Abstract
Molten salts serve as effective high-temperature heat transfer fluids and thermal storage media used in a wide range of energy generation and storage facilities, including concentrated solar power plants, molten salt reactors and high-temperature batteries. However, at the salt-metal interfaces, a complex interplay of charge-transfer reactions involving various metal ions, generated either as fission products or through corrosion of structural materials, takes place. Simultaneously, there is a mass transport of ions or atoms within the molten salt and the parent alloys. The precise physical and chemical mechanisms leading to the diverse morphological changes in these materials remain unclear. To address this knowledge gap, this work employed a combination of synchrotron X-ray nanotomography and electron microscopy to study the morphological and chemical evolution of Ni-20Cr in molten KCl-MgCl2, while considering the influence of metal ions (Ni2+, Ce3+, and Eu3+) and variations in salt composition. Our research suggests that the interplay between interfacial diffusivity and reactivity determines the morphological evolution. The summary of the associated mass transport and reaction processes presented in this work is a step forward toward achieving a fundamental comprehension of the interactions between molten salts and alloys. Overall, the findings offer valuable insights for predicting the diverse chemical and structural alterations experienced by alloys in molten salt environments, thus aiding in the development of protective strategies for future applications involving molten salts.
Original language | English |
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Pages (from-to) | 45606-45618 |
Number of pages | 13 |
Journal | ACS Applied Materials and Interfaces |
Volume | 16 |
Issue number | 34 |
DOIs | |
State | Published - Aug 28 2024 |
Funding
This work was supported as part of the Molten Salts in Extreme Environments (MSEE) Energy Frontier Research Center, funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences. BNL, INL, and ORNL are operated under DOE contracts DE-SC0012704, DE-AC07-05ID14517, and DE-AC05-00OR22725, respectively. Work at Stony Brook University, the University of Tennessee and the University of Michigan was supported by MSEE through subcontracts from BNL. This research used resources and the Full Field X-ray Imaging (FXI, 18-ID) and Quick X-ray Absorption and Scattering (QAS, 7-BM) beamlines of the National Synchrotron Light Source II, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Brookhaven National Laboratory under Contract DE-SC0012704. We thank Dr. James Wishart, Dr. Simon Pimblott, Prof. Adrien Couet and Prof. Anatoly Frenkel for helpful discussions as part of the MSEE activities, as well as their great insights contributing to the interpretations and future planned work mentioned in this manuscript. We thank Bobby Layne for helping with the heater and experimental setup. Current Chen-Wiegart group members are acknowledged for helping with the experiments: Xiaoyin Zheng, Varun Ravi Kankanallu and Cheng-Chu Chung.
Funders | Funder number |
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Basic Energy Sciences | |
University of Tennessee | |
U.S. Department of Energy | |
Office of Science | |
University of Michigan | |
MSEE | |
Brookhaven National Laboratory | DE-SC0012704, 18-ID |
Brookhaven National Laboratory |
Keywords
- STEM
- TXM
- dealloying
- high-temperature corrosion
- materials kinetics