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Pair Contact Process withDiffusion
Uwe Tauber, Olivier Deloubriere and Frederic van Wijland
Department of Physics, Virginia Polytechnic Institute and State University,Blacksburg, Virginia, USA.
ITF, Utrecht ; LPT, Orsay and Pole Matiere et Systemes Complexes, ParisVII.
1Non-Equilibrium Statistical Physics in Low Dimensions and Reaction Diffusion Sys-tems, Dresden, 22/09/2003 – 10/10/2003
Outline
•Motivations
•PCPD (definition, known facts)
•State of the art
•Systematic study of fluctuations (technical)
•Consequences for the critical behavior
•Other processes
Phase transitions in NonEquilibrium Steady-States
•Understanding NESS
•Long-range order without macroscopic currents
•Universality
•Absence of rationalized classification
Absorbing State Transitions
•A particular subclass
•Transition from an active state to a frozen state (possibly degenerate)
•Specific analytical and numerical difficulties
•Experimental issue
Pair Contact Process with Diffusion
•Contact ProcessA → 2A, A → ∅
with exclusion, without diffusion;
•Pair Contact Process
2A → 3A, 2A → ∅
with exclusion, without diffusion;
•�
�
�
�Pair Contact Process with Diffusion
2Aλ→ 3A, 2A
k→ ∅
with exclusion, with diffusion;
•Higher order processes
•Coupling to conserved modes
Known analytical facts about the PCPD
•Mean-field equation of the local density field ρ(x, t) = 〈nA(x, t)〉:
∂tρ = D∆xρ − 2kρ2 + λρ2(1 − ρ)︸ ︷︷ ︸
λρ2−λ′ρ3
•Predicted phase diagram
•For k ≥ kc the system falls into an absorbing, particle-free, state.
•For k < kc it reaches a stationary nonzero density
ρ(∞) =λ − 2k
λ′∼ ∆β , ∆ = kc − k
•At k = kc,
ρ(t) =1√2λ′t
∼ t−δ
•Relaxation to the absorbing state is as 1/t
•Relaxation to the active state is exponentially fast, with typical timeτ ∼ ∆−2.
•Correlation length in the active phase is ξ ∼ τ 1/2.
•β = 1, δ = 1/2, ν = 1 and z = 2.
•�
�
�
�Keep in mind the λ′ dependence.
Relevant questions
•Upper critical dimension above which mean-field is valid
•Critical properties below dc
– .New universality class?
– .or known one, like the contact process or the parity conservingone.
– .Understanding why simulations are difficult.
Answers from the simulation experts in d = 2
•G. Odor, M.C. Marques and M.A. Santos (2002): Effective exponentδ
0.48 ≤ δ ≤ 0.55
depending on the diffusion constant.
•H. Chate (2003): Again a slightly faster-than-mean-field decay atcriticality.
•Similar behavior for P. Grassberger (19??).
• Probably mean-field with strong corrections. Hints at dc = 2.
Answers from the simulation experts in d = 1
•Odor, Chate, Kockelkoren: There is an independent universality classwith δ = 0.20.
•Carlon, Barkema: This is the Directed Percolation (or Contact Pro-cess) class.
•All: z ' 1.7 � 2.
•All: Absorbing phase follows A + A → ∅ kinetics. There is an entirecritical line.
•Barkema, Chate: The density of p-uplets scales with time as theparticle density.
•Dornic, Chate: Anticorrelations, which are present in the absorbingphase do not survive up to the critical point.
Analytic strategies
•Howard, Tauber: without mutual exclusion of particles there is nei-ther a critical point (see poster by Paessens and Schutz) nor a steady-state and there are an infinite number of generated vertices;
•Hinrichsen: Phenomenological Langevin equations for ρ(x, t). Doesthis exist? How to choose the noise?
∂tρ = ∆ρ + (λ − 2k)ρ2 − λ′ρ3 + η
〈η(x, t)η(x′, t′)〉 = ...ρ2δ(t − t′)δ(d)(x − x′)
Master equation
•P (n = {ni}, t) is the probability to observe the microscopic config-uration of occupation numbers n.
•|Ψ〉 ≡ ∑
n P (n, t)|n〉.
•Master equation
∂tP (n) =∑
n′
W (n′ → n)P (n′) −∑
n′
W (n → n′)P (n)
is equivalent tod|Ψ〉dt
= −H|Ψ〉
with appropriately chosen H.
• Examples:
Hannihilation = k∑
x
(a†2
x − 1)a2
x
Bosonic field theory with built-in exclusion
• H may evolve only |0〉 or |1〉 states.
• Spin chain formulation not convenient when nonintegrable (all phasetransitions in d ≥ 1, all in d ≥ 2).
