Ternary silicide formation from Ni-Pt, Ni-Pd and Pt-Pd alloys on Si(100): Nucleation and solid solubility of the monosilicides

被引:10
作者
Schrauwen, A. [1 ]
Demeulemeester, J. [1 ]
Deduytsche, D. [2 ]
Devulder, W. [2 ,4 ]
Detavernier, C. [2 ]
Comrie, C. M. [3 ]
Temst, K. [1 ]
Vantomme, A. [1 ]
机构
[1] Katholieke Univ Leuven, Inst Kern Stralingsfys, Celestijnenlaan 200 D, B-3001 Leuven, Belgium
[2] Univ Ghent, Dept Solid State Sci, B-9000 Ghent, Belgium
[3] Natl Res Fdn, iThemba LABS, POB 772, ZA-7129 Somerset West, South Africa
[4] IMEC, Kapeldreef 75, B-3001 Leuven, Belgium
基金
新加坡国家研究基金会;
关键词
Ternary silicides; Solid solubility; Nucleation; Crystalline phase formation; Atomic redistribution; THERMAL-STABILITY; PHASE-SEPARATION; MIXING ENTROPY; THIN-FILMS; DIFFUSION; BILAYERS; ELEMENTS; SI; TI;
D O I
10.1016/j.actamat.2017.03.022
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The solid solubility of the isomorphous monosilicides during the silicide reaction of Ni-Pt, Ni-Pd and Pt-Pd alloys on Si(100) is comparatively studied in the full composition range. Our study reveals that PtSi and PdSi, exhibiting a minor lattice mismatch, directly form a solid solution. In contrast, for larger differences in lattice parameters such as is the case for NiSi-PtSi and NiSi-PdSi, the mutually soluble phases coexist, prior to the formation of a solid solution at increased temperatures. Hence, it appears that the direct formation of a ternary monosilicide solid solution is inherently related to the lattice mismatch of the binary monosilicides. This finding provides an explanation for important differences observed in the elemental redistribution between the three systems, considered to be very similar up to now. Moreover, the different formation of a solid solution results in a fundamentally different nucleation of PdSi: while Ni lowers the nucleation barrier by reducing the contribution of the interface energy, Pt strongly increases the entropy of mixing which triggers the formation of the Pd-monosilicide at surprisingly low temperatures. Our results show that the lattice mismatch is a crucial parameter and determines the phase formation sequence and elemental redistribution during the silicide reaction. (C) 2017 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:19 / 27
页数:9
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