Open Access Article
Sarafa A. Iyaniwura
a,
Mingfeng Qiu
b and
Zhiwei Peng
*c
aVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington 98109, USA. E-mail: iyaniwura@aims.ac.za
bSchool of Mathematics and Statistics, University of Canterbury, Christchurch 8140, New Zealand. E-mail: mingfeng.qiu@canterbury.ac.nz
cDepartment of Chemical and Materials Engineering, University of Alberta, Edmonton, Alberta T6G 1H9, Canada. E-mail: zhiwei.peng@ualberta.ca
First published on 15th June 2026
Chiral active Brownian particles (CABPs) are self-propelled agents with intrinsic rotational dynamics, giving rise to circular trajectories commonly observed in biological and synthetic microswimmers. Understanding how CABPs explore confined environments and locate targets is crucial for characterizing transport, search efficiency, and reaction processes in physical and biological systems. We study the escape dynamics of CABPs from one- and two-dimensional confined domains. In one dimension, we consider intervals with either two absorbing boundaries or a reflecting boundary on one side and an absorbing boundary on the other, and derive closed-form asymptotic solutions in the high-chirality regime, revealing the quantitative scaling of the mean first passage time (MFPT) as a function of particle rotation speed (chirality). In two dimensions, we analyze escape from a disk containing one absorbing arc or two symmetric absorbing arcs. By numerically solving the governing partial differential equations, we compute the MFPT for CABPs to escape the domains as a function of the particle's initial orientation, self-propulsion speed, angular velocity, and domain geometry. Our results show that, depending on the parameters and geometry, the MFPT can exhibit non-monotonic behavior as a function of chirality. A minimal escape time exists at an intermediate value of chirality, where the rotational time scale balances the active swimming time scale, redirecting a particle towards the exit which would otherwise be blocked due to unfavorable initial orientation. Our work offers a comprehensive characterization of CABP escape dynamics in canonical confinements and identifies chirality as a key control parameter for transport and search in confined physical and biological systems.
CABPs can be used as a simple model for understanding active biological systems where chirality is important. Many microorganisms exhibit either intrinsic or emergent chiral swimming trajectories due to asymmetric flagellar motion, cell shape, and/or swimmer-boundary hydrodynamic interactions. These chiral dynamics enable microorganisms to navigate complex environments, respond to chemical gradients, and interact with surfaces in specialized ways.16,17 Chiral motility has also been linked to biological processes such as biofilm formation, tissue organization, and immune cell migration.18,19 Insights from dynamics of CABPs can thus deepen our understanding of how motile cells exploit chirality for ecological fitness and adaptation. Moreover, these principles may inform the design of synthetic active systems for targeted drug delivery, microfluidic transport, and environmental sensing.20,21
Understanding transport and first-encounter statistics in active systems is central to many problems, from target search, chemotaxis, and infection spread to designing micro-robotic search strategies. The mean first passage time (MFPT), which quantifies the expected time for a particle to reach a target or exit a domain for the first time, is a fundamental metric for these processes. For achiral active Brownian particles (e.g., ABPs) exhibiting translational persistence, MFPT has been extensively studied, revealing how directional persistence, stochastic fluctuations, and domain geometry influence search efficiency.22–26 However, chirality qualitatively modifies trajectories, so first-passage statistics in that context often deviate from achiral models.
Despite growing interest, quantitative theory for the MFPT of CABPs remains scarce. Existing studies have typically focused on passive and non-chiral active particles,26–30 and have not examined the effects of chirality and rotational velocity—factors that can qualitatively alter search dynamics and first-passage behavior. Another relevant study compares ABPs and run-and-tumble particles near flat boundaries,23 providing useful insights into boundary interactions, but such analyses likewise exclude chirality and do not extend to first-passage problems in more complex geometries. Environmental complexity has also been shown to strongly influence first-passage dynamics, as demonstrated in systems with passive crowders,31 yet these investigations remain largely focused on ABPs. A notable exception is recent work on the narrow escape problem for CABPs.14 Using Brownian dynamics (BD) simulations, Upadhyaya and Akella14 showed that the MFPT of CABPs is a non-monotonic function of chirality and exhibits a minimum at a finite chirality. While this represents an important step toward understanding first-passage phenomena in chiral systems, it focuses on specific boundary conditions and narrow escape scenarios, leaving open fundamental questions about how chirality modulates MFPTs across diverse geometries and parameter regimes. In particular, it remains unclear whether the observed optimal escape is specific to narrow escape settings or reflects a more general behavior of CABPs.
In this paper, we employ a backward Fokker–Planck equation to investigate the optimal escape dynamics of CABPs across a range of one- and two-dimensional geometries, with the goal of elucidating systematically how domain geometry and boundary conditions influence the escape of these particles. We begin by analyzing CABPs in one-dimensional (1D) domains, first considering a finite interval bounded by two absorbing ends, which provides fundamental insight into how chirality and persistence shape escape times in the simplest setting. We then examine a modified 1D geometry in which one boundary is absorbing and the other reflecting, allowing us to isolate the influence of asymmetric boundary conditions on the escape time. For either case, we provide a complete asymptotic theory to characterize CABP escape behavior in 1D at high chirality, which has not yet been available from existing theoretical or computational results. At intermediate chirality, we use numerical simulations to study the escape times. Building on these results, we extend our analysis to two dimensions (2D) by considering CABPs escaping from a circular domain (a disk region) containing one or two openings on its boundary. In this context, we investigate how swim speed, chirality, and opening size modulate escape times, and how chirality interacts with geometric constraints to enhance or hinder escape.
Here we briefly outline the theoretical framework before detailed analysis. Let P(x, q, t) denote the probability density of finding a CABP at position x with orientation q at time t; it is governed by the Fokker–Planck equation:
![]() | (1) |
[P] = −∇·(UsqP) + Dx∇2P − ∇R·(ΩP) + DR∇R2P. Here Us is the swim speed, q denotes the swimming direction (q·q = 1), Dx is the translational diffusivity, Ω is the angular velocity, DR is the rotational diffusivity,
is the translational gradient operator, and
is the rotational gradient operator. The inverse of DR defines the reorientation time, τR = 1/DR. If Ω = 0, one recovers the dynamics of ABPs, which is achiral.
