Non-destructive determination of local strain with 100-nanometre spatial resolution

被引:104
|
作者
Di Fonzo, S
Jark, W
Lagomarsino, S
Giannini, C
De Caro, L
Cedola, A
Müller, M
机构
[1] Sincrotrone Trieste, I-34012 Trieste, Italy
[2] CNR, Ist Elettron Stato Solido, I-00156 Rome, Italy
[3] Ctr Nazl Ric & Sviluppo Mat, PASTIS, I-72100 Brindisi, Italy
[4] ESRF, F-38043 Grenoble, France
关键词
D O I
10.1038/35001035
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Structure sizes of similar to 180 mm are now standard in microelectronics, and state-of-the-art fabrication techniques can reduce these to just a few tens of nanometres (ref. 1). But at these length scales, the strain induced at interfaces can locally distort the crystal lattice, which may in turn affect device performance in an unpredictable way. A means of non-destructively characterizing such strain fields with high spatial resolution and sensitivity is therefore highly desirable. One approach is to use Raman spectroscopy(2), but this is limited by the intrinsic similar to 0.5-mu m resolution limit of visible light probes. Techniques based on electron-beam diffraction can achieve the desired nanometre-scale resolution But either they require complex sample preparation procedures(3) (which may alter the original strain field) or they are sensitive to distortional (but not dilational) strain within only the top few tens of nanometres of the sample surface(4,5). X-rays, on the other hand, have a much greater penetration depth, but have not hitherto achieved strain analysis with sub-micrometre resolution(6). Here we describe a magnifying diffraction imaging procedure for X-rays which achieves a spatial resolution of 100 nm in one dimension and a sensitivity of 10(-4) for relative lattice variations. We demonstrate the suitability of this procedure for strain analysis by measuring the strain depth profiles beneath oxidized lines on silicon crystals.
引用
收藏
页码:638 / 640
页数:3
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