Correlation between bonding structure and microstructure in fullerenelike carbon nitride thin films -: art. no. 125414

被引:37
作者
Gago, R
Jiménez, I
Neidhardt, J
Abendroth, B
Caretti, I
Hultman, L
Möller, W
机构
[1] Rossendorf Inc, Forschungszentrum Rossendorf EV, Inst Ion Beam Phys & Mat Res, D-01314 Dresden, Germany
[2] CSIC, Inst Ciencia & Tecnol Polimeros, E-28006 Madrid, Spain
[3] Linkoping Univ, IFM, Dept Phys, Thin Film Phys Div, S-58183 Linkoping, Sweden
[4] CSIC, Inst Ciencia Mat Madrid, E-28049 Madrid, Spain
关键词
D O I
10.1103/PhysRevB.71.125414
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The bonding structure of highly ordered fullerenelike (FL) carbon nitride (CNx) thin films has been assessed by x-ray absorption near-edge spectroscopy (XANES). Samples with different degrees of FL character have been analyzed to discern spectral signatures related to the FL microstructure. The XANES spectra of FL-CNx films resemble that of graphitic CNx, evidencing the sp(2) hybridization of both C and N atoms. The FL structure-is achieved with the promotion of N in threefold positions over pyridinelike and cyanidelike bonding environments. In addition, the relative pi*sigma* XANES intensity ratio at the C(1s) edge is independent of the FL character, while it decreases similar to 40% at the N(1s) edge with the formation of FL arrangements. This result indicates that there is no appreciable introduction of C-sp(3) hybrids with the development of FL structures and, additionally, that a different spatial localization of pi electrons at C and N sites takes place in curved graphitic structures. The latter has implications for the elastic properties of graphene sheets and could, as such, explain the outstanding elastic properties of FL-CNx.
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