The true corrugation of a h-BN nanomesh layer

TL;DR

This study accurately measures the true atomic corrugation and bonding distances of a hexagonal boron nitride nanomesh on rhodium using photoelectron diffraction, resolving previous discrepancies from other methods.

Contribution

It introduces a high-precision, core-sensitive photoelectron diffraction technique to determine the nanomesh's structure, providing quantitative data on corrugation and atomic buckling.

Findings

Peak-to-peak corrugation amplitude of 0.80 Å

Bonding distance to substrate of 2.20 Å

Boron and nitrogen buckling of 0.07 Å

Abstract

Hexagonal boron nitride (h-BN) nanomesh, a two-dimensional insulating monolayer, grown on the (111) surface of rhodium exhibits an intriguing hexagonal corrugation pattern with a lattice constant of 3.2 nm. Despite numerous experimental and theoretical studies no quantitative agreement has been found on some details of the adsorption geometry such as the corrugation amplitude. The issue highlights the differences in chemical and electronic environment in the strongly bound pore regions and the weakly bound wire regions of the corrugated structure. For reliable results it is important to probe the structure with a method that is intrinsically sensitive to the position of the atomic cores rather than the electron density of states. In this work, we determine the corrugation of h-BN nanomesh from angle- and energy-resolved photoelectron diffraction measurements with chemical state resolution. By combining the results from angle and energy scans and comparing them to multiple-scattering simulations true adsorbate-substrate distance can be measured with high precision, avoiding pitfalls of apparent topography observed in scanning probe techniques. Our experimental results give accurate values for the peak to peak corrugation amplitude (0.80 A), the bonding distance to the substrate (2.20 A) and the buckling of the boron and nitrogen atoms in the strongly bound pore regions (0.07 A). The results are important for the development of theoretical methods involving the quantitative description of van der Waals systems like it requires the understanding of the physics of two-dimensional sp2 layers.