Next Article in Journal
Evolution of Hypoequilibrium States in Steepest Entropy Ascent Models for Nonequilibrium Quantum Thermodynamics
Previous Article in Journal
Security as a Natural Law: A Quantum-Inspired Hypothesis for Information Persistence
Previous Article in Special Issue
Open and Periodic Boundary Conditions in Statistical Mechanics: A Case Study of the Antiferromagnetic Ising Chain
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Exact Solution of the Glauber–Ising Model on the Finite-Length Semi-Open Chain

1
Laboratoire de Physique et Chimie Théoriques (CNRS UMR 7019), Université de Lorraine Nancy, P.O. Box 70239, F-54506 Vandœuvre-lès-Nancy, France
2
Centro de Física Teórica e Computacional, Universidade de Lisboa, Campo Grande, P-1749-016 Lisboa, Portugal
Entropy 2026, 28(7), 771; https://doi.org/10.3390/e28070771
Submission received: 15 June 2026 / Revised: 1 July 2026 / Accepted: 5 July 2026 / Published: 7 July 2026
(This article belongs to the Special Issue Ising Model—100 Years Old and Still Attractive)

Abstract

The exact time–space correlation function of the 1 D Glauber–Ising model, quenched to temperature T = 0 and on a semi-open lattice of finite size N, is obtained. This also enables deducing the exact empty-interval probability of the dual 1 D coagulation–diffusion process on a periodic finite ring and reproducing the long-time decay of the particle concentration. These results are consistent with the generic expectations of dynamical finite-size scaling theory.

1. Introduction

Physical ageing phenomena [1,2] may arise in a many-body system after a quench, typically from a disordered initial state, either onto a critical point where at least two physical phases become indistinguishable or else into a phase coexistence region where two macroscopic physical phases coexist. In both cases, the after-quench dynamics is a slow one, which may come from the effects of critical-point fluctuations or else from the competition between relaxation towards at least two distinct physical states. Microscopically, the system separates into many (correlated or ordered) clusters whose mean size ( t ) is growing with time. The phenomenology of physical ageing is contained in its three defining properties, namely [3]
1.
Slow dynamics (relaxations are slower than might be described by simple exponentials);
2.
Absence of time-translation invariance;
3.
Dynamical scaling.
  • These are reflected in the properties of the (coarse-grained) order parameter ϕ = ϕ ( t , r ) ), which depends on the time t and the space coordinates r . For a disordered initial state, the average order parameter vanishes, viz. ϕ ( t , r ) = 0 . One of the most frequently studied observables is the correlation function Its Fourier transform, the structure function, can be measured in scattering experiments.)
    C ( t ; r ) = ϕ ( t , r ) ϕ ( t , 0 ) = t b F C | r | t 1 / z
    whose scaling is specified here for an algebraically growing domain size ( t ) t 1 / z and then defines the dynamical exponent z . The exponent b is an ageing exponent, but in what follows we shall restrict ourselves to cases where b = 0 . For a non-conserved order parameter and short-ranged interactions, one has z = 2 [4,5,6]. (For a conserved order parameter, one speaks of phase separation and z takes different values [5,6]. Long-range interactions lead to further modifications [5,7,8,9,10,11].) Up to metric scale factors, the form of the scaling function F C is generically expected to be universal, hence independent of most of the ‘details’ of the underlying microscopic physics; see [4,12,13,14,15,16] for reviews. The theoretical task of finding the form of F C is also of practical importance since a priori knowledge of F C permits long-time predictions on the basis of short-time data.
The universality of functions such as F C permits their study via well-chosen and mathematically extremely simplified models. In this context, the celebrated 1 D  Ising model continues to play an important role. It is defined on a chain Λ Z with spin variables σ n = ± 1 attached to each of its sites. At equilibrium, it is specified through the Hamiltonian [17,18]
H = n Λ σ n σ n + 1
where the exchange coupling was normalized to unity. Because of its short-ranged interactions, in one dimension, there is no equilibrium phase transition at any non-vanishing temperature T > 0 [18]. We shall be interested here in some of its non-equilibrium dynamical properties (a slow Glauber–Ising dynamics in a ferrimagnetic chain made from Co+ ions and organic radical spins that are strongly antiferromagnetically coupled was studied experimentally, e.g., [19,20,21,22]). Such a dynamics, at temperature T, may be created in a heat-bath formulation by selecting randomly, at each time step Δ t , a site n Λ whose spin σ n is updated according to the Glauber rule [23], with the rate [24]
σ n ( t ) ± 1 with probability 1 2 1 ± tanh σ n 1 ( t ) + σ n + 1 ( t ) T
Clearly, the temperature T is a property of the heat bath. In one spatial dimension, Glauber’s rule has the remarkable and attractive feature that local spin-observables, such as local magnetization, local correlators and so on, satisfy closed equations of motion, which can be studied analytically, rather than infinite uncoupled hierarchies of equations of motion [25], which arise generically. Specifically, on a discrete chain, the single-time correlator is C n ( t ) : = σ n ( t ) σ 0 ( t ) , where the average is over the thermal histories defined by Equation (3). The correlator obeys the (rescaled) equation of motion [23,24,26,27,28], with the short-hand 0 γ = tanh ( 2 / T ) 1
t C n ( t ) = 2 C n ( t ) + γ C n 1 ( t ) + C n + 1 ( t ) when n 0 , C 0 ( t ) = 1
which only contains correlators C n ( t ) at different sites but does not contain any reference to higher multi-point correlators. For an initially disordered system, one has C n ( 0 ) = δ n , 0 [23,24].
Various aspects of this model have been thoroughly analyzed many times [23,24,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43], notably for T = 0 , where updates that would lead to an increase in H are forbidden. Because of the competition between the two stationary and absorbing states where all spins are either + 1 or 1 , the T = 0 -dynamics becomes slow and obeys dynamical scaling with the exponent z = 2 (a rigorous new bound on the spectral gap implies for all T T c the improved bound z 2 [44]). In doing so, a main issue is the appropriate treatment of the constraint C 0 ( t ) = 1 , which precludes the immediate application of Fourier series. A recently introduced possibility to treat this uses spatial symmetry properties [45,46], which provides a convenient way to treat the model in a finite and periodic lattice. Here we shall consider how to extend this idea to a chain that is open on one end (following an idea from [23]), find the exact correlation function in this case, and analyze how the finite-size effects will modify the scaling (1) of the infinite-size system, especially for a case when spatial translation invariance does not hold. This will also enable studying the influence of the boundary conditions on the form of the scaling function. One of the aims of this study is to provide an explicitly worked out case to serve as a background for more generic studies. One issue will be how to insert the results to be obtained in the context of finite-size scaling [47,48], especially for dynamics [49].
Another aspect of this problem arises from the link of the Glauber–Ising model with stochastic reaction–diffusion processes [50]. Here we shall focus on the 1 D coagulation–diffusion process, mainly studied via the so-called empty-interval method, e.g., [29,35,42,45,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68]. Each site of the lattice is either empty or occupied by a single particle A. Particles can randomly hop to a nearest-neighbor site, and, if that site already happens to be occupied, the two particles undergo, with probability one, a coagulation reaction A + A A . In one dimension, the particle concentration decays (For brief overviews on experimental results in 1 D we refer to [62,64] and Refs. therein.) for long times as c ( t ) t 1 / 2 [66], which makes it (i) a slow process (of which in principle the ageing can be analysed) with anomalous transport and (ii) is distinct from mean-field theories that hold for dimensions d > 2 and would give c MF ( t ) t 1 [13]. It is long established that this process is dual to the Glauber–Ising model at T = 0 [50,69]. We are interested in extending this to finite lattices with N sites. For technical simplicity, we shall admit a continuum limit throughout, which in principle holds for sufficiently large distances | x | = n a with respect to the lattice constant a . On finite systems, this continuum assumption will work for sufficiently large lattice sizes N that the large-distance limit mentioned above can sensibly be taken. As we shall show, the correlation function C ( t ; x ) on a semi-open lattice in the Glauber–Ising model corresponds to the empty-interval probability E ( t , x ) on a periodic ring in the diffusion–coagulation process, from which observables such as the concentration c ( t ) can be found.
This paper is organized as follows. Section 2 first recalls the treatment of a finite periodic chain in the Glauber–Ising model before the semi-open geometry is defined and then solved through an extension of the spatial symmetry method. We also discuss if/when a natural-looking short-cut towards the scaling function is applicable. In Section 3 we shall show that the correlation function C ( t ; x ) of the semi-open Glauber–Ising model can be reinterpreted as the empty-interval probability E ( t , x ) of diffusion–coagulation on a periodic ring. The conclusions are given in Section 4. Three appendices contain the technical details of the calculations.

