Hollow polysiloxane nanostructures based on pressure-induced film expansion
Source abstract
Abstract
Superhydrophobicity has gained extensive interest in academia and industry. One of the most facile ways of creating superhydrophobic surfaces is the surface-initiated synthesis of 1D polysiloxane nanostructures known as silicone nanofilaments. However, physicochemical details of their synthesis process remain a puzzle, and studies so far have fallen short in explaining the ways in which the 3D film growth transforms into 1D objects. From the observation of hollow cylindrical polysiloxane nanostructures, this study proposes a growth model based on pressure-induced uniaxial elongation of a partially cross-linked polysiloxane film. The pressure build-up is caused by gaseous by-products of hydrolysis and condensation reactions. The presented model aims to promote the understanding of the growth processes, and could thus facilitate the design of robust superhydrophobic coatings onto various surfaces. Furthermore, it is envisioned that novel applications utilizing the tubular nature of the nanostructures could emerge. This article contains supporting information that is available online.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Surface Modification and Superhydrophobicity · Advanced Sensor and Energy Harvesting Materials · Aerogels and thermal insulation
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Staff scientist, Nanomicroscopy Center, Aalto University School of Science, Espoo, Finland
Undergraduate student, Department of Applied Physics, Aalto University School of Science, Espoo, Finland
Graduate student, Department of Applied Physics, Aalto University School of Science, Espoo, Finland
Professor, Department of Applied Physics, Aalto University School of Science, Espoo, Finland
References (33)
Show source-provided references
1. 10.1021/la950418o10.1021/la950418o ↗
2. 10.1007/s00425005009610.1007/s004250050096 ↗
3. 10.1006/jcis.1998.581310.1006/jcis.1998.5813 ↗
4. 10.1016/j.cis.2009.11.00110.1016/j.cis.2009.11.001 ↗
5. 10.1039/c1sm05849e10.1039/c1sm05849e ↗
6. 10.1006/anbo.1997.040010.1006/anbo.1997.0400 ↗
7. 10.1016/j.cocis.2006.06.00210.1016/j.cocis.2006.06.002 ↗
8. 10.1146/annurev.matsci.38.060407.13243410.1146/annurev.matsci.38.060407.132434 ↗
9. 10.1073/pnas.120432810910.1073/pnas.1204328109 ↗
10. 10.1039/tf944400054610.1039/tf9444000546 ↗
11. 10.1002/adma.20100312910.1002/adma.201003129 ↗
12. 10.1016/j.apsusc.2006.12.11810.1016/j.apsusc.2006.12.118 ↗
13. 10.1016/j.colsurfa.2007.02.03310.1016/j.colsurfa.2007.02.033 ↗
14. 10.1002/adma.20050203010.1002/adma.200502030 ↗
15. 10.1021/ja062943n10.1021/ja062943n ↗
16. 10.1021/la063604a10.1021/la063604a ↗
17. 10.1163/156856108X30516510.1163/156856108X305165 ↗
18. 10.1021/la801595m10.1021/la801595m ↗
19. 10.1088/0957-4484/19/34/34560310.1088/0957-4484/19/34/345603 ↗
20. 10.1021/jp811462210.1021/jp8114622 ↗
21. 10.1039/c1py00246e10.1039/c1py00246e ↗
22. 10.1016/j.apsusc.2012.04.08410.1016/j.apsusc.2012.04.084 ↗
23. 10.1080/01932691.2011.58448310.1080/01932691.2011.584483 ↗
24. 10.1021/am400025z10.1021/am400025z ↗
25. 10.1002/cphc.20120099510.1002/cphc.201200995 ↗
26. 10.1021/cm400851k10.1021/cm400851k ↗
27. 10.1021/la702529710.1021/la7025297 ↗
28. 10.1039/C3PY01293J10.1039/C3PY01293J ↗
29. 10.1021/la400009m10.1021/la400009m ↗
30. 10.1021/la001780s10.1021/la001780s ↗
31. 10.1088/0026-1394/41/3/00510.1088/0026-1394/41/3/005 ↗
32. 10.1021/cr040369x10.1021/cr040369x ↗
33. Hearn E. J. · 1997