Future brain-machine interfaces, prosthetics, and intelligent soft robotics will require integrating artificial neuromorphic devices with biological systems. Due to their poor biocompatibility, circuit complexity, low energy efficiency, and operating principles fundamentally different from the ion signal modulation of biology, traditional Silicon-based neuromorphic implementations have limited bio-integration potential. Here, we report the first organic electrochemical neurons (OECNs) with ion-modulated spiking, based on all-printed complementary organic electrochemical transistors. We demonstrate facile bio-integration of OECNs with Venus Flytrap (Dionaea muscipula) to induce lobe closure upon input stimuli. The OECNs can also be integrated with all-printed organic electrochemical synapses (OECSs), exhibiting short-term plasticity with paired-pulse facilitation and long-term plasticity with retention >1000 s, facilitating Hebbian learning. These soft and flexible OECNs operate below 0.6 V and respond to multiple stimuli, defining a new vista for localized artificial neuronal systems possible to integrate with bio-signaling systems of plants, invertebrates, and vertebrates.
Research advancement in brain-machine interfaces, implantable/wearable devices, prosthetics, and intelligent soft robotics calls for close interaction between and integration of technology into nature. Since the fundamental building elements of life differ significantly from those utilized in electronic devices, the ability to link an artificial device with a biological system is crucial to the success of these domains. Neuromorphic systems1 that borrow design concepts from biological signaling systems promise to bridge this gap. Although several software-based neuromorphic algorithms have been integrated into biomedical systems2,3, hardware-based systems4 that intimately interface with living tissues, evolve its function based on biological feedback5,6, and utilize event-based sensing7,8, and processing capabilities of the biological systems are ultimately necessary. However, circuits and devices made of silicon (Si)7,9,10,11, commonly used in hardware neural networks and neural interfaces, suffer from several drawbacks such as rigidity, poor biocompatibility, the requirement for numerous circuit elements, and operation mechanisms that are fundamentally orthogonal to those of biological systems, making bio-integration difficult.
On the other hand, organic semiconductors are becoming a competitive alternative in this field, as seen by their growing applications in artificial synapses12,13,14,15,16,17, nervetronics18,19, and neural interfaces20,21,22. Their structural kinship with biomolecules makes them ideal for bioelectronic applications23,24. Organic semiconductors are solution-processable, biocompatible, biodegradable, soft, and conformable from a structural standpoint. Furthermore, they can also be easily functionalized to offer specialized excitation, sensing, and actuation capabilities, and they support the transport of both the electronic and ionic signals25,26. Since biological neurons communicate with each other through a regulated flux and polarization of ionic species, organic materials are an obvious choice for creating devices that replicate biological activities due to their ability to couple ionic polarization to the modulation of electronic charge transport.
Despite the success of organic materials in emulating neuromorphic functions and artificial nerves, there have been limited attempts to fabricate and bio-integrate artificial neurons, which are essential to enable spike-based information encoding that closely mirrors the processing strategies used by biological systems. Recently reported artificial neurons based on organic field-effect transistors (OFETs)27 are promising in this regard. However, they require high voltage (5V) inputs for operation, which is an obvious critical issue when integrating with biology. In addition, as in the case of Si, their operation mechanism is fundamentally different from the ion-based mechanisms found in biological systems, making bio-integration, sensing, and response feedback difficult.
Organic electrochemical transistors (OECTs), which are modulated by a gate-driven ionic doping/de-doping of the organic bulk channel material25, resemble the ion-driven processes and dynamics of biological systems. Compared to OFETs, OECTs operate at considerably lower voltages (<1 V), have a higher transconductance, maintain excellent threshold voltage stability, demonstrate strong ion concentration-dependent switching properties28, and are in general highly biocompatible29. Aside from their use as chemical, physical, and biochemical sensors, they have been implemented as artificial synaptic devices12,14,16,17,30 that exhibit both long and short-term plasticity. The robust device architecture and the solubility of the organic materials in benign solvents have also enabled the facile fabrication of large-scale printed OECT-based digital circuits31,32,33. These properties make OECTs the ideal candidates for developing printed, biocompatible artificial spiking neural circuits with ion-mediated spiking mechanisms closely resembling the signaling characteristics of biological systems.
