Chemical heterogeneity enhances hydrogen resistance in high-strength steels

The antagonism between strength and resistance to hydrogen embrittlement in metallic materials is an intrinsic obstacle to the design of lightweight yet reliable structural components operated in hydrogen-containing environments. Economical and scalable microstructural solutions to this challenge mu...

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Veröffentlicht in:Nature materials 2021-12, Vol.20 (12), p.1629-1634
Hauptverfasser: Sun, Binhan, Lu, Wenjun, Gault, Baptiste, Ding, Ran, Makineni, Surendra Kumar, Wan, Di, Wu, Chun-Hung, Chen, Hao, Ponge, Dirk, Raabe, Dierk
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Sprache:eng
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Zusammenfassung:The antagonism between strength and resistance to hydrogen embrittlement in metallic materials is an intrinsic obstacle to the design of lightweight yet reliable structural components operated in hydrogen-containing environments. Economical and scalable microstructural solutions to this challenge must be found. Here, we introduce a counterintuitive strategy to exploit the typically undesired chemical heterogeneity within the material’s microstructure that enables local enhancement of crack resistance and local hydrogen trapping. We use this approach in a manganese-containing high-strength steel and produce a high dispersion of manganese-rich zones within the microstructure. These solute-rich buffer regions allow for local micro-tuning of the phase stability, arresting hydrogen-induced microcracks and thus interrupting the percolation of hydrogen-assisted damage. This results in a superior hydrogen embrittlement resistance (better by a factor of two) without sacrificing the material’s strength and ductility. The strategy of exploiting chemical heterogeneities, rather than avoiding them, broadens the horizon for microstructure engineering via advanced thermomechanical processing. Typically undesired chemically heterogeneous microstructures are shown to enhance the resistance of high-strength steel against hydrogen embrittlement, with no loss in strength or ductility.
ISSN:1476-1122
1476-4660
DOI:10.1038/s41563-021-01050-y