Effect of encapsulated atoms on the electronic structure of the fullerene cage:: A case study on La2@C78 and Ti2C2@C78 via ultraviolet photoelectron spectroscopy

被引:20
作者
Hino, Shojun [1 ]
Kato, Masayuki
Yoshimura, Daisuke
Moribe, Hiroe
Umemoto, Hisashi
Ito, Yasuhiro
Sugai, Toshiki
Shinohara, Hisanori
Otani, Minoru
Yoshimoto, Yoshihide
Okada, Susumu
机构
[1] Ehime Univ, Grad Sch Sci & Engn, Matsuyama, Ehime 7908577, Japan
[2] Chiba Univ, Grad Sch Sci & Technol, Chiba 2638522, Japan
[3] Inst Mol Sci, UVSOR, Okazaki, Aichi 4448585, Japan
[4] Nagoya Univ, Res Ctr Mat Sci, Nagoya, Aichi 4648602, Japan
[5] Nagoya Univ, Grad Sch Sci, Nagoya, Aichi 4648602, Japan
[6] Univ Tokyo, Inst Solid State Phys, Kashiwa, Chiba 2778581, Japan
[7] Univ Tsukuba, Ctr Computat Sci, Tsukuba, Ibaraki 3058571, Japan
[8] Japan Sci & Technol Agcy, CREST, Kawaguchi, Saitama 3320012, Japan
关键词
D O I
10.1103/PhysRevB.75.125418
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Ultraviolet photoelectron spectra (UPS) of metallofullerene, La-2@C-78 were measured using a synchrotron-radiation light source. Its spectral onset energy was 0.70 eV below the Fermi level, indicating the semiconductive nature of this metallofullerene. The UPS consisted of numerous crests and troughs. Further, a change in intensity upon tuning the excitation energy was observed; however, the intensity of the change was not as large as those observed for other fullerenes. The UPS of La-2@C-78 differ considerably from those of Ti2C2@C-78, although they are thought to have the same cage structure. Herein, this difference is explored using density-functional theory, and the origin of this difference was determined to be the hybridization of the pi-electron wave functions.
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页数:5
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