Published October 2007 | Version v1
Journal article

Transition metal co-precipitation mechanisms in silicon

  • 1. Department of Materials Science and Engineering, University of California, Berkeley and Materials Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States)
  • 2. Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States)
  • 3. Advanced Photon Source, Argonne National Laboratory, Argonne, IL 60439 (United States)

Description

Formation mechanisms of precipitates containing multiple-metal species in silicon are elucidated by nano-scale morphology and phase investigations performed by synchrotron-based X-ray microprobe techniques. Precipitates formed at low (655 deg. C) and high (1200 deg. C+) temperatures exhibit distinguishing features indicative of unique formation mechanisms. After lower-temperature annealing, co-localized single-metal silicide phases are observed, consistent with classical models predicting that dissolved, supersaturated metal atoms will precipitate into solid second-phase particles. Precise precipitate morphologies are found to depend on the local crystallographic environment. In precipitates formed during slow cooling from higher-temperature anneals, nano-scale phase separation and intermetallic phases are evident, suggestive of a high-temperature transition through a liquid phase. Based on experimental results and phase diagram information, it is proposed that under certain conditions, liquid metal-silicon droplets may form within the silicon matrix, possibly with the potential to getter additional metal atoms via liquid-solid segregation

Availability note (English)

Available from http://dx.doi.org/10.1016/j.actamat.2007.07.030

Additional details

Identifiers

DOI
10.1016/j.actamat.2007.07.030;
PII
S1359-6454(07)00483-1;

Publishing Information

Journal Title
Acta Materialia
Journal Volume
55
Journal Issue
18
Journal Page Range
p. 6119-6126
ISSN
1359-6454
CODEN
ACMAFD

Optional Information

Copyright
Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.