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Molecular beam study of the adsorption and desorption of hydrogen sulfide on Au{100}

机译:硫化氢在Au {100}上的吸附和解吸的分子束研究

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The adsorption and desorption of hydrogen sulfide on clean reconstructed Au{100}-(5 * 20) and sulfided gold, denoted by Au{100}-(1 * 1)-SH, has been studied with a combination of temperature programmed desorption (TPD), low energy electron diffraction (LEED), Auger electron spectroscopy (AES), and molecular beam (MB) methods. Precursor-mediated adsorption kinetics were observed for the adsorption of H_2S on the Au{100)-(5 * 20) between 80 and 100 K. The H_2S adsorbs reversibly into a weakly bound physisorbed state, which desorbs at approx 107 K. At 110 K reversible Langmuir adsorption into the precursor state was observed for H_2S on the Au{100}-(5 * 20). The Au{100}-(1 * 1)-SH was prepared by electron irradiation of H_2S adsorbed on the Au{100}-(5 * 20) substrate. In sharp contrast with the precursor adsorption kinetics observed on the clean Au{100}-(5 * 20) surface, the adsorption kinetics for H_2S from Au{100}-(1 * 1)-SH and H_2S adsorbed on Au{100}-(1 * 1)-SH showed additional features at higher temperatures which were associated with the disproportionation of chemisorbed HS(ad). Finally, we have identified a new sulfided gold surface, denoted Au{100}-(2 * 2)-S which was prepared by annealing the Au{100}-(1 * 1)-SH to remove adsorbed hydrogen.
机译:结合程序升温脱附,研究了纯净重构的Au {100}-(5 * 20)和硫化金(以Au {100}-(1 * 1)-SH表示)上硫化氢的吸附和解吸( TPD),低能电子衍射(LEED),俄歇电子能谱(AES)和分子束(MB)方法。在80至100 K之间,观察到前体介导的H_2S在Au {100)-(5 * 20)上的吸附动力学。H_2S可逆地吸附成弱结合的物理吸附状态,在约107 K时解吸。110。对于Au {100}-(5 * 20)上的H_2S,观察到K可逆的朗缪尔吸附成前体状态。通过对吸附在Au {100}-(5 * 20)衬底上的H_2S进行电子辐照来制备Au {100}-(1 * 1)-SH。与在干净的Au {100}-(5 * 20)表面观察到的前驱体吸附动力学形成鲜明对比,Au {100}-(1 * 1)-SH对H_2S的吸附动力学和在Au {100}上吸附的H_2S -(1 * 1)-SH在较高温度下显示出其他特征,这些特征与化学吸附的HS(ad)的歧化有关。最后,我们确定了一个新的硫化金表面,称为Au {100}-(2 * 2)-S,该表面是通过对Au {100}-(1 * 1)-SH进行退火以去除吸附的氢而制备的。

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