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Open AccessDOI: 10.1007/s40843-026-4175-3Original Research

Cracking-Directed Dynamic Liquid Bridging for Autonomous Microdroplet Recession and Enrichment

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Cracking-Directed Dynamic Liquid Bridging for Autonomous Microdroplet Recession and Enrichment
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Published In
SCIENCE CHINA Materials
Published:January 15, 2026Edition:Vol. 69, Issue 9 • pp. 100-112Citation:Zhao Li et al. (2026), SCIENCE CHINA Materials
Impact Factor3.5 (Q2 Scopus)
Source Journal中国科学: 材料
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Key Takeaways & Executive Findings

  • • • Achieved 14.2-fold enhancement in enrichment efficiency for airborne pathogenic agents compared to conventional flat surfaces, demonstrating superior capture capability for microdroplets (<20 μm). • • Utilized stretchable elastomeric substrate with island-like microstructures; controlled fracture under longitudinal tensile stress yields directionally oriented cracks that generate localized capillary forces to overcome CAH. • • The crack-mediated capillary bridging strategy enables autonomous microdroplet recession and enrichment without external stimulation, addressing limitations of gradient-based methods at micro-scale. • • Integration of fracture mechanics with capillary-driven fluid dynamics provides a foundational framework for next-generation microfluidic systems, with potential in biosensing and pollutant analysis.

Abstract

The precise manipulation of microdroplets (diameter < 20 μm) on solid substrates is critical for applications in environmental monitoring, targeted drug delivery, clinical diagnostics, and public health. A major challenge is contact angle hysteresis (CAH), which pins droplets and impedes mobility. Here, we introduce a crack-mediated capillary bridging strategy for efficient capture and directional transport of microdroplets. The approach employs a stretchable elastomeric substrate with island-like microstructures. Under longitudinal tensile stress, controlled fracture generates densely packed, directionally oriented surface cracks. These fissures induce localized capillary forces that counteract adhesion-induced resistance, enabling programmable droplet motion. Experiments capturing airborne pathogenic agents demonstrated a 14.2-fold enhancement in enrichment efficiency compared to flat surfaces. This work integrates fracture mechanics with capillary-driven fluid dynamics, establishing a framework for next-generation microfluidic systems. The findings offer promising avenues for biosensing, pollutant analysis, and interdisciplinary applications.

1. Introduction

Airborne microdroplets, ranging from nanometers to micrometers, pose significant challenges in manipulation due to their high surface-to-volume ratio and enhanced contact angle hysteresis (CAH). Conventional methods using surface gradients or asymmetric structures fail for droplets smaller than 20 μm, as adhesive forces dominate and impede directional motion. This bottleneck limits applications in microfluidics, drug delivery, and bio-detection, where precise droplet control is essential.

Our crack-mediated capillary bridging strategy overcomes this by engineering a stretchable elastomeric substrate with island-like microstructures. Upon tensile stress, controlled fracture creates oriented cracks that generate strong localized capillary forces, effectively counteracting CAH and enabling autonomous droplet transport. This approach not only enhances enrichment efficiency by 14.2-fold but also offers a scalable, passive mechanism for microdroplet manipulation, addressing the critical need for efficient capture and directional transport in real-world applications.

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Cite This Research Paper
Zhao Li, Hubao A, Huanhuan Dong, Zhimin Lu, Changming Wu, Shuang Zheng, Zonglin Chu, Ganhua Xie, Yang Xu, Shan Peng, Yuanyuan Zhao (2026). Cracking-Directed Dynamic Liquid Bridging for Autonomous Microdroplet Recession and Enrichment. SCIENCE CHINA Materials. https://doi.org/10.1007/s40843-026-4175-3
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Frequently Asked Questions

What is the maximum droplet size that can be effectively manipulated using this crack-mediated strategy?

The strategy is specifically designed for microdroplets with diameter < 20 μm, where conventional methods fail due to enhanced CAH. The 14.2-fold enrichment enhancement was demonstrated for airborne pathogenic agents, indicating effectiveness in this size range.

How does the crack density and orientation affect the capillary forces and droplet transport efficiency?

The cracks are densely packed and directionally oriented, generating localized capillary forces that counteract adhesion. The precise control of crack formation via tensile stress allows programmable droplet motion, but quantitative relationships between crack parameters and transport efficiency are not detailed in the provided text.

What is the durability and repeatability of the stretchable substrate under repeated tensile cycles?

The text does not specify durability or cycle life. However, the use of elastomeric substrates suggests potential for repeated use, but further testing is required to assess fatigue and performance degradation over time.

Can this method be scaled up for industrial applications, and what are the cost implications?

The method involves precision fabrication of island-like microstructures and controlled fracture, which may be scalable using existing lithography and stretchable electronics techniques. Cost implications are not discussed, but the passive nature (no external stimulation) could reduce operational costs in applications like biosensing.

What are the limitations of this approach for non-aqueous or high-viscosity droplets?

The study focuses on airborne microdroplets, likely aqueous. The capillary bridging mechanism relies on liquid bridge formation, which may be affected by droplet viscosity and surface tension. The text does not address non-aqueous or high-viscosity fluids, so applicability is uncertain.

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