2. Correlation Functions on a Finite Chain

We now describe the calculation of the spin correlation function, which will be conducted throughout in the continuum limit such that C n ( t ) C ( t ; x ) . We shall also restrict to T = 0 since this is the only situation where dynamical scaling holds and slow dynamics occurs.

2.1. Periodic Chain

We begin by recalling the result in the 1 D Glauber–Ising model on a periodic ring with N sites [46]. One purpose of this subsection is to briefly recall the technique we use here, and we shall emphasize later the differences with respect to the semi-open chain. In the continuum limit, one has from (4) for the correlation function C ( t ; x ) the following equation of motion, together with the boundary conditions
t C ( t ; x ) = x 2 C ( t ; x ) ; C ( t ; 0 ) = C ( t ; N ) = 1
and where 0 x N . The first of these constraints comes from the Ising constraint in (4) and the second one comes from the periodicity. Rather than dealing with these directly, we recognize first that the physical correlation function C ( t ; x ) is even in x. This means that we can restrict to positive values of x only such that C ( t ; x ) with negative spatial arguments becomes available for purely mathematical purposes. This permits treating the two constraints in (5) by using an analytic continuation to negative values of x. From now on, C ( t ; x ) will denote that analytically continued function. Only at the very end do we revert to the physical correlation function by making the substitution x | x | . The analytic continuation is expressed explicitly as follows [46]:
C ( t ; x ) = 2 C ( t ; x ) , C ( t ; x ) = C ( t ; N x ) C ( t ; x + 2 N ) = C ( t ; x )
Clearly, the spatial symmetries (6) reproduce the constraints in (5). Together, these can be shown to imply that the analytically continued function C ( t ; x ) is periodic in the spatial coordinate x, with period 2 N ; see (6). In this way, the physically motivated constraints are embedded into spatial symmetry properties of the analytically continued function C ( t ; x ) . Hence, for the analytically continued function, one has the Fourier series representation [70]
C ( t ; x ) = k = C ˜ ( t ; k ) e i π k x N , C ˜ ( t ; k ) = 1 2 N N N d x C ( t ; x ) e i π k x N
and now the equation of motion (5) can indeed be solved in Fourier space. A straightforward calculation leads, for the physical correlation function, to [46]
C ( t ; x ) = 1 2 N 0 N d x 2 ϑ 3 π 2 | x | + x N , e π 2 t / N 2 + C ( 0 ; x ) ϑ 3 π 2 | x | x N , e π 2 t / N 2 ϑ 3 π 2 | x | + x N , e π 2 t / N 2
where ϑ 3 is a Jacobi theta function [71]. It follows that both the physical constraints as well as the required periodicity properties (6) are indeed satisfied if they only hold for the initial correlator C ( 0 ; x ) . If the initial correlation function decays with x, for example, C ( 0 ; x ) | x | for large | x | and with > 0 , the term is irrelevant in the sense that it merely gives rise to corrections to the leading finite-size scaling limit behavior [26,46]. For example, for a fully disordered initial state with C ( 0 ; x ) δ ( x ) , this correction term in the second line of (8) vanishes. The finite-size scaling behavior is obtained by simultaneously taking the limits t , | x | and N but such that the (finite-size) scaling variables
u = | x | t 1 / 2 , v = N t 1 / 2
are kept finite. This scaling limit also arises naturally for a fully disordered initial state (In general, an initial correlator C ( 0 ; x ) in (8) breaks dynamical scaling.) where C ( 0 ; x ) δ ( x ) . Then one may re-cast the physical single-time correlator (1) as
C ( t ; x ) = F C per u , v = F C per | x | t , N t = 0 1 d u ϑ 3 π 2 u + π 2 | x | N , e π 2 t / N 2 = 1 2 π 0 | x | / N d v ϑ 2 π v , e 4 π 2 t / N 2
where ϑ 2 is another Jacobi theta function [71] that is distinct from ϑ 3 . This form is in generic agreement with the expectation of dynamical finite-size scaling [49]. The expression (10) gives the explicit finite-size scaling functions for the single-time correlator in terms of the finite-size scaling variables | x | / N and t / N 2 for a periodic chain of length N (The generic form is quite analogous to existing analytical results in the spherical model in 2 < d < 4 dimensions, with periodic boundary conditions and quenched to T < T c [72]; see the discussion in Section 2.2 below).

2.2. Semi-Open Chain

Our focus shall be on the semi-open chain; see Figure 1. In contrast to the periodic ring considered in Section 2.1, spatial translation invariance no longer holds true. In one spatial dimension, previous results with open boundary conditions include finite-size scaling studies on the critical relaxation times in the Glauber–Ising model [36] or on the particle density in asymmetric exclusion models via algebraic techniques, e.g., [42,73,74,75]. To our knowledge, this is the first study of finite-size scaling for free boundary conditions on time–space correlation functions in the Glauber–Ising model. In Figure 1, we indicate that the correlation function C n ( t ) = C n ( t ) should be considered as being of a central spin at fixed position n = 0 and another one n sites away. This is symmetric in n, and we can therefore consider n 0 without restriction on the generality (the only restriction we admit is that the site n = 0 is at the center of the interval [ N , N ] ). Then we can also speak of the correlation function C n ( t ) = σ 0 ( t ) σ n ( t ) between an Ising spin fixed at the leftmost edge of the interval [ 0 , N ] and another spin at site n to the right. We shall use this picture from now on. Specifically, consider that, at the leftmost edge, an Ising spin is fixed, and we look for the correlator C n ( t ) = σ 0 ( t ) σ n ( t ) with another spin at site n to the right. The chain is open at the right end because of the requirement C N ( t ) = 0 . In the continuum limit, we have (with 0 x < N )
t C ( t ; x ) = 1 2 x 2 C ( t ; x ) ; C ( t ; 0 ) = 1 , C ( t ; N ) = 0
Since the left spin is considered fixed, changes in C ( t ; x ) only arise from the motion of the right spin. This leads to a reduction in the diffusion constant by a factor 2 in comparison to the periodic case (5) where both spins are mobile (consideration of two mobile spins would require using correlators with two spatial variables, in the spirit of [57], but is beyond the scope of the present work). Rather than dealing with these two constraints directly, we shall implement them via spatial symmetries in an analytically continued function C ( t ; x ) in the same spirit as for the periodic case above. But, in contrast to Section 2.1, these conditions are chosen to be
C ( t ; x ) = 2 C ( t ; x ) , C ( t ; x ) = 1 x N + B ( t ; x )
The first of these solves the first constraint. From the definition (12) of the function B ( t ; x ) , the second constraint implies
B ( t ; ± N ) = B ( t ; 0 ) = 0
In addition, combination with the first property (12) proves that, on the interval [ N , N ] , the function B is anti-symmetric (as shown in Appendix A)
B ( t ; x ) = B ( t ; x )
Since B ( t ; ± N ) = 0 vanishes at the extremities of the interval [ N , N ] , it can be considered to be of spatial period 2 N (in spite of the absence of spatial translation invariance, we have satisfied once more the conditions for a Fourier analysis to be applicable [70] (Kap. 4)). Furthermore, it admits a Fourier representation
B ( t ; x ) = k = 1 b k ( t ) sin π N k x , b k ( t ) = 1 N N N d x B ( t ; x ) sin π N k x
which is the analogue of (7) above. Then the equation of motion (11) can be solved in Fourier space, and we find (see Appendix A for the details)
C ( t ; x ) = 1 0 | x | / N d u ϑ 3 π 2 u , e π 2 2 t N 2 + 1 2 N 0 N d x C ( 0 ; x ) ϑ 3 π 2 | x | x N , e π 2 2 t N 2 ϑ 3 π 2 | x | + x N , e π 2 2 t N 2
where finally the analytically continued function is reduced to the physical correlation function C ( t ; x ) by making at the very end the substitution x | x | . This gives the exact expression for the correlation function C ( t ; x ) between an Ising spin at the center of the open segment [ N , N ] and another spin at the position N x N subject to Glauber dynamics and such that the correlation function is forced to vanish C ( t ; ± N ) = 0 at the end of the segment; see Figure 1. Up to a trivial re-scaling in time (which comes from the rescaled equations of motion) the corrections to the leading scaling forms for both the periodic and semi-open lattices are the same. It follows that the discussion of the irrelevance of spatially decaying initial correlators can be taken over from the periodic case (8) in Section 2.1 and hence also holds for the semi-open chain. The leading scaling contributions can be cast into their final forms
C semi ( t ; x ) = 1 0 | x | / N d v ϑ 3 π 2 v , e π 2 2 t N 2
C per ( t ; x ) = 1 2 π 0 | x | / N d v ϑ 2 π v , e 4 π 2 t N 2
which depend on the finite-size scaling variables | x | / N and t / N 2 . They are both consistent with the generic expectations of dynamical finite-size scaling [49] in the sense that we can write the correlation functions (17) as C ( t ; x ; N ) = F C | x | t , N t , which generalizes (1), and where the universal scaling functions F C are boundary-condition-dependent. The existence of a second argument is the new feature of finite geometries.
Figure 2 illustrates these scaling functions: the semi-open correlator (17a) in Figure 2a and the periodic correlator (17b) in Figure 2b over against the finite-size scaling variable | x | / N . A common aspect is that the functional forms of these correlators not only depend on the second finite-size scaling variable N / t but on the boundary conditions as well. At first sight, their behavior is clearly quite distinct (notice that the qualitative shape of the curves in Figure 2b is similar to that found for the spherical model in 2 < d < 4 dimensions, quenched to temperature T < T c [72]). Upon closer inspection, it appears that the behavior of the semi-open correlator (17a) in the interval 0 | x | N 1 is quite analogous, although not identical, to the behavior of the periodic correlator (17b) in the interval 0 | x | N 1 2 (this also illustrates that the condition C ( t ; N ) = 0 does not eliminate the possibilities of short-range order, analogously to the periodic case). Here the distinct boundary conditions C semi ( t ; ± N ) = 0 and C per ( t ; ± N ) = 1 are of essential influence. For example, at x = N , the semi-open correlator vanishes exactly, whereas, in the periodic case, at x = 1 2 N , the correlator tends to zero exponentially fast with increasing N. On the other hand, if one considers, as in the inset of Figure 2a, the dependence of C ( t ; x ) on the bulk scaling variable x / t , the scaling functions are close to those of the spatially infinite system, viz. C semi ( t ; x ) = erfc | x | 2 t , if N / t is large enough (analogously, for periodic boundary conditions in the limit N / t , the curves converge towards the correlator C per ( t ; x ) = erfc | x | 2 t [31]. Conversely, if | x | N 1 , one finds a linear decay whose slope approaches that of the infinite-size system for sufficiently large N / t . Deviations from the infinite-size curve first become visible for large values of | x | t . Since the model is made from ‘hard’ Ising spins, one finds a cusp at x = 0 (see Figure 2), usually referred to as Porod’s law [4]. In contrast, such a cusp does not exist for ‘soft’ spins, as in, for example, the spherical model, where the correlator is rounded off at x = 0 ([72], Figure 1a).

