Answers are grounded in this paper and cite their sources.
First-principles study reveals high storage capacity and ultrafast ion diffusion for B4C4N2 monolayers, indicating strong potential as a universal battery anode.
With the growing demand for high-performance electrode materials in electrochemical energy storage devices, two-dimensional (2D) materials have demonstrated significant potential in the field of alkali metal ion batteries due to their unique structural advantages. In this study, first-principles density functional theory calculations were employed to systematically evaluate the application prospects of the novel B 4 C 4 N 2 monolayer as an anode material for Li + , Na + and K + ion batteries. Multidimensional validation, including phonon spectra, binding energies, ab initio molecular dynamics (AIMD) simulations and elastic constants, indicates that B 4 C 4 N 2 possesses excellent intrinsic structural stability, maintaining an intact 2D framework even at high temperatures of 1000 K and under saturated ion loading. Electronic structure analysis reveals its intrinsic metallic nature, with covalent-metallic hybrid bonding ensuring efficient charge transport. In terms of ion storage, B 4 C 4 N 2 exhibits moderate chemical adsorption for Li, Na and K, whilst achieving maximum theoretical specific capacities of 1347.91 and 1123.26 mAh·g −1 . Notably, the minimum diffusion energy barrier for K + on the B 4 C 4 N 2 surface is merely 0.069 eV, demonstrating virtually unimpeded migration kinetics. These results indicate that B 4 C 4 N 2 combines high specific capacity, ultra-fast ion diffusion and a robust structural framework, making it a highly promising universal anode material for multi-alkali metal ion batteries.
No takes yet. Share an insight, caveat, or question.
Fu et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: