An organic/inorganic light-emitting diode (LED) consisting of n-type vertically aligned ZnO nanowires (NWs) and p-type proton acid doped polyaniline (PANi) is reported. The device was fabricated on flexible indium-tin-oxide (ITO) coated polyethylene terephthalate (PET) substrate. A broad blue light emission band ranging from 390 nm to 450 nm was observed in the electroluminescence (EL) spectra of the device, which was related to the interface recombination of electrons in the conduction band of ZnO NWs and holes in the polaron level of PANi. The turn-on voltage of the device is ~3.5 V, lower than most of ZnO NWs based LED devices. In combination with the easy fabrication, flexibility, low power consumption, and mechanical robustness, this novel device is very promising in the application of blue LEDs.

1. Introduction

ZnO, especially in its nanostructured form, has been considered to be attractive for applications in ultraviolet (UV) lasers [1], LEDs [24], and solar cells [5] because of the wide band gap and high exciton binding energy. However, it remains critical and challenging to fabricate high quality ZnO with stable p-type conductivity because of the intrinsically n-type nature. The difficulty in doping ZnO to p-type polarity has led the researchers to seek to create heterojunctions with other p-type semiconductors to enable the use of ZnO in all kinds of electronic devices. Many efforts have been made to grow n-type ZnO on p-type substrates, but usually the quality of such heterojunctions is limited by the lattice mismatch. P-type conducting polymer has many advantages including easy fabrication, flexibility, and tunable carrier densities. Various LEDs based on ZnO NWs/p-type polymer heterostructures have been reported in the literature [3, 4]; however, blue LED is still quite limited [6].

In this work, a blue LED device consisting of vertically aligned ZnO NWs and p-type conducting PANi heterojunction was fabricated. PANi was selected as the hole conducting layer because of its facile synthetic process, good environmental stability, easy conductivity control, and cheap production in large quantities. The structure of the LED device was schematically illustrated in Figure 1. Vertically aligned ZnO NWs are used as the light emission units, and proton doped PANi is used as the hole-transporting layer. Au film serves as the top electrode, and ITO is the bottom electrode. The function of polymethyl methacrylate (PMMA) is to form a smooth surface for PANi coating. A broad blue light emission band ranging from 390 nm to 450 nm was observed from the EL spectra of the ZnO NWs/PANi heterojunction LED. The origins of the blue emission were also discussed in this paper.

2. Experimental

For the LED device fabrication, ZnO NW arrays were grown on ITO coated PET substrate using a low temperature hydrothermal method. Equimolar (0.05 M) of hydrated zinc nitrate (Zn(NO3)2A · 6H2O) and hexamethylenetetramine (HMT) was used as the precursor. The reaction was carried out at 90°C for 6 hours. After growth the as-grown NW forest was infiltrated with 5% (weight percent) PMMA solution (in toluene) to provide a smooth film for subsequent PANi coating. Then oxygen plasma etching was applied to remove excessive PMMA and expose the NW tips for junction formation with PANi. HCl doped PANi dissolved in dimethylformamide (DMF) was spin coated on top of ZnO NW tips. The device was then baked at 60°C for 10 hours to completely remove the organic solvents. Finally Au top electrode with the thickness of 150 nm was deposited using e-beam evaporation with the deposition rate of 0.1 nm/s.

The morphologies and microstructures of the as-synthesized ZnO NW arrays were examined using scanning electron microscope (SEM, FEI Quanta FEG), transmission electron microscope (TEM, FEI G30), and X-ray diffraction pattern (XRD, Bruker D8 Advance). Electrical properties of the devices were examined using semiconducting characterization system (SCS, Keithley 4200) equipped with a probe station (Cascade M 150). The photoluminescence (PL) and EL spectra were detected using a FS 920 type spectrometer (Edinburgh).

3. Results and Discussions

From the SEM image of the as-grown ZnO NW arrays (Figure 2(a)), it can be seen that ZnO NWs are uniformly distributed on the PET substrate and primarily vertically aligned. The diameter of ZnO NWs ranges from 80 nm to 130 nm, and the average height is around 3 μm. The TEM image of a randomly picked individual NW is shown in Figure 2(b). Clearly, the NW has uniform diameter of 110 nm throughout the entire length. The selected area diffraction pattern shown in the inset of Figure 2(b) demonstrates that the NWs are single crystalline with preferred growth direction. Strong (0002) diffraction peak centered at 34.4° can be observed from XRD pattern of the NW arrays (Figure 2(c)), suggesting that the NWs are highly ordered along -axis with the lattice spacing of 0.52 nm. No other impurity peaks or ITO related peaks are observed. The PL spectra of the as-grown ZnO NW arrays are presented in Figure 2(d). The strong ultraviolet emission peak centered at 383 nm is the intrinsic luminesce of ZnO NWs. The defect related visible emission at around 500 nm is much weaker than the UV peak, indicating that ZnO NWs are of high degree of crystalline quality with few defects.

Figure 3(a) shows the top-view SEM image of the surface of the device after PANi deposition. The bright spots represent the tips of ZnO NWs, and the dark area is the space between NWs solidly filled with PMMA. Obviously the NWs are well separated, demonstrating that no agglomerations occurred during the polymer infiltration process. The density of the NW tips can be estimated to be 14 NW/μm2. Figure 3(b) shows the current-voltage (IV) characteristics of the ZnO NWs/PANi heterostructure LED device. The IV curve clearly shows nonlinear increase of the current under the forward bias, which indicates the formation of p-n junction between ZnO NWs and PANi. The turn-on voltage of the device is around 1.3 V, as shown in Figure 3(b).

The EL spectra of the ZnO NWs/PANi heterojunction LED device were measured under different forward biasing voltages (2 V, 3.5 V, 5 V, and 6.5 V). As is shown in Figure 4(a), the light emission is too low to be detected when the forward bias is below 2 V. However when the bias voltage is larger than 3.5 V, a broad blue light emission band spreading through 390 nm to 450 nm can be observed. Obviously, this band is neither related with the near band edge nor to the deep level emission of ZnO NWs. Blue LEDs based on ZnO NWs/p-GaN [2] and ZnO NWs/PFO [7] heterojunctions have been reported before; however, the emission is often dominated by the p-type conducting layer instead of ZnO NWs. To understand the origins of the blue light emission of ZnO NWs/PANi device, the energy band diagrams of all the layers were schematically illustrated in Figure 4(b). Doping caused a self-localized polaron band in PANi, existing as a defect band in the bandgap (3.4 eV) between the valence band and the conduction band. It is half-filled and has a significant band width (~1.1 eV) [810]. When a forward bias is applied, electrons in the conduction band of the ZnO NWs will be driven to move towards the PANi. Also the holes in the polaron band of PANi will move towards ZnO because of the relatively low energy barrier. The electrons and holes recombine at the interface of the p-n junction and produce a photon. The emission wavelength in the EL spectra must be corresponding with the bandgap between the conduction band of ZnO and the polaron band of PANi, although the exact position of the polaron band was not found in the literaturs.

Several other features can also be found from the EL spectra. First, the turn-on voltage of ZnO NWs/PANi heterostructure is substantially lower compared with other ZnO NWs based LED devices. For example, the turn-on voltage is 10 V for ZnO NWs/p-type GaN film hybrid junction [2] and 6 V for ZnO NWs/p-Si junction [11]. The small turn-on voltage can be attributed to the low carrier injection barriers (Figure 4(b)). Second, the blue emission peak is increasingly broadened, and the intensity is enhanced with the increase of the bias voltage. The broad blue light-emitting range suggests that the emission behavior is complicated and must be related to the polaