On-Surface Synthesis of a Pure and Long-Range-Ordered Titanium(IV)-Porphyrin Contact Layer on Titanium Dioxide
Giacomo Lovat, Daniel Forrer, Mikel Abadia, Marcos Dominguez, Maurizio, Casarin, Celia Rogero, Andrea Vittadini, Luca Floreano

TL;DR
This study demonstrates the controlled synthesis and characterization of a pure, long-range-ordered titanium(IV)-porphyrin monolayer on TiO2(110), revealing its stability and potential for photovoltaic applications.
Contribution
It introduces a method to create a stable, ordered titanium(IV)-porphyrin monolayer on TiO2 and analyzes its self-metalation process and thermal stability.
Findings
Monolayer forms a commensurate phase at saturation coverage.
Self-metalation occurs at 100°C, complete by 200°C.
The monolayer remains stable up to 300°C.
Abstract
We show the possibility of tailoring the molecular arrangement, as well as the chemical and structural modifications, of porphyrins at the monolayer saturation coverage on TiO2(110) by Synchrotron photoemission, electron diffraction, STM topography and DFT calculations. Free-base tetra-phenyl-porphyrins (2H-TPP) adsorb on the oxygen rows, where they can spontaneously capture two additional hydrogen atoms at their iminic nitrogens (4H-TPP). Both 2H-TPP and 4H-TPP molecules aggregate into a commensurate phase at the saturation coverage of one monolayer. Upon sample heating, a self-metalation reaction sets in at 100C, yielding full metalation of the saturated monolayer at ~200C. The Ti atoms are extracted from the substrate and, by simultaneous dehydrogenation of the pyrrolic nitrogen atoms, incorporated into the porphyrin macrocycle, where they remain coordinated to two oxygen atoms…
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