2.3. A Short-Cut Towards Dynamical Scaling?

Given that scaling approaches often allow for a rapid and simple derivation of (universal) scaling functions, it is tempting to try such a scaling approach for the solution of the equation of motion (11) and with its associated boundary conditions. One might try one’s hand at a simple scaling ansatz of the form
C scal ( t ; x ) = F | x | t ; u = | x | t
which should hold in the scaling limit where simultaneously t , x but u is kept finite [76]. Inserting the ansatz into (11) readily gives the differential equation
F ( u ) + u F ( u ) = 0 F ( u ) = F 0 + F 1 0 u d u e u 2 / 2
and where the two constants F 0 , 1 are to be found from the boundary conditions F ( 0 ) = 1 and F ( N / t ) = 0 , implied by (11). This yields
C scal ( t ; x ) = 1 0 x / t d u e u 2 / 2 0 N / t d u e u 2 / 2 = 1 erf x 2 t erf N 2 t = erfc x 2 t erfc N 2 t 1 erfc N 2 t
where erf ( x ) is the error function [71] (7.1.1) and erfc ( x ) = 1 erf ( x ) is the complementary error function. Of course, such a scaling solution will be independent of any initial correlator C ( 0 ; x ) . Since, for large arguments erfc ( x ) x 0 that are exponentially fast [71], the solution (20) certainly has the attractive feature that, for N / t 1 , one recovers the exactly known scaling function C scal ( t ; x ) erfc x 2 t of the spatially infinite system [31]. We also observe that the final result (20) agrees once more with the generic expectations of dynamical finite-size scaling [49] since it depends on both variables x t and N t , although from the original ansatz (18) one might have expected a different result.
Does the approach leading to (20) represent a useful short-cut in order to obtain the exact physical correlation function? If that were so, comparison with the exact solution (17a) would imply the mathematical identity
f ( x , y ) : = erf x erf y = ? 0 x / y d u ϑ 3 π 2 u , e π 2 / 4 y 2 = 2 y π 0 x / y d u e y u 2 / 2 ϑ 3 i u y , e 4 y 2
where the last relation is a consequence of the modular transformation
ϑ 3 π u , e π t = t 1 / 2 exp π u 2 t ϑ 3 i π u t , e π / t
which follows from Poisson’s resummation formula [77,78] of the Jacobi theta function ϑ 3 π 2 u , q = ϑ 3 π 2 ( 2 u ) , q = k Z q k 2 cos ( π u k ) [71] (16.27.3).
In Figure 3 numerical tests of the conjectured relation (21) are shown. In the left panel, essentially the dependence on x of the function f ( x , y ) is displayed for several values of y. The full curves show the left-hand side of (21) as it follows from C scal , whereas the points show the right-hand side of (21) as it follows from C semi . Clearly, for sufficiently large y, excellent agreement is found and the points fall very nicely onto the full lines of the same color. However, when y 2 , notable deviations appear, which are particularly notable around y 1 . The right panel illustrates this further by showing f ( x , y ) as a function of y for several values of x / y . Again, for sufficiently large y, one observes very good agreement (the points fall clearly onto the full lines of the same color and deviations should be exponentially small), but C scal and C semi lead to different results for small values of y, which appears to be most strong around y 1 . The same effect can also be seen in Figure 2a, where the dashed gray lines give C scal ( t ; x ) for two values of N / t . For the larger one (blue curve), there is very good agreement with the exact result (17a). However, for the smaller one (green curve), deviations are notable, although the curves are qualitatively similar.
Hence the proposed identity (21) only holds approximately in the region y 2 . The intriguing and simple short-cut towards a finite-size scaling function only produces an approximate result, probably since the ansatz (18) merely depends on the single scaling variable u . Comparison with the exact result (17a) shows this to be an over-simplification [49]. Still, the quantitative agreement of the simple form (20) with the exact result (17a) is not so bad (see Figure 2a), and the simplicity of its derivation might become useful for a quick orientation in more complicated models. Implicitly, in the scaling approach described here, one has admitted that N / t 1 , but Figure 3 shows that the cross-over, when the length scale ( t ) t becomes comparable to N, is not completely captured.

