Electronic structure of Pd-based bulk metallic glasses

被引:23
作者
Alamgir, FM
Jain, H
Schwarz, RB
Jin, O
Williams, DB
机构
[1] Lehigh Univ, Dept Mat Sci & Engn, Bethlehem, PA 18015 USA
[2] Univ Calif Los Alamos Natl Lab, Los Alamos, NM 87545 USA
关键词
D O I
10.1016/S0022-3093(00)00192-7
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
From high-resolution X-ray photoelectron spectroscopy (XPS) of PdxNi(80-x)P20 bulk metallic glasses (BMGs) we observe bonding states in the ternary glasses that cannot be simulated by linear combinations of the valence bands of the binaries. Thus, the bonding in the ternary glasses is qualitatively different from those of the binary alloys of this composition range. Further, we observe that there are more such states in Pd40Ni40P20 than in Pd40.5Cu40.5P19, explaining the greater glass-formability of the former. Within the bulk glass formation range, 30 less than or equal to x less than or equal to 60, the valence band of the most stable glass, Pd40Ni40P20, is found to be a linear combination of those of the glasses at the extremes of this range. Comparison of XPS core level binding energies of glasses and crystals in PdxNi(80-x)P20 show that the electronic structure of glasses is closest to that of the corresponding crystals at x = 30, which agrees with a minimum in the heat of crystallization for this composition. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:289 / 293
页数:5
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