Aging in the one-dimensional coagulation-diffusion process Xavier - - PowerPoint PPT Presentation

aging in the one dimensional coagulation diffusion process
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Aging in the one-dimensional coagulation-diffusion process Xavier - - PowerPoint PPT Presentation

Aging in the one-dimensional coagulation-diffusion process Xavier Durang , Jean Yves Fortin, Malte Henkel IJL, Universit e Henri Poincar e Nancy I XD, Fortin, Del Biondo, Henkel, Richert, J. Stat. Mech 2010 XD, Fortin, Henkel J. Stat. Mech


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Aging in the one-dimensional coagulation-diffusion process

Xavier Durang, Jean Yves Fortin, Malte Henkel

IJL, Universit´ e Henri Poincar´ e Nancy I

XD, Fortin, Del Biondo, Henkel, Richert, J. Stat. Mech 2010 XD, Fortin, Henkel J. Stat. Mech 2011

Dresden, MPI, LAFNES11

15 juillet 2011

Xavier Durang, Jean Yves Fortin, Malte Henkel

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Contents

1 Introduction

Ageing phenomena : from simple magnets to directed percolation Two-time observables, Fluctuation-Dissipation ratio Model

2 One-time quantities

Training example (Method used) Influence of the initial conditions

3 Two-time functions

Generalisation of the empty-interval method Ageing exponents

4 Fluctuation-dissipation ratio 5 Conclusion Xavier Durang, Jean Yves Fortin, Malte Henkel

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I.1 Ageing

Struik 1978

Three defining properties of ageing :

  • 1. observe slow relaxation after quenching PVC from melt to low T
  • 2. creep curves depend on waiting time te (or s) and creep time t
  • 3. find master curve for all (t, te) −

→ dynamical scaling

Quench

Constraint Measure s t time Xavier Durang, Jean Yves Fortin, Malte Henkel

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t = t1 t = t2 > t1

magnet T < Tc − → ordered cluster magnet T = Tc − → correlated cluster critical contact process

diffusion, A → 2A, A → φ

= ⇒ cluster dilution

voter model, contact process,. . .

Characteristic length scale : L(t) ∼ t1/z

Xavier Durang, Jean Yves Fortin, Malte Henkel

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I.2 Two-time observables

time-dependent order-parameter φ(t, r) (Directed percolation : φ =part. density) two-time correlator C(t, s) := φ(t, r)φ(s, r) − φ(t, r) φ(s, r) two-time response R(t, s) := δ φ(t, r) δh(s, r)

  • h=0

(Directed percolation : h(t) = creation of part.) t : observation time, s : waiting time Scaling regime : t ≫ s ≫ τmicro (For simple magnets) C(t, s) = s−bfC t s

  • , R(t, s) = s−1−afR

t s

  • Asymptotics : fC,R(y) ∼ y−λC,R/z for y ≫ 1

λC : autocorrelation exponent, λR : autoresponse exponent, z : dynamical exponent, a, b : ageing exponents

Xavier Durang, Jean Yves Fortin, Malte Henkel

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I.3 Fluctuation dissipation ratio

Usually λR = λC

The fluctuation-dissipation ratio (fdr)

Cugliandolo, Kurchan, Parisi ’94

X(t, s) := TR(t, s) ∂C(t, s)/∂s X∞ = lim

s→∞

  • lim

t→∞ X(t, s)

  • Godr`

eche & Luck 00

measures the distance to the equilibrium : Xeq = X(t − s) = 1. a = b valid when systems satisfy detailed balance Contact process 1 + a = b : ⇐ = rapidity-reversal symmetry of stationary state

  • f cp ⇒ specific property !

= ⇒ try new form of FDR !

Enss et. al. 04

Ξ(t, s) := R(t, s) C(t, s) = fR(t/s) fC(t/s) , Ξ∞ := lim

s→∞

  • lim

t→∞ Ξ(t, s)

  • Universality of Ξ∞ proven to one-loop order.

Baumann & Gambassi 07 Xavier Durang, Jean Yves Fortin, Malte Henkel

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I.4 Coagulation-diffusion process

AIM : to test these scaling predictions on an exactly solvable model without detailed balance Model : One dimensional lattice of spacing a

D D Coagulation Diffusion

(diffusion and coagulation can occur in both directions) Space translation invariance Absence of detailed balance Absorbing phase Stationary state

Xavier Durang, Jean Yves Fortin, Malte Henkel

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II.1 Empty interval method : training example

Particle concentration : c(t) = Pr({•; t})

  • D. ben Avraham et al. 90

n empty sites

En(t) : time-dependent probability of having an interval of n consecutive empty sites at time t c(t) = E1(t) − E0(t) continuum limit (x=na) − → c(t) = − ∂xE(x, t)|x=0 Equation of motion For n > 1 ∂tEn(t) = (2D/a2) (En−1 − 2En + En+1) For n = 1 ∂tE1(t) = (2D/a2)

  • 1 − 2E1(t) + E2(t)
  • This gives the constraint : E0(t) = 1

Equation of motion in the continuum limit (x = na) ∂tE(x, t) = 2D∂xxE(x, t), and E(0, t) = 1.