We define the MFPT, T(x, q), as the mean time it takes for CABPs initially located at position x with orientation q to escape a domain. This quantity is governed by a backward Fokker–Planck equation, which reads
†[T] = −1,
| (2) |
† = Usq·∇ + Dx∇2 + Ω·∇R + DR∇R2 is the adjoint operator of
.32 Alternatively, one can obtain eqn (2) using a random walk approach.29,33
ϕex + sin
ϕey, where ex and ey are the unit basis vectors in the x and y directions, respectively. The angular velocity is defined as Ω = Ωez, where ez = ex × ey is the unit vector along the z axis, perpendicular to the x–y plane, and Ω is the magnitude of the angular velocity.
To make eqn (2) non-dimensional, we scale time by the swim timescale τs = L/Us and length by L. The non-dimensional form of eqn (2) is given by
![]() | (3) |
= T/τs,
= x/L, Pe = UsL/Dx, χ = ΩL/Us, and β = L/(UsτR), with the MFPT
≡
(
,ϕ) depending on the dimensionless initial position
and orientation ϕ of the CABP. Here, Pe compares the diffusive timescale L2/Dx to the swim timescale L/Us, χ compares the swim timescale with the rotational timescale 1/Ω, and β represents the ratio of the swim timescale to the reorientation time τR. Equivalently, β quantifies the ratio between the domain size L and the persistence length ℓ = UsτR. Throughout this article, we refer to χ as the chirality and only need to consider χ ≥ 0. The boundary conditions in
are given by
(±1,ϕ) = 0. Periodic boundary conditions are enforced for ϕ:
(
,0) =
(
,2π).
![]() | (4) |
Substituting the expansion in (4) into the PDE in (3) and collecting terms in powers of χ, at leading order O(1), we have ∂
0/∂ϕ = 0, which implies that
0 is independent of the initial angular orientation of the particle and depends only on its initial position, i.e.,
0 ≡
0(
). At order O(1/χ), we obtain
![]() | (5) |
Integrating the PDE in eqn (5) over ϕ and applying the periodic boundary conditions for
0 and
1, we obtain
![]() | (6) |
0(
= ±1) = 0. We note that the appearance of Pe in eqn (6) is due to non-dimensionalization. In dimensional form, this PDE is equivalent to Dx∂2TPBP/(∂x2) = −1, which governs the MFPT of PBPs. This is consistent with the expected behavior of CABPs, whose dynamics recover those of PBPs in the limit χ → ∞. The analytic solution to eqn (6) with the corresponding absorbing boundary conditions is
![]() | (7) |
Substituting
0 into eqn (5) the ∂2
0/∂ϕ2 = 0 term varnishes. Solving the resulting equation for
1, we obtain
1 = Pe![]() sin ϕ,
| (8) |
0, this O(1/χ) bulk correction introduces an orientation-dependent escape time such that
1(±1,ϕ) = ±Pe
sin
ϕ that violates the absorbing boundary conditions
1(±1,ϕ) = 0. This mismatch implies the formation of boundary layers near the exits as χ → ∞. The boundary-layer thickness scales as
, which is set by the balance between translational diffusion and chiral rotation,
. We therefore revise the outer bulk expansion given in eqn (4) as
![]() | (9) |
We note the introduction of an O(1/χ3/2) correction term in the asymptotic expansion of the outer solution. This term is required to ensure consistent matching between the bulk and boundary layer solutions. Substituting the expansion in eqn (9) into eqn (3), we obtain the equation governing
3/2:
![]() | (10) |
The solutions to
0 and
1 are given in eqn (7) and (8), respectively. From eqn (10), we have
3/2 ≡
3/2(
). Collecting terms from eqn (3) at O(1/χ3/2) gives
. As before, integrating over ϕ and using the periodic boundary conditions for
5/2, together with the fact that
3/2 depends only on
, yields
.
To resolve the behavior near
= 1, we introduce a stretched boundary-layer coordinate
. Defining the boundary-layer solution as
(s,ϕ) =
(
,ϕ), we obtain
![]() | (11) |
In addition to the absorbing boundary,
must match the bulk solution as s → +∞. Employing Van Dyke's matching rule,34 we substitute eqn (7) and (8) into the the bulk expansion in eqn (9), and express the resulting solution in terms of the boundary-layer coordinate s, yielding
![]() | (12) |
3/2(1) ≡
3/2(
= 1). Observing the form of the bulk solution in eqn (12), we seek a boundary-layer solution of the form
![]() | (13) |
1/2 ∼ Pes,
, and
3/2 ∼ −Pes
sin
ϕ +
3/2 (1) as s → ∞.
Inserting the expansion in eqn (13) into eqn (11), we obtain
![]() | (14) |
1/2 = Pes. At O(1/χ), we have
![]() | (15) |
We solve eqn (15) to obtain
![]() | (16) |
. The first term recovers the local expansion of the outer bulk solution near the exit, while the second term represents the boundary-layer correction. This correction takes the form of a damped oscillation that decays exponentially into the bulk with a characteristic dimensionless penetration depth of λ−1.
At O(1/χ3/2), the governing equation is given by
![]() | (17) |
Substituting
1/2 = Pes and
1 in eqn (16) into the PDE in eqn (17), and solving the resulting equation, we obtain
![]() | (18) |
| H(η,θ) = e−η[cos(η + θ) + sin(η + θ)]. | (19) |
Noting that H(η, θ) → 0 as η → ∞ and comparing eqn (17) with eqn (18),
3/2(1) is uniquely determined as −Peλ/2. It is now clear that the presence of the nonzero constant −Peλ/2 in the limit s → ∞ necessitates an O(χ−3/2) correction in the bulk region to satisfy the matching condition.
Owing to symmetry, the boundary-layer solutions near the left exit can be readily derived. Near
= −1, we define
and obtain
![]() | (20) |
From this, we have
3/2(−1) = −Peλ/2. Since
3/2(±1) = −Peλ/2, the equation
admits a constant solution given by
3/2 = −Peλ/2.
