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arXiv:2407.01692 · Physical Review Letters

Clifford Dressed Time-Dependent Variational Principle

Antonio Francesco Mello, Alessandro Santini, Guglielmo Lami, Jacopo De Nardis, Mario Collura

Published Apr 15, 2025• 20 citations
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Abstract

We propose an enhanced time-dependent variational principle (TDVP) algorithm for matrix product states that integrates Clifford disentangling techniques to efficiently manage entanglement growth. By leveraging the Clifford group, which maps Pauli strings to other Pauli strings while maintaining low computational complexity, we introduce a Clifford dressed single-site 1-TDVP scheme. During the TDVP integration, we apply a global Clifford transformation as needed to reduce entanglement by iteratively sweeping over two-qubit Clifford unitaries that connect neighboring sites in a checkerboard pattern. We validate the new algorithm numerically using various quantum many-body models, including both integrable and nonintegrable systems. Our results demonstrate that the Clifford dressed TDVP significantly improves entanglement management and computational efficiency, achieving higher accuracy, extended simulation times, and enhanced precision in computed observables compared to standard TDVP approaches. Additionally, we propose incorporating Clifford gates directly within the two-site 2-TDVP scheme.

DOI
10.1103/physrevlett.134.150403

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We propose an enhanced time-dependent variational principle (TDVP) algorithm for matrix product states that integrates Clifford disentangling techniques to efficiently manage entanglement growth. By leveraging the Clifford group, which maps Pauli strings to other Pauli strings while maintaining low computational complexity, we introduce a Clifford dressed single-site 1-TDVP scheme. During the TDVP integration, we apply a global Clifford transformation as needed to reduce entanglement by iteratively sweeping over two-qubit Clifford unitaries that connect neighboring sites in a checkerboard pattern. We validate the new algorithm numerically using various quantum many-body models, including both integrable and nonintegrable systems. Our results demonstrate that the Clifford dressed TDVP significantly improves entanglement management and computational efficiency, achieving higher accuracy, extended simulation times, and enhanced precision in computed observables compared to standard TDVP approaches. Additionally, we propose incorporating Clifford gates directly within the two-site 2-TDVP scheme.
We extend the recently introduced Clifford-dressed time-dependent variational principle (TDVP) to efficiently compute many-body wave-function amplitudes in the computational basis. This advancement enhances the study of Loschmidt echoes, which generally require accurate calculations of the overlap between the evolved state and the initial wave function. By incorporating Clifford-disentangling gates during TDVP evolution, our method effectively controls entanglement growth while keeping the computation of these amplitudes accessible. Specifically, it reduces the problem to evaluating the overlap between a matrix product state (MPS) and a stabilizer state, a task that remains computationally feasible within the proposed framework. To demonstrate the effectiveness of this approach, we first benchmark it on the one-dimensional transverse-field Ising model. We then apply it to more challenging scenarios, including a nonintegrable next-to-nearest-neighbor Ising chain and a two-dimensional Ising model. Our results highlight the versatility and efficiency of the Clifford-augmented MPS, showcasing its capability to go beyond the evaluation of simple expectation values. This makes it a powerful tool for exploring various aspects of many-body quantum dynamics.
The recently proposed Clifford circuits augmented matrix product states (CA-MPSs) [X. Qian, J. Huang, and M. Qin, Phys. Rev. Lett. 133, 190402 (2024)PRLTAO0031-900710.1103/PhysRevLett.133.190402] seamlessly augment density matrix renormalization groups with Clifford circuits. In CA-MPSs, the entanglement from stabilizers is transferred to the Clifford circuits, which can be easily handled according to the Gottesman-Knill theorem. As a result, an MPS needs only to deal with the nonstabilizer entanglement, which largely reduces the bond dimension and the resource required for the accurate simulation of many-body systems. In this Letter, we generalize CA-MPSs to the framework of the time-dependent variational principle (TDVP) for time evolution simulations. In this method, we apply Clifford circuits to the resulting MPS in each TDVP step with a two-site sweeping process similar as in density matrix renormalization groups, aiming at reducing the entanglement entropy in the MPS, and the Hamiltonian is transformed accordingly using the chosen Clifford circuits. Similar as in CA-MPSs, the Clifford circuits does not increase the number of terms in the Hamiltonian, which makes the overhead very small in the new method. We test this method in XXZ chain, 2D Heisenberg model, and Kitaev honeycomb model. The results show that the Clifford circuits augmented TDVP method can reduce the entanglement entropy in the time evolution process and hence makes the simulation reliable for a longer time. The Clifford circuits augmented time-dependent variational principle provides a useful tool for the simulation of the time evolution process of many-body systems in the future.