Xavier Durang, Jean Yves Fortin, Malte Henkel

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II.2 Solution by analytical continuation

Assume that the differential equation is valid for n ≤ 0 E(x, t) = ∞

−∞

dx′ √πℓ0 exp

  • − 1

ℓ02 (x − x′)2 E(x′, 0). where ℓ0 is the scaling length ℓ0 := √ 8Dt . Take into account the constraint : E0(t) = 1. For n = 0 ∂tE0(t) = (2D/a2) (E−1 − 2E0 + E1) = 0 E−1(t) = 2E0(t) − E1(t) = 2 − E1(t) Redefine the meaning of E(n, 0) for negative n such that E−n(t) = 2 − En(t) and E(−x, t) = 2 − E(x, t)

Xavier Durang, Jean Yves Fortin, Malte Henkel

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II.3 General expression for the particle concentration

One-empty-interval probability E(x, t) = erfc(x/ℓ0) + +∞ dx′ √πℓ0 E(x′, 0)

  • e

1 ℓ02 (x−x′)2

− e

1 ℓ02 (x+x′)2

. Hierarchy Particle concentration c(t) = 2 √πℓ0

  • 1 −

∞ dxE(xℓ0, 0)2xe−x2 c(t) = 2 √πℓ0 + o(1/ℓ0) ∼ t−1/2 Independent of initial condition → very well known result

Xavier Durang, Jean Yves Fortin, Malte Henkel

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  • II. 4 One-time Correlation funtion

Connected correlator : C(d, t) = Pr(• d •, t) − Pr(•, t)Pr(•, t) Two-interval probability

n d m

En1,n2,d(t) : time-dependent probability of having two intervals of n1 and n2 consecutive empty sites distant from d at time t Continuum limit (x = n1a, y = n2a, z = da) C(z, t) = ∂2

xyE(x, y, z, t)

  • x=0,y=0 − ∂xE(x, t)|x=0 ∂yE(y, t)|y=0

Xavier Durang, Jean Yves Fortin, Malte Henkel

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II.5 One-time correlation function

Equation of motion : (only for x, y and z positive) ∂tE(x, y, z, t) = 2D

  • ∂2

x + ∂2 y + ∂2 z −

  • ∂x∂z + ∂y∂z
  • E(x, y, z, t)

with compatibility conditions (ex : E(x, 0, d, t) = E(x, t)). Decomposition of the solution as a sum of three terms : E(x, y, z, t) = E (0)(x, y, z, t) + E (1)(x, y, z, t) + E (2)(x, y, z, t)

1

E (0)(x, y, z, t) is independent of the initial conditions

2

E (1)(x, y, z, t) depends on the initial one-interval probability

3

E (2)(x, y, z, t) depends on the initial two-intervals probability

→ System initially filled with particles

E(x, y, z; t) = E (0)(x, y, z, t) = erfc x ℓ0

  • erfc

y ℓ0

  • +erfc

z ℓ0

  • erfc

x + y + z ℓ0

  • − erfc

x + z ℓ0

  • erfc

y + z ℓ0

  • Xavier Durang, Jean Yves Fortin, Malte Henkel
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II.6 One-time correlation function

Correlation function C(z, t) = ∂2

xyE(x, y, z, t)

  • x=0,y=0 − ∂xE(x, t)|x=0 ∂yE(y, t)|y=0

In the case of an initially completely filled system, E(x, 0) = 0 and E(x, y, z, 0) = 0, we obtain dynamical scaling with ℓ0 = √ 8Dt. Connected correlator C(z, t) =

  • 2

√πℓ0 2 f (z/ℓ0) with f (y) = −e−2y2 + √πye−y2erfc(y)

  • D. ben Avraham, 1998

exact in asymptotic regime for all initial conditions.

