You are on page 1of 5

Multi-gate organic neuron transistors for

spatiotemporal information processing


Cite as: Appl. Phys. Lett. 110, 083302 (2017); https://doi.org/10.1063/1.4977069
Submitted: 07 December 2016 • Accepted: 07 February 2017 • Published Online: 23 February 2017

Chuan Qian, Ling-an Kong, Junliang Yang, et al.

ARTICLES YOU MAY BE INTERESTED IN

Electrolyte-gated transistors for synaptic electronics, neuromorphic computing, and


adaptable biointerfacing
Applied Physics Reviews 7, 011307 (2020); https://doi.org/10.1063/1.5122249

Synaptic plasticity functions in an organic electrochemical transistor


Applied Physics Letters 107, 263302 (2015); https://doi.org/10.1063/1.4938553

A comprehensive review on emerging artificial neuromorphic devices


Applied Physics Reviews 7, 011312 (2020); https://doi.org/10.1063/1.5118217

Appl. Phys. Lett. 110, 083302 (2017); https://doi.org/10.1063/1.4977069 110, 083302

© 2017 Author(s).
APPLIED PHYSICS LETTERS 110, 083302 (2017)

Multi-gate organic neuron transistors for spatiotemporal information


processing
Chuan Qian,1 Ling-an Kong,1 Junliang Yang,1 Yongli Gao,1,2,a) and Jia Sun1,a)
1
Hunan Key Laboratory for Super Microstructure and Ultrafast Process, School of Physics and Electronics,
Central South University, Changsha, Hunan 410083, People’s Republic of China
2
Department of Physics and Astronomy, University of Rochester, Rochester, New York 14627, USA
(Received 7 December 2016; accepted 7 February 2017; published online 23 February 2017)
Due to similar transmission characteristics of biological synaptic activities, neuromorphic
behaviors simulated by organic electrochemical transistors (OECTs) is of great interest. In this
letter, the fabrication and performance of multi-gate poly(3-hexylthiophene) (P3HT) OECTs with
ion-gel gating are reported. The neuromorphic behaviors, such as dendrite correlated excitatory
postsynaptic current (EPSC), paired pulse facilitation, and modulation, were simulated in the
OECTs. These behaviors were observed to depend on the degree of temporal correlation and dis-
tance between the in-plane-gate and the channel. More importantly, by using dendritic integration
from two different gates, spatiotemporally correlated outputs were also emulated. The spatial orien-
tations of the input pulse are defined, and changing the orientation will result in a change in the
EPSC amplitude. Our results provide a way to construct spatiotemporally neural network based on
multi-gate OECTs. Published by AIP Publishing. [http://dx.doi.org/10.1063/1.4977069]

