Depth dependence of {311} defect dissolution

被引:22
作者
Venezia, VC
Kalyanaraman, R
Gossmann, HJL
Rafferty, CS
Werner, P
机构
[1] Oak Ridge Natl Lab, Div Solid State, Oak Ridge, TN 37831 USA
[2] Bell Labs, Lucent Technol, Murray Hill, NJ 07974 USA
[3] Max Planck Inst Microstruct Phys, D-06120 Halle Saale, Germany
关键词
D O I
10.1063/1.1392972
中图分类号
O59 [应用物理学];
学科分类号
摘要
A deep band of {311} defects was created 520 nm below the silicon surface with a 350 keV Si implant followed by a cluster-forming rapid thermal anneal (800 degreesC, 1000 s). Chemical etching was used to vary the depth to the surface of the {311}-defect band. Afterwards, the defect dissolution was investigated at 750 degreesC for different times. Varying the depth in this fashion assures that only the depth and no other feature of the cluster distribution is changed. The {311} defects were analyzed by plan-view, transmission electron microscopy. We show that the dissolution time of the {311}-defect band varies linearly with depth, confirming that surface recombination controls the dissolution and is consistent with analogous observations of transient enhanced diffusion. (C) 2001 American Institute of Physics.
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收藏
页码:1429 / 1431
页数:3
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