Search results for "Physics - Chemical Physics"

showing 10 items of 172 documents

High pressure crystal structures of orthovanadates and their properties

2020

Pressure-induced phase transitions in orthovanadates have led to interesting physical phenomena. The observed transitions usually involve large volume collapses and drastic changes in the electronic and vibrational properties of the materials. In some cases, the phase transitions implicate coordination changes in vanadium, which has important consequences in the physical properties of vanadates. In this Perspective, we explore the current knowledge of the behavior of MVO4 vanadates under compression. In particular, we summarize studies of the structural, vibrational, and electronic properties and a few illustrative examples of high-pressure research in the compounds of interest are discusse…

010302 applied physicsChemical Physics (physics.chem-ph)Phase transitionCondensed Matter - Materials ScienceMaterials scienceGeneral Physics and AstronomyMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences02 engineering and technologyApplied Physics (physics.app-ph)Physics - Applied Physics021001 nanoscience & nanotechnology01 natural sciencesEngineering physicsHigh pressurePhysical phenomenaPhysics - Chemical Physics0103 physical sciences0210 nano-technologyElectronic properties
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Few layer 2D pnictogens catalyze the alkylation of soft nucleophiles with esters

2019

Group 15 elements in zero oxidation state (P, As, Sb and Bi), also called pnictogens, are rarely used in catalysis due to the difficulties associated in preparing well–structured and stable materials. Here, we report on the synthesis of highly exfoliated, few layer 2D phosphorene and antimonene in zero oxidation state, suspended in an ionic liquid, with the native atoms ready to interact with external reagents while avoiding aerobic or aqueous decomposition pathways, and on their use as efficient catalysts for the alkylation of nucleophiles with esters. The few layer pnictogen material circumvents the extremely harsh reaction conditions associated to previous superacid–catalyzed alkylations…

0301 basic medicineCatàlisi heterogèniaScienceFOS: Physical sciencesGeneral Physics and Astronomy02 engineering and technologyAlkylationIonic liquidGeneral Biochemistry Genetics and Molecular BiologyArticleCatalysis03 medical and health scienceschemistry.chemical_compoundNucleophileOxidation stateAntimonenePhysics - Chemical PhysicsQUIMICA ANALITICAlcsh:ScienceMaterialsChemical Physics (physics.chem-ph)MultidisciplinaryAqueous solutionChemistryPnictogensPhosphoreneQGeneral Chemistry021001 nanoscience & nanotechnologyCombinatorial chemistryPhosphorene030104 developmental biologyReagentddc:540Ionic liquidlcsh:QCatalyst0210 nano-technologyNature Communications
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Electronic signature of the instantaneous asymmetry in the first coordination shell of liquid water

2013

Interpretation of the X-ray spectra of water as evidence for its asymmetric structure has challenged the conventional symmetric nearly-tetrahedral model and initiated an intense debate about the order and symmetry of the hydrogen bond network in water. Here, we present new insights into the nature of local interactions in water obtained using a novel energy decomposition method. Our simulations reveal that while a water molecule forms, on average, two strong donor and two strong acceptor bonds, there is a significant asymmetry in the energy of these contacts. We demonstrate that this asymmetry is a result of small instantaneous distortions of hydrogen bonds, which appear as fluctuations on …

Absorption spectroscopymedia_common.quotation_subjectShell (structure)FOS: Physical sciencesGeneral Physics and AstronomyCondensed Matter - Soft Condensed Matter010402 general chemistry01 natural sciencesAsymmetryMolecular physicsGeneral Biochemistry Genetics and Molecular BiologySpectral linePhysics - Chemical Physics0103 physical sciencesMoleculeCondensed Matter - Statistical Mechanicsmedia_commonChemical Physics (physics.chem-ph)PhysicsMultidisciplinaryStatistical Mechanics (cond-mat.stat-mech)010304 chemical physicsHydrogen bondGeneral ChemistryComputational Physics (physics.comp-ph)AcceptorSymmetry (physics)0104 chemical sciencesCondensed Matter - Other Condensed MatterSoft Condensed Matter (cond-mat.soft)Physics - Computational PhysicsOther Condensed Matter (cond-mat.other)
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Orientation and Alignment Echoes

2015

We present one of the simplest classical systems featuring the echo phenomenon---a collection of randomly oriented free rotors with dispersed rotational velocities. Following excitation by a pair of time-delayed impulsive kicks, the mean orientation or alignment of the ensemble exhibits multiple echoes and fractional echoes. We elucidate the mechanism of the echo formation by the kick-induced filamentation of phase space, and provide the first experimental demonstration of classical alignment echoes in a thermal gas of ${\mathrm{CO}}_{2}$ molecules excited by a pair of femtosecond laser pulses.

