TY - JOUR
T1 - Bonding nature of C60 adsorbed on Si(111) 7 × 7 and Si(100) 2 × 1 surfaces studied by HREELS and PES
AU - Suto, S.
AU - Sakamoto, K.
AU - Kondo, D.
AU - Wakita, T.
AU - Kimura, A.
AU - Kakizaki, A.
N1 - Funding Information:
The authors would like to thank Professor Wakio Uchida for his valuable discussions. This work was supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture and the Kurata Research Grant.
PY - 1999/6/1
Y1 - 1999/6/1
N2 - We report here the measurements of vibrational excitation spectra, valence band spectra and C 1s core level spectra of C60 molecules adsorbed on Si(111) 7 × 7 and Si(100) 2 × 1 surfaces, using high-resolution electron energy loss spectroscopy (HREELS) and photoelectron spectroscopy (PES). At a coverage between 1 and 0.25 ML, HREELS and PES measurements show that the interaction is as weak as the van der Waals interaction on both surfaces. At a coverage lower than 0.25 ML, some contradictory results are obtained by HREELS and PES. With HREELS, the softening of several vibrational modes is observed on the Si(111) 7 × 7 surface, but no indication of softening is observed on the Si(100) 2 × 1 surface. The charge transfer scheme explains the softening well. These results by HREELS indicate that the nature of the bonding is ionic on the Si(111) 7 × 7 surface and of the van der Waals type on the Si(100) 2 × 1 surface. In contrast, the bonding states between C60 molecules and Si substrates are clearly observed at 2.4 eV on both surfaces with PES. The PES measurements indicate that the interaction has a covalent character on the Si(111) 7 × 7 surface, and that it is in between covalent and ionic, i.e. not purely ionic or at the covalent limit, on the Si(100) 2 × 1 surface. We will discuss the nature of the interaction manifested by HREELS and PES measurements in comparison with the spectra of C60 molecules adsorbed on metal surfaces.
AB - We report here the measurements of vibrational excitation spectra, valence band spectra and C 1s core level spectra of C60 molecules adsorbed on Si(111) 7 × 7 and Si(100) 2 × 1 surfaces, using high-resolution electron energy loss spectroscopy (HREELS) and photoelectron spectroscopy (PES). At a coverage between 1 and 0.25 ML, HREELS and PES measurements show that the interaction is as weak as the van der Waals interaction on both surfaces. At a coverage lower than 0.25 ML, some contradictory results are obtained by HREELS and PES. With HREELS, the softening of several vibrational modes is observed on the Si(111) 7 × 7 surface, but no indication of softening is observed on the Si(100) 2 × 1 surface. The charge transfer scheme explains the softening well. These results by HREELS indicate that the nature of the bonding is ionic on the Si(111) 7 × 7 surface and of the van der Waals type on the Si(100) 2 × 1 surface. In contrast, the bonding states between C60 molecules and Si substrates are clearly observed at 2.4 eV on both surfaces with PES. The PES measurements indicate that the interaction has a covalent character on the Si(111) 7 × 7 surface, and that it is in between covalent and ionic, i.e. not purely ionic or at the covalent limit, on the Si(100) 2 × 1 surface. We will discuss the nature of the interaction manifested by HREELS and PES measurements in comparison with the spectra of C60 molecules adsorbed on metal surfaces.
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U2 - 10.1016/S0039-6028(99)00238-1
DO - 10.1016/S0039-6028(99)00238-1
M3 - Conference article
AN - SCOPUS:0033149525
SN - 0039-6028
VL - 427-428
SP - 85
EP - 90
JO - Surface Science
JF - Surface Science
T2 - Proceedings of the 1998 9th International Conference on Vibrations at Surfaces (VAS9)
Y2 - 12 October 1998 through 16 October 1998
ER -