Sequential lithium deposition on hexagonal boron nitride monolayer on Ir(111): Identifying intercalation and adsorption

TL;DR

This study investigates how lithium atoms deposit on hexagonal boron nitride monolayers on Ir(111), revealing intercalation and adsorption behaviors that influence electronic properties and substrate decoupling.

Contribution

It provides detailed insights into the sequential intercalation and adsorption of lithium on hBN/Ir(111), highlighting the effects on band structure and surface corrugation.

Findings

Li intercalates under hBN at low coverages, causing significant band shifts.

Intercalated Li decouples hBN from the substrate and reduces moiré corrugation.

Further Li adsorption on top diminishes charge and band shifts due to Coulomb repulsion.

Abstract

Stepwise deposition of Li atoms onto hexagonal boron nitride (hBN) monolayer on Ir(111) is investigated by means of angle-resolved photoemission spectroscopy and low-energy electron diffraction. Sequential Li deposition progressively shifts the band structure of hBN to higher binding energies due to the induction of a variable electric potential originating from electronic charge donation by alkali atoms. At small coverages, Li atoms preferably intercalate under the hBN layer, where they are highly charged and give rise to a large initial shift of the band structure. Additionally, intercalated Li atoms effectively decouple hBN from the substrate and consequently reduce its moir\'e corrugation. As the deposition progresses further, Li atoms also adsorb on top of hBN, and the average effective charge of both intercalated and adsorbed Li atoms progressively diminishes due to the Coulomb repulsion penalty, which is partially screened by the metal substrate in the intercalated subsystem. This gives rise to a saturation of the respective electric potential and the band structure shift, and elaborates on the pathways and limitations of chemical functionalization of epitaxial hBN systems with charge donating species.