TY - JOUR
T1 - High-Gain Chemically Gated Organic Electrochemical Transistor
AU - Tan, Siew Ting Melissa
AU - Giovannitti, Alexander
AU - Melianas, Armantas
AU - Moser, Maximilian
AU - Cotts, Benjamin L.
AU - Singh, Devan
AU - McCulloch, Iain
AU - Salleo, Alberto
N1 - KAUST Repository Item: Exported on 2021-03-08
Acknowledgements: The authors thank the Dionne lab for access to their UV–vis spectrometer and the Soft and Hybrid Materials Facility in the Stanford Nano Shared Facilities for access to the rheometer and profilometer. A.G. and A.S. acknowledge funding from the TomKat Center for Sustainable Energy at Stanford University. A.S. and M.T. gratefully acknowledge support from the National Science Foundation Award CBET #1 804 915. A.M. gratefully acknowledges support from the Knut and Alice Wallenberg Foundation (KAW 2016.0494) for Postdoctoral Research at Stanford University. Part of this work was performed at the Stanford Nano Shared Facilities (SNSF), supported by the National Science Foundation under award ECCS–1542152.
PY - 2021/3/3
Y1 - 2021/3/3
N2 - Organic electrochemical transistors (OECTs) have exhibited promising performance as transducers and amplifiers of low potentials due to their exceptional transconductance, enabled by the volumetric charging of organic mixed ionic/electronic conductors (OMIECs) employed as the channel material. OECT performance in aqueous electrolytes as well as the OMIECs’ redox activity has spurred a myriad of studies employing OECTs as chemical transducers. However, the OECT's large (potentiometrically derived) transconductance is not fully leveraged in common approaches that directly conduct chemical reactions amperometrically within the OECT electrolyte with direct charge transfer between the analyte and the OMIEC, which results in sub-unity transduction of gate to drain current. Hence, amperometric OECTs do not truly display current gains in the traditional sense, falling short of the expected transistor performance. This study demonstrates an alternative device architecture that separates chemical transduction and amplification processes on two different electrochemical cells. This approach fully utilizes the OECT's large transconductance to achieve current gains of 103 and current modulations of four orders of magnitude. This transduction mechanism represents a general approach enabling high-gain chemical OECT transducers.
AB - Organic electrochemical transistors (OECTs) have exhibited promising performance as transducers and amplifiers of low potentials due to their exceptional transconductance, enabled by the volumetric charging of organic mixed ionic/electronic conductors (OMIECs) employed as the channel material. OECT performance in aqueous electrolytes as well as the OMIECs’ redox activity has spurred a myriad of studies employing OECTs as chemical transducers. However, the OECT's large (potentiometrically derived) transconductance is not fully leveraged in common approaches that directly conduct chemical reactions amperometrically within the OECT electrolyte with direct charge transfer between the analyte and the OMIEC, which results in sub-unity transduction of gate to drain current. Hence, amperometric OECTs do not truly display current gains in the traditional sense, falling short of the expected transistor performance. This study demonstrates an alternative device architecture that separates chemical transduction and amplification processes on two different electrochemical cells. This approach fully utilizes the OECT's large transconductance to achieve current gains of 103 and current modulations of four orders of magnitude. This transduction mechanism represents a general approach enabling high-gain chemical OECT transducers.
UR - http://hdl.handle.net/10754/667932
UR - https://onlinelibrary.wiley.com/doi/10.1002/adfm.202010868
U2 - 10.1002/adfm.202010868
DO - 10.1002/adfm.202010868
M3 - Article
SN - 1616-301X
SP - 2010868
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -