اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدDMRG Simulation of the SU(3) AFM Heisenberg Model
192
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We analyze the antiferromagnetic $text{SU}(3)$ Heisenberg chain by means of the Density Matrix Renormalization Group (DMRG). The results confirm that the model is critical and the computation of its central charge and the scaling dimensions of the first excited states show that the underlying low energy conformal field theory is the $text{SU}(3)_1$ Wess-Zumino-Novikov-Witten model.
قيم البحث
اقرأ أيضاً
The DMRG method is applied to integrable models of antiferromagnetic spin chains for fundamental and higher representations of SU(2), SU(3), and SU(4). From the low energy spectrum and the entanglement entropy, we compute the central charge and the
primary field scaling dimensions. These parameters allow us to identify uniquely the Wess-Zumino-Witten models capturing the low energy sectors of the models we consider.
In the Density Matrix Renormalization Group (DMRG) algorithm, Hamiltonian symmetries play an important role. Using symmetries, the matrix representation of the Hamiltonian can be blocked. Diagonalizing each matrix block is more efficient than diagona
lizing the original matrix. This paper explains how the the DMRG++ code has been extended to handle the non-local SU(2) symmetry in a model independent way. Improvements in CPU times compared to runs with only local symmetries are discussed for the one-orbital Hubbard model, and for a two-orbital Hubbard model for iron-based superconductors. The computational bottleneck of the algorithm and the use of shared memory parallelization are also addressed.
A zero-site density matrix renormalization algorithm (DMRG0) is proposed to minimize the energy of matrix product states (MPS). Instead of the site tensors themselves, we propose to optimize sequentially the message tensors between neighbor sites, wh
ich contain the singular values of the bipartition. This leads to a local minimization step that is independent of the physical dimension of the site. Conceptually, it separates the optimization and decimation steps in DMRG. Furthermore, we introduce two new global perturbations based on the optimal low-rank correction to the current state, which are used to avoid local minima. They are determined variationally as the MPS closest to the one-step correction of the Lanczos or Jacobi-Davidson eigensolver, respectively. These perturbations mainly decrease the energy and are free of hand-tuned parameters. Compared to existing single-site enrichment proposals, our approach gives similar convergence ratios per sweep while the computations are cheaper by construction. Our methods may be useful in systems with many physical degrees of freedom per lattice site. We test our approach on the periodic Heisenberg spin chain for various spins, and on free electrons on the lattice.
We have studied the magnetization reversal process in FM/AFM bilayer structures through of spin dynamics simulation. It has been observed that the magnetization behavior is different at each branch of the hysteresis loop as well as the exchange-bias
behavior. On the descending branch a sudden change of the magnetization is observed while on the ascending branch is observed a bland change of the magnetization. The occurrence of the asymmetry in the hysteresis loop and the variation in the exchange-bias is due to anisotropy which is introduced only in the coupling between ferromagnetic (FM) and antiferromagnetic (AFM) layers.
Conflicting predictions have been made for the ground state of the SU(3) Heisenberg model on the honeycomb lattice: Tensor network simulations found a plaquette order [Zhao et al, Phys. Rev. B 85, 134416 (2012)], where singlets are formed on hexagons
, while linear flavor-wave theory (LFWT) suggested a dimerized, color ordered state [Lee and Yang, Phys. Rev. B 85, 100402 (2012)]. In this work we show that the former state is the true ground state by a systematic study with infinite projected-entangled pair states (iPEPS), for which the accuracy can be systematically controlled by the so-called bond dimension $D$. Both competing states can be reproduced with iPEPS by using different unit cell sizes. For small $D$ the dimer state has a lower variational energy than the plaquette state, however, for large $D$ it is the latter which becomes energetically favorable. The plaquette formation is also confirmed by exact diagonalizations and variational Monte Carlo studies, according to which both the dimerized and plaquette states are non-chiral flux states.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