Xavier Durang, Jean Yves Fortin, Malte Henkel

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II.7 Correction to the leading behaviour

Time evolution of C(z; t) for an initial one-interval probability E(x; 0) = exp(−x) and z = 1/2

10 100

t

0,01 0,1

  • C(z=1/2,t)

C

(0)(z,t)

C

(0)(z,t)+C (1)(z,t)

C

(0)(z,t)+C (1)(z,t)+C (2)(z,t)

Full black solid line : leading contribution Algebraic behaviour when t large |C(z, t)| ∼ t−1. Red dashed line includes the effect of one-interval contribution Dashed-dotted line includes all contributions

Hierarchy :

  • C (0)(1/2, t)
  • C (1)(1/2, t)
  • C (2)(1/2, t)
  • Xavier Durang, Jean Yves Fortin, Malte Henkel
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III.1 Two-times functions

We want to evaluate connected correlation C(z; t, s) and response R(z; t, s) functions (t ≥ s) using the interval probability method In the discrete space, their definition are C(d; t, s) = Pr({•; t} d {•; s}) − Pr(•; t)Pr(•; s) If we add a particle at a given site at time s : R(d; t, s) = Pr({•; t} d {•; s}) − Pr(•; t) = δ φ(t, r) δh(s, r)

  • h=0

φ = part. density and h(t) = creation of part.

n d

Mixed-interval probability F(n, d; t, s) = Pr({ n ; t} d {•; s})

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.2 Mixed-interval probability

Two-time correlation C(z; t, s) = lim

a→0

C(d; t, s) a = −∂xF(x, z; t, s)|x=0 ∼ 1/L2 Two-time response, G has the same definition than F R(z; t, s) = lim

a→0

R(d; t, s) a = −∂xG(x, z; t, s)|x=0 ∼ 1/L Initial conditions at t = s F(x, z; s, s) = lim

a→0

1 aF(n, d; s, s) = −∂yE(x, y, z; s)|y=0 G(x, z; s, s) = lim

a→0 G(n, d; s, s) = E(x; s)

F and G are different because of their initial conditions at t = s

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.3 Equation of motion

In the continuum limit and for x and z positive variables ∂tF(x, z; t, s) = 2D

  • ∂2

x + 1

2∂2

z − ∂x∂z

  • F(x, z; t, s)

Symmetries between positive and negative variables F(−x < 0, z; s, s) = 2c0(s) − F(x, z − x; s, s) F(x, −z < 0; s, s) = θ(z − x)F(x, z − x; s, s)) F(−x < 0, −z < 0; s, s) = 2c0(s) − F(x, z; s, s) with c0(s) = c(s) for F and c0(s) = 1 for G

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.4 Response function

Expression for an initially filled system

R(z; t, s) = 2 πℓ1ℓ0

  • R+ dx′
  • erfc

x′ − 2z ℓ1

  • + erfc

x′ + 2z ℓ1

  • exp
  • − x′2(ℓ2

0 + ℓ2 1)

ℓ2

0ℓ2 1

  • + 2

πℓ2

1

e−2z2/ℓ2

1

  • R+ dx′
  • exp
  • − 2(z − x′)2

ℓ2

1

  • + exp
  • − 2(z + x′)2

ℓ2

1

  • erfc

x′ ℓ0

2 √πℓ0

Analogous expression for the correlation function but much more lengthy.

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.5 Response function

Discrete numerical simulations on a chain of 512 sites with s = 10 and D = 1/2 versus analytical expressions

10 100 1000 t 0,0001 0,001 0,01 0,1 1 R(t,s;r) s=10 100 t 0,001 0,01 0,1 1 t s=100

Full line : analytical solution ; symbols : simulation r = [0, 1, 2, 3] from top to bottom

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.6 Auto-correlator and auto-response

Autocorrelator

y = t/s C(ys, s) = 4 πℓ2

  • 1
  • y 2 − 1

+

  • 2(y − 1)

π(1 + y) tan−1

2 √y − 1

2 π√y tan−1 1 √y

1 1 + y

  • := 1

s fC(y) = 1 sb fC(y)

in agreement with P.Mayer and P. Sollich 2007

Autoresponse

R(ys, s) = 2 √πℓ0

2 π√y − 1 tan−1

2 √y − 1

2 π√y tan−1 1 √y

  • := 1

√s fR(y) = 1 s1+a fR(y)

Exponents λC = λR = 4, a = −1/2 and b = 1

Xavier Durang, Jean Yves Fortin, Malte Henkel

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IV.1 Fluctuation-dissipation ratio

Question What’s the relation between R and C ? a = b detailed balance → Usual definition of the fluctuation-dissipation ratio X(t, s) = TR(t, s) ∂sC(t, s)

L.F. Cugliandolo and al. 1994

1 + a = b directed percolation → Ξ(t, s) := R(t, s) C(t, s) = fR(t/s) fC(t/s) , Ξ∞ := lim

s→∞

  • lim

t→∞ Ξ(t, s)

  • here b = 1 and a = −1/2 → 3/2 + a = b, therefore we define

another ratio Ξ(t, s) = R(t, s) √ 8D∂s−1/2C(t, s)

Xavier Durang, Jean Yves Fortin, Malte Henkel

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IV.2 New forms of fluctuation-dissipation relations ?

