Hybrid Field-Effect Transistors and Photodetectors Based on Organic Semiconductor and CsPbI₃ Perovskite Nanorods Bilayer Structure

Abstract

The outstanding performances of nanostructured all-inorganic CsPbX₃ (X = I, Br, Cl) perovskites in optoelectronic applications can be attributed to their unique combination of a suitable bandgap, high absorption coefficient, and long carrier lifetime, which are desirable for photodetectors. However, the photosensing performances of the CsPbI₃ nanomaterials are limited by their low charge-transport efficiency. In this study, a phototransistor with a bilayer structure of an organic semiconductor layer of 2,7-dioctyl [1] benzothieno[3,2-b] [1] benzothiophene and CsPbI₃ nanorod layer was fabricated. The high-quality CsPbI₃ nanorod layer obtained using a simple dip-coating method provided decent transistor performance of the hybrid transistor device. The perovskite layer efficiently absorbs light, while the organic semiconductor layer acts as a transport channel for injected photogenerated carriers and provides gate modulation. The hybrid phototransistor exhibits high performance owing to the synergistic function of the photogating effect and field effect in the transistor, with a photoresponsivity as high as 4300 A W⁻¹, ultra-high photosensitivity of 2.2 × 10⁶, and excellent stability over 1 month. This study provides a strategy to combine the advantages of perovskite nanorods and organic semiconductors in fabrication of high-performance photodetectors.

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Highlights

• A high-performance phototransistor with an organic semiconductor and CsPbI₃ perovskite nanorod hybrid structure was fabricated and characterized.

• The perovskite layer efficiently absorbs the input illumination, while the organic semiconductor layer acts as a transport channel for injected photogenerated carriers and provides gate tuning.

• The hybrid phototransistor exhibits high performance with a photoresponsivity as high as 4300 A W⁻¹, ultra-high photosensitivity of 2.2 × 10⁶, and long-term stability of 1 month.

Introduction

Recently, organometal halide perovskites have attracted a significant interest in the field of optoelectronics owing to their desirable electronic and optoelectronic properties, such as strong and broad light absorption, weakly bound excitons, long-range-balanced electron/hole transport lengths, and low-cost fabrication [1, 2]. These characteristics make them widely use in solar cells [3, 4], light-emitting diodes (LEDs) [5, 6], lasing [7], and photodetectors [8–10]. However, these perovskite materials usually have a low long-term stability owing to the environmental degradation of organic cations within the materials from moisture and heat [11, 12]. In contrast, all-inorganic CsPbX₃ (X = I, Br, Cl) perovskites exhibit decent stabilities; among them, the CsPbI₃ perovskite exhibited unique properties with a suitable bandgap, high quantum efficiency, and long radiative lifetime [13, 14]. However, this material has two phases: cubic phase and orthorhombic phase. The black cubic phase is stable above 300 °C; it quickly undergoes phase transformation into the wider-bandgap (3.01 eV) orthorhombic phase upon cooling to room temperature. This phase transformation largely limited its applications. In order to overcome this problem, low-dimensional CsPbI₃ perovskites, including quantum dots, nanowires, nanorods, and nanoplates, have been prepared. Owing to both surface and nanoeffects, as the size of the perovskite material is reduced to the nanoscale, the phase stability can significantly differ from that in the bulk counterpart [15–18].

Owing to the outstanding characteristics including few grain boundaries, large specific surface area, low charge carrier rate, long charge carrier lifetime, and high surface-to-volume ratio, one-dimensional (1D) CsPbI₃ nanorods are promising materials for photodetector devices [19–23]. For example, Yang et al. [22] reported superior photodetectors based on a single CsPbI₃ nanorod with an ultra-fast response and high stability. Tang et al. [23] demonstrated a simple method for the synthesis of CsPb(Br/I)₃ nanorods; the photosensitivity of the nanorod-based photodetectors could reach up to 10³. Owing to the charge-transport limitation in the perovskite layers, the CsPbI₃ nanorod-based photodetectors exhibited a relatively low photoresponsivity (R) [24].

