Abstract
Molybdenum disulfide (MoS2) has attracted a great attention as an excellent 2D material for future optoelectronic devices. Here, a novel MoS2 tribotronic phototransistor is developed by a conjunction of a MoS2 phototransistor and a triboelectric nanogenerator (TENG) in sliding mode. When an external friction layer produces a relative sliding on the device, the induced positive charges on the back gate of the MoS2 phototransistor act as a “gate” to increase the channel conductivity as the traditional back gate voltage does. With the sliding distance increases, the photoresponsivity of the device is drastically enhanced from 221.0 to 727.8 A W−1 at the 100 mW cm−2 UV excitation intensity and 1 V bias voltage. This work has extended the emerging tribotronics to the field of photodetection based on 2D material, and demonstrated a new way to realize the adjustable photoelectric devices with high photoresponsivity via human interfacing.
Keywords: MoS2, photoresponsivity, phototransistor, triboelectric nanogenerator, tribotronics
1. Introduction
Recently, because of the intriguing electrical,1 piezoelectric,2, 3 and optical4, 5, 6 properties, molybdenum disulfide (MoS2) has attracted a great interest for the researchers. As a typical 2D material, the bulk MoS2 consists of lamellar S–Mo–S atoms units bonded by weakly van der Waals forces, facilitating cleavage of the crystals using the mechanical exfoliation technique or the liquid‐phase method.7, 8, 9 Bulk MoS2 is an indirect‐gap semiconductor with a bandgap of 1.2 eV, while monolayer MoS2 is a direct‐gap semiconductor with a bandgap of 1.8 eV.8, 10, 11 Field effect transistors using MoS2 as semiconductor channel material have exhibited excellent performances, such as high current ON/OFF ratio (107–108), high electron mobility (≈200 cm2 V−1 S−1) and low sub‐threshold swing (74 mV dec−1),1, 12 which have a wide range of potential practical applications in the field of gas sensor,13, 14 amplifiers,15 and logic circuits.16 To date, a series of phototransistors based on multilayer MoS2 has been reported with broad spectral response from ultraviolet to infrared and high photoresponsivity (880 A W−1) and optical gain (V ds = 8 V, V gs = −70 V),4 indicating that MoS2 is a promising building‐block for the optoelectronic devices. However, in order to enhance the photoresponsivity of MoS2 phototransistors, a high gate bias or large drain–source bias voltage usually needs to be applied to increase the photocurrent, resulting in extra energy dissipation or the increased dark current. A direct adjusting mechanism is not available for interfacing the external environment and phototransistors.
Since 2012, based on the universally known triboelectrification and electrostatic induction effects, the innovative triboelectric nanogenerator (TENG) has been successfully invented to convert ambient mechanical energy into electricity.17, 18, 19, 20, 21 The TENG has been extensively utilized in microenergy,22, 23 macroenergy,24, 25 active sensors,26, 27, 28, 29 and triboelectric‐charge‐controlled devices.30, 31 In 2014, an interesting new field of tribotronics was introduced, which uses electrostatic potential created by TENG as a “gate” voltage to control charge carrier transport in the semiconductor.32 By now, several tribotronic devices have been experimentally demonstrated including logic circuits,33 organic LED,34 memory,35 and phototransistors,36 especially smart tactile switch based on MoS2 tribotronic transistor.37
Here in this work, we developed a novel MoS2 tribotronic phototransistor by coupling of a MoS2 phototransistor and a sliding mode TENG. The photoresponsivity of the MoS2 tribotronic phototransistor can be enhanced considerably by a relative sliding between the bottom friction layer and the device. With the sliding distance increasing, electrons flow from the aluminum electrode on the bottom of the fluorinated ethylene propylene (FEP) film to the source electrode and an inner gate voltage is formed, resulting in the increased Femi level of the semiconducting MoS2. Consequently, the energy bands of the MoS2 will bend downwards and the barrier height between the electrode and the MoS2 will be lowered, resulting in increased separation and transport of the photogenerated carriers under illumination. Under an illumination of 100 mW cm−2 excitation intensity and 1 V bias voltage, with the sliding range of 8 mm, the photoresponsivity of the device is drastically enhanced from 221.0 to 727.8 A W−1. This work has extended the emerging tribotronics to the field of photodetection based on 2D material, and demonstrated a new way to realize adjustable photoelectric devices with high photoresponsivity via human interfacing.
