材料科学
生物电子学
跨导
佩多:嘘
离子液体
兴奋剂
光电子学
晶体管
有机电子学
柔性电子器件
纳米技术
导电聚合物
离子
聚合物
电压
生物传感器
电气工程
复合材料
有机化学
催化作用
工程类
化学
图层(电子)
作者
Xihu Wu,Abhijith Surendran,Jieun Ko,Oliver Filonik,Eva M. Herzig,Peter Müller‐Buschbaum,Wei Lin Leong
标识
DOI:10.1002/adma.201805544
摘要
Abstract Organic electrochemical transistors (OECTs) are highly attractive for applications ranging from circuit elements and neuromorphic devices to transducers for biological sensing, and the archetypal channel material is poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate), PEDOT:PSS. The operation of OECTs involves the doping and dedoping of a conjugated polymer due to ion intercalation under the application of a gate voltage. However, the challenge is the trade‐off in morphology for mixed conduction since good electronic charge transport requires a high degree of ordering among PEDOT chains, while efficient ion uptake and volumetric doping necessitates open and loose packing of the polymer chains. Ionic‐liquid‐doped PEDOT:PSS that overcomes this limitation is demonstrated. Ionic‐liquid‐doped OECTs show high transconductance, fast transient response, and high device stability over 3600 switching cycles. The OECTs are further capable of having good ion sensitivity and robust toward physical deformation. These findings pave the way for higher performance bioelectronics and flexible/wearable electronics.
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