Abstract

The present study focuses on the interaction of C60 with the surfaces of highly oriented pyrolitic graphite (HOPG) and sp2-bonded boron nitride (BN). The nanocrystalline BN film was deposited by mass selected ion beams and features an sp2-bonded surface layer, which covers a cubic phase BN film. The first part of the experiment is the sequential deposition of C60, which is monitored by photoelectron spectroscopy in the x-ray (XPS) and ultraviolet (UPS) regime. The growth of the C60 layer on HOPG is close to a layer-by-layer growth mode, but on the BN surface island growth is favored. No charge transfer or chemical reaction (e.g., carbide formation) between the fullerene layer, and the underlying substrate is observed in either case. In the second part of the experiment the samples are heated at a rate of 10 K/min while simultaneously recording the UPS VB spectra. The complete desorption of C60 from the HOPG surface occurs in a small temperature interval between 510–530 K. For the sp2 BN surface the majority of C60 desorbs around 493 K, about half a monolayer (ML) remains, and the C60 concentration decreases gradually with increasing temperature; less than a tenth of a ML can be detected even at 1000 K. The first desorption event at 493 K is attributable to the multilayer desorption from islands. The remaining C60 directly in contact with the BN surface is then removed in a large temperature interval between 500 and 1000 K which indicates the presence of a multitude of adsorption sites. The presence of C60 on the BN film surface also induces a band bending and related B 1s and N 1s core level shifts. An upward band bending is present in the C60 overlayer, which indicates that defects are responsible for the pinning of the Fermi level at the interface.

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