Abstract
A neuro-bionic device based on a two-dimensional Ti.sub.3C.sub.2 material is provided. The device includes a Pt/Ti/SiO.sub.2/Si substrate, a neuro-bionic layer formed on a Pt film layer of the Pt/Ti/SiO.sub.2/Si substrate, and an Al electrode layer formed on the neuro-bionic layer. The neuro-bionic layer is made of a two-dimensional Ti.sub.3C.sub.2 material. The neuro-bionic device of the present invention is prepared by an evaporating coating method and a drop-coating method. The preparation process is relatively simple. The prepared device can successfully simulate the characteristics of synapse. More importantly, the resistance of the device can be modulated continuously under a scanning of a pulse sequence with pulse width and interval of 10 ns, which is beneficial to the application of the device in the ultrafast synapse simulation.
Claims
1. A neuro-bionic device, comprising: a Pt/Ti/SiO.sub.2/Si substrate, a neuro-bionic layer formed directly on a Pt film layer of the Pt/Ti/SiO.sub.2/Si substrate, the neuro-bionic layer is made of a two-dimensional Ti.sub.3C.sub.2 material, and an Al electrode layer formed directly on the neuro-bionic layer, the Al electrode layer comprises a plurality of circular electrodes uniformly distributed on the neuro-bionic layer, and a diameter of each circular electrode of the plurality of circular electrodes is 80 μm-300 μm; wherein the neuro-bionic device is an electronic artificial synapse device configured to provide spike-timing-dependent plasticity and paired pulse facilitation.
2. The neuro-bionic device according to claim 1, wherein the neuro-bionic layer is prepared by a drop-coating method, and a thickness of the neuro-bionic layer is 5 nm-200 nm.
3. The neuro-bionic device according to claim 1, wherein the Al electrode layer is prepared by an evaporation method and the diameter of each circular electrode of the plurality of circular electrodes is 90 μm.
4. The neuro-bionic device according to claim 3, wherein a thickness of each of the plurality of circular electrodes is 50 nm-200 nm.
5. The neuro-bionic device according to claim 1 wherein the Pt/Ti/SiO.sub.2/Si substrate comprises a Si layer, a SiO.sub.2 layer, a Ti layer and a Pt film layer from bottom to top.
6. The neuro-bionic device according to claim 1, wherein the Al electrode layer is configured to simulate a pre-synaptic membrane of a synapse.
7. The neuro-bionic device according to claim 1, wherein the Pt film layer is configured to simulate a post-synaptic membrane of the synapse.
8. The neuro-bionic device according to claim 1, wherein the artificial synapse device is configured to be controlled by applying a series of pulse sequences with different amplitudes and widths.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) FIG. 1 is a structural diagram of a neuro-bionic device of the present invention.
(2) FIG. 2 is a structural diagram of an evaporation coating machine for preparing a neuro-bionic device.
(3) FIG. 3 shows a voltage-current characteristic curve of a neuro-bionic device of the present invention scanned under a voltage ranging from −6 V to 6 V at a limiting current of 300 μA.
(4) FIG. 4 shows a voltage-current characteristic curve of a neuro-bionic device of the present invention scanned under a voltage ranging from 0 V to 6 V at a limiting current of 50 μA.
(5) FIG. 5 shows a pulse waveform of an Au electrode layer of contrast example 1 when applied with a series of pulse sequences with different pulse widths.
(6) FIG. 6 is a diagram showing a change of a relationship between a resistance and a pulse scanning number of an Au electrode layer of contrast example 1 when applied with a series of pulse sequences with different pulse widths.
(7) FIG. 7 shows a pulse waveform of an Al electrode layer of a neuro-bionic device of the present invention when applied with a series of pulse sequences with different pulse widths.
(8) FIG. 8 is a diagram showing a change of a relationship between a resistance and a pulse sequence number of an Al electrode layer of a neuro-bionic device of the present invention when applied with a series of pulse sequences with different pulse widths.
(9) FIG. 9 shows a diagram of a simulation of a spike-timing dependent plasticity (STDP) by a neuro-bionic device of the present invention.
(10) FIG. 10 shows a diagram of a simulation of a paired pulse facilitation (PPF) by a neuro-bionic device of the present invention.
DETAILED DESCRIPTION
Embodiment 1
(11) As shown in FIG. 1, the neuro-bionic device of the present invention includes the Pt/Ti/SiO.sub.2/Si substrate 1 at the bottom, the neuro-bionic layer 2 formed on the Pt/Ti/SiO.sub.2/Si substrate 1, and the Al electrode layer 3 formed on the neuro-bionic layer 2. The Pt/Ti/SiO.sub.2/Si substrate 1 includes the Si layer at the bottom, the SiO.sub.2 layer on the Si layer, the Ti layer on the SiO.sub.2 layer, and the Pt film layer on the Ti layer at the top. The neuro-bionic layer 2 is located on the Pt film layer.
(12) The neuro-bionic layer 2 is a two-dimensional Ti.sub.3C.sub.2 material with a thickness of 150 nm.
(13) The Al electrode layer 3 includes a plurality of uniformly distributed circular electrodes with a diameter of 90 μm, and a thickness of each circular electrode is 150 nm.
(14) The method of preparing the neuro-bionic device shown in FIG. 1 includes the following steps:
(15) (1) forming a neuro-bionic layer on a Pt/Ti/SiO.sub.2/Si substrate
(16) {circle around (1)} the Pt/Ti/SiO.sub.2/Si substrate is washed with acetone under an ultrasonic wave for 10 minutes, put into alcohol for an ultrasonic washing for 10 minutes, put into deionized water using a tweezer for an ultrasonic washing for 5 minutes, and finally placed on a dustless test paper and dried with nitrogen for storage;
(17) {circle around (2)} prepared Ti.sub.3C.sub.2 powder is dissolved in deionized water at a concentration of 5 mg/mL for shaking evenly, and then dissociated by the ultrasound wave for 30 minutes;
(18) {circle around (3)} a solution after an ultrasonic treatment is taken out, and rinsed with nitrogen for sealing;
(19) {circle around (4)} the solution is taken using a pasteur pipette, and drop coated on a Pt film layer of the Pt/Ti/SiO.sub.2/Si substrate, and the Pt/Ti/SiO.sub.2/Si substrate is placed overnight in a closed space filled with nitrogen to form the neuro-bionic layer with a thickness of 150 nm;
(20) (2) preparing an Al electrode on the neuro-bionic layer
(21) {circle around (1)} as shown in FIG. 2, the cavity 4 of the evaporation coating machine is opened, then the prepared neuro-bionic layer is placed on a mask with an aperture diameter of 90 and the mask is fixed on the substrate table 5 of the evaporation coating machine, the aluminum strip 7 having a length of 1.5 cm is placed into the molybdenum bar 6;
(22) {circle around (2)} a bell jar pressure and a system pressure of the evaporation coating machine is adjusted to 1.5 Pa by a mechanical pump, then the mechanical pump is converted into a diffusion pump state for a preheating for 60 minutes, and after the preheating, the bell jar pressure is adjusted to 3×10.sup.−3 Pa;
(23) {circle around (3)} when a vacuum degree reaches 3×10.sup.−3 Pa, the evaporation coating machine is adjusted to an evaporation state, and a workpiece is rotated;
(24) {circle around (4)} an evaporation bombardment voltage is increased slowly, when a reading of an evaporation bombardment ammeter is 50 A, an evaporation coating is performed to obtain the Al electrode having a thickness of 150 nm.
Contrast Example 1
(25) The Al electrode layer is replaced by the Au electrode layer, and other parameters and preparation methods remain unchanged. The neuro-bionic device with the top layer of Au electrode layer is obtained.
Embodiment 2
(26) The performance of the devices in Embodiment 1 and contrast example 1 are tested respectively.
(27) As shown in FIG. 3, a voltage ranging from −6 V to 6 V is applied to the Al electrode layer of the neuro-bionic device in Embodiment 1 of the present invention. The voltage is increased from 0 V to 6 V, and then gradually reduced to 0 V, then, the voltage changes from 0 V to −6 V, and then changes gradually to 0 V. When the scanning voltage reaches about 4 V, the device suddenly changes from a high-resistance state to a low-resistance state. At this time, the resistance value of the neuro-bionic device remains at the low-resistance state. When the negative voltage applied on the Al electrode layer is increased to −4 V, the neuro-bionic device suddenly changes from the low-resistance state to the high-resistance state, and the device remains at the high-resistance state until the scanning voltage returns to 0 V.
(28) As shown in FIG. 4, a low limiting current of 50 μA is used for voltage scanning the neuro-bionic device in Embodiment 1. The forward voltage is applied to the Al electrode layer, and the voltage is increased from 0 V to 6 V, and then gradually reduced to 0 V. The continuous changing voltage is used for scanning. When the voltage reaches about 4 V, the resistance value of the neuro-bionic device changes slowly from a high-resistance state to a low-resistance state. This change is more conducive to the simulation of synaptic function.
