Photoemission study of electronic structure evolution across the metal-insulator transition of heavily B-doped diamond

被引:6
作者
Okazaki, H. [1 ,2 ]
Arakane, T. [3 ]
Sugawara, K. [4 ]
Sato, T. [3 ]
Takahashi, T. [3 ,4 ]
Wakita, T. [1 ,2 ]
Hirai, M. [1 ]
Muraoka, Y. [1 ,2 ]
Takano, Y. [5 ]
Ishii, S. [5 ]
Iriyama, S. [6 ]
Kawarada, H. [6 ]
Yokoya, T. [1 ,2 ]
机构
[1] Okayama Univ, Grad Sch Nat Sci & Technol, Okayama 7008530, Japan
[2] Japan Sci & Technol Agcy, Okayama 7008530, Japan
[3] Tohoku Univ, Dept Phys, Sendai, Miyagi 9808578, Japan
[4] Tohoku Univ, Adv Inst Mat Res, WPI Res Ctr, Sendai, Miyagi 9808577, Japan
[5] Natl Inst Mat Sci, Tsukuba, Ibaraki 3050047, Japan
[6] Waseda Univ, Sch Sci & Engn, Shinjuku Ku, Tokyo 1698555, Japan
关键词
Semiconductors; Superconductors; Photoelectron spectroscopy; SUPERCONDUCTING DIAMOND; BAND;
D O I
10.1016/j.jpcs.2010.10.052
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We studied the electronic structure evolution of heavily B-doped diamond films across the metal-insulator transition (MIT) using ultraviolet photoemission spectroscopy (UPS). From high-temperature UPS, through which electronic states near the Fermi level (E(F)) up to similar to 5k(B)T can be observed (k(B) is the Boltzmann constant and T the temperature), we observed the carrier concentration dependence of spectral shapes near E(F). Using another carrier concentration dependent UPS, we found that the change in energy position of sp-band of the diamond valence band, which corresponds to the shift of E(F), can be explained by the degenerate semiconductor model, indicating that the diamond valence band is responsible for the metallic states for samples with concentrations above MIT. We discuss a possible electronic structure evolution across MIT. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:582 / 584
页数:3
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