• Incorporate exclusion at least for the branching process:
i
Ai+1
Ai+2
∅ →i
Ai+1
Ai+2
A
H = λ[
1 − a†i+2δni+2,0 − δni+2,0ai+2
]
δni,1δni+1,1δni+2,0
• Exact mapping to a field theory: normal order, replace creation a†x
and annihilation ax operators by fields a(x, t) and a(x, t).
Interaction vertices (bare action)
branching and exclusion
branching
annihilation and branching
Bubbles everywhere
=
a2a5
•Problem: all branching processes
2A → (n + 2)A, n ≥ 1
are wildly generated;
•Big problem: all of them are equally relevant;
•Renormalizable theory?
+
+ +...
= + +
u3
2
u1u2u3
u2
2u2
u2
u3u1
Simple functional RG
• Write the action in the form
Sinteraction =
∫
∑
n≥1
unana2 +∑
n≥1
vnana3
• Identify dc = 2 as the upper critical dimension, and set ε = 2 − d.
• Microscopic couplings are
u1 = 2k − λ, u2 = k − 2λ
• DefineU(x) =
∑
n≥1
unxn
V (x) =∑
n≥1
vnxn (irrelevant)
• Sit at space scale e` and define scale-dependent couplings:
U(x, `) =∑
n≥1
un(`)xn
• Sit at space scale e` and define scale-dependent couplings:
U(x, `) =∑
n≥1
un(`)xn
•�
�
�
�Beautiful miracle
∂`U = εU − 1
2U∂2
xU
with ε = 2 − d.
•Neither the field nor the diffusion constant pick up any anomalousdimension.
Analysis of the flow
• Fixed function is
G∗(x) = ∆x + εx2, ∆ = a constant
• Effective action at the fixed point is
S =
∫[∆aa2 + εa2a2
]
• Problem: such an effective action does not yield the expected phasediagram.
•�
�
�
�Do not throw all irrelevant couplings
• Keep those that are responsible for producing a nontrivial phasediagram.
A dangerously irrelevant coupling
•RG irrelevance is not synonymous for physical irrelevance.
•To one-loop,
∂`V = (−2 + 2ε)V − 1
2∂2
xV U − 3
2V ∂2
xU
•Among the infinite number of couplings flowing to 0 only one reallymatters.
•The v1(0) = λ′ eventually flows to zero as
v1(`) ∝ exp(y`), y = −2 − ε + 3 ln4
3ε2 + O(ε2)
•Find the effective equation of state at scale e` with v1 and solve it.
Critical behavior of the PCPD near dc = 2
• Critical exponents:
δ =1
2− 3
4ε2 +
3
4ln
4
3ε2 + O(ε3)
β = 1 − 2ε + O(ε2)
ν = 1 +1
2ε + O(ε2)
• But there are two results valid to all orders in ε:
z = 2, η = 0
and a hyperscaling relation
β =2δ
d − 2δ
• Relaxation to the absorbing state follows the annihilation kinetics(as t−d/2).
PCPD at the upper dc
• Logarithmic corrections in every corner.
• Active phase:
ρ(t → ∞) ∼ ∆ ln2 ∆, ξ ∼ 1
∆ ln1/2 ∆
• Critical point:
ρ(t) ∼ ln3/2 t
t1/2
• Relaxation to the absorbing state:
ρ(t) ∼ ln t
t
Critical comments
• Do the initial conditions lie in the basin of attraction of our fixedpoint?
• Couplings eventually responsible for anticorrelations starts in a pos-itive correlation region.
• Weird things happening at finite ε? Note the bad convergence ofthe ε expansion. Or is it just bad luck?
Comparison with numerical results
•Agreement that dc = 2.
•But the faster-than-mean-field decay in d = 2 is a sign that asymp-totics might not be reached.
•Needless to say both exact results on the exponents disagree withexisting simulations.
•Anticorrelations at variance with the clustering observed in all simu-lations.
Triplet Contact Process with Diffusion
•Triplets involved:
3Aλ→ 4A, 3A
k→ ∅with exclusion, with diffusion;
•dc = 1,
ρ(t) ∼ ln4/3 t
t1/3
•Quite consistent with δ = 0.27 in Kockelkoren-Chate’s simulations.is mean-field in d = 1.
•Similar but higher order processes are mean-field down to d = 1.
Conserved Pair Contact Process with Diffusion
• Idea: introduce an auxiliary species tuned to ensure conservation ofparticles. For instance
2A + Bλ→ 3A, 2A
k→ 2B
• The auxiliary species may be diffusing (faster or slower than theorder parameter) or static.
• Number of accessible absorbing states may become infinite.
• First order transition for DA < DB .
• Discrepancies with simulations expected to be even stronger, but forDA > DB ≥ 0 all exponents are known exactly
d ≤ 2, δ =d
4, z = 2
Final comments
•Approaching a complete classification of absorbing phase transitions.
•Hope to bring some measurable quantities in d = 2 and a couple ofexact results in d = 1 or 2.
•Numerical issue.