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Charge-transfer and structure in C-60 adsorption on metal surfaces

机译:C-60在金属表面吸附的电荷转移和结构

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摘要

The charge state and structure of C60 monolayers deposited on Au(110), polycrystalline Ag, and Ni(110) have been investigated by electron-energy-loss spectroscopy and low-energy electron diffraction. The vibrational excitation spectra have been used to obtain a quantitative determination of the molecular charge state of the adsorbed C60 molecules. On both the Au(110) and Ag surfaces the charge transfer from the surface to the C60 is found to be (1±1) electrons and that on Ni(110) is (2±1) electrons. These estimates are supported by the metallic nature of the low-energy (0–7.5 eV) electronic excitations of the monolayers. For submonolayer coverages of C60, rectangular overlayer phases are observed on Ni(110) in contrast to the close-packed islands seen on the other metals. This difference in the low-coverage structure can be related to differing substrate-adsorbate interactions, directly reflected by the C60 charge state.
机译:通过电子-能量损失谱和低能电子衍射研究了沉积在Au(110),多晶Ag和Ni(110)上的C60单层的电荷状态和结构。振动激发光谱已用于获得吸附的C60分子的分子电荷状态的定量测定。在Au(110)和Ag表面上,从表面到C60的电荷转移都是(1±1)电子,而Ni(110)上的电荷转移是(2±1)电子。这些估计得到了单层低能(0–7.5 eV)电子激发的金属性质的支持。对于C60的亚单层覆盖,与在其他金属上看到的密堆积岛相反,在Ni(110)上观察到矩形覆盖相。低覆盖率结构的这种差异可能与不同的底物与被吸附物的相互作用有关,直接由C60电荷状态反映出来。

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