RESUMO
We introduce a new paradigm for scaling simulations with projected entangled-pair states (PEPS) for critical strongly correlated systems, allowing for reliable extrapolations of PEPS data with relatively small bond dimensions D. The key ingredient consists of using the effective correlation length ξ for inducing a collapse of data points, f(D,χ)=f(ξ(D,χ)), for arbitrary values of D and the environment bond dimension χ. As such we circumvent the need for extrapolations in χ and can use many distinct data points for a fixed value of D. Here, we need that the PEPSs have been optimized using a fixed-χ gradient method, which can be achieved using a novel tensor-network algorithm for finding fixed points of 2D transfer matrices, or by using the formalism of backwards differentiation. We test our hypothesis on the critical 3D dimer model, the 3D classical Ising model, and the 2D quantum Heisenberg model.
RESUMO
Doubts have been raised on the representation of chiral spin liquids exhibiting topological order in terms of projected entangled pair states (PEPSs). Here, starting from a simple spin-1/2 chiral frustrated Heisenberg model, we show that a faithful representation of the chiral spin liquid phase is in fact possible in terms of a generic PEPS upon variational optimization. We find a perfectly chiral gapless edge mode and a rapid decay of correlation functions at short distances consistent with a bulk gap, concomitant with a gossamer long-range tail originating from a PEPS bulk-edge correspondence. For increasing bond dimension, (i) the rapid decrease of spurious features-SU(2) symmetry breaking and long-range tails in correlations-together with (ii) a faster convergence of the ground state energy as compared to state-of-the-art cylinder matrix-product state simulations involving far more variational parameters, prove the fundamental relevance of the PEPS ansatz for simulating systems with chiral topological order.