Organic semiconductors (OSCs) are promising materials with large potentials in next-generation flexible electronic and photoelectronic devices owing to their attractive advantages of easily tunable bandgap, simple synthesis, low cost, and resolvability [25–31]. 2,7-Dioctyl [1] benzothieno[3,2-b] [1] benzothiophene (C8BTBT) is an excellent OSC material, which does not respond to visible light, and has a good air stability and high hole-carrier mobility [32–34]. In this study, C8BTBT/CsPbI₃ nanorod bilayer films were produced and used to fabricate high-performance phototransistors. The gate-tunable hybrid transistor devices illuminated by white light exhibited an outstanding photosensing performance with an R as high as 4.3 × 10³ A W⁻¹ and ultra-high I_photo/I_dark ratio of 2.2 × 10⁶. Furthermore, the hybrid phototransistors possessed an excellent long-term stability when stored under ambient conditions for more than 1 month. Therefore, this study reveals a simple approach to fabricate hybrid phototransistors with comprehensive advantages including a simple fabrication, enhanced photosensitivity, and high stability.

Experimental Methods

Chemicals

C8BTBT (98%, Suna Tech Inc), Cs₂CO₃ (99.9%, Adamas), lead iodide (PbI₂, 99.99%, Sigma-Aldrich), 1-octadecene (ODE, 90%, Energy Chemical), oleylamine (OA, 90%, Energy Chemical), oleylamine (OAm, 70%, Energy Chemical), and octane (99.9%, Sigma-Aldrich) were used without further purification.

Preparation of CsPbI₃ Nanorod

CsPbI₃ nanorods were synthesized using the ligand-assisted method [23, 35]. Cs₂CO₃ (0.40 g, 1.23 mmol) was added to a 50-mL round-bottom flask along with OA (1.5 mL) and ODE (25 mL) and stirred under vacuum for 1 h at 120 °C. The flask was filled with Ar. Subsequently, all Cs₂CO₃ reacted with the OA when the solution was clear. PbI₂ (1.00 g, 2.17 mmol) and ODE (50 mL) were loaded into a 150-mL round-bottom flask and dried under vacuum at 120 °C for 1 h. Ar was then flowed into the flask. OA and OAm (5 mL each) were injected at 120 °C. The PbI₂ completely dissolved, leading to the formation of a clear solution. The Cs-oleate solution (~ 0.046 M, 5.9 mL), prepared as described above, was injected and the reaction mixture was quenched by immersion of the flask into an ice bath after a 5-min reaction. The crude nanorod solution was added into 200 mL methyl acetate and centrifuged at 8000 rpm for 5 min. The precipitates were dispersed in 6 mL hexane and 20 mL methyl acetate and then centrifuged at 8000 rpm for 2 min. The nanorods were dispersed in 10 mL of hexane and centrifuged again at 4000 rpm for 5 min. Finally, the as-prepared nanorods were dispersed in octane for further use.

Device Fabrication

Heavily n-doped Si wafers with a thermally grown 300-nm-thick SiO₂ layer were used as substrates. Before device fabrication, the substrates were cleaned using ultra-sonication consecutively with acetone, isopropanol, and deionized water for 30 min and finally dried by N₂. The pre-cleaned substrates were immersed into a CsPbI₃ nanorod solution (~ 20 mg mL⁻¹ in octane) and pulled out at an optimized speed of 5 μm s⁻¹ (SYDC-100H DIP COATER). The samples were then placed under vacuum for 2 h. A 30-nm-thick C8BTBT film was then deposited by vacuum evaporation, and 50-nm-thick Au source/drain electrodes on top of the hybrid films were thermally evaporated by shadow masks with a channel length of 5 μm and channel width of 1 mm. For the pure-CsPbI₃-nanorod-based photodetectors, the nanorod solution was drop-cast directly on Si/SiO₂ substrates with pre-patterned gold electrodes, followed by drying under vacuum for 1 h.

