Improved Correlation Optimized Virtual Orbital Algorithm for Plane-Wave Full Configuration Interaction Calculations

Full configuration interaction (FCI) calculations have historically faced significant challenges in dealing with periodic systems. The plane-wave basis sets are valued for their efficiency and broad applicability in various computational physics and chemistry simulations. Because of their natural periodicity, the plane-wave basis sets offer a potential solution to this problem. Moreover, FCI can address the limitations of widely used methods, such as density functional theory (DFT) with plane-wave basis sets, in accurately describing strongly correlated systems. However, the large basis set nature of the plane-wave makes them unsuitable for direct application in FCI calculations. To address this challenge, we propose an improved algorithm based on the correlation-optimized virtual orbital (COVOS) framework. By incorporating rotational matrices to enhance the active space dimension and optimizing orbitals through iterative coupled processes, we successfully compress the extensive plane-wave basis set into a manageable number of virtual orbitals suitable for FCI calculations while retaining most of the original basis set characteristics. We apply this method to supercell calculations and potential energy curves of periodic metallic systems. To further validate our approach, we test it on nonperiodic small molecular systems and compare the results with those obtained from DFT, second-order Møller-Plesset perturbation theory (MP2), random phase approximation (RPA), FCI calculations using the 6-31G or cc-pVDZ basis sets, and the original COVOS algorithm. The improved COVOS framework demonstrates significant advantages in convergence and correlation description over the original method. Furthermore, we observe metal divergence issues in MP2 calculations for certain metallic systems and note that RPA may overestimate the correlation energy of such systems. These findings underscore the importance of achieving FCI calculations with plane-wave basis sets.

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Journal
Journal of Chemical Theory and Computation
Published
2025-06-13
DOI
https://doi.org/10.1021/acs.jctc.5c00586
Primary Topic
Advanced Chemical Physics Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Improved Correlation Optimized Virtual Orbital Algorithm for Plane-Wave Full Configuration Interaction Calculations

Zhenlin Zhang, Wei Hu, Zhiyuan Zhang, Jinlong Yang et al.
1 links
Journal of Chemical Theory and Computation
Advanced Chemical Physics Studies
article

Improved Correlation Optimized Virtual Orbital Algorithm for Plane-Wave Full Configuration Interaction Calculations

Zhenlin Zhang, Wei Hu, Zhiyuan Zhang, Jinlong Yang, Yuduan Lin, Yingzhou Li, Mengdi Qiu
article en

Abstract

Full configuration interaction (FCI) calculations have historically faced significant challenges in dealing with periodic systems. The plane-wave basis sets are valued for their efficiency and broad applicability in various computational physics and chemistry simulations. Because of their natural periodicity, the plane-wave basis sets offer a potential solution to this problem. Moreover, FCI can address the limitations of widely used methods, such as density functional theory (DFT) with plane-wave basis sets, in accurately describing strongly correlated systems. However, the large basis set nature of the plane-wave makes them unsuitable for direct application in FCI calculations. To address this challenge, we propose an improved algorithm based on the correlation-optimized virtual orbital (COVOS) framework. By incorporating rotational matrices to enhance the active space dimension and optimizing orbitals through iterative coupled processes, we successfully compress the extensive plane-wave basis set into a manageable number of virtual orbitals suitable for FCI calculations while retaining most of the original basis set characteristics. We apply this method to supercell calculations and potential energy curves of periodic metallic systems. To further validate our approach, we test it on nonperiodic small molecular systems and compare the results with those obtained from DFT, second-order Møller-Plesset perturbation theory (MP2), random phase approximation (RPA), FCI calculations using the 6-31G or cc-pVDZ basis sets, and the original COVOS algorithm. The improved COVOS framework demonstrates significant advantages in convergence and correlation description over the original method. Furthermore, we observe metal divergence issues in MP2 calculations for certain metallic systems and note that RPA may overestimate the correlation energy of such systems. These findings underscore the importance of achieving FCI calculations with plane-wave basis sets.

Journal of Chemical Theory and ComputationVol. 21(13)
University of Science and Technology of China (CN), Fudan University (CN), Hefei National Center for Physical Sciences at Nanoscale (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, Science and Technology Commission of Shanghai Municipality, Natural Science Foundation of Anhui Province, National Key Research and Development Program of China, Anhui Provincial Key Research and Development Plan
Affordable and clean energy
Openalex Percentile: Top 90%
Advanced Chemical Physics Studies
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