生物电子学
材料科学
超分子化学
生物相容性
纳米技术
聚合物
导电聚合物
离子键合
超分子聚合物
制作
生物传感器
分子
复合材料
有机化学
化学
冶金
离子
替代医学
病理
医学
作者
Stephen J. K. O’Neill,Zehuan Huang,Mohammed Ahmed,Alexander J. Boys,Santiago Velasco‐Bosom,Jiaxuan Li,Róisı́n M. Owens,Jade A. McCune,George G. Malliaras,Oren A. Scherman
标识
DOI:10.1002/adma.202207634
摘要
Abstract Addressing the mechanical mismatch between biological tissue and traditional electronic materials remains a major challenge in bioelectronics. While rigidity of such materials limits biocompatibility, supramolecular polymer networks can harmoniously interface with biological tissues as they are soft, wet, and stretchable. Here, an electrically conductive supramolecular polymer network that simultaneously exhibits both electronic and ionic conductivity while maintaining tissue‐mimetic mechanical properties, providing an ideal electronic interface with the human body, is introduced. Rational design of an ultrahigh affinity host–guest ternary complex led to binding affinities (>10 13 M ‐2 ) of over an order of magnitude greater than previous reports. Embedding these complexes as dynamic cross‐links, coupled with in situ synthesis of a conducting polymer, resulted in electrically conductive supramolecular polymer networks with tissue‐mimetic Young's moduli (<5 kPa), high stretchability (>500%), rapid self‐recovery and high water content (>84%). Achieving such properties enabled fabrication of intrinsically‐stretchable stand‐alone bioelectrodes, capable of accurately monitoring electromyography signals, free from any rigid materials.
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