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Updated: May 28, 2026

Generation and Coherent Control of Pulsed Quantum Frequency Combs
Published on: June 8, 2018
Accurate, Full-Dimensional Computations of Thousands of Complex Vibrational Eigenstates with Tree Tensor Network
Henrik R Larsson1, Brieuc Le Dé1, Gino E Gamboni2
1Department of Chemistry and Biochemistry, University of California, Merced, California 95343, United States.
None:
Tree tensor network states (TTNSs) combined with the density matrix renormalization group (DMRG) are emerging as powerful tools for vibrational and vibronic structure simulations in molecules with strong coupling and fluxionality. In this Perspective, we discuss how TTNS methods enable accurate, full-dimensional computations of thousands of eigenstates for molecular systems ranging from quartic-force-field benchmarks to molecules with strong vibronic coupling and protonated water clusters as large as the 33-dimensional Eigen ion, H3O+·(H2O)3. We emphasize the close connection and interoperability between DMRG-based TTNS methods and the multilayer multiconfiguration time-dependent Hartree method (ML-MCTDH), which share the same underlying ansatz. We also highlight practical challenges of predictive simulations, including robust error estimation, convergence of observables such as infrared intensities, and optimization of tensor network tree structures. Finally, we outline recent advances toward direct targeting of excited states and discuss opportunities for broader applications in molecular spectroscopy and quantum dynamics.
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