The organic electrochemical transistor (OECT) is an organic electronic device which functions like a transistor. The current flowing through the device is controlled by the exchange of ions between an electrolyte and the OECT channel composed of an organic conductor or semiconductor. [1] The exchange of ions is driven by a voltage applied to the gate electrode which is in ionic contact with the channel through the electrolyte. The migration of ions between the channel and the electrolyte is accompanied by electrochemical redox reactions occurring in the channel material. The electrochemical redox of the channel along with ion migration changes the conductivity of the channel in a process called electrochemical doping. OECTs are being explored for applications in biosensors, bioelectronics and large-area, low-cost electronics. OECTs can also be used as multi-bit memory devices that mimic the synaptic functionalities of the brain. For this reason, OECTs can be also being investigated as elements in neuromorphic computing applications.
OECTs consist of a semiconductor or even conductor thin-film (the channel), usually made of a conjugated polymer, which is in direct contact with an electrolyte. [2] Source and drain electrodes establish electrical contact to the channel, while a gate electrode establishes electrical contact to the electrolyte. The electrolyte can be liquid, gel, or solid. In the most common biasing configuration, the source is grounded and a voltage (drain voltage) is applied to the drain. This causes a current to flow (drain current), due to electronic charge (usually holes) present in the channel. When a voltage is applied to the gate, ions from the electrolyte are injected in the channel and change the electronic charge density, and hence the drain current. When the gate voltage is removed, the injected ions return to the electrolyte and the drain current goes back to its original value. However, some channel materials can hold the migrated ions even after removing the gate voltage enabling their use as memory devices.
OECTs commonly use PEDOT:PSS as the channel material, and work in the depletion mode. [3] The organic semiconductor PEDOT is doped p-type by the sulfonate anions of present in PSS [4] and hence PEDOT:PSS exhibits a high electronic conductivity. When no gate voltage is applied, a high drain current flows through the highly conductive channel, and the OECT is said to be in the ON state. When a positive voltage is applied to the gate, cations from the electrolyte are injected into the PEDOT:PSS channel, where they compensate the negative charge on the sulfonate anions. This leads to electrochemical reduction of PEDOT from its oxidised state to its neutral state resulting in de-doping of the OECT channel. The OECT is then said to be in the OFF state. [1] Accumulation mode OECTs, based on intrinsic organic semiconductors (for example p(g2T-TT)), have also been described. [5] [6]
OECTs are different from electrolyte-gated field-effect transistors. In the latter type of device, ions do not penetrate into the channel, but rather accumulate near its surface (or near the surface of a dielectric layer, when such a layer is deposited on the channel). [7] This induces accumulation of electronic charge inside the channel, near the surface. In contrast, in OECTs, ions are injected into the channel and change the electronic charge density throughout its entire volume. As a result of this bulk coupling between ionic and electronic charge, OECTs show a very high transconductance [8] along with an outstanding intrinsic gain. [9] The disadvantage of OECTs is that they are slow, as they are limited by the inherently slow migration of ions into and out of the channel. However, micro-fabricated OECTs show response times of the order of hundreds of microseconds. [10] Accurate simulation of OECTs is possible using the drift-diffusion model. [11]
OECTs were first developed in the 80’s by the group of Mark Wrighton. [12] They are currently the focus of intense development for applications in bioelectronics, [13] and in large-area, low-cost electronics. [14] Advantages such as straightforward fabrication and miniaturization, compatibility with low-cost printing techniques, [15] [16] compatibility with a wide range of mechanical supports (including fibers, [17] paper, [18] plastic [19] and elastomer [20] ), and stability in aqueous environments, led to their use in a variety of applications in biosensors. [21] [22] Moreover, their high transconductance makes OECTs powerful amplifying transducers. [23] OECTs have been used to detect ions, [24] [25] neurotransmitters, [9] metabolites, [26] [27] DNA, [28] pathogenic organisms, [29] as well as to probe cell adhesion, [30] measure the integrity of barrier tissue, [31] detect epileptic activity in rats, [32] and interface with electrically active cells and tissues. [33] [34] [35]
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Poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) is a polymer mixture of two ionomers. One component in this mixture is made up of polystyrene sulfonate which is a sulfonated polystyrene. Part of the sulfonyl groups are deprotonated and carry a negative charge. The other component poly(3,4-ethylenedioxythiophene) (PEDOT) is a conjugated polymer and carries positive charges and is based on polythiophene. Together the charged macromolecules form a macromolecular salt.
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Róisín Owens is a professor in the Department of Chemical Engineering and Biotechnology, University of Cambridge and a Fellow of Newnham College, Cambridge. Her research investigates new engineering technology for biological applications with a focus on organic bioelectronics, developing electroactive materials that can be used between physical transducers and soft biological tissues.
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