Combining the time-dependent variational principle (TDVP) algorithm with the parallelization scheme introduced by Stoudenmire and White for the density matrix renormalization group (DMRG), we present the first parallel matrix product state (MPS) algorithm capable of time evolving one-dimensional (1D) quantum lattice systems with long-range interactions. We benchmark the accuracy and performance of the algorithm by simulating quenches in the long-range Ising and XY models. We show that our code scales well up to 32 processes, with parallel efficiencies as high as 8686%86. Finally, we calculate the dynamical correlation function of a 201-site Heisenberg XXX spin chain with 1/r21/{r}^{2}1/r2 interactions, which is challenging to compute sequentially. These results pave the way for the application of tensor networks to increasingly complex many-body systems.
We present a controlled bond expansion (CBE) approach to simulate quantum dynamics based on the time-dependent variational principle (TDVP) for matrix product states. Our method alleviates the numerical difficulties of the standard, fixed-rank one-site TDVP integrator by increasing bond dimensions on the fly to reduce the projection error. This is achieved in an economical, local fashion, requiring only minor modifications of standard one-site TDVP implementations. We illustrate the performance and accuracy of CBE-TDVP with several numerical examples on finite quantum lattices, including new results on bipolaron formation in the Peierls-Hubbard model and spin pumping via adiabatic flux insertion in a chiral spin liquid.
Entanglement is a key bottleneck limiting the efficiency of tensor-network and quantum simulations of molecular electronic structures. Here, we systematically assess and extend Clifford disentanglers as a structure-preserving approach to entanglement reduction: they can modify the entanglement structure of qubit wavefunctions while retaining the Pauli-string form of qubit Hamiltonians. To enable a practical search over Clifford transformations, we classify Clifford operators by their action on the Schmidt spectrum across a bipartition, reducing the two- and four-qubit search spaces to 20 and 91392 representatives, respectively. Embedded in an iterative Clifford-augmented matrix product state framework, these transformations reduce the energy errors at fixed bond dimension for the molecular test cases studied and mitigate the dependence on orbital orderings and fermion-to-qubit mappings. We further show that Clifford disentanglers can also benefit quantum simulations such as the shallow-circuit variational quantum eigensolver calculations. Together, these results establish Clifford disentanglers as a useful structure-preserving entanglement-engineering tool for tensor-network and quantum simulations of molecular electronic structure, while also clarifying their correlation dependence and motivating future developments.
In recent years, the time-dependent variational principle (TDVP) method based on the matrix product state (MPS) wave function formulation has shown its great power in performing large-scale quantum dynamics simulations for realistic chemical systems with strong electron-vibration interactions. In this work, we propose a stochastic adaptive single-site TDVP (SA-1TDVP) scheme to evolve the bond-dimension adaptively, which can integrate the traditional advantages of both the high efficiency of the single-site TDVP (1TDVP) variant and the high accuracy of the two-site TDVP (2TDVP) variant. Based on the assumption that the level statistics of entanglement Hamiltonians, which originate from the reduced density matrices of the MPS method, follows a Poisson or Wigner distribution, as generically predicted by random-matrix theory, additional random singular values are generated to expand the bond-dimension automatically. Tests on simulating the vibrationally resolved quantum dynamics and absorption spectra in the pyrazine molecule and perylene bisimide (PBI) J-aggregate trimer as well as a spin-1/2 Heisenberg chain show that it can be automatic and as accurate as 2TDVP but reduce the computational time remarkably.