Quantitative thermodynamic analyses of nucleation, evolution and stabilization of surface nanobubbles

Lili Lan; Yongcai Pan; Liang Zhao; Binghai Wen

Home/Archive/arXiv

arXiv · 2502.02916

Quantitative thermodynamic analyses of nucleation, evolution and stabilization of surface nanobubbles

Lili Lan·Yongcai Pan·Liang Zhao·Binghai Wen

View original source ↗Read source document ↗Export metadata ↓

Abstract

Surface nanobubbles are complex micro- and nanoscale fluid systems. While thermodynamics is believed to dominate nanobubble dynamics, the precise mechanism by which nanobubble evolution is driven by thermodynamics remains unclear. It is essential to understand how nanobubble nucleation and growth, nanoscale contact line movement, and gas diffusion across the liquid-bubble interface are simultaneously driven by the change in free energy, leading to the ultimate thermodynamic equilibrium of surface nanobubble systems. In this paper, we first propose a quantitative theoretical model to elucidate the thermodynamic dominance behind the dynamics and stability of the fluid system with surface nanobubbles. The present model demonstrates that thermodynamic non-equilibrium drives the gas diffusion and the contact line motion of surface nanobubbles. Overcoming the nucleation energy barrier is crucial for bubble nucleation and growth. Surface nanobubbles evolve towards the reduction of the system's free energy and stabilize at the state with minimum free energy. The thermodynamic equilibrium is accompanied by the mechanical equilibrium at the contact line and the gas diffusion equilibrium at the liquid-bubble interface, and the theoretical results are in excellent agreement with the nanobubble morphology observed in experiments. The study highlights the significant influence of gas properties and ambient conditions in promoting bubble nucleation and stability.

Explore related subjects

cond-mat.soft physics.comp-ph physics.flu-dyn

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

Lili Lan, Yongcai Pan, Liang Zhao, Binghai Wen. 2025-02-05. Quantitative thermodynamic analyses of nucleation, evolution and stabilization of surface nanobubbles. https://arxiv.org/abs/2502.02916

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

arXiv2026

Transient Elasticity -- A Unifying Framework for Thixotropy, Polymers, and Granular Media

Thixotropic yield stress fluids, such as paint or ketchup, are traditionally viewed as elastic structures that, under shear rates, break into viscous liquids with lumps, and reconnect at rest. An alternative framework is presented here: Upon shear, structural destruction is incomplete, leaving sufficient connections. As a result, elasticity fundamentally underlies their non-Newtonian behavior, though they do appear purely viscous under a steady shear, displaying little direct evidence of elastic rebound---same as granular media and polymers. Consequently, all three are described by the same set of evolution equations, differing only in their parameters. These equations are set up by starting from solid dynamics and allowing the elastic strain $\varepsilon^e$ to relax, which in effect interpolates between solid and fluid behavior, appropriate for systems that display both types of behavior. Incorporating in addition a two-temperature framework, tracking how energy is dissipated in two consecutive stages, yields the nonlinear model of Transient Elasticity (TE). It describes an elasticity that is transient in time yet persistent under shear. Previously validated for polymers and granular media, TE is here applied to thixotropic yield-stress fluids. As shown, it successfully accounts for a wide range of characteristic phenomena, including over- and undershoot, viscosity bifurcation, shear banding, and oscillatory rheography. Given its appropriateness across structurally diverse systems, TE offers a unified, surprisingly general account of non-Newtonian phenomena.

cond-mat.soft↗

arXiv2026

Linear and nonlinear active microrheology of viscous, viscoelastic, and elastic media: A fluid particle dynamics approach

Active microrheology is an effective tool to determine the rheological properties of viscous, viscoelastic, or elastic materials on microscopic length scales. The positional response of an embedded probe particle to an externally applied oscillating driving force allows to indirectly characterize the properties of the surrounding media. We aim to explore the linear and nonlinear response of probe particles in a microrheological setup of planar geometry. For this purpose, we extend the computational method of fluid particle dynamics from viscous fluid-like to viscoelastic and elastic media, including nonlinear regimes. We consider a system confined by solid walls. In this case, we validate the approach by quantifying the linear response in terms of a Jeffreys model. Increasing the amplitude of the driving force, we observe distinct nonlinear effects. They include distorted stress-strain curves and a gradual net drift of probe particles initially positioned close to a wall. This drift vanishes in the viscous fluid-like and elastic solid-like limits, but is manifest for intermediate viscoelastic systems. We further address a setup of two probe particles in the absence of walls. They experience reciprocal pairwise oscillatory forcing. Here, nonlinearities in viscoelastic systems induce a net drift gradually moving the particles further apart from each other. Comparing with real setups, our implementation of the driving force is in line with experimental setups of optical tweezers or active magnetic microrheology.

cond-mat.soft↗

arXiv2026

Reinterpreting ultrafast experiments on supercooled water: Glass transition versus liquid-liquid criticality

Water's anomalous properties have been hypothesized to originate from a liquid-liquid critical point in the supercooled regime, separating high- and low-density liquid states. Experimental verification remains challenging due to rapid crystallization under these conditions. A recent study reported evidence for such a transition, based primarily on a pronounced increase in the heat capacity of rapidly heated low-density amorphous ice. Here, we show that this heat capacity increase can be explained without invoking a liquid-liquid transition. By combining simulations using a machine-learning potential trained on the state-of-the-art MB-pol water model, combined with the Tool-Narayanaswamy-Moynihan (TNM) model of the glass transition, we demonstrate that the observed signal can arise instead from a dynamical effect induced by the mobilization of rotational and translational molecular degrees of freedom during ultrafast heating. We further show that our findings are fully consistent with recent electron diffraction measurements showing structural arrest of supercooled water close to our predicted glass-transition temperature. These results provide an alternative interpretation of the experimental observations and highlight the importance of nonequilibrium glassy dynamics in the interpretation of the behavior of supercooled water on ultra-short time scales.

cond-mat.soft↗