Return to the non-equilibrium scaling forms

C(t, s) = L(s)−bzFC t s

  • = s−bfC

t s

  • R(t, s)

= L(s)−az−zFR t s

  • = s−1−afR

t s

  • time-dependent length scale :

L(s) = (ϑs)1/z

Xavier Durang, Jean Yves Fortin, Malte Henkel

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IV.3 Generalisation ?

Ξ(t, s) := ϑ1+a−b R(t, s) ∂1+a−b

s

C(t, s) use Riemann-Liouville fractional derivative ∂α

s

ϑ−1 is a characteristic time for the passage into the scaling behaviour. contains two situations :

1

critical systems with detailed balance (a = b holds true and ϑ → T becomes the equilibrium temperature)

2

critical particle-reaction models with a + 1 = b

in the limit y = t/s ≫ 1, the function Ξ tends towards an universal limit Ξ∞. for the coagulation diffusion process : Ξ∞ =

3π 6π−16

Xavier Durang, Jean Yves Fortin, Malte Henkel

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Conclusion

Ageing in the 1D coagulation-diffusion process quite analogous to what have been seen in simple magnets Exactly solvable model allow us to verify the expected scaling forms Tool : generalized empty interval method We find the one-time and two-time correlation functions for any given initial conditions Proposal of a new FDR Physical meaning of Ξ ?

Xavier Durang, Jean Yves Fortin, Malte Henkel

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Xavier Durang, Jean Yves Fortin, Malte Henkel

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Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.3 Quantum representation

Empty site |0 >i= 1

  • Filled site |1 >i=

1

  • Operators of creation and destruction

d†

i =

1 1

  • , di =

1

  • di|0 >i= 0, di|1 >i= |0 >i, d†

i |0 >i= |1 >i, d† i |1 >i= |1 >i

Particle number operator ni = d†

i di and hole operator

hi = 1 − ni Initial state : |P(0) >=

  • {αi=0,1}

P({αi}, t = 0) ⊗i |αi > Ground state : < G| = ⊗i{ 1

1

  • }

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.4 Quantum representation

Hamiltonian H = −Γ

  • i
  • d†

i+1di + d† i−1di

  • + µ
  • i

ni µ = 2Γ is the chemical potential such that < G|H = 0 and P(t) =< G|P(t) >= 1 Empty-interval operator X(1, n) :=

  • i=1,n

(1 − ni) =

  • i=1,n

hi. Mixed function is represented by the expectation value G(n, d; t, s) =< G|X(1, n)e−H(t−s)d†

n+d+1e−Hs|P(0) >

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.3 Equations of motion

Same equation for F and G ∂tF(n, d; t, s) = Γ [F(n + 1, d; t, s) + F(n + 1, d − 1; t, s) + F(n − 1, d; t, s) + F(n − 1, d + 1; t, s) − 4F(n, d; t, s)] In the continuum limit ∂tF(x, z; t, s) = 2D

  • ∂2

x + 1

2∂2

z − ∂x∂z

  • F(x, z; t, s)

General solution F(x, z; t, s) =

  • R2

2dx′dz′ πℓ2

1

Wℓ1(x − x′, z − z′)F(x′, z′; s, s), Wℓ1(x − x′, z − z′) = e

− 2

ℓ2 1 [(x−x′+z−z′)2−(z−z′)2]

with ℓ1 =

  • 8D(t − s) and ℓ0 =

√ 8Ds

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.4 Symmetries

We have to rewrite the former integrals in terms of physical domain (x > 0, z > 0) We obtain, using the constraints imposed by the differential equation of motion F(−x < 0, z; s, s) = 2c0(s) − F(x, z − x; s, s) F(x, −z < 0; s, s) = θ(z − x)F(x, z − x; s, s)) F(−x < 0, −z < 0; s, s) = 2c0(s) − F(x, z; s, s) with c0(s) = c(s) for F and c0(s) = 1 for G

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.8 Correlation function

Discrete numerical simulations on a chain of 512 sites with s = 10 and D = 1/2 versus analytical expressions

100 1000 t 0,0001 0,001 0,01 0,1 s=100 10 100 1000 t 0,0001 0,001 0,01 0,1 C(t,s;r) s=10

The full line are the analytical solution while the symbols are the simulations Black curves are z = 0 and red curves are for z = 3

