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arXiv:2609.17121

Floquet Theory and Average Hamiltonian Theory Revisited: Equivalence, Convergence and Applications to NMR

Antonia J. Bock, Matthias Ernst, Götz S. Uhrig

quant-phphysics.chem-phSubmitted Sep 15, 2026• Announced Sep 16, 2026• 0 citations
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Abstract

An accurate theoretical treatment of periodically driven quantum systems is crucial for various fields in the exact sciences, for instance Nuclear Magnetic Resonance (NMR) spectroscopy. Conventionally, either average Hamiltonian theory or Floquet theory is used to predict or describe experimental outcomes, such as the time evolution or the spectra yielding the information of the sample under study. A detailed analysis of the equivalence of these two approaches with an emphasis on applications in NMR will help to improve the theoretical understanding of NMR experiments. In this work, we identify the Floquet-Magnus expansion as essential to prove the mathematical equivalence of Floquet theory and average Hamiltonian theory. We advocate a calculation scheme which is less prone to algebraic mistakes because explicit integration is avoided. On this basis, we provide the first four orders of both theories. We further examine their applicability to some experiments in NMR. As examples, we investigate the Bloch-Siegert shift and dipolar coupled spin systems under magic-angle spinning. Based on our analysis, we recommend the use of the Floquet-Van Vleck approach including both the effective Hamiltonian and the kick operator. The consistent separation of secular and non-secular contributions appears to be especially advantageous for numerical robustness. Its accuracy is about three times better than the one provided by average Hamiltonian theory despite their formal equivalence. Our findings provide important insights into the theoretical background of Floquet theory and average Hamiltonian theory. This includes the extent of their algebraic and perturbative equivalence, with an emphasis on how these findings are of relevance in the analysis of solid-state NMR experiments.

DOI
10.5194/mr-2026-10
Comments
32 pages, 13 figures

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An accurate theoretical treatment of periodically driven quantum systems is crucial for various fields in the exact sciences, for instance Nuclear Magnetic Resonance (NMR) spectroscopy. Conventionally, either average Hamiltonian theory or Floquet theory is used to predict or describe experimental outcomes, such as the time evolution or the spectra yielding the information of the sample under study. A detailed analysis of the equivalence of these two approaches with an emphasis on applications in NMR will help to improve the theoretical understanding of NMR experiments.
In this work, we identify the Floquet-Magnus expansion as essential to prove the mathematical equivalence of Floquet theory and average Hamiltonian theory. We advocate a calculation scheme which is less prone to algebraic mistakes because explicit integration is avoided. On this basis, we provide the first four orders of both theories. We further examine their applicability to some experiments in NMR. As examples, we investigate the Bloch-Siegert shift and dipolar coupled spin systems under magic-angle spinning.
Based on our analysis, we recommend the use of the Floquet-Van Vleck approach including both the effective Hamiltonian and the kick operator. The consistent separation of secular and non-secular contributions appears to be especially advantageous for numerical robustness. Its accuracy is about three times better than the one provided by average Hamiltonian theory despite their formal equivalence.
Our findings provide important insights into the theoretical background of Floquet theory and average Hamiltonian theory. This includes the extent of their algebraic and perturbative equivalence, with an emphasis on how these findings are of relevance in the analysis of solid-state NMR experiments.
This article presents the application of continuous Floquet theory in solid-state nuclear magnetic resonance (NMR). Continuous Floquet theory extends the traditional Floquet theory to non-continuous Hamiltonians, enabling the description of observable effects not fully captured by the traditional Floquet theory due to its requirement for a periodic Hamiltonian. We present closed-form expressions for computing first- and second-order effective Hamiltonians, streamlining integration with the traditional Floquet theory and facilitating application in NMR experiments featuring multiple modulation frequencies. Subsequently, we show examples of the practical application of continuous Floquet theory by investigating several solid-state NMR experiments. These examples illustrate the importance of the duration of the pulse scheme regarding the width of the resonance conditions and the near-resonance behavior.
In this paper, we revisit, from different perspectives, the applications of Floquet–Magnus expansion (FME) and Fer expansion (FE) in NMR and physics. We use these expansion schemes for the calculation of effective Hamiltonians and propagators. We found that the FME is related to the FE. While both approaches are powerful methods, there are subtle differences between them. To understand the differences, we performed explicit calculation on various problems, namely, Bloch–Siegert shift, Cross Polarization (CP) and Continuous Waves (CW). We put the work in a prospect that is related to spin physics in order to make the calculation more general. As the propagator from the FME takes the form of the evolution operator, which removes the constraint of a stroboscopic observation, we appreciated the effects of time-evolution under Hamiltonians with different orders separately.
This article presents the application of continuous Floquet theory in solid-state NMR. Continuous Floquet theory extends traditional Floquet theory to non-continuous Hamiltonians, enabling the description of observable effects not fully captured by traditional Floquet theory due to its requirement for a periodic Hamiltonian. We present closed-form expressions for computing first and second-order effective Hamiltonians, streamlining integration with traditional Floquet theory and facilitating application in NMR experiments featuring multiple modulation frequencies. Subsequently, we show examples of the practical application of Continuous Floquet theory by investigating several solid-state NMR experiments. These examples illustrate the importance of the duration of the pulse scheme regarding the width of the resonance conditions and the near-resonance behavior.
The work in this thesis presents an operator-based Floquet formalism which can be used to describe a Hamiltonian with multiple time dependencies, i.e. multiple basic frequencies in solid-state Nuclear Magnetic Resonance (NMR) experiments.In solid-state NMR, the time dependence can be caused for example by magic-angle spinning (MAS) where the sample is rotated about a specific (magic) angle with respect to the static field, thus averaging all anisotropic spin interactions.Radio-frequency irradiation, which is
Quantum mechanical Floquet theory, a powerful tool for the solution of Schrödinger equations with a periodically time-dependent Hamiltonian is formalized by the systematic usage of the Floquet Hilbert space, the Floquet density operator, Floquet detection operators, and of the Floquet Liouville space. A concise description is obtained that is useful in analytical calculations and for computer simulations. It is implemented in the context of the general computational environment ‘GAMMA’. Simplified expressions are derived for single-axis and double-axis sample-spinning experiments in NMR.
Comprehending the dynamical behaviour of quantum systems driven by time-varying Hamiltonians is particularly difficult. Systems with as little as two energy levels are not yet fully understood. Since the inception of Magnus’ expansion in 1954, no fundamentally novel mathematical method for solving the quantum equations of motion with a time-varying Hamiltonian has been devised. We report here of an entirely different non-perturbative approach, termed path-sum, which is always guaranteed to converge, yields the exact analytical solution in a finite number of steps for finite systems and is invariant under scale transformations. We solve for the dynamics of all two-level systems as well as of many-body Hamiltonians with a particular emphasis on NMR applications (Bloch-Siegert effect and N-spin systems involving the dipolar Hamiltonian and spin diffusion).