Here, we report the first organic electrochemical neurons (OECNs), based on all-printed complementary OECTs. The OECNs exhibit several neuronal characteristics, including ionic concentration-dependent spiking, and spike-timing-dependent plasticity (STDP) on integration with printed organic electrochemical synapses (OECSs). It responds to a wide range of input currents (0.1–10 µA), resulting in frequency modulation of over 450%. For the first time, we utilize the ionic concentration-dependent switching characteristics of the transistor to modulate the frequency of spiking to a large extent analogous to biological systems and demonstrate its integration with Venus Flytrap (Dionaea muscipula). The electrochemical transistors enable chemical modulation of the spiking behavior, which is impossible in OFET-based or Si-based CMOS neurons. The all-printed OECSs, which form and evolve in operando by electropolymerizing the monomer precursor of a polymeric mixed ion-electron conductor, exhibits two different modes of operation based on ionic doping and electropolymerization-induced conductivity modulation. This dual-mode of conductance modulation enables short-term plasticity with paired-pulse facilitation and long-term plasticity with retention of over 1000 seconds, facilitating symmetric Hebbian learning upon integration with the OECN. We anticipate that the OECNs’ soft nature, ability to be printed on flexible substrates, ion-modulated spiking and multi-stimuli response will open new avenues for facile integration with biological neural networks and applications in event-based sensors.
Printed organic electrochemical transistors
We chose the Axon-Hillock (A-H) circuit1 (Fig. 1b) to fabricate leaky integrate and fire (LIF) type spiking OECN because it is the most compact model suitable for spiking neural networks (SNNs) and event-based sensors. The components of the circuit, made of n-type and p-type OECTs, are the Amplifying block and the resetting transistor Treset (Fig. 1b, c). The complementary OECTs (c-OECT) – made of the hole-transporting glycolated polythiophene (P(g42T-T), p-type) and the electron-transporting poly(benzimidazobenzophenanthroline) (BBL, n-type) – were fabricated by a combination of screen printing and spray coating techniques, as described in the Methods section (Fig. 1d). The OECTs have lateral Ag/AgCl gate configuration with screen-printed carbon and silver electrodes on a polyethylene terephthalate (PET) substrate. The silver underlayer decreases the line resistance while the carbon acts as a chemically inert layer to contact the polymer semiconductor. Owing to the volumetric bulk conductivity of the OECT channel material, it is easier to achieve a balanced driving strength between the p-type and n-type transistors by modulating the thickness of the semiconductor layer as opposed to complementary OFET-based circuits where the channel width/length of transistors must be altered to achieve the same. With the same device geometry (W = 2000 μm, L = 200 μm), the thicknesses of P(g42T-T) and BBL are 20 nm and 250 nm, respectively, to obtain the same driving strength (ON-state current ~50 μA at VGS = VDS = ± 0.6 V) as shown in Supplementary Figure 1. A c-OECT inverter, comprising a pair of P(g42T-T) and BBL OECTs, is made to build the amplifying block in the A-H circuit (Supplementary Figure 2). The maximum DC voltage gain of the inverter is 26 (V/V) and we can reach nearly 200 (V/V) by cascading two inverters to form the amplifying block34. The fully printed OECN is shown in Fig. 1b and a typical spike firing of printed OECNs is presented in Fig. 1f.
Organic electrochemical neurons, analogy with the biological neuron and bio-integration
The operational mechanism of OECNs resembles that of the biological nerve cell35,36 (Fig. 1a). At rest, the extracellular side of a nerve cell has excess positive charge, and the intracellular side has excess negative charge maintained by the insulating property of the lipid cell membrane which acts as a barrier to charges except at the non-gated and voltage-gated ion channels (Na, K, Ca, and Cl). Thus, the cell’s resting potential is negative and is closest to the K+ Nernst potential (−75 mV) as these are the most permeable species at rest. Any influx of Na+ is counterbalanced by the efflux of K+ to maintain the membrane potential constant. As the membrane is depolarized near the action potential threshold, voltage-gated Na+ channels open rapidly, resulting in an increased influx of Na+, which serves as positive feedback, further depolarizing the membrane and moving the potential close to the Na+ Nernst potential (+55 mV), resulting in a spike (Fig. 1e).
Analogous to the operation of nerve cell, a spike is generated in the OECN circuit by integration of the current injected into the input terminal (Iin). As shown in Fig. 1b, c and f, the integration of the current is carried out by the capacitor Cmem which increases the voltage Vmem gradually, and upon reaching a specific threshold value, a nerve pulse is fired at Vout. This is enabled by the noninverting amplifier block A and the positive feedback capacitor Cf. The amplifier gain increases rapidly after reaching its transition voltage VT, which is related to the threshold voltage of P(g42T-T) and BBL OECTs. The capacitor Cmem can be charged linearly until VT is reached, but if the current supply is removed before reaching this threshold, the built-up voltage will sink to the ground similar to failed initiations in the biological neuron (Fig. 1e). If Vmem reaches VT, the amplifier turns on and the Vout increases. A change in the Vout value will result in a change in the input voltage Vmem enabled by the capacitance-voltage divider circuit implemented by Cf and Cmem. A small change in the input will further increase the Vout, leading to a feedback sequence and an exponential increase of voltage, resulting in the action potential generation. A similar positive feedback loop is achieved in a biological neuron by voltage-gated Na+ channels, resulting in further depolarization and opening of even more gated channels causing an exponential increase of cytoplasmic voltage until it is closer to the Nernst potential of Na+. Once the potential reaches this value, Na+ channels close, and K+ channels open, leading to an efflux of K+ and a restoration of the membrane potential to the resting value by the process called repolarization. These processes are repeated in the adjacent regions in the membrane and the action potential is propagated.
The resetting transistor Treset works analogously to the voltage-dependent potassium channels in the nerve cell. When Vout is high enough, Treset turns on, and the capacitance Cmem discharges through the Treset, resulting in a reduction of Vmem. Once Vmem reduces to the threshold voltage of the amplifier VT, the feedback loop is initiated again, resulting in a significant reduction in Vout for a slight change in Vmem. Thus, Vout reduces to zero, and the Treset turns off, resulting in termination of the nerve pulse, and the cycle is repeated.
The membrane capacitance plays a crucial role in the speed of the conduction of the action potential in a biological neuron36. A lower membrane capacitance results in faster propagation because it is easier to change the potential of the adjacent region as fewer charges are sufficient to change it (∆V = ∆Q/C) compared to a membrane with higher capacitance. In nerve cells, this reduction in capacitance is facilitated by wrapping an insulating layer called myelin over the axon. Analogous to this, the OECN spike frequency and width can be modulated by altering the Cmem and Cf capacitances in the circuit. Figure 2a, b and Supplementary Figure 3 shows the modulation of the frequency and the full width at half maximum (FWHM) of the spikes of the OECN with capacitance for a constant input current of 1 μA. A lower capacitance value reduces the charging time to reach the spiking threshold voltage and results in higher frequency spikes. With Cmem = Cf = 100 nF, the firing frequency approaches 0.1 Hz, which matches the low firing rate of certain single neurons37. Similarly, the peak width will depend on the discharging time of the capacitors through the resetting transistor Treset. Hence, the FWHM will be higher for higher capacitance values. It is noted that there is no further increase in frequencies on reducing the capacitances (Cmem = Cf) below 100 nF, probably due to limits imposed by the intrinsic overlap capacitances of the printed OECTs.
To further investigate the firing frequency dependence on the OECT performance, we built SPICE models for both p-type and n-type OECTs (Supplementary Figure 5). The simulated transient behaviors of both p-/n-type OECTs were matched with measured results (rise time (tr) ~230–390 ms34) by choosing the appropriate value of capacitance C1, as shown in Supplementary Figure 6 and 7a. The simulated neuron spiking frequency reaches 48 mHz, 75 mHz, and 85 mHz for Cmem = Cf = 6.8 μF, 1 μF, and 100 nF, respectively at an input current of 1 μA (Supplementary Figure 7b–d), showing excellent match with the experimental results (Fig. 2a). Further improving the OECT switching speed, by reducing the channel dimensions, could enable higher firing frequency. For tr = 0.5–1 ms for both p-/n-type OECTs, typical of short-channel photolithographically-made OECTs38, the simulated firing frequency reaches 95 Hz for Cmem = Cf = 2 nF and 1 μA current input (Supplementary Figure 8). Such a relatively high and biologically plausible frequency could mimic most neural firing rates (Supplementary Figure 4)39. Strategies for reaching such high spiking frequency by reducing the device dimensions are discussed in Supplementary Note 1.