3. Coagulation–Diffusion Process

The 1 D Glauber–Ising model at temperature T = 0 is dual [50,69] to the coagulation–diffusion process of particles of a single species A, and provided diffusion A + Ø D Ø + A and coagulation A + A D A + Ø , Ø + A occur with the same rate (if the rates are different, the universal long-time exponent c ( t ) t 1 / 2 is kept but the associated amplitude will be modified, e.g., [79]. This is in agreement with experimental results, e.g., [62] and Refs. therein). In the exact solution, a central quantity is the empty-interval probability E n ( t ) [45,52,55,56,57,60], which is the probability to find an interval of n subsequent empty sites. Under the stated conditions, E n ( t ) obeys a closed set of equations of motion. In the continuum limit, one rather deals with a function E ( t , x ) , which obeys the well-known equation of motion [35,53]
t E ( t , x ) = 2 D x 2 E ( t , x ) , E ( t , 0 ) = 1 , E ( t , N ) = 0
Herein, the last condition holds if the particles are moving on a ring of N sites. If initially there is at least one particle in the system, the last particle that has survived the coagulation reactions cannot decay because of the lack of a reaction partner. On a ring of N sites, the largest empty interval can have N 1 sites. The other constraint follows since only nearest-neighbor particles can undergo a coagulation reaction. In what follows, we shall always scale to D = 1 .
Clearly, the equations of motion (11) and (23), along with their constraints, are identical up to a trivial re-scaling t 4 t when going from the semi-open Glauber–Ising model to the coagulation–diffusion process. On a periodic ring of size N, the empty-interval probability can be read off from the previous discussion
E ( t , x ) = 1 0 x / N d u ϑ 3 π 2 u , e π 2 2 4 t N 2 + 1 2 N 0 N d x E ( 0 , x ) ϑ 3 π 2 x x N , e π 2 2 4 t N 2 ϑ 3 π 2 x + x N , e π 2 2 4 t N 2
This is the precise statement of the duality with Glauber–Ising chain mentioned in Section 1 for the case of finite chains with N sites. One of the quantities of interest is the time-dependent particle concentration, which follows directly once E ( t , x ) is known [35,53] and reads
c ( t ) = E ( t , x ) x x = 0 = 1 N ϑ 3 0 , e 2 π 2 t N 2 + 1 2 N 0 N d x E ( 0 , x ) x ϑ 3 π 2 x + x N , e 2 π 2 t / N 2 ϑ 3 π 2 x x N , e 2 π 2 t / N 2 x = 0
Herein, the first term does reproduce the well-known analytic result by Krebs et al. in their Equation (6.7) [60]. We point out that their result was derived on a discrete lattice (see their Equation (6.6) [60]) and a continuum limit was merely taken at the very end of their calculation (their solution also contains corrections to scaling that come from the discreteness of the lattice) [60]. This observation already serves as a useful cross-check of our calculational technique in Section 2.2, including the use of the continuum limit right from the beginning.
The empty-interval probability can be expressed as
E ( t , x ) = x N d x P ( t , x )
where P ( t , x ) = Pr x ; t is the probability to find an empty interval of size x bounded on the left by a particle. Carrying out the partial integration in (25) leads to a more compact expression for the time-dependent density (as derived in Appendix B)
c ( t ) = 0 1 d u P ( 0 , N u ) ϑ 3 π 2 u , e 2 π 2 t N 2
If initially the particles are uncorrelated and have the infinite-volume concentration c eq , the initial probabilities on a finite ring may be chosen as
P ( 0 , x ) = c eq e c eq x 1 e c eq N , E ( 0 , x ) = e c eq x e c eq N 1 e c eq N
The distribution E ( 0 , x ) obeys the two constraints (23), as it should. On a finite lattice of size N, c eq = c eq ( c 0 , N ) must be chosen such that the initial concentration indeed takes the desired value c 0 = c eq / ( 1 e c eq N ) , consistent with P ( 0 , 0 ) = c 0 . Physical arguments for this form for initially uncorrelated particles of concentration c 0 are recalled in Appendix C.
Alternatively, one may also start from the initial distribution [76]
P ( 0 , x ) = c 0 1 x N c 0 N 1 , E ( 0 , x ) = e c 0 N ln 1 x / N
which obeys the same boundary conditions as the choice (28). Then the concentration can be found via
c ( t ) = c 0 0 1 d u u c 0 N 1 ϑ 4 π 2 u , e 2 π 2 t N 2
with the theta function ϑ 4 [71]. The scaling solution (the leading part in (25)) implicitly starts with an initial value c 0 = 1 , and the modular transformation (22) produces the expected long-time decay c ( t ) 2 π t 1 / 2 . If an initial concentration c 0 < 1 is chosen, the concentration c ( t ) will initially decay more slowly than the scaling solution and will cross over to the scaling decay once the more rapidly decaying scaling solution has become close to it.
We have restricted attention here to the mere calculation of time-dependent concentrations c ( t ) . The study of many-point particle correlation functions requires the analysis of many-hole probabilities, e.g., following the lines of [45,56,57].

4. Conclusions

Even a century after its introduction [17,18], and after a long history of having fruitfully stimulated many different insights into phase transitions at and far from equilibrium (for historical reviews, see [80,81,82,83,84,85]), the “Ising model still thrives” [86]. We have studied some aspects of the celebrated Glauber–Ising dynamics [23], which in turn has become quite time-honored itself. The Glauber–Ising dynamics in 1 D is rightly famous since it is one of the rare cases where the usually infinite hierarchy of coupled equations of motion [25,87] naturally decouples and thus becomes available to methods of analytical study. This feature has furnished explicit examples in Ising model contexts for a long time.
In the continuum limit, time–space-dependent correlation functions C ( t ; x ) then obey simple diffusion equations but are still subject to boundary conditions, which prevent a totally straightforward solution, viz. in terms of Fourier analysis. Much of the body of work in the past decades has been on how to treat these. Our main innovation in this work has been to show how to use spatial symmetries to recast the problem into one where Fourier series methods can indeed be used and then to show how this applies in the case of non-periodic boundary conditions on finite lattices of size N. The results presented here can immediately be used as initial conditions for the calculation of two-time correlators and the exploration of novel finite-size effects therein [88,89]. We also hope that these techniques may become useful in different applications in the future, which may involve more general interactions, surface magnetic fields and/or more general boundary conditions. Similarly, in the related coagulation–diffusion process, it should be possible to consider particle currents at the boundaries [57] or to extend the techniques at hand towards the analysis of correlation functions. Again, the boundary conditions that arise in the equations of motion for the empty-interval probabilities E ( t , x ) were long considered so difficult that attention was shifted to other observables that are easier to analyze [35,53].
Explicit results were shown in Figure 2 and satisfactorily enter into the generic and expected context of dynamical finite-size scaling [49]. This also provided the opportunity to test a proposal for a short-cut towards the dynamical finite-size scaling functions, which, although not exact, still satisfy dynamical finite-size scaling and might become of heuristic value in more complicated systems. Numerical work will now be needed to further understand which aspects are specific to the 1 D Glauber–Ising dynamics and which ones permit further generalization. At the very least, our result should serve as a benchmark for future numerical studies. Long-standing relations with integrable quantum chains [29,42] point towards possible extensions regarding quantum dynamics [68,90,91].

Funding

This work was supported by the French ANR-PRME UNIOPEN (ANR-22-CE30-0004-01).

Data Availability Statement

No new data were created or analyzed in this study.

Acknowledgments

It is a pleasure to thank J.-Y. Fortin for useful discussions.

Conflicts of Interest

The author declare no conflicts of interest.

