Abstract
Owing to the conductance-adjustable performance, the emerging two-terminal memristors are promising candidates for artificial synapses and brain-spired neuromorphic computing. Although memristors based on molybdenum disulfide (MoS2) have displayed outstanding performance, such as thermal stability and high energy efficiency, reports on memristors based on MoS2 as the functional layer to simulate synaptic behavior are limited. Herein, a homologous Mo2C/MoS2-based memristor is prepared by partially sulfuring two-dimensional Mo2C crystal. The memristor shows good stability, excellent retention (~104 s) and endurance (>100 cycles), and a high ON/OFF ratio (>103). Moreover, for comprehensively mimicking biological synapses, the essential synaptic functions of the device are systematically analyzed, including paired-pulse facilitation (PPF), short-term plasticity (STP), long-term plasticity (LTP), long-term depression (LTD), and the transitions from STP to LTP. Notably, this artificial synapse could keep a high-level stable memory for a long time (60 s) after repeated stimulation. These results prove that our device is highly desirable for biological synapses, which show great potential for application in future high-density storage and neuromorphic computing systems.
Introduction
Inspired by highly connected and extremely energy-efficient biological neural system, researchers have put forward a computing system consisting of artificial neurons1,2, which can not only solve the bottleneck effectively that computers based on Von-Neumann architecture are facing, but lead to a generation of powerful computing paradigms3,4. Among various devices used for mimicking synapses, including memristors5,6, complementary metal-oxide-semiconductor transistors7,8 and phase change memories9, memristors have been considered as one of the most promising electronic devices for neuromorphic computing owing to their intrinsic capability to remember historical states10,11,12,13. As a representative of transition metal dichalcogenides (TMDCs), MoS2 is widely applied in various devices such as memristors14,15, field-effect transistors16,17, and photodetectors18,19 due to its abundant sulfur vacancies, semiconductor characteristics and tunable bandgap. Currently, MoS2-based memristors have reached some performance milestones and achieved some intriguing applications20,21,22,23. For instance, due to the atomic-scale thickness and electrochemical metallization (ECM), the switching voltage of the MoS2 double-layer memristor can be lowered to 0.1–0.2 V20. A fully printed Ag/MoS2/Ag memristor exhibits a high switching ratio of 107, a wide range of tunable resistance states of 10–1010 Ω, and a switching energy of 4.5 fJ per transition set21. With high-quality crystal, an atomically sharp interface, and the assistance of oxygen atoms doping, the MoS2-based memristor shows excellent switching performance with an endurance of up to 107 and an operating temperature of 340 °C22. In addition, four-terminal lateral memristors with artificial engineered grain boundaries in monolayer MoS2 can not only respond to electric and light stimulation simultaneously, but also imitate biological learning and cognitive processes as well as image perception and processing23. In all, most of the reported MoS2 memristors have outstanding switching performance and tunable window voltages, compared with those using transition metal oxides (TMOs) as functional materials. However, reports on memristors with MoS2 as the functional layer to simulate synaptic behavior are limited, and transition from short-term plasticity (STP) to long-term plasticity (LTP) based on MoS2 synaptic also need further investigation24,25,26,27.
For an electronic device based on two-dimensional (2D) materials, its performance can be greatly improved by reducing the contact resistance and potential barrier between the active layer and the electrodes. There have been various strategies to solve the problem of large contact resistance between semiconductor materials and metal electrodes, such as phase engineering28, doping29, inserting a tunneling layer into the interface to form a metal-insulator-semiconductor contact structure30, and using graphene/soft-landed metals as vdW-interfaced electrodes31. Similarly, for memristors, using the above methods to optimize the contact between the memristive layer and the electrodes can also improve their performance. For example, by introducing graphene as contact electrodes, the MoS2−xOx-based memristor could switch in more than 100 ns and over 2 × 107 cycles. This high switching performance is primarily benefitted from a high-quality interface between graphene and MoS2−xOx22. By forming a variable-barrier WSe2/graphene Schottky junction, the WOx-based memristor exhibits gate-tunable memristive switching characteristics with programming voltages of 0.2–0.5 V, and implements fundamental synaptic functions32. In addition, the InSe2-based memristor fabricated by van der Waals electrodes integration has an ultralow set/reset voltage of 0.12 /0.04 V, which is attributed to the atomically clean and sharp interface between electrodes and the channel33. Mo2C, as a metallic 2D material with low work function (3.8 eV), can improve the contact with semiconductor materials34,35,36. It has been reported that an excellent contact resistance as low as 2.1 kΩ·μm could be formed between Mo2C and MoS234. Moreover, by inserting Mo2C between the metal electrodes and 2D MoOx, the contact barrier is lowered and the performance of two-terminal MoOx-based device is enhanced37. Hence, it is appealing and significant to design a Mo2C/MoS2-based memristor and study its application in mimicking synapses by inserting Mo2C into the contact interface.