(29) As shown in FIG. 5, continuous pulses with different pulse widths are applied to the Au electrode layer of the neuro-bionic device in the contrast example 1, and the pulse widths are 50 ns, 100 ns, 150 ns, respectively. The pulse data obtained from the oscilloscope are shown in FIG. 5. We can see that the amplitude of the device changes slowly with the change of the number of pulses. With the change of pulse width, the amplitude increase of the neuro-bionic device shows a different trend. However, when the pulse width is reduced to 10 ns, the device cannot be turned on for adjustment.
(30) As shown in FIG. 6, the pulse sequence is continuously applied to the Au electrode layer of the neuro-bionic device in the contrast example 1. The same positive pulse sequence is applied to the Al electrode layer, and the amplitude is 6 V. The pulse widths are 50 ns, 100 ns and 150 ns, respectively. By the continuous pulse scanning, the resistance is reduced until the resistance is slowly reduced to a low-resistance state and remains stable. The figure shows the relationship between the resistance and the amplitude of the device. It can be seen that when the pulse width is gradually increased on the Au electrode layer of the device while other conditions remain unchanged, the number of pulses required for the device to change from high resistance to low resistance is different, thus the conductance changes obviously.
(31) The same pulse test is performed on the neuro-bionic device of Embodiment 1, as shown in FIG. 7 and FIG. 8. It is found that the amplitude of the neuro-bionic device using the Al electrode layer is reduced to 2 V. More importantly, the pulse interval of the pulse sequences can be reduced to 10 ns for continuous regulation, which is helpful for the application of ultrafast neural modulation.
(32) As shown in FIG. 7, the continuous pulse sequences with different pulse widths of 10 ns, 20 ns and 30 ns are respectively applied to the Al electrode layer, the original pulse data are shown in FIG. 7.
(33) As shown in FIG. 8, the pulse sequence is continuously applied to the Al electrode layer of the neuro-bionic device, and the amplitude and interval of the pulse sequence are 2 V and 10 ns, respectively. The pulse widths are 10 ns, 20 ns and 30 ns, respectively. By applying the pulse sequence, the resistance is slowly reduced to the low-resistance state and remains stable. FIG. 8 shows the relationship between the resistance value and the amplitude. When the pulse width is gradually increased on the Al electrode layer of the device while other conditions remain unchanged, the number of pulses required for the device to change from high resistance to low resistance is different, thus the conductance changes obviously. Moreover, it can be clearly seen that the device using the Al electrode can be modulated under a pulse sequence with a pulse width of 10 ns. This is beneficial to the application in the field of ultrafast neural bionics.
(34) As shown in FIG. 9, the spike-timing dependent plasticity (STDP) of the neuro-bionic device is stimulated. Specifically, Δt is the relative time difference between the pulse and the input and output neurons. When the pre-synaptic peak appears before the post-synaptic peak, Δt>0, the long-term potentiation (LTP) occurs. On the contrary, when the pre-synaptic peak appears after the post-synaptic peak, Δt<0, the long-term depression (LTD) occurs. FIG. 9 shows the relationship between synaptic weight ΔW and time interval Δt. ΔW is defined as the percentage change of the conductance of the device after the occurrence of STDP. Specifically, ΔW=G2−G1/G1×100%. In addition, it can be seen from the diagram that the smaller the Δt, the greater the change of synaptic weight. In the present embodiment, the STDP function in the biological synapse is perfectly reproduced.
(35) As shown in FIG. 10, the paired pulse facilitation (PPF) of the neuro-bionic device is stimulated. The PPF curve in FIG. 10 is fitted by the following equation: PPF=(G.sub.2−G.sub.1)/G.sub.1×100%=C.sub.1exp(−t/τ.sub.1)+C.sub.2exp(−t/τ.sub.2). In this equation, G.sub.1 and G.sub.2 are the conductance values after the first and second pulses, respectively. The two fitting time constants, τ.sub.1 and τ.sub.2, correspond to the fast decaying and slow decaying, respectively, which are similar to the characteristic relaxation time observed in biological synapses. In the present embodiment, τ.sub.1 and τ.sub.2 are respectively equal to 392 ns and 400 ns. Therefore, the memory effect is enhanced by well controlling the pulse pair and decreasing the pulse interval, which is similar to the behavior of biological synapses.
