Highly Conductive and Fatigue‐Free Flexible Copper Film Electrode Fabricated by a Facile Dry Transfer Technique
Source abstract
Abstract
Abstract The flexible electrodes with excellent electrical and mechanical performance play critical and fundamental roles in the wearable electronics. In this work, highly conductive and fatigue‐free flexible copper thin‐film electrodes on polyethylene terephthalate substrate are successfully fabricated by a facile, nondestructive, and heat‐resistant dry transfer technique. Before the transfer process, the interface adhesive strength and electrical resistivity of Cu films on SiO2+Si substrates are weakened and optimized. The flexible copper film electrode exhibits extremely low electrical resistivity (ρ = 3.1 µΩ cm), which is much superior to the flexible film electrodes fabricated through using the paste agent. Additionally, the fatigue experimental results show that the film electrode possesses excellent flexibility with a bending radius of 10 mm over 500 cycles due to the formation of the special microwavy structure, and is competent for a service environment with alternating temperature (−40–110 °C). It presents that the outstanding performance of flexible Cu film electrode is competent for most wearable electronics. The preparation of the advanced film electrode accelerates progress of the flexible electronics.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Conducting polymers and applications · Nanomaterials and Printing Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering Beihang University No.37 Xueyuan Road Beijing 100191 China
School of Energy and Power Engineering Beihang University No.37 Xueyuan Road Beijing 100191 China
Beijing Key Laboratory for Advanced Functional Materials and Thin Film Technology Beijing 100191 China
Funding
National Natural Science Foundation of China
References (41)
Show source-provided references
1. 10.1002/aenm.20160049010.1002/aenm.201600490 ↗
2. 10.1016/j.nanoen.2016.07.00910.1016/j.nanoen.2016.07.009 ↗
3. 10.3390/s1611171510.3390/s16111715 ↗
4. Park J. · ACS Nano · 2014 · 8 · 9
5. 10.1002/admi.20170049710.1002/admi.201700497 ↗
6. 10.1016/j.matdes.2016.12.04310.1016/j.matdes.2016.12.043 ↗
7. 10.1002/admi.20170050210.1002/admi.201700502 ↗
8. 10.1039/C6TA03537J10.1039/C6TA03537J ↗
9. 10.1039/C6TA05319J10.1039/C6TA05319J ↗
10. 10.1016/j.surfcoat.2016.05.05810.1016/j.surfcoat.2016.05.058 ↗
11. XXXX
12. 10.1007/s10853-015-9198-310.1007/s10853-015-9198-3 ↗
13. 10.1002/adma.20140586410.1002/adma.201405864 ↗
14. 10.1021/nn800434d10.1021/nn800434d ↗
15. 10.1016/j.snb.2009.09.02410.1016/j.snb.2009.09.024 ↗
16. 10.1016/j.jpowsour.2016.11.02810.1016/j.jpowsour.2016.11.028 ↗
17. 10.1088/1757-899X/137/1/01206010.1088/1757-899X/137/1/012060 ↗
18. 10.1002/admi.20160119810.1002/admi.201601198 ↗
19. 10.1021/nn502702a10.1021/nn502702a ↗
20. 10.1039/C6NR04056J10.1039/C6NR04056J ↗
21. 10.1039/C4TC01959H10.1039/C4TC01959H ↗
22. 10.1002/aelm.20160031410.1002/aelm.201600314 ↗
23. 10.1021/acsami.6b0905610.1021/acsami.6b09056 ↗
24. 10.1088/0957-4484/23/48/48570410.1088/0957-4484/23/48/485704 ↗
25. 10.1146/annurev.matsci.30.1.15910.1146/annurev.matsci.30.1.159 ↗
26. 10.1109/TADVP.2006.88477410.1109/TADVP.2006.884774 ↗
27. 10.1007/s11664-002-0120-910.1007/s11664-002-0120-9 ↗
28. Lee J. · J. Korean Phys. Soc. · 2004 · 44 · 1177
29. 10.1021/acsami.6b0138910.1021/acsami.6b01389 ↗
30. 10.1021/nn503758710.1021/nn5037587 ↗
31. 10.1007/s11340-006-9346-410.1007/s11340-006-9346-4 ↗
32. 10.1021/acsami.6b0049910.1021/acsami.6b00499 ↗
33. 10.1016/j.sna.2016.04.05910.1016/j.sna.2016.04.059 ↗
34. 10.1021/acs.nanolett.6b0293110.1021/acs.nanolett.6b02931 ↗
35. 10.1016/j.apsusc.2010.08.10310.1016/j.apsusc.2010.08.103 ↗
36. 10.1088/0957-4484/23/3/03560310.1088/0957-4484/23/3/035603 ↗
37. 10.1016/j.surfcoat.2006.01.04710.1016/j.surfcoat.2006.01.047 ↗
38. 10.1021/am405314s10.1021/am405314s ↗
39. 10.1016/S0143-7496(03)00068-X10.1016/S0143-7496(03)00068-X ↗
40. 10.1126/science.118238310.1126/science.1182383 ↗
41. 10.1002/adfm.20160071310.1002/adfm.201600713 ↗