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Molecular conductance versus inductive effects of axial ligands on the electrocatalytic activity of self-assembled iron phthalocyanines: The oxygen reduction reaction

机译:分子导率与轴向配体对自组装铁酞菁电催化活性的诱导效应:氧还原反应

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The construction of self-assembled iron phthalocyanine (FePc) systems on gold electrodes modified by self-assembled monolayers (SAMs) is becoming an interesting strategy for obtaining electrocatalytic molecular building blocks for the oxygen reduction reaction (ORR). In this work, we have measured the conductance of pyridiniums axial ligands at the single molecule level using the scanning tunneling microscope-based break-junction method (STM-Break Junction) to study the role of the axial ligand on the activity of the self-assembled FePc systems on a gold electrode surface. The electron-pulling effect of pyridinium axial ligands is known to increase the electrocatalytic activity of FePc for the oxygen reduction reaction (ORR). We have used these systems as a platform for carrying out a comparative study for understanding the real influence of the proximal axial ligands. Further, these ligands act as molecular wires between the gold electrode surface and the FePc molecule. The pyridinium molecules were synthesized following a series of structural variations using a basic molecular backbone. From conductance measurements obtained for each pyridinium molecule, it was possible to establish that electron transport through each pyridinium does not influence the activity of FePc for ORR in alkaline media. In addition, the DFT calculations shows that the axial ligand in FePc modifies its catalytic activity by decreasing the binding energy of O-2 to the Fe site. (C) 2019 Elsevier Ltd. All rights reserved.
机译:通过自组装单层(SAMS)改性的金电极上的自组装铁酞菁(FEPC)系统的构建成为获得氧还原反应(ORR)的电催化分子结构块的有趣策略。在这项工作中,我们使用基于扫描的隧道显微镜的断裂 - 结法(STM-断裂结)测量了单分子水平的吡啶轴配体的电导,以研究轴向配体对自我活性的作用在金电极表面上组装FEPC系统。已知吡啶轴配体的电子拉动效果增加FEPC的电催化活性用于氧还原反应(ORR)。我们使用这些系统作为执行比较研究的平台,以了解近端轴向配体的真正影响。此外,这些配体充当金电极表面和FEPC分子之间的分子线。在使用基本分子骨架的一系列结构变化之后合成吡啶鎓分子。从每个吡啶分子获得的电导测量中,可以通过每个吡啶的电子传输建立电子输送不会影响碱性介质中FEPC的FEPC的活性。此外,DFT计算表明FEPC中的轴向配体通过将O-2的结合能量降低到Fe位点来改变其催化活性。 (c)2019 Elsevier Ltd.保留所有权利。

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