Here, a strategy for fabricating vertical two-terminal memristor based on Mo2C/MoS2 heterostructure is proposed, by which Mo2C is partially sulfurized to obtain a seamless interface. The device based on this homologous heterostructure exhibits stable memristive performance with retention time up to 104 s, endurance up to 100 cycles, and on/off ratio up to 103. Meanwhile, it can be used to simulate biological synaptic functions, including paired-pulse facilitation (PPF), STP, LTP, and long-term depression (LTD). Furthermore, the regulation of PPF and the transitions from STP to LTP by applying continuous pulses have been discussed systematically. It is found that the artificial synapse can maintain a high level of memory after the end of the stimulation for a long time, that is, the memristor can maintain stable long-term memory. Therefore, the proposed device is a promising candidate for high-density storage and neuromorphic computing applications.
Results
Fabrication and characterization of the Mo2C/MoS2 heterostructure
The Mo2C/MoS2 heterostructure is prepared by controlling sulfurization of 2D Mo2C crystal, which is synthesized by CVD, as reported in our early work36. After sulfurization, several layers on the top surface of Mo2C could convert to MoS2, and form an integrated Mo2C/MoS2 heterostructure, as illustrated in Fig. 1a. After deposition of the top electrode (Ni/Au) at the surface of MoS2 and the bottom electrode (Ni/Au) on the p++ Si substrate (Fig. 1b), the heterostructure can be directly used as a memristor. Detailed fabricating process of materials and devices is described in Methods. The optical microscope (OM) image displays that the as-grown 2D Mo2C crystal is mainly in a regular hexagon with the size of ~15 μm (Fig. 1c). More morphology and structural characteristics of the Mo2C are shown in Supplementary Fig. 1. Atomic force microscopy (AFM) results show that the thickness and surface roughness of the Mo2C is about 84 nm and 1.05 nm, respectively, indicating the excellent flatness of multilayer 2D Mo2C (Fig. 1d).
a Schematic illustration of the Mo2C/MoS2 heterostructure. b Schematic illustration of the measurement of the electrical properties of the device, where Ni/Au electrodes are deposited on the surface of MoS2 and Si substrate, respectively. c OM, and d AFM image of the as grown 2D Mo2C crystal. e OM, f Raman spectra, g Raman mapping of the intensity at the peak of 410.5 cm−1, and h XPS of the 2D Mo2C/MoS2heterostructure.
The Mo2C/MoS2 heterostructure becomes darker after sulfurization, while it maintains the same hexagonal shape as the pristine Mo2C (Fig. 1e). It suggests that the sulfurization process did not destroy the morphology and structure of the sample. The degree of sulfurization of the sample can be controlled by changing the sulfurization temperature and time during CVD process, similar to the oxidation of Mo2C crystal36. Figure 1f shows the Raman spectra of the Mo2C/MoS2. Compared with the Raman spectra of the Mo2C (Supplementary Fig. 1), additional characteristic peaks at 182.1, 380.3, 410.5, 457.6, and 635.2 cm−1 are collected for the Mo2C/MoS2, while the characteristic peak (143.5 cm-1) of B3g mode for Mo2C is significantly weakened. The peak at 380.3 cm−1 corresponds to \({{{\mathrm{E}}}}_{2g}^1\) mode of MoS2, resulting from the opposite vibration of two S atoms with respect to the Mo atom. The peak at 410.5 cm−1 represents A1g mode, which is associated with the out-of-plane vibration of only S atoms in opposite directions38. Besides, the peaks at 182.1, 457.6, and 635.2 cm−1 are resulted from the resonance Raman (RR) scattering38. These results indicate that the surface layers of Mo2C have been successfully converted to MoS2. Moreover, the Raman mapping images of the Mo2C/MoS2 heterostructure at its characteristic peak show a uniform intensity distribution, indicating the homogeneity of the as-synthesized MoS2 on Mo2C (Fig. 1g and Supplementary Fig. 2). X-ray photoelectron spectroscopy (XPS) results further confirm the formation of the Mo2C/MoS2 heterostructure, as shown in Fig. 1h. The high-resolution Mo 3d XPS of the Mo2C/MoS2 heterostructure presents the doublet peaks of Mo2+ (228.6 and 231.8 eV), and Mo4+ (229.5 and 232.7 eV), which mean the coexistence of Mo2C and MoS2, respectively36,39. The weak signal of MoO3 (doublet peaks of Mo6+ at 233.1 and 236.7 eV) is due to the bonding of Mo atoms with O atoms in the air. The XPS survey spectra and high-resolution of C1s