Unraveling the Band Structure and Orbital Character of a π‐Conjugated 2D Graphdiyne‐Based Organometallic Network

Graphdiyne-based carbon systems generate intriguing layered sp–sp2 organometallic lattices, characterized by flexible acetylenic groups connecting planar carbon units through metal centers. At their thinnest limit, they can result in 2D organometallic networks exhibiting unique quantum properties and even confining the surface states of the substrate, which is of great importance for fundamental studies. In this work, the on-surface synthesis of a highly crystalline 2D organometallic network grown on Ag(111) is presented. The electronic structure of this mixed honeycomb-kagome arrangement – investigated by angle-resolved photoemission spectroscopy and scanning tunneling spectroscopy – reveals a strong electronic conjugation within the network, leading to the formation of two intense electronic band-manifolds. In comparison to theoretical density functional theory calculations, it is observed that these bands exhibit a well-defined orbital character that can be associated with distinct regions of the sp–sp2 monomers. Moreover, it is found that the halogen by-products resulting from the network formation locally affect the pore-confined states, causing a significant energy shift. This work contributes to the understanding of the growth and electronic structure of graphdiyne-like 2D networks, providing insights into the development of novel carbon materials beyond graphene with tailored properties.