Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

A Remarkable Application of Zassenhaus Formula to Quantum Physics and Chemistry

Louis Jourdan, Patrick Cassam‐Chenaï

Published Aug 23, 2025• 0 citations
OpenAlex

Abstract

We show that the Zassenhaus decomposition for the exponential of the sum of two non-commuting operators, simplifies drastically when these operators satisfy a simple condition, called the no-mixed adjoint property. An important application to a unitary Coupled Cluster method is presented. The latter method is particularly promising in quantum chemistry and the simple formula obtained in this work, demonstrates that it will be perfectly adapted to a quantum computer implementation.

Related papers

A Remarkable Application of Zassenhaus Formula to Strongly Correlated Electron Systems

Louis Jourdan, Patrick Cassam‐Chenaï

We show that the Zassenhaus decomposition for the exponential of the sum of two non-commuting operators, simplifies drastically when these operators satisfy a simple condition, called the no-mixed adjoint property. An important application to a Unitary Coupled Cluster method for strongly correlated electron systems is presented. This ansatz requires no Trotterization and is exact on a quantum computer with a finite number of Givens gate equals to the number of free parameters. The formulas obtained in this work also shed light on why and when optimization after Trotterization gives exact solutions in disentangled forms of unitary coupled cluster.

arXiv:2510.24364•Quantum•Apr 8, 2026•0 citations

Analytical evaluation of the numerical coefficients in the Zassenhaus product formula and its applications to quantum and statistical mechanics

Mauro Bologna

This paper studies the exponential of the sum of two non-commuting operators as an infinite product of exponential operators involving repeated commutators of increasing order. It will be shown how to determine the two coefficients in front of the nested commutators in the Zassenhaus formula. The knowledge of one coefficient is enough to generate closed formulas that have several applications in solving problems ranging from linear differential equations and quantum mechanics to non-linear differential equations.

arXiv:1804.01125•Progress of Theoretical and Experimental Physics•Mar 28, 2019•2 citations

Error bounds for the truncated Baker--Campbell--Hausdorff and Zassenhaus formulas in unitary problems

A. Arnal, F. Casas, J. L. Ruiz-Benito

The Baker--Campbell--Hausdorff (BCH) formula plays a critical role in many branches of mathematics and physics. It expresses the logarithm of the product of exponentials of non-commuting operators as an infinite series of nested commutators of the operators involved. The Zassenhaus formula is the dual of the BCH formula: the exponential of a sum of operators is written as an infinite product of exponentials involving the operators and their commutators. In practical computations, however, one typically has to truncate the expansions, and so understanding the error committed by the resulting approximations and eventually providing suitable bounds for this error is of paramount interest. In this work we present a general strategy to derive rigorous error bounds and explicit error constants for the BCH and Zassenhaus formulas when the operators involved are skew-adjoint, as is the case for quantum evolution problems.

math-phCross-listedarXiv:2607.07692•Jul 9, 2026

Operator Relationship between Conventional Coupled Cluster and Unitary Coupled Cluster

James K. Freericks

The chemistry community has long sought the exact relationship between the conventional and the unitary coupled cluster ansatz for a single-reference system, especially given the interest in performing quantum chemistry on quantum computers. In this work, we show how one can use the operator manipulations given by the exponential disentangling identity and the Hadamard lemma to relate the factorized form of the unitary coupled-cluster approximation to a factorized form of the conventional coupled cluster approximation (the factorized form is required, because some amplitudes are operator-valued and do not commute with other terms). By employing the Trotter product formula, one can then relate the factorized form to the standard form of the unitary coupled cluster ansatz. The operator dependence of the factorized form of the coupled cluster approximation can also be removed at the expense of requiring even more higher-rank operators, finally yielding the conventional coupled cluster. The algebraic manipulations of this approach are daunting to carry out by hand, but can be automated on a computer for small enough systems.

arXiv:2201.11881•Symmetry•Feb 28, 2022•11 citations

New perspectives on unitary coupled‐cluster theory

Andrew G. Taube, Rodney J. Bartlett

Abstract The advantages and possibilities of a unitary coupled‐cluster (CC) theory are examined. It is shown that using a unitary parameterization of the wave function guarantees agreement between a sum‐over‐states polarization propagator and response theory calculation of properties of arbitrary order, as opposed to the case in conventional CC theory. Then, using the Zassenhaus expansion for noncommuting exponential operators, explicit diagrams for an extensive and variational method based on unitary CC theory are derived. Possible extensions to the approximations developed are discussed as well. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2006

International Journal of Quantum Chemistry•Jan 1, 2006•253 citations

Qubit Coupled Cluster Method: A Systematic Approach to Quantum Chemistry on a Quantum Computer

