Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/96785
Title: On valence electron density, energy dissipation and plasticity of bulk metallic glasses
Authors: Pang, Jianjun
Tan, M. J.
Liew, K. M.
Keywords: DRNTU::Engineering::Mechanical engineering
Issue Date: 2012
Source: Pang, J. J., Tan, M. J., & Liew, K. M. (2012). On valence electron density, energy dissipation and plasticity of bulk metallic glasses. Journal of Alloys and Compounds.
Series/Report no.: Journal of alloys and compounds
Abstract: In conventional crystalline alloys, valence electron density (VED) is one of the most significant factors in determining their phase stability and mechanical properties. Extending the concept to metallic glasses (MGs), it is found, not totally surprisingly, that their mechanical properties are VED-dependent as in crystalline alloys. Interestingly, the whole VED region can be separated into two zones: Zone 1 consists of Mg-, Ca-, and RE-based (RE for rare earth) alloys; Zone 2 consists of the rest of MGs. In either zone, for each type of MGs, Poisson's ratio generally decreases as VED increases. From the energy dissipation viewpoint proposed recently, the amorphous plasticity is closely related to the activation energy for the operation of shear-transformation-zones (STZs). Smaller STZ activation energy suggests higher ductility because STZs with lower activation energy are able to convert deformation work more efficiently into configurational energy rather than heat, which yields mechanical softening and advances the growth of shear bands (SBs). Following this model, it is revealed that the activation energies for STZ operation and crystallization are certainly proportional to VED. Thus, it is understood that, in Zone 2, MGs have a smaller VED and hence lower activation energies which are favorable for ductility and Poisson's ratio. In Zone 1, MGs have the lowest VED but apparent brittleness because either of low glass transition temperature and poor resistance to oxidation or of a large fraction of covalent bonds.
URI: https://hdl.handle.net/10356/96785
http://hdl.handle.net/10220/11664
ISSN: 0925-8388
DOI: 10.1016/j.jallcom.2012.03.036
Rights: © 2012 Elsevier B.V.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:MAE Journal Articles

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