Grafting, self-organization and reactivity of double-decker rare-earth phthalocyanine

Unveiling the interplay of semiconducting organic molecules with their environment, such as inorganic materials or atmospheric gas, is the first step to designing hybrid devices with tailored optical, electronic or magnetic properties. The present article focuses on a double-decker lutetium phthalocyanine known as an intrinsic semiconducting molecule, holding a Lu ion in its center, sandwiched between two phthalocyanine rings. Carrying out experimental investigations by means of electron spectroscopies, X-ray diffraction and scanning probe microscopies together with advanced ab initio computations, allows us to unveil how this molecule interacts with weakly or highly reactive surfaces. Our studies reveal that a molecule–surface interaction is evidenced when molecules are deposited on bare silicon or on gold surfaces together with a charge transferred from the substrate to the molecule, affecting to a higher extent the lower ring of the molecule. A new packing of the molecules on gold surfaces is proposed: an eclipse configuration in which molecules are flat and parallel to the surface, even for thick films of several hundreds of nanometers. Surprisingly, a robust tolerance of the double-decker phthalocyanine toward oxygen molecules is demonstrated, leading to weak chemisorption of oxygen below 100 K.

[1]  E. Llobet,et al.  A tungsten oxide–lutetium bisphthalocyanine n–p–n heterojunction: from nanomaterials to a new transducer for chemo-sensing , 2019, Journal of Materials Chemistry C.

[2]  R. Resel,et al.  New Quadratic Self-Assembly of Double-Decker Phthalocyanine on Gold(111) Surface: From Macroscopic to Microscopic Scale , 2018, The Journal of Physical Chemistry C.

[3]  N. Witkowski,et al.  High Tolerance of Double-Decker Phthalocyanine toward Molecular Oxygen , 2018, The Journal of Physical Chemistry C.

[4]  M. Mateos,et al.  Comprehensive Study of Poly(2,3,5,6-tetrafluoroaniline): From Electrosynthesis to Heterojunctions and Ammonia Sensing. , 2018, ACS applied materials & interfaces.

[5]  Junsheng Yu,et al.  Emission Spectral Stability Modification of Tandem Organic Light-Emitting Diodes through Controlling Charge-Carrier Migration and Outcoupling Efficiency at Intermediate/Emitting Unit Interface , 2018, ACS Omega.

[6]  P. Saalfrank,et al.  Control of Oxidation and Spin State in a Single-Molecule Junction. , 2018, ACS nano.

[7]  W. Wernsdorfer,et al.  Molecular spin qudits for quantum algorithms. , 2017, Chemical Society reviews.

[8]  N. Takagi,et al.  Single-molecule quantum dot as a Kondo simulator , 2017, Nature Communications.

[9]  C. Grazioli,et al.  When the Grafting of Double Decker Phthalocyanines on Si(100)-2 × 1 Partly Affects the Molecular Electronic Structure , 2016 .

[10]  M. Ivanovic,et al.  Electronic structure at transition metal phthalocyanine-transition metal oxide interfaces: Cobalt phthalocyanine on epitaxial MnO films. , 2015, The Journal of chemical physics.

[11]  Yaw-Wen Yang,et al.  A direct Fe-O coordination at the FePc/MoO(x) interface investigated by XPS and NEXAFS spectroscopies. , 2015, Physical chemistry chemical physics : PCCP.

[12]  M. Pourkashanian,et al.  DFT study of the oxygen reduction reaction on iron, cobalt and manganese macrocycle active sites , 2014 .

[13]  O. Schmidt,et al.  Determination of the Charge Transport Mechanisms in Ultrathin Copper Phthalocyanine Vertical Heterojunctions , 2014 .

[14]  C. Grazioli,et al.  Experimental and theoretical study of electronic structure of lutetium bi-phthalocyanine. , 2013, The Journal of chemical physics.

[15]  A. Verdini,et al.  Tuning the catalytic activity of Ag(110)-supported Fe phthalocyanine in the oxygen reduction reaction. , 2012, Nature materials.

[16]  M. Hietschold,et al.  Investigation of Ultrathin Layers of Bis(phthalocyaninato)lutetium(III) on Graphite , 2012, 1312.6509.

[17]  M. Knupfer,et al.  Initial growth of lutetium(III) bis-phthalocyanine on Ag(111) surface. , 2011, Journal of the American Chemical Society.

[18]  Chongwu Zhou,et al.  Continuous, highly flexible, and transparent graphene films by chemical vapor deposition for organic photovoltaics. , 2010, ACS nano.

