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showing 10 items of 18071 documents

TDDFT Analysis of Optical Properties of Thiol Monolayer-Protected Gold and Intermetallic Silver–Gold Au144(SR)60 and Au84Ag60(SR)60 Clusters

2014

The optical absorption spectra of atomistic model structures for experimentally isolated all-gold Au144(SR)60 and intermetallic Au84Ag60(SR)60 clusters are systematically analyzed from linear-response time-dependent density functional theory (LR-TDDFT) and time-dependent density functional perturbation theory (TD-DFPT) calculations. The computed spectra, utilizing the atomistic model for Au144(SR)60 published by us in 2009, reproduce closely the experimental observations for corresponding isolated compounds, reported previously by Kumara and Dass in 2011. A collective dipole oscillation within the metal cores of the all-gold and intermetallic clusters is formed as response to light in the v…

ta114ChemistryIntermetallicTime-dependent density functional theoryMolecular physicsSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMetalDipoleGeneral Energyvisual_artMonolayervisual_art.visual_art_mediumDensity functional theoryPhysical and Theoretical ChemistrySurface plasmon resonanceAtomic physicsta116The Journal of Physical Chemistry C
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Vibrational Perturbations and Ligand–Layer Coupling in a Single Crystal of Au144(SC2H4Ph)60 Nanocluster

2015

We have determined vibrational signatures and optical gap of the Au144(PET)60 (PET: phenylethylthiol, SC2H4Ph) nanocluster solvated in deuterated dichloromethane (DCM-D2, CD2Cl2) and in a single crystal. For crystals, solid-state (13)C NMR and X-ray diffraction were also measured. A revised value of 2200 cm(-1) (0.27 eV) was obtained for the optical gap in both phases. The vibrational spectra of solvated AU144(PET)60 closely resembles that of neat PET, while the crystalline-state spectrum exhibits significant inhomogeneous spectral broadening, frequency shifts, intensity transfer between vibrational modes, and an increase in the overtone and combination transition intensities. Spectral broa…

ta114ChemistryOvertoneta221Analytical chemistryOvertone bandMolecular physicsHot bandCrystalMolecular vibrationGeneral Materials SciencePhysical and Theoretical ChemistryRotational–vibrational couplingSingle crystalta116Doppler broadeningThe Journal of Physical Chemistry Letters
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Molecule-like photodynamics of Au102(pMBA)44 nanocluster.

2015

Photophysical properties of a water-soluble cluster Au102(pMBA)44 (pMBA = para-mercaptobenzoic acid) are studied by ultrafast time-resolved mid-IR spectroscopy and density functional theory calculations in order to distinguish between molecular and metallic behavior. In the mid-IR transient absorption studies, visible or near-infrared light is used to electronically excite the sample, and the subsequent relaxation is monitored by studying the transient absorption of a vibrational mode in the ligands. Based on these studies, a complete picture of energy relaxation dynamics is obtained: (1) 0.5-1.5 ps electronic relaxation, (2) 6.8 ps vibrational cooling, (3) intersystem crossing from the low…

ta114ChemistryRelaxation (NMR)General EngineeringGeneral Physics and Astronomytransient absorptionInternal conversion (chemistry)PhotochemistryMolecular physicselectronic relaxationvibrational spectroscopyIntersystem crossinggold nanoclusterUltrafast laser spectroscopyGeneral Materials ScienceDensity functional theoryTriplet stateSpectroscopyGround stateta116femtosecondACS nano
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Optical Properties of Monolayer-Protected Aluminum Clusters: Time-Dependent Density Functional Theory Study

2015

We examine the electronic and optical properties of experimentally known monolayer-protected aluminum clusters Al4(C5H5)4, Al50(C5Me5)12, and Al69(N(SiMe3)2)183– using time-dependent density functional theory. By comparing Al4(C5H5)4 and the theoretical Al4(N(SiMe3)2)4 cluster, we observe significant changes in the optical absorption spectra caused by different hybridization between metal core and ligands. Using these initial observations, we explain the calculated spectra of Al50(C5Me5)12 and Al69(N(SiMe3)2)183–. Al50(C5Me5)12 shows a structured spectrum with clear regions of low-intensity core-to-core transitions followed by high-intensity ligand-to-core transitions due to its high symmet…

ta114Chemistrychemistry.chemical_elementTime-dependent density functional theorySpectral lineSymmetry (physics)3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsaluminum clustersMetalCrystallographytime-dependent density functional theoryGeneral EnergyAluminiumvisual_artMonolayervisual_art.visual_art_mediumCluster (physics)Density functional theoryPhysical and Theoretical Chemistryta116Journal of Physical Chemistry C
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Symmetry breaking in ligand-protected gold clusters probed by nonlinear optics

2016

The first hyperpolarizabilities of [Au25(SR)18](-1/0) and Au38(SR)24 clusters were determined by Hyper-Rayleigh Scattering. A strong dependence on the molecular symmetry was observed, and we explore two strategies to destroy the center of inversion in [Au25(SR)18](-1/0), protection by chiral ligands and alloying of the cluster with silver. This may open new avenues to applications of Au : SR clusters in second-order nonlinear optics.

ta114Condensed matter physicsligandsChemistryScatteringLigandnonlinear opticsNonlinear optics02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologygold clusters01 natural sciencesMolecular physics0104 chemical sciencesmolecular symmetryMolecular symmetryCluster (physics)General Materials ScienceSymmetry breaking0210 nano-technologyta116Nanoscale
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A DFT Study of Linear Gold–Thiolate Superclusters Absorbing in the Therapeutic NIR Window

