Cesium Clustering and Fluoroberyllate Network Disruption in FLiBe: A Total Scattering and Molecular Dynamics Study

Abstract

Several next-generation fission reactor designs employ molten salts such as FLiBe (2LiF-BeF$_2$), with some concepts using fuel dissolved directly in the salt. During operation, fission products such as cesium will accumulate in the salt mixture, potentially leading to an evolution of the thermophysical properties underpinned by the atomic structure. To understand the structural perturbations in FLiBe with 5 mol% CsF, we conducted X-ray and neutron diffraction measurements, refined empirical potential structure refinement (EPSR) models against the experimental data, and compared the resulting structure with neural network molecular dynamics (NNMD) simulations. Comparisons of the EPSR and NNMD structures distinguishes features constrained by the scattering data from those that remain model dependent. The new Cs-bearing correlations account for the changes in the total structure factor and pair-distribution function, while the FLiBe correlations remain minimally altered. We find that Cs slightly disrupts the intermediate-range fluoroberyllate network, increasing the fraction of free fluorine ions, while the local coordination remains largely unchanged. The Cs ions within FLiBe cluster extensively, with BeF$_4^{2-}$ tetrahedra bridging neighboring cesium environments. In contrast to the minor structural perturbations in the liquid, the addition of 5 mol% CsF suppressed the formation of the crystalline Li2BeF4 phase at room temperature, with the phase appearing only above 180C upon heating. These experimentally constrained structural features provide a benchmark for atomistic models used to predict the behavior and properties of fission-product-containing FLiBe.