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Ion beam modification of the Ni-Si solid-phase reaction: The influence of substrate damage and nitrogen impurities introduced by ion implantation

材料科学 硅化物 极点图 卢瑟福背散射光谱法 纹理(宇宙学) 成核 基质(水族馆) 离子束 无定形固体 分析化学(期刊) 杂质 离子注入 相(物质) 薄膜 结晶学 离子 冶金 纳米技术 化学 海洋学 有机化学 色谱法 人工智能 地质学 计算机科学 图像(数学)
作者
K. van Stiphout,Filip Geenen,Nuno M. Santos,S. M. C. Miranda,Vincent Joly,J. Demeulemeester,Cristian Mocuta,C.M. Comrie,Christophe Detavernier,L. M. C. Pereira,K. Temst,A. Vantomme
出处
期刊:Journal of Physics D [IOP Publishing]
卷期号:54 (1): 015307-015307 被引量:7
标识
DOI:10.1088/1361-6463/abb046
摘要

Abstract We report on the growth of thin NiSi films via the thermal reaction of Ni layers (13–35 nm) with Si(100) substrates modified by ion implantation. By introducing substrate damage or nitrogen impurities prior to the solid-phase reaction, several properties of the NiSi films can be modified: the formation temperature, texture, diffusion-limited growth rate and morphological stability. As some of the modifications to the NiSi films are rooted in the early silicide phases preceding the NiSi phase, particularly its formation temperature, special attention is devoted to the growth of the amorphous Ni-Si alloy and the crystalline δ -Ni 2 Si and θ -Ni 2 Si phases. We employed a number of experimental techniques, including in situ synchrotron x-ray diffraction (XRD), in situ Rutherford backscattering spectrometry (RBS), in situ sheet resistance measurements, ex situ ion beam channelling and ex situ pole figure measurements. We show that both the formation temperature of the NiSi films and the intensity of epitaxial and axiotaxial components of the NiSi texture can be either lowered or raised by selecting appropriate implantation conditions. Agglomeration of the NiSi films at high temperature (> 700 °C) can be slowed down, either by slowing down the mobility of the Ni and Si atoms, or by removing the morphologically destabilizing axiotaxial texture. Our results emphasize the strong interwoven nature of phase formation, texture and morphological degradation. We illustrate that the kinetics of the early stages of thin film reactions consist of more than just diffusion, i.e. nucleation can also play a crucial role.
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