2. Principle and Characteristics
2.1. Structure of the MoS2 Tribotronic Phototransistor
The basic structure of the MoS2 tribotronic phototransistor is composed of a MoS2 phototransistor and a TENG in sliding mode, as schematically illustrated in Figure [qv: 1]a. A few‐layer MoS2 was prepared on degenerately doped p‐type silicon substrate with 300 nm thick SiO2 by using the Scotch tape‐based mechanical exfoliation method. Subsequently, UV lithography and electron beam evaporation were used for the fabrication of source and drain electrodes (5 nm Cr/50 nm Au) on MoS2 flakes. An aluminum (Al) film was deposited on the bottom surface of the silicon substrate with a thickness of about 100 nm, serving as a gate electrode. The bottom friction layer, which acts as a free‐sliding layer, consists of a 20 μm thick FEP film (10 mm × 10 mm) attached on a 50 μm thick Al foil. In order to increase the effective surface area and improve the triboelectric charge density, the surface of the FEP was etched by inductively coupled plasma (ICP) (Figure S1, Supporting Information). To keep its stability, the device was packaged with a layer of 30 nm thick Al2O3 by atomic layer deposition (ALD). Figure 1b shows the atomic force microscopy (AFM) image of the MoS2 flake used in this device. The left inset presents that the height of the MoS2 flake along the black line is about 8 nm. The conduction channel length and width is 3 μm and 5 μm, respectively.
Figure 1.

Schematic illustration of a MoS2 tribotronic phototransistor. a) Structure of a MoS2 tribotronic phototransistor based on a MoS2 phototransistor and a triboelectric nanogenerator in sliding mode. b) Atomic force microscope (AFM) image of the MoS2 flake used in this device. Inset: Cross‐sectional plot along the black line and the height of the flake is 8 nm.
2.2. Characteristics of the MoS2 Phototransistor
The characteristics of the MoS2 phototransistor were measured by a semiconductor parameter analyzer (Keithley 4200) and shielded probe station at room temperature. As shown in Figure [qv: 2]a, the drain–source current (I ds) varies nearly linearly with V ds under different V gs from −10 to 10 V. Figure 2b shows the I ds−V gs transfer curves at the drain bias voltage of 1 V, and the current ON/OFF ratio of the device is about 103. The device exhibits the excellent n‐type transistor properties, which are similar to the previous reports of the MoS2 transistor.1 Without gate voltage, the typical I ds–V ds characteristics of the MoS2 phototransistor under the dark and different excitation light intensity (λ = 365 nm) are shown in Figure 2c. It is presented that the phototransistor is very sensitive to the excitation light intensity and the drain–source current increases with the increasing illumination. When the illumination increases from dark to 400 mW cm−2, the I ds increase from 0.72 to 15.46 μA at a drain voltage of 5 V, enhancing about 21 times. The relationships between the photocurrent (I ph = I light−I dark) and the excitation light intensity under different drain voltages are plotted in Figure 2d, which indicate that the photocurrent increases with the excitation light intensity increasing. The photocurrent in different wavelengths and the response time of the MoS2 phototransistor are shown in Figures S2 and S3 (Supporting Information), respectively. The measured results distinctly demonstrated that the MoS2 has good photosensitive prosperity and can be used as semiconductor channel material in phototransistor.
Figure 2.

Characteristics of the MoS2 phototransistor. a) I ds–V ds output characteristics at different V gs without illumination. b) I ds–V gs transfer characteristics without illumination (V ds = 1 V). c) I ds–V ds output characteristics at different UV excitation light intensity (λ = 365 nm) (V gs = 0 V). d) Photocurrent as a function of UV excitation light intensity (λ = 365 nm) at different V ds (V gs = 0 V).
