کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5348476 | 1503621 | 2015 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Fabrication and characterization of periodic arrays of epitaxial Ni-silicide nanocontacts on (1Â 1Â 0)Si
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی تئوریک و عملی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
In this study, we report on the fabrication and characterization of periodic Ni and Ni-silicide nanocontact arrays on (1 1 0)Si substrates. From transmission electron microscopy and selected-area electron diffraction analysis, it is found that the epitaxial NiSi2 is the first and the only silicide phase formed in the nanoscale Ni contact/(1 1 0)Si sample after annealing at a temperature as low as 300 °C, demonstrating that the nanoscale Ni contact is more favorable for the epitaxial growth of NiSi2 phase on (1 1 0)Si. The orientation relationship between the epitaxial NiSi2 nanocontacts and the (1 1 0)Si substrate is identified as [1 1 0]NiSi2//[1 1 0]Si and (1¯11¯)NiSi2//(1¯11¯)Si. For the samples annealed at higher temperatures, all the epitaxial NiSi2 nanocontacts formed on (1 1 0)Si are anisotropic in shape and elongated along the crystallographic 11¯0 directions. The observed results can be attributed to the higher surface area to volume ratio of Ni nanocontacts and the faster growth rate along the ã1 1 0ã directions than along other directions. The size and periodicity of the nanocontacts can be readily controlled by adjusting the diameter of the colloidal nanosphere template. The self-assembled approach proposed here will provide the capability to fabricate other highly-ordered metal silicide nanocontact arrays and may offer potential applications in constructing silicide-based nanodevices.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Surface Science - Volume 343, 15 July 2015, Pages 88-93
Journal: Applied Surface Science - Volume 343, 15 July 2015, Pages 88-93
نویسندگان
S.L. Cheng, L.H. Chang, C.F. Chuang, H. Chen,