Hubbard-corrected DFT energy functionals: the LDA+U description of correlated systems (1309.3355v1)

Abstract: The aim of this review article is to assess the descriptive capabilities of the Hubbard-rooted LDA+U method and to clarify the conditions under which it can be expected to be most predictive. The paper illustrates the theoretical foundation of LDA+U and prototypical applications to the study of correlated materials, discusses the most relevant approximations used in its formulation, and makes a comparison with other approaches also developed for similar purposes. Open "issues" of the method are also discussed, including the calculation of the electronic couplings (the Hubbard U), the precise expression of the corrective functional and the possibility to use LDA+U for other classes of materials. The second part of the article presents recent extensions to the method and illustrates the significant improvements they have obtained in the description of several classes of different systems. The conclusive section finally discusses possible future developments of LDA+U to further enlarge its predictive power and its range of applicability.

• The paper presents the LDA+U method as a Hubbard correction to standard DFT, improving the treatment of electron localization in strongly correlated systems.
• It details the derivation of LDA+U from the Hubbard model and systematically evaluates its performance across transition metal oxides and mixed-valence compounds.
• It discusses extensions like LDA+U+V and LDA+U+J, highlighting future improvements in U parameter determination and broader applicability in materials design.

Overview of "Hubbard-corrected DFT energy functionals: the LDA+U description of correlated systems"

The paper "Hubbard-corrected DFT energy functionals: the LDA+U description of correlated systems" provides a critical review of the method known as LDA+U, an extension of the Local Density Approximation (LDA) within Density Functional Theory (DFT), incorporating Hubbard corrections for improved treatment of electronic localization and correlation effects in materials. The authors, Burak Himmetoglu, Andrea Floris, Stefano de Gironcoli, and Matteo Cococcioni, aim to elucidate the strengths and limitations of the LDA+U approach, identifying conditions under which it can provide predictive results for correlated systems.

Key Points and Theoretical Foundations

The paper begins by acknowledging the significant role of DFT as a computational tool for electronic structure calculations despite its limitations in dealing with systems exhibiting strong electronic correlations. Traditional LDA and GGA (Generalized Gradient Approximation) tend to over-delocalize electrons, failing to accurately capture the ground state properties of Mott insulators and other systems with localized electrons.

LDA+U addresses these limitations by introducing a Hubbard-like term to the DFT Hamiltonian. This term corrects the tendency of LDA to over-delocalize the electrons in localized states such as d or f orbitals, providing a more realistic description of on-site electron-electron interactions. The paper explores the formulation of the LDA+U method, illustrating its derivation from the Hubbard model and detailing its application to various material systems.

Numerical Results and Claims

One of the strengths of the paper is its systematic examination of the numerical results obtained using LDA+U across different systems. It critically examines the Hubbard U parameter's role, a key factor in the accuracy of LDA+U results, discussing various computational methods for its determination, including linear-response calculations.

The authors provide examples of systems where LDA+U yields significant improvements over standard DFT, particularly in reproducing the insulating ground state of transition metal oxides and the mixed-valence compounds' charge ordering. The paper also discusses the limitations and potential pitfalls of LDA+U, such as its somewhat empirical nature and the challenges associated with determining the U parameter consistently for a wide range of materials.

Extensions and Future Developments

Further sections of the paper discuss recent extensions to the Hubbard-corrected functionals, including LDA+U+V, which incorporates inter-site interactions, and LDA+U+J, addressing magnetic interactions. These extensions aim to broaden the applicability of the method to systems where simple on-site corrections are insufficient, such as in covalent systems or materials with complex magnetic ordering.

The authors speculate on future developments in the field, pointing towards a more systematic approach to choose the U parameter and improve the functional's generality, thus enhancing the method's accuracy and predictive power across diverse classes of materials.

Implications and Conclusion

The paper concludes by emphasizing the practical implications of LDA+U in computational material science. It highlights the method's suitability for high-throughput calculations and its potential role in materials design and discovery despite its limitations. The discussion underscores the importance of a critical assessment of LDA+U's applicability based on the specific characteristics of the system under paper.

In summary, this paper offers an in-depth analysis of the LDA+U method, evaluating its utility and guiding its application in studying correlated electron systems. By reviewing its theoretical underpinnings, numerical successes, and limitations, the authors provide a comprehensive resource aimed at advancing the understanding and application of Hubbard-corrected DFT methods in the research community.