• Media type: E-Article
  • Title: Properties of Porphyrin- and Phthalocyanin-Monolayers at Metal-Electrolyte Interfaces
  • Contributor: Wandelt, Klaus R.
  • imprint: The Electrochemical Society, 2014
  • Published in: ECS Meeting Abstracts
  • Language: Not determined
  • DOI: 10.1149/ma2014-01/35/1336
  • ISSN: 2151-2043
  • Keywords: General Medicine
  • Origination:
  • Footnote:
  • Description: <jats:p>The adsorption of organic layers on solid surfaces is a promising route to produce surfaces of designed functionality. In this lecture an overview will be given about state-of-the-art investigations of the structural and chemical properties of porphyrin- and phthalocyanin-monolayers adsorbed electrochemically in the form of their molecular cations on anion-modified single-crystal metal electrode surfaces as a function of the nature of the metal (copper, gold), the kind of the pread-sorbed anions (chloride, iodide, sulfate), the symmetry of the surface ((100), (111)), and the electro-chemical potential, using besides classical electrochemical methods Electrochemical Scanning Tunneling Microscopy (EC-STM), and ex-situ Synchrotron X-Ray Photoelectron Spectroscopy (S-XPS). Particular attention will be paid to the self-assembly- vs. template-effects in the structure formation process, to structural phase transitions as a function of electrochemical potential, as well as to the chemical reactivity of selected porphyrins and phthalocyanins. Fig. 1b shows 5,10,15,20-Tetrakis(4-trimethylammonio-phenyl)porphyrin molecules adsorbed on a Cl-precovered Cu(111) surface. Instead of the <jats:italic>threefold</jats:italic> symmetry of the substrate (Fig. 1a) the molecules self-assemble into a <jats:italic>square</jats:italic> molecular superlattice (Fig.1b) [1]. Fig.2 shows coexisting square and hexagonal structure domains of 3-pyridyloxy-appended phthalocyanine on iodide precovered Cu(100) [2]. </jats:p> <jats:p>References</jats:p> <jats:p>[1] Thanh Hai Phan,<jats:sup> </jats:sup>Tomasz Kosmala, and Klaus Wandelt, in preparation</jats:p> <jats:p>[2] Thanh Hai Phan,<jats:sup> </jats:sup>Stephan Breuer, Uwe Hahn, DucThanh Pham, Tomás Torres,<jats:sup> </jats:sup>and Klaus Wandelt, </jats:p> <jats:p> J.Phys.Chem.C, submitted</jats:p> <jats:p> <jats:bold>Fig. 1</jats:bold> 5,10,15,20-Tetrakis(4-trimethylammonio-phenyl)porphyrin <jats:bold>Fig. 2</jats:bold> 3-pyridyloxy-phthalocyanine</jats:p> <jats:p> on Cl-precovered Cu(111) [1] on iodide precovered Cu(100) [2]. </jats:p> <jats:p> </jats:p> <jats:p> <jats:inline-formula> <jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="1336fig1.jpeg" xlink:type="simple" /> </jats:inline-formula> </jats:p>
  • Access State: Open Access