Selective Metallization Induced by Laser Activation: Fabricating Metallized Patterns on Polymer via Metal Oxide Composite
Source abstract
Abstract
Recently, metallization on polymer substrates has been given more attention due to its outstanding properties of both plastics and metals. In this study, the metal oxide composite of copper–chromium oxide (CuO·Cr 2 O 3 ) was incorporated into the polymer matrix to design a good laser direct structuring (LDS) material, and the well-defined copper pattern (thickness =10 μm) was successfully fabricated through selective metallization based on 1064 nm near-infrared pulsed laser activation and electroless copper plating. We also prepared polymer composites incorporated with CuO and Cr 2 O 3; however, these two polymer composites both had very poor capacity of selective metallization, which has no practical value for LDS technology. In our work, the key reasons causing the above results were systematically studied and elucidated using XPS, UV–vis–IR, optical microscopy, SEM, contact angle, ATR FTIR, and so on. The results showed that 54.0% Cu 2+ in the polymer composite of CuO·Cr 2 O 3 (the amount =5 wt %) is reduced to Cu 0 (elemental copper) after laser activation (irradiation); however, this value is only 26.8% for the polymer composite of CuO (the amount =5 wt %). It was confirmed that to achieve a successful selective metallization after laser activation, not only was the new formed Cu 0 (the catalytic seeds) the crucial factor, but the number of generated Cu 0 catalytic seeds was also important. These two factors codetermined the final results of the selective metallization. The CuO·Cr 2 O 3 is very suitable for applications of fabricating metallic patterns (e.g., metal decoration, circuit) on the inherent pure black or bright black polymer materials via LDS technology, which has a prospect of large-scale industrial applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Surface Roughness and Optical Measurements · Electrodeposition and Electroless Coatings · Laser-Ablation Synthesis of Nanoparticles
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Polymer Materials Engineering of China, Polymer Research Institute, Sichuan University, Chengdu 610065, China
Funding
National Natural Science Foundation of China · Outstanding Youth Foundation of Sichuan Province · State Key Laboratory of Polymer Materials Engineering, Sichuan University
References (37)
Show source-provided references
1. 10.1021/am201605q10.1021/am201605q ↗
2. 10.1016/j.apsusc.2013.04.11710.1016/j.apsusc.2013.04.117 ↗
3. 10.1016/j.apsusc.2013.04.03510.1016/j.apsusc.2013.04.035 ↗
4. 10.1016/j.apsusc.2013.06.10810.1016/j.apsusc.2013.06.108 ↗
5. 10.1021/am403780610.1021/am4037806 ↗
6. 10.1016/j.mee.2014.09.00310.1016/j.mee.2014.09.003 ↗
7. 10.1016/j.matlet.2007.07.05510.1016/j.matlet.2007.07.055 ↗
8. 10.1016/j.matlet.2009.01.00610.1016/j.matlet.2009.01.006 ↗
9. 10.1021/am800121d10.1021/am800121d ↗
10. 10.1016/j.surfcoat.2011.08.06410.1016/j.surfcoat.2011.08.064 ↗
11. 10.1039/c3tc32146k10.1039/c3tc32146k ↗
12. 10.1021/acsami.5b0959610.1021/acsami.5b09596 ↗
13. 10.1021/acs.langmuir.6b0111810.1021/acs.langmuir.6b01118 ↗
14. 10.1016/j.optmat.2009.02.01610.1016/j.optmat.2009.02.016 ↗
15. 10.1016/j.jmatprotec.2005.04.07510.1016/j.jmatprotec.2005.04.075 ↗
16. 10.1021/am100907j10.1021/am100907j ↗
17. 10.1016/j.surfcoat.2013.02.05010.1016/j.surfcoat.2013.02.050 ↗
18. 10.1016/j.surfcoat.2014.04.00510.1016/j.surfcoat.2014.04.005 ↗
19. 10.1007/s12034-014-0615-z10.1007/s12034-014-0615-z ↗
20. 10.1016/j.matlet.2015.02.01810.1016/j.matlet.2015.02.018 ↗
21. 10.1016/j.cej.2016.05.11410.1016/j.cej.2016.05.114 ↗
22. 10.1016/j.surfcoat.2014.10.01510.1016/j.surfcoat.2014.10.015 ↗
23. 10.1021/acsami.6b1130510.1021/acsami.6b11305 ↗
24. 10.1021/acsami.5b1024310.1021/acsami.5b10243 ↗
25. 10.1063/1.33672810.1063/1.336728 ↗
26. Makee T. J. · Plast. Technol. · 1996 · 35 · 11
27. 10.1016/S0169-4332(02)01239-410.1016/S0169-4332(02)01239-4 ↗
28. 10.1007/s00339-006-3856-x10.1007/s00339-006-3856-x ↗
29. 10.1006/jcat.1998.209410.1006/jcat.1998.2094 ↗
30. 10.1016/j.jcat.2011.09.03010.1016/j.jcat.2011.09.030 ↗
31. 10.1021/ja406820f10.1021/ja406820f ↗
32. 10.1039/b906352h10.1039/b906352h ↗
33. 10.1016/S0032-3861(02)00152-010.1016/S0032-3861(02)00152-0 ↗
34. 10.1016/j.aca.2014.07.02110.1016/j.aca.2014.07.021 ↗
35. 10.1016/S0141-3910(01)00093-310.1016/S0141-3910(01)00093-3 ↗
36. 10.1016/S0924-2031(01)00111-410.1016/S0924-2031(01)00111-4 ↗
37. 10.3390/polym203017410.3390/polym2030174 ↗