Characterizations and Measurements

The surface morphologies of the CsPbI₃ nanorod films were investigated by an atomic force microscope (AFM, SEIKO SPA-300HV) operated in the tapping mode. Ultraviolet–visible (UV–Vis) absorption spectra of thin films on quartz substrates were acquired using a Cary 60 UV–Vis spectrometer (Agilent Technologies). Powder X-ray diffraction (XRD) was performed using a DX-2700 X-ray diffractometer (Dandong Haoyunan Instrument Co. Ltd) with Cu K_α radiation (1.54 Å) at 40 kV and 50 mA. Transmission electron microscopy (TEM) and high-resolution TEM (HRTEM) images were recorded with a JEOL JEM-2100F TEM operated at 200 kV. The performances of the photodetectors were studied using a Keithley 4200 SCS. Monochromatic lights with different wavelengths were provided by a 300-W xenon lamp filtered with a double-grating monochromator (Omno 330150, Beijing NBeT, China). All of the measurements were taken in air at room temperature.

Results and Discussion

Figure 1a shows a TEM image of the as-synthesized CsPbI₃ nanorods, indicating that the perovskites have a highly pure morphology with uniformly distributed diameters and lengths, with average values of ~ 10 and ~ 100 nm, respectively. The HRTEM image of the nanorods (Fig. 1b) shows an interplanar distance of 0.62 nm, which is consistent with the (100) plane of the cubic-phase CsPbI₃ perovskite [36]. As shown in Fig. 1c, the structure of the CsPbI₃ nanorods was studied using XRD, further confirming the cubic phase [37]. In this study, CsPbI₃ nanorod thin films were fabricated by a one-step dip-coating method. An AFM analysis showed that the surface roughness R_a was approximately 0.87 nm (Fig. 1d). The film was sufficiently thin for a well alignment of the OSC molecules deposited on it, which provides the decent transistor performance of the hybrid device [38, 39]. A layer of C8BTBT was then evaporated on the CsPbI₃ nanorod layer. The surface roughness of the CsPbI₃ nanorod layer was essential for a high device performance.

Fig. 1.

a TEM image, b HRTEM image, and c XRD patterns of CsPbI₃ nanorods. d AFM image of the CsPbI₃ nanorod film. The inset image presents a height profile of the film surface. e UV–Vis absorption spectra of CsPbI₃ nanorods, C8BTBT, and C8BTBT/CsPbI₃ nanorod films. f Energy level diagrams of C8BTBT and CsPbI₃ nanorods

An additional benefit of the use of C8BTBT as the OSC is that C8BTBT does not strongly adsorb visible light and hence has no responsivity to visible light, while the CsPbI₃ nanorods have a broad absorption in both UV and visible regions. When the device was illuminated by visible light, only the CsPbI₃ nanorods could act as the light adsorption materials, while C8BTBT acted only as a charge-transport material. It is beneficial to understand the underlying sensing mechanism of our devices. Figure 1e shows the UV–Vis absorbance spectra of a CsPbI₃ nanorod film, C8BTBT film, and C8BTBT/CsPbI₃ nanorod hybrid film. Although there was an intense absorption peak observed around 365 nm, the pure C8BTBT film did not exhibit an obvious absorption in the range of 400–800 nm. In contrast, the CsPbI₃ nanorod film exhibited a strong and broad absorption in both UV and visible regions. The spectrum of the hybrid film included the absorptions of the C8BTBT and CsPbI₃ nanorod films; the superimposed effect of the hybrid film obviously enhanced its light-absorption range.

