Dynamic healing-assembly for biocompatible, biodegradable, stretchable and self-healing triboelectric nanogenerators

Ao Shen, Huixia Xuan, Yujie Jia, Shijia Gu, Rasoul Esmaeely Neisiany, Wenmiao Shu, Wei Sun*, Zhengwei You*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)
18 Downloads (Pure)

Abstract

Triboelectric nanogenerators (TENGs) have great potential as power sources for on-skin and implantable electronics. However, most existing TENGs are not suitable for the above applications due to limited material choices, often characterized by rigidity, susceptibility to damage, biological incompatibility, and non-biodegradability. Herein, we developed a simple self-healing assembly strategy based on introducing dynamic Cu(II)-dimethylglyoxime-urethane groups into a biocompatible and biodegradable polyurethane elastomer, to simultaneously address the above obstacles. The coordination of Cu2+ with dynamic bonds significantly enhanced the mechanical properties of elastomer, resulting in a modulus of 9.4 MPa and toughness of 40.2 MJ/m3. These bonds also gave the elastomer skin-like self-healing capabilities, achieving a healing efficiency of 77.5 % at 80 °C. Subsequently, a highly stretchable and integrated triboelectric nanogenerator (Cu-POU TENG) with self-healing capabilities was developed. The Cu-POU TENG with an effective area of 1.5 × 1.5 cm2 produced an open-circuit voltage of 38 V in single-electrode mode. The Cu-POU TENG could restore its original electrical properties through self-healing after mechanical damage. Furthermore, the Cu-POU TENG exhibited biocompatibility and biodegradability, making it suitable for on-skin and implantable electronics. Notably, the Cu-POU TENG maintained a stable voltage output throughout the degradation process. The integration of self-healing feature enabled a sophisticated structure, allowing the Cu-POU TENG to function effectively as a motion sensor for tracking body movement. This Cu-POU TENG holds great potential for applications in on-skin and implantable electronics.

Original languageEnglish
Article number151896
Number of pages11
JournalChemical Engineering Journal
Volume491
Early online date11 May 2024
DOIs
Publication statusPublished - 1 Jul 2024

Funding

This study was financially supported by the National Key Research and Development Program of China (2021YFC2400802, 2021YFC2101800), the National Natural Science Foundation of China (52173117, 52002059, 21991123, 52303178), Ningbo 2025 Science and Technology Major Project (2019B10068), Science and Technology Commission of Shanghai Municipality (20DZ2254900 and 20DZ2270800), the China Postdoctoral Science Foundation (2023M740585), Shanghai Sailing Program (23YF1400500), UK Engineering and Physical Sciences Research Council (EPSRC) (EP/X033686/1).

Keywords

  • bioelectronics
  • elastomer
  • polyurethane
  • self-healing
  • stretchable electronics

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