Vitrification of a monatomic metallic liquid

被引:195
作者
Bhat, M. H.
Molinero, V.
Soignard, E.
Solomon, V. C.
Sastry, S.
Yarger, J. L.
Angell, C. A. [1 ]
机构
[1] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
[2] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
[3] Jawaharlal Nehru Ctr Adv Sci Res, Bangalore 560064, Karnataka, India
基金
美国国家科学基金会;
关键词
D O I
10.1038/nature06044
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although the majority of glasses in use in technology are complex mixtures of oxides or chalcogenides, there are numerous examples of pure substances - 'glassformers' - that also fail to crystallize during cooling. Most glassformers are organic molecular systems, but there are important inorganic examples too(1,2), such as silicon dioxide and elemental selenium ( the latter being polymeric). Bulk metallic glasses can now be made(3); but, with the exception of Zr50Cu50 ( ref. 4), they require multiple components to avoid crystallization during normal liquid cooling. Two-component 'metglasses' can often be achieved by hyperquenching, but this has not hitherto been achieved with a single- component system. Glasses form when crystal nucleation rates are slow, although the factors that create the slow nucleation conditions are not well understood. Here we apply the insights gained in a recent molecular dynamics simulation study(5) to create conditions for successful vitrification of metallic liquid germanium. Our results also provide micrographic evidence for a rare polyamorphic transition preceding crystallization of the diamond cubic phase.
引用
收藏
页码:787 / U3
页数:5
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