TY - JOUR
T1 - Ultrasonic-Induced Synthesis of Underwater Adhesive and Antiswelling Hydrogel for Strain Sensor
AU - Wang, Siying
AU - Wang, Leichen
AU - Qu, Xinyu
AU - Lei, Bing
AU - Zhao, Ye
AU - Wang, Qian
AU - Wang, Wenjun
AU - Shao, Jinjun
AU - Dong, Xiaochen
N1 - Publisher Copyright:
© 2022 American Chemical Society
PY - 2022
Y1 - 2022
N2 - To perceive the human body's multienvironmental mobility, intelligent flexible electronic equipment with an underwater motion monitoring function has potential research value in the field of intelligent detection. Hydrogels are widely used in the field of flexible electronics for their unique three-dimensional polymer networks. Due to the instinctive hydrophilicity of hydrogels, the swelling of hydrogels underwater and the formation of hydration coating on the surface become the primary obstacles to underwater applications. Herein, a hydrogel sensor that can achieve underwater utilization was prepared through copolymerization between hydrophobic and hydrophilic polymer monomers. The synergistic impact of electrostatic interaction, metal coordination, and hydrogen bonding ensured the hydrogel's remarkable underwater adhesive ability to a variety of substrates. The hydrophobic micelles and self-hydrophobization process induced from ultrasonic dispersion in the polymer matrix gave an outstanding hydrophobic performance (water contact angle of 130.4°) and antiswelling property (swelling ratio of 26% after 72 h of immersion), presenting unprecedented underwater adaptability. The above-mentioned hydrogel could be assembled into a flexible hydrogel sensor with satisfactory sensitivity (gauge factor of 0.44), ultrafast response rate (106 ms), and excellent cyclic stability, demonstrating accurate monitoring of complex human motions in water and air.
AB - To perceive the human body's multienvironmental mobility, intelligent flexible electronic equipment with an underwater motion monitoring function has potential research value in the field of intelligent detection. Hydrogels are widely used in the field of flexible electronics for their unique three-dimensional polymer networks. Due to the instinctive hydrophilicity of hydrogels, the swelling of hydrogels underwater and the formation of hydration coating on the surface become the primary obstacles to underwater applications. Herein, a hydrogel sensor that can achieve underwater utilization was prepared through copolymerization between hydrophobic and hydrophilic polymer monomers. The synergistic impact of electrostatic interaction, metal coordination, and hydrogen bonding ensured the hydrogel's remarkable underwater adhesive ability to a variety of substrates. The hydrophobic micelles and self-hydrophobization process induced from ultrasonic dispersion in the polymer matrix gave an outstanding hydrophobic performance (water contact angle of 130.4°) and antiswelling property (swelling ratio of 26% after 72 h of immersion), presenting unprecedented underwater adaptability. The above-mentioned hydrogel could be assembled into a flexible hydrogel sensor with satisfactory sensitivity (gauge factor of 0.44), ultrafast response rate (106 ms), and excellent cyclic stability, demonstrating accurate monitoring of complex human motions in water and air.
KW - antiswelling
KW - flexible electronics
KW - hydrogel
KW - underwater adhesion
KW - underwater application
UR - http://www.scopus.com/inward/record.url?scp=85141645676&partnerID=8YFLogxK
U2 - 10.1021/ACSAMI.2C16388
DO - 10.1021/ACSAMI.2C16388
M3 - 文章
AN - SCOPUS:85141645676
SN - 1944-8244
VL - 14
SP - 50256
EP - 50265
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 44
ER -