2.3. Characteristics of the MoS2 Tribotronic Phototransistor
The characteristics of the MoS2 tribotronic phototransistor are investigated independently, as shown in Figure [qv: 3], by applying different sliding distances. The testing set for the device is shown in Figure 3a. The phototransistor is fastened on a linear motor, which can accurately control the sliding distance of the device. The bottom friction layer is supported by an arclic plate mounted on a fixed bracket and the surface of the FEP keeps closely contact with the aluminum film on the bottom of the device. The defined sliding distance between the bottom friction layer and the device is labeled as d. Figure 3b shows the I ds−V ds characteristics of the MoS2 tribotronic phototransistor at different sliding distances without illumination and external gate voltage. It is observed that the drain‐source current is increased with the increasing of the sliding distances d. The drain–source current for different sliding distances with 200 mW cm−2 excitation intensity and 1 V bias voltage are shown in Figure 3c. In the original state, the device is contacted with the whole bottom friction layer and the sliding distance d is 0 mm. Driven by the programmed linear motor with a fixed frequency, the device moves back and forth to a certain distance from the original position. With the sliding distance from 0 to 8 mm, the change in drain–source current are uniform and stable, and the drain–source current can increase from 1.05 to 3.24 μA, nearly for three times enhancement. It is demonstrated that the changing of the sliding distance can effectively and stably tune the drain‐source current as well as the photocurrent. The photoresponsivity is defined as I ph/P ill, where P ill is the illumination power on the phototransistor. The photoresponsivity of the MoS2 tribotronic phototransistor versus sliding distance d is plotted in the inset of Figure 3c, which is increased from 48.81 to 83.19 A W−1 with sliding distance of 8 mm. The generated positive gate voltage corresponding to the different sliding distance is shown in Figure S4 (Supporting Information). It is distinctly illustrated that the TENG can effectively improve the phototransistor and the photoresponsivity. Compared with the output and transfer characteristics of the MoS2 phototransistor with external gate voltage source in Figure 2a,b, the characteristics of the MoS2 tribotronic phototransistor has been successfully adjusted and enhanced by the sliding electrification, which has the same effect as applying a gate voltage.
Figure 3.

Characteristics of the MoS2 tribotronic phototransistor. a) Optical graph of the testing set for the device. The phototransistor is fastened on a linear motor while the bottom friction layer mounted on a fixed bracket. The sliding distance between the bottom friction layer and the device is labeled as d. b) I ds–V ds output characteristics as a function of d without illumination. c) I ds at different sliding distances with 200 mW cm−2 excitation intensity and 1 V bias voltage. The photoresponsivity versus d is plotted in the inset.
2.4. Tribotronic Enhanced Photoresponsivity of the MoS2 Phototransistor under Different Excitation Intensity
I ds–V ds curves with the different excitation intensity of 10, 100, and 400 mW cm−2 are shown in Figure [qv: 4]a–c at different sliding distances. The I ds–V ds curves are almost linear and show an increase of drain–source current with the increasing of the sliding distance and excitation intensity. To quantificationally study the relationship between the photoresponsivity and excitation intensity at different sliding distances, the plot of photoresponsivity and the excitation intensity with 1 V drain voltage are interpreted in Figure 4d. Under the 0 mm sliding distance and 10 mW cm−2 illumination, the photoresponsivity is 221.03 A W−1 with 1 V drain voltage while increasing to 727.87 A W−1 with the sliding distance of 8 mm, which demonstrates that the sliding distance plays an important role in tuning the photoresponsivity of the MoS2 phototransistor. I ds–V ds curves with the excitation intensity of 50 and 200 mW cm−2, and the plot of photoresponsivity and the excitation intensity with different drain voltages are also shown in Figures S5 and S6 (Supporting Information), respectively, in which the MoS2 tribotronic phototransistor has similar characteristics. It is noted that the photoresponsivity and enhanced value by triboelectrification both decrease with the increasing of the excitation intensity, owing to the saturation of trap states either in the MoS2 or at the interface between the MoS2 and substrate.
Figure 4.

Tribotronic enhanced photoresponsivity of the MoS2 phototransistor under different excitation intensity. a–c) I ds–V ds curves with the different excitation intensity of 10, 100, and 400 mW cm−2, respectively. d) Photoresponsivity relative to excitation intensity at different sliding distances (V ds = 1 V).
