Egger Larissa, Hollerer Michael, Kern Christian S, Herrmann Hannes, Hurdax Philipp, Haags Anja, Yang Xiaosheng, Gottwald Alexander, Richter Mathias, Soubatch Serguei, Tautz F Stefan, Koller Georg, Puschnig Peter, Ramsey Michael G, Sterrer Martin
Institute of Physics, NAWI Graz, University of Graz, Universitätsplatz 5, 8010, Graz, Austria.
Peter Grünberg Institute (PGI-3), Forschungszentrum Jülich, 52425, Jülich, Germany.
Angew Chem Int Ed Engl. 2021 Mar 1;60(10):5078-5082. doi: 10.1002/anie.202015187. Epub 2021 Jan 14.
Metalation and self-metalation reactions of porphyrins on oxide surfaces have recently gained interest. The mechanism of porphyrin self-metalation on oxides is, however, far from being understood. Herein, we show by a combination of results obtained with scanning tunneling microscopy, photoemission spectroscopy, and DFT computations, that the self-metalation of 2H-tetraphenylporphyrin on the surface of ultrathin MgO(001) films is promoted by charge transfer. By tuning the work function of the MgO(001)/Ag(001) substrate, we are able to control the charge and the metalation state of the porphyrin molecules on the surface.
卟啉在氧化物表面的金属化和自金属化反应近来备受关注。然而,卟啉在氧化物上的自金属化机理仍远未明晰。在此,我们通过扫描隧道显微镜、光电子能谱和密度泛函理论计算相结合的结果表明,电荷转移促进了2H-四苯基卟啉在超薄MgO(001)薄膜表面的自金属化。通过调节MgO(001)/Ag(001)衬底的功函数,我们能够控制表面卟啉分子的电荷和金属化状态。