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GPAW: An open Python package for electronic structure calculations

delete2024-03-07
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OA
AI
J
Jens Jørgen Mortensen *
A
Ask Hjorth Larsen
M
Mikael Kuisma
A
Aleksei V. Ivanov
A
Alireza Taghizadeh
A
Andrew A. Peterson
A
Anubhab Haldar
A
Asmus Ougaard Dohn
C
C. Schäfer
E
Elvar Örn Jónsson
E
Eric Hermes
F
Fredrik Nilsson
G
Georg Kastlunger
G
Gianluca Levi
H
Hannes Jónsson
H
Hannu Häkkinen
J
Jakub Fojt
J
Jiban Kangsabanik
J
Joachim Sødequist
J
Jouko Lehtomäki
J
Julian Heske
J
Jussi Enkovaara
K
Kirsten T. Winther
M
Marcin Dułak
M
Marko Melander
M
Martin Ovesen
M
Martti Louhivuori
M
Michael Walter
M
Morten N. Gjerding
O
Olga Lopez‐Acevedo
P
Paul Erhart
R
Robert Warmbier
R
Rolf Würdemann
S
Sami Kaappa
S
Simone Latini
T
Tara M. Boland
T
Thomas Bligaard
T
Thorbjørn Skovhus
T
Toma Susi
T
Tristan Maxson
T
Tuomas Rossi
陈熙 (Xi Chen)
Y
Yorick L. A. Schmerwitz
J
Jakob Schiøtz
T
Thomas Olsen
K
Karsten W. Jacobsen
K
Kristian S. Thygesen
DOI:10.1063/5.0182685delete
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Abstract

Abstract

En 中文
We review the GPAW open-source Python package for electronic structure calculations. GPAW is based on the projector-augmented wave method and can solve the self-consistent density functional theory (DFT) equations using three different wave-function representations, namely real-space grids, plane waves, and numerical atomic orbitals. The three representations are complementary and mutually independent and can be connected by transformations via the real-space grid. This multi-basis feature renders GPAW highly versatile and unique among similar codes. By virtue of its modular structure, the GPAW code constitutes an ideal platform for the implementation of new features and methodologies. Moreover, it is well integrated with the Atomic Simulation Environment (ASE), providing a flexible and dynamic user interface. In addition to ground-state DFT calculations, GPAW supports many-body GW band structures, optical excitations from the Bethe-Salpeter Equation, variational calculations of excited states in molecules and solids via direct optimization, and real-time propagation of the Kohn-Sham equations within time-dependent DFT. A range of more advanced methods to describe magnetic excitations and non-collinear magnetism in solids are also now available. In addition, GPAW can calculate non-linear optical tensors of solids, charged crystal point defects, and much more. Recently, support for graphics processing unit (GPU) acceleration has been achieved with minor modifications to the GPAW code thanks to the CuPy library. We end the review with an outlook, describing some future plans for GPAW.
Keywords:
DENSITY-FUNCTIONAL THEORY
SELF-INTERACTION CORRECTION
RANDOM-PHASE-APPROXIMATION
TOTAL-ENERGY CALCULATIONS
CHARGE-TRANSFER EXCITATIONS
SURFACE-PLASMON RESONANCE
TRANSFER EXCITED-STATES
FINDING SADDLE-POINTS
ELASTIC BAND METHOD
1ST-PRINCIPLES CALCULATIONS

Journal

Journal of Chemical Physics cover
Journal of Chemical Physics
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3.1
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7.2W
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23.2W

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