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UV-laser-induced desorption of NO from the pure and modified Cr2O3(0001) surfaces: spin effects in surface-state-induced desorption

机译:紫外激光诱导的纯和改性Cr2O3(0001)表面NO的解吸:表面状态诱导的解吸中的自旋效应

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Abstract: We shall report the UV-laser induced desorption of NO/Cr$- 2$/O$-3$/(0001) and the coadsorbate system NO/K/Cr$-2$/O$- 3$/(0001). Resonance enhanced multiphoton ionization was used for state selective detection of the desorbing NO after excitation with pulses of nanosecond duration and desorption laser energies between 3.5 eV and 6.4 eV. There are two adsorbate species of NO, a chemisorbed and a physisorbed species. We shall focus on data of the chemisorbed species. The main emphasis within this paper will be put on electron spin effects, particularly the preferential population of a fast translational desorption channel for the $+2$/$Pi$- 3/2$/ state observed specifically in connection with surface state induced processes at desorption energies of 5.0 eV. For those processes changes within the final state distributions of desorbing NO are fond when modifying the electronic surface structure via adsorption of small amounts of potassium.!25
机译:摘要:我们将报告紫外激光诱导的NO / Cr $ -2 $ / O $ -3 $ /(0001)和共吸附系统NO / K / Cr $ -2 $ / O $ -3 $ /( 0001)。共振增强多光子电离用于以纳秒持续时间的脉冲和3.5 eV至6.4 eV之间的解吸激光能量激发后的解吸NO的状态选择性检测。 NO有两种吸附物,一种是化学吸附物,一种是物理吸附物。我们将专注于化学吸附物质的数据。本文中的主要重点将放在电子自旋效应上,尤其是在与表面态诱导过程有关的情况下观察到的对于$ + 2 $ / $ Pi $ -3 / 2 $ /状态的快速平移解吸通道的优先种群。解吸能量为5.0 eV。对于那些过程,当通过少量钾的吸附来改变电子表面结构时,会喜欢脱附NO的最终状态分布内的变化。25

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