journal article·2026-04

Self‐Healing Metal Circuits via Controlled Electrochemical Migration: Turning A Reliability Hazard Into an Automatically Triggered and Repeatable Repair Strategy

Fei Gao, Wei Jie Mo, Ze Ping Zhang, Min Zhi Rong, Ming Qiu Zhang

Advanced Functional Materials· Volume 36· Issue 32
Publisher page

Abstract

ABSTRACT Achieving repeatable self‐healing without human intervention in metal circuits remains a critical challenge. Here, we repurpose electrochemical migration, typically a reliability hazard, into a controlled mechanism for intrinsic conductive self‐healing. By optimizing structure of flexible printed circuit boards (PCBs), directional electrochemical migration is allowed to bridge mechanically damaged traces self‐driven by the operational voltage of the PCB itself. The PCBs comprises a healable supramolecular substrate (consists of linear polyurethane and hyperbranched oligomer (LPU/HBO)), Ag circuits, a polyvinyl alcohol isolation layer, gelatin/glycerol/KNO 3 colloidal electrolyte, and an LPU/HBO encapsulation layer. Upon damage, capillary action drives the electrolyte infiltration into cracks, and then promote electrochemical migration between severed wires under working voltage, autonomously reconnecting fractures via metallic dendrite growth. The self‐healing procedure is repeatable, restoring ≈ 100% current in several hours at room temperature, while metal trace can withstand up to 350,000 bending cycles. This work transforms electrochemical migration from a failure mode into a sustainable self‐healing strategy, advancing flexible electronics toward long‐term reliability.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Polymer composites and self-healing · Advanced Sensor and Energy Harvesting Materials · Nanomaterials and Printing Technologies

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

Affiliations

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, GD HPPC Lab, School of Chemistry Sun Yat‐Sen University 132 Waihuan East Road Guangzhou Guangdong China

Funding

National Natural Science Foundation of China

References (65)

