Quantum Information reveals that orbital-wise correlation is essentially classical in Natural Orbitals

TL;DR

This study shows that orbital-wise electron correlations in molecular wavefunctions are mainly classical when analyzed with Natural Orbitals, which could simplify quantum chemistry computations.

Contribution

It demonstrates that using Natural Orbitals significantly reduces the quantum nature of correlations, suggesting a new approach to simplify quantum chemical calculations.

Findings

Correlation differences decrease by ~100-fold with Natural Orbitals

Wavefunction correlations are predominantly classical in Natural Orbitals

Implications for simplifying quantum chemistry computations

Abstract

The intersection of Quantum Chemistry and Quantum Computing has led to significant advancements in understanding the potential of using quantum devices for the efficient calculation of molecular energies. Simultaneously, this intersection is enhancing the comprehension of quantum chemical properties through the use of quantum computing and quantum information tools. This paper tackles a key question in this relationship: Is the nature of the orbital-wise electron correlations in wavefunctions of realistic prototypical cases classical or quantum? We delve into this inquiry with a comprehensive examination of molecular wavefunctions using Shannon and von Neumann entropies, alongside classical and quantum information theory. Our analysis reveals a notable distinction between classical and quantum mutual information in molecular systems when analyzed with Hartree-Fock canonical orbitals. However, this difference decreases dramatically, by approximately 100-fold, when Natural Orbitals are used as reference. This finding suggests that wavefunction correlations, when viewed through the appropriate orbital basis, are predominantly classical. This insight indicates that computational tasks in quantum chemistry could be significantly simplified by employing Natural Orbitals. Consequently, our study underscores the importance of using Natural Orbitals to accurately assess molecular wavefunction correlations and to avoid their overestimation. In summary, our results suggest a promising path for computational simplification in quantum chemistry, advocating for the wider adoption of Natural Orbitals and raising questions about the actual computational complexity of the multi-body problem in quantum chemistry.