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The escape dynamics of sticky particles from textured surfaces is poorly understood despite importance to various scientific and technological domains. In this work, we address this challenge by investigating the escape time of adsorbates from prevalent surface topographies, including holes/pits, pillars, and grooves. Analytical expressions for the probability density function and the mean of the escape time are derived. A particularly interesting scenario is that of very deep and narrow confining spaces within the surface. In this case, the joint effect of the entrapment and stickiness prolongs the escape time, resulting in an effective desorption rate that is dramatically lower than that of the untextured surface. This rate is shown to abide a universal scaling law, which couples the equilibrium constants of adsorption with the relevant confining length scales. While our results are analytical and exact, we also present an approximation for deep and narrow cavities based on an effective description of one dimensional diffusion that is punctuated by motionless adsorption events. This simple and physically motivated approximation provides high-accuracy predictions within its range of validity and works relatively well even for cavities of intermediate depth. All theoretical results are corroborated with extensive Monte-Carlo simulations., Comment: 19 pages, 8 figures

Adsorption to a surface, reversible-binding, and trapping are all prevalent scenarios where particles exhibit "stickiness". Escape and first-passage times are known to be drastically affected, but detailed understanding of this phenomenon remains illusive. To tackle this problem, we develop an analytical approach to the escape of a diffusing particle from a domain of arbitrary shape, size, and surface reactivity. This is used to elucidate the effect of stickiness on the escape time from a slab domain: revealing how adsorption and desorption rates affect the mean and variance, and providing a novel approach to infer these rates from measurements. Moreover, as any smooth boundary is locally flat, slab results are leveraged to devise a numerically efficient scheme for simulating sticky boundaries in arbitrary domains. Generalizing our analysis to higher dimensions reveals that the mean escape time abides a general structure that is independent of the dimensionality of the problem. This letter thus offers a new starting point for analytical and numerical studies of stickiness and its role in escape, first-passage, and diffusion-controlled reactions., Comment: 5 Pages + 13 appendices pages, 4 + 3 figures

Gated first-passage processes, where completion depends on both hitting a target and satisfying additional constraints, are prevalent across various fields. Despite their significance, analytical solutions to basic problems remain unknown, e.g. the detection time of a diffusing particle by a gated interval, disk, or sphere. In this paper, we elucidate the challenges posed by continuous gated first-passage processes and present a renewal framework to overcome them. This framework offers a unified approach for a wide range of problems, including those with single-point, half-line, and interval targets. The latter have so far evaded exact solutions. Our analysis reveals that solutions to gated problems can be obtained directly from the ungated dynamics. This, in turn, reveals universal properties and asymptotic behaviors, shedding light on cryptic intermediate-time regimes and refining the notion of high-crypticity for continuous-space gated processes. Moreover, we extend our formalism to higher dimensions, showcasing its versatility and applicability. Overall, this work provides valuable insights into the dynamics of continuous gated first-passage processes and offers analytical tools for studying them across diverse domains., Comment: 26 pages, 6 figures

First-passage times provide invaluable insight into fundamental properties of stochastic processes. Yet, various forms of gating mask first-passage times and differentiate them from actual detection times. For instance, imperfect conditions may intermittently gate our ability to observe a system of interest, such that exact first-passage instances might be missed. In other cases, e.g., certain chemical reactions, direct observation of the molecules involved is virtually impossible, but the reaction event itself can be detected. However, this instance need not coincide with the first collision time since some molecular encounters are infertile and hence gated. Motivated by the challenge posed by such real-life situations we develop a universal -- model-free -- framework for the inference of first-passage times from the detection times of gated first-passage processes. In addition, when the underlying laws of motions are known, our framework also provides a way to infer physically meaningful parameters, e.g. diffusion coefficients. Finally, we show how to infer the gating rates themselves via the hitherto overlooked short-time regime of the measured detection times. The robustness of our approach and its insensitivity to underlying details are illustrated in several settings of physical relevance.

Adsorption is the accumulation of a solute at an interface that is formed between a solution and an additional gas, liquid, or solid phase. The macroscopic theory of adsorption dates back more than a century and is now well-established. Yet, despite recent advancements, a detailed and self-contained theory of single-particle adsorption is still lacking. Here, we bridge this gap by developing a microscopic theory of adsorption kinetics, from which the macroscopic properties follow directly. One of our central achievements is the derivation of the microsopic version of the seminal Ward-Tordai relation which connects the surface and subsurface adsorbate concentrations via a universal equation that holds for arbitrary adsorption dynamics. Furthermore, we present a microscopic interpretation of the Ward-Tordai relation which, in turn, allows us to generalize it to arbitrary dimension, geometry and initial conditions. The power of our approach is showcased on a set of hitherto unsolved adsorption problems to which we present exact analytical solutions. The framework developed herein sheds fresh light on the fundamentals of adsorption kinetics, which opens new research avenues in surface science with applications to artificial and biological sensing and to the design of nano-scale devices., Comment: 23 pages, 6 figures

How much time does it take two molecules to react? If a reaction occurs upon contact, the answer to this question boils down to the classic first-passage time problem: find the time it takes the two molecules to meet. However, this is not always the case as molecules switch stochastically between reactive and non-reactive states. The reaction is then said to be "gated" by the internal states of the molecules involved which could have a dramatic influence on kinetics. A unified, continuous-time, approach to gated reactions on networks was presented in [Phys. Rev. Lett. 127, 018301, 2021]. Here, we build on this recent advancement and develop an analogous discrete-time version of the theory. Similar to continuous-time, we employ a renewal approach to show that the gated reaction time can always be expressed in terms of the corresponding ungated first-passage and return times; which yields formulas for the generating function of the gated reaction-time distribution and its corresponding mean and variance. In cases where the mean reaction time diverges, we show that the long-time asymptotics of the gated problem is inherited from its ungated counterpart. However, when molecules spend most of their time non-reactive, an interim regime of slower power-law decay emerges prior to the terminal asymptotics. The discretization of time also gives rise to resonances and anti-resonances, which were absent from the continuous time picture. These features are illustrated using two case studies that also demonstrate how the general approach presented herein greatly simplifies the analysis of gated reactions.

For two molecules to react they first have to meet. Yet, reaction times are rarely on par with the first-passage times that govern such molecular encounters. A prime reason for this discrepancy is stochastic transitions between reactive and non-reactive molecular states, which results in effective gating of product formation and altered reaction kinetics. To better understand this phenomenon we develop a unifying approach to gated reactions on networks. We first show that the mean and distribution of the gated reaction time can always be expressed in terms of ungated first-passage and return times. This relation between gated and ungated kinetics is then explored to reveal universal features of gated reactions. The latter are exemplified using a diverse set of case studies which are also used to expose the exotic kinetics that arises due to molecular gating.