Understanding the Interaction of the Porphyrin Macrocycle to Reactive Metal Substrates: Structure, Bonding, and Adatom Capture

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• 作者：Matthew S. Dyer ; Abel Robin ; Sam Haq ; Rasmita Raval ; Mats Persson ; Jiří Klimeš
• 刊名：ACS Nano
• 出版年：2011
• 出版时间：March 22, 2011
• 年：2011
• 卷：5
• 期：3
• 页码：1831-1838
• 全文大小：939K
• 年卷期：0
• ISSN：1936-086X

文摘

We investigate the adsorption and conformation of free-base porphines on Cu(110) using STM, reflection absorption infrared spectroscopy, and periodic DFT calculations in order to understand how the central polypyrrole macrocycle, common to all porphyrins, interacts with a reactive metal surface. We find that the macrocycle forms a chemisorption bond with the surface, arising from electron donation into down-shifted and nearly degenerate unoccupied porphine π-orbitals accompanied with electron back-donation from molecular π-orbitals. Our calculations show that van der Waals interactions give rise to an overall increase in the adsorption energy but only minor changes in the adsorption geometry and electronic structure. In addition, we observe copper adatoms being weakly attracted to adsorbed porphines at specific molecular sites. These results provide important insights into porphyrin−surface interactions that, ultimately, will govern the design of robust surface-mounted molecular devices based on this important class of molecules.