α-Borophene Nanoribbons: Edge-Dependent Metallic and Magnetic Properties for Low-Dimensional Nanoelectronics

We present a comprehensive first-principles study of nanoribbons made from the α-borophene sheet. This study looks at how edge shape, ribbon width, and magnetic ordering affect their structural, electronic, and transport properties. Ribbons cut along armchair (ac) and zigzag (zz) directions with various edge designs-armchair (a), single (s), and double (d) chains-are all stable. The double chain "dd" edges have the highest binding energies and the lowest edge energies, which aligns with near-bulk coordination. Our analysis of electronic structure and ballistic transport shows strong metallic characteristics in almost all configurations. Only the narrowest "3-ad" ribbon shows a small energy gap that disappears as the width increases. Zigzag ribbons ("zz") display edge magnetism that depends on width, changing from non-magnetic to antiferromagnetic and finally to ferromagnetic states. Their spin-resolved transmission demonstrates clear spin filtering with polarization exceeding about 40%. Edge passivation affects these properties: hydrogen and fluorine reduce the "zz" edge magnetic moments and spin transport, while oxygen maintains finite magnetism. Near the Fermi level, many ribbons allow for multiple conducting channels. This feature supports low-resistance charge flow even for widths below 10 nm, while higher-energy transmission shows greater dependence on width. These findings position α-borophene nanoribbons as promising one-dimensional components for nanoelectronic connections and spintronic devices, combining high stability, adjustable edge magnetism, and strong metallic conduction.