A striking feature of this OECN, especially when compared to Si-based or OFET-based spiking neurons, is the ability to control the spiking frequency directly by modulating the ion concentration of the electrolyte. It is observed that the amplifier transition voltage VT shifts from 0.5 V to 0.2 V as a function of the ion concentration in the electrolyte (10−4 to 1 M, Supplementary Figure 9). This shift originates from the threshold voltage dependence of the individual transistors on the ion concentration—the transfer curves of the n-OECTs shift toward lower positive values on increasing the concentration (Supplementary Figure 10), resulting in a shift in VT. A low transition voltage of the amplifier means that the Vmem has to reach a lower value to initiate the exponential rise in Vout and the positive feedback in the neuron, thus resulting in a higher spiking frequency. The spiking frequency can be increased by 25% on increasing the electrolyte concentration (Fig. 2c). This is also associated with a concurrent reduction in the FWHM of the spikes.
A spiking neuron is generally characterized by its output response for a range of injected currents. The Frequency-Current (F-I) curves of the OECN at two different capacitance configurations are shown in Fig. 2d. Similar to the leaky behavior of the biological neurons that require that the membrane voltage exceeds a given threshold to generate a pulse, the OECN circuit does not fire below a specific current threshold value. In the Cmem = Cf = 100 nF configuration, a current below 100 nA cannot charge the capacitors enough to reach the spiking threshold (Fig. 2e and Supplementary Figure 11). The frequency can be modulated from 46 mHz at 300 nA to 274 mHz at 10 μA as the capacitors can be charged faster at higher currents bringing the Vmem closer to the threshold value faster. Further increase in current does not increase the spiking frequency and is limited by the inverter delay time. The VDD of the inverter can also modulate the spiking frequency of the OECN as shown in Supplementary Figure 12.
Low power consumption is crucial for the application of the circuit in SNNs and event-based sensors. The primary source of power dissipation in this circuit is the amplifying block. Hence, the dynamic power consumption of the circuit is the product of IDD,dynamic and VDD. Since the inverter can be operated at a low operating voltage of 0.6 V and the maximum value of IDD dynamic is 25 μA, the maximum dynamic power consumption is 15 μW. This value is lower than the dynamic power consumption of 40 μW reported in OFET-based Axon-Hillock circuit. Furthermore, the power consumption of the OECN can be reduced to much lower values by reducing the channel dimensions by lithographic techniques, which will reduce the current flowing through the OECT. A smaller channel will also increase the response time of the OECT and enable a lower FWHM of the spike to reduce energy consumption.
A monolithically integrated version of the neuron is fabricated by replacing the external capacitors with printed ones based on lateral carbon electrodes (Fig. 1c) and 1 M NaCl as the electrolyte. The characteristics of the fully printed neuron are similar to those discussed above, albeit that it spikes at a slightly lower frequency (Supplementary Figure 13). It is observed that the electrolyte concentration of the capacitor does not change the spiking frequency of the neuron (Supplementary Figure 14). Interestingly, the spiking characteristics remain unchanged even in the absence of the capacitors indicating that the internal capacitance of the circuit induced by the OECTs is larger than the carbon electrode-based capacitors and is sufficient to act as Cmem, eliminating the need for additional capacitors as required in Si-based circuits.
As a demonstration of the bio-integration capability of the OECN, we interfaced this fully printed neuron with a Venus Flytrap (Dionaea muscipula). Venus Flytraps (VFTs) have a thigmonastic response and catch insects by closing the lobes when their mechanosensitive hairs are mechanically elicited. Physical stimulation of the hairs triggers the release of Ca2+ in the cytosol40. For the trap to close, the cytosolic Ca2+ concentration must reach a putative threshold which is typically obtained by stimulating the hair twice within a time interval approximately lower than 30 sec. Trap closure can also be induced by electrical stimulation, including DC stimulation, direct charge injection41,42, AC stimulation, and capacitive induced current flow43, making it ideal for integration with the artificial neuron. We used Ag/AgCl electrodes to feed the output of the OECN to the lobes of the VFT with the ground of OECN connected to the lobe and the Vout to the midrib. The detailed experimental setup is described in the Methods section and Supplementary Figure 16. Injection of a high current (10 µA) results in a higher frequency (100 mHz) output of the OECN, resulting in the closure of the VFT (Supplementary Video 1). In contrast, a lower current input (2 µA) causes the OECN to spike at a lower frequency (44 mHz) and does not induce closure (Supplementary Video 2, Fig. 2f). We hypothesize the cytosolic Ca2+ threshold is met only when the OECN output frequency is high, while at a lower frequency, the cytosolic Ca2+ remains below the threshold required to close the VFT. The possibility of modulating the plant’s electrophysiology using the OECN opens up new avenues for integration of artificial neuromorphic devices and various biological systems. For example, the unique ability of OECTs to sense multiple biological, physical, and chemical signals enables multiple sensory detection, and their possible fusion in the neuron itself allows the development of novel bio-integrable event-based sensors with sensory fusion. In addition, the ion-based operation mechanism enables facile integration and feedback from biological systems. However, the main advantage of OECNs over other modulation techniques will be the capability for supervised or unsupervised learning at the sensor level. For this, the integration of OECNs with organic artificial synapses is inevitable. Here, we utilize printed organic electrochemical synapses (OECSs) based on electropolymerization mechanism to enable the same, as discussed in the next sections.