are shown in Supplementary Fig. 3. Thus, a uniform Mo2C/MoS2 heterostructure has been fabricated by the sulfurization of the 2D Mo2C crystal. To further demonstrate the interface characteristics of Mo2C/MoS2 heterostructure, the samples are analyzed by high-resolution transmission electron microscope (HRTEM). From the HRTEM images of the cross-sectional of Mo2C/MoS2 (Supplementary Fig. 4), it can be seen that there is a very clear boundary between Mo2C and MoS2, indicating its seamless structure (Supplementary Fig. 4b). In addition, the Mo2C crystal maintains original single structure with d-spacing of 3.7 Å, which is in consistent with the (110) plane of Mo2C (Supplementary Fig. 4c)40. In the MoS2 region, the major d-spacing is 3.1 Å corresponding to the (004) plane (Supplementary Fig. 4d). This further confirms the structural transition of the samples from Mo2C to MoS2.
Electrical characterizations of the memristor
To examine the switching performance of the Mo2C/MoS2-based memristor, the samples are systematically tested for their electrical properties. Figure 2a shows the typical bipolar current-voltage (I-V) curve of the device. During the test, a forward voltage is applied between the top electrode (connected with MoS2) and the bottom electrode. Initially, the device requires an electroforming process with a larger sweep voltage (−8 to 8 V) to achieve the switching process between the high-resistance state (HRS, i.e., OFF state) and the low-resistance state (LRS, i.e., ON state). Then, the device can operate at lower voltages, such as a smaller sweep voltage (−4 to 4 V) for the 1st switching process (Fig. 2a). The process of ON switching is defined as SET, where the voltage is about 2.9 V. Next, an opposite-polarity bias sweep is applied to bring the device back to the HRS at the voltage of proximately −3 V (defined as RESET). Linear I-V curves of electroforming and 1st switching process are displayed in Supplementary Fig. 5. It can be calculated that the power consumption of the device is 0.16 mW. It is essential to verify the reliability and nonvolatility of our device as a memristor, so 100 consecutive cycles of sweep voltage from −4 to 4 V are employed to the device (Fig. 2b). As a result, the memristor could maintain stable switching behaviors of HRS and LRS in 100 cycles. At a higher sweep voltage of −8 to 8 V, the device also exhibits high stability (Supplementary Fig. 5c), which indicates that the memristor has a wide operating voltage. Figure 2c displays the distribution of SET and RESET voltage of 100 cycles, the corresponding standard deviation (σ) of which are 0.45 and 0.35 V, respectively. Additionally, it is found that the memristor possesses threshold voltages with a mean value of 2.83 and −3.04 V, which are larger than other reported vertical memristors12,41,42,43. Such large threshold voltages are attributed to large activation energy and migration of sulfur ions in MoS244,45,46. The device at a sweep voltage from −8 to 8 V shows a resistance of 106 and 103 Ω at HRS and LRS, respectively. The resistance for both states maintains steady during the sweep cycles (Fig. 2d). The cumulative probability of the HRS and LRS resistance is further calculated and shown in Fig. 2e. It exhibits HRS/LRS ratio of ≈103 in all cycles, indicating the reproducibility of such a memristor during cycle-to-cycle measurement. Supplementary Fig. 6 displays the distribution and cumulative probability of HRS and LRS at a sweep voltage from −4 to 4 V. Figure 2f illustrates the retention characterization of LRS and HRS after applying the corresponding pulse (amplitude:8 V for SET and −8 V for RESET, read voltage: 0.1 V), which shows no noticeable change during the test time (>104 s), indicating the reliable nonvolatility of the memristor. It is worth noting that the HRS/LRS ratio for endurance statistics is bigger than that for retention statistic due to the difference of the read voltage.
a I-V switching curves of the device. The green and red line represents the electroforming and the 1st switching process, respectively. b I-V curves of the device for 100 consecutive cycles of sweep volatges. c The distribution of Set voltage and Reset voltage during 100 cycles. d Endurance characteristics undergoing 100 SET/RESET switching cycles. e Cumulative probability plots of HRS and LRS. f Retention performance of LRS and HRS after Set and Reset operations. The pulse voltages and read voltages are 8/−8 V, and 0.1 V, respectively.
