Paket: nwchem (7.0.2-4)

[ Källkod: nwchem  ]

High-performance computational chemistry software (default MPI)

NWChem is a computational chemistry program package. It provides methods which are scalable both in their ability to treat large scientific computational chemistry problems efficiently, and in their use of available parallel computing resources from high-performance parallel supercomputers to conventional workstation clusters.

NWChem can handle:

 * Molecular electronic structure methods using gaussian
   basis functions for high-accuracy calculations of molecules
 * Pseudopotentials plane-wave electronic structure methods for calculating
   molecules, liquids, crystals, surfaces, semi-conductors or metals
 * Ab-initio and classical molecular dynamics simulations
 * Mixed quantum-classical simulations
 * Parallel scaling to thousands of processors

Features include:

 * Molecular electronic structure methods, analytic second derivatives:
  - Restricted/unrestricted Hartree-Fock (RHF, UHF)
  - Restricted Density Functional Theory (DFT) using many local,
    non-local (gradient-corrected) or hybrid (local, non-local, and HF)
    exchange-correlation potentials
 * Molecular electronic structure methods, analytic gradients:
  - Restricted open-shell Hartree-Fock (ROHF)
  - Unrestricted Density Functional Theory (DFT)
  - Second-order Moeller-Plesset perturbation theory (MP2), using RHF and UHF
    reference
  - MP2 with resolution of the identity approximation (RI-MP2)
  - Complete active space SCF (CASSCF)
  - Time-Dependent Density Functional Theory (TDDFT)
 * Molecular electronic structure methods, single-point energies:
  - MP2 spin-component scaled approach (SCS-MP2)
  - Coupled cluster singles and doubles, triples or pertubative triples
    (CCSD, CCSDT, CCSD(T)), with RHF and UHF reference
  - Configuration interaction (CISD, CISDT, and CISDTQ)
  - Second-order approximate coupled-cluster singles doubles (CC2)
  - State-specific multireference coupled cluster methods (MRCC)
    (Brillouin-Wigner (BW-MRCC) and Mukherjee (Mk-MRCC) approaches)
 * Further molecular electronic structure features:
  - Geometry optimization including transition state searches, constraints
    and minimum energy paths (via the Nudged Elastic Band (NEB) and Zero
    Temperature String methods)
  - Vibrational frequencies
  - Equation-of-motion (EOM)-CCSD, EOM-CCSDT, EOM-CCSD(T), CC2,
    Configuration-Interaction singles (CIS), time-dependent HF (TDHF) and
    TDDFT, for excited states with RHF, UHF, RDFT, or UDFT reference
  - Solvatisation using the Conductor-like screening model (COSMO) for RHF,
    ROHF and DFT, including analytical gradients
  - Hybrid calculations using the two- and three-layer ONIOM method
  - Relativistic effects via spin-free and spin-orbit one-electron
    Douglas-Kroll and zeroth-order regular approximations (ZORA) and
    one-electron spin-orbit effects for DFT via spin-orbit potentials
 * Pseudopotential plane-wave electronic structure:
  - Pseudopotential Plane-Wave (PSPW), Projector Augmented Wave (PAW) or band
    structure methods for calculating molecules, liquids, crystals, surfaces,
    semi-conductors or metals
  - Geometry/unit cell optimization including transition state searches
  - Vibrational frequencies
  - LDA, PBE96, and PBE0 exchange-correlation potentials (restricted and
    unrestricted)
  - SIC, pert-OEP, Hartree-Fock, and hybrid functionals (restricted and
    unrestricted)
  - Hamann, Troullier-Martins and Hartwigsen-Goedecker-Hutter norm-conserving
    pseudopotentials with semicore corrections
  - Wavefunction, density, electrostatic and Wannier plotting
  - Band structure and density of states generation
 * Car-Parrinello ab-initio molecular dynamics (CPMD):
  - Constant energy and constant temperature dynamics
  - Verlet algorithm for integration
  - Geometry constraints in cartesian coordinates
 * Classical molecular dynamics (MD):
  - Single configuration energy evaluation
  - Energy minimization
  - Molecular dynamics simulation
  - Free energy simulation (multistep thermodynamic perturbation (MSTP) or
    multiconfiguration thermodynamic integration (MCTI) methods with options
    of single and/or dual topologies, double wide sampling, and separation-
    shifted scaling)
  - Force fields providing effective pair potentials, first order
    polarization, self consistent polarization, smooth particle mesh Ewald
    (SPME), periodic boundary conditions and SHAKE constraints
 * Mixed quantum-classical:
  - Mixed quantum-mechanics and molecular-mechanics (QM/MM) minimizations and
    molecular dynamics simulations
  - Quantum molecular dynamics simulation by using any of the quantum
    mechanical methods capable of returning gradients.

This package provides example input scripts and depends on nwchem built for the default MPI implementation for the architecture.

The default MPI is openmpi for most debian systems. OpenMPI has known problems running nwchem over multiple nodes. If you need to compute large molecules using cluster computation, you may want to use the MPICH build provided by nwchem-mpich instead.

Märken: Field: Chemistry, Role: Program

Andra paket besläktade med nwchem

• dep: mpi-default-bin

  Standard MPI runtime programs (metapackage)

• dep: nwchem-openmpi

  High-performance computational chemistry software (OpenMPI build)

  eller nwchem-mpich

  High-performance computational chemistry software (MPICH build)

  eller nwchem-openmpi

  High-performance computational chemistry software (OpenMPI build)

Hämta nwchem

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