Printed organic electrochemical synapses
The OECSs are fabricated on the same printed electrode architecture as described for OECNs. The synaptic channel is formed by electropolymerizing a zwitterionic monomer precursor of a conducting polymer (2-(2,5-bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)thiophen-3-yl)ethyl(2-(trimethylammonio)ethyl) phosphate, ETE-PC), similar to our previous reports on evolvable OECTs using the anionic sulfonated form of this monomer, ETE-S12,13 (Fig. 3a, b). The zwitterionic nature of the ETE-PC side chain enables better interaction with the PET substrate compared to ETE-S and results in the formation of a conductive channel when −0.6 V is applied to the gate. The OECT characteristics are reported in Supplementary Figure 17. Figure 3a shows the analogy between a biological synapse and the printed OECS. The voltage applied to the Ag/AgCl gate of the OECT represents the presynaptic input and the current response to a presynaptic input, measured between source and drain, is the postsynaptic output referred to as the Excitatory and the Inhibitory Post Synaptic Current (EPSC and IPSC). Like a biological synapse, the OECS operates in 2 modes—short-term and long-term plasticity modes. The ionic accumulation in the poly-ETE-PC channel during the gate-induced doping/dedoping in the absence of ETE-PC monomer results in a short-term increase/decrease in channel conductance on the timescale of several seconds. This process, caused by the accumulation of ions in the channel is similar to the short-term synaptic facilitation (ms to s), which occurs in biological synapses encountering repeated action potentials due to the accumulation of excess Ca2+ and neurotransmitters. Figure 3c depicts the evolution of the EPSC with time on the application of gate pulses with a duration of 1 s. The EPSC can be modulated by tuning gate bias from −0.05 V to −0.2 V, showing an excitatory effect for over 100 s. The OECS also exhibits Paired Pulse Facilitation (PPF)/Paired Pulse Depression (PPD) with the peak of the EPSC/IPSC increasing/decreasing on successive application of presynaptic spikes (Fig. 3d). PPF is essential for decoding temporal information in biological systems. PPF indices of the OECS decay exponentially with the pulse intervals and is similar to the signaling characteristics of biological systems (Fig. 3e).
A long-term increase in conductivity of OECS is achieved by electropolymerizing additional ETE-PC in the channel through the application of gate voltage pulses of −0.6 V for a duration of 1 s (Fig. 3f). This process is analogous to the N-methyl-D-aspartate (NMDA) receptor-mediated insertion of new receptors in the biological synapse, leading to a long-lasting increase in synaptic strength (minutes to hours and more). A total of 150 distinct states are demonstrated in the OECS, with state retention of more than 1000 s (Fig. 3g). This retention is significantly higher than other OECT-based synapses and eliminates the need for external switches to achieve state retention15. Long-term depression (LTD) can be initiated in the synapse by over-oxidizing the channel, which is obtained by applying sufficiently high gate voltage pulses of −2 V for durations of 1 s in the absence of ETE-PC. However, LTD is highly nonlinear compared to a more linear LTP in this OECS. The need to remove the monomer solution to over-oxidize the channel hinders fast reversibility of the process and alternative approaches to induce long-term depression in the system are under investigation (see Supplementary Note 4).
