TY - JOUR
T1 - Self-Healable Reprocessable Triboelectric Nanogenerators Fabricated with Vitrimeric Poly(hindered Urea) Networks
AU - Patel, Twinkal
AU - Kim, Minsoo P.
AU - Park, Junyoung
AU - Lee, Tae Hee
AU - Nellepalli, Pothanagandhi
AU - Noh, Seung Man
AU - Jung, Hyun Wook
AU - Ko, Hyunhyub
AU - Oh, Jung Kwon
N1 - Funding Information:
This work is supported from Natural Science and Engineering Research Council (NSERC) in Canada through Discovery Grant (RGPIN/4989-2016) and Canada Research Chair (CRC) (950-231058) Award, National Research Foundation (NRF) of Korea (2019R1I1A1A01060653), and Ministry of Trade, Industry, and Energy (10067082). J.K.O. is entitled Tier II CRC in Nanobioscience (renewed in 2016). The Office of the VP Research at Concordia University is also acknowledged for stipends for T.P. through Team Accelerate Grant and P.N. through Horizon Postdoctoral Fellowship. The authors thank Dr. Heng Wang at Concordia Center of Composite (ConCom) for his helpful suggestions with rheometer operation.
Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/9/22
Y1 - 2020/9/22
N2 - In recent years, the advent of highly deformable and healable electronics is exciting and promising for next-generation electronic devices. In particular, self-healable triboelectric nanogenerators (SH-TENGs) serve as promising candidates based on the combination of the triboelectric effect, electrostatic induction, and self-healing action. However, the majority of SH-TENGs have been devised with weak polymeric networks that are healed with reversible supramolecular interactions or disulfides, thus resulting in poor mechanical properties and low resistance to creeping. To address this issue, we demonstrate the integration of mechanically strong and self-healable poly(hindered urea) (PHU) network in the fabrication of effective TENGs. The designed PHU network is flexible but shows greater mechanical property of tensile strength as high as 1.7 MPa at break. The network is capable of self-healing quickly and repeatedly as well as being reprocessable under mild conditions, enabling the recovery of triboelectric performances after the complete healing of the damaged surfaces. Furthermore, the interfacial-polarization-induced enhancement of dielectric constant endows our SH-TENG with the highest triboelectric output performance (169.9 V/cm2) among the reported healable TENGs. This work presents an avenue to the development of mechanical energy-harvesting devices and self-powered sensors with excellent stretchability, high recoverability, and good mechanical strength.
AB - In recent years, the advent of highly deformable and healable electronics is exciting and promising for next-generation electronic devices. In particular, self-healable triboelectric nanogenerators (SH-TENGs) serve as promising candidates based on the combination of the triboelectric effect, electrostatic induction, and self-healing action. However, the majority of SH-TENGs have been devised with weak polymeric networks that are healed with reversible supramolecular interactions or disulfides, thus resulting in poor mechanical properties and low resistance to creeping. To address this issue, we demonstrate the integration of mechanically strong and self-healable poly(hindered urea) (PHU) network in the fabrication of effective TENGs. The designed PHU network is flexible but shows greater mechanical property of tensile strength as high as 1.7 MPa at break. The network is capable of self-healing quickly and repeatedly as well as being reprocessable under mild conditions, enabling the recovery of triboelectric performances after the complete healing of the damaged surfaces. Furthermore, the interfacial-polarization-induced enhancement of dielectric constant endows our SH-TENG with the highest triboelectric output performance (169.9 V/cm2) among the reported healable TENGs. This work presents an avenue to the development of mechanical energy-harvesting devices and self-powered sensors with excellent stretchability, high recoverability, and good mechanical strength.
KW - dynamic bulky urea chemistry
KW - interfacial polarization
KW - poly(hindered urea)
KW - reprocessability
KW - self-healing
KW - triboelectric device
UR - http://www.scopus.com/inward/record.url?scp=85091602095&partnerID=8YFLogxK
U2 - 10.1021/acsnano.0c03819
DO - 10.1021/acsnano.0c03819
M3 - Article
C2 - 32840992
AN - SCOPUS:85091602095
SN - 1936-0851
VL - 14
SP - 11442
EP - 11451
JO - ACS Nano
JF - ACS Nano
IS - 9
ER -