Various forms of ecological monitoring and disease diagnosis rely upon the detection of amphiphiles, including lipids, lipopolysaccharides, and lipoproteins, at ultralow concentrations in small droplets. Although assays based on droplets’ wettability provide promising options in some cases, their reliance on the measurements of surface and bulk properties of whole droplets (e.g., contact angles, surface tensions) makes it difficult to monitor trace amounts of these amphiphiles within small-volume samples. Here, we report a design principle in which self-assembled monolayer–functionalized microstructured surfaces coated with silicone oil create locally disordered regions within a droplet’s contact lines to effectively concentrate amphiphiles within the areas that dominate the droplet static friction. Remarkably, such surfaces enable the ultrasensitive, naked-eye detection of amphiphiles through changes in the droplets’ sliding angles, even when the concentration is four to five orders of magnitude below their critical micelle concentration. We develop a thermodynamic model to explain the partitioning of amphiphiles at the contact line by their cooperative association within the disordered, loosely packed regions of the self-assembled monolayer. Based on this local analyte concentrating effect, we showcase laboratory-on-a-chip surfaces with positionally dependent pinning forces capable of both detecting industrially and biologically relevant amphiphiles (e.g., bacterial endotoxins), as well as sorting aqueous droplets into discrete groups based on their amphiphile concentrations. Furthermore, we demonstrate that the sliding behavior of amphiphile-laden aqueous droplets provides insight into the amphiphile’s effective length, thereby allowing these surfaces to discriminate between analytes with highly disparate molecular sizes.
Self‐propulsion of highly wetting liquids is important in heat exchanger, air conditioning, and refrigeration systems. However, it is challenging to achieve such a spontaneous motion as these liquids tend to wet all the surfaces due to their ultralow surface tensions. Despite that extensive asymmetric surface structures and gradient chemical coatings are developed for directional droplet transport, they will be flooded and covered by these liquids. Here, this challenge is addressed by creating a gradient quasi‐liquid surface to achieve the self‐propulsion of droplets with surface tensions down to 10.0 mN m−1. Such a surface engineered by tethering flexible polymers with gradient grafting density shows ultralow contact angle hysteresis (<1o) to highly wetting liquids. Thus, the surface can simultaneously provide sufficient driving forces through the gradient wettability and negligible retention forces through the slippery boundary lubrication for spontaneous droplet movement. Moreover, continual self‐propulsion of tiny droplets is achieved by spraying highly wetting liquids in simulated condensation conditions and demonstrates that adding temperature gradient can further accelerate the self‐propulsion. The study provides a new paradigm to promote passive removal of highly wetting droplets, leading to potential impacts in enhancing condensation heat transfer regardless of surface orientations.
more » « less- Award ID(s):
- 1929677
- NSF-PAR ID:
- 10452911
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Functional Materials
- Volume:
- 31
- Issue:
- 13
- ISSN:
- 1616-301X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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