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Adsorption and decomposition of nickelocene on Ag(100): a high-resolution electron energy loss spectroscopy and temperature programmed desorption study

机译:在Ni(100)上吸附和分解二茂镍:高分辨率电子能量损失光谱和程序升温脱附研究

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摘要

Nickelocene adsorption and decomposition on the Ag(100) surface were studied with temperature programmed desorption and high resolution electron energy loss spectroscopy. At monolayer coverages on the relatively inert Ag(100) surface at 175 K, nickelocene physisorbs molecularly, with its molecular axis perpendicular to the surface plane. Nickelocene begins decomposing to adsorbed cyclopentadienyl and nickel at 225 K. Molecular desorption is only observed from multilayer material, at 210 K, or from the first monolayer if adjacent surface sites for decomposition are not available. The cyclopentadienyl decomposes through disproportionation to cyclopentadiene, which desorbs, and adsorbed nickel and carbon fragments on the Ag(100) surface with a maximum at 525 K.
机译:用程序升温脱附和高分辨率电子能量损失谱研究了镍在Ag(100)表面的吸附和分解。在相对惰性的Ag(100)表面在175 K的单层覆盖率下,全新世会分子发生物理吸附,其分子轴垂直于表面。镍茂在225 K下开始分解为吸附的环戊二烯基和镍。只有在没有相邻的分解表面位置时,才能从210 K的多层材料或第一个单层观察到分子解吸。环戊二烯基通过歧化分解为环戊二烯,后者以525 K的最大速度吸附和吸附Ag(100)表面上的镍和碳碎片。

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