2.5. Principle Discussion on the MoS2 Tribotronic Phototransistor
The working principle of the MoS2 tribotronic phototransistor is based on the coupling effects of triboelectrification, electrostatic induction, and field effect, which is schematically shown in Figure [qv: 5]. In the original state of Figure 5a, a drain voltage is applied without illumination on the device. The aluminum friction layer on the back of the device and the whole FEP friction layer fully overlap and intimately contact with each other. Owing to the different triboelectric polarity of the FEP and aluminum, the electrons are injected from the aluminum friction layer into the surface of the FEP, giving rise to the FEP film with negative charges and the aluminum friction layer with equal positive charges in the saturated state. As shown in the energy band diagram, owing to the different work function of the semiconductor and the metal, the equilibrium state forms upon the contact between Au/Cr and MoS2, forming a new quasi‐Fermi level. At this moment, the gate voltage is zero and conduction channel width is not influenced because the negative and positive charges on the surface of the two friction layers are fully balanced. When the FEP friction layer with the negatively charged surface slides with the aluminum friction layer by an external force (Figure 5b), some triboelectric charges lose constraint due to the decrease in the contact surface area, which will generate an electric field parallel to the sliding direction, and induce the electron flow from the aluminum electrode on the bottom of the FEP film to the source electrode. Consequently, an inner electric field voltage across the gate and source electrode is formed and an enhancement zone is formed in the n‐type MoS2 channel, which is similar to applying a positive voltage on the back gate of the MoS2 phototransistor. At the same time, the Femi level of the semiconducting MoS2 will be increased due to the inner gate voltage. The energy bands of the MoS2 will bend downwards and the barrier height between the electrode and the MoS2 will be lowered, giving rise to an increased photogenerated carriers passing through the channel under illumination.4, 5, 6 With the continuing increase of the sliding distance of the bottom FEP friction layer, as shown in Figure 5c, more photogenerated charges can be separated and efficiently passing through the channel, producing a higher photocurrent.
Figure 5.

Working principle of the MoS2 tribotronic phototransistor. a) Initial state of the MoS2 tribotronic phototransistor at a bias voltage without illumination and sliding distance. b–d) The schematic interpretation and corresponding band diagrams of the MoS2 tribotronic phototransistor at different sliding distances with illumination.
Thereafter, when the bottom FEP friction layer slides backward (Figure 5d), the charged surfaces begin to get in contact again and the electrons flow back from the drain electrode to the aluminum electrode on the bottom of the FEP film, resulting in decrease of the induced positive gate voltage and photocurrent. Once the two friction layers overlap again, there will be no separated charges, and the MoS2 phototransistor returns to the original state in Figure 5a. In this entire cycle, it is demonstrated that the inner gate voltage can be created and effectively tune the photocurrent of the MoS2 phototransistor by the sliding distance between the two friction layers, which has the same effect as applying an external gate voltage.
3. Conclusion
In summary, a MoS2 tribotronic phototransistor by coupling of a MoS2 phototransistor and a TENG in sliding mode has been fabricated for the first time, and the tribotronic enhanced optoelectric characteristics are investigated in details. With the horizontally sliding of the two friction layers, the drain–source current is increased from 0.72 to 3.85 μA at a 5 V bias voltage without illumination in place of the traditional gate voltage. Furthermore, the photoresponsivity of the MoS2 phototransistor can be effectively enhanced from 221.03 to 727.87 A W−1 with 1 V drain voltage by the induced inner electrostatic potential of the sliding electrification. By introducing 2D material‐based photoelectronics into the new fields of tribotronics, a novel and effective way has been developed to improve the photoresponsivity of the device for photodetection, which may has important prospects in human–computer interaction, touching optoelectronics and internet of things.
4. Experimental Section
Characterization: The surface morphology of PTFE film was characterized by scanning electron microscope (SEM, FEI‐8020). A common Hg–Xe lamp (LC8‐TLSX1046C03) was used in the experiment. The diameter of beam spot is 10 mm, which illuminates the whole device. The experimental scheme is shown in Figure S7 (Supporting Information).
Supporting information
As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re‐organized for online delivery, but are not copy‐edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors.