2015

A series of linear clusters up to an aspect ratio of 1:6, formed as multimers of smaller clusters with an icosahedral Au13(5+) core having an eight-electron superatom configuration, are computationally predicted to have a greatly enhanced size-dependent absorption in the near-infrared (NIR) region extending to the biologically important NIR window. A novel structural model is presented for the previously isolated thiol-stabilized Au54(SR)30 cluster, where the metal core is formed as a heterodimer of the cores of the known Au25(SR)18(-/0) and Au38(SR)24 clusters.

ta114Icosahedral symmetryChemistrySuperatomNanotechnologyAspect ratio (image)MetalCore (optical fiber)Crystallographyvisual_artvisual_art.visual_art_mediumCluster (physics)General Materials ScienceDensity functional theoryPhysical and Theoretical ChemistryAbsorption (electromagnetic radiation)ta116The Journal of Physical Chemistry Letters
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One-pot synthesis and characterization of subnanometre-size benzotriazolate protected copper clusters

2012

A simple one-pot method for the preparation of subnanometre-size benzotriazolate (BTA) protected copper clusters, Cu(n)BTA(m), is reported. The clusters were analyzed by optical and infrared spectroscopy, mass spectrometry and transmission electron microscopy together with computational methods. We suggest a structural motif where the copper core of the Cu(n)BTA(m) clusters is protected by BTA-Cu(i)-BTA units.

ta114Inorganic chemistryOne-pot synthesischemistry.chemical_elementInfrared spectroscopyTriazolesMass spectrometryCopperCharacterization (materials science)CrystallographychemistryCoordination ComplexesTransmission electron microscopyQuantum TheorySpectrophotometry UltravioletGeneral Materials ScienceStructural motifta116CopperNanoscale
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The Role of the Anchor Atom in the Ligand of the Monolayer-Protected Au25(XR)18– Nanocluster

2015

We present a density functional theory (DFT) investigation on the role of the anchor atom and ligand on the structural, electronic, and optical properties of the anionic Au25(XR)18– nanocluster (X = S, Se, Te; R = H, CH3, and (CH2)2Ph). Substituting the anchor atom with other group 16 elements induces subtle changes in the Au–Au and Au–X bond lengths and polarization of the covalent bond. The changes in the electronic structure based on substituting both the anchor and R groups are presented through careful analysis of the density of states and theoretical determined optical spectra. We give a detailed side-by-side comparison into the structural, electronic, and optical properties of Au25(X…

ta114LigandChemistryligandsElectronic structureanchor atomsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBond lengthCrystallographyGeneral EnergyCovalent bondComputational chemistryAtomMonolayerDensity of statesDensity functional theoryPhysical and Theoretical Chemistryta116gold nanoclustersJournal of Physical Chemistry C
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Design of a Cleaning Program for a PV Plant Based on Analysis of Energy Losses

2015

Solar photovoltaic (PV) energy has grown significantly over the past few years. However, despite the increase in installed capacity, this energy source still raises important concerns related to the variability of power production. The short-term effects such as cloud shadowing and supply interruptions, as well as long-term effects such as dust accumulation, seasonal variation, and ageing of PV modules, can cause variability of power production. Therefore, the analysis of all the variability sources in order to provide statistically consistent power production data is an important challenge. This study presents a methodology to analyze data from a PV plant in order to have an independent ev…

ta213digital signal processingta1172Photovoltaic systemEnvironmental engineeringSeasonalityCondensed Matter Physicsmedicine.diseaseElectronic Optical and Magnetic MaterialsPower (physics)Nameplate capacityenvironmental factorsphotovoltaic systemsmedicineGrid-connected photovoltaic power systemEnvironmental scienceProduction (economics)Electrical and Electronic EngineeringEnergy sourceta218Energy (signal processing)IEEE Journal of Photovoltaics
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Crystal Structures and Density Functional Theory Calculations of o-and p-Nitroaniline Derivatives: Combined Effect of Hydrogen Bonding and aromatic i…

2013

The interplay of strong and weak hydrogen bonds, dipole–dipole interactions, and aromatic interactions of o- and p-nitroaniline derivatives was studied by combining crystal structure analysis and density functional theory (DFT) calculations. Crystal structures of four 2-nitroaniline derivatives, 2-((2-nitrophenyl)amino)ethyl methanesulfonate (1A), 2-((2-nitrophenyl)amino)ethyl 4-methylbenzenesulfonate (2A), N,N′-((1,3-phenylenebis(oxy))bis(ethane-2,1-diyl))bis(2-nitroaniline) (3A), and N-(2-chloroethyl)-2-nitroaniline (4A), and crystal structures of three 4-nitroaniline derivatives, 2-((4-nitrophenyl)amino)ethyl methanesulfonate (1B), 2-((4-nitrophenyl)amino)ethyl 4-methylbenzenesulfonate (…

ta214Ethyl methanesulfonateta114Hydrogen bondIntermolecular forceAromaticityGeneral ChemistryCrystal structureCondensed Matter PhysicsRing (chemistry)Nitroanilinechemistry.chemical_compoundCrystallographychemistryComputational chemistryGeneral Materials ScienceDensity functional theoryta116Crystal Growth and Design
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