Organic semiconductors offer unique features such as transformed from dendrites. Therefore, it is important to
low cost, flexibility, and large-area process properties, and study the spatiotemporal synaptic response and to extract its
many electronic devices based on organic semiconductors global properties and configuration.
have been developed, including organic light-emitting diodes, In this letter, we demonstrate the fabrication of organic
organic photovoltaics, and organic field-effect transistors.1–6 neuron transistors with a multi-gate dendritic input array.
In recent years, organic electrochemical transistors (OECTs) EPSC is shown to be dependent on the degree of temporal
have attracted considerable interest in bioelectronics and correlation and distance between the in-plane-gate and the
sensing.7,8 OECTs are organic transistor devices that use an channel. More importantly, spatiotemporally correlated out-
electrolyte as the dielectric material and form extremely high puts were also emulated by using dendritic integration. The
specific capacitance of the electric-double-layer (EDL), typi- spatial orientations are defined by the geometry of dendritic
cally larger than 1 lF/cm2.9,10 As a result, OECTs can be array, and changing the orientation will result in a change in
operated at very low voltages (typically below 2.0 V) to the EPSC amplitude.
derive a large number of charges in the channel. It is known Figure 1(a) shows a simple picture of a biological synap-
that the synaptic activities are achieved via various ionic tic integration in a neuron.17 The pre-synaptic neuron can
fluxes,11,12 and the OECTs transmit a signal based on the transmit many synaptic input signals from a different den-
motion of ions.13 It is therefore possible that the OECT can drite to a synapse, which occurs via the motion of chemical
be used for emulating biological synaptic behaviors due to ions from the pre-neuron to the post-neuron. Figure 1(b) dis-
their similar transmission characteristics. In this context, a plays the device structure of an ion-gel coupling P3HT neu-
few endeavors have been reported that utilized OECTs ron transistor with a multi-in-plane-gate structure on the
in artificial synaptic devices.13–16 Recently, Malliaras and 200 nm-SiO2/Si (Si-Mat, Silicon Materials) substrate. The
his group have first demonstrated the fabrication of OECTs multi-dendritic input structure of neuron is thought to be
based artificial synapses by using liquid electrolyte gating.14 very useful for enriching information transmission and the
Importantly, the function of spatial synaptic mapping and computational ability. To mimic neuromorphic functions,
integration was achieved in these devices.15 However, with the P3HT is considered as post-neuron, ion-gel as pre-
liquid electrolyte, the electrolyte-ion-polarization-induced neuron, in-plane Au electrodes as the dendrite, and conduc-
leakage current could distort the drain current in the channel. tance of channel as the synaptic weight. Polymer P3HT is
Xu et al. have reported organic nanowire synaptic transistors purchased from Sigma-Aldrich, which was dissolved in
with ultralow energy consumption.16 Most recently, our dichlorobenzene (15 mg/ml). After being spin-coated, P3HT
group has demonstrated that solid-state ion-gel laterally gated films were cured at 50  C for 2 h. Thermally deposited Au
OECTs can be used for the simulation of biological synapses. electrodes through a micrometer sized carbon fiber shadow
Although some important behaviors are successfully mim- mask on the top of the P3HT film were used as the source,
icked in artificial synapses, such as excitatory postsynaptic drain, and in-plane-gate, which define a channel with a
current (EPSC), paired pulse facilitation (PPF), synaptic fil- length of 6 lm and with a width of 200 lm. The preparation
ter, and synaptic plasticity, an essential aspect of neuron of the ion-gel films (P(VDF-HFP) þ [EMI][TFSA]) followed
network is still untouched that many synaptic inputs are the previous method, and the gels were then transferred to
the device as the gate dielectric by employing “cut and stick”
a)
Electronic addresses: ygao@csu.edu.cn and jiasun@csu.edu.cn processes.18 Electrical performance of the transistors and

0003-6951/2017/110(8)/083302/4/$30.00 110, 083302-1 Published by AIP Publishing.


083302-2 Qian et al. Appl. Phys. Lett. 110, 083302 (2017)

