Synapses are the fundamental units in the biological nervous system, which play an important role in transmitting, processing, and memorizing information.
Fig. 1a shows a schematic diagram of the synapse. After receiving an electrical impulse, the presynaptic membrane generates an action potential, enhancing its permeability to calcium ions [
21]. Then, calcium ions enter the presynaptic membrane and trigger the release of neurotransmitters into the synaptic cleft. The neurotransmitters diffuse and interact with receptors on the postsynaptic membrane, thereby changing its ion permeability. The postsynaptic current will be generated after ions enter the postsynaptic membrane, thus forming information transmission. Inspired by this, an OECT was demonstrated (
Fig. 1b), in which the gate terminal, channel, and ions in the dielectric layer corresponded to the presynaptic membrane, postsynaptic membrane, and neurotransmitters, respectively. The channel layer adopts poly(3, 4-ethylene dioxythiophene): poly(styrene sulfonate) (PEDOT: PSS) doped with [MTEOA][MeOSO
3] ionic liquid (
Fig. 1c). The morphology and electrical properties of PEDOT: PSS can be modulated by the ion doping of [MTEOA][MeOSO
3], which is beneficial for carrier transport [
35]. Fig. S1 (Supporting information) shows the morphology and thickness of the channel layer characterized by atomic force microscopy (AFM). The smooth surface and continuous structure of the channel layer ensure good contact with the subsequently deposited dielectric layer. Normally, the PHPMA and PEI blend polymer system that contains many dynamic hydrogen bonds can be served as the polymer electrolyte of OECTs for achieving self-healing characteristic, while these hydrogen bonds in the blend polymer system cannot be readily moved into the channel layer (
Fig. 1c) [
33]. Therefore, the [MTEOA][MeOSO
3] containing hydroxyl groups was skillfully added into the PHPMA and PEI blend polymer system, which increased the number of ions that can migrate to dope the channel. X-ray photoelectron spectroscopy (XPS) was employed to characterize the [MTEOA][MeOSO
3] in the polymer electrolyte. The obtained sulfur (S) 2p spectrum indicated the presence of the S element in the [MTEOA][MeOSO
3] (Fig. S2 in Supporting information). Fig. S3 (Supporting information) displays the Fourier transform infrared (FTIR) spectrum of the polymer electrolyte, which reveals the presence of C=O stretching vibration in the PHPMA at 1721 cm
−1, N–H bending vibration in the PEI at 1560 cm
−1, and –CH
2 symmetric and antisymmetric stretching vibrations at 2848 and 2933 cm
−1, respectively. The hydrogen bond of O–H and N–H is confirmed at 3213 cm
−1, which is the foundation for the self-healing performance of the polymer electrolyte.
Fig. 1d illustrates the self-healing process of the polymer electrolyte with the thickness of about 193 µm (Fig. S4 in Supporting information). A blade was used to scratch the surface of the polymer electrolyte, creating a wound about 10 µm wide. The scratches vanished after heating the damaged polymer electrolyte for 5 min at 50 ℃, demonstrating its rapid and outstanding self-healing ability. To further explore the self-healing ability of the polymer electrolyte after scratching, the ionic conductivity of the electrolyte was investigated by electrochemical impedance spectroscopy. The polymer electrolyte between the two planar electrodes was completely cut. As depicted in Fig. S5 (Supporting information), the ionic conductivity after self-healing was 2.89 × 10
−3 S/m, which demonstrated almost no attenuation compared with that before damage (2.98 × 10
−3 S/m). Besides, an electric double layer with the effective capacitance of 50.57 nF at the frequency of 25 Hz was formed owing to the migration of ions in the polymer electrolyte to electrodes under an electric field (
Fig. 1e). The effective capacitance decreased as the frequency of the electric field increased originating from the low ion migration rate in the polymer electrolyte responding to the electric field with high frequency.
Fig. 1f and Fig. S6 (Supporting information) depict the transfer and output curves of the OECT, respectively. The device resembled an enhancement-mode transistor that remained off when the
VGS was set at 0 V. The contact between the PEI in the polymer electrolyte and PEDOT: PSS induced a redox reaction that converted PEDOT
+ to PEDOT
0 and compensated PSS
− by the amine group of PEI, which resulted in a dedoped process that decreased the conductance of PEDOT: PSS, forming a semiconducting channel with reduced charge transport [
36–
39]. Besides, as the ionic liquid proportion increased and the PEI proportion decreased, the threshold voltage of the OECT gradually shifted to the positive direction, transforming from an enhancement mode to a depletion mode (Fig. S7 in Supporting information). It should be noticed that synaptic behaviors can be simulated in the off-state of the enhancement-mode transistor, which can further decrease the energy consumption. In addition, with the decrease of the proportion of ionic liquid in the polymer dielectric, the on-state current of the OECT decreased. Therefore, the polymer electrolyte with the mass ratio of ionic liquid to blend polymer component of 50% as the dielectric layer of OECTs in this work.