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首页> 外文期刊>Physical chemistry chemical physics: PCCP >In situ STM investigation of spinodal decomposition and surface alloying during underpotential deposition of Cd on Au(111) from an ionic liquid
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In situ STM investigation of spinodal decomposition and surface alloying during underpotential deposition of Cd on Au(111) from an ionic liquid

机译:原位STM研究从离子液体中Au(111)上Cd的欠电位沉积过程中的旋节线分解和表面合金化

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摘要

The electrodeposition and anodic dissolution of Cd on Au(111) in an acidic chloroaluminate ionic liquid (MBIC - AlCl3, 42 : 58 mol%) have been investigated by cyclic voltammetry and in situ STM. In the Cd underpotential deposition region, various nanostructures can be distinguished. At a potential of 0.95 V vs. Al/Al(III), a transformation from a well ordered AlCl4- adlayer to a (root 3 x root 19) superstructure, presumably due to Cd - AlCl4- coadsorption, is observed. Reducing the potential to 0.45 V, surface alloying of Cd and Au occurs, which is evidenced for the first time by typical spinodal structures occurring both during deposition and dissolution of the surface alloy layer having a hexagonal structure. At still lower potentials below 0.21 V, a layer-by-layer growth of bulk Cd sets in.
机译:通过循环伏安法和原位STM研究了Cd在酸性氯铝酸盐离子液体(MBIC-AlCl3,42:58 mol%)中在Au(111)上的电沉积和阳极溶解。在Cd电位不足的沉积区域中,可以区分出各种纳米结构。在相对于Al / Al(III)为0.95 V的电势下,观察到可能是由于Cd-AlCl4-共吸附,导致从有序的AlCl4-吸附层转变为(根3 x根19)超结构。将电势降低到0.45 V,会发生Cd和Au的表面合金化,这首次通过具有六方结构的表面合金层的沉积和溶解过程中同时出现的典型旋节线结构来证明。在低于0.21 V的较低电势下,块状Cd逐层生长。

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