TY - JOUR
T1 - Ultrastretchable and Stable Strain Sensors Based on Antifreezing and Self-Healing Ionic Organohydrogels for Human Motion Monitoring
AU - Wu, Jin
AU - Wu, Zixuan
AU - Lu, Xing
AU - Han, Songjia
AU - Yang, Bo Ru
AU - Gui, Xuchun
AU - Tao, Kai
AU - Miao, Jianmin
AU - Liu, Chuan
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/3/6
Y1 - 2019/3/6
N2 - Ionic hydrogels, a class of intrinsically stretchable and conductive materials, are widely used in soft electronics. However, the easy freezing and drying of water-based hydrogels significantly limit their long-term stability. Here, a facile solvent-replacement strategy is developed to fabricate ethylene glycol (Eg)/glycerol (Gl)-water binary antifreezing and antidrying organohydrogels for ultrastretchable and sensitive strain sensing within a wide temperature range. Because of the ready formation of strong hydrogen bonds between Eg/Gl and water molecules, the organohydrogels gain exceptional freezing and drying tolerance with retained deformability, conductivity, and self-healing ability even stay at extreme temperature for a long time. Thus, the fabricated strain sensor displays a gauge factor of 6, which is much higher than previously reported values for hydrogel-based strain sensors. Furthermore, the strain sensor exhibits a relatively wide strain range (0.5-950%) even at -18 °C. Various human motions with different strain levels are monitored by the strain sensor with good stability and repeatability from -18 to 25 °C. The organohydrogels maintained the strain sensing capability when exposed to ambient air for nine months. This work provides new insight into the fabrication of stable, ultrastretchable, and ultrasensitive strain sensors using chemically modified organohydrogel for emerging wearable electronics.
AB - Ionic hydrogels, a class of intrinsically stretchable and conductive materials, are widely used in soft electronics. However, the easy freezing and drying of water-based hydrogels significantly limit their long-term stability. Here, a facile solvent-replacement strategy is developed to fabricate ethylene glycol (Eg)/glycerol (Gl)-water binary antifreezing and antidrying organohydrogels for ultrastretchable and sensitive strain sensing within a wide temperature range. Because of the ready formation of strong hydrogen bonds between Eg/Gl and water molecules, the organohydrogels gain exceptional freezing and drying tolerance with retained deformability, conductivity, and self-healing ability even stay at extreme temperature for a long time. Thus, the fabricated strain sensor displays a gauge factor of 6, which is much higher than previously reported values for hydrogel-based strain sensors. Furthermore, the strain sensor exhibits a relatively wide strain range (0.5-950%) even at -18 °C. Various human motions with different strain levels are monitored by the strain sensor with good stability and repeatability from -18 to 25 °C. The organohydrogels maintained the strain sensing capability when exposed to ambient air for nine months. This work provides new insight into the fabrication of stable, ultrastretchable, and ultrasensitive strain sensors using chemically modified organohydrogel for emerging wearable electronics.
KW - antidrying
KW - antifreezing organohydrogels
KW - human motion detection
KW - self-healing
KW - stretchable strain sensor
UR - http://www.scopus.com/inward/record.url?scp=85062347790&partnerID=8YFLogxK
U2 - 10.1021/acsami.8b20267
DO - 10.1021/acsami.8b20267
M3 - 文章
C2 - 30763515
AN - SCOPUS:85062347790
SN - 1944-8244
VL - 11
SP - 9405
EP - 9414
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 9
ER -