0000000001311140

AUTHOR

Xiao-ye Wang

showing 10 related works from this author

π-Extended Pyrene-Fused Double [7]Carbohelicene as a Chiral Polycyclic Aromatic Hydrocarbon

2019

A π-extended double [7]carbohelicene 2 with fused pyrene units was synthesized, revealing considerable intra- and intermolecular π–π interactions as confirmed with X-ray crystallography. As compared to the previous double [7]carbohelicene 1, the π-extended homologue 2 demonstrated considerably red-shifted absorption with an onset at 645 nm (1: 550 nm) corresponding to a smaller optical gap of 1.90 eV (1: 2.25 eV). A broad near-infrared emission from 600 to 900 nm with a large Stokes shift of ∼100 nm (2.3 × 103 cm–1) was recorded for 2, implying formation of an intramolecular excimer upon excitation, which was corroborated with femtosecond transient absorption spectroscopy. Moreover, 2 revea…

General Chemistry010402 general chemistry01 natural sciencesBiochemistryArticleCatalysis0104 chemical sciencesChiral column chromatographysymbols.namesakeCrystallographychemistry.chemical_compoundColloid and Surface ChemistrychemistryStokes shiftIntramolecular forceUltrafast laser spectroscopysymbolsPyreneDensity functional theorySpectroscopyIsomerizationJournal of the American Chemical Society
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Polycyclic aromatic chains on metals and insulating layers by repetitive [3+2] cycloadditions

2020

The vast potential of organic materials for electronic, optoelectronic and spintronic devices entails substantial interest in the fabrication of π-conjugated systems with tailored functionality directly at insulating interfaces. On-surface fabrication of such materials on non-metal surfaces remains to be demonstrated with high yield and selectivity. Here we present the synthesis of polyaromatic chains on metallic substrates, insulating layers, and in the solid state. Scanning probe microscopy shows the formation of azaullazine repeating units on Au(111), Ag(111), and h-BN/Cu(111), stemming from intermolecular homo-coupling via cycloaddition reactions of CN-substituted polycyclic aromatic az…

Materials scienceFabricationScienceGeneral Physics and Astronomy02 engineering and technologyConjugated system010402 general chemistry01 natural sciencesArticleGeneral Biochemistry Genetics and Molecular Biologylaw.inventionchemistry.chemical_compoundScanning probe microscopylawDehydrogenationon-surface synthesislcsh:Science13-dipolar cycloadditionschemistry.chemical_classificationMultidisciplinaryalgorithmGrapheneQgrapheneazomethine ylidesGeneral ChemistryPolymer021001 nanoscience & nanotechnologyCycloadditionddc:0104 chemical sciencesCU(111)total-energy calculationschemistryChemical engineeringboron-nitrideBoron nitrideazide-alkyne cycloadditionlcsh:QMaterials chemistrydehalogenation0210 nano-technology
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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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Bottom-Up, On-Surface-Synthesized Armchair Graphene Nanoribbons for Ultra-High-Power Micro-Supercapacitors

2020

Bottom-up-synthesized graphene nanoribbons (GNRs) with excellent electronic properties are promising materials for energy storage systems. Herein, we report bottom-up-synthesized GNR films employed as electrode materials for micro-supercapacitors (MSCs). The micro-device delivers an excellent volumetric capacitance and an ultra-high power density. The electrochemical performance of MSCs could be correlated with the charge carrier mobility within the differently employed GNRs, as determined by pump–probe terahertz spectroscopy studies.

Supercapacitorbusiness.industryCharge carrier mobilityChemistryCommunicationGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciences7. Clean energyBiochemistryCatalysisEnergy storage0104 chemical sciencesTerahertz spectroscopy and technologyPower (physics)Colloid and Surface ChemistryOptoelectronicsbusinessGraphene nanoribbonsPower densityJournal of the American Chemical Society
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Regioselective Hydrogenation of a 60-Carbon Nanographene Molecule toward a Circumbiphenyl Core.

2019

Regioselective peripheral hydrogenation of a nanographene molecule with 60 contiguous sp2 carbons provides unprecedented access to peralkylated circumbiphenyl (1). Conversion to the circumbiphenyl core structure was unambiguously validated by MALDI-TOF mass spectrometry, NMR, FT-IR, and Raman spectroscopy. UV–vis absorption spectra and DFT calculations demonstrated the significant change of the optoelectronic properties upon peripheral hydrogenation. Stimulated emission from 1, observed via ultrafast transient absorption measurements, indicates potential as an optical gain material.

