SU-8-Induced Strong Bonding of Polymer Ligands to Flexible Substrates via in Situ Cross-Linked Reaction for Improved Surface Metallization and Fast Fabrication of High-Quality Flexible Circuits
Source abstract
Abstract
On account of in situ cross-linked reaction of epoxy SU-8 with poly(4-vinylpyridine) (P4VP) and its strong reactive bonding ability with different pretreated substrates, we developed a simple universal one-step solution-based coating method for fast surface modification of various objects. Through this method, a layer of P4VP molecules with controllable thickness can be tethered tightly onto substrates with the assistance of SU-8. P4VP molecules possess a lot of pyridine ligands to immobilize transitional metal ions that can behave as the catalyst of electroless copper plating for surface metallization while functioning as the adhesion-promoting layer between the substrate and deposited metal. Attributed to interpenetrated entanglement of P4VP molecules and as-deposited metal, ultrathick (>7 μm) strongly adhesive high-quality copper layer can be formed on flexible substrates without any delamination. Then through laser printer to print toner mask, a variety of designed circuits can be easily fabricated on modified flexible PET substrate.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanofabrication and Lithography Techniques · Force Microscopy Techniques and Applications · Molecular Junctions and Nanostructures
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Mechanical and Materials Engineering, The University of Western Ontario, London, Ontario N6A 5B9, Canada
Department of Electronic and Information Engineering, South China University of Technology, Guangzhou 510641, P. R. China
Funding
Natural Sciences and Engineering Research Council of Canada
References (28)
Show source-provided references
1. 10.1038/nature0249810.1038/nature02498 ↗
2. 10.1126/science.120615710.1126/science.1206157 ↗
3. 10.1002/adma.20060222310.1002/adma.200602223 ↗
4. 10.1002/adma.20130118410.1002/adma.201301184 ↗
5. 10.1021/ja908433p10.1021/ja908433p ↗
6. 10.1039/C3TC31740D10.1039/C3TC31740D ↗
7. 10.1021/am100016310.1021/am1000163 ↗
8. 10.1149/1.349358510.1149/1.3493585 ↗
9. 10.1021/la060891+10.1021/la060891+ ↗
10. 10.1002/adfm.20110004110.1002/adfm.201100041 ↗
11. 10.1002/cphc.20110056210.1002/cphc.201100562 ↗
12. 10.1021/la051538r10.1021/la051538r ↗
13. 10.1021/am405539r10.1021/am405539r ↗
14. 10.1002/marc.20040046210.1002/marc.200400462 ↗
15. 10.1021/la010755z10.1021/la010755z ↗
16. 10.1021/la404251h10.1021/la404251h ↗
17. 10.1149/1.151291510.1149/1.1512915 ↗
18. 10.1016/S0169-4332(02)00473-710.1016/S0169-4332(02)00473-7 ↗
19. 10.1021/jp013236d10.1021/jp013236d ↗
20. 10.1002/marc.1986.03007010710.1002/marc.1986.030070107 ↗
21. 10.1002/apmc.1986.05142010210.1002/apmc.1986.051420102 ↗
22. 10.1007/s10853-005-1732-210.1007/s10853-005-1732-2 ↗
23. 10.1002/adma.20140105310.1002/adma.201401053 ↗
24. 10.1021/am800121d10.1021/am800121d ↗
25. 10.1002/adfm.20120354410.1002/adfm.201203544 ↗
26. 10.1021/ja908433p10.1021/ja908433p ↗
27. 10.1021/am404620y10.1021/am404620y ↗
28. 10.1021/acsnano.5b0508210.1021/acsnano.5b05082 ↗