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Chebyshev matrix product state approach for spectral functions

Andreas Holzner, Andreas Weichselbaum, Ian P. McCulloch, Ulrich Schollwöck, and Jan von Delft
Phys. Rev. B 83, 195115 – Published 10 May 2011

Abstract

We show that recursively generated Chebyshev expansions offer numerically efficient representations for calculating zero-temperature spectral functions of one-dimensional lattice models using matrix product state (MPS) methods. The main features of this Chebyshev matrix product state (CheMPS) approach are as follows: (i) it achieves uniform resolution over the spectral function’s entire spectral width; (ii) it can exploit the fact that the latter can be much smaller than the model’s many-body bandwidth; (iii) it offers a well-controlled broadening scheme that allows finite-size effects to be either resolved or smeared out, as desired; (iv) it is based on using MPS tools to recursively calculate a succession of Chebyshev vectors |tn, (v) the entanglement entropies of which were found to remain bounded with increasing recursion order n for all cases analyzed here; and (vi) it distributes the total entanglement entropy that accumulates with increasing n over the set of Chebyshev vectors |tn, which need not be combined into a single vector. In this way, the growth in entanglement entropy that usually limits density matrix renormalization group (DMRG) approaches is packaged into conveniently manageable units. We present zero-temperature CheMPS results for the structure factor of spin-12 antiferromagnetic Heisenberg chains and perform a detailed finite-size analysis. Making comparisons to three benchmark methods, we find that CheMPS (a) yields results comparable in quality to those of correction-vector DMRG, at dramatically reduced numerical cost; (b) agrees well with Bethe ansatz results for an infinite system, within the limitations expected for numerics on finite systems; and (c) can also be applied in the time domain, where it has potential to serve as a viable alternative to time-dependent DMRG (in particular, at finite temperatures). Finally, we present a detailed error analysis of CheMPS for the case of the noninteracting resonant level model.

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  • Received 29 January 2011

DOI:https://doi.org/10.1103/PhysRevB.83.195115

©2011 American Physical Society

Authors & Affiliations

Andreas Holzner1, Andreas Weichselbaum1, Ian P. McCulloch2, Ulrich Schollwöck1, and Jan von Delft1

  • 1Physics Department, Arnold Sommerfeld Center for Theoretical Physics, and Center for NanoScience, Ludwig-Maximilians-Universität München, D-80333 München, Germany
  • 2School of Physical Sciences, University of Queensland, Brisbane, Queensland 4072, Australia

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Issue

Vol. 83, Iss. 19 — 15 May 2011

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