From a free electron gas to confined states: A mixed island of PTCDA and copper phthalocyanine on Ag(111)

• Alfred J. Weymouth,
• Emily Roche and
• Franz J. Giessibl

Beilstein J. Nanotechnol. 2022, 13, 1572–1577, doi:10.3762/bjnano.13.131

• gas (2DEG). We investigated mixed islands of PTCDA and copper phthalocyanine (CuPc) to study the change in the electronic state with the addition of an electron donor. We no longer observe a 2DEG state and instead identify states at 0.46 and 0.79 V. While one state appears in dI/dV images as an array

• of one-dimensional quantum wells, our analysis shows that this state does not act as a free electron gas and that the features are instead localized above individual PTCDA molecules. Keywords: AFM; copper phthalocyanine; dI/dV; PTCDA; STM; Introduction Organic semiconductor devices typically

• Information File 1. A natural complement to PTCDA is copper phthalocyanine (CuPc) for several reasons: First, CuPc and PTCDA together can form an organic light-emitting diode with PTCDA as the acceptor [14]. Second, CuPc [15] and PTCDA both lie flat on metal surfaces at submonolayer coverage, enabling high

Revealing local structural properties of an atomically thin MoSe₂ surface using optical microscopy

• Lin Pan,
• Peng Miao,
• Anke Horneber,
• Alfred J. Meixner,
• Pierre-Michel Adam and
• Dai Zhang

Beilstein J. Nanotechnol. 2022, 13, 572–581, doi:10.3762/bjnano.13.49

• molybdenum diselenide (MoSe2) flake as surface-enhanced Raman spectroscopy (SERS) platform, we demonstrate the dependency of the Raman enhancement on laser beam polarization and local structure using copper phthalocyanine (CuPc) as probe. Second harmonic generation (SHG) and photoluminescence spectroscopy

• dichalcogenide. Keywords: copper phthalocyanine; local structure; molybdenum diselenide; optical spectroscopy; surface-enhanced Raman spectroscopy; Introduction Two-dimensional (2D) materials have garnered interest for the next generation of optoelectronic and electrochemical devices, mainly owing to their

The influence of an interfacial hBN layer on the fluorescence of an organic molecule

• Christine Brülke,
• Oliver Bauer and
• Moritz M. Sokolowski

Beilstein J. Nanotechnol. 2020, 11, 1663–1684, doi:10.3762/bjnano.11.149

• , causing an enhancement by a factor of not more than 102–103 [46]. Recently, hBN has gained interest as a SERS substrate [49]. In a comparative study on 2DMs on SiO2 it was shown that hBN had an enhancement effect on the Raman modes of adsorbed copper phthalocyanine molecules [50]. The effect was explained

Growth of a self-assembled monolayer decoupled from the substrate: nucleation on-command using buffer layers

• Robby Reynaerts,
• Kunal S. Mali and
• Steven De Feyter

Beilstein J. Nanotechnol. 2020, 11, 1291–1302, doi:10.3762/bjnano.11.113

• symmetry of the underlying alkane layer [27]. Buffer layers of tetratriacontane [25] and tridecylamine [31] were used to template the self-assembly of copper phthalocyanine. Room temperature STM measurements revealed that the adsorption as well as the diffusion of clusters of CuPc molecules was strongly

Adsorption of iron tetraphenylporphyrin on (111) surfaces of coinage metals: a density functional theory study

• Hao Tang,
• Nathalie Tarrat,
• Véronique Langlais and
• Yongfeng Wang

Beilstein J. Nanotechnol. 2017, 8, 2484–2491, doi:10.3762/bjnano.8.248

• agreement with the experimental one (5.35 eV) [23]. After the adsorption, the work function was reduced to 4.19 eV. This value is consistent with that measured on copper phthalocyanine (CuPc) adsorbed on Au(111) [24]. Adsorption on Ag(111) and Cu(111) surfaces It is well known for large organic molecules

Electronic structure, transport, and collective effects in molecular layered systems