Appendix A. Finite-Size Correlation Function

Details of the derivation of the correlation function (16) are presented.
We start from the equation of motion (11) and its two accompanying constraints for the semi-open finite chain; see Figure 1. These are parameterized using (12). Combining these leads to the condition
1 x N + B ( t ; x ) = 2 1 x N + B ( t ; x )
which, upon simplification, produces the anti-symmetry condition (14). Hence the unknown function B ( t ; x ) is periodic on the interval [ N , N ] and can be cast into a Fourier series (14) [70]. This implies, for the Fourier coefficients b k ( t ) ,
t b k ( t ) = 1 2 π k N 2 b k ( t ) b k ( t ) = b k ( 0 ) exp 1 2 π k N 2 t
and furthermore the integral representation
B ( t ; x ) = 1 N N N d x B ( 0 ; x ) k = 1 exp 1 2 π k N 2 t sin π N k x sin π N k x
Since C ( t ; x ) = 1 x N + B ( t ; x ) , we find, for the analytically continued correlator,
C ( t ; x ) = 1 x N + 1 N N N d x C ( 0 ; x ) 1 + x N k = 1 e 1 2 π k N 2 t sin π N k x sin π N k x
Since the last factor is odd in x , the constant term in parentheses does not contribute to the integral. We then have the decomposition
C ( t ; x ) = 1 x N + 1 N 0 N d x C ( 0 ; x ) k = 1 e 1 2 π k N 2 t sin π N k x sin π N k x + 1 N 0 N d x C ( 0 ; x ) = 2 C ( 0 ; x ) k = 1 e 1 2 π k N 2 t sin π N k x sin π N k x + 1 N N N d x x N k = 1 e 1 2 π k N 2 t sin π N k x sin π N k x
= 1 x N 2 N 0 N d x k = 1 e 1 2 π k N 2 t sin π N k x sin π N k x 2 N 0 N d x C ( 0 ; x ) k = 1 e 1 2 π k N 2 t 1 2 cos π N ( x + x ) k cos π N ( x x ) k + 1 N N N d x x N k = 1 e 1 2 π k N 2 t sin π N k x sin π N k x
= : 1 x N + T 1 + T 2 + T 3
where the first continuation (12) is applied to the second line of (A5a) and [71] (4.3.31) was used in the second line of (A5b).
With the help of the identity
0 1 d u sin π k u = 0 ; k even 2 π k ; k odd
the first term in (A5c) becomes
T 1 = 2 N 0 N d x k = 1 e 1 2 π k N 2 t sin π N k x sin π N k x = 2 k = 1 e 1 2 π k N 2 t sin π N k x 0 1 d u sin π k u = 4 π k = 0 e π 2 t 2 N 2 2 k + 1 2 1 2 k + 1 sin π x N 2 k + 1
Next, the identity
1 1 d u u sin π k u = 2 π k ( 1 ) k
gives for the third term
T 3 = k = 1 e 1 2 π k N 2 t sin π N k x 1 N N N d x x N sin π N k x = k = 1 e π 2 t 2 N 2 k 2 2 π k ( 1 ) k sin π x N k
such that both terms together turn into
T 1 + T 3 = 4 π k = 0 e π 2 t 2 N 2 2 k + 1 2 1 2 k + 1 sin π x N 2 k + 1 2 π k = 1 e π 2 t 2 N 2 k 2 ( 1 ) k k sin π x N k = 4 π + 2 π k = 0 e π 2 t 2 N 2 2 k + 1 2 2 k + 1 sin π x N 2 k + 1 2 π k = 1 e π 2 t 2 N 2 2 k 2 2 k sin π x N 2 k = 2 π k = 1 e π 2 t 2 N 2 k 2 1 k sin π x N k
where, in the first line, the second sum is decomposed into odd and even integers, and, in the second line, a partial cancellation arises before the two sums can be gathered together again. With the identity 0 x d x cos π x N k = N π k sin π k N x , this becomes
T 1 + T 3 = 2 π π N 0 x d x k = 1 e π 2 t 2 N 2 k 2 cos π x N k = x N 1 N 0 x d x ϑ 3 π 2 x N , e π 2 2 N 2 t
and with the Jacobi theta function ϑ 3 [71] (16.27.3). This contribution is independent of the initial correlator. Finally, the second term
T 2 = 1 N 0 N d x C ( 0 ; x ) k = 1 e 1 2 π k N 2 t cos π N ( x + x ) k cos π N ( x x ) k = 1 2 N 0 N d x C ( 0 ; x ) ϑ 3 π 2 x + x N , e π 2 t / 2 N 2 ϑ 3 π 2 x x N , e π 2 t / 2 N 2
can be expressed in terms of the Jacobi theta function ϑ 3 as well. In particular, T 2 vanishes for an uncorrelated initial condition C ( 0 ; x ) δ ( x ) .
Insertion of the results (A9) and (A10) into (A5c) produces (16) in the text, where we also substituted x | x | in order to retrieve the physical correlation function.

Appendix B. Particle Density in the Coagulation–Diffusion Process

Equation (27) is derived. This is based on the known empty-interval probability (24) and the fact that the average time-dependent concentration can be found as the derivative c ( t ) = x E ( t , x ) x = 0 [53].
We begin by considering the contribution related to the initial probability in (24). Standard trigonometric identities give
x ϑ 3 π 2 x x N , e 2 π 2 t / N 2 ϑ 3 π 2 x + x N , e 2 π 2 t / N 2 x = 0 = 2 k = 1 e 2 π 2 t / N 2 k 2 x cos π N ( x x ) k cos π N ( x x ) k x = 0 = 4 k = 1 e 2 π 2 t / N 2 k 2 x sin π N x k sin π N x k x = 0 = 4 π N k = 1 e 2 π 2 t / N 2 k 2 k cos π N x k = 1 sin π N x k x = 0
This is then inserted into the calculation of the concentration
c ( t ) = E ( t , x ) x x = 0 = 1 N ϑ 3 0 , e 2 π 2 t / N 2 2 π N 2 0 N d x E ( 0 , x ) k = 1 e 2 π 2 t / N 2 k 2 k sin π N x k = 1 N ϑ 3 0 , e 2 π 2 t / N 2 + 2 N k = 1 e 2 π 2 t / N 2 k 2 0 N d x E ( 0 , x ) x cos π N x k = 1 N ϑ 3 0 , e 2 π 2 t / N 2 + 2 N k = 1 e 2 π 2 t / N 2 k 2 E ( 0 , x ) cos π N x k 0 N 0 N d x E ( 0 , x ) x cos π N x k
after a partial integration. With the boundary conditions E ( 0 , 0 ) = 1 , E ( 0 , N ) = 0 of the empty-interval probability, the concentration becomes
c ( t ) = 1 N ϑ 3 0 , e 2 π 2 t / N 2 + 2 N k = 1 e 2 π 2 t / N 2 k 2 1 0 N d x E ( 0 , x ) x cos π N x k = 1 N 1 + 2 k = 1 e 2 π 2 t / N 2 k 2 2 k = 1 e 2 π 2 t / N 2 k 2 1 N 0 N d x E ( 0 , x ) x 1 + 1 + 2 k = 1 e 2 π 2 t / N 2 k 2 cos π N x k = 1 N + 1 N 0 N d x E ( 0 , x ) x 1 N 0 N d x E ( 0 , x ) x ϑ 3 π 2 x N , e 2 π 2 t / N 2
To evaluate the second integral further, we recall that
E ( t , x ) = x N d x P ( t , x ) ; P ( t , x ) = Pr ( x ; t ) = probability of empty section of size x , bounded on the left by a particle
and hence P ( t , x ) = x E ( t , x ) . The usefulness of this quantity was pointed out by Durang et al. [45]. The first integral in (A13) is treated using the same boundary conditions as above. This finally implies
c ( t ) = 1 N + 1 N E ( 0 , N ) E ( 0 , 0 ) + 1 N 0 N d x P ( 0 , x ) ϑ 3 π 2 x N , e 2 π 2 t / N 2 = 1 N 0 N d x P ( 0 , x ) ϑ 3 π 2 x N , e 2 π 2 t / N 2
which is the assertion stated in the text.

