NMR Studies of Nitrogen Doping in the 4H Polytype of Silicon Carbide: Site Assignments and Spin−Lattice Relaxation

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• 作者：J. Stephen Hartman ; Bob Berno ; Paul Hazendonk ; Christopher W. Kirby ; Eric Ye ; Josef Zwanziger ; Alex D. Bain
• 刊名：Journal of Physical Chemistry C
• 出版年：2009
• 出版时间：August 20, 2009
• 年：2009
• 卷：113
• 期：33
• 页码：15024-15036
• 全文大小：369K
• 年卷期：v.113,no.33(August 20, 2009)
• ISSN：1932-7455

文摘

Nitrogen doping in silicon carbide converts an insulator to a wide-band gap semiconductor with many potential uses. Most doping studies have involved the 4H and 6H polytypes, which alone among the many known hexagonal SiC polytypes are commercially available as large single crystals. Nitrogen doping makes ¹³C and ²⁹Si NMR spin−lattice relaxation much more efficient, presumably by donating unpaired electron density to the conduction band. However the effect is site-specific. We now report a huge site-specific difference in relaxation efficiency, a factor of 60, between the two carbon sites in the 4H polytype. Because the relaxation of the undoped material is extremely slow, such measurements provide a very sensitive probe of differences in local electronic structure at the sites. The crystallographic sites differ only in their next-nearest neighbors because the first neighbors are always tetrahedral, and the only difference between the fast- and slow-relaxing carbon sites, out to the second-neighbor positions, is a rotation through 60° of three of the second-neighbor atoms. We have previously reported similar but less extreme site-specific differences in ¹³C relaxation behavior in the 6H polytype. Interpretation of these results requires firm assignments of the ¹³C and ²⁹Si signals in both polytypes to the specific crystallographic sites: three in the 6H and two in the 4H polytype. This has been problematic because all peaks have equal intensities in both polytypes. We propose new peak assignments, correcting the different literature reports. The new assignments are based on a combination of electronic structure calculations, ¹³C-to-²⁹Si cross-polarization experiments, and chemical shift anisotropy studies.