MARGINAL FERMI LIQUID IN STRONGLY CORRELATED SPIN SYSTEMS

1994 ◽  
Vol 08 (14n15) ◽  
pp. 859-869
Author(s):  
A. P. PROTOGENOV ◽  
D. A. RYNDYK
Keyword(s):  
Excitation Spectrum ◽  
Fermi Liquid ◽  
Degrees Of Freedom ◽  
Chemical Potential ◽  
Collective Excitation ◽  
Spin Systems ◽  
Strongly Correlated ◽  
Band Center ◽  
Marginal Fermi Liquid ◽  
Self Consistent

We consider the consequences of the separation of spin and charge degrees of freedom in 2 + 1 D strongly correlated spin systems. Self-consistent spin and charge motions induced by doping in sites of ground and dual lattices form such a spectrum of quasiparticles which together with the dispersionless character of the collective excitation spectrum and the chemical potential pinning in the band center yield the necessary behavior to support the theory of marginal Fermi liquid formulated by C. M. Varma et al. (Phys. Rev. Lett.63, 1996 (1989)).

scholarly journals A Segregated Approach for Modeling the Electrochemistry in the 3-D Microstructure of Li-Ion Batteries and Its Acceleration Using Block Preconditioners

2021 ◽  
Vol 86 (3) ◽  
Author(s):  
Jeffery M. Allen ◽  
Justin Chang ◽  
Francois L. E. Usseglio-Viretta ◽  
Peter Graf ◽  
Kandler Smith
Keyword(s):  
Degrees Of Freedom ◽  
Electrode Materials ◽  
Lithium Ion ◽  
Automotive Application ◽  
System Of Equations ◽  
Strongly Correlated ◽  
Electrolyte Depletion ◽  
Li Ion ◽  
Block Preconditioners ◽  
Electrochemical Model

AbstractBattery performance is strongly correlated with electrode microstructure. Electrode materials for lithium-ion batteries have complex microstructure geometries that require millions of degrees of freedom to solve the electrochemical system at the microstructure scale. A fast-iterative solver with an appropriate preconditioner is then required to simulate large representative volume in a reasonable time. In this work, a finite element electrochemical model is developed to resolve the concentration and potential within the electrode active materials and the electrolyte domains at the microstructure scale, with an emphasis on numerical stability and scaling performances. The block Gauss-Seidel (BGS) numerical method is implemented because the system of equations within the electrodes is coupled only through the nonlinear Butler–Volmer equation, which governs the electrochemical reaction at the interface between the domains. The best solution strategy found in this work consists of splitting the system into two blocks—one for the concentration and one for the potential field—and then performing block generalized minimal residual preconditioned with algebraic multigrid, using the FEniCS and the Portable, Extensible Toolkit for Scientific Computation libraries. Significant improvements in terms of time to solution (six times faster) and memory usage (halving) are achieved compared with the MUltifrontal Massively Parallel sparse direct Solver. Additionally, BGS experiences decent strong parallel scaling within the electrode domains. Last, the system of equations is modified to specifically address numerical instability induced by electrolyte depletion, which is particularly valuable for simulating fast-charge scenarios relevant for automotive application.

scholarly journals Complex Langevin calculations in QCD at finite density

2020 ◽  
Vol 2020 (10) ◽  
Author(s):  
Yuta Ito ◽  
Hideo Matsufuru ◽  
Yusuke Namekawa ◽  
Jun Nishimura ◽  
Shinji Shimasaki ◽  
...  
Keyword(s):  
Degrees Of Freedom ◽  
Chemical Potential ◽  
Expansion Method ◽  
Finite Density ◽  
Fermi Sphere ◽  
Expectation Value ◽  
Sign Problem ◽  
Zero Momentum ◽  
Effective Theories ◽  
Severe Sign

Abstract We demonstrate that the complex Langevin method (CLM) enables calculations in QCD at finite density in a parameter regime in which conventional methods, such as the density of states method and the Taylor expansion method, are not applicable due to the severe sign problem. Here we use the plaquette gauge action with β = 5.7 and four-flavor staggered fermions with degenerate quark mass ma = 0.01 and nonzero quark chemical potential μ. We confirm that a sufficient condition for correct convergence is satisfied for μ/T = 5.2 − 7.2 on a 83 × 16 lattice and μ/T = 1.6 − 9.6 on a 163 × 32 lattice. In particular, the expectation value of the quark number is found to have a plateau with respect to μ with the height of 24 for both lattices. This plateau can be understood from the Fermi distribution of quarks, and its height coincides with the degrees of freedom of a single quark with zero momentum, which is 3 (color) × 4 (flavor) × 2 (spin) = 24. Our results may be viewed as the first step towards the formation of the Fermi sphere, which plays a crucial role in color superconductivity conjectured from effective theories.