In a brain, the spatiotemporal synaptic response in corti-


cal neurons is a significant part in the formation of dynamic
cell assemblies.22 Information processing is spatiotemporal,
and the neuron network is very complicated, in which many
synaptic inputs are transformed from dendrites of pre-neuron
to post-neuron. The outputs are sensitive to both the timing
and the location of inputs.23,24 Both the spike pulse duration
and distances between the in-plane-gate and the channel
(dendrite to post-synapse) will contribute to a change in
EPSC. The spatiotemporal synaptic response in P3HT-based
neuron transistors is shown in Figure 2(a), which is a 3-D-
scatter plot, describing the EPSCs as a function of pulse
duration of 30 to 100 ms and the dendrite to post-synapse
distance of 1.08 to 2.64 mm. Each point is the average value
of six peak EPSCs. The point with 100 ms duration and
1.08 mm distance between dendrite and post-synapse is
extracted from Figure 1(c). With the increased duration,
more and more ions move onto the interface of ion-gel/semi-
conductor,13 and the average peak EPSC is increased from
1.79 lA to 7.89 lA. Moreover, with 100 ms duration and
2.64 mm distance, the average peak EPSC is just 2.33 lA,
3.4 times smaller than the value with 100 ms duration and
1.08 mm distance. It is known that the ion-gel electrolyte
FIG. 1. (a) A simple schematic picture of a biological synaptic integration in resistivity and the area covered by ion-gel are constant val-
a neuron. (b) Schematic illustrations of the P3HT-based neuron transistor ues. If the gate-to-channel distance is larger, fewer ions will
with a multi-in-plane-gate structure. (c) EPSCs triggered by six pre-synaptic diffuse to the ion-gel/P3HT interface, and the Ids in the chan-
spikes (2.0 V, 90 ms) applied at the gate electrode 1 are shown as a func-
nel will be relatively small.15 The temporal response depends
tion of time.
on the distance between the in-plane-gate and the channel.
neuromorphic behaviors were measured by a semiconductor
parameter characterization system (Keithley 4200 SCS) in
air and at room temperature.
For the organic electrochemical transistor, under a gate
electric field, the drain current is controlled by the injection of
ions from an electrolyte into a semiconductor channel.13 The
transfer and output characteristic curves of the device are
shown in Figure S1 (supplementary material). When the gate
voltage is decreased from 2.0 V to 2.0 V with a low source-
drain voltage of 1.0 V, the Ids increases from 1.5  107 A
to 1.1  105 A. To represent the synaptic strength in our
organic neuromorphic devices, a potential spike signal is
applied on the arbitrary gate electrode, which can trigger the
motion of [TFSA]– ions from ion-gel to the P3HT film and a
peak EPSC in the channel.13 Figure 1(c) shows the typical
temporal response of the organic neuron transistors to six
2.0 V pre-synaptic spikes (interval is about 3 s) applied on
G1 electrode with 100 ms duration. Because the devices are
reliable and the P3HT layer is reversibly de-doped to its initial
state under gate voltage back to 2.0 V, the peak EPSC is rela-
tively stable, and the average value of six peak EPSCs is about
7.89 lA. All the synaptic simulations are measured with a con-
stant potential Vds ¼ 0.5 V applied on the source-drain elec-
trodes. EPSCs recorded in response to the train of pulses
(interval is about 50 ms) are shown in Figure S2 (supplemen-
tary material). When the interval is shortened to 50 ms, the FIG. 2. (a) Spatiotemporal EPSC response in P3HT-based neuron transis-
short-term plasticity (STP) and self-tuning are reproduced, tors. A 3-D-scatter plot describing the EPSCs as a function of pulse duration
which are discussed in the biological system.19–21 As the and the distance between the in-plane-gate and the channel (dendrite to post-
synapse). (b) Paired-pulse facilitation ratio as a function of interval (Dt) and
pulses applied, the peak EPSC is initially hypersensitive and
the distance between in-plane-gate and channel. The inset in (b) shows
subsequently adapts to the stimulation. After the end of the EPSCs triggered by paired pulses applied at the gate electrode 1 with the
train of pulses, the EPSC is back to the initial level. pulse Dt of 50 ms.
083302-3 Qian et al. Appl. Phys. Lett. 110, 083302 (2017)

