We have performed cascade genetic algorithm and ab initio atomistic thermodynamics under the framework of first-principles density functional theory to study the (meta-)stability of a wide range of LixNy clusters. We found that hybrid xc-functional is essential to address this problem as a local/semi-local functional simply fails even to predict a qualitative prediction. Most importantly, we find that though in bulk Lithium Nitride, Li rich phase, i.e. Li3N, is the stable stoichiometry, in small LixNy clusters N-rich phases are more stable at thermodynamic equilibrium. We further show a that these N-rich clusters are promising hydrogen storage material because of their easy adsorption and desorption ability at respectively low (< 300K) and moderately high temperature (> 600K).
@article{arxiv.1506.06566,
title = {Exploring N-rich phases in LixNy clusters for hydrogen storage at nano-scale},
author = {Amrita Bhattacharya and Saswata Bhattacharya},
journal= {arXiv preprint arXiv:1506.06566},
year = {2021}
}