Electron spectroscopy of nanodiamond surface states

被引:28
|
作者
Belobrov, PI [1 ]
Bursill, LA
Maslakov, KI
Dementjev, AP
机构
[1] Russian Acad Sci, SB, Inst Biophys, Mol Architecture Grp, Krasnoyarsk 660036, Russia
[2] Krasnoyarsk State Tech Univ, UNESCO Chair, Krasnoyarsk 660036, Russia
[3] Univ Melbourne, Sch Phys, Parkville, Vic 3010, Australia
[4] IV Kurchatov Atom Energy Inst, RRC, Moscow 123182, Russia
关键词
nanodiamond; surface states; PEELS; XPS; Auger electron spectroscopy;
D O I
10.1016/S0169-4332(03)00287-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electronic states of nanodiamond (ND) were investigated by PEELS, XPS and CKVV Auger spectra. Parallel electron energy loss spectra (PEELS) show that the electrons inside of ND particles are sp(3) hybridized but there is a surface layer containing distinct hybridized states. The CKVV Auger spectra imply that the HOMO of the ND surface has a shift of 2.5 eV from natural diamond levels of sigma(p) up to the Fermi level. Hydrogen (H) treatment of natural diamond surface produces a chemical state indistinguishable from that of ND surfaces using CKVV. The ND electronic structure forms sigma(s)(1)sigma(p)(2)pi(1) surface states without overlapping of pi-levels. Surface electronic states, including surface plasmons, as well as phonon-related electronic states of the ND surface are also interesting and may also be important for field emission mechanisms from the nanostructured diamond surface. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:169 / 177
页数:9
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