RESUMEN
We report on the fabrication of solution-processed organic phototransistors (OPTs) based on perylenebis(dicarboximide)s (PDIs). We found that the responsivity to the photoillumination depends on the transistor's channel length and that it can be tuned by varying the device geometry. The analysis of different morphologies of the active semiconducting layer revealed that single PDI fibers exhibit the higher photoresponse when compared to more poorly organized films. The highest responsivity value of 4.08 ± 1.65 × 10(5) A/W was achieved on a multifiber-based OPT. These findings represent a step forward toward the use of organic based phototransistors as photosensors.
Asunto(s)
Perileno/química , Transistores Electrónicos , Luz , Estructura Molecular , Perileno/análogos & derivados , Procesos FototróficosRESUMEN
We report on a combined scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), and density functional theory (DFT) study on the surface-assisted assembly of the hexaiodo-substituted macrocycle cyclohexa-m-phenylene (CHP) toward covalently bonded polyphenylene networks on Cu(111), Au(111), and Ag(111) surfaces. STM and XPS indicate room temperature dehalogenation of CHP on either surface, leading to surface-stabilized CHP radicals (CHPRs) and coadsorbed iodine. Subsequent covalent intermolecular bond formation between CHPRs is thermally activated and is found to proceed at different temperatures on the three coinage metals. The resulting polyphenylene networks differ significantly in morphology on the three substrates: On Cu, the networks are dominated by "open" branched structures, on the Au surface a mixture of branched and small domains of compact network clusters are observed, and highly ordered and dense polyphenylene networks form on the Ag surface. Ab initio DFT calculations allow one to elucidate the diffusion and coupling mechanisms of CHPRs on the Cu(111) and Ag(111) surfaces. On Cu, the energy barrier for diffusion is significantly higher than the one for covalent intermolecular bond formation, whereas on Ag the reverse relation holds. By using a Monte Carlo simulation, we show that different balances between diffusion and intermolecular coupling determine the observed branched and compact polyphenylene networks on the Cu and Ag surface, respectively, demonstrating that the choice of the substrate plays a crucial role in the formation of two-dimensional polymers.
RESUMEN
The development of a detailed theoretical understanding of surface-supported supramolecular networks is important for designing novel organic nanodevices. By comparing with STM experiments, we show that van der Waals corrections to density functional theory (DFT) in the generalized gradient approximation (GGA) are mandatory to correctly reproduce the electronic and geometric structure of a prototypical system of this kind, the self-assembled hydrogen bonded network formed by 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) and 4,4''-diamino-p-terphenyl (DATP) deposited on Au(111). Our results reproduce both the network structure and its higher stability with respect to homomolecular networks. By successful comparison with the experiments, we demonstrate that dispersive interactions must be taken into account when rationally designing organic semiconductor nanostructures on a metallic substrate. DFT-GGA alone would fail in predicting geometric and electronic properties for weakly bounded large organic adsorbates on coinage metal surfaces.
RESUMEN
Interest in thermal and chemical stability of surface-supported organic networks has stimulated recent attempts to covalently interlink adsorbed molecular species into extended nanostructures. We show, using low-temperature scanning tunneling microscopy, that imidization of anhydrides and amines adsorbed on Au(111) can be thermally initiated under controlled ultrahigh vacuum conditions. Using two types of amine-functionalized polyphenyl molecules together with the organic semiconductor PTCDA, monolayer thick linear polymeric strands and a porous polymeric network with nanoscale dimensions are obtained.
Asunto(s)
Oro/química , Membranas Artificiales , Resinas Sintéticas/química , Aminas/síntesis química , Aminas/química , Anhídridos/química , Enlace de Hidrógeno , Microscopía de Túnel de Rastreo/métodos , Estructura Molecular , Tamaño de la Partícula , Perileno/análogos & derivados , Perileno/química , Porosidad , Propiedades de Superficie , Temperatura , Triazinas/químicaRESUMEN
We show, using scanning tunneling microscopy, how a coupling motif based on self-complementary helical aromatic units is able to drive the formation of a chiral porous supramolecular network and chains based on lateral aromatic interactions in two dimensions.
RESUMEN
A novel semiconducting benzothiadiazole (BTZ)-thiophene (T) co-oligomer having an unprecedented BTZ-T alternated motif has been synthesized and self-assembled into micrometer sized fibers by simple solution processing. The electrical properties of these low-dimensional architectures have been characterized by integrating them in an organic field-effect transistor.