Appendix C. Initial States in the Coagulation–Diffusion Process

Physical arguments to justify the use of Equation (28) are recalled.
This is done in the context of particles hopping freely on a lattice [53]. At equilibrium, one has a state of maximal entropy, and particle distribution is random (Poissonian). It may be described in terms of the so-called interparticle distribution function (ipdf) p eq ( x ) . A Poissonian distribution is exponential p eq ( x ) = c e c x [53] with the particle concentration c. On the other hand, for finite times t, the ipdf p ( t , x ) is related to the empty-interval probability E ( t , x ) , namely [35,53]
c ( t ) p ( t , x ) = 2 E ( t , x ) x 2 , P ( t , x ) = E ( t , x ) x = Pr ( x ; t )
where c ( t ) is the time-dependent concentration and P ( t , x ) the probability to find an empty interval of size x, bounded on the left by a particle. Clearly, c ( t ) p ( t , x ) = x P ( t , x ) .
If one has at equilibrium a Poissonian distribution, encoded via p eq ( x ) = c eq e c eq x , it is clear that P eq ( x ) = c eq e c eq x is Poissonian as well. For a spatially infinite system, which for large times relaxes towards equilibrium with c ( t ) c eq , one has
E ( , x ) = E eq ( x ) = x d x P eq ( x ) = x d x c eq e c eq x = e c eq x
reproducing the well-known form for independent particles of concentration 0 < c eq 1 [35,52].
On a finite chain of length L, at equilibrium, the ipdf is expected to be of the form
p eq ( x ) = p 0 c eq e c eq x
and should be normalized according to 0 L d x p eq ( x ) = ! 1 . This fixes p 0 such that
p eq ( x ) = c eq e c eq x 1 e c eq L = P eq ( x )
and hence
E eq ( x ) = x L d x P eq ( x ) = c eq 1 e c eq L x L d x e c eq x = e c eq x e c eq L 1 e c eq L
which is (28) in the text.
One may also obtain this form via reversible coagulation–decoagulation, which, besides single-particle diffusion A + Ø Ø + A , also contains the reversible reactions A + A A [55]. Therein, the empty-interval probability E ( t , x ) obeys the equation
t E ( t , x ) = 2 x 2 E ( t , x ) + v x E ( t , x )
with the decoagulation rate v. At equilibrium, one has E ( t , x ) t E eq ( x ) and t E eq ( x ) = 0 . With the boundary conditions E eq ( 0 ) = 1 and E eq ( L ) = 0 , one readily obtains [52,55]
E eq ( x ) = e v 2 x e v 2 L 1 e v 2 L
The state (28) may be achieved as follows: begin with the reversible coagulation–decoagulation process and relax it towards equilibrium, choosing v = v ( c 0 , L ) by solving c 0 = v 2 / 1 e v L / 2 for v to obtain the desired concentration c 0 ; see Figure A1. Having fixed this configuration, the rate v for decoagulation A 2 A is set to zero and the state (A22) so prepared is taken as the initial state, at time t = 0 , for the subsequent irreversible coagulation–diffusion process.
Alternatively, one may also consider the statistics of a hole of n sites on a lattice of size L. This leads to the initial configuration [76]
E ( 0 , x ) = E ( 0 , x ) = e c 0 N ln 1 x / N , P ( 0 , x ) = E ( 0 , x ) x = c 0 1 x N c 0 N 1
where c 0 = P ( 0 , 0 ) is the initial concentration. This satisfies the same boundary conditions as the initial configuration prepared above and is stated in (29) in the text.
Figure A1. Choice of the parameter v = v ( c 0 , L ) required for achieving the desired initial concentration c 0 for L = [ 4 , 8 , 16 ] from bottom to top.
Figure A1. Choice of the parameter v = v ( c 0 , L ) required for achieving the desired initial concentration c 0 for L = [ 4 , 8 , 16 ] from bottom to top.
Entropy 28 00771 g0a1