Using the bulk and boundary-layer solutions, we construct a composite asymptotic solution as
![]() | (21) |
F1 = Pe[![]() sin ϕ − e−λs sin(ϕ + λs) + e−λz sin(ϕ + λz)],
| (22) |
![]() | (23) |
In eqn (22) and (23),
,
,
, and the function H(η,θ) is as defined in eqn (19). We note that the asymptotic solution in eqn (21) is independent of β. For particles initially located at the midpoint of the interval (
= 0), the Pe![[x with combining macron]](https://www.rsc.org/images/entities/i_char_0078_0304.gif)
sin
ϕ term in eqn (22) vanishes, yielding
![]() | (24) |
(0,ϕ) is independent of ϕ, at least up to O(1/χ3/2). In the bulk, for
= 0 or ϕ = 0,π, the first correction to the passive result is at O(1/χ3/2), whereas for
≠ 0 and ϕ ≠ 0,π, it is at O(1/χ).
To validate the asymptotic solution in eqn (21), we solve the full problem [eqn (3)] numerically using a finite element method (FEM) implemented in FreeFem++.35 We compute the MFPT from FEM for χ = 50, Pe = 1, and β = 0.1. In Fig. 2(a), we compare the correction terms beyond leading order, namely (T − TPBP)/τs = F1/χ + F3/2/χ3/2 (solid lines), with those obtained from FEM (markers). For FEM, the corresponding result is defined as (Tnum − TPBP)/τs, where Tnum denotes the full numerical solution of the MFPT. As shown in Fig. 2(a), the asymptotic solution agrees very well with the full numerical solution over the entire x-domain for different values of ϕ.
![]() | ||
| Fig. 2 Asymptotic solutions for the MFPT of CABPs in a 1D interval with absorbing boundaries. (a) Comparison between the full numerical (FEM; solid lines) and asymptotic (markers) solutions for (T − TPBP)/τs. The plotted asymptotic solution [see eqn (21)] is given by (T − TPBP)/τs = F1/χ + F3/2/χ3/2. (b) Contour plot showing the MFPT obtained from the three-term asymptotic solution in eqn (21). For both (a) and (b), Pe = 1, χ = 50, and β = 0.1. | ||
In Fig. 2(a), we present the MFPT correction relative to PBPs for several initial orientations ϕ as a function of initial location
= x/L. Owing to the symmetry of the domain and equations, it suffices to consider 0 <
< 1 and −π/2 < ϕ < π/2. As ϕ increases from negative to positive values, CABPs transition continuously from facilitated to hindered transport regimes. For χ > 0, CABPs rotate counterclockwise. Although the particle initially sits closer to the right exit (
> 0), for ϕ > 0 the rotation steers it further upward, which may cause it to miss the right boundary. As a result, escape through the right exit is generally delayed. On the other hand, for ϕ < 0, the particle's orientation is further steered toward the right exit as the particle approaches the exit, thereby facilitating escape. We note that there is a delicate balance between chirality, swim-induced escape, and Brownian diffusion. Taking ϕ = 0 as an example, propulsion-accelerated escape is only effective when the particle is sufficiently close to the exit, otherwise the chirality-induced rotation may oversteer the particle's orientation before it reaches the boundary. In that case, the particle has not yet escaped while its orientation has already reversed (ϕ > π/2). If the particle starts exactly at the exit, MFPT is zero. As a result, for a fixed ϕ, the quantity (T − TPBP)/τs exhibits a non-monotonic dependence on
[see Fig. 2(a)].
At the midpoint of the interval, the asymptotic solution [at least up to O(1/χ3/2)] in this high-chirality regime is independent of ϕ; therefore, the curves for different ϕ intersect at
= 0. From eqn (24), it follows that (T − TPBP)/τs ∼ −Peλ/(2χ3/2) ≈ −0.0047 for Pe = 1 and χ = 50 [Fig. 2(a)].
Our asymptotic theory and Fig. 2(a) highlight the fine structure of the dependence of the MFPT of CABPs on the initial orientation angle of the particles in the high chirality regime, although this dependence is generally weak. Notice the small magnitude of the correction to the MFPT evidenced in Fig. 2(a). Indeed the MFPT of CABPs is, to leading order, identical to that of PBPs [see first term in eqn (21)]. This is demonstrated in Fig. 2(b) where we show a contour plot of the MFPT for CABPs obtained from the three-term asymptotic solution in eqn (21) as a function of the initial position and orientation of the particles, for χ = 50 and Pe = 1. Here the MFPT is normalized by the constant swimming time scale τs to provide a global view of the actual magnitude of escape time. As expected, overall escape is slower when a particle starts closer to the midpoint.
![]() | ||
Fig. 3 Scaled MFPT as a function of chirality (χ) for CABPs in a 1D interval with absorbing boundaries, computed using BD (see Appendix A.3) and FEM. We plot T( ,ϕ) normalized by the passive MFPT TPBP, i.e., T/TPBP, for particles starting at x = 0 under three initial-orientation conditions: (a) ϕ = 0 (right-pointing), (b) ϕ = π/2 (orientation perpendicular to the exits), and (c) ϕ uniformly random, and for three swim speed: Pe = 1 (red circles), Pe = 10 (blue diamonds), and Pe = 20 (green squares). In each case, TPBP is computed from eqn (7). For all results, β = 0.1. The dashed lines indicate the high-chirality solution given in eqn (26). The FEM and BD solutions have excellent agreement and cannot be distinguished visually. | ||
In Fig. 3, we show the MFPT for CABPs normalized by that of PBPs, i.e., T/TPBP, for particles starting at
= 0 as a function of χ. Results are shown for varying Péclet numbers (Pe = 1, Pe = 10, and Pe = 20) and initial orientations: right-pointing [ϕ = 0, Fig. 3(a)], perpendicular to the exits [ϕ = π/2, Fig. 3(b)], and uniformly random ϕ [Fig. 3(c)]. For uniformly random initial orientations, we define
![]() | (25) |
For ABPs (χ = 0) and CABPs with weak chirality, the MFPT decreases with increasing Pe since particles can exit from both ends of the interval. Increasing Pe corresponds to a lower translational diffusivity, thereby enhancing escape driven by self-propulsion. In contrast, when χ becomes large, the MFPT converges to that of PBPs at leading-order for all values of Pe, consistent with our asymptotic analysis in the high-chirality regime (Section 2.1.1). Using eqn (24), we obtain the analytical solution
![]() | (26) |
. For Pe = 10 and Pe = 20, this large-χ limit is indicated by the dashed lines in Fig. 3(c).