• Torsten Hahn,
• Tim Ludwig,
• Carsten Timm and
• Jens Kortus

Beilstein J. Nanotechnol. 2017, 8, 2094–2105, doi:10.3762/bjnano.8.209

• heterostructures for organic device applications is exemplified by the targeted engineering of the electronic properties of phthalocyanine-based systems. The transport properties of two different phthalocyanine systems, a pure copper phthalocyanine (CoPc) and a flourinated copper phthalocyanine–manganese

• similar fluorinated copper phthalocyanine (F16CoPc), has demonstrated the occurrence of hybridization [11]. It was proved that a local charge transfer which affects only the transition-metal centers changes the charge state of the transition metal and is directly related to a change of its magnetic moment

Energy-level alignment at interfaces between manganese phthalocyanine and C₆₀

• Daniel Waas,
• Florian Rückerl,
• Martin Knupfer and
• Bernd Büchner

Beilstein J. Nanotechnol. 2017, 8, 927–932, doi:10.3762/bjnano.8.94

• phthalocyanine-based (model) devices have been realized [28][29][30][31][32][33]. In particular, organic photovoltaic cells containing, e.g., copper phthalocyanine (CuPc) can be found rather frequently in the literature [28][30][34][35][36]. There, the charge separation at interfaces between the phthalocyanine

• of more than 1 eV at the interface, while the energy positions of the LUMOs are much closer. These values are significantly different from those found for the interface between copper phthalocyanine (CuPc) and C60, where the HOMO offset was reported to be about 0.9 eV [51], while the LUMO offset can

Ordering of Zn-centered porphyrin and phthalocyanine on TiO₂(011): STM studies

• Piotr Olszowski,
• Lukasz Zajac,
• Szymon Godlewski,
• Bartosz Such,
• Rémy Pawlak,
• Antoine Hinaut,
• Res Jöhr,
• Thilo Glatzel,
• Ernst Meyer and
• Marek Szymonski

Beilstein J. Nanotechnol. 2017, 8, 99–107, doi:10.3762/bjnano.8.11

• studied copper phthalocyanine (CuPc) and ZnTPP heterostructures. It was found that the central metal atom may play some role in ordering and growth of phthalocyanine/ZnTPP heterostructures, causing differences in stability of upright standing ZnPc versus CuPc molecular chains at given thermal annealing

• have shown that copper phthalocyanine (CuPc) molecules deposited on rutile (011) could form ordered planar nanostructures up to a complete monolayer coverage. At higher deposition, this wetting layer of planar molecules became covered with 2-dimensional (2D) molecular islands which could be stabilized

Layered composites of PEDOT/PSS/nanoparticles and PEDOT/PSS/phthalocyanines as electron mediators for sensors and biosensors

• Celia García-Hernández,
• Cristina García-Cabezón,
• Fernando Martín-Pedrosa,
• José Antonio De Saja and
• María Luz Rodríguez-Méndez

Beilstein J. Nanotechnol. 2016, 7, 1948–1959, doi:10.3762/bjnano.7.186

• electrodes chemically modified with PEDOT/PSS towards catechol and hydroquinone sensing have been successfully improved by combining layers of PEDOT/PSS with layers of a secondary electrocatalytic material such as gold nanoparticles (PEDOT/PSS/AuNPs), copper phthalocyanine (PEDOT/PSS/CuPc) or lutetium

• EMs, three different materials with different characteristics and electrocatalytic activity towards phenols were tested, including gold nanoparticles (AuNPs), a copper phthalocyanine (CuPc) (a p-type semiconductor) and a lutetium bisphthalocyanine (LuPc2) (a sandwich-type derivative with free radical

Scanning probe microscopy studies on the adsorption of selected molecular dyes on titania

• Jakub S. Prauzner-Bechcicki,
• Lukasz Zajac,
• Piotr Olszowski,
• Res Jöhr,
• Antoine Hinaut,
• Thilo Glatzel,
• Bartosz Such,
• Ernst Meyer and
• Marek Szymonski