RESUMEN
We report on the formation of photoconductive self-assembled fibres by solvent induced precipitation of a HBC-PMI donor-acceptor dyad. Kelvin Probe Force Microscopy revealed that upon illumination with white light the surface potential of the fibres shifted to negative values due to a build-up of negative charge. When integrated in a field-effect transistor (FET) configuration, the devices can be turned 'on' much more efficiently using light than conventional bias triggered field-effect, suggesting that these structures could be used for the fabrication of light sensing devices. Such a double gating represents an important step towards bi-functional organic FETs, in which the current through the junction can be modulated both optically (by photoexcitation) and electrically (by gate control).
RESUMEN
Atomically thin sheets of sp(2)-hybridized carbon--graphene--have enormous potential for applications in future electronic devices. Particularly promising are nanostructured (sub)units of graphene, the electronic properties of which can be tuned by changing the spatial extent or the specific edge termination of the carbon network. Processability and precise tailoring of graphene-derived structures are, however, still major obstacles in developing applications; both bottom-up and top-down routes are presently under investigation in attempts to overcome this limitation. Here, we propose a surface chemical route that allows for the atomically precise fabrication of tailored nanographenes from polyphenylene precursors. The cyclodehydrogenation of a prototypical polyphenylene on Cu(111) is studied using scanning tunnelling microscopy and density functional theory. We find that the thermally induced cyclodehydrogenation proceeds via several intermediate steps, two of which can be stabilized on the surface, yielding unprecedented insight into a dehydrogenative intramolecular aryl-aryl coupling reaction.
Asunto(s)
Grafito/síntesis química , Electrónica , Electrones , Hidrogenación , Nanoestructuras , Polímeros/química , Propiedades de SuperficieRESUMEN
The reactions of 3,4,9,10-perylenetetracarboxylic dianhydride with 4,4'-diamino-p-terphenyl and with 2,4,6-tris(4-aminophenyl)-1,3,5-triazine on an Au(111) surface have been followed by low-temperature UHV-STM in the range of 300 to 700 K at coverages of up to one monolayer. Well-ordered, H-bonded structures are observed even after annealing at temperatures up to 470 K, while above 550 K reaction is initiated with evidence of amic acid intermediates. At higher temperatures, full imidisation leads to a covalently linked, surface polyimide networks. There is evidence of gold reconstruction playing a role in the early stages of imidisation and signs of limited order in the final polyimide. With the diamine as precursor, 1D-interconnectivity results, while with the triamine as partner, full 2D-connectivity is possible. In contrast to the situation in the bulk, the intermediate amic acid seems to be less stable and iso-imides are common in the final networks, as witnessed by the conformation of the product and the prevalence of triangular features in the case of the polyimide formed from the triamine precursor.
Asunto(s)
Anhídridos/síntesis química , Oro/química , Imidas/síntesis química , Perileno/análogos & derivados , Polímeros/síntesis química , Triazinas/síntesis química , Isomerismo , Microscopía de Túnel de Rastreo/métodos , Perileno/síntesis química , Propiedades de Superficie , Temperatura , Compuestos de Terfenilo/síntesis química , VacioRESUMEN
The quest for miniaturization of organic nanostructures is fueled by their possible applications in future nanoscale electronic devices. Here we show how a range of nanostructures of reduced dimensionality of the organic semiconductor PTCDA can be realized on Au(111) by intermixing the latter with hydrogen bonding spacer molecules. The purpose of the spacers is to separate nanounits of pure PTCDA, using hydrogen bonds between the anhydride end of PTCDA and amine groups of the spacers. A highly regular array of potential quantum dots can be realized by this approach.
Asunto(s)
Cristalización/métodos , Electroquímica/métodos , Nanoestructuras/química , Nanoestructuras/ultraestructura , Nanotecnología/métodos , Compuestos Orgánicos/química , Semiconductores , Sustancias Macromoleculares/química , Ensayo de Materiales , Conformación Molecular , Tamaño de la Partícula , Propiedades de SuperficieRESUMEN
We demonstrate, by surface-assisted coupling of specifically designed molecular building blocks, the fabrication of regular two-dimensional polyphenylene networks with single-atom wide pores and sub-nanometer periodicity.