Influence of chemical disorder on energy dissipation and defect evolution in concentrated solid solution alloys

Yanwen Zhang, G. Malcolm Stocks, Ke Jin, Chenyang Lu, Hongbin Bei, Brian C. Sales, Lumin Wang, Laurent K. Béland, Roger E. Stoller, German D. Samolyuk, Magdalena Caro, Alfredo Caro, William J. Weber

Research output: Contribution to journalArticlepeer-review

553 Scopus citations

Abstract

A grand challenge in materials research is to understand complex electronic correlation and non-equilibrium atomic interactions, and how such intrinsic properties and dynamic processes affect energy transfer and defect evolution in irradiated materials. Here we report that chemical disorder, with an increasing number of principal elements and/or altered concentrations of specific elements, in single-phase concentrated solid solution alloys can lead to substantial reduction in electron mean free path and orders of magnitude decrease in electrical and thermal conductivity. The subsequently slow energy dissipation affects defect dynamics at the early stages, and consequentially may result in less deleterious defects. Suppressed damage accumulation with increasing chemical disorder from pure nickel to binary and to more complex quaternary solid solutions is observed. Understanding and controlling energy dissipation and defect dynamics by altering alloy complexity may pave the way for new design principles of radiation-tolerant structural alloys for energy applications.

Original languageEnglish
Article number8736
JournalNature Communications
Volume6
DOIs
StatePublished - Oct 28 2015

Funding

This work was supported as part of the Energy Dissipation to Defect Evolution (EDDE), an Energy Frontier Research Center funded by the US Department of Energy, Office of Sciences, Basic Energy Sciences. B.C.S. was supported by the Department of Energy, Office of Science, BES, Materials Sciences and Engineering Division. L.K.B. acknowledges additional support from a fellowship awarded by the Fonds Québécois de recherche Nature et Technologies. Ion beam work was performed at the University of Tennessee– Oak Ridge National Laboratory Ion Beam Materials Laboratory (IBML) located at the campus of the University of Tennessee, Knoxville. Electronic structure calculations were performed in collaboration with Markus Däne at the Lawrence Livermore National Laboratory, which is operated by Lawrence Livermore National Security, LLC, for the U.S. Department of Energy, National Nuclear Security Administration under Contract DE-AC52-07NA27344. This simulation used resources of the National Energy Research Scientific Computing Center, supported by the Office of Science, US Department of Energy, under Contract No. DEAC02-05CH11231.

FundersFunder number
Office of Sciences
US Department of Energy
U.S. Department of Energy
Office of Science
Basic Energy Sciences
Fonds Québécois de la Recherche sur la Nature et les TechnologiesDEAC02-05CH11231

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