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基于多壁碳纳米管与阳离子乙酰芘部分在水溶液中的强相互作用的水的电催化氧化阳极制备策略

Anode Preparation Strategies for the Electrocatalytic Oxidation of Water Based on Strong Interactions between Multiwalled Carbon Nanotubes and Cationic Acetylammonium Pyrene Moieties in Aqueous Solutions.

作者信息

Koelewijn Jacobus M, Lutz Martin, Detz Remko J, Reek Joost N H

机构信息

Van 't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH, Amsterdam, The Netherlands.

Crystal and Structural Chemistry Bijvoet Center for Biomolecular Research, Utrecht University, Padualaan 8, 3584 CH, Utrecht, The Netherlands.

出版信息

Chempluschem. 2016 Oct;81(10):1098-1106. doi: 10.1002/cplu.201600235.

Abstract

A strategy is reported for the immobilization of iridium-based water oxidation catalyst 3 onto fluorine-doped tin oxide (FTO) anodes evaluated for the electrocatalytic oxidation of H O. The strategy is based on noncovalent π-π interactions between multiwalled carbon nanotubes (MWCNTs) and the cationic acetylammonium pyrene moiety (Pyr ) covalently attached to a NHC IrCpCl catalytically active center (NHC=N-heterocyclic carbene, Cp=C Me ). The dispersive properties of the Pyr moiety in compound 3 leads to the formation of stable MWCNT dispersions in aqueous solutions. In addition, the MWCNT/3 assembly shows activity in the Ce -driven oxidation of H O. FTO/MWCNT/3 anodes show increased current densities when used as a working electrode for the electrocatalytic oxidation of H O. At higher anodic polarizations initially high current densities were achieved; however, these currents prove to be non-sustained due to delamination and degradation of the catalytically active surface. The immobilization strategy is limited to applications below 1.4 V vs normal hydrogen electrode (NHE) as oxidation of the pyrene backbone is evident at higher potentials.

摘要

报道了一种将铱基水氧化催化剂3固定在氟掺杂氧化锡(FTO)阳极上的策略,该阳极用于评估H₂O的电催化氧化。该策略基于多壁碳纳米管(MWCNT)与共价连接到NHC IrCpCl催化活性中心(NHC = N-杂环卡宾,Cp = C₅Me₅)的阳离子乙酰铵芘部分(Pyr⁺)之间的非共价π-π相互作用。化合物3中Pyr⁺部分的分散特性导致在水溶液中形成稳定的MWCNT分散体。此外,MWCNT/3组件在Ce⁴⁺驱动的H₂O氧化中表现出活性。当用作H₂O电催化氧化的工作电极时,FTO/MWCNT/3阳极显示出更高的电流密度。在较高的阳极极化下,最初实现了高电流密度;然而,由于催化活性表面的分层和降解,这些电流被证明是不可持续的。该固定策略仅限于相对于标准氢电极(NHE)低于1.4 V的应用,因为在较高电位下芘主链的氧化很明显。

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