Tailoring the Superatomic Characteristics and Optical Behavior of Metal-Free Boron Clusters via Ligand Engineering.

It is of great importance to understand how the number and type of ligands influence the properties of clusters through ligand engineering, as this knowledge is crucial for the rational design and optimization of functional materials. Herein, the geometrical structures, binding energies, and electronic properties of nonmetallic B (n = 20 and 40) clusters with CO, PEt, F, NO, and CN ligands are systematically explored based on density functional theory (DFT) calculations. Our findings demonstrate that the CO ligand acts as an electron donor when attached to these two boron clusters, in contrast to their role as electron acceptors in interactions with metal oxide and metal chalcogenide clusters. This emphasizes the necessity of considering the intrinsic properties of the host cluster when modifying with ligands. Moreover, it was observed that substituting PEt with F, NO, or CN converted the B cluster from an electron acceptor to an electron donor, thereby demonstrating the versatility in tuning the redox characteristics of boron clusters by selecting appropriate ligands. Intriguingly, the attachment of the PEt, F, NO, and CN ligands to B can significantly modulate the electronic properties of B to realize the formation of metal-free superalkali (B(PEt), n = 3-5) and superhalogen (BF, BNO and BCN) clusters. Furthermore, the structure, stability, and optical absorption of the charge transfer complex B(PEt)BF were analyzed. This complex has been identified as an efficient material for harvesting visible light. Our findings provide insights into the effects of ligand variations on boron cluster functionalities, offering a new perspective for the design of advanced materials with tailored cluster properties through ligand engineering.