A schematic band diagram of the CsPbI₃ nanorods and C8BTBT is shown in Fig. 1f. The values of the conduction band (CB) and valence band (VB) of perovskite are at − 3.45 and − 5.44 eV, respectively [40]. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels of C8BTBT are − 5.39 and − 1.55 eV, respectively [41]. Therefore, the CsPbI₃ perovskite and C8BTBT form a type-II heterojunction [42]. The VB of CsPbI₃ aligns well with the HOMO of C8BTBT, facilitating the injection of photogenerated holes from the perovskite into the OSC. Furthermore, the high LUMO energy level of C8BTBT effectively blocks electrons and prevents them diffusing into the OSC layer, thus efficiently reducing the photogenerated charge recombination.

The schematic diagram of the C8BTBT/CsPbI₃ nanorod-based phototransistor is illustrated in Fig. 2a. Heavily n-doped silicon wafers coated with a 300-nm-thick SiO₂ surface layer (capacitance: 10 nF cm⁻²) were used as the substrates and gate electrodes. The CsPbI₃ perovskites were employed as the light absorber, while the OSC was used to facilitate the separation and transport of photogenerated electron–hole pairs. Au source/drain electrodes (50 nm) were thermally evaporated through shadow masks with a channel length of 5 μm and channel width of 1 mm. A power-tunable white LED with a wavelength range of 400–800 nm was used as the illumination source. As the photon energy (1.55–3.10 eV) was smaller than the bandgap of C8BTBT (3.84 eV), the OSC layer exhibited a limited photosensitive performance to the white light (Fig. S1). As shown in Fig. S2, the spectral response of the external quantum efficiency (EQE = Rhc/λe), where hc/λ is the photon energy, closely follows the absorption spectrum of the C8BTBT/CsPbI₃ nanorod hybrid film. The output curves of the hybrid phototransistors were obtained in a dark state and under illumination of 10 mW cm⁻², as shown in Fig. 2b, c, respectively. The devices exhibited p-type transistor I_D–V_D characteristics in the dark state and under illumination, displaying both linear and saturation regions. The cut-off V_G of the device was − 40 V in the dark state. At the same applied voltage, the illumination increased the drain current and modulated the cut-off voltage of the device.

Fig. 2.

a Schematic diagram of the C8BTBT/CsPbI₃ nanorod-based phototransistor. I_D–V_D transistor characteristics of the hybrid phototransistor under a fixed illumination power intensity: b in the dark state and c under a white-light illumination of 10 mW cm⁻². d Transfer characteristics (V_D = −30 V) under different illumination power densities. e Photocurrent as a function of the illumination power density for different gate voltages

Figure 2d shows the transfer curves (I_D–V_G) of the hybrid phototransistors with a gate voltage sweeping from − 60 to 20 V and fixed drain voltage of − 30 V under illuminations of 0.05, 0.5, 1.5, 5, and 10 mW cm⁻² and in the dark state, suggesting a typical p-type semiconductor behavior. The photocurrent (I_photo= I_light − I_dark) significantly enhanced with the increase in the illumination power density (Fig. 2e). The results show that a larger applied gate voltage leads to a larger increase in the photocurrent for the p-type phototransistors. Therefore, the photosensitive performances of the devices can be modulated by applying different gate voltages. Devices based on pure CsPbI₃ nanorods were also fabricated by drop casting directly on Si/SiO₂ substrates with pre-patterned gold electrodes; the I–V curves of the devices in the dark state and under an illumination of 5 mW cm⁻² are shown in Fig. S3. The hybrid phototransistors exhibited not only a higher photocurrent, but also a significantly larger photocurrent to dark current ratio than those of the pure CsPbI₃ nanorod devices, although the pure CsPbI₃ nanorod devices exhibited a relatively high response speed [43].