References

  1. Arceri, F.; Landes, F.P.; Berthier, L.; Biroli, G. A statistical mechanics perspective on glasses and ageing. In Encyclopedia of Complexity and Systems Science; Meyers, R.A., Ed.; Springer: Berlin/Heidelberg, Germany, 2021. [Google Scholar]
  2. Vincent, E. Spin glass experiments. In Encyclopedia of Condensed Matter Physics; Chakraborty, T., Ed.; Oxford University Press: Oxford, UK, 2024; Volume 2, pp. 371–387. [Google Scholar]
  3. Struik, L.C.E. Physical Ageing in Amorphous Polymers and Other Materials; Elsevier: Amsterdam, The Netherlands, 1978. [Google Scholar]
  4. Bray, A.J. Theory of phase-ordering kinetics. Adv. Phys. 1994, 43, 357. [Google Scholar] [CrossRef]
  5. Bray, A.J.; Rutenberg, A.D. Growth laws for phase ordering. Phys. Rev. 1994, E49, R27. [Google Scholar] [CrossRef]
  6. Rutenberg, A.D.; Bray, A.J. Energy-scaling approach to phase-ordering growth laws. Phys. Rev. E 1995, 51, 5499. [Google Scholar]
  7. Christiansen, H.; Majumder, S.; Henkel, M.; Janke, W. Ageing in the long-range Ising model. Phys. Rev. Lett. 2020, 125, 180601. [Google Scholar] [CrossRef] [PubMed]
  8. Christiansen, H.; Majumder, S.; Janke, W. Zero-temperature coarsening in the two-dimensional long-range Ising model. Phys. Rev. E 2021, 103, 052122. [Google Scholar] [PubMed]
  9. Corberi, F.; Lippiello, E.; Politi, P. One-dimensional phase-ordering in the Ising model with space-decaying interactions. J. Stat. Phys. 2019, 176, 510. [Google Scholar]
  10. Corberi, F.; Lippiello, E.; Politi, P. Universality in the time correlations of the long-range 1D Ising model. J. Stat. Mech. 2019, 2019, 074002. [Google Scholar] [CrossRef]
  11. Müller, F.; Christiansen, H.; Janke, W. Non-universality in ageing during phase-separation of the two-dimensional long-range Ising model. Phys. Rev. Lett. 2024, 133, 237102. [Google Scholar] [PubMed]
  12. Cugliandolo, L.F.; Barrat, J.-L.; Feiglman, M.; Kurchan, J.; Dalibard, J. (Eds.) Slow Relaxations and Non-Equilibrium Dynamics in Condensed Matter; Les Houches LXXVII; Springer: Berlin/Heidelberg, Germany, 2003; pp. 367–521. [Google Scholar]
  13. Henkel, M.; Hinrichsen, H.; Lübeck, S. Non-Equilibrium Phase Transitions Volume 1: Absorbing Phase Transitions; Springer: Berlin/Heidelberg, Germany, 2009. [Google Scholar]
  14. Henkel, M.; Pleimling, M. Non-Equilibrium Phase Transitions Volume 2: Ageing and Dynamical Scaling Far from Equilibrium; Springer: Berlin/Heidelberg, Germany, 2010. [Google Scholar]
  15. Puri, S.; Wadhawan, V. (Eds.) Kinetics of Phase Transitions; Taylor and Francis: London, UK, 2009. [Google Scholar]
  16. Täuber, U.C. Critical Dynamics: A Field-Theory Approach to Equilibrium and Non-Equilibrium Scaling Behaviour; Cambridge University Press: Cambridge, UK, 2014. [Google Scholar]
  17. Lenz, W. Beiträge zum Verständnis der magnetischen Eigenschaften in festen Körpern. Phys. Z. 1920, 21, 613. [Google Scholar]
  18. Ising, E. Beitrag zur Theorie des Ferromagnetismus. Z. Phys. 1925, 31, 253. [Google Scholar] [CrossRef]
  19. Caneschi, A.; Gatteschi, D.; Lalioti, N.; Sangregorio, C.; Sessoli, R.; Venturi, G.; Vindigni, A.; Rettori, A.; Pini, M.G.; Novak, M.A. Glauber slow dynamics of the magnetization in a molecular Ising chain. Europhys. Lett. 2002, 58, 771. [Google Scholar] [CrossRef]
  20. Ceglarska, M.; Böhme, M.; Neumann, T.; Plass, W.; Näther, C.; Rams, M. Magnetic investigations of monocrystalline [Co(NCS)2(L)2]n: New insights into single-chain relaxations. Phys. Chem. Chem. Phys. 2021, 23, 10281. [Google Scholar] [PubMed]
  21. Foltyn, M.; Pinkowicz, D.; Rams, M. Magnetic relaxation in a Co(II) based quasi-one dimensional Ising spin system. J. Mag. Mag. Mat. 2023, 584, 171069. [Google Scholar]
  22. Pini, M.G.; Rettori, A. Effect of antiferromagnetic exchange interactions on the Glauber dynamics of one-dimensional Ising models. Phys. Rev. B 2007, 76, 064407. [Google Scholar] [CrossRef]
  23. Glauber, R. Time-dependent statistics of the Ising model. J. Math. Phys. 1963, 4, 294. [Google Scholar] [CrossRef]
  24. Godrèche, C.; Luck, J.-M. Response of non-equilibrium systems at criticality: Exact results for the Glauber-Ising chain. J. Phys. A Math. Gen. 2000, 33, 1151. [Google Scholar]
  25. Kreuzer, H.J. Non-Equilibrium Thermodynamics and Its Statistical Foundations; Oxford University Press: Oxford, UK, 1986. [Google Scholar]
  26. Henkel, M.; Schütz, G.M. On the universality of the fluctuation-dissipation ratio in non-equilibrium critical dynamics. J. Phys. A Math. Gen. 2004, 37, 591. [Google Scholar]
  27. Lippiello, E.; Zannetti, M. Fluctuation dissipation ratio in the one-dimensional kinetic Ising model. Phys. Rev. E 2000, 61, 3369. [Google Scholar] [CrossRef]
  28. Mayer, P.; Sollich, P. General solution for multispin two-time correlation and response functions in the Glauber-Ising chain. J. Phys. A Math. Gen. 2004, 37, 9. [Google Scholar]
  29. Alcaraz, F.C.; Droz, M.; Henkel, M.; Rittenberg, V. Reaction-diffusion processes, critical dynamics and quantum chains. Ann. Phys. 1994, 230, 250. [Google Scholar] [CrossRef]
  30. Aliev, M.A. Generating function of spin correlations functions for kinetic Glauber-Ising model with time-dependent transition rates. J. Math. Phys. 2009, 50, 083302. [Google Scholar]
  31. Bray, A.J. Phase-ordering dynamics in one dimension. In Non-Equilibrium Statistical Mechanics in One Dimension; Privman, V., Ed.; Cambridge University Press: Cambridge, UK, 1997; pp. 143–165. [Google Scholar]
  32. Felderhof, B.U. Spin relaxation in the Ising chain. Rep. Math. Phys. 1971, 1, 215, Erratum in Rep. Math. Phys. 1971, 2, 151. [Google Scholar] [CrossRef]
  33. Godrèche, C. Dynamics of the directed Ising chain. J. Stat. Mech. 2011, 2011, P04005. [Google Scholar] [CrossRef]
  34. Godrèche, C.; Luck, J.-M. The Glauber-Ising chain under low-temperature protocols. J. Phys. A Math. Theor. 2022, 55, 495001. [Google Scholar]
  35. Krapivsky, P.L.; Redner, S.; Ben-Naim, E. A Kinetic View of Statistical Physics; Cambridge University Press: Cambridge, UK, 2010. [Google Scholar]
  36. Luscombe, J.H.; Luban, M.; Reynolds, J.P. Finite-size scaling of the Glauber model of critical dynamics. Phys. Rev. E 1996, 53, 5852. [Google Scholar] [CrossRef]
  37. Mayer, P.; Berthier, L.; Garrahan, J.P.; Sollich, P. Fluctuation-dissipation relations in the non-equilibrium critical dynamics of Ising models. Phys. Rev. E 2003, 68, 016116. [Google Scholar]
  38. Mayer, P.; Sollich, P.; Berthier, L.; Garrahan, J.P. Dynamic heterogeneity in the Glauber-Ising chain. J. Stat. Mech. 2005, 2005, P05002. [Google Scholar]
  39. Monthus, C.; Garel, T. Dynamics of Ising models near zero temperature: Real-space renormalization approach. J. Stat. Mech. 2013, 2013, P02037. [Google Scholar] [CrossRef][Green Version]
  40. Prados, A.; Brey, J.J.; Sánchez-Rey, B. Ageing in the one-dimensional Ising model with Glauber dynamics. Europhys. Lett. 1997, 40, 13. [Google Scholar] [CrossRef]
  41. Schütz, G.M.; Domany, E. Phase transitions in an exactly soluble one-dimensional exclusion process. J. Stat. Phys. 1993, 72, 277. [Google Scholar] [CrossRef]
  42. Schütz, G.M. Exactly solvable models for many-body systems far from equilibrium. In Phase Transitions and Critical Phenomena; Domb, C., Lebowitz, J.L., Eds.; Academic: London, UK, 2001; Volume 19, pp. 3–251. [Google Scholar]
  43. Verley, G.; Chétrite, R.; Lacoste, D. Modified fluctuation-dissipation theorem near non-equilibrium states and applications to the Glauber-Ising chain. J. Stat. Mech. 2011, 2011, P10025. [Google Scholar]
  44. Masaoka, R.; Soejima, T.; Watanabe, H. Rigorous lower bound of the dynamical critical exponent of the Ising model. J. Stat. Phys. 2025, 192, 76. [Google Scholar] [CrossRef]
  45. Durang, X.; Fortin, J.-Y.; del Biondo, D.; Henkel, M.; Richert, J. Exact correlations in the one-dimensional coagulation-diffusion process by the empty-interval method. J. Stat. Mech. 2010, 2010, P04002. [Google Scholar]
  46. Henkel, M. Finite-size scaling in the ageing dynamics of the 1D Glauber-Ising model. Entropy 2025, 27, 139. [Google Scholar] [PubMed]
  47. Fisher, M.E. The theory of critical-point singularities. In Critical Phenomena, Proceedings of the 51st International School of Physics “Enrico Fermi"; Green, M.S., Ed.; Academic Press: London, UK, 1971; p. 1. [Google Scholar]
  48. Barber, M.N. Finite-size scaling. In Phase Transitions and Critical Phenomena; Domb, C., Lebowitz, J.L., Eds.; Academic Press: London, UK, 1983; Volume 8, p. 146. [Google Scholar]
  49. Suzuki, M. Static and dynamic finite-size scaling theory based on the renormalization-group approach. Prog. Theor. Phys. 1977, 58, 1142. [Google Scholar]
  50. Siggia, E. Pseudospin formulation of kinetic Ising models. Phys. Rev. B 1977, 16, 2319. [Google Scholar] [CrossRef]
  51. Afzal, N.; Waugh, J.; Pleimling, M. Ageing processes in reversible reaction–diffusion systems: Monte Carlo simulations. J. Stat. Mech. 2011, 2011, P06006. [Google Scholar] [CrossRef]
  52. Ben Avraham, D.; Burschka, M.; Doering, C.R. Statics and dynamics of a diffusion-limited reaction: Anomalous kinetics, non-equilibrium self-ordering, and a dynamic transition. J. Stat. Phys. 1990, 60, 695. [Google Scholar]
  53. Ben Avraham, D.; Havlin, S. Diffusion and Reactions in Fractals and Disordered Systems; Cambridge University Press: Cambridge, UK, 2000. [Google Scholar]
  54. Crampé, N. Analytical results for a coagulation/decoagulation model on an inhomogeneous lattice. Sci. Post. Phys. 2017, 2, 006. [Google Scholar] [CrossRef][Green Version]