For a fixed Pe, the MFPT increases monotonically with χ for right-pointing particles [see Fig. 3(a)]. Physically, increasing χ enhances the rate of rotation, thereby reducing the effective swimming persistence. As a result, particle escape mediated by self-propulsion is increasingly suppressed. We note that, by symmetry, left-pointing particles exhibit the same MFPT behavior as right-pointing particles.
In contrast, for particles initially oriented perpendicular to the exits [ϕ = π/2; see Fig. 3(b)], there exists an intermediate value of χ that minimizes the MFPT. In this scenario, the MFPT initially decreases as χ increases, reaches a minimum, and then increases for larger χ values. For χ = 0, ABPs oriented toward the wall typically spend a time of order τR reorienting before they are able to swim toward the absorbing boundary. When χ is small, particles can acquire a non-zero horizontal velocity, allowing them to escape more quickly compared to ABPs. In the limit χ → ∞, self-propulsion no longer contributes to directed motion, and escape occurs purely via Brownian motion. An optimum is obtained when the swim timescale is comparable to the timescale of rotation due to chirality, L/Us ≈ 1/Ω, which gives χ ≈ 1.
When the initial orientation of the particles is uniformly random, the MFPT profile represents an average of the MFPTs for right-pointing particles and for particles oriented perpendicular to the boundaries. Upon averaging over the orientations [see Fig. 3(c)], the non-monotonicity in χ becomes much less pronounced compared to Fig. 3(b) for top-pointing particles.
While uniformly random initial orientations may better represent realistic scenarios, it is instructive to examine how the MFPT depends more generally on the initial orientation. Fig. 4 shows contour plots of the MFPT for CABPs in a 1D interval with absorbing boundaries as a function of the initial position and orientation of the particles, for different chirality. In all cases, the swim speed is fixed at Pe = 10, and β = 0.1. When χ = 0 (achiral), the MFPT is maximized when particles start at the center of the domain (
= 0) and are oriented perpendicularly to the boundaries, with the MFPT profile symmetric about ϕ = π. As the starting position moves toward the right boundary (
= 1), the MFPT increases for orientations pointing toward the left boundary (ϕ ≈ π) [see Fig. 4(a)]. Conversely, for particles starting near the left boundary, the MFPT increases for orientations pointing toward the right boundary, with the symmetry preserved about ϕ = π. As expected for χ = 0, particles starting very close to a boundary exhibit the maximum MFPT when initially oriented directly toward the opposite boundary.
A similar trend is observed for χ = 1 [Fig. 4(b)], which yields the lowest maximum MFPT among the values of χ considered in Fig. 4. As χ increases further, the MFPT maximum remains near the center of the domain but becomes less sensitive to the initial orientation [Fig. 4(c) and (d)]. For large χ, the MFPT converges to that of PBPs, as shown for χ = 100 in Fig. 4(d), where it is maximized at
= 0 and decreases monotonically and symmetrically as the starting position approaches either boundary, independent of orientation.
The MFPT for the CABP to escape the domain in this configuration is parameterized analogously to that of the symmetric interval with absorbing boundaries at both ends. Consequently, the governing non-dimensional PDE for the MFPT is identical to eqn (3), but with boundary conditions adapted to the mixed (reflecting–absorbing) domain geometry:
![]() | (27) |
= −1 enforces a zero flux of probability at the left boundary, and the absorbing condition at
= 1 indicates certain escape upon reaching the right boundary. We also impose a periodic boundary condition for ϕ:
(
,0) =
(
,2π).
0 as in eqn (6), but now solved with the boundary conditions in eqn (27). Solving this boundary-value problem (BVP) yields an explicit expression for the leading-order MFPT in the limit χ → ∞:
![]() | (28) |
0 into eqn (5) and solving, we obtain
1 = Pe(1 + )sin ϕ + a( ),
| (29) |
) is an unknown function of
.Near the right absorbing boundary, we again introduce the stretched boundary-layer coordinate
. We express the bulk expansion
0 +
1/χ + ⋯ in terms of the boundary-layer coordinate s and expand it in a series as χ → ∞, yielding
![]() | (30) |
= 1). The boundary-layer equation and asymptotic expansion are identical to those in the case where both boundaries are absorbing; they are given by eqn (11) and (13), respectively. The distinction lies solely in the matching conditions:
1/2 ∼ 2Pes and
1 ∼ a(1) − Pes2/2 + 2Pe
sin
ϕ as s → ∞. Solving the boundary-layer equations subject to these matching conditions yields
![]() | (31) |
A necessary condition for the above solution is that a(1) = 0.
Near the left reflecting boundary, we introduce the stretched boundary-layer coordinate
. Similar to eqn (30), we express the outer solution in terms of z to obtain
![]() | (32) |
This suggests a boundary-layer expansion of the form
![]() | (33) |
0 ∼ 2Pe and
1 ∼ a(−1) − Pez2/2 as z → ∞. Substituting eqn (33) into the boundary-layer PDE (11) and solving each order in turn, subject to these matching conditions, yields
![]() | (34) |
) = 0.
At O(1/χ3/2), the governing equation for the right boundary layer remains the same as eqn (17). Substituting the solutions in eqn (31) into eqn (17) and solving the resulting equation, we obtain the solution for
3/2 at the right boundary layer, given by
![]() | (35) |
3/2(1) = −Peλ. Similarly, at the left boundary layer, the solution at O(1/χ3/2) is
3/2(z,ϕ) = Pez sin ϕ + 3/2(−1) + λH(λz,ϕ).
| (36) |
We note that the left solution given in eqn (36) still contains the undetermined constant
3/2(−1). To solve the BVP
[cf. eqn (10)], we need an additional boundary condition. In the Appendix, we show that this condition is provided by the solvability condition for the left boundary layer at the next order. The solvability requires that
. With this, one can readily solve the BVP to obtain
![]() | (37) |
We then calculate the value of
3/2 at the left boundary as
3/2(−1) = −2Peλ, which uniquely determines the solution given in eqn (36).
