journal article·2022-03-25

Scalable Nanofabrication of T-Shape Nanopillars Based on Polystyrene/Polyphenylsilsequioxane Films Showing Broadband Antireflection and Super-omniphobicity

Shuijing Wang, Hongdou Li, Rong Xia, Yaqing Xie, Yang Li, Haixiong Ge, Chunhua Lu

ACS Applied Nano Materials· Volume 5· Issue 3
Publisher page

Abstract

The ability to create antireflective super-omniphobic surfaces is important for various optoelectronic applications, which is still a challenge. The combination design of sub-wavelength nanoscale structures for antireflection and re-entrant structures for super-omniphobicity is an effective way to obtain super-omniphobicity and antireflection simultaneously. However, due to the inclination of droplets to strike to the bottom and the complicated craftsmanship, obtaining efficient nanoscale re-entrant super-omniphobic surfaces is difficult, which limits the compatibility of antireflection and super-omniphobicity. Herein, disordered nanoscale T-shape pillars are utilized to obtain the broadband antireflection, non-iridescence, and super-omniphobicity. A simple and repetitive method is reported for large-area scalable fabrication of disordered nanoscale T-shape pillars on glass based on a maskless phase separation lithographic approach. The kinetic roles of Laplace pressure, viscous force, and saturated vapor pressure in the super-omniphobicity are demonstrated by investigating the effect of feature size, interval, area fraction and pillar height of the T-shape nanopillars, liquid surface tension, viscosity, etc. The effects of feature size, interval, and height on the antireflection and the optical behavior on the T-shape nanopillars are also investigated. Although the cap of T-shape nanopillars could bring scattering loss when light touches on the cap range with a large incident angle, broadband antireflection is still obtained. As a demonstration, T-shape nanopillars exhibiting super-omniphobicity (static water contact angle of 160 ± 1.0° and ethyl alcohol contact angle of 162 ± 0.5°), high transparency (94%), broadband antireflection (347–780 nm), and non-iridescence are obtained. Our proposed method provides a simple, rapid, and low-cost process to explore the ability of nanoscale re-entrant structures for compatibility of broadband antireflection and super-omniphobicity, with promising practical application in self-cleaning optoelectronic surfaces.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Surface Modification and Superhydrophobicity · Silicone and Siloxane Chemistry · Fluid Dynamics and Thin Films

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

College of Materials Science and Engineering, Nanjing Tech University, Nanjing, Jiangsu 210009, P. R. China

State Key Laboratory of Materials-Orient Chemical Engineering, Nanjing Tech University, Nanjing, Jiangsu 210009, P. R. China

Jiangsu Collaborative Innovation Center for Advanced Inorganic Function Composites, Nanjing Tech University, Nanjing, Jiangsu 210009, P. R. China

Department of Materials Science and Engineering, College of Engineering and Applied Sciences, Nanjing University, Nanjing, Jiangsu 210093, P. R. China

National Laboratory of Solid State Microstructures, Nanjing University, Nanjing, Jiangsu 210093, P. R. China

Funding

Jiangsu Provincial Key Research and Development Program · Ministry of Science and Technology of the People's Republic of China · Six Talent Peaks Project in Jiangsu Province · National Natural Science Foundation of China · Priority Academic Program Development of Jiangsu Higher Education Institutions

References (48)

Show source-provided references
1. 10.1021/acsnano.8b0560010.1021/acsnano.8b05600 ↗
2. 10.1039/C6CS00751A10.1039/C6CS00751A ↗
3. 10.1002/adem.20160087910.1002/adem.201600879 ↗
4. 10.1021/am509135310.1021/am5091353 ↗
5. Lin M. F. · Adv. Mater. Technol. · 2016 · 2 · 160018610.1002/admt.201600186 ↗
6. 10.1126/science.114832610.1126/science.1148326 ↗
7. 10.1039/C7TA03248J10.1039/C7TA03248J ↗
8. 10.1002/adfm.20170741510.1002/adfm.201707415 ↗
9. 10.1002/smll.20190461210.1002/smll.201904612 ↗
10. 10.1021/acsami.7b0352610.1021/acsami.7b03526 ↗
11. 10.1021/acsnano.8b0509910.1021/acsnano.8b05099 ↗
12. 10.1002/adma.20180010310.1002/adma.201800103 ↗
13. 10.1126/sciadv.aat497810.1126/sciadv.aat4978 ↗
14. 10.1021/acsnano.6b0671510.1021/acsnano.6b06715 ↗
15. 10.1039/C9MH00589G10.1039/C9MH00589G ↗
16. 10.1021/la703401f10.1021/la703401f ↗
17. 10.1021/jp407039910.1021/jp4070399 ↗
18. 10.1038/nnano.2007.38910.1038/nnano.2007.389 ↗
19. 10.1016/j.mser.2010.04.00110.1016/j.mser.2010.04.001 ↗
20. 10.1021/acsami.0c0082310.1021/acsami.0c00823 ↗
21. 10.1021/acsami.0c1877610.1021/acsami.0c18776 ↗
22. 10.1016/j.jcis.2019.06.10610.1016/j.jcis.2019.06.106 ↗
23. 10.1002/adfm.20190435010.1002/adfm.201904350 ↗
24. 10.1016/j.bios.2018.06.06010.1016/j.bios.2018.06.060 ↗
25. 10.1021/acsami.8b1102010.1021/acsami.8b11020 ↗
26. 10.1016/j.solener.2017.12.02310.1016/j.solener.2017.12.023 ↗
27. 10.1021/acsnano.0c0346310.1021/acsnano.0c03463 ↗
28. 10.1021/acsami.0c1246510.1021/acsami.0c12465 ↗
29. 10.1039/C8RA00414E10.1039/C8RA00414E ↗
30. 10.1039/c4tc00063c10.1039/c4tc00063c ↗
31. 10.1038/s41598-018-26119-810.1038/s41598-018-26119-8 ↗
32. 10.3390/ma1404086710.3390/ma14040867 ↗
33. 10.1002/adfm.20090105210.1002/adfm.200901052 ↗
34. 10.1016/j.apsusc.2018.07.01710.1016/j.apsusc.2018.07.017 ↗
35. 10.1021/acs.langmuir.6b0044710.1021/acs.langmuir.6b00447 ↗
36. 10.1007/s10765-015-1907-210.1007/s10765-015-1907-2 ↗
37. 10.1007/s10570-019-02338-810.1007/s10570-019-02338-8 ↗
38. 10.1080/0193269080250071910.1080/01932690802500719 ↗
39. 10.1021/am404317c10.1021/am404317c ↗
40. 10.1016/j.cis.2008.10.00210.1016/j.cis.2008.10.002 ↗
41. Akira K. · Jpn. J. Appl. Phys. · 2006 · 45 · 542910.1143/JJAP.45.5429 ↗
42. 10.1021/je00019a01610.1021/je00019a016 ↗
43. Thompson W. T. · Philos. Mag. · 1871 · 42 · 44810.1080/14786447108640606 ↗
44. John A. R. · Phys. Chem. C · 2012 · 116 · 863410.1021/jp300166h ↗
45. 10.1002/adfm.20180727510.1002/adfm.201807275 ↗
46. 10.1016/j.jaerosci.2019.10546210.1016/j.jaerosci.2019.105462 ↗
47. Alison B. · Spectrosc. Radiat. Transf. · 2018 · 221 · 6110.1016/j.jqsrt.2018.09.026 ↗
48. 10.1038/ncomms696310.1038/ncomms6963 ↗