With the increase in the light power density, the threshold voltage positively shifted. The ΔV_th is plotted as a function of the incident illumination power density in Fig. 3a. It can be fitted with ΔV_th = αP^β, yielding β ≈ 0.24, where β is the power factor. The well-fitted line indicates that the shift of the threshold voltage was attributed to the photogating effect [44]. When the illumination power density increased, the ΔV_th tended to saturate, indicating that the photogenerated carriers in the light-absorber layer almost reached their maximum density. The μ of the device can be calculated from the saturation region of the transfer curve (Eq. 1) [45],

$$\mu =\frac{2L}{W{C}_i}{\left(\frac{\partial \sqrt{I_D}}{\partial V_G}\right)}^2$$ 1

Figure S4 shows the illumination power density dependence of the normalized mobility. The μ slightly changed with the increase in the illumination power density; the field-effect mobility of the hybrid phototransistors can be regarded as a constant. Therefore, the enhancement in the photocurrent is attributed to the positively shifted threshold voltage rather than to change in the field-effect mobility. As shown in Fig. 3b, electron–hole pairs are generated only in the CsPbI₃ nanorod layer when white light is incident on the device and dissociated into electrons and holes near the junction between the CsPbI₃ nanorod and C8BTBT layers. The photogenerated holes in the perovskite layer can easily transfer to the C8BTBT layer, while the photoexcited electrons accumulated in the perovskite layer. When the hybrid devices are in the on-state, the photovoltaic effect is dominant as photo-voltage is induced by the large number of accumulated electrons under the source, and the illumination leads to a photoinduced positive shift of the threshold voltage, leading to a significant increase in the photocurrent. When the hybrid devices are in the off-state, the channel current exhibits a relatively small increase with the optical power owing to a photoconductive effect (Fig. S5) [46, 47].

Fig. 3.

a Shift of the threshold voltage of the hybrid phototransistor as a function of the illumination power density. b Schematic of the photo-generated carrier transport in the hybrid phototransistor under illumination

One of the important criteria of efficacy for phototransistors is the responsivity R, which can be expressed as Eq. 2:

$$R=\frac{I_{\text{photo}}}{\mathit{PS}}$$ 2

where P is the incident illumination power density on the channel of the device, and S is the working area of the device. The values of R reveal to what extent the optical power is converted into photocurrent. The gate voltage dependences of the R for the devices illuminated with various light intensities are plotted in Fig. 4a, indicating that the R increased with the negative shift of the gate voltage when the devices were in the on-state. Figure 4b shows the illumination power density dependence of the R; the R decreased linearly with the incident power density (r² = 0.99). An R as high as 4300 A W⁻¹ can be obtained at V_G = −60 V, V_D = −30 V, as shown in Fig. 4b, which is comparable to the performances of the best perovskite-based photodetectors [22].

Fig. 4.

a Responsivity of the hybrid phototransistor as a function of the gate voltage for different illumination power densities. b Illumination power density dependence of the responsivity at V_G = −60 V, V_D = −30 V. c I_photo/I_dark ratio as a function of the gate voltage for different illumination power densities. d Illumination-power-density dependence of the I_photo/I_dark ratio at V_G = −60 V, V_D = −30 V. e Photoswitching characteristics of the hybrid phototransistor under an alternating dark and light illumination (0.5 mW cm⁻²) at V_G = −30 V, V_D = −30 V. f Transfer curves of the fresh hybrid phototransistor and device stored at an atmospheric environment (average temperature of 0 °C and average relative humidity of 50%) for 1 month