To analyze the underlying conduction mechanism of the memristor, we have plotted and fitted the I-V curves by I∝Vα corresponding to HRS and LRS of the electroforming process (Fig. 3a and b), respectively. The results show that the I-V curve can be divided into three regions according to the value of α, which represents the slope of the curve. The conduction mechanism of the sample in this work conforms to the space charge limited conduction (SCLC)47,48,49. At low voltage, it exhibits ohmic conductive behaviors, implying that the concentration of thermally generated free carriers is larger than that of the injected carriers. With the increasing voltage, the current gradually increases, and the slope (α) is >2 as the voltage is larger than 4 V. It indicates that the injected charge density exceeds the intrinsic free carrier density and Child’s law becomes the main conductive mechanism. Afterwards, the device is reset to LRS and the fitting result is similar to that of HRS. Note that the conductive filament is usually formed by activating metal ions, such as Cu and Ag, driven by external bias in ECM mechanism-based memristors20,50. In contrast, the memristor in this work is based on inert electrodes -Ni/Au, which cannot be ionized under electric field and is not easy to adsorb oxygen atoms. Thus, we claim that our memristor is likely to be a valance change memory (VCM) device12,22,51, in which sulfur vacancies move to form conductive channels. Figure 3c illustrates the distribution of sulfur vacancies during HRS and LRS. When a forward electric field is applied to the device, a large number of sulfur vacancies appear in MoS2 layers due to the migration of sulfur ions. Therefore, the conductive channels are formed, leading to the conversion from HRS to LRS. For the rupture of conductive channels that reset the device back to the HRS, it is ascribed to the reverse diffusion of sulfur ions to fill sulfur vacancies under a reverse electric field. A similar mechanism of MoS2-based memristor is also confirmed by in situ characteristics of sulfur vacancies, which are reported by other previous works42,52,53.
Artificial synaptic characteristics of the memristor
The memristor based on the Mo2C/MoS2 heterostructure can also be used for simulating synaptic behaviors. As five continuous positive and negative sweep voltages are applied to the device, the conductance increases (decreases) with positive (negative) sweep voltages (Fig. 4a). It means gradual changes of the conductance under continuous voltage stimulations, which is analogous to the behavior of biosynapse, reflecting a successively variable of synaptic weight54. Usually, as two consecutive pulses are successively applied to a memristor, the phenomenon in which the second pulse generates a larger postsynaptic current (PSC) than the first one is called PPF55. Obviously, the memristor in this work exhibits an obvious PPF characteristic when they are applied two continuous pulses, as shown in Fig. 4b. Note that PPF index is expressed by:
Where I1 and I2 are the PSC corresponding to the first and second pulse, respectively. Accordingly, PPF index in Fig. 4b is about 47.4%. In addition, the enhancement of the PSC is related to the parameter of pulses, including the interval, width and amplitude. In Fig. 4c, a pair of positive pulses with interval varying from 20 to 1000 ms is applied to another device. It is found that the value of the PPF index gradually decreases with the increasing time interval, which is in agreement with the behavior of biological synapses. Furthermore, the PPF index can be fitted by a double-phase exponential function (pink line in Fig. 4c):
where t is the pulse interval time, C1 and C2 are the initial facilitation magnitudes, τ1 and τ2 are the characteristic relaxation time55. The results show that τ1 and τ2, are about 145.4 and 932.0 ms, corresponding to the fast and slow facilitation terms, respectively. Figure 4d exhibits the post-tetanic potentiation (PTP) index versus the interval time with ten consecutive pulses applied to the device. Here, the PTP index is defined as:
Where I1 and I10 are the PSC corresponding to the first and tenth pulse, respectively. Similar to the PPF, the index of PTP also decreases with increasing pulse intervals. However, the PTP index is larger than the PPF index. As applying pulses with different widths and amplitudes on the device, it also exhibits behavior similar to biosynapse (Fig. 4e, f). As the pulse width increases, the PPF index first increases and then reaches saturation. And the increasing amplitude triggers the linear increase of PPF index. The increasing trend in both cases is due to the presence of more sulfur vacancies in the material.
a Variations of voltage and current with respect to sweep cycles. b Emulations of PPF behaviors. The test parameters are pulse amplitude of 8 V, width of 100 ms, interval of 100 ms, and read voltage of 0.1 V. c The PPF indexes at different pulse interval, which varies from 20 to 1000 ms. d The PTP indexes versus pulse interval, which varies from 20 to 1600 ms. The PPF indexes versus pulse (e) width, and (f) magnitude, which varies from 10 to 800 ms, and from 4 to 10 V, respectively.