Integration of organic electrochemical neurons and synapses
In biological synapses, the synaptic strength does not change for every presynaptic input, as that would quickly saturate the synaptic strength, making any learning impossible. Time correlations between pre- and postsynaptic neuronal spikes form the basis for long-term increases/decreases in synaptic plasticity, known as spike-timing-dependent plasticity (STDP), enabling associative learning. Here, we demonstrate symmetric Hebbian-type STDP with maximum change in synaptic strength when pre- and postsynaptic signals coincide and a lower change in strength (conductivity) when the timing of the pulses is mismatched. Figure 4a–c shows the configuration of the pre- and postsynaptic terminals and the characteristic spikes applied to each terminal. Voltage pulses are chosen such that the maximum voltage difference (0.6 V), which is required for electropolymerization, is applied only when both pre- and postsynaptic spikes overlap. The extent of the overlap, which reaches a maximum when the spikes are applied simultaneously, determines the change in channel conductance. The changes in conductance are normalized by the initial channel conductance to present the data in percentage changes in weights. A difference in the timing of the spikes results in a reduced time duration of the spike overlap, and hence lower increase in synaptic strength. This process is analogous to the NMDA receptor-activated insertion of new receptors in synapse leading to LTP; NMDA acts as a biological ‘AND’ gate and only opens when presynaptic spikes cause glutamate to bind to it, and postsynaptic spike removes the Mg2+ blockade. Since electropolymerization can occur even at millisecond time scales, the STDP behavior can be tuned to match biological time scales by optimizing the pulse duration and amplitude.
To further illustrate the significance of the OECN and OECS, we demonstrate a simple neuro-synaptic system with Hebbian learning using a single synaptic transistor connected to the OECN (Fig. 4d). Instead of excitatory current input to the neuron, a voltage is applied to the synapse, which is converted to current based on its synaptic strength, resulting in modulation of the spiking frequency (Supplementary Figure 20). Since the gate and drain of the synaptic ETE-PC-based OECT are kept at a common voltage of 0.5 V, it operates in the fully depleted mode with low conductivity. The presynaptic pulses of magnitude −0.8 V and duration of 1 s are applied to the synapse at predefined delays of 0, 5, and 10 s with respect to the time when the value of Vmem is maximum. Any delay between the two results in a lower rate of electropolymerization and lower or no change in the spiking of the postsynaptic neuron (Fig. 4e, f). The Vmem of the neuron generates the postsynaptic feedback to the synapse. If the presynaptic input arrives in sync with the maximum value of Vmem, there is a maximum voltage difference across the synapse (0.68 V) for electropolymerization to take place, and the synaptic strength increases significantly. This results in an increase in the firing frequency of the neuron from 22 mHz to 30 mHz, as shown in Fig. 4g, demonstrating the concept of ‘neurons which fire together wire together’ put forward by Hebb44. Si-based systems require complicated circuits with multiple transistors to emulate STDP behavior. Hence, the demonstration of Hebbian learning in this organic electrochemical neuro-synaptic system is an important step and can be extended to build more complicated sensory and processing systems with local learning capabilities.
We have demonstrated the first OECT-based spiking neuron, here made from an all-printed c-OECT technology, and its integration with printed OECT-based artificial synapses exhibiting a range of learning behaviors, including long-term and short-term potentiation and depression and STDP. A neuro-synaptic system with STDP is demonstrated with much fewer elements in comparison to Si-based circuits. The OECT-based circuit can be printed on large scale31 and with high manufacturing yield45, which greatly simplifies the production protocol, as the driving strengths of p- and n-type transistors can be matched easily by tuning the thickness of the semiconductor layers. The neuron can be fully printed on flexible substrates and operates at a much lower power compared to OFET-based circuits and can thus enable the development of distributed low-cost smart labels for the future Internet of Things (IoT). The spiking frequency of the OECN can be modulated by changing the input current, membrane capacitance, and voltage input to the amplifier. The properties mentioned above and the ability to tune the frequency of spiking via modulation of electrolyte concentration, which is unique to this OECN, offer facile integration with biological systems that work by similar mechanisms and facilitate the development of future implantable devices. We demonstrate this possibility by interfacing the OECN with a Venus Flytrap to induce the closure of its lobes based on the neuron’s firing frequency. Furthermore, we demonstrate the integration of the OECN with an OECS with Hebbian learning capabilities. This, along with the unique ability of the OECTs to sense multiple biological, physical, and chemical signals, enables multiple sensory detection. The possibility to fuse multiple sensing elements in the neuron itself could enable the development of novel bio-integrable event-based sensors for applications ranging from smart neuromorphic labels for IoT packaging and continuous body health monitoring (i.e., wearable electronics) to brain-machine interfaces. Our findings open for the possibility to integrate localized artificial neurosynaptic systems, composed of OECNs and OECSs, with the signaling systems of plants, and with the diffusive, peripheral, and central nervous systems of invertebrates and vertebrates, respectively.
