4.8 Article

Ultra-High Electrical Conductivity in Filler-Free Polymeric Hydrogels Toward Thermoelectrics and Electromagnetic Interference Shielding

期刊

ADVANCED MATERIALS
卷 34, 期 12, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202109904

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资金

  1. National Natural Science Foundation of China [51876151]
  2. Key Research and Development Program in Shaanxi Province of China [2021GXLH-Z-056]
  3. Fundamental Research Funds for the Central Universities
  4. World-Class Universities (Disciplines)
  5. Characteristic Development Guidance Funds for the Central Universities [PY3A010]
  6. Xi'an Jiaotong University [QY1J003]
  7. HPC platform, Xi'an Jiaotong University
  8. H2 Cluster in XJTU

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This study reports highly conductive PEDOT:PSS hydrogels without any conductive filler, which exhibit about 8 times higher conductivity than polymeric hydrogels without conductive filler in literature. These hydrogels not only show enhanced thermoelectric output power and electromagnetic interference shielding efficiency, but also have stretchable, self-healing, and shape/size-tunable properties, which are desirable for hydrogel bioelectronics and wearable organic devices.
Conducting hydrogels have attracted much attention for the emerging field of hydrogel bioelectronics, especially poly(3,4-ethylenedioxythiophene): poly(styrene sulfonate) (PEDOT:PSS) based hydrogels, because of their great biocompatibility and stability. However, the electrical conductivities of hydrogels are often lower than 1 S cm(-1 )which are not suitable for digital circuits or applications in bioelec txonics. Introducing conductive inorganic fillers into the hydrogels can improve their electrical conductivities. However, it may lead to compromises in compliance, biocompatibility, deformability, biodegradability, etc. Herein, a series of highly conductive ionic liquid (IL) doped PEDOT:PSS hydrogels without any conductive fillers is reported. These hydrogels exhibit high conductivities up to approximate to 305 S cm(-1), which is approximate to 8 times higher than the record of polymeric hydrogels without conductive fillers in literature. The high electrical conductivity results in enhanced areal thermoelectric output power for hydrogel-based thermoelectric devices, and high specific electromagnetic interference (EMI) shielding efficiency which is about an order in magnitude higher than that of state-of-the-art conductive hydrogels in literature. Furthermore, these stretchable (strain >30%) hydrogels exhibit fast self-healing, and shape/size-tunable properties, which are desirable for hydrogel bioelectronics and wearable organic devices. The results indicate that these highly conductive hydrogels are promising in applications such as sensing, thermoelectrics, EMI shielding, etc.

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