Simultaneous Oxygen and Boron Trifluoride Functionalization of Hexagonal Boron Nitride: A Designer Cathode Material for Energy Storage

TL;DR

This paper explores covalent functionalization of hexagonal boron nitride with oxygen and boron trifluoride to create potential cathode materials for high-energy, fast-charging batteries, based on band structure calculations.

Contribution

It introduces new functionalization methods for h-BN that could lead to advanced cathode materials with high voltage and energy density.

Findings

Functionalized h-BN can become metallic, enhancing conductivity.

Potential for batteries with voltages of 2.1-5.6 V and energy densities of 800-1200 Wh/kg.

Open surfaces allow fast ionic diffusion for Li, Na, and Mg ions.

Abstract

Covalent functionalization is a way to tune the electrochemical properties of hexagonal boron nitride (h-BN) monolayers. The wide band gap insulator h-BN may become metallic conductor upon functionalization with strong oxidants, such as fluorosulfonyl radicals ($\cdot$OSO$_2$F), as known since 1978 [N. Bartlett et al., J. Chem. Soc. Chem. Comm. {\bf 5}, 200 (1978)], with electrical conductivity of 1.5 S/cm [C. Shen et al., J. Solid State Chem. {\bf 147}, 74 (1999)] that greatly surpasses commercial cathode material Li$_{x}$CoO$_{2}$ while retaining excellent ionic conductivity. Functionalized boron nitrides (FBN-s) have great potential for cathode applications in energy storage devices, for example in solid state batteries. While fluorosulfonyl functionalization is unlikely to result in rechargeable cathodes, similarly to graphene fluoride (CF$_x$), some other FBN-s discussed here may do. In the present work, fluorene, oxygen and combined oxygen and boron trifluoride functionalizations are studied, on the basis of band structure calculations. Due to the open surfaces of FBN-s, fast ionic diffusion with Li, Na and Mg ions is possible, enabling batteries with voltages of 2.1-5.6 V, theoretical energy densities of 800-1200 Wh/kg and fast charge and discharge.