Using the bulk and boundary-layer solutions, we construct a composite asymptotic solution for the MFPT of CABPs in the interval, given by
![]() | (38) |
0(
,ϕ) is given in eqn (28),
1(
,ϕ) is given in eqn (29), and
3/2(
,ϕ) is given in eqn (37). Here, G1 and G3/2 are defined as follows:
G1 = −2Pee−λs sin(λs + ϕ),
| (39) |
![]() | (40) |
In Fig. 6(a), we compare (T − TPBP)/τs obtained from the full FEM solution against the asymptotic prediction, given by (
1 + G1)/χ + (
3/2 + G3/2)/χ3/2 via eqn (38). The asymptotic solution shows excellent agreement with the FEM result across the entire x-domain for all values of ϕ considered. As in the case with absorbing boundaries at both ends, we observe a non-monotonic dependence on
. Similarly, as ϕ increases from negative to positive values, CABPs undergo a continuous transition from facilitated to hindered transport regimes (cf. Fig. 2).
![]() | ||
Fig. 6 Asymptotic solutions for the MFPT of CABPs in a 1D interval with reflecting left and absorbing right boundaries. (a) Comparison between the full numerical (FEM; solid lines) and asymptotic (markers) solutions for (T − TPBP)/τs. The plotted asymptotic solution [see eqn (38)] is given by (T − TPBP)/τs = (G1 + 1)/χ + (G3/2 + 3/2)/χ3/2. (b) Contour plot showing the MFPT obtained from the three-term asymptotic solution in eqn (38). For both (a) and (b), Pe = 1, χ = 50, and β = 0.1. The asymptotic and full solutions in panel (a) have excellent agreement. | ||
In Fig. 6(b), we show a contour plot of the MFPT for CABPs obtained from the three-term asymptotic solution in eqn (38) as a function of the initial position and orientation of the particles, for χ = 50 and Pe = 1. In the high-chirality regime, the MFPT of CABPs is, to leading order, identical to that of PBPs [see first term in eqn (38)]. The presence of higher-order correction terms introduces a weak dependence of the MFPT on the particle orientation ϕ.
Since the left boundary is reflecting, the MFPT attains its maximum there; evaluating the composite solution at
= −1 yields
![]() | (41) |
Notably, the O(1/χ) terms in eqn (38) vanish at
= −1, so the leading correction to the passive result appears at O(1/χ3/2). Furthermore, the MFPT of CABPs at the reflecting boundary is slighted reduced compared to that of PBPs, thanks to the coupling of swimming and chiral rotation assisting the particle steering away from the wall.
The computed MFPT for CABPs is presented in Fig. 7 and 8. Fig. 7 shows the normalized MFPT, T/TPBP, as a function of chirality, for particles starting at the midpoint of the interval (
= 0) with varying initial orientations and different Péclet numbers. In Fig. 7(a), we show the MFPT for particles initially oriented to the right (ϕ = 0). The MFPT profile closely resembles that of the symmetric interval with absorbing boundaries at both ends [see Fig. 3(a)], increasing monotonically with χ. Although the ratios in Fig. 3(a) and 7(a) suggest that T/TPBP is lower for the interval with a left reflecting boundary, this does not imply that the absolute MFPT is smaller, since the passive MFPTs for the two domain configurations differ.
![]() | ||
| Fig. 7 Scaled MFPT as a function of chirality (χ) for CABPs in a 1D interval with reflecting left and absorbing right boundaries, computed using FEM. We plot T/TPBP for particles starting at x = 0 under three initial-orientation conditions: (a) ϕ = 0 (right-pointing), (b) ϕ = π (left-pointing), and (c) ϕ uniformly random, and for three swim speed: Pe = 1 (red circles), Pe = 10 (blue diamonds), and Pe = 20 (green squares). In each case, TPBP is computed from eqn (28). For all results, β = 0.1. Note the differing y-axis limits in panels (a)–(c). The dashed lines in panel (c) indicate the high-chirality asymptotic solution given in eqn (43). | ||
So far, the MFPT computed across all scenarios and both 1D domain configurations as a function of χ shows that the MFPT for CABPs is generally less than or equal to that of PBPs [see Fig. 3(a)–(c) and 7(a)]. However, Fig. 7(b) presents a contrasting case: when particles start oriented toward the reflecting boundary (left-pointing), the MFPT for CABPs is greater than that of PBPs for all values of Pe when χ is very small, as indicated by T/TPBP > 1. In this small-χ regime, the escape is dominated by the achiral active Brownian dynamics. ABPs initially oriented towards the left wall become trapped there and must rely on rotational Brownian diffusion to reorient away from the wall. As χ increases, the MFPT decreases for all values of Pe. For Pe = 1 (red circles), this decrease is monotonic, and the MFPT converges to that of PBPs as χ → ∞. For higher swim speeds, Pe = 10 and Pe = 20, the MFPT exhibits non-monotonic behavior: it initially decreases as χ increases, reaches a minimum, and then increases again with further increases in χ, eventually converging to the MFPT for PBPs as χ → ∞. For these larger values of Pe, the MFPT for CABPs drops below that of PBPs over a range of χ.
In Fig. 7(c), we show the results for particles with uniformly random initial orientations, which effectively average the behaviors observed in Fig. 7(a) and (b). In this case, the MFPT exhibits a minimum at an intermediate value of χ. Unlike the symmetric interval with uniformly random orientations [cf. Fig. 3(c)], where CABPs consistently have MFPTs below the passive MFPT (T/TPBP < 1) for all Pe, in the left reflecting boundary configuration, the MFPT for CABPs exceeds that of PBPs at Pe = 1, but is lower for higher swim speeds (Pe = 10 and Pe = 20). For all swim speeds, the variation in T/TPBP with increasing χ is more pronounced for the reflecting-left boundary configuration, highlighting the influence of boundary type on the MFPT as a function of chirality.
In the high-chirality regime, applying eqn (38) at the domain midpoint (
= 0) yields the asymptotic expansion
![]() | (42) |
We note that the order of the leading correction to the passive result depends on the initial orientation angle. When sin
ϕ = 0, as shown in Fig. 7(a) and (b), the first nonzero correction arises at O(1/χ3/2); for sin
ϕ ≠ 0, it appears at O(1/χ). For CABPs with an initially uniform orientational distribution, the O(1/χ) term vanishes, yielding
![]() | (43) |
This asymptotic result is shown as dashed lines in Fig. 7(c), exhibiting excellent agreement with the numerical results in the high-chirality regime.