Atomic Physics (physics.atom-ph)FOS: Physical sciencesGeneral Physics and AstronomyPhysics - Classical PhysicsPhysics - Atomic Physicslaw.inventionOpticsFilamentationlawPhysics - Chemical PhysicsChemical Physics (physics.chem-ph)Physics[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics][PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]business.industry[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]Echo (computing)Classical Physics (physics.class-ph)LaserOrientation (vector space)Phase spaceExcited stateFemtosecondAtomic physicsbusinessExcitationPhysics - OpticsOptics (physics.optics)Physical Review Letters
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Experimental benchmarking of quantum control in zero-field nuclear magnetic resonance

2017

Zero-field nuclear magnetic resonance (NMR) provides complementary analysis modalities to those of high-field NMR and allows for ultra-high-resolution spectroscopy and measurement of untruncated spin-spin interactions. Unlike for the high-field case, however, universal quantum control -- the ability to perform arbitrary unitary operations -- has not been experimentally demonstrated in zero-field NMR. This is because the Larmor frequency for all spins is identically zero at zero field, making it challenging to individually address different spin species. We realize a composite-pulse technique for arbitrary independent rotations of $^1$H and $^{13}$C spins in a two-spin system. Quantum-inform…

Atomic Physics (physics.atom-ph)FOS: Physical sciencesQuantum simulator02 engineering and technology01 natural sciencesPhysics - Atomic PhysicsNuclear magnetic resonanceControlled NOT gatePhysics - Chemical Physics0103 physical sciencesQuantum metrology010306 general physicsSpin (physics)Chemical Physics (physics.chem-ph)Larmor precessionPhysicsQuantum PhysicsMultidisciplinarySpins500Nuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnologyCondensed Matter::Strongly Correlated Electronsddc:500Quantum Physics (quant-ph)0210 nano-technologyRealization (systems)
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Measurement of untruncated nuclear spin interactions via zero- to ultralow-field nuclear magnetic resonance

2015

Zero- to ultra-low-field nuclear magnetic resonance (ZULF NMR) provides a new regime for the measurement of nuclear spin-spin interactions free from effects of large magnetic fields, such as truncation of terms that do not commute with the Zeeman Hamiltonian. One such interaction, the magnetic dipole-dipole coupling, is a valuable source of spatial information in NMR, though many terms are unobservable in high-field NMR, and the coupling averages to zero under isotropic molecular tumbling. Under partial alignment, this information is retained in the form of so-called residual dipolar couplings. We report zero- to ultra-low-field NMR measurements of residual dipolar couplings in acetonitrile…

Atomic Physics (physics.atom-ph)Fluids & Plasmasphysics.chem-phFOS: Physical sciences010402 general chemistryJ-couplingphysics.atom-ph01 natural sciencesPhysics - Atomic Physicssymbols.namesakeEngineeringNuclear magnetic resonancequant-phPhysics - Chemical Physics0103 physical sciencesMagnetization transfer010306 general physicsChemical Physics (physics.chem-ph)PhysicsQuantum PhysicsZeeman effectCondensed matter physicsCondensed Matter Physics0104 chemical sciences3. Good healthElectronic Optical and Magnetic MaterialsMagnetic fieldSolid-state nuclear magnetic resonanceResidual dipolar couplingPhysical SciencesChemical SciencessymbolsQuantum Physics (quant-ph)Two-dimensional nuclear magnetic resonance spectroscopyMagnetic dipole–dipole interaction
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Compact two-electron wave function for bond dissociation and Van der Waals interactions: A natural amplitude assessment

