Improving the precision of forces in real-space pseudopotential density functional theory

被引:0
|
作者
Roller, Deena [1 ]
Rappe, Andrew M. [2 ]
Kronik, Leeor [1 ]
Hellman, Olle [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Chem & Mat Sci, IL-76100 Rehovot, Israel
[2] Univ Penn, Dept Chem, Philadelphia, PA 10104 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2024年 / 161卷 / 07期
基金
瑞典研究理事会;
关键词
ELECTRONIC-STRUCTURE CALCULATIONS;
D O I
10.1063/5.0218715
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The high-order finite difference real-space pseudopotential density functional theory (DFT) approach is a valuable method for large-scale, massively parallel DFT calculations. A significant challenge in the approach is the oscillating "egg-box" error introduced by aliasing associated with a coarse grid spacing. To address this issue while minimizing computational cost, we developed a finite difference interpolation (FDI) scheme [Roller et al., J. Chem. Theory Comput. 19, 3889 (2023)] as a means of exploiting the high resolution of the pseudopotential to reduce egg-box effects systematically. Here, we show an implementation of this method in the PARSEC code and examine the practical utility of the combination of FDI with additional methods for improving force precision and/or reducing its computational cost, including orbital-based forces, compensating charges (namely, adding and subtracting a judiciously chosen charge density such that the total density is unaltered), and a modified spatial domain in which the real-space grid is defined. Using selected small molecules, as well as metallic Li, as test cases, we show that a combination of all four aspects leads to a significant reduction in computational cost while retaining a high level of precision that supports accurate structures and vibrational spectra, as well as stable and accurate molecular dynamics runs.
引用
收藏
页数:13
相关论文
共 50 条
  • [41] Chemical Bonding in Large Systems Using Projected Population Analysis from Real-Space Density Functional Theory Calculations
    Ramakrishnan, Kartick
    Nori, Sai Krishna Kishore
    Lee, Seung-Cheol
    Das, Gour P.
    Bhattacharjee, Satadeep
    Motamarri, Phani
    JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2023, 19 (13) : 4216 - 4231
  • [42] The Sternheimer approach to all-electron real-space density-functional perturbation theory with atomic basis set
    Shang, Honghui
    AIP ADVANCES, 2021, 11 (01)
  • [43] Real-Space Density Functional Theory on Graphical Processing Units: Computational Approach and Comparison to Gaussian Basis Set Methods
    Andrade, Xavier
    Aspuru-Guzik, Alan
    JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2013, 9 (10) : 4360 - 4373
  • [44] A real-space perturbation theory for electronic correlation
    Manby, FR
    Knowles, PJ
    CHEMICAL PHYSICS LETTERS, 1999, 310 (5-6) : 561 - 567
  • [45] ACCURATE DENSITY FUNCTIONAL FOR THE ENERGY - REAL-SPACE CUTOFF OF THE GRADIENT EXPANSION FOR THE EXCHANGE HOLE
    PERDEW, JP
    PHYSICAL REVIEW LETTERS, 1985, 55 (16) : 1665 - 1668
  • [46] DENSITY-FUNCTIONAL MOLECULAR-DYNAMICS WITH REAL-SPACE FINITE-DIFFERENCE
    HOSHI, T
    ARAI, M
    FUJIWARA, T
    PHYSICAL REVIEW B, 1995, 52 (08) : R5459 - R5462
  • [47] IMPROVING CRYSTALLOGRAPHIC MACROMOLECULAR IMAGES - THE REAL-SPACE APPROACH
    PODJARNY, AD
    BHAT, TN
    ZWICK, M
    ANNUAL REVIEW OF BIOPHYSICS AND BIOPHYSICAL CHEMISTRY, 1987, 16 : 351 - 373
  • [48] Efficient single-grid and multi-grid solvers for real-space orbital-free density functional theory
    Bu, Ling-Ze
    Wang, Wei
    COMPUTER PHYSICS COMMUNICATIONS, 2023, 290
  • [49] Real-space density profile reconstruction of stacked voids
    Pisani, A.
    Lavaux, G.
    Sutter, P. M.
    Wandelt, B. D.
    MONTHLY NOTICES OF THE ROYAL ASTRONOMICAL SOCIETY, 2014, 443 (04) : 3238 - 3250
  • [50] Self-consistent DFT plus U method for real-space time-dependent density functional theory calculations
    Tancogne-Dejean, Nicolas
    Oliveira, Micael J. T.
    Rubio, Angel
    PHYSICAL REVIEW B, 2017, 96 (24)