It is instructive to compare Tuni for particles starting from the midpoint (
= 0) under two boundary conditions: both ends absorbing, and a reflecting left boundary with an absorbing right boundary. While TPBP(
= 0) differs between the two cases, the two-term asymptotic solution for the scaled MFPT, Tuni(
= 0)/TPBP(
= 0) coincides for both boundary conditions [cf. eqn (26) and (43)]. We note that this is not generally true for an arbitrary
, which reflects precisely the interplay between asymmetric confinement, chirality and activity.
Next, we present contour plots of the MFPT for CABPs in the 1D interval with a left reflecting boundary, as functions of the initial position and orientation of the particles in Fig. 8. The physical parameters are Pe = 10 and β = 0.1. Each subplot corresponds to a different fixed value of chirality χ. For χ = 0 [see Fig. 8(a)], the MFPT corresponds to that of standard ABPs. In this case, the MFPT is maximized when particles are initially oriented toward the reflecting boundary and located at x/L = −1 (i.e., ϕ/π = 1), and it decreases symmetrically as the initial orientation deviates from this direction. Generally, for a fixed initial orientation, the MFPT decreases as the starting position moves closer to the absorbing boundary at x/L = 1. This behavior is intuitive, as particles near the absorbing boundary are more likely to escape quickly. We further note that for ϕ = π, ABPs initially swim toward the wall before reorienting and eventually exiting. If the Péclet number is large, the transit time from the bulk to the left wall is short, and the MFPT is therefore dominated by the reorientation process at the wall. Consequently, for large Pe (e.g., Pe = 10) and ϕ = π, T/τs exhibits a plateau before decreasing to zero, consistent with the absorbing boundary condition at the right exit (see also Fig. 12 in Appendix A.2).
As χ increases from zero, the particles begin to spin in the counterclockwise direction (since χ > 0). This rotational motion significantly affects their overall dynamics, as reflected in the MFPT required to escape the domain [see Fig. 8(b)–(e)]. Notably, for small χ [see Fig. 8(b); see also Fig. 13 in Appendix A.2], the previously symmetric contour begins to distort, and a pronounced asymmetry emerges as χ increases further [see Fig. 8(c) and (d)]. Owing to the counterclockwise rotation, the location of the maximum MFPT at the left wall shifts to orientations with ϕ < π. This arises because particles starting with ϕ < π are advected by chirality toward the left wall, which increases their residence time before reaching the escape-favorable orientation window |ϕ| < π/2. On the other hand, for ϕ > π, rotational motion carries particles directly into this escape window, allowing for faster escape. Additionally, the maximum MFPT [see the color bars in Fig. 8(a)–(d)] decreases relative to the χ = 0 (ABP) case, indicating that rotational dynamics reduce the worst-case escape time. Physically, the worst-case scenario for ABPs corresponds to orientations pointing toward the left wall, where particles become effectively trapped by persistent propulsion. Chirality introduces rotational dynamics that break this trapping by reorienting particles, thereby enhancing escape and reducing the MFPT.
As mentioned earlier, when CABPs rotate rapidly, their directed motion becomes increasingly disrupted, and their behavior approaches that of PBPs, as χ → ∞. This transition is evident in the contour plots in Fig. 8(e) (χ = 10) and Fig. 8(f) (χ = 100). For χ = 10, the influence of the initial orientation on the MFPT is already significantly reduced compared to lower values of χ. In this case, the escape dynamics is largely dominated by chirality, which is characterized in Section 2.2.1. For χ = 100, effect of persistent propulsion becomes negligible. In this regime, the MFPT is determined primarily by the particle's initial position, rather than its orientation or swim speed, which is characteristic of PBPs and consistent with the results for the symmetric domain shown in Fig. 4(d), and our asymptotic analysis.
Lastly, we note from Fig. 3 and 7 that the MFPT for CABPs decreases as the particle swim speed increases, i.e., as Pe increases. This trend is expected, as higher activity enhances the ability of particles to escape from the domain regardless of boundary type, consistent with previous findings for ABPs.27 Although this is not immediately evident from the computed ratio T/TPBP in all cases, the MFPT for CABPs is higher in the interval with a left reflecting boundary than in the symmetric domain with absorbing boundaries at both ends. This is also expected, since particles in the symmetric domain can exit from either boundary, whereas those in the domain with a left-reflecting boundary can only exit through the right boundary. This difference is apparent when comparing the results in Fig. 2(b) and 4 with Fig. 6(b) and 8.
![]() | (44) |
In analyzing the MFPT in this geometry, we consider two configurations: (i) a disk with a single absorbing arc, and (ii) a disk with two symmetric absorbing arcs (Fig. 9). For each configuration, the MFPT is computed using FEM as a function of the Péclet number (Pe) and chirality (χ).
![]() | (45) |
( = 1,θ,ϕ) = 0 for θ ∈ Θe,
| (46) |
![]() | (47) |
= r/R, and
is the non-dimensional gradient operator. As in the 1D cases, q = cos
ϕex + sin
ϕey.
The MFPT for a CABP starting at the center of the disk with a uniformly random initial orientation is shown in Fig. 10, plotted as a function of chirality χ for different values of Pe. These results extend the analysis of Section 2.2, which considered a CABP in a 1D interval with a reflecting boundary on the left and an absorbing boundary on the right, to the 2D setting. In particular, the configuration shown in Fig. 10(a) for θe = π/2 is analogous to that in Fig. 7(c) for the 1D case.
As in the 1D case, there exists an intermediate value of χ that minimizes the MFPT. This minimum is sharp at large Péclet numbers, as shown for Pe = 10 in Fig. 10(a). In the large-Pe regime, the minimum is set by the balance R/Us ≈ 1/Ω, which again gives χ ≈ 1. As Pe decreases, translational Brownian motion becomes increasingly important, and the minimum becomes both shallower and broader. This behavior reflects a generic trade-off: at low Pe, diffusive transport reduces the sensitivity of the MFPT to the chiral dynamics set by χ. Put differently, the reduction in MFPT due to optimal chirality is most pronounced for highly active particles.
