Surface degradation mechanisms in a eutectic high entropy alloy at microstructural length-scales and correlation with phase-specific work function
High entropy alloys represent a new paradigm of structural alloy design consisting of (near) equal proportions of constituent elements resulting in a number of attractive properties. In particular, eutectic high entropy alloys offer a remarkable combination of high strength and good ductility from t...
Gespeichert in:
Veröffentlicht in: | Npj Materials degradation 2019-04, Vol.3 (1), Article 16 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | High entropy alloys represent a new paradigm of structural alloy design consisting of (near) equal proportions of constituent elements resulting in a number of attractive properties. In particular, eutectic high entropy alloys offer a remarkable combination of high strength and good ductility from the synergistic contribution of each phase in the eutectic, thereby circumventing the strength-ductility trade-off in conventional structural materials. In the present study, wear and corrosion behavior were evaluated for the AlCoCrFeNi
2.1
eutectic high entropy alloy consisting of BCC (B2), and FCC (L1
2
) lamellae. A transition from adhesive to oxidative wear was observed in reciprocating wear analysis. The L1
2
phase with lower hardness preferentially deformed during the wear test. The ratio of hardness to modulus was almost two times higher for the B2 phase as compared to L1
2
. The overall corrosion resistance of the eutectic high entropy alloy was comparable to 304 stainless steel in 3.5 wt% NaCl solution. However, detailed microscopy revealed preferential dissolution of the B2 phase. Phase-specific scanning kelvin probe analysis showed relatively higher electropositivity for the B2 phase as compared with L1
2
, supporting the selective corrosion and higher coefficient of friction of B2. |
---|---|
ISSN: | 2397-2106 2397-2106 |
DOI: | 10.1038/s41529-019-0079-0 |