In Situ Investigation of Structural Evolution in Zr46Cu46Al8 and Zr56Cu36Al8 Bulk Metallic Glasses During Isothermal Annealing

Xuelian Wu, Xiyang Li, Zhenduo Wu, Xun-Li Wang, Xiaoya Wei, Jie Zhou, Zhaoping Lu, Elliot Paul Gilbert, Zhengming Sun, Jianxiang Ding*, Dongming Liu*, Chenchen Yuan*, Si Lan*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

The crystallization kinetics of Zr46Cu46Al8 and Zr56Cu36Al8 bulk metallic glasses (BMGs) during isothermal annealing in the supercooled liquid region has been studied using in situ simultaneous differential scanning calorimetry (DSC) and small-angle neutron scattering (SANS) technique. Zr46Cu46Al8, known for its good glass forming ability (GFA), exhibits a complex crystallization pathway. Initially, a transition region emerges, eventually evolving into the thermodynamically stable crystalline phase of Cu10Zr7, facilitated by continuous chemical redistribution at the late stage of annealing. In contrast, Zr56Cu36Al8 , a poor glass former, crystallizes directly into the thermodynamically stable crystalline phase of CuZr2 in a single step, with no observed chemical redistribution. Overall, the results suggest that continuous chemical redistribution following structural ordering may contribute to stabilizing the amorphous state and improving the thermal stability of BMGs. This study highlights the critical role of chemical redistribution in the crystallization of BMGs and introduces a new perspective for assessing their GFAs.

© 2024 The Minerals, Metals & Materials Society
Original languageEnglish
Pages (from-to)6917-1924
JournalJOM
Volume76
Online published7 Aug 2024
DOIs
Publication statusPublished - Dec 2024

Funding

This work was supported by the Research Grants Council of Hong Kong Special Administrative Region, Project N_CityU173/22. S. Lan acknowledges the supports by the National Natural Science Foundation of China (Grant Nos. 52222104, 12261160364). Z.D. Wu acknowledges the financial support by the National Natural Science Foundation of China (Grant No. 52201190) and the open research fund of Songshan Lake Materials Laboratory (Grant No. 2022SLABFN19). C.C. Yuan acknowledges the financial support by the National Natural Science Foundation of China (Grant No. 52071078). X.L. Wu acknowledges the Start-up Fund from Anhui University of Technology (Grant No. DT2300000362). We acknowledge the support of the Australian Centre for Neutron Scattering, Australian Nuclear Science and Technology Organization, through proposal number 4707 in providing the neutron-scattering research facilities.

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