Show source-provided references
1. Harper C. A. · 2005
2. Lau J. H. · 2010
3. 10.1016/j.progpolymsci.2023.10172410.1016/j.progpolymsci.2023.101724 ↗
4. 10.1007/s10118-024-3076-x10.1007/s10118-024-3076-x ↗
5. 10.1016/j.mtnano.2025.10061910.1016/j.mtnano.2025.100619 ↗
6. 10.1016/j.cej.2024.15297110.1016/j.cej.2024.152971 ↗
7. 10.1039/C5CC00262A10.1039/C5CC00262A ↗
8. 10.1038/s41928‐025‐01389‐z10.1038/s41928‐025‐01389‐z ↗
9. 10.1002/adfm.20241246110.1002/adfm.202412461 ↗
10. 10.1002/adfm.20170069010.1002/adfm.201700690 ↗
11. 10.1002/adma.20110288810.1002/adma.201102888 ↗
12. 10.1016/j.nanoen.2019.10389810.1016/j.nanoen.2019.103898 ↗
13. 10.1002/aelm.20160013610.1002/aelm.201600136 ↗
14. 10.1021/acsami.1c1585510.1021/acsami.1c15855 ↗
15. 10.6703/IJASE.202409_21(4).00510.6703/IJASE.202409_21(4).005 ↗
16. 10.1021/acsami.8b0888410.1021/acsami.8b08884 ↗
17. 10.1002/adma.20120130610.1002/adma.201201306 ↗
18. 10.1016/j.progpolymsci.2018.03.00210.1016/j.progpolymsci.2018.03.002 ↗
19. 10.1021/am504829z10.1021/am504829z ↗
20. 10.1002/advs.20180010110.1002/advs.201800101 ↗
21. 10.2528/PIERC2501210610.2528/PIERC25012106 ↗
22. 10.1002/ange.20140514510.1002/ange.201405145 ↗
23. 10.1038/s41467‐018‐05238‐w10.1038/s41467‐018‐05238‐w ↗
24. 10.1016/j.nanoen.2023.10923910.1016/j.nanoen.2023.109239 ↗
25. 10.1103/PhysRevApplied.11.01405710.1103/PhysRevApplied.11.014057 ↗
26. 10.1007/s10118‐021‐2627‐710.1007/s10118‐021‐2627‐7 ↗
27. 10.1021/acsnano.4c1830910.1021/acsnano.4c18309 ↗
28. 10.1021/acs.nanolett.5b0314010.1021/acs.nanolett.5b03140 ↗
29. 10.1021/acsami.0c1447210.1021/acsami.0c14472 ↗
30. 10.1038/s41467‐024‐53957‐010.1038/s41467‐024‐53957‐0 ↗
31. 10.1002/adfm.20200353310.1002/adfm.202003533 ↗
32. 10.1016/j.nanoen.2023.10923910.1016/j.nanoen.2023.109239 ↗
33. 10.1002/adma.20120019610.1002/adma.201200196 ↗
34. 10.1038/s41598‐019‐55801‐810.1038/s41598‐019‐55801‐8 ↗
35. 10.1002/adfm.20100015910.1002/adfm.201000159 ↗
36. 10.1007/s40820‐023‐01043‐310.1007/s40820‐023‐01043‐3 ↗
37. 10.1021/acs.nanolett.3c0367010.1021/acs.nanolett.3c03670 ↗
38. 10.1016/j.nanoen.2019.06.02310.1016/j.nanoen.2019.06.023 ↗
39. 10.1002/eem2.1244810.1002/eem2.12448 ↗
40. 10.1016/j.apmt.2021.10115110.1016/j.apmt.2021.101151 ↗
41. 10.1007/s10854‐011‐0435‐510.1007/s10854‐011‐0435‐5 ↗
42. 10.1016/j.microrel.2006.07.08010.1016/j.microrel.2006.07.080 ↗
43. 10.1149/1.210040110.1149/1.2100401 ↗
44. 10.1007/s11664‐008‐0491‐710.1007/s11664‐008‐0491‐7 ↗
45. 10.1109/95.46515910.1109/95.465159 ↗
46. 10.1007/s40195‐020‐01102‐310.1007/s40195‐020‐01102‐3 ↗
47. 10.1149/1.210040110.1149/1.2100401 ↗
48. 10.1021/ma062636210.1021/ma0626362 ↗
49. 10.1039/C6GC01096B10.1039/C6GC01096B ↗
50. 10.1039/C0JM03810E10.1039/C0JM03810E ↗
51. 10.1016/j.xcrp.2021.10037910.1016/j.xcrp.2021.100379 ↗
52. 10.1038/nature0666910.1038/nature06669 ↗
53. 10.1016/j.polymer.2014.06.06410.1016/j.polymer.2014.06.064 ↗
54. 10.1002/adfm.20231251110.1002/adfm.202312511 ↗
55. 10.1016/j.polymertesting.2012.08.00910.1016/j.polymertesting.2012.08.009 ↗
56. 10.1016/j.polymer.2005.10.10710.1016/j.polymer.2005.10.107 ↗
57. 10.1016/j.electacta.2005.02.14510.1016/j.electacta.2005.02.145 ↗
58. 10.1021/acsaem.9b0196510.1021/acsaem.9b01965 ↗
59. 10.1039/C3TA14237J10.1039/C3TA14237J ↗
60. 10.1023/A:101797343259210.1023/A:1017973432592 ↗
61. 10.1080/14786435.2014.90675510.1080/14786435.2014.906755 ↗
62. 10.1038/s41467‐025‐60800‐710.1038/s41467‐025‐60800‐7 ↗
63. 10.1016/0013‐4686(83)85163‐910.1016/0013‐4686(83)85163‐9 ↗
64. 10.1080/21663831.2015.110587610.1080/21663831.2015.1105876 ↗
65. 10.1002/adma.20240100710.1002/adma.202401007 ↗