2014

Electron correlations in molecules can be divided in short range dynamical correlations, long range Van der Waals type interactions and near degeneracy static correlations. In this work we analyze for a one-dimensional model of a two-electron system how these three types of correlations can be incorporated in a simple wave function of restricted functional form consisting of an orbital product multiplied by a single correlation function $f(r_{12})$ depending on the interelectronic distance $r_{12}$. Since the three types of correlations mentioned lead to different signatures in terms of the natural orbital (NO) amplitudes in two-electron systems we make an analysis of the wave function in t…

Atomic Physics (physics.atom-ph)General Physics and AstronomyFOS: Physical sciencesPhysics - Atomic Physicssymbols.namesakeCondensed Matter - Strongly Correlated ElectronsAtomic orbitalQuantum mechanicsPhysics - Chemical PhysicsPhysics::Atomic PhysicsSDG 7 - Affordable and Clean EnergyPhysical and Theoretical ChemistryWave functionAnsatzPhysicsChemical Physics (physics.chem-ph)Quantum Physics/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energyta114Electronic correlationStrongly Correlated Electrons (cond-mat.str-el)Computational Physics (physics.comp-ph)Diatomic molecule3. Good healthBond lengthAmplitudesymbolsvan der Waals forceQuantum Physics (quant-ph)Physics - Computational Physics
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Generalized Many-Body Expanded Full Configuration Interaction Theory

2019

Facilitated by a rigorous partitioning of a molecular system's orbital basis into two fundamental subspaces - a reference and an expansion space, both with orbitals of unspecified occupancy - we generalize our recently introduced many-body expanded full configuration interaction (MBE-FCI) method to allow for electron-rich model and molecular systems dominated by both weak and strong correlation to be addressed. By employing minimal or even empty reference spaces, we show through calculations on the one-dimensional Hubbard model with up to 46 lattice sites, the chromium dimer, and the benzene molecule how near-exact results may be obtained in a entirely unbiased manner for chemical and physi…

Chemical Physics (physics.chem-ph)010304 chemical physicsBasis (linear algebra)Computer scienceFOS: Physical sciences010402 general chemistrySpace (mathematics)01 natural sciencesFull configuration interactionMany body0104 chemical sciencesTheoretical physicsAtomic orbitalPhysics - Chemical Physics0103 physical sciencesGeneral Materials ScienceAstrophysics::Earth and Planetary AstrophysicsPhysical and Theoretical Chemistry
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Assessment of the accuracy of coupled cluster perturbation theory for open-shell systems. II. Quadruples expansions

2016

We extend our assessment of the potential of perturbative coupled cluster (CC) expansions for a test set of open-shell atoms and organic radicals to the description of quadruple excitations. Namely, the second- through sixth-order models of the recently proposed CCSDT(Q-n) quadruples series [J. Chem. Phys. 140, 064108 (2014)] are compared to the prominent CCSDT(Q) and lambda-CCSDT(Q) models. From a comparison of the models in terms of their recovery of total CC singles, doubles, triples, and quadruples (CCSDTQ) energies, we find that the performance of the CCSDT(Q-n) models is independent of the reference used (unrestricted or restricted (open-shell) Hartree-Fock), in contrast to the CCSDT(…

Chemical Physics (physics.chem-ph)010304 chemical physicsPhysics - Chemical Physics0103 physical sciencesFOS: Physical sciencesGeneral Physics and AstronomyPhysical and Theoretical Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesThe Journal of Chemical Physics
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Many-Body Expanded Full Configuration Interaction. II. Strongly Correlated Regime

2019

In this second part of our series on the recently proposed many-body expanded full configuration interaction (MBE-FCI) method, we introduce the concept of multideterminantal expansion references. Through theoretical arguments and numerical validations, the use of this class of starting points is shown to result in a focussed compression of the MBE decomposition of the FCI energy, thus allowing chemical problems dominated by strong correlation to be addressed by the method. The general applicability and performance enhancements of MBE-FCI are verified for standard stress tests such as the bond dissociations in H$_2$O, N$_2$, C$_2$, and a linear H$_{10}$ chain. Furthermore, the benefits of em…

Chemical Physics (physics.chem-ph)010304 chemical physicsThe RenaissanceFOS: Physical sciences010402 general chemistry01 natural sciencesFull configuration interactionMany body0104 chemical sciencesComputer Science ApplicationsFormalism (philosophy of mathematics)Physics - Chemical Physics0103 physical sciencesStatistical physicsPhysical and Theoretical ChemistryGround state
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