0000000000282937

AUTHOR

Pascal Ruffieux

showing 14 related works from this author

A Universal Length-Dependent Vibrational Mode in Graphene Nanoribbons

2019

Graphene nanoribbons (GNRs) have attracted considerable interest as their atomically tunable structure makes them promising candidates for future electronic devices. However, obtaining detailed information about the length of GNRs has been challenging and typically relies on low-temperature scanning tunneling microscopy. Such methods are ill-suited for practical device application and characterization. In contrast, Raman spectroscopy is a sensitive method for the characterization of GNRs, in particular for investigating their width and structure. Here, we report on a length-dependent, Raman active low-energy vibrational mode that is present in atomically precise, bottom-up synthesized armch…

530 Physicssubstrate transferSTMFOS: Physical sciencesGeneral Physics and Astronomy02 engineering and technology010402 general chemistryDFT01 natural sciencessymbols.namesakegraphene nanoribbons; Raman spectroscopy; length-dependent mode; STM; substrate transfer; vibrational modes; DFT540 ChemistryMesoscale and Nanoscale Physics (cond-mat.mes-hall)General Materials Sciencevibrational modesCondensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale Physicsbusiness.industryGeneral EngineeringMode (statistics)Materials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnology3. Good health0104 chemical sciencesMolecular vibrationRaman spectroscopysymbols570 Life sciences; biologyOptoelectronicslength-dependent mode0210 nano-technologybusinessRaman spectroscopyGraphene nanoribbonsgraphene nanoribbons
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On-Surface Synthesis of Unsaturated Carbon Nanostructures with Regularly Fused Pentagon–Heptagon Pairs

2020

Multiple fused pentagon-heptagon pairs are frequently found as defects at the grain boundaries of the hexagonal graphene lattice and are suggested to have a fundamental influence on graphene-related materials. However, the construction of sp2-carbon skeletons with multiple regularly fused pentagon-heptagon pairs is challenging. In this work, we found that the pentagon-heptagon skeleton of azulene was rearranged during the thermal reaction of an azulene-incorporated organometallic polymer on Au(111). The resulting sp2-carbon frameworks were characterized by high-resolution scanning probe microscopy techniques and feature novel polycyclic architectures composed of multiple regularly fused pen…

ChemistryGraphene530 PhysicsCommunicationAromaticityGeneral ChemistryElectronic structureAzulene010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceslaw.inventionchemistry.chemical_compoundScanning probe microscopyCrystallographyColloid and Surface ChemistrylawLattice (order)540 ChemistryGrain boundaryHeptagonPhysics::Chemical PhysicsJournal of the American Chemical Society
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Chemical Vapor Deposition Synthesis and Terahertz Photoconductivity of Low-Band-Gap N = 9 Armchair Graphene Nanoribbons.

2017

Recent advances in bottom-up synthesis of atomically defined graphene nanoribbons (GNRs) with various microstructures and properties have demonstrated their promise in electronic and optoelectronic devices. Here we synthesized N = 9 armchair graphene nanoribbons (9-AGNRs) with a low optical band gap of ∼1.0 eV and extended absorption into the infrared range by an efficient chemical vapor deposition process. Time-resolved terahertz spectroscopy was employed to characterize the photoconductivity in 9-AGNRs and revealed their high intrinsic charge-carrier mobility of approximately 350 cm2·V-1·s-1.

Band gapInfraredChemistryTerahertz radiationPhotoconductivityNanotechnology02 engineering and technologyGeneral ChemistryChemical vapor depositionPhysik (inkl. Astronomie)010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences7. Clean energyBiochemistryCatalysis0104 chemical sciencesTerahertz spectroscopy and technologyColloid and Surface Chemistry0210 nano-technologyAbsorption (electromagnetic radiation)Graphene nanoribbonsJournal of the American Chemical Society
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Large-Cavity Coronoids with Different Inner and Outer Edge Structures

2020

Coronoids, polycyclic aromatic hydrocarbons with geometrically defined cavities, are promising model structures of porous graphene. Here, we report the on-surface synthesis of C168 and C140 coronoids, referred to as [6]- and [5]coronoid, respectively, using 5,9-dibromo-14-phenylbenzo[m]tetraphene as the precursor. These coronoids entail large cavities (>1 nm) with inner zigzag edges, distinct from their outer armchair edges. While [6]coronoid is planar, [5]coronoid is not. Low-temperature scanning tunneling microscopy/spectroscopy and noncontact atomic force microscopy unveil structural and electronic properties in accordance with those obtained from density functional theory calculation…

Chemistry530 PhysicsPorous grapheneCommunicationAromaticityGeneral ChemistryEdge (geometry)010402 general chemistry01 natural sciencesBiochemistryMolecular physicsCatalysis0104 chemical scienceslaw.inventionColloid and Surface ChemistryPlanarZigzaglaw540 ChemistryDensity functional theoryScanning tunneling microscopeSpectroscopyJournal of the American Chemical Society
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Optimized substrates and measurement approaches for Raman spectroscopy of graphene nanoribbons