With the distance increasing from 1.08 to 2.64 mm, the slope
of the spatiotemporal synaptic integration curve decrease from
about 0.028 lA/ms to 0.087 lA/ms, thus to evoke a large
response, a longer pulse duration time is needed. The EPSCs
depend both on spatial and temporal characteristics of dendritic
inputs, which are important for neural network construction.
We emulated the paired-pulse facilitation (PPF) with the
in-plane-gate and the channel distance in the organic neuron
transistors. The behavior of PPF is a kind of STP and very
important for neural activities.25,26 The inset in Figure 2(b)
shows that EPSCs triggered by paired pulses applied at the
gate electrode 1 with the pulse Dt of 50 ms and the channel
current are measured as a function of time. A1 and A2 are the
peak EPSCs of the first and second spikes, respectively. A2
is facilitated by the residual ions triggered by the first spike.
The PPF ratio of two amplitudes (A2/A1) as a function of
interval (Dt) and the dendrite to post-synapse distance is
shown in Figure 2(b). The pulse Dt and the dendrite to post-
synapse distance for PPF measurement were ranged from
50 to 800 ms and 1.08 to 2.64 mm. A2/A1 shows a distance-
dependent weight, especially when the Dt is smaller than
200 ms. When Dt ¼ 50 ms, the A2/A1 reaches the top point in
FIG. 3. (a) The modulatory effect of VM and Vpulse is plotted as a 3-D-scatter
each line. The maximum value of 149.2% is obtained when plot. (b) Dendrite to post-synapse distance-dependent EPSCs of the ion-gel
the distance is 1.08 mm. When the distance is increased to gated organic neuron transistors with two in-plane spike inputs applied
2.64 mm, the value is reduced to 117.1%. With a nearer loca- at the two gate electrodes with same dendrite to post-synapse distance,
simultaneously.
tion away from the channel, the residual ions triggered by
dendrites in a short time are much more. With the interval
lengthened to 800 ms, the A2 is almost equal to A1, and most studied. A schematic image is shown in Figure S3 (supple-
of the ions triggered by the first spike are back to the ion-gel mentary material): the two inputs are applied at the two gate
for three kinds of distance. electrodes with the same dendrite to post-synapse distance,
Under changing conditions, synaptic modulation pro- simultaneously. Figure 3(b) shows the distance correlated
vides flexibility to operate, which is a ubiquitous phenome- average peak EPSCs of the integration of two in-plane pre-
non in physiological systems.27 The realization of dynamic synaptic inputs. Pre-synaptic inputs are applied at the gate
synaptic behaviors by using modulation voltage (VM) is very electrodes 1 and 2, the vertical distance between channel and
useful for understanding the principle of neural networks and gate electrode 1 or 2 is 1.08 mm, and the average peak EPSC
guiding the innovation of neural circuits.28,29 Especially, is about 2.768 lA; inputs applied at the gate electrodes 5 and
Professor Ren’s group has demonstrated the dynamic 6, the vertical distance between channel and gate electrode
synaptic plasticity by using the modulation voltage of the 5 or 6 is 2.64 mm, and the average peak EPSC is about
back gate.29 For our organic neuron transistors, the output 1.482 lA. The peak EPSC shows a linear relationship with
response can be tuned in a wide range by the VM of the in- the distance between dendrite and post-synapse, which
plane gate. As shown in Figure 3(a), the modulatory effect of meshes well with the experimental finding in Figure 2(a) with
VM and Vpulse is plotted as a 3-D-scatter plot. To mimic the single input.
modulation behavior, ten pre-synaptic spikes of VPulse with a The neurons in primary visual cortex have strong tuning
duration time of 50 ms are applied on the G1 electrode, and to a small set of stimuli, and the neuronal responses can dis-
the constant modulation voltage (VM) is applied on the G2 criminate small changes in colors, spatial frequencies, and
electrode, simultaneously. Each point in Figure 3(a) is the visual orientations.30 In our study, the spatiotemporal den-
average of the ten peaks. Without modulation of VM and dritic integration with correlated inputs can be illustrated by
when the VPulse is set to 1 V, there are limited holes spatial orientations. Figure 4(b) shows the schematic image
increased in the channel and the average of peak EPSCs is of the ion-gel gated organic neuron transistors with two in-
just about 1.9 lA; when the VPulse and VM are both set to plane pre-synaptic inputs applied at the gate electrode 0 and
2 V, many ions move onto the interface of ion-gel/semicon- another gate electrode x (x ¼ 16), simultaneously. The spa-
ductor to modulate the peak EPSC, and the value is up to tial orientations of the input pulse are defined by the angle
16.08 lA. When more negative voltage is applied on the mod- ranging from 0 to 180 . The gate electrode 0 is defined as
ulatory terminal, a more obvious modulatory effect of VM and the common endpoint of each angle, the line between the
Vpulse is observed, and the average of peak EPSCs has about gate electrodes 0 and 5 as the common ray, and the line
eight times of increasing magnitude. Modulation may reflect between the gate electrodes 0 and x as the other ray. EPSC
a change in the relationship between spatiotemporal synaptic triggered by eight pre-synaptic spikes (2.0 V) applied at
input and output. The influences of distance between the in- the gate electrodes 0 and 5 is shown versus time with the
plane gate and the channel on the spatiotemporally correlated duration of 50 ms in Figure 4(a). When the input spikes trig-
outputs from two different dendritic positions were also gered simultaneously on two dendrites, the EPSC in the
083302-4 Qian et al. Appl. Phys. Lett. 110, 083302 (2017)