For ABPs or CABPs with small χ, the escape dynamics are effectively governed by standard ABP behavior. In contrast to the 1D case—where the MFPT decreases monotonically with increasing Pe—the 2D results exhibit a more intricate dependence on Pe. Specifically, for small or vanishing χ, the MFPT is larger for Pe = 2 than for Pe = 1. For ABPs, this non-monotonic dependence of the MFPT on Pe has been discussed in Iyaniwura & Peng;29 the MFPT distribution as a function of Pe and rotational Brownian motion has also been studied theoretically in a circular region with the boundary being entirely absorbing.28
To examine the dependence of the MFPT on the size of the absorbing arc, in Fig. 10(b) we show the MFPT for several values of the absorbing arc half-angle θe (θe = π/8, π/4, π/2) at a fixed value of Pe = 10. Increasing θe corresponds to enlarging the absorbing arc, thereby increasing the likelihood that a particle encounters the escape window along the boundary; as a result, the MFPT decreases monotonically with increasing θe. As discussed earlier, for large Pe, the optimality arises from the balance R/Us ≈ 1/Ω. Consequently, the chirality that minimizes the MFPT is largely independent of the size of the absorbing arc. Therefore, the drop in the MFPT becomes more pronounced with a smaller window size.
Similar to the 1D case [Fig. 7(c)] is that the MFPT of CABPs, and of ABPs in the small chirality limit, can be shorter or longer than that of PBPs as shown in Fig. 10. This again reflects the competition previously described: particles with unfavorable initial orientations are more likely to encounter the reflecting boundary first and may even become trapped, whereas those oriented toward the exit can escape more rapidly due to active swimming. This competition is further modulated by the swimming speed Pe and the size of the opening θe.
As shown in Fig. 11(a), for Pe = 10, the MFPT exhibits a non-monotonic dependence on χ. In contrast to the one-arc case, this non-monotonicity is largely absent at lower Pe, as illustrated for Pe = 1 and Pe = 2 in Fig. 11(a). With two exits, particles can escape from either side, which reduces geometric constraints on the dynamics, similar to the 1D cases. As a result, only highly active particles—those that tend to become trapped along the reflecting portions of the boundary—benefit significantly from an optimal chirality.
Lastly, Fig. 11(b) shows the MFPT for a CABP escaping the disk for Pe = 10 and θe = π/8, π/4, π/2. As in the single-arc case, the MFPT decreases monotonically with increasing arc length, and the optimal χ that minimizes the MFPT is largely independent of the absorbing arc length. However, the dependence on the chirality χ differs qualitatively from the single-arc geometry. Specifically, for a disk with one absorbing arc, the MFPT is smaller in the limit χ → ∞ than in the limit χ → 0 for all values of θe considered. In contrast, for two symmetric absorbing arcs, the MFPT is lower as χ → 0 than as χ → ∞.
Since the dynamics of CABPs approach those of ABPs as χ → 0 and those of PBPs as χ → ∞, these results imply that ABPs escape more slowly than PBPs in the single-arc geometry, but more rapidly in the two-arc geometry. In the single-arc case, ABPs tend to become trapped near the reflecting boundary, which increases their residence time in the domain before reaching the exit. In contrast, with two exits, they can reach the boundaries more efficiently; sliding along the reflecting segments on either side eventually leads to an exit, enhancing escape efficiency.33 Note that this is similar to the contrast between 1D cases with absorbing/absorbing and reflecting/absorbing boundaries.
A central finding of this work is the existence of an optimal chirality that minimizes the MFPT, a feature that is especially pronounced for CABPs at large Péclet numbers. Primarily for CABPs with unfavorable initial orientations, the optimality arises when the time of reorientation towards the exit, thanks to chirality, matches the time to transit the confinement domain through active swimming. It is generally independent of geometric dimensions (1D or 2D) and escape configurations (single or double symmetric exits). This universality highlights chirality as a robust control parameter that can be tuned to minimize escape times across a broad class of confined geometries, with practical implications for the design of synthetic microswimmer systems in which the rotation rate can be controlled externally, for instance through magnetic fields or geometric confinement.36–38 This perspective draws a natural connection to studies of microswimmers in corrugated or periodically structured environments, where boundary curvature and shape have been shown to modulate swimmer trajectories and transport.26,33,39–41 The present results suggest that chirality introduces a control parameter in addition to boundary curvature. The interplay between chirality and boundary geometry can therefore give rise to non-trivial transport behavior.21
In the high-chirality regime (χ ≫ 1), the MFPT approaches that of PBPs to leading order. In 1D using asymptotic expansions, we have systematically resolved the structure of CABP escape time compared to its PBP limit, uncovering a delicate interaction among chirality, swim-induced escape, and Brownian diffusion. Meanwhile, this recovery of passive-like behavior reflects the fact that strong chirality suppresses persistent swimming and reduces net directed transport. Thus, while intermediate chirality enhances escape efficiency, excessive chirality is detrimental, underscoring the importance of tuning chirality to its optimal value.
The initial orientation ϕ of the particles plays a qualitatively distinct role in shaping the MFPT depending on the boundary configuration. In the fully absorbing case, the MFPT transitions smoothly between facilitated escape, when the particle is initially directed toward either exit and self-propulsion immediately drives it toward an absorbing boundary, and hindered escape, when it starts perpendicular to the boundaries and must first reorient before making productive progress toward an exit, a process governed by rotational diffusion and therefore costly in time. In the mixed boundary case, the maximum MFPT occurs when the particle starts pointing toward the reflecting boundary, since self-propulsion initially drives it away from the only available exit, effectively increasing the distance the particle must cover before escaping; as chirality increases, the orientation associated with this maximum rotates continuously in the direction of the chiral angular drift, reflecting the systematic bias that chirality introduces into the particle's trajectory. In both cases, the sensitivity of the MFPT to ϕ diminishes with increasing chirality and vanishes as χ → ∞: rapid chiral rotation causes the self-propulsion direction to precess rapidly through all angles, averaging out any directional bias over timescales short compared to the escape time, erasing the memory of the initial orientation, and recovering the isotropic MFPT of a passive Brownian particle independent of ϕ.
