Self-metalation of monophosphonic acid tetraphenylporphyrin on TiO2(110)-(1×1)

Fernández CC, Wechsler D, Lytken O, Steinrück HP, Williams FJ (2022)


Publication Type: Journal article

Publication year: 2022

Journal

Book Volume: 717

Article Number: 122005

DOI: 10.1016/j.susc.2021.122005

Abstract

Fundamental studies on the interaction of porphyrin molecules with oxide surfaces are important due to the relevance of these systems in emerging technologies. In this work, we used X-ray photoelectron spectroscopy (XPS) to study the interaction of solution-deposited monophosphonic acid tetraphenylporphyrin (MPTPP) molecules with well-defined rutile TiO2(110)-(1×1) surfaces as a function of coverage and temperature. We found that molecules adsorb mainly in their free-base form with some molecules protonating on the surface at room temperature. In agreement with the behavior of carboxylic acid functionalized porphyrin molecules, raising the temperature results in porphyrin self-metalation and the temperature onset for self-metalation shifts to higher values as the coverage is increased. Furthermore, we found that self-metalation is accompanied by surface reduction, and we propose a mechanism based on the formation of oxygen vacancies driven by water desorption. Our findings contribute towards the understanding of the rich surface chemistry that porphyrin molecules have on oxide surfaces.

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How to cite

APA:

Fernández, C.C., Wechsler, D., Lytken, O., Steinrück, H.-P., & Williams, F.J. (2022). Self-metalation of monophosphonic acid tetraphenylporphyrin on TiO2(110)-(1×1). Surface Science, 717. https://dx.doi.org/10.1016/j.susc.2021.122005

MLA:

Fernández, Cynthia C., et al. "Self-metalation of monophosphonic acid tetraphenylporphyrin on TiO2(110)-(1×1)." Surface Science 717 (2022).

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