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.9 Response function

Expression for an initially filled system

R(z; t, s) = 2 πℓ1ℓ0

  • R+ dx′
  • erfc

x′ − 2z ℓ1

  • + erfc

x′ + 2z ℓ1

  • exp
  • − x′2(ℓ2

0 + ℓ2 1)

ℓ2

0ℓ2 1

  • + 2

πℓ2

1

e−2z2/ℓ2

1

  • R+ dx′
  • exp
  • − 2(z − x′)2

ℓ2

1

  • + exp
  • − 2(z + x′)2

ℓ2

1

  • erfc

x′ ℓ0

2 √πℓ0

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.12 Auto-correlation and auto-response functions

C(0; t, s) = C(t, s) = 1 sb fC(y = t/s) := 1 s fC(y = t/s) R(0; t, s) = R(t, s) = 1 s1+a fR(y = t/s) := 1 √s fR(y = t/s) Asymptotically fC(y) ≃ (2D)−1 (1 − 8/(3π))π−1y−2 + ( 16

5 π − 1/2)π−1y−3

which gives the exponent λC = 4. Asymptotically fR(y) ≃ (2D)−1/2 4

3π−3/2y−2 + 8 15π−3/2y−3

which gives the exponent λR = 4.

Xavier Durang, Jean Yves Fortin, Malte Henkel

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III.13 Asymptotic behavior

fC behaves asymptotically like fC(y) ≃ (2D)−1

  • (1 − 8/(3π))π−1y−2 + (16

5 π − 1/2)π−1y−3

  • with the dynamical exponent z = 2, which gives the exponent

λC = 4. fR behaves asymptotically like fR(y) ≃ (2D)−1/2 4 3π−3/2y−2 + 8 15π−3/2y−3

  • which gives the exponent λR = 4

Xavier Durang, Jean Yves Fortin, Malte Henkel

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IV.4 Behaviour of Ξ(t, s) for the coagulation-diffusion process

1 10 100 1000

t/s

~ 3.307 3 2 3.5 2.5

Ξ(t,s)

The behaviour is not monotonous while in models such that a + 1 = b or a = b it seems to be generically the case.

Xavier Durang, Jean Yves Fortin, Malte Henkel

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IV.3 Model with a + 3/2 = b (Coagulation-diffusion)

We use the Riemann representation for fractional derivatives with negative arguments ∂−ν ∂s−ν ϕ(s) = 1 Γ(ν) s (s − u)ν−1ϕ(u) du Asymptotic limits when t ≫ s ≫ 1 C(t, s) ≃ aC t−2s and R(t, s) ≃ aR t−2s3/2 with aC = (2D)−1(3π − 8)/3π−2 and aR = (2D)−1/24/3π−3/2 then the FDR in the asymptotic limit t ≫ s ≫ 1 reads X∞ = lim

y≫1 X(t, s) =

3π 6π − 16 ≃ 3.307

Xavier Durang, Jean Yves Fortin, Malte Henkel

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IV.2 Models

model reactions Diffusion nmax BCPD A → 2A A → ∅ diffusion ∞ BCPL A → 2A A → ∅ L´ evy flight ∞ FA A → 2A 2A → A none 1 contact process A → 2A A → ∅ diffusion 1 NEKIM 2A → ∅ A ↔ 3A diffusion 1

Xavier Durang, Jean Yves Fortin, Malte Henkel

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model d b, a Ξ∞ Ref. BCPD > 0 b = a 1/2

  • F. Baumann

BCPL > 0 b = a 1/2

  • X. Durang

FA 1 b = a −3π/(6π − 16)

  • P. Mayer

contact process 1 b = 1 + a 1.15(5) (directed perco.) 4 − ε b = 1 + a 2 − ε( 119

240 − π2 60 )

  • F. Baumann

NEKIM 1 b = 1 + a ≈ 0.1

  • G. Odor

coag.-diff. 1 b = 3/2 + a 3π/(6π − 16) this work

Xavier Durang, Jean Yves Fortin, Malte Henkel

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Models with a = b contains critical systems with detailed balance (FA model) in systems without detailed balance, we use X(t, s) = R(s, s) ∂sC(s, s) −1 R(t, s) ∂sC(t, s) = X t s

→ X∞ since there is no longer reference to an equilibrium temperature Models with 1 + a = b Limit value Ξ∞ is directly universal since the dependence one the scale ϑ drops out In the stationary state, one has Ξ−1

stat = 0

In the directed percolation class, the universality of Ξ∞ has been proven to one-loop order.

  • F. Baumann and al. 2007

Xavier Durang, Jean Yves Fortin, Malte Henkel