In order to show the characteristic of PSC, pulses trains of the device with different amplitudes, widths and intervals are performed (Supplementary Fig. 7). When the amplitude of pulses increases from 6 V to 10 V, the initial current is larger and PSC increases more significantly. In addition, the regulation of current by pulse width shows the same trend as that of pulse amplitude. However, a larger pulse interval leads to a smaller final current. In short, PSC could be well regulated by different amplitude, width, and interval of pulse trains, which facilitates obtaining ideal PSC under suitable pulse stimulation, thus broadening the application of memristors in synapses.
The ability to modulate and retain the synaptic weight over time is defined as synaptic plasticity, namely synaptic potentiation, which represents the level of learning and memory and is divided into STP and LTP56,57,58. Note that short-term depression (STD) and LTD are depression of synaptic weight59. To simulate the LTP and LTD of the proposed device, 20 positive and 20 negative pulses are applied in sequential. The PSC response indicates that the artificial synapses can be bidirectionally regulated by a sequence of positive or negative pulses, which is suitable for application in more complex deep neural networks (Fig. 5a and Supplementary Fig. 8). From previous results about PPF simulations, synaptic plasticity can also be modulated by pulse interval. As shown in Fig. 5b, it could exhibit either STP or LTP using pulses with different intervals (Δt = 100 ms or 500 ms).
a PSC values with the increasing of pulse number (pulse amplitude of 8/−8 V, width of 100 ms, interval of 100 ms, and read voltage of 0.1 V), mimicking potentiation/depression behaviors of a biological synapse. b PSC values versus the pulse number at pulse interval of 100 ms and 500 ms. c Pulse curves for the device after application of a sequence of presynaptic pulses with different width (100 and 300 ms), and same pulse interval of 100 ms. d Retention curves for synaptic weight after different numbers of identical presynaptic pulses (pulse amplitude of 8 V, width of 1000 ms, interval of 1000 ms and read voltage of 1 V). e The distribution of time constants obtained by fitting. f Comparison of time constants for different memristors.
Compared with STP representing short-term memory, LTP is a permanent memory formed by repeated training based on short-term memory, corresponding to the lasting change of synaptic weight. Therefore, two pulse trains with the same interval (100 ms) and different widths (50 ms and 200 ms) are sequentially applied to the device. The result illustrates that pulse trains with wider widths lead to larger PSC after the stimulation, that is, the device can be switched from STP to LTP (Fig. 5c). Through sufficient repeated training, the transition from STP to LTP can also be achieved, resembling the biological synapse. To obtain this transition, we attach pulses with different numbers (5, 10, 20, 40, and 80) to the device and then use a voltage of 1 V to read current within 60 s. As shown in Fig. 5d, the normalized synaptic weight decreases rapidly at the beginning, then decreases slowly, and finally reaches a relatively stable level, indicating a similar trend with the human-memory “forgetting (or retention) curve” in psychology. The decay process and the final synaptic weight can be regarded as STP and LTP, respectively. With the increase of pulse number, the synaptic weight for LTP can be increased from 35% to 77%, suggesting the transition from short- to long-term memory. The experimental decay can be fitted by a double exponential decay function as follows
where y0 is the current offset, C3 and C4 are the fit constants, τ3 and τ4 are the time constants54. The fitting result is shown in Fig. 5e, where τ3 and τ4 are significantly different from τ1 and τ2 in Eq. (2) related to PPF. The decay of the former undergoes repeated pulse stimulation, resulting in more sulfur vacancies accumulating and longer duration time, representing LTP. However, the latter only undergoes two pulses stimulation and the concentration difference of sulfur vacancies is smaller, representing STP. The distribution of τ3 and τ4 obtained by fitting are shown in Fig. 5e. τ3 and τ4 increase from 2.38 to 6.53 s and from 17.25 to 124.31 s, respectively, indicating a decreasing forgetting rate which further verifies the slower relaxation of synaptic weight by applying more pulses. Figure 5f compares the time constant τ4 representing the degree of forgetting in this paper with the time constants in other reports. The results show that our device has a very low level of forgetting under the same pulse stimulation, implying a clear advantage in learning ability12,54,60,61,62,63,64,65,66.