In the 2D setting, the MFPT was analyzed numerically across both absorbing arc configurations. A key finding is that the configuration of absorbing arcs can qualitatively alter the escape dynamics beyond a simple rescaling, even when the total absorbing arc length is held fixed between the two configurations. In particular, unlike the 1D case where the MFPT varies monotonically with swim speed across all chirality values considered, the 2D single-arc configuration exhibits a non-monotonic dependence of the MFPT on swim speed at low chirality. No such behavior was observed in the two-arc configuration, where the MFPT varies monotonically with swim speed across the full range of chirality values considered. These results demonstrate that the number and placement of absorbing arcs in 2D or 3D can qualitatively alter the relationship between swim speed and escape time, even when the total absorbing arc length is held fixed. Unlike in 1D, particles in 2D or 3D are more likely to remain trapped for longer at a reflecting boundary. In a 1D interval, even a small deviation from the normal orientation to the wall allows the particle to slide along the boundary and eventually escape. In higher dimensions, however, particles must undergo a more substantial reorientation before they can move away from the boundary and reach the exit. As an example, this can be seen by comparing Fig. 3(c) and 11(b), where the non-monotonicity is more pronounced in the 2D case.
Furthermore, in both configurations, the optimal chirality that minimizes the MFPT is found to be independent of the absorbing arc length, suggesting that this optimality is a robust geometric feature of the escape dynamics rather than a boundary-size effect. However, the results for these two configurations differ qualitatively in the limiting behavior of the MFPT: for a single absorbing arc, the MFPT is smaller as χ → ∞ than as χ → 0, whereas for two symmetric absorbing arcs the opposite holds, with the MFPT being lower as χ → 0 than as χ → ∞. This qualitative reversal underscores the role of domain geometry in determining whether high or low chirality is more detrimental to escape.
Despite the in-depth analysis carried out in this work, several avenues remain open for future investigation. The present model assumes a uniform translational diffusion coefficient and a fixed swim speed; relaxing these assumptions to account for spatially varying diffusivity or chirality would broaden the applicability of the framework to experimentally relevant systems. A natural extension is also the case of multiple absorbing windows with arbitrary placement and size, beyond the symmetric two-arc configuration considered here, particularly in the context of modeling cell membrane transport or drug delivery in complex environments.
Another natural extension of this work is the narrow escape problem for a CABP confined to a 2D disk with a fully reflecting boundary, where the absorbing targets consist of one or more small traps of size ε ≪ 1 located in the interior of the disk.42–44 A key question is whether closed-form asymptotic solutions can be derived in this setting. Extending this analysis to CABPs would reveal how chirality and swim speed modify the asymptotic behavior of the MFPT as ε → 0, and whether the optimal chirality identified in the present work persists in this interior trap setting. This extension is relevant to applications such as the targeting of drug-carrying microswimmers to specific receptor sites, and the arrival of reactive molecules at localized catalytic sites within a confined cellular environment.
Overall, the results presented in this work establish a quantitative framework for understanding how chirality modulates escape dynamics in confined active matter systems. A key outcome is the identification of an optimal chirality that minimizes the MFPT, positioning chirality as a robust control parameter for modulating the motion of active particles. This shows that chirality could be leveraged in synthetic microswimmer systems to achieve targeted transport, with potential applications in drug delivery, microfluidics, and biomedical engineering, and provides a foundation for future studies of escape dynamics in more complex environments relevant to biological and synthetic microswimmers.
3/2, we need to first obtain the bulk solution at O(1/χ2). From the regular expansion given in eqn (9), we obtain
![]() | (48) |
Inserting eqn (29) into the above equation and integrating yields
![]() | (49) |
) remains to be determined.
For the boundary layer near the reflecting wall on the left, the matching condition is then given by
![]() | (50) |
![]() | (51) |
1 and
3/2 are given by eqn (34) and (36), respectively.
At O(1/χ2), we obtain
![]() | (52) |
![]() | (53) |
Comparing this solution with the matching condition given in eqn (50), we conclude that
. We note that, at this stage, b(−1) remains undetermined. Integrating the BVP,
, together with the boundary conditions
3/2(1) = −Peλ and
, we obtain
![]() | (54) |
![]() | ||
| Fig. 12 MFPT of ABPs (χ = 0) in a 1D interval with reflecting left and absorbing right boundaries as a function of the initial position (x/L). Other parameters are Pe = 10 and β = 0.1. The corresponding contour plot for the MFPT as a function of x/L and ϕ is given in Fig. 8(a). | ||
![]() | ||
| Fig. 13 MFPT of CABPs in a 1D interval with reflecting left and absorbing right boundaries as a function of the initial orientation. For all results, the starting particle position x/L = −1. That is, the particles start from the left reflecting wall. Other parameters are Pe = 10 and β = 0.1. See Fig. 8(a)–(c) for the corresponding contour plots for the MFPT as a function of x/L and ϕ. | ||
In Fig. 12, we plot the scaled MFPT, T/τs, as a function of the position for different values of the orientation angle ϕ. For ϕ = 0, the particle initially points towards the exit. As the starting position shifts from left to right, the MFPT decreases monotonically. For ϕ = π, the particle initially points towards the reflecting wall. In this case, the MFPT exhibits a plateau before it eventually decreases to zero as x/L approaches the exit.
In Fig. 13, we plot the scaled MFPT, T/τs, as a function of the initial orientation angle ϕ for different values of chirality. The initial particle position x/L = −1, i.e., the particle starts from the reflecting left wall. For ABPs (χ = 0), the maximum is attained at ϕ = π, corresponding to a particle initially oriented toward the reflecting left wall. In this configuration, the particle is initially stuck at the wall and must rely on rotational Brownian motion to reorient away from it. As chirality increases, the location of the maximum shifts towards smaller ϕ.
xn+1 = xn + Us cos(ϕn)Δt + ΔxB,
| (55a) |
| ϕn+1 = ϕn + ΩΔt + ΔϕB, | (55b) |
For all simulations, a sufficiently small time step is used to resolve all the physical timescales in the system. To ensure good statistics, all simulations are performed with 200
000 particles. For each particle, the simulation is terminated upon reaching the absorbing boundary, and the corresponding first-passage time is recorded. The mean first passage time can be easily computed by an appropriate ensemble average.
For CABPs in a 2D disk, in addition to eqn (55), the equation of motion for the y-coordinate reads
yn+1 = yn + Us sin(ϕn)Δt + ΔyB.
| (56) |
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