Magnetic ordering of itinerant systems ; the role of kinetic exchange interaction

نویسندگان

  • G. Górski
  • J. Mizia
چکیده

The possibility of ferromagnetic ordering is revisited in the band model. The coherent potential approximation decoupling has been used for the strong on-site Coulomb interaction. The driving forces towards the ferromagnetism are the on-site and inter-site molecular fields coming from different Coulomb interactions. Another driving force is the lowering of the kinetic energy with growing magnetic moment coming from the dependence of the hopping in-tegrals on occupation of the neighboring sites involved in hopping. This effect is described by the hopping interaction, ∆t , and by what we call the exchange-hopping interaction, t ex. The exchange-hopping interaction, which is the difference in hopping integrals for different occupation of neighboring lattice sites, acts in analogous way to the Hund's magnetic exchange interaction. The results are calculated for semi-elliptic density of states (DOS) and for the distorted semi-elliptic DOS with the maximum around the Fermi energy. They show a natural tendency towards the magnetic ordering at the end of the 3d row for the DOS with maximum density around the Fermi energy , when the hopping integrals grow with the occupation of the neighboring lattice sites.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Antiferromagnetic ordering of itinerant systems in modified mean-field theory

This is an analysis of the itinerant model for antiferromagnetism, in which is included both on-site and inter-site electron correlations. We also consider the band degeneration, which brings into the Hamiltonian the on-site exchange interactions. The Green function technique is used and the coherent potential approximation (CPA) decoupling for the on-site Coulomb repulsion. This decoupling com...

متن کامل

Study of the self-organization of spin-polarized atomic clusters on a solid rare gas surface

Exchange interaction is responsible for both covalent bonding and ferromagnetism in both localized and itinerant electron systems. Nevertheless, crystalline structures are not apparently affected by a change of electron magnetic state in most systems. In these systems, the exchange coupling constant J can be treated as constant to the first order during a magnetic transition. Coupling between t...

متن کامل

Pressure-tuned spin and charge ordering in an itinerant antiferromagnet.

Elemental chromium orders antiferromagnetically near room temperature, but the ordering temperature can be driven to zero by applying large pressures. We combine diamond anvil cell and synchrotron x-ray diffraction techniques to measure directly the spin and charge order in the pure metal at the approach to its quantum critical point. Both spin and charge order are suppressed exponentially with...

متن کامل

Non - Degenerate Ground State in the Antiferromagnetic Double - Exchange Model on a Triangular Lattice

In order to study effects of frustration in an itinerant electron system, we investigate ground states of the antiferromagnetic double-exchange model on a triangular lattice. In this model, pseudo-spins are coupled to electron transfer integrals in such a way that antiparallel configurations of pseudo-spins gain kinetic energies. Although the antiferromagnetic Ising model on a triangular lattic...

متن کامل

خواص الکتریکی و مغناطیسی ترکیب فرومغناطیس- ابررسانای Ru(Gd1.5-xPrx)Ce0.5Sr2Cu2O10-δ

  Coexistence of superconductivity and magnetic ordering or their mutually exclusive existence in solids is one of the fundamental problems of solid state physics. To determine the effect of Pr substitution for Gd on electrical and magnetic properties of RuGd1.5Ce0.5Sr2Cu2O10-δ (Ru-1222), Ru(Gd1.5-xPrx)Ce0.5Sr2Cu2O10-δ with x=0.0, 0.01, 0.03, 0.03 3 , 0.04, 0.05, 0.06, 0.1 have been prepared by...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2004