First-principles study of lithium aluminosilicate glass scintillators.

Radiation sensors are an important enabling technology in several fields, such as medicine, scientific research, energy, defence, meteorology, and homeland security. Glass-based scintillators have been in use for more than 50 years and offer many benefits, including their ability to respond to different types of radiation, and to be readily formed into various shapes. There is, however, the prospect to develop new and improved glass scintillators, with low self-absorption, low refractive indices, and high radiative recombination rates. To investigate the factors limiting the improvement of glass scintillator properties, this work provides insight from atomic scale simulations of the cerium-doped lithium aluminosilicate (SiO2-Al2O3-MgO-Li2O-Ce2O3) glass scintillator system. Three glass compositions were studied using molecular dynamics and density functional theory to investigate the effect of the ratio (with RAl/M = [0.1, 0.8 and 1.2]) on the structural and electronic properties. For a ratio RAl/M > 1, it has been shown that glasses with increased polymerization allow for more effective incorporation of Ce3+ cations. The structural analysis also showed that the bond order of Al-O can be affected in the presence of a lithium-rich environment. Electronic density of states and Bader charge analysis indicate a decline in the population of localized trapping states with increasing RAl/M. This suggests a higher probability of radiative recombination which can increase the photon yield of these scintillators. These findings provide valuable guidance for optimizing Li-glasses in neutron detection systems by highlighting the intricate challenges.

Optimization of a new interatomic potential to investigate the thermodynamic properties of hypo-stoichiometric mixed oxide fuel U1-y Pu y O2-x.

The behaviour of stoichiometric U1-y Pu y O2 compounds used as nuclear fuel is relatively well understood. Conversely, the effects of stoichiometry deviation on fuel performance and fuel stability are intricate and poorly studied. In order to investigate what affect these have on the thermophysical properties of hypo-stoichiometric U1-y Pu y O2-x mixed oxide fuel, new interaction parameters based on the many-body CRG (Cooper-Rushton-Grimes) potential formalism were optimized. The new potential has been fitted to match experimental lattice parameters of U0.70Pu0.30O1.99 (O/M = 1.99) and U0.70Pu0.30O1.97 (O/M = 1.97), where M represents the total amount of metallic cations, through a rigorous procedure combining classical molecular dynamic and classical molecular Monte Carlo simulation methods. This new potential provides an excellent description of the U1-y Pu y O2-x system. Concerning lattice parameter, although fitted on only one Pu content (30%) and two stoichiometries (1.99 and 1.97), our potential allows good predictions compared to available experimental results as well as to available recommendations in wide ranges of O/M ratio, Pu content and temperature. For the U0.70Pu0.30O2-x hypo-stoichiometric system (30% Pu content and O/M ratio ranging from 1.94 to 2.00), some direct properties (lattice parameter and enthalpy) and some derivative properties (linear thermal expansion coefficient and specific heat) were systematically investigated from room temperature up to the expected melting temperatures and a good agreement with experiments is found. Moreover, our potential shows good transferability to the plutonium sesquioxide Pu2O3 system.

Thermophysical properties and oxygen transport in (Thx,Pu1-x)O2.

Using Molecular Dynamics, this paper investigates the thermophysical properties and oxygen transport of (Thx,Pu1-x)O2 (0 ≤ x ≤ 1) between 300-3500 K. In particular, the superionic transition is investigated and viewed via the thermal dependence of lattice parameter, linear thermal expansion coefficient, enthalpy and specific heat at constant pressure. Oxygen diffusivity and activation enthalpy are also investigated. Below the superionic temperature an increase of oxygen diffusivity for certain compositions of (Thx,Pu1-x)O2 compared to the pure end members is predicted. Oxygen defect formation enthalpies are also examined, as they underpin the superionic transition temperature and the increase in oxygen diffusivity. The increase in oxygen diffusivity for (Thx,Pu1-x)O2 is explained in terms of lower oxygen defect formation enthalpies for (Thx,Pu1-x)O2 than PuO2 and ThO2, while links are drawn between the superionic transition temperature and oxygen Frenkel disorder.

Development of Xe and Kr empirical potentials for CeO2, ThO2, UO2 and PuO2, combining DFT with high temperature MD.