2019

The on-surface synthesis of graphene nanoribbons (GNRs) allows for the fabrication of atomically precise narrow GNRs. Despite their exceptional properties which can be tuned by ribbon width and edge structure, significant challenges remain for GNR processing and characterization. In this contribution, we use Raman spectroscopy to characterize different types of GNRs on their growth substrate and to track their quality upon substrate transfer. We present a Raman-optimized (RO) device substrate and an optimized mapping approach that allows for acquisition of high-resolution Raman spectra, achieving enhancement factors as high as 120 with respect to signals measured on standard SiO2/Si substra…

Fabrication530 PhysicsFOS: Physical sciences02 engineering and technologySubstrate (electronics)01 natural sciencessymbols.namesakeQuality (physics)540 Chemistry0103 physical sciencesRibbon010302 applied physicsCondensed Matter - Materials Sciencebusiness.industryMaterials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCharacterization (materials science)Molecular vibrationsymbols570 Life sciences; biologyOptoelectronics0210 nano-technologybusinessRaman spectroscopyGraphene nanoribbons
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On-Surface Synthesis of Antiaromatic and Open-Shell Indeno[2,1- b ]fluorene Polymers and Their Lateral Fusion into Porous Ribbons

2019

Polycyclic hydrocarbons have received great attention due to their potential role in organic electronics and, for open-shell systems with unpaired electron densities, in spintronics and da-ta storage. However, the intrinsic instability of polyradical hydrocarbons severely limits de-tailed investigations of their electronic structure. Here, we report the on-surface synthesis of conjugated polymers consisting of indeno[2,1-b]fluorene units, which are antiaromatic and open-shell biradicaloids. The observed reaction products, which also include a non-benzenoid porous ribbon arising from lateral fusion of unprotected indeno[2,1-b]fluorene chains, have been characterized via low temperature scann…

Materials science530 PhysicsBand gapFOS: Physical sciencesConjugated systemFluorene010402 general chemistry01 natural sciencesBiochemistryCatalysislaw.inventionchemistry.chemical_compoundColloid and Surface Chemistrylaw540 ChemistryOrganic electronicsCondensed Matter - Materials ScienceSpintronicsMaterials Science (cond-mat.mtrl-sci)General Chemistry0104 chemical sciencesUnpaired electronchemistryChemical physicsScanning tunneling microscopeAntiaromaticityJournal of the American Chemical Society
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On-surface Synthesis of a Chiral Graphene Nanoribbon with Mixed Edge Structure.

2020

Abstract Chiral graphene nanoribbons represent an important class of graphene nanomaterials with varying combinations of armchair and zigzag edges conferring them unique structure‐dependent electronic properties. Here, we describe the on‐surface synthesis of an unprecedented cove‐edge chiral GNR with a benzo‐fused backbone on a Au(111) surface using 2,6‐dibromo‐1,5‐diphenylnaphthalene as precursor. The initial precursor self‐assembly and the formation of the chiral GNRs upon annealing are revealed, along with a relatively small electronic bandgap of approximately 1.6 eV, by scanning tunnelling microscopy and spectroscopy.

Band gapAnnealing (metallurgy)530 Physics010402 general chemistry01 natural sciencesBiochemistrygraphene nanoribbonNanomaterialslaw.inventionlawchiral edge540 Chemistrypolycyclic aromatic hydrocarbonon-surface synthesisSpectroscopyQuantum tunnelling010405 organic chemistryChemistryGraphenescanning tunneling microscopy and spectroscopyCommunicationOrganic ChemistryGeneral ChemistryCommunications0104 chemical sciencesZigzagChemical physics570 Life sciences; biologyGraphene nanoribbonsChemistry, an Asian journal
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Overcoming Steric Hindrance in Aryl‐Aryl Homocoupling via On‐Surface Copolymerization

2019

On-surface synthesis is a unique tool for growing low-dimensional carbon nanomaterials with precise structural control down to the atomic level. This novel approach relies on carefully designed precursor molecules, which are deposited on suitable substrates and activated to ultimately form the desired nanostructures. One of the most applied reactions to covalently interlink molecular precursors is dehalogenative aryl-aryl coupling. Despite the versatility of this approach, many unsuccessful attempts are also known, most of them associated to the poor capability of the activated precursors to couple to each other. Such failure is often related to the steric hindrance between reactants, which…

Steric effectsArylIntermolecular force02 engineering and technologyConjugated system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryAtomic and Molecular Physics and Optics0104 chemical sciencesNanomaterialschemistry.chemical_compoundAdsorptionchemistryCovalent bond540 ChemistryCopolymer570 Life sciences; biologyPhysical and Theoretical Chemistry0210 nano-technologyChemPhysChem
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On-Surface Synthesis of Dibenzohexacenohexacene and Dibenzopentaphenoheptaphene