Beilstein J. Nanotechnol. 2016, 7, 1642–1653, doi:10.3762/bjnano.7.156

• [33][43][44][45][46][47] and to investigate the heteromolecular systems in which phthalocyanine molecules formed a second layer [48][49]. Copper phthalocyanine (CuPc) appears to be the most extensively studied Pc derivative on titania surfaces [27][33][43][46]. Other accounts refer to CoPc/TiO2(110

Effects of spin–orbit coupling and many-body correlations in STM transport through copper phthalocyanine

• Benjamin Siegert,
• Andrea Donarini and
• Milena Grifoni

Beilstein J. Nanotechnol. 2015, 6, 2452–2462, doi:10.3762/bjnano.6.254

• of metallorganic compounds, such as the widely studied metal phthalocyanines [7][8], exhibit sizeable magnetic anisotropy induced by the interplay of electronic correlations and SOI. Indeed, in an X-ray magnetic circular dichroism (XMCD) analysis copper phthalocyanine (CuPc) was found to exhibit

• splitting of former degenerate levels and a magnetic anisotropy, which can be captured by an effective low-energy spin Hamiltonian. We show that scanning tunneling microscopy-based magnetoconductance measurements can yield clear signatures of both these SOI-induced effects. Keywords: anisotropy; copper

• phthalocyanine; magnetotransport; spin–orbit interaction; scanning tunneling microscopy (STM); Introduction Spin–orbit interaction (SOI) can play a major role in molecular spintronics. For example, in combination with the configuration of the non-magnetic component (organic ligand), it is known to be essential

Vibration-mediated Kondo transport in molecular junctions: conductance evolution during mechanical stretching

• David Rakhmilevitch and
• Oren Tal

Beilstein J. Nanotechnol. 2015, 6, 2417–2422, doi:10.3762/bjnano.6.249

• in a molecular junction. Recently, vibration-mediated Kondo transport was demonstrated in junctions consisting of a copper–phthalocyanine (CuPc; Figure 1b) molecule suspended between silver (Ag) electrodes [23]. In the current work we use similar junctions realized in a break junction setup, to

• ) Differential conductance vs applied bias voltage (dI/dV vs V) measured for a silver/copper–phthalocyanine (Ag/CuPc) molecular junction. The spectrum exhibits a zero-bias Kondo peak accompanied by vibration-mediated Kondo side peaks [23]. Inset: A vibration-induced differential conductance step occurring in the

Localized surface plasmon resonances in nanostructures to enhance nonlinear vibrational spectroscopies: towards an astonishing molecular sensitivity

• Dan Lis and
• Francesca Cecchet

Beilstein J. Nanotechnol. 2014, 5, 2275–2292, doi:10.3762/bjnano.5.237

• enhancement of the non-resonant SFG intensity from the metallic surface itself was mentioned to be greater than 104. Later in 1999, the authors demonstrated the feasibility to use a similar plasmonic substrate to amplify the resonant SFG signals of copper phthalocyanine and fullerene films adsorbed onto the

Pyrite nanoparticles as a Fenton-like reagent for in situ remediation of organic pollutants

• Carolina Gil-Lozano,
• Elisabeth Losa-Adams,
• Alfonso F.-Dávila and
• Luis Gago-Duport

Beilstein J. Nanotechnol. 2014, 5, 855–864, doi:10.3762/bjnano.5.97

• The Fenton reaction is the most widely used advanced oxidation process (AOP) for wastewater treatment. This study reports on the use of pyrite nanoparticles and microparticles as Fenton reagents for the oxidative degradation of copper phthalocyanine (CuPc) as a representative contaminant. Upon

• alternative to conventional Fenton procedures for use in wastewater treatment, avoiding the potential risks caused by the release of heavy metals upon dissolution of natural pyrites. Keywords: copper phthalocyanine; Fenton-like reagent; hydrogen peroxide; nanoparticles; pyrite; Introduction There has been

• remains poorly studied and, to the best of our knowledge, has never been used to remove dyes from textile wastewater. In this work, we compared synthetic pyrite nanoparticles to naturally derived pyrite microparticles for their efficiency in the oxidative degradation of copper phthalocyanine (CuPc), a