Microstructural evolution and stability of (Fe1-xVx)3Al alloys in relation to the electronic structure.

被引:40
|
作者
Botton, GA
Nishino, Y
Humphreys, CJ
机构
[1] Nat Resources Canada, Mat Technol Lab, Ottawa, ON K1A 0G1, Canada
[2] Nagoya Inst Technol, Dept Mat Sci & Engn, Showa Ku, Nagoya, Aichi 4668555, Japan
[3] Univ Cambridge, Dept Mat Sci & Met, Cambridge CB2 3QZ, England
基金
英国工程与自然科学研究理事会;
关键词
aluminides; miscellaneous; bonding; defects; antiphase domains; electronic structure; calculation; phase stability; prediction; spectroscopic methods; various;
D O I
10.1016/S0966-9795(00)00043-1
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The evolution of the microstructure of (Fe1-xVx)(3)Al alloys in the D0(3) structure has been studied as function of composition by transmission electron microscopy. The domain size of the D03 structure significantly increases as V is added to the alloy. An increase in long range order parameter is also shown. This microstructural evolution is discussed in terms of the increased second nearest neighbor interactions induced by the V additions. Electronic structure calculations are also presented in this paper. The density of states shows a strong pseudogap for the Fe2VAl compound and thus strong hybridization induced by the alloying element. This electronic structure feature is discussed in terms of interesting physical properties of the system and in relation to the density of states, stability and properties of similar compounds [Fe2MAl (M = Ti, Cr, Mn)]. Electron energy loss spectra of the Al L2-3 edge show that the strong hybridization induced by V does not affect the unoccupied Al s and d states. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1209 / 1214
页数:6
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