Absorption spectroscopyChemistryCommunicationChemistry (all)RegioselectivityGeneral Chemistry010402 general chemistryMass spectrometryPhotochemistryCatalysis; Chemistry (all); Biochemistry; Colloid and Surface Chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCatalysissymbols.namesakeColloid and Surface ChemistryUltrafast laser spectroscopysymbolsMoleculeStimulated emissionRaman spectroscopyJournal 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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Synthesis of Graphene Nanoribbons by Ambient-Pressure Chemical Vapor Deposition and Device Integration

2016

Graphene nanoribbons (GNRs), quasi-one-dimensional graphene strips, have shown great potential for nanoscale electronics, optoelectronics, and photonics. Atomically precise GNRs can be "bottom-up" synthesized by surface-assisted assembly of molecular building blocks under ultra-high-vacuum conditions. However, large-scale and efficient synthesis of such GNRs at low cost remains a significant challenge. Here we report an efficient "bottom-up" chemical vapor deposition (CVD) process for inexpensive and high-throughput growth of structurally defined GNRs with varying structures under ambient-pressure conditions. The high quality of our CVD-grown GNRs is validated by a combination of different …

FabricationBAND-GAPNanotechnologyHETEROJUNCTIONSORGANIC FIELD EFFECT TRANSISTORS02 engineering and technologyChemical vapor deposition010402 general chemistry01 natural sciencesBiochemistryCatalysislaw.inventionColloid and Surface ChemistrylawNanoscopic scaleNANOGRAPHENESPECTROSCOPYbusiness.industryChemistryGrapheneTransistorGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesgraphene nanoribbon CVD HREELS spectroscopy electronic propertiesGRAPHENE NANORIBBONSPhotonics0210 nano-technologybusinessGraphene nanoribbonsAmbient pressure
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Chemisorption of Atomically Precise 42-Carbon Graphene Quantum Dots on Metal Oxide Films Greatly Accelerates Interfacial Electron Transfer

2019

Graphene quantum dots (GQDs) are emerging as environmentally friendly, low-cost, and highly tunable building blocks in solar energy conversion architectures, such as solar (fuel) cells. Specifically, GQDs constitute a promising alternative for organometallic dyes in sensitized oxide systems. Current sensitized solar cells employing atomically precise GQDs are based on physisorbed sensitizers, with typically limited efficiencies. Chemisorption has been pointed out as a solution to boost photoconversion efficiencies, by allowing improved control over sensitizer surface coverage and sensitizer-oxide coupling strength. Here, employing time-resolved THz spectroscopy, we demonstrate that chemisor…

LetterMaterials scienceGrapheneOxidechemistry.chemical_elementNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundElectron transferchemistryQuantum dotlawChemisorptionSurface modificationGeneral Materials SciencePhysical and Theoretical Chemistry0210 nano-technologyMesoporous materialCarbonThe Journal of Physical Chemistry Letters
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CCDC 1914718: Experimental Crystal Structure Determination

2019

Related Article: Yunbin Hu, Giuseppe M. Paternò, Xiao-Ye Wang, Xin-Chang Wang, Michele Guizzardi, Qiang Chen, Dieter Schollmeyer, Xiao-Yu Cao, Giulio Cerullo, Francesco Scotognella, Klaus Müllen, Akimitsu Narita|2019|J.Am.Chem.Soc.|141|12797|doi:10.1021/jacs.9b05610

Space GroupCrystallographypyrene-fused double [7]carbohelicene methanedithione solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1521825: Experimental Crystal Structure Determination

2016

Related Article: Zongping Chen, Wen Zhang, Carlos-Andres Palma, Alberto Lodi Rizzini, Bilu Liu, Ahmad Abbas, Nils Richter, Leonardo Martini, Xiao-Ye Wang, Nicola Cavani, Hao Lu, Neeraj Mishra, Camilla Coletti, Reinhard Berger, Florian Klappenberger, Mathias Kläui, Andrea Candini, Marco Affronte, Chongwu Zhou, Valentina De Renzi, Umberto del Pennino, Johannes V. Barth, Hans Joachim Räder, Akimitsu Narita, Xinliang Feng, and Klaus Müllen|2016|J.Am.Chem.Soc.|138|15488|doi:10.1021/jacs.6b10374

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters4-(611-dibromo-14-diphenyl-3-(thiophen-3-yl)triphenylen-2-yl)pyridineExperimental 3D Coordinates
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