Another important parameter to evaluate the performance of the phototransistor is the photocurrent to dark current ratio (I_photo/I_dark). Figure 4c shows the I_photo/I_dark ratio as a function of the gate voltage of the hybrid devices under various illumination intensities. When the devices were in the off-state under a sub-threshold voltage, the I_photo/I_dark ratio increased with the increase in gate voltage, owing to the increased photocurrent with a contribution from the positively shifted threshold voltage. When the phototransistors were turned on by applying more negative gate voltages, a significant decrease in the I_photo/I_dark ratio could be observed; the ratio disparities of the devices, caused by the different illumination intensities, rapidly diminished, as the electrical contribution to the charge carrier generation was dominant after the threshold was reached [48, 49]. The maximum I_photo/I_dark ratio significantly increased with the incident illumination power increased; it could reach a value as high as 2.2 × 10⁶ under a gate voltage around − 30 V when the power density of the white light was 10 mW cm⁻², as shown in Fig. 4d, which is among the highest values of previously reported perovskite-based photodetectors. The temporal photoresponses of the C8BTBT/CsPbI₃ nanorod phototransistors were measured under an illumination of 0.5 mW cm⁻² at V_G = −30 V, V_D = −30 V. Figure 4e shows the pulsed laser illumination (top) and temporal response of the photocurrent (bottom). The hybrid devices exhibited a good on–off switching. As shown in Fig. S6, an abrupt increase in the drain current can be observed when the hybrid devices were exposed to white light; the I_photo/I_dark ratio was close to that in Fig. 4e. Owing to the high-level electron trapping capability in the CsPbI₃ nanorod layer and at the C8BTBT/CsPbI₃ nanorod interface, the trapped electrons remain in the thin film for a very long time with a low recombination rate and it is hard to reset the devices in a short time after removal of the incident light, keeping the devices in a metastable state with a high conductivity, leading to a decrease in the large drain current with a long relaxation time. The time responses of the photocurrent increase and decay were dominated by two components, which can be fitted with a double-exponential function (Eqs. 3 and 4) [44]:

$$\mathrm{\Delta }{I}_D=\mathrm{\Delta }{I}_{1}exp(1-t/{\tau }_1)+\mathrm{\Delta }{I}_{2}exp(1-t/{\tau }_2)$$ 3

$$\mathrm{\Delta }{I}_D=\mathrm{\Delta }{I}_3(-exp(-t/{\tau }_3))+\mathrm{\Delta }{I}_4(-exp(-t/{\tau }_4))$$ 4

where ΔI is the change in the channel current and τ is the time constant (Fig. S7). The small relaxation times τ₁ (0.63) and τ₃ (0.54) correspond to the lifetime of holes in the CsPbI₃ nanorod layer before they transferred to the C8BTBT layer, whereas the large relaxation times τ₂ (4.24) and τ₄ (9.62) represent the charge transfer between CsPbI₃ nanorods [50].

The long-term stabilities of the hybrid phototransistors were also studied. As shown in Fig. 4f, the transfer curves of the hybrid phototransistors after they were stored in an atmospheric environment (average temperature of 20 °C and average relative humidity of 50%) for 1 month were almost perfectly overlapped with those of the fresh samples, indicating their excellent stabilities with respect to oxygen and moisture. Furthermore, Table S1 presents key parameters of the hybrid devices, compared with those of recently reported low-dimensional all-inorganic perovskite-based photodetectors; the photosensitivity, responsivity, and stability values of our devices are among the highest reported values. The excellent stabilities of the devices can be mainly attributed to the following factors. First, C8BTBT is an excellent OSC material possessing a good air stability. Second, 1D all-inorganic perovskites with a better crystallization tend to have higher stabilities than those of the organic–inorganic hybrid counterparts. Third, the OSC layer fabricated in the upper part of the hybrid layers protects the perovskite layer from atmospheric moisture.

Conclusion

We demonstrated high-performance phototransistors based on the C8BTBT/CsPbI₃ nanorod hybrid layers with high photosensitive performances and long-term stabilities in ambient conditions. The high-quality perovskite films were necessary to provide the desirable device performance. The perovskite layer could efficiently absorb the input illumination and generate a large amount of charge carriers, while a transport channel for the injection of photogenerated carriers and gate-tuning property was provided by the OSC layer. Owing to the photogating effect, the gate-tunable hybrid devices illuminated by white light exhibited outstanding photosensitivity performances with an R as high as 4300 A W⁻¹ and ultra-high I_photo/I_dark ratio of 2.2 × 10⁶, significantly higher than those of most of the previously reported perovskite-based photodetectors. Furthermore, the hybrid phototransistors possessed long-term stabilities owing to the high stabilities of the two materials and device structure under ambient conditions. Therefore, this study provides a strategy to combine the advantages of perovskite semiconductors and OSCs to obtain high-performance photodetectors.

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