Supplementary
Acknowledgements
Y.P. and F.X. contributed equally to this work. The project was supported by National Natural Science Foundation of China (Grant Nos. 51475099, 51432005, and 5151101243), the “thousands talents” program for the pioneer researcher and his innovation team, China, and the Youth Innovation Promotion Association, CAS. The authors also thank Libo Chen and Limin Zhang for the helpful discussions.
Pang Y., Xue F., Wang L., Chen J., Luo J., Jiang T., Zhang C., Wang Z. L. (2016). Tribotronic Enhanced Photoresponsivity of a MoS2 Phototransistor. Adv. Sci., 3: 1500419. doi: 10.1002/advs.201500419
References
- 1. Radisavljevic B., Radenovic A., Brivio J., Giacometti V., Kis A., Nat. Nanotechnol. 2011, 6, 147. [DOI] [PubMed] [Google Scholar]
- 2. Wu W., Wang L., Li Y., Zhang F., Lin L., Niu S., Chenet D., Zhang X., Hao Y., Heinz T. F., Hone J., Wang Z. L., Nature 2014, 514, 470. [DOI] [PubMed] [Google Scholar]
- 3. Zhu H., Wang Y., Xiao J., Liu M., Xiong S., Wong Z. J., Ye Z., Ye Y., Yin X., Zhang X., Nat. Nanotechnol. 2015, 10, 151. [DOI] [PubMed] [Google Scholar]
- 4. Lopez‐Sanchez O., Lembke D., Kayci M., Radenovic A., Kis A., Nat. Nanotechnol. 2013, 8, 497. [DOI] [PubMed] [Google Scholar]
- 5. Yin Z., Li H., Jiang L., Shi Y., Sun Y., Lu G., Zhang Q., Chen X., Zhang H., ACS Nano 2012, 6, 74. [DOI] [PubMed] [Google Scholar]
- 6. Wang X., Wang P., Wang J., Hu W., Zhou X., Guo N., Huang H., Sun S., Shen H., Lin T., Tang M., Liao L., Jiang A., Sun J., Meng X., Chen X., Lu W., Chu J., Adv. Mater. 2015, 27, 6575. [DOI] [PubMed] [Google Scholar]
- 7. Liu H., Guo H., Yang T., Zhang Z., Kumamoto Y., Shen C. C., Hsu Y. T., Li L. J., Saito R., Kawata S., Phys. Chem. Chem. Phys. 2015, 17, 14561. [DOI] [PubMed] [Google Scholar]
- 8. Splendiani A., Sun L., Zhang Y., Li T., Kim J., Chim C. Y., Galli G., Wang F., Nano Lett. 2010, 10, 1271. [DOI] [PubMed] [Google Scholar]
- 9. Nguyen E. P., Carey B. J., Daeneke T., Ou J. Z., Latham K., Zhuiykov S., Kalantar‐zadeh K., Chem. Mater. 2015, 27, 53. [Google Scholar]
- 10. Han S. W., Kwon H., Kim S. K., Ryu S., Yun W. S., Kim D. H., Hwang J. H., Kang J. S., Baik J., Shin H. J., Hong S. C., Phys. Rev. B 2011, 84, 045409. [Google Scholar]
- 11. Ganatra R., Zhang Q., ACS Nano 2014, 8, 4074. [DOI] [PubMed] [Google Scholar]
- 12. Liu H., Neal A. T., Ye P. D., ACS Nano 2012, 6, 8563. [DOI] [PubMed] [Google Scholar]
- 13. Wu S., Zeng Z., He Q., Wang Z., Wang S. J., Du Y., Yin Z., Sun X., Chen W., Zhang H., Small 2012, 8, 2264. [DOI] [PubMed] [Google Scholar]
- 14. Li H., Yin Z., He Q., Li H., Huang X., Lu G., Fam D. W., Tok A. I., Zhang Q., Zhang H., Small 2012, 8, 63. [DOI] [PubMed] [Google Scholar]
- 15. Radisavljevic B., Whitwick M. B., Kis A., Appl. Phys. Lett. 2012, 101, 043103. [Google Scholar]
