Delaying Ice and Frost Formation Using Phase‐Switching Liquids
Source abstract
Abstract
Abstract Preventing water droplets from transitioning to ice is advantageous for numerous applications. It is demonstrated that the use of certain phase‐change materials, which are in liquid state under ambient conditions and have melting point higher than the freezing point of water, referred herein as phase‐switching liquids (PSLs), can impede condensation–frosting lasting up to 300 and 15 times longer in bulk and surface infused state, respectively, compared to conventional surfaces under identical environmental conditions. The freezing delay is primarily a consequence of the release of trapped latent heat due to condensation, but is also affected by the solidified PSL surface morphology and its miscibility in water. Regardless of surface chemistry, PSL‐infused textured surfaces exhibit low droplet adhesion when operated below the corresponding melting point of the solidified PSLs, engendering ice and frost repellency even on hydrophilic substrates. Additionally, solidified PSL surfaces display varying degrees of optical transparency, can repel a variety of liquids, and self‐heal upon physical damage.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Surface Modification and Superhydrophobicity · Icing and De-icing Technologies · Smart Materials for Construction
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Mechanical & Industrial Engineering University of Illinois at Chicago Chicago IL 60607 USA
PMMH/ESPCI & CNRS UMR 7636 Universités Paris 6 & Paris 7 10 rue Vauquelin 75005 Paris France
Funding
The Branco Weiss Fellowship – Society in Science · University of Illinois at Urbana-Champaign · National Science Foundation
References (28)
Show source-provided references
1. 10.1063/1.141618610.1063/1.1416186 ↗
2. 10.1021/nn406522n10.1021/nn406522n ↗
3. 10.1038/natrevmats.2015.310.1038/natrevmats.2015.3 ↗
4. 10.1021/la902882b10.1021/la902882b ↗
5. 10.1021/nn103214q10.1021/nn103214q ↗
6. 10.1021/la104762g10.1021/la104762g ↗
7. 10.1002/adma.20110441210.1002/adma.201104412 ↗
8. 10.1039/C3NR06644D10.1039/C3NR06644D ↗
9. 10.1021/la104277q10.1021/la104277q ↗
10. 10.1063/1.352451310.1063/1.3524513 ↗
11. 10.1038/nature1044710.1038/nature10447 ↗
12. 10.1021/nn302310q10.1021/nn302310q ↗
13. 10.1021/la400801s10.1021/la400801s ↗
14. 10.1080/15567265.2016.125600710.1080/15567265.2016.1256007 ↗
15. 10.1016/j.rser.2007.10.00510.1016/j.rser.2007.10.005 ↗
16. 10.1103/PhysRevLett.68.6410.1103/PhysRevLett.68.64 ↗
17. 10.1021/la504850x10.1021/la504850x ↗
18. Hinds W. C. · 1999
19. 10.1103/PhysRevA.44.827110.1103/PhysRevA.44.8271 ↗
20. 10.1021/acs.langmuir.8b0145010.1021/acs.langmuir.8b01450 ↗
21. 10.1016/0169-8095(95)00015-J10.1016/0169-8095(95)00015-J ↗
22. 10.1021/ja00387a01310.1021/ja00387a013 ↗
23. 10.1039/jm994040097710.1039/jm9940400977 ↗
24. 10.1063/1.166980710.1063/1.1669807 ↗
25. 10.1002/jps.260055082210.1002/jps.2600550822 ↗
26. 10.1021/nn305504810.1021/nn3055048 ↗
27. 10.1209/0295-5075/101/1600910.1209/0295-5075/101/16009 ↗
28. 10.1039/C2SM27032C10.1039/C2SM27032C ↗