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Chemisorption and dissociation of O_2 on Pd(111) studied by STM

机译:STM研究O_2在Pd(111)上的化学吸附和解离

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The adsorption and dissociation of O_2 on Pd(111) at low coverage was studied in a variable temperature scanning tunneling microscope (STM) in the range from 25 to 210 K. Below 60 K the diffusion rate is negligible and individual molecules appear as slightly elongated 5 pm protrusions surrounded by 10 pm depressions at low bias voltage (≈200 mV). The molecules predominantly appear in three distinct orientations and closely resemble the peroxide species observed on Pt(111). A small fraction of the molecules occupy a second binding configuration at 25 K, appearing similar to the dominant species but with opposite orientations. No molecules resembling the superoxide precursor state on Pt(111) were observed. Both thermal activation and interaction with the STM tip induce rotation between the three orientations of each molecule, as well as displacement to adjacent sites and conversion between the two binding ge- ometries. The molecules order in p(2 x 2) clusters, which grow in size upon annealing to 100 K. Rotational disorder is observed within the islands below 60 K. but not at higher temperature due to rapid rotation. Near 120 K, thermal O_2 dissociation occurs primarily at the periphery of islands and at active sites associated with impurities beneath the Pd surface.
机译:在25至210 K范围内的可变温度扫描隧道显微镜(STM)中研究了低覆盖率下Od在Pd(111)上的吸附和解离。在60 K以下,扩散速率可忽略不计,单个分子表现为略长的在低偏置电压(≈200mV)下,有5 pm的突起被10 pm的凹陷所包围。该分子主要以三个不同的方向出现,并且与在Pt(111)上观察到的过氧化物种类非常相似。一小部分分子在25 K处占据第二个结合构型,看起来与优势种相似,但方向相反。没有观察到类似于Pt(111)上超氧化物前体状态的分子。热激活和与STM尖端的相互作用都引起每个分子三个方向之间的旋转,以及向相邻位点的位移和两个结合几何结构之间的转化。分子以p(2 x 2)簇的顺序排列,在退火至100 K时大小会增长。在60 K以下的岛中观察到旋转紊乱,但由于快速旋转,在更高的温度下观察不到。在120 K附近,热离解主要发生在岛的外围以及与Pd表面下的杂质相关的活性位点。

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