FIG. 4. (a) EPSCs triggered by eight pre-synaptic spikes (2.0 V) applied at the gate electrodes 0 and 5 are shown versus time with a duration of 50 ms.
(b) Schematic image of the ion-gel gated organic neuron transistors with two in-plane pre-synaptic inputs applied at the gate electrode 0 and another gate elec-
trode x (x ¼ 1–6), simultaneously. The spatial orientations of the input pulse are defined by the angle range from 0 to 180 . The gate electrode 0 is defined as
the common endpoint of each angle, the line between the gate electrodes 0 and 5 as the common ray, and the line between the gate electrodes 0 and x as the
other ray. (c) Polar diagram of the EPSCs for different spatial orientations of the input pulse.

1
channel can be observed, and the average value is about S. Reineke, F. Lindner, G. Schwartz, N. Seidler, K. Walzer, B. L€ ussem,
1.38 lA. Figure 4(c) shows the Polar diagram of the EPSCs and K. Leo, Nature 459, 234 (2009).
2
W. Lee, D. Kim, J. Rivnay, N. Matsuhisa, T. Lonjaret, T. Yokota, H.
for different spatial orientations of the input pulse. Each Yawo, M. Sekino, G. G. Malliaras, and T. Someya, Adv. Mater. 28, 9722
point is the average of the eight peaks, and the average val- (2016).
3
ues are demonstrated in Table S1 (supplementary material). C. Qian, J. Sun, L. Zhang, H. Huang, J. Yang, and Y. Gao, J. Phys. Chem.
When the orientation angle is 129.8 , the maximum tuning C 119, 14965 (2015).
4
C. Qian, J. Sun, L. Zhang, H. Xie, H. Huang, J. Yang, and Y. Gao, Synth.
response (2.22 lA) is obtained. The average peak EPSC is Met. 210, 336 (2015).
gradually increased with the orientation angle changed from 5
J. Xiong, B. Yang, J. Yuan, L. Fan, X. Hu, H. Xie, L. Lyu, R. Cui, Y. Zou,
0 to 50.2 or from 180 to 129.8 , which is similar to the 6
C. Zhou, D. Niu, Y. Gao, and J. Yang, Org. Electron. 17, 253 (2015).
orientation tuning curve in the primary visual cortex.31 The W. L. Huang, B. C. Yang, J. Sun, B. Liu, J. L. Yang, Y. P. Zou, J. Xiong,
C. H. Zhou, and Y. L. Gao, Org. Electron. 15, 1050 (2014).
multi-gate organic neuron transistors have a symmetrical 7
S. P. White, K. D. Dorfman, and C. D. Frisbie, Anal. Chem. 87, 1861
arrangement of gate array, but the average peak EPSC trig- (2015).
8
gered simultaneously on the gate electrodes 0 and x (2, 4, S. P. White, S. Sreevatsan, C. D. Frisbie, and K. D. Dorfman, ACS
and 6) is larger than the average peak EPSC triggered on the Sensors 1, 1213 (2016).
9
O. Larsson, E. Said, M. Berggren, and X. Crispin, Adv. Funct. Mater. 19,
gate electrode 0 and corresponding x (1, 3, 5). The peak 3334 (2009).
EPSC follows the empirical formula of I / A=d, where d is 10
S. H. Kim, K. Hong, W. Xie, K. H. Lee, S. Zhang, T. P. Lodge, and C. D.
the distance from the gate to drain electrode; A is constant in Frisbie, Adv. Mater. 25, 1822 (2013).
11
this comparison, dependent on electrode area, electrolyte R. S. Zucker, Annu. Rev. Neurosci. 12, 13 (1989).
