Formation of Supernarrow Borophene Nanoribbons

Borophenes have sparked considerable interest owing to their fascinating physical characteristics and diverse polymorphism. However, borophene nanoribbons (BNRs) with widths less than 2 nm have not been achieved. Herein, we report the experimental realization of supernarrow BNRs. Combining scanning tunneling microscopy imaging with density functional theory modeling and ab initio molecular dynamics simulations, we demonstrate that, under the applied growth conditions, boron atoms can penetrate the outermost layer of Au(111) and form BNRs composed of a pair of zigzag (2,2) boron rows. The BNRs have a width self-contained to similar to 1 nm and dipoles at the edges to keep them separated. They are embedded in the outermost Au layer and shielded on top by the evacuated Au atoms, free of the need for post-passivation. Scanning tunneling spectroscopy reveals distinct edge states, primarily attributed to the localized spin at the BNRs' zigzag edges. This work adds a new member to the boron material family and introduces a new physical feature to borophenes. The formation of supernarrow borophene nanoribbons has been experimentally realized. The ribbons have a uniform width of similar to 10 & Aring; and can be as long as 200 & Aring;. They are embedded in the outermost layer of Au(111) and shielded on top by evacuated Au atoms. Distinct edge states are revealed from the ribbons, which are primarily attributed to the localized spin at their zigzag edges. image