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Exploring Electrosorption at Iron Electrode with in Situ Surface-Enhanced Infrared Absorption Spectroscopy

机译:用原位表面增强红外吸收光谱研究铁电极上的电吸附

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摘要

Surface-enhanced infrared absorption spectroscopy (SEI-RAS) in attenuated total reflection (ATR) configuration has been extended to the Fe electrode/electrolyte interface in neutral and weakly acidic solutions for the first time. The SEIRA-active Fe film electrode was obtained through a potentiostatic electrodeposition of a virtually pinhole-free 40 nm-thick Fe overfilm onto a 60 nm-thick Au underfilm chemically predeposited on the reflecting plane of an ATR Si prism. The infrared absorption for CO adlayer at the Fe film electrode measured with ATR-SEIRAS was enhanced by a factor of larger than 34, as compared to that at a Fe bulk electrode with external infrared absorption spectroscopy in the literature. More importantly, the unipolar band shape enabled the reliable determination of the Stark tuning rates of CO adlayer at Fe electrode. In situ ATR-SEIRAS was also applied to study the electrosorption of a typical corrosion inhibitor benzotriazole (BTAH) on Fe electrode as a function of potential, providing additional spectral information at positive potentials in support of the formation of a polymer-like surface complex Fe~(II)_(m)(BTA)_(n) as the corrosion-resistant layer.
机译:衰减全反射(ATR)配置的表面增强红外吸收光谱(SEI-RAS)首次扩展到中性和弱酸性溶液中的Fe电极/电解质界面。 SEIRA活性Fe膜电极是通过将几乎无针孔的40 nm厚的Fe上膜恒电位电沉积到化学沉积在ATR Si棱镜反射平面上的60 nm厚的Au底膜上而获得的。与文献中具有外部红外吸收光谱的Fe块状电极相比,用ATR-SEIRAS测量的Fe膜电极上的CO附加层的红外吸收增强了34倍以上。更重要的是,单极性带的形状能够可靠地确定Fe电极上CO附加层的Stark调谐速率。原位ATR-SEIRAS还用于研究典型缓蚀剂苯并三唑(BTAH)在Fe电极上的电吸附与电势的关系,在正电势下提供额外的光谱信息,以支持形成类似聚合物的表面络合物Fe 〜(II)_(m)(BTA)_(n)作为耐腐蚀层。

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