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Collective diffusion of the interacting surface gas

Collective diffusion of the interacting surface gas. M agdalena Załuska-Kotur Institute of Physics, Polish Academy of Sciences. Random walk. Diffusion coefficient D. Collective diffusion. + mass conservation. local density. Equilibrium distribution. c – microstate. Local density.

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Collective diffusion of the interacting surface gas

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  1. Collective diffusion ofthe interactingsurface gas MagdalenaZałuska-Kotur Institute of Physics, Polish Academy of Sciences

  2. Random walk Diffusion coefficientD

  3. Collective diffusion + mass conservation local density

  4. Equilibrium distribution c – microstate Local density The model –noninteractinglattice gas

  5. Noninteracting system single particle result

  6. Single particlediffusion – noninteracting gas. for small k Do=Wa2

  7. Interacting particles

  8. Interacting particles –2D system with repulsive interactions J’=3/4J Square lattice

  9. Questions • How diffusion depends on interactions? • How minima of the density-diffusion plot are related to the phase diagram? • Where are phase transition points? • Are there some other characteristic points?

  10. Example - hexagonal lattice - repulsion kT=0.25J kT=0.5J kT=J

  11. J’=2J Attraction J<0 T=0.89Tc Tc=1.8|J|/k J’=J J’=0 J’=J J>0 J’=2J Repulsion J=0

  12. Experimental results - Pb/Cu(100)

  13. Simulation methods • Harmonic density perturbation • Step profile decay

  14. kT=0.25J kT=0.5J kT=J

  15. Profile evolution Boltzmann –Matano method

  16. Definition of transitionrates

  17. The model Equilibrium distribution c – microstate Detailed balance condition

  18. Possible approaches - QCA Hierarchy of equations

  19. X Analysis of microscopic equations. Local density X L - lattice sites + periodic boundary conditions

  20. For N=2 when reference particle jumps =1 otherwise Fourier transformation of master equation.

  21. Eigenvalue of matrix M Approximation: Eigenvalue Limit

  22. one interaction constant J x - number of bonds Approximate eigenvector for interacting gas

  23. ( ) Definition of transition rates in 1D system Possible transitions

  24. Diffusion coefficient of 1D system Grand canonical regime Low temperature approximation

  25. Diffusion coefficient - repulsive interactions p=2,10,100

  26. Diffusion coefficient - repulsive - QCA p=2,10,100

  27. Activation energy –repulsive interactions

  28. Diffusion coefficient - attractive interactions p=0.5,0.3,0.1

  29. Diffusion coefficient - attractive QCA p=0.5,0.3,0.1

  30. Activation energy – attractive interactions

  31. Eigenvector for random state Initial configuration

  32. Repulsive far from equilibrium case θ ν p=100 θ

  33. J’ J 2x2 ordering –definition of transitionrates M. A. Załuska-Kotur Z.W.Gortel – to be published

  34. Equilibrium probability strong repulsion Diagonal matrix

  35. * * Components of eigenvector Primary configurations: Secondary configurations (average of neighbouring primary ones):

  36. Result Upper line: Lower line:

  37. J’=3/4J Ordered phase

  38. Other parameters – kT/J=0.3

  39. Otherparameters – kT/J’=0.4

  40. Other parameters – J’=0

  41. Summary • New approach to the collective diffusion problem, based on many-body function description– analytic theory. • Exact solution for noninteracting system. • Collective diffusion in 1D system with nearest neighbor attractive and repulsiveinteractions. • Diffusion coefficient in 2D lattice gas of2X2 ordered phase with repulsive forces. • Agrement with numerical results • Numerical approaches: step density profile evolution and harmonic density perturbation decay methods

  42. Possible applications Analysis of • Far from equlibrium systems. • More complex interactions – long range • Surfaces with steps • Phase transitions

  43. J’=2J J=J’ J’=2J J=0

  44. j x i Jak dyfuzja zależy od oddziaływań? Gaz cząstek na dwuwymiarowej sieci Szybkość przeskoków jednocząstkowych Einit,(i)- lokalna energia jednocząstkowa Ebar (ij) - energia cząstki w punkcie siodłowym

  45. Analysis of microscopic equations. Local density

  46. 1D -- z=2 for small k Do=Wa2

  47. = n1 –n2 Calculation for s clusters Y: Łukasz Badowski, M. A. Załuska-Kotur – to be published

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