Electron Microscopy of the Tin-oxide Nanolayer Formed on the Surface of Sn-Ag-Cu Alloys

3rd International Conference on Functional Materials Science 2016

Sosiati, H.^1 ; Kuwano, N.^2 ; Hata, S.^3

Department of Mechanical Engineering, Faculty of Engineering, Universitas Muhammadiyah Yogyakarta, Yogyakarta

55183, Indonesia^1

Mechanical Precision Engineering, Malaysia-Japan International Institute of Technology (MJIIT), University of Technology Malaysia (UTM), International Campus, Jalan Semarak, Kualalumpur

54100, Malaysia^2

Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, Kasuga, Fukuoka

816-8580, Japan^3

关键词: Atmospheric oxidation;    Cross-sectional TEM;    Fast fourier transformation (FFT);    High resolution;    High temperature;    Oxidation mechanisms;    Sn-3.0ag-0.5cu solders;    Specimen surfaces;   

Others  :  https://iopscience.iop.org/article/10.1088/1757-899X/196/1/012006/pdf
DOI  :  10.1088/1757-899X/196/1/012006

来源: IOP

【 摘 要 】

Sn-Ag-Cu alloy used in the present study is commercial Sn-3.0Ag-0.5Cu solder ball alloys with a diameter of 400 and 300 μm which were long term atmospheric oxidized for about 6 years (specimen-1) and under high temperature/humidity at 85°C and relative humidity of 85% for 2140 h, respectively. Morphologies and nanostructure of the oxide nanolayers formed on the surface of Sn-Ag-Cu alloys were studied from the interface of the oxide film and the tin substrate by transmission electron microscopy (TEM) to verify the oxidation mechanism. Cross-sectional TEM specimens were prepared using a focused-ion-beam (FIB) micro-sampling technique. Before the FIB fabrication, the specimen surface was coated with carbon (C) and tungsten (W) films. Inhomogeneous thickness of tin-oxide nanolayer formed on specimen-1 and specimen-2 were fluctuated between 20-40 nm and 40-50 nm, respectively. The nanolayer on specimen-1, however, consists of polycrystalline SnO and SnO2, whereas the one on the specimen-2 comprises of polycrystalline SnO2. High resolution (HRTEM) image and fast Fourier transformation (FFT) spectra corresponding to the interface and the substrate areas have confirmed those results. The results verify that at very long atmospheric oxidation Sn was gradually oxidized to be SnO (Sn2+) and then SnO2(Sn4+), in which SnO is present at the region closed to interface between Sn-substrate and the tin-oxide layer. At high temperature oxidation, however, Sn was completely oxidized to be SnO2.