The polyethylene terephtalate (PET) substrate Polifoil Bias is purchased from Policrom Screen. Ag 5000, DuPont Silver Ink is used for printed interconnects. Carbon ink 7102 printing paste from DuPont is used for the electrode contacts. Insulating ink (5018, DuPont) is used for electrode isolation. PQ-10, PSSNa, and BBL were purchased from Sigma-Aldrich and used as received. The P(g42T-T) and BBL inks are fabricated through a solvent exchange method. P(g42T-T) (30 mg) dissolved in chloroform (15 mL) is added dropwise to isopropanol (75 mL) under high speed stirring (1500 rpm) to obtain bright blue nanoparticles of P(g42T-T). BBL (30 mg) dissolved in methanesulfonic acid (15 mL) is added dropwise to isopropanol (75 mL) under high-speed stirring (1500 rpm) to obtain dark purple BBL nanoparticles. The P(g42T-T) and BBL nanoparticles are respectively collected by centrifugation (5000 rpm, 30 min) and washed in IPA six times until neutral. The neutral P(g42T-T) and BBL nanoparticles are re-dispersed in IPA to obtain dispersion inks (about 0.006 mg/mL for P(g42T-T) and 0.1 mg/mL for BBL)34,46.
Fabrication of OECTs
Flatbed sheet-fed screen-printing equipment (DEK Horizon 03iX) is used to deposit all materials on top of PET plastic substrates. To form the contacts, a layer of carbon is first deposited on the substrate. This is followed by the Ag 5000 silver ink deposition and the insulating layer of 5018 ink, which is UV-cured to define the channel and the gate. Ag/AgCl ink is blade coated through a shadow mask and annealed at 120οC for 10 min to form the gate. The P(g42T-T) and BBL layers are deposited by spray-casting in air through a shadow mask, using a standard HD-130 air-brush (0.3 mm) at an atomization air pressure of 1 bar34.
All the OECT characterizations are carried out in a semiconductor parameter analyzer (Keithley 4200 SCS) at a temperature of around 20 °C and a relative humidity of around 45%.
Simulation of OECTs and OECNs
The SPICE models of p-type and n-type OECTs are developed in B2 SPICE (EMAG Technologies Inc.). Both models are built based on the measured transfer characteristics and transient switching characteristics of printed OECTs. The simulation of OECNs gives the membrane voltage (Vmem) and the output of the Amplifier A (Vout) in the OECN circuits.
Venus Flytrap measurement setup
Venus Flytraps (Dionaea muscipula, VFTs) were purchased from Plantagen (Norrköping, Sweden) and kept in greenhouse conditions (day/night temperature of 28/22.5 °C, 12 h photoperiod, 60% relative humidity, 400 ppm CO2). Ag/AgCl electrodes were prepared by coating two Ag wires (AGW1030, World Precision Instruments) with AgCl and insulating them with Teflon heat shrink tubing, leaving the electrode tips open. To electrically stimulate the VFT, the positive stimulation electrode was placed on the midrib and the ground or negative electrode was attached on the lobe, via a conductive gel (SignaGel, Parker Laboratories, Inc., NJ, USA) to ensure stable electrical contact. The positive stimulation electrode was electrically integrated with the output of the OECN and the two ground terminals were connected together to close the circuit. The Action Potential signals at different frequencies were then supplied by the OECN to induce the VFT trap closure.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
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This work was financially supported by the Knut and Alice Wallenberg foundation, the Swedish Research Council (2016-03979, 2018-06197, and 2020-03243), the Swedish Foundation for Strategic Research (RMX18-0083, FFL18-0101), ÅForsk (18-313 and 19-310), Olle Engkvists Stiftelse (204-0256), VINNOVA (2020-05223), the European Research Council (834677 “e-NeuroPharma” ERC-2018-ADG), the European Commission through the FET-OPEN project MITICS (GA-964677), and the Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linköping University (Faculty Grant SFO-Mat-LiU 2009-00971). R.O. and D.B. are supported by MultiPark, a strategic research area at Lund University.
Open access funding provided by Linköping University.
C.-Y.Y., M.B., and S.F. are the founder of n-Ink AB. The other authors declare no competing interests.
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Harikesh, P.C., Yang, CY., Tu, D. et al. Organic electrochemical neurons and synapses with ion mediated spiking. Nat Commun 13, 901 (2022). https://doi.org/10.1038/s41467-022-28483-6