- 16. Radisavljevic B., Whitwick M. B., Kis A., ACS Nano 2011, 5, 9934. [DOI] [PubMed] [Google Scholar]
- 17. Fan F. R., Tian Z. Q., Wang Z. L., Nano Energy 2012, 1, 328. [Google Scholar]
- 18. Zhang C., Zhou T., Tang W., Han C. B., Zhang L. M., Wang Z. L., Adv. Energy Mater. 2014, 4, 1301798. [Google Scholar]
- 19. Zhou T., Zhang C., Han C. B., Fan F. R., Tang W., Wang Z. L., ACS Appl. Mater. Interfaces 2014, 6, 14695. [DOI] [PubMed] [Google Scholar]
- 20. Zhang C., Tang W., Han C. B., Fan F. R., Wang Z. L., Adv. Mater. 2014, 26, 3580. [DOI] [PubMed] [Google Scholar]
- 21. Wang Z. L., ACS Nano 2013, 7, 9533. [DOI] [PubMed] [Google Scholar]
- 22. Han C. B., Du W. M., Zhang C., Tang W., Zhang L. M., Wang Z. L., Nano Energy 2014, 6, 59. [Google Scholar]
- 23. Tang W., Han C. B., Zhang C., Wang Z. L., Nano Energy 2014, 9, 121. [Google Scholar]
- 24. Jiang T., Zhang L. M., Chen X. Y., Han C. B., Tang W., Zhang C., Xu L., Wang Z. L., ACS Nano 2015. 9, 12562. [DOI] [PubMed] [Google Scholar]
- 25. Chen J., Yang J., Li Z. L., Fan X., Zi Y. L., Jing Q. S., Guo H. Y., Wen Z., Pradel K. C., Niu S. M., Wang Z. L., ACS Nano 2015, 9, 3324. [DOI] [PubMed] [Google Scholar]
- 26. Pang Y. K., Li X. H., Chen M. X., Han C. B., Zhang C., Wang Z. L., ACS Appl. Mater. Interfaces 2015, 7, 19076. [DOI] [PubMed] [Google Scholar]
- 27. Zhang L. M., Xue F., Du W. M., Han C. B., Zhang C., Wang Z. L., Nano Res. 2014, 7, 1215. [Google Scholar]
- 28. Han C. B., Zhang C., Li X. H., Zhang L. M., Zhou T., Hu W., Wang Z. L., Nano Energy 2014, 9, 325. [Google Scholar]
- 29. Luo J. J., Fan F. R., Zhou T., Tang W., Xue F., Wang Z. L., Extreme Mech. Lett. 2015, 2, 28. [Google Scholar]
- 30. Zhang C., Tang W., Pang Y. K., Han C. B., Wang Z. L., Adv. Mater. 2015, 27, 719. [DOI] [PubMed] [Google Scholar]
- 31. Han C. B., Zhang C., Tian J. J., Li X. H., Zhang L. M., Li Z., Wang Z. L., Nano Res. 2015, 8, 219. [Google Scholar]
- 32. Zhang C., Tang W., Zhang L. M., Han C. B., Wang Z. L., ACS Nano 2014, 8, 8702. [DOI] [PubMed] [Google Scholar]
- 33. Zhang C., Zhang, Zhang L. M., Han C. B., Wang Z. L., Adv. Mater. 2015, 27, 3533. [DOI] [PubMed] [Google Scholar]
- 34. Zhang C., Li J., Han C. B., Zhang L. M., Chen X. Y., Wang L. D., Dong G. F., Wang Z. L., Adv. Funct. Mater. 2015, 25, 5625. [Google Scholar]
- 35. Li J., Zhang C., Duan L., Zhang L. M., Wang L. D., Dong G. F., Wang Z. L., Adv. Mater. 2016, 28,106 . [DOI] [PubMed] [Google Scholar]
- 36. Zhang C., Zhang Z. H., Yang X., Zhou T., Han C. B., Wang Z. L.,Adv. Funct. Mater. 2015, DOI:10.1002/adfm.201504919. [Google Scholar]
- 37. Xue F., Chen L. B., Wang L. F., Pang Y. P., Chen J., Zhang C., Wang Z. L., Adv. Funct. Mater. 2015, DOI:10.1002/adfm.201504485. [Google Scholar]
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