Clarifying the Adsorption of Triphenylamine on Au(111): Filling the HOMO-LUMO Gap

In this article, we analyze the electronic structure modifications of triphenylamine (TPA), a well-known electron donor molecule widely used in photovoltaics and optoelectronics, upon deposition on Au(111) at a monolayer coverage. A detailed study was carried out by synchrotron radiation-based photoelectron spectroscopy, near-edge X-ray absorption fine structure (NEXAFS) spectroscopy, scanning tunneling microscopy (STM), and ab initio calculations. We detect a new feature in the pre-edge energy region of the N K-edge NEXAFS spectrum that extends over 3 eV, which we assign to transitions involving new electronic states. According to our calculations, upon adsorption, a number of new unoccupied electronic states fill the energy region between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of the free TPA molecule and give rise to the new feature the pre-edge region of the NEXAFS spectrum. This finding highlights the occurrence of a considerable modification of the electronic structure of TPA. The appearance of new states in the HOMO-LUMO gap of TPA when adsorbed on Au(111) has crucial implications for the design of molecular nanoelectronic devices based on similar donor systems.

Automated summary

In this article, the electronic structure modifications of triphenylamine (TPA) upon adsorption on Au(111) at a monolayer coverage are analyzed using various experimental and computational methods. The appearance of new unoccupied electronic states between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of free TPA indicates a considerable modification of its electronic structure. This finding has crucial implications for the design of molecular nanoelectronic devices based on similar donor systems.