The development of embedded atom method (EAM) many-body potentials for actinide oxides and associated mixed oxide (MOX) systems has motivated the development of a complementary parameter set for gas-actinide and gas-oxygen interactions. A comprehensive set of density functional theory (DFT) calculations were used to study Xe and Kr incorporation at a number of sites in CeO2, ThO2, UO2 and PuO2. These structures were used to fit a potential, which was used to generate molecular dynamics (MD) configurations incorporating Xe and Kr at 300 K, 1500 K, 3000 K and 5000 K. Subsequent matching to the forces predicted by DFT for these MD configurations was used to refine the potential set. This fitting approach ensured weighted fitting to configurations that are thermodynamically significant over a broad temperature range, while avoiding computationally expensive DFT-MD calculations. The resultant gas potentials were validated against DFT trapping energies and are suitable for simulating combinations of Xe and Kr in solid solutions of CeO2, ThO2, UO2 and PuO2, providing a powerful tool for the atomistic simulation of conventional nuclear reactor fuel UO2 as well as advanced MOX fuels.

Genetics of superionic conductivity in lithium lanthanum titanates.

The self-diffusion of ions is a fundamental mass transport process in solids and has a profound impact on the performance of electrochemical devices such as the solid oxide fuel cell, batteries and electrolysers. The perovskite system lithium lanthanum titanate, La2/3-xLi3xTiO3 (LLTO) has been the subject of much academic interest as it displays very high lattice conductivity for a solid state Li conductor; making it a material of great technological interest for deployment in safe durable mobile power applications. However, so far, a clear picture of the structural features that lead to efficient ion diffusion pathways in LLTO, has not been fully developed. In this work we show that a genetic algorithm in conjunction with molecular dynamics can be employed to elucidate diffusion mechanisms in systems such as LLTO. Based on our simulations we provide evidence that there is a three-dimensional percolated network of Li diffusion pathways. The present approach not only reproduces experimental ionic conductivity results but the method also promises straightforward investigation and optimisation of the properties relating to superionic conductivity in materials such as LLTO. Furthermore, this method could be used to provide insights into related materials with structural disorder.

Thermal conductivity and energetic recoils in UO2 using a many-body potential model.

Classical molecular dynamics simulations have been performed on uranium dioxide (UO2) employing a recently developed many-body potential model. Thermal conductivities are computed for a defect free UO2 lattice and a radiation-damaged, defect containing lattice at 300 K, 1000 K and 1500 K. Defects significantly degrade the thermal conductivity of UO2 as does the presence of amorphous UO2, which has a largely temperature independent thermal conductivity of ∼1.4 Wm(-1) K(-1). The model yields a pre-melting superionic transition temperature at 2600 K, very close to the experimental value and the mechanical melting temperature of 3600 K, slightly lower than those generated with other empirical potentials. The average threshold displacement energy was calculated to be 37 eV. Although the spatial extent of a 1 keV U cascade is very similar to those generated with other empirical potentials and the number of Frenkel pairs generated is close to that from the Basak potential, the vacancy and interstitial cluster distribution is different.

Impact of uniaxial strain and doping on oxygen diffusion in CeO2.

Doped ceria is an important electrolyte for solid oxide fuel cell applications. Molecular dynamics simulations have been used to investigate the impact of uniaxial strain along the <100> directions and rare-earth doping (Yb, Er, Ho, Dy, Gd, Sm, Nd, and La) on oxygen diffusion. We introduce a new potential model that is able to describe the thermal expansion and elastic properties of ceria to give excellent agreement with experimental data. We calculate the activation energy of oxygen migration in the temperature range 900-1900 K for both unstrained and rare-earth doped ceria systems under tensile strain. Uniaxial strain has a considerable effect in lowering the activation energies of oxygen migration. A more pronounced increase in oxygen diffusivities is predicted at the lower end of the temperature range for all the dopants considered.

A many-body potential approach to modelling the thermomechanical properties of actinide oxides.

A many-body potential model for the description of actinide oxide systems, which is robust at high temperatures, is reported for the first time. The embedded atom method is used to describe many-body interactions ensuring good reproduction of a range of thermophysical properties (lattice parameter, bulk modulus, enthalpy and specific heat) between 300 and 3000 K for AmO2, CeO2, CmO2, NpO2, ThO2, PuO2 and UO2. Additionally, the model predicts a melting point for UO2 between 3000 and 3100 K, in close agreement with experiment. Oxygen-oxygen interactions are fixed across the actinide oxide series because it facilitates the modelling of oxide solid solutions. The new potential is also used to predict the energies of Schottky and Frenkel pair disorder processes.