scholarly journals Chemical potential and quantum Hall ferromagnetism in bilayer graphene

Science ◽  
2014 ◽  
Vol 345 (6192) ◽  
pp. 58-61 ◽  
Author(s):  
Kayoung Lee ◽  
Babak Fallahazad ◽  
Jiamin Xue ◽  
David C. Dillen ◽  
Kyounghwan Kim ◽  
...  
Keyword(s):  
Degrees Of Freedom ◽  
Chemical Potential ◽  
Hexagonal Boron Nitride ◽  
Quantum Hall ◽  
Bilayer Graphene ◽  
Zero Magnetic Field ◽  
High Magnetic Fields ◽  
Complex Interplay ◽  
Electron Hole ◽  
Quantum Hall State

Bilayer graphene has a distinctive electronic structure influenced by a complex interplay between various degrees of freedom. We probed its chemical potential using double bilayer graphene heterostructures, separated by a hexagonal boron nitride dielectric. The chemical potential has a nonlinear carrier density dependence and bears signatures of electron-electron interactions. The data allowed a direct measurement of the electric field–induced bandgap at zero magnetic field, the orbital Landau level (LL) energies, and the broken-symmetry quantum Hall state gaps at high magnetic fields. We observe spin-to-valley polarized transitions for all half-filled LLs, as well as emerging phases at filling factors ν = 0 and ν = ±2. Furthermore, the data reveal interaction-driven negative compressibility and electron-hole asymmetry in N = 0, 1 LLs.

A DOMAIN MODEL OF CUPRATES

1994 ◽  
Vol 08 (22) ◽  
pp. 3083-3094 ◽  
Author(s):  
V. DALLACASA
Keyword(s):  
Fermi Liquid ◽  
Characteristic Length ◽  
Domain Model ◽  
Linear Temperature Dependence ◽  
Arbitrary Length ◽  
Linear Temperature ◽  
Bcs Model ◽  
Marginal Fermi Liquid ◽  
System Length ◽  
Enhanced Superconductivity

We have investigated the occurrence of superconductivity in a Fermi liquid of finite volume, under the assumption of a sharp surface, by solving numerically (at arbitrary length) and analytically (at the smallest lengths) the Cooper–BCS model. We find that this model can predict enhanced superconductivity with respect to the bulk BCS model when the system length L ≪ L0, in which L0 is a characteristic length. Under the same conditions the normal state is found to behave anomalously with respect to the conventional Fermi liquid, with a linear temperature dependence of the resistivity and marginal Fermi liquid properties. The results are used to implement a domain model of high T c superconductors.

scholarly journals Self-Consistent Calculation of Particle-Hole Diagrams on the Matsubara Frequency: Flex Approximation

1997 ◽  
Vol 08 (05) ◽  
pp. 1145-1158
Author(s):  
J. J. Rodríguez-Núñez ◽  
S. Schafroth
Keyword(s):  
Hubbard Model ◽  
Imaginary Part ◽  
Chemical Potential ◽  
Order Approximation ◽  
The Self ◽  
Green Functions ◽  
Matsubara Frequency ◽  
Self Energy ◽  
Peak Structure ◽  
Self Consistent

We implement the numerical method of summing Green function diagrams on the Matsubara frequency axis for the fluctuation exchange (FLEX) approximation. Our method has previously been applied to the attractive Hubbard model for low density. Here we apply our numerical algorithm to the Hubbard model close to half filling (ρ =0.40), and for T/t = 0.03, in order to study the dynamics of one- and two-particle Green functions. For the values of the chosen parameters we see the formation of three branches which we associate with the two-peak structure in the imaginary part of the self-energy. From the imaginary part of the self-energy we conclude that our system is a Fermi liquid (for the temperature investigated here), since Im Σ( k , ω) ≈ w2 around the chemical potential. We have compared our fully self-consistent FLEX solutions with a lower order approximation where the internal Green functions are approximated by free Green functions. These two approches, i.e., the fully self-consistent and the non-self-consistent ones give different results for the parameters considered here. However, they have similar global results for small densities.

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