[19]  Shuang Chen,et al.  Charge transport in stacking metal and metal‐free phthalocyanine iodides. Effects of packing, dopants, external electric field, central metals, core modification, and substitutions , 2009, J. Comput. Chem..

[20]  S. Sakaki,et al.  Direct observation of the energy gap in lutetium bisphthalocyanine thin films , 2009 .

[21]  M. Yamashita,et al.  Low-Temperature Scanning Tunneling Microscopy Investigation of Bis(phthalocyaninato)yttrium Growth on Au(111): From Individual Molecules to Two-Dimensional Domains , 2009 .

[22]  J. Saja,et al.  On the effect of ammonia and wet atmospheres on the conducting properties of different lutetium bisphthalocyanine thin films , 2008 .

[23]  H. Steinrück,et al.  NO-induced reversible switching of the electronic interaction between a porphyrin-coordinated cobalt ion and a silver surface. , 2007, Journal of the American Chemical Society.

[24]  S. Du,et al.  Epitaxial Growth of Iron Phthalocyanine at the Initial Stage on Au(111) Surface , 2007 .

[25]  O. Pluchery,et al.  RAS : An efficient probe to characterize Si(001)-(2 x 1) surfaces , 2006 .

[26]  Yi Luo,et al.  The electronic structure of iron phthalocyanine probed by photoelectron and x-ray absorption spectroscopies and density functional theory calculations. , 2006, The Journal of chemical physics.

[27]  M. Casu,et al.  Growth mode and molecular orientation of phthalocyanine molecules on metal single crystal substrates: A NEXAFS and XPS study , 2006 .

[28]  M. L. Rodriguez-Mendez,et al.  Sensors based on double-decker rare earth phthalocyanines. , 2005, Advances in colloid and interface science.

[29]  N. Witkowski,et al.  Optical response of clean and hydrogen-covered vicinal Si(001)2 × 1 surfaces , 2004 .

[30]  M. Takada,et al.  Low temperature scanning tunneling microscopy of phthalocyanine multilayers on Au(1 1 1) surfaces , 2004 .

[31]  B. Delley,et al.  Photoemission and theoretical investigations on NO2 doping of copper phthalocyanine thin films , 2004 .

[32]  K. W. Hipps,et al.  Scanning tunneling microscopy of 1, 2, and 3 layers of electroactive compounds. , 2003, Ultramicroscopy.

[33]  L. Lozzi,et al.  Interaction of naphthalocyanine with oxygen and with Si(111)7×7: an in-situ X-ray photoelectron spectroscopy study , 1999 .

[34]  K. W. Hipps,et al.  Scanning Tunneling Microscopy of Metal Phthalocyanines: d6 and d8 Cases , 1997 .

[35]  C. Maleysson,et al.  Gaseous oxidation and compensating reduction of lutetium bis-phthalocyanine and lutetium phthalo-naphthalocyanine films , 1995 .

[36]  Anders Nilsson,et al.  Physisorbed, chemisorbed and dissociated O2 on Pt(111) studied by different core level spectroscopy methods , 1995 .

[37]  B. I. Craig,et al.  Structures of small hydrocarbons adsorbed on Si(001) and Si terminated β-SiC(001) , 1992 .

[38]  P. Petit Magnetism of lutetium bisphthalocyanine , 1992 .

[39]  W. Göpel,et al.  Growth and electronic properties of ultrathin lutetium–diphthalocyanine films studied by electron spectroscopy , 1991 .

[40]  Ertl,et al.  Scanning tunneling microscopy observations on the reconstructed Au(111) surface: Atomic structure, long-range superstructure, rotational domains, and surface defects. , 1990, Physical review. B, Condensed matter.

[41]  J. Simon,et al.  Electrical properties of rare earth bisphthalocyanine and bisnaphthalocyanine complexes , 1990 .

[42]  Jacques Simon,et al.  Field-effect transistors based on intrinsic molecular semiconductors , 1990 .

[43]  J. Brédas,et al.  Electronic structure of phthalocyanines : Theoretical investigation of the optical properties of phthalocyanine monomers, dimers, and crystals , 1990 .

[44]  J. Simon,et al.  Near infrared absorption spectra of lanthanide bis-phthalocyanines , 1987 .

[45]  J. Fischer,et al.  Synthesis, structure, and spectroscopic and magnetic properties of lutetium(III) phthalocyanine derivatives: LuPc2.CH2Cl2 and [LuPc(OAc)(H2O)2].H2O.2CH3OH , 1985 .