2021

We report the on-surface synthesis and gas-phase theoretical studies of two novel nanographenes, namely, dibenzohexacenohexacene and dibenzopentaphenoheptaphene, using 8,8′-dibromo-5,5′-bibenzo[rst]pentaphene as a precursor. These nanographenes display a combination of armchair and zigzag edges, as shown by noncontact atomic force microscopy (nc-AFM), and their electronic properties are elucidated by density functional theory (DFT) calculations which reveal relatively low HOMO-LUMO energy gaps of about 1.75 eV.

Surface (mathematics)chemistry.chemical_classificationchemistry010405 organic chemistryComputational chemistryPolycyclic aromatic hydrocarbonPolycyclicaromatichydrocarbonOn-surfacesynthesisGeneral Chemistry010402 general chemistry01 natural sciencesNanographene0104 chemical sciencesBulletin of the Chemical Society of Japan
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On-Surface Synthesis of Oligo(indenoindene)

2020

Fully conjugated ladder polymers (CLP) possess unique optical and electronic properties, and are considered promis-ing materials for applications in (opto)electronic devices. Poly(indenoindene) is a CLP consisting of an alternating array of five- and six-membered rings, which has remained elusive so far. Here, we report an on-surface synthesis of oligo(indenoindene) on Au(111). Its structure and a low elec-tronic bandgap have been elucidated by low-temperature scanning tunneling microscopy and spectroscopy and non-contact atomic force microscopy, complemented by density functional theory calculations. Achieving defect-free seg-ments of oligo(indenoindene) offers an exclusive insight into th…

chemistry.chemical_classificationBand gapAtomic force microscopy530 PhysicsElectronic bandNanotechnologyGeneral ChemistryPolymerConjugated system010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceslaw.inventionColloid and Surface Chemistrychemistrylaw540 ChemistryDensity functional theoryScanning tunneling microscopeSpectroscopy
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Optical Imaging and Spectroscopy of Atomically Precise Armchair Graphene Nanoribbons

2019

We report the optical imaging and absorption spectroscopy on atomically precise armchair graphene nanoribbons (GNRs) on insulating fused silica substrates. This is achieved by controlling light polarization on macroscopically aligned GNRs which greatly enhances the optical contrast of the submonolayer GNRs on the insulating substrates. We measure the linear absorption spectra of 7-armchair and 9-armchair GNRs in this study, and the experimental data agree qualitatively with ab inito calculation results. The polarization spectroscopy technique enables an unambiguous optical identification of GNRs and provides a rapid tool to characterize the transferred film over a large area.

Optical contrastAbsorption spectroscopy530 Physicsbusiness.industryMechanical EngineeringBioengineering02 engineering and technologyGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsPolarization (waves)Optical imaging540 Chemistry570 Life sciences; biologyOptoelectronicsGeneral Materials ScienceOptical identification0210 nano-technologybusinessSpectroscopyAb initoGraphene nanoribbonsNano Letters
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CCDC 2021698: Experimental Crystal Structure Determination

2020

Related Article: Ashok Keerthi, Carlos Sánchez‐Sánchez, Okan Deniz, Pascal Ruffieux, Dieter Schollmeyer, Xinliang Feng, Akimitsu Narita, Roman Fasel, Klaus Müllen|2020|Chem.Asian J.|15|3807|doi:10.1002/asia.202001008

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters26-dibromo-15-diphenylnaphthaleneExperimental 3D Coordinates
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CCDC 1980964: Experimental Crystal Structure Determination

2020

Related Article: Marco Di Giovannantonio, Qiang Chen, José I. Urgel, Pascal Ruffieux, Carlo A. Pignedoli, Akimitsu Narita, Klaus Müllen, Roman Fasel|2020|J.Am.Chem.Soc.|142|12925|doi:10.1021/jacs.0c05701

Space GroupCrystallographyCrystal SystemCrystal Structure44''-dibromo-2'35'-trimethyl-11':4'1''-terphenylCell ParametersExperimental 3D Coordinates
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CCDC 1903872: Experimental Crystal Structure Determination

2019

Related Article: Marco Di Giovannantonio, Kristjan Eimre, Aliaksandr V. Yakutovich, Qiang Chen, Shantanu Mishra, José I. Urgel, Carlo A. Pignedoli, Pascal Ruffieux, Klaus Müllen, Akimitsu Narita, Roman Fasel|2019|J.Am.Chem.Soc.|141|12346|doi:10.1021/jacs.9b05335

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters44''-dibromo-4'6'-dimethyl-11':3'1''-terphenylExperimental 3D Coordinates
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