Discussion
In summary, a two-terminal memristor based on Mo2C/MoS2 heterostructure was fabricated. The device exhibits excellent stability, retention, endurance, and a high HRS/LRS ratio, which is attributed to the good contact brought by introducing Mo2C. In addition, we indirectly proved that the memristive mechanism is the formation and destruction of conductive channels associated with sulfur vacancies under the electric field. Moreover, the memristor successfully mimicked main biological synaptic functions, including PPF, STP, LTP, LTD, and STP to LTP transitions. The device can not only possess a lower forgetting rate, but also maintain a stable long-term memory under repeated stimulation. Therefore, it can be concluded that our memristor is an excellent candidate for an artificial synapse, which shows great potential in high-density storage and neuromorphic computing applications.
Methods
Growth and transfer of Mo2C
The 2D Mo2C was synthesized by CVD, as reported by our previous work36. First, a piece of Cu foil (120 μm in thickness) as the growth substrate was placed on top of a Mo foil (thickness of 50 μm). Then they were put in the middle of the quartz reactor. Before the growth, Cu/Mo foil was heated to 1100 °C in 50 min under a mixture of Ar (200 sccm) and H2 (100 sccm), then annealed for 25 min. Subsequently, the 2D Mo2C was grown for 60 min by introducing CH4 (3 sccm). After growth, the Mo2C was transferred onto a p++ Si substrate with low resistance by the polydimethylsiloxane (PDMS) assisted transfer method.
Preparation of the Mo2C/MoS2 hybrid structure
The Mo2C/MoS2 hybrid structure was synthesized by sulfurization of 2D Mo2C. First, the obtained Mo2C on Si substrate was put in the middle of the quartz reactor, while sulfur powders (Alfa Aesar, precipitated, 99.5%) in moderation were put in the upstream of the heating zone. Then, the tube furnace was heated from ambient temperature to 350 °C under a mixture of Ar (200 sccm) and H2 (100sccm) in 60 min. Subsequently, the supply of H2 was cut off and the flow rate of Ar was set as 60 sccm. The temperature of the reactor was raised from 350 °C to 720 °C in 20 min, and the heating temperature of the sulfur powders was set to 170 °C. After the sulfurization for 60 min, a Mo2C/MoS2 heterostructure was obtained on the Si substrate.
Sample characterization and measurement of the device
The morphology, composition, and crystal structure of the Mo2C and the Mo2C/MoS2 hybrid were characterized by SEM (Hitachi S-4800), AFM (Bruker Dimension), OM (HORIBA JY HR800), and XPS (Thermo-VG Scientific, ESCALAB 250Xi). Raman spectra and mapping were collected using HORIBA JY HR800 with a 633 nm exciting laser. TEM images were obtained by Tecnai, G2 F30. With massless photolithography, two square windows with area of 64 μm2 and 3.6 × 105 μm2 were carved in the middle of the Mo2C/MoS2 sample and the surface of the Si substrate, respectively, followed by depositing Ni/Au of 20/65 nm as electrodes. The electrical characteristics, including DC and pulse measurement, were tested using a probe station with KEYSIGHT B2902A.
Data availability
Additional data related to this paper may be requested from the authors.
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Acknowledgements
This work was financially supported by the National Natural Science Foundation of China (grant no. 52072415) and Guangdong Basic and Applied Basic Research Foundation (grant nos. 2021A1515012387, and 2021A1515110980).
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The preparation of Mo2C, and Mo2C/MoS2 hybrid structure was completed by X.T., L.L.Y. and B.H.L.; the fabrication of devices completed by X.T., J.H.H. and B.H.L.; the characterization 2D materials were carried out by S.D.Y. and R.L.Y.; the test of memristors and artificial synapse were implemented by X.T., L.L.Y. and J.H.H.; the device structure design, and performance analysis were completed by W.J.C., Z.P.Z., Z.K.T. and X.C.G.; X.C.G. and X.T. contributed to the writing and polishing of the manuscript; X.C.G. supervised the overall research.
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Tang, X., Yang, L., Huang, J. et al. Controlling sulfurization of 2D Mo2C crystal for Mo2C/MoS2-based memristor and artificial synapse. npj Flex Electron 6, 93 (2022). https://doi.org/10.1038/s41528-022-00227-y
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DOI: https://doi.org/10.1038/s41528-022-00227-y