  55. Doering, C.R.; Burschka, M.A. Long crossover times in a finite system. Phys. Rev. Lett. 1990, 64, 245. [Google Scholar] [CrossRef] [PubMed]
  56. Durang, X.; Fortin, J.-Y.; Henkel, M. Exact two-time correlation and response functions in the one-dimensional coagulation-diffusion process by the empty-interval-particle method. J. Stat. Mech. 2011, P02030. [Google Scholar]
  57. Fortin, J.-Y. Crossover properties of a one-dimensional reaction-diffusion process with a transport current. J. Stat. Mech. 2014, 2014, P09033. [Google Scholar]
  58. Henkel, M.; Orlandini, E.; Schütz, G.M. Equivalences between stochastic systems. J. Phys. A Math. Theor. 1995, 28, 6335. [Google Scholar] [CrossRef]
  59. Hinrichsen, H.; Rittenberg, V.; Simon, H. Universality properties of the stationary states in the one-dimensional coagulation-diffusion model with external particle input. J. Stat. Phys. 1997, 86, 1023. [Google Scholar]
  60. Krebs, K.; Pfannmüller, M.P.; Wehefritz, B.; Hinrichsen, H. Finite-size scaling studies of one-dimensional reaction-diffusion systems. Part I. Analytical results. J. Stat. Phys. 1994, 78, 1429. [Google Scholar]
  61. Krebs, K.; Pfannmüller, M.P.; Simon, H.; Wehefritz, B. Finite-size scaling studies of one-dimensional reaction-diffusions systems. Part II. Numerical Methods. J. Stat. Phys. 1994, 78, 1471. [Google Scholar]
  62. Shapoval, D.; Dudka, M.; Durang, X.; Henkel, M. Crossover between diffusion-limited and reaction-limited regimes in the coagulation–diffusion process. J. Phys. A Math. Theor. 2018, 51, 425002. [Google Scholar]
  63. Fortin, J.-Y.; Durang, X.; Choi, M.Y. Limited coagulation-diffusion dynamics in inflating spaces. Eur. Phys. J. 2020, B93, 175. [Google Scholar]
  64. Li, R.; Ding, Q.; Cui, W. Scaling crossovers in non-equilibrium critical dynamics. J. Phys. A Math. Theor. 2025, 58, 385004. [Google Scholar] [CrossRef]
  65. Simon, H. Concentration for one and two-species one-dimensional reaction-diffusion systems. J. Phys. A Math. Theor. 1995, 28, 6585. [Google Scholar]
  66. Toussaint, D.; Wilczek, F. Particle-antiparticle annihilation in diffusive motion. J. Chem. Phys. 1983, 78, 2642. [Google Scholar]
  67. Turban, L.; Fortin, J.-Y. Reaction-diffusion on the fully-connected lattice. J. Phys. A Math. Theor. 2018, 51, 145001. [Google Scholar]
  68. Zahra, A.; Dubail, J.; Schütz, G.M. Emergent hydrodynamics in an exclusion-process with long-range interactions. Sci. Post. Phys. 2026, 20, 141. [Google Scholar]
  69. Santos, J.E. The duality relation between Glauber dynamics and the diffusion–annihilation model as a similarity transformation. J. Phys. A Math. Gen. 1997, 30, 3249. [Google Scholar]
  70. Hildebrand, S. Analysis 1, 2nd ed.; Springer: Berlin/Heidelberg, Germany, 2006. [Google Scholar]
  71. Abramowitz, M.; Stegun, I.A. Handbook of Mathematical Functions; Dover: New York, NY, USA, 1965. [Google Scholar]
  72. Henkel, M. Non-equilibrium relaxations: Ageing and finite-size effects. Condens. Matt. Phys. 2023, 26, 13501. [Google Scholar]
  73. Derrida, B.; Domany, E.; Mukamel, D. An exact solution of a one-dimensional asymmetric exclusion model with open boundaries. J. Stat. Phys. 1992, 69, 667. [Google Scholar] [CrossRef]
  74. Derrida, B.; Evans, M.R.; Hakim, V.; Pasquier, V. Exact solution of a 1D asymmetric exclusion model using a matrix formulation. J. Phys. A Math. Gen. 1993, 26, 1493. [Google Scholar] [CrossRef]
  75. Schütz, G.M. Dynamic matrix ansatz for integrable reaction-diffusion processes. Eur. Phys. J. B Condens. Matter Complex Syst. 1998, 5, 589. [Google Scholar] [CrossRef][Green Version]
  76. Fortin, J.-Y. (Laboratoire de Physique et Chimie Théoriques, University of Lorraine, Vandoeuvre-lès-Nancy, France). Personal communication, 2026.
  77. Itzykson, C.; Drouffe, J.-M. Théorie Statistique des Champs; InterEditions/Editionsdu CNRS: Paris, France, 1989; Volume 2. [Google Scholar]
  78. Itzykson, C.; Drouffe, J.-M. Statistical Field Theory; Cambridge University Press: Cambridge, UK, 1989; Volume 2. [Google Scholar]
  79. Ódor, G. Phase transition of the one-dimensional coagulation-production process. Phys. Rev. E 2001, 63, 067104. [Google Scholar]
  80. Berche, B.; Henkel, M.; Kenna, R. Fenômenos críticos: 150 anos desde Cagniard de la Tour. Rev. Bras. Ensino Física 2009, 31, 2602. [Google Scholar] [CrossRef]
  81. Berche, B.; Henkel, M.; Kenna, R. Critical phenomena: 150 years since Cagniard de la Tour. J. Phys. Stud. 2009, 13, 3201. [Google Scholar] [CrossRef]
  82. Folk, R. The survival of Ernst Ising and the struggle to solve his model. In Order, Disorder and Criticality; Holovatch, Y., Ed.; World Scientific: Singapore, 2023; Volume 7, pp. 1–77. [Google Scholar]
  83. Folk, R.; Berche, B.; Kenna, R.; Holovatch, Y. Ernst Ising’s Doctoral Thesis; World Scientific: Singapore, 2026. [Google Scholar]
  84. Girolami, G.S. A brief history of thermodynamics, as illustrated by books and people. J. Chem. Eng. Data 2020, 65, 298. [Google Scholar]
  85. Niss, M. History of the Lenz-Ising model 1920–1950: From ferromagnetic to cooperative phenomena. Arch. Hist. Exact. Sci. 2005, 59, 267. [Google Scholar]
  86. Fisher, M.E. Simple Ising models still thrive! Phys. A Stat. Mech. Its Appl. 1981, 106, 28. [Google Scholar] [CrossRef]
  87. Pottier, N. Physique Statistique hors D’équilibre; CNRS Éditions/EDP Sciences: Paris, France, 2007. [Google Scholar]
  88. Henkel, M. Physical ageing from generalised time-translation-invariance. Nucl. Phys. B 2025, 1017, 116968. [Google Scholar] [CrossRef]
  89. Warkotsch, D.; Janke, W.; Henkel, M. Harnessing finite-size effects to gauge ageing in the 2D Ising model. J. Stat. Mech. 2026; in press.
  90. Bouchoule, I.; Dubail, J. Une approche hydrodynamique pour décrire les gaz de bosons unidimensionnels. Comptes Rendus Phys. 2026, 27, 253. [Google Scholar]
  91. Malvania, N.; Zhang, Y.; Le, Y.; Dubail, J.; Rigol, M.; Weiss, D.S. Generalized hydrodynamics in strongly interacting 1D Bose gases. Science 2021, 373, 1129–1133. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Semi-open segment with N sites. On the left, an Ising spin is kept fixed and the time-dependent correlator C n ( t ) with another spin at site 0 < n < N is studied. The constraints C 0 ( t ) = 1 and C N ( t ) = 0 are applied.
Figure 1. Semi-open segment with N sites. On the left, an Ising spin is kept fixed and the time-dependent correlator C n ( t ) with another spin at site 0 < n < N is studied. The constraints C 0 ( t ) = 1 and C N ( t ) = 0 are applied.
Entropy 28 00771 g001
Figure 2. Finite-size scaling in the 1 D Glauber–Ising model at T = 0 on a finite chain for (a) semi-open and (b) periodic boundary conditions. The main plots display the dependence of the correlation function C ( t ; x ) on the finite-size scaling variable x / N for several fixed values of N / t . The inset in (a) shows the dependence of C ( t ; x ) on the bulk scaling variable x / t for the same values of N / t . The dotted line in the inset is the infinite-size correlation function C ( t ; x ) = erfc ( | x | / 2 t ) . The dashed gray lines in (a) give the approximate scaling function C scal ( t ; x ) according to (20).
Figure 2. Finite-size scaling in the 1 D Glauber–Ising model at T = 0 on a finite chain for (a) semi-open and (b) periodic boundary conditions. The main plots display the dependence of the correlation function C ( t ; x ) on the finite-size scaling variable x / N for several fixed values of N / t . The inset in (a) shows the dependence of C ( t ; x ) on the bulk scaling variable x / t for the same values of N / t . The dotted line in the inset is the infinite-size correlation function C ( t ; x ) = erfc ( | x | / 2 t ) . The dashed gray lines in (a) give the approximate scaling function C scal ( t ; x ) according to (20).
Entropy 28 00771 g002
Figure 3. Test of the identity (21), conjectured from the correlation scaling function of the finite-size semi-open 1 D Glauber–Ising model. Full curves come from the simplified scaling expression derived from C scal . Points are derived from the exact solution C semi . The (left) panel shows the dependence on x / y for several values of y. The (right) panel shows the dependence on y for several values of x / y .
Figure 3. Test of the identity (21), conjectured from the correlation scaling function of the finite-size semi-open 1 D Glauber–Ising model. Full curves come from the simplified scaling expression derived from C scal . Points are derived from the exact solution C semi . The (left) panel shows the dependence on x / y for several values of y. The (right) panel shows the dependence on y for several values of x / y .
Entropy 28 00771 g003
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Henkel, M. Exact Solution of the Glauber–Ising Model on the Finite-Length Semi-Open Chain. Entropy 2026, 28, 771. https://doi.org/10.3390/e28070771

AMA Style

Henkel M. Exact Solution of the Glauber–Ising Model on the Finite-Length Semi-Open Chain. Entropy. 2026; 28(7):771. https://doi.org/10.3390/e28070771

Chicago/Turabian Style

Henkel, Malte. 2026. "Exact Solution of the Glauber–Ising Model on the Finite-Length Semi-Open Chain" Entropy 28, no. 7: 771. https://doi.org/10.3390/e28070771

APA Style

Henkel, M. (2026). Exact Solution of the Glauber–Ising Model on the Finite-Length Semi-Open Chain. Entropy, 28(7), 771. https://doi.org/10.3390/e28070771

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop