On-Surface Synthesis of a Pure and Long-Range-Ordered Titanium(IV)-Porphyrin Contact Layer on Titanium Dioxide

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 underneath. Neither the adsorption geometry (on-bridge, atop the oxygen rows) nor the molecular arrangement change across the self-metalation transition up to 300C. On one side, the robustness of this saturation phase makes it a promising system for its implementation into applications for photocatalysis and photovoltaic devices. On the other side, the possible manifestation of metal exchange with the very reactive Ti atoms must be taken into account when designing porphyrin-sensitized solar cells since the critical temperature for the onset of self-metalation is very close to the normal operating temperature of photovoltaic devices.