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在厌氧条件下,通过离子液体中双(三氟甲基磺酰)亚胺阴离子的电化学氧化生成用于甲醇氧化的铂催化剂。

Generated Platinum Catalyst for Methanol Oxidation via Electrochemical Oxidation of Bis(trifluoromethylsulfonyl)imide Anion in Ionic Liquids at Anaerobic Condition.

作者信息

Tang Yongan, Wang Zhe, Chi Xiaowei, Sevilla Michael D, Zeng Xiangqun

机构信息

Department of Chemistry, Oakland University, Rochester, Michigan 48309, United States.

出版信息

J Phys Chem C Nanomater Interfaces. 2016 Jan 21;120(2):1004-1012. doi: 10.1021/acs.jpcc.5b09777. Epub 2015 Dec 14.

DOI:10.1021/acs.jpcc.5b09777
PMID:29034058
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5640268/
Abstract

The bis(trifluoromethylsulfonyl)imide anion is widely used as an ionic liquid anion due to its electrochemical stability and wide electrochemical potential window at aerobic conditions. Here we report an innovative strategy by directly oxidizing bis(trifluoromethylsulfonyl)imide anion to form a radical electrocatalyst on platinum electrode at anaerobic condition. The generated radical catalyst was shown to catalytically and selectively promote the electrooxidation of methanol to form methoxyl radical, in which the formation potential was drastically decreased with the existence of bis(trifluoromethylsulfonyl)imide radical. The electrochemically generated radical catalyst not only facilitates the oxidation of methanol but also provides good selectivity. The unique double layer structure of the 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([Bmpy][NTf]) likely excludes the diffusion of larger molar mass molecules onto the electrode surface and enables the highly selective methanol oxidation at this IL-electrode interface. Cyclic voltammetry (CV) experiments were used to systematically characterize the details of the electrochemical processes with and without methanol in several other ILs, and a mechanism of the chemical and redox processes was proposed. This study provides a promising new approach for utilizing the unique properties of ionic liquids not only as solvents and electrolytes but also as the medium for generation of electrocatalysts to promote methanol redox reactions for practical applications.

摘要

双(三氟甲基磺酰)亚胺阴离子因其电化学稳定性以及在有氧条件下较宽的电化学势窗而被广泛用作离子液体阴离子。在此,我们报道一种创新策略,即在厌氧条件下通过直接氧化双(三氟甲基磺酰)亚胺阴离子在铂电极上形成一种自由基电催化剂。所生成的自由基催化剂被证明能催化并选择性地促进甲醇电氧化形成甲氧基自由基,其中在双(三氟甲基磺酰)亚胺自由基存在的情况下,形成电位大幅降低。电化学产生的自由基催化剂不仅促进甲醇氧化,还具有良好的选择性。1-丁基-1-甲基吡咯烷鎓双(三氟甲基磺酰)亚胺([Bmpy][NTf])独特的双层结构可能会阻止较大摩尔质量分子扩散到电极表面,并使得在该离子液体-电极界面能够高度选择性地氧化甲醇。循环伏安法(CV)实验用于系统地表征在其他几种离子液体中有甲醇和无甲醇时电化学过程的细节,并提出了化学和氧化还原过程的机理。这项研究提供了一种有前景的新方法,不仅利用离子液体的独特性质作为溶剂和电解质,还将其作为生成电催化剂的介质,以促进甲醇氧化还原反应用于实际应用。

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