Ilya G. Ryabinkin, Tzu-Ching Yen, Scott N. Genin +1 more

A unitary coupled cluster (UCC) form for the wave function in the variational quantum eigensolver has been suggested as a systematic way to go beyond the mean-field approximation and include electron correlation in solving quantum chemistry problems on a quantum computer. Although being exact in the limit of including all possible coupled cluster excitations, practically, the accuracy of this approach depends on the number and type of terms are included in the wave function parametrization. Another difficulty of UCC is a growth of the number of simultaneously entangled qubits even at the fixed Fermionic excitation rank. Not all quantum computing architectures can cope with this growth. To address both problems, we introduce a qubit coupled cluster (QCC) method that starts directly in the qubit space and uses energy response estimates for ranking the importance of individual entanglers for the variational energy minimization. Also, we provide an exact factorization of a unitary rotation of more than two qubits to a product of two-qubit unitary rotations. Thus, the QCC method with the factorization technique can be limited to only two-qubit entanglement gates and allows for very efficient use of quantum resources in terms of the number of coupled cluster operators. The method performance is illustrated by calculating ground-state potential energy curves of H 2 and LiH molecules with chemical accuracy, ≤1 kcal/mol, and a symmetric water dissociation curve.

arXiv:1809.03827•Journal of Chemical Theory and Computation•Nov 14, 2018•285 citations
We show that the Zassenhaus decomposition for the exponential of the sum of two non-commuting operators, simplifies drastically when these operators satisfy a simple condition, called the no-mixed adjoint property. An important application to a unitary Coupled Cluster method is presented. The latter method is particularly promising in quantum chemistry and the simple formula obtained in this work, demonstrates that it will be perfectly adapted to a quantum computer implementation.
We show that the Zassenhaus decomposition for the exponential of the sum of two non-commuting operators, simplifies drastically when these operators satisfy a simple condition, called the no-mixed adjoint property. An important application to a Unitary Coupled Cluster method for strongly correlated electron systems is presented. This ansatz requires no Trotterization and is exact on a quantum computer with a finite number of Givens gate equals to the number of free parameters. The formulas obtained in this work also shed light on why and when optimization after Trotterization gives exact solutions in disentangled forms of unitary coupled cluster.
This paper studies the exponential of the sum of two non-commuting operators as an infinite product of exponential operators involving repeated commutators of increasing order. It will be shown how to determine the two coefficients in front of the nested commutators in the Zassenhaus formula. The knowledge of one coefficient is enough to generate closed formulas that have several applications in solving problems ranging from linear differential equations and quantum mechanics to non-linear differential equations.
The Baker--Campbell--Hausdorff (BCH) formula plays a critical role in many branches of mathematics and physics. It expresses the logarithm of the product of exponentials of non-commuting operators as an infinite series of nested commutators of the operators involved. The Zassenhaus formula is the dual of the BCH formula: the exponential of a sum of operators is written as an infinite product of exponentials involving the operators and their commutators. In practical computations, however, one typically has to truncate the expansions, and so understanding the error committed by the resulting approximations and eventually providing suitable bounds for this error is of paramount interest. In this work we present a general strategy to derive rigorous error bounds and explicit error constants for the BCH and Zassenhaus formulas when the operators involved are skew-adjoint, as is the case for quantum evolution problems.
The chemistry community has long sought the exact relationship between the conventional and the unitary coupled cluster ansatz for a single-reference system, especially given the interest in performing quantum chemistry on quantum computers. In this work, we show how one can use the operator manipulations given by the exponential disentangling identity and the Hadamard lemma to relate the factorized form of the unitary coupled-cluster approximation to a factorized form of the conventional coupled cluster approximation (the factorized form is required, because some amplitudes are operator-valued and do not commute with other terms). By employing the Trotter product formula, one can then relate the factorized form to the standard form of the unitary coupled cluster ansatz. The operator dependence of the factorized form of the coupled cluster approximation can also be removed at the expense of requiring even more higher-rank operators, finally yielding the conventional coupled cluster. The algebraic manipulations of this approach are daunting to carry out by hand, but can be automated on a computer for small enough systems.
Abstract The advantages and possibilities of a unitary coupled‐cluster (CC) theory are examined. It is shown that using a unitary parameterization of the wave function guarantees agreement between a sum‐over‐states polarization propagator and response theory calculation of properties of arbitrary order, as opposed to the case in conventional CC theory. Then, using the Zassenhaus expansion for noncommuting exponential operators, explicit diagrams for an extensive and variational method based on unitary CC theory are derived. Possible extensions to the approximations developed are discussed as well. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2006
A unitary coupled cluster (UCC) form for the wave function in the variational quantum eigensolver has been suggested as a systematic way to go beyond the mean-field approximation and include electron correlation in solving quantum chemistry problems on a quantum computer. Although being exact in the limit of including all possible coupled cluster excitations, practically, the accuracy of this approach depends on the number and type of terms are included in the wave function parametrization. Another difficulty of UCC is a growth of the number of simultaneously entangled qubits even at the fixed Fermionic excitation rank. Not all quantum computing architectures can cope with this growth. To address both problems, we introduce a qubit coupled cluster (QCC) method that starts directly in the qubit space and uses energy response estimates for ranking the importance of individual entanglers for the variational energy minimization. Also, we provide an exact factorization of a unitary rotation of more than two qubits to a product of two-qubit unitary rotations. Thus, the QCC method with the factorization technique can be limited to only two-qubit entanglement gates and allows for very efficient use of quantum resources in terms of the number of coupled cluster operators. The method performance is illustrated by calculating ground-state potential energy curves of H 2 and LiH molecules with chemical accuracy, ≤1 kcal/mol, and a symmetric water dissociation curve.