12
L. A. Kong, J. Sun, C. Qian, G. Gou, Y. He, J. Yang, and Y. Gao, Org.
resistivity, and pre-synaptic spike.15 Thus, increased ampli- Electron. 39, 64 (2016).
tudes of peak EPSC are measured for the gates, which are 13
C. Qian, J. Sun, L.-a. Kong, G. Gou, J. Yang, J. He, Y. Gao, and Q. Wan,
closer to the drain electrode. ACS Appl. Mater. Interfaces 8, 26169 (2016).
14
P. Gkoupidenis, N. Schaefer, B. Garlan, and G. G. Malliaras, Adv. Mater.
In summary, the fabrication and performance of artifi-
27, 7176 (2015).
cial neuron transistors based on multi-gate OECTs with ion- 15
P. Gkoupidenis, D. A. Koutsouras, T. Lonjaret, J. A. Fairfield, and G. G.
gel dielectrics are reported. The neuromorphic behaviors are Malliaras, Sci. Rep. 6, 27007 (2016).
16
dependent on the degree of temporal correlation and distance W. Xu, S. Y. Min, H. Hwang, and T. W. Lee, Sci. Adv. 2, e1501326
(2016).
between in-plane-gate and channel. Furthermore, by using 17
D. Kuzum, S. Yu, and H. P. Wong, Nanotechnology 24, 382001
dendritic integration from two different gates, spatiotempo- (2013).
rally correlated outputs were also emulated. The spatial ori- 18
K. H. Lee, M. S. Kang, S. Zhang, Y. Gu, T. P. Lodge, and C. D. Frisbie,
entations of the input pulse are defined, and changing the Adv. Mater. 24, 4457 (2012).
19
M. V. Tsodyks and H. Markram, Proc. Natl. Acad. Sci. U. S. A. 94, 719
orientation will result in the change in the EPSC amplitude.
(1997).
Our results provide a way to construct a complicated neural 20
J. A. Varela, K. Sen, J. Gibson, J. Fost, L. Abbott, and S. B. Nelson,
network based on spatiotemporal correlated multi-gate J. Neurosci. 17, 7926 (1997).
21
OECTs. G. G. Turrigiano, Cell 135, 422 (2008).
22
R. Azouz, J. Neurophysiol. 94, 2785 (2005).
23
G. Ariav, A. Polsky, and J. Schiller, J. Neurosci. 23, 7750 (2003).
See supplementary material for transfer and output char- 24
A. Polsky, B. W. Mel, and J. Schiller, Nat. Neurosci. 7, 621 (2004).
25
acteristic curves of P3HT-based OFET, related characteriza- D. V. Buonomano, J. Neurosci. 20, 1129 (2000).
26
tions, and setup. D. V. Buonomano and W. Maass, Nat. Rev. Neurosci. 10, 113 (2009).
27
S. Martin, P. Grimwood, and R. Morris, Annu. Rev. Neurosci. 23, 649
(2000).
This work was supported by the National Natural 28
C. Wan, L. Q. Zhu, Y. H. Liu, P. Feng, L. P. Liu, H. L. Cao, P. Xiao, Y.
Science Foundation of China (61306085, 11334014) and the Shi, and Q. Wan, Ad. Mater. 28, 3557 (2016).
29
Fundamental Research Funds for the Central Universities of H. Tian, W. Mi, X. Wang, H. Zhao, Q. Xie, C. Li, Y. Li, Y. Yang, and T.
Ren, Nano Lett. 15, 8013 (2015).
Central South University (2016zzts018). Y. G. acknowledges 30
D. H. Hubel, T. N. Wiesel, and M. P. Stryker, J. Comp. Neurol. 177, 361
the support by National Science Foundation DMR-1303742 (1978).
31
and CBET-1437656. R. Shapley, M. Hawken, and D. L. Ringach, Neuron 38, 689 (2003).

You might also like