-8 on the substrate. Interestingly, the size, shape, and position of the film on the substrate replicated those of the working electrode, showing the applicability of this approach to the patterned deposition of a ZIF-8 film. In addition, film thickness could be easily controlled in the range of tens to hundreds of nanometers by adjusting the potential application conditions. This electrochemistry-induced method will provide a simple means for the patterned formation of a MOF film of controlled thickness on an insulator without metal precoating and thus will open the possibility of designing unique devices for various applications including chemical sensing and separations.

Abstract Image

电化学诱导在绝缘体衬底上直接沉积纳米级咪唑酸沸石骨架-8薄膜
电化学方法作为控制电极上金属有机骨架(mof)薄膜的方法已经被探索,但很少用于在绝缘体表面形成绝缘体薄膜。在此,我们报告了一种基于电化学的方法,将沸石咪唑酸框架-8 (ZIF-8)薄膜直接沉积到绝缘体表面。在含有ZnCl2和2-甲基咪唑的甲醇溶液中,在绝缘体上方距离约为100 μm的电极上发生阴极反应,形成薄膜。系统研究了电极和绝缘体材料、外加电位、电极-衬底距离、沉积时间和沉积循环次数等因素对沉积机理的影响。这些测量结果与假设的机制一致,包括在配体去质子化的工作电极上阴极碱的产生,中间物质的形成,它们向底物的扩散,以及在底物上形成ZIF-8。有趣的是,薄膜在衬底上的大小、形状和位置与工作电极的大小、形状和位置相同,表明了这种方法对ZIF-8薄膜的图图化沉积的适用性。此外,通过调整潜在的应用条件,可以很容易地将薄膜厚度控制在几十到几百纳米的范围内。这种电化学诱导的方法将为在没有金属预涂层的绝缘体上形成厚度可控的MOF薄膜提供一种简单的方法,从而为设计包括化学传感和分离在内的各种应用的独特设备提供可能性。
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来源期刊
Crystal Growth & Design
Crystal Growth & Design 化学-材料科学:综合
CiteScore
6.30
自引率
10.50%
发文量
650
审稿时长
1.9 months
期刊介绍: The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials. Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.
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