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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Scanning Tunneling Microscopy Study of Formate Species Synthesized from CO_2 Hydrogenation and Prepared by Adsorption of Formic Acid over Cu(111)
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Scanning Tunneling Microscopy Study of Formate Species Synthesized from CO_2 Hydrogenation and Prepared by Adsorption of Formic Acid over Cu(111)

机译:甲酸在Cu(111)上吸附制备的CO_2加氢合成甲虫的扫描隧道显微镜研究

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摘要

The adsorption strucrture of formate species on Cu(111), prepared by two different methods, was studied using ultrahigh vacuum scanning tunneling microscopy (UHV-STM0, that is, the synthesis by the hydrogenation of CO_2 at atmospheric pressure and the adsorption of formic acid onan oxygen-prencovered Cu(111), Linear chains of formate molecules were imaged by the hydrogenation of CO_2 by STM at low formate coverage wtih the distance to the nearest neighbor of the formate species estimated to be 5.0 +- 0.2 A, twice that of the nearest Cu-Cu neighbor. The adsorption phase of formate thus grows linearly at the initial stage by an anisotropic attractive interaction between the formate species. The ordered structure of the formate species changed inte order of p(2 x 4), c(2 x 8), (7 x 7), p(2 x 3), (5 x 5), and c(2 x 4) with increasing fomate coverage, indicating that various ordered structures appeared corresponding to the small change in the formate coverage. All the formate structures, except for (7 x 7) and (5 x 5), consisted of the same chain as observed at low coverage, with the distance between the formate chains decreasing as the formate coverage increased. A repulsive interaction thus acts between the formate chains, resulting in a lowering of the adsorption energy of the formate species as reported inteh literature. On the other hand, (4 x 40) and (3 x ~7/_2) structures were observed upon exposing the Cu(111) surface ot formic acid at 2 and 15 L, respectively, showing no chain structure of the formate species. At low formate coverage, no molecular image was observed, indicating that the formate species difuses more rapidly than the scanning of the STM tip. Thus, the adsorption structure of formate on Cu(111) was found to be different depending on the preparation method. It is suggested that the difference in the adsorption structure strongly influences the rate constant of the previously reported formate decomposition.
机译:使用超高真空扫描隧道显微镜(UHV-STM0)研究了两种不同方法制备的甲酸类物质在Cu(111)上的吸附结构,即在大气压力下通过CO_2加氢合成和甲酸的吸附在一个用氧气清除的Cu(111)上,通过STM在低甲酸盐覆盖率下通过CO_2加氢使甲酸盐分子的线性链成像,与甲酸盐物种的最近邻的距离估计为5.0 +-0.2 A,是甲酸盐分子的两倍。最接近的Cu-Cu邻居,因此甲酸盐的吸附相在初始阶段通过甲酸盐之间的各向异性吸引相互作用线性增长,甲酸盐的有序结构以p(2 x 4),c(2)的顺序变化x 8),(7 x 7),p(2 x 3),(5 x 5)和c(2 x 4)随着泡沫覆盖率的增加,表明出现了各种有序结构,与甲酸覆盖率的小变化相对应。所有有孔的结构,例如(7 x 7)和(5 x 5)除外,其组成与低覆盖率时观察到的链相同,甲酸盐链之间的距离随甲酸盐覆盖率的增加而减小。因此,甲酸链之间发生排斥相互作用,导致文献中报道的甲酸物种的吸附能降低。另一方面,将甲酸的Cu(111)表面分别暴露于2 L和15 L时观察到(4 x 40)和(3 x〜7 / _2)结构,表明没有甲酸分子的链结构。在较低的甲酸覆盖率下,未观察到分子图像,这表明甲酸种类比STM尖端的扫描扩散更快。因此,根据制备方法,发现甲酸在Cu(111)上的吸附结构不同。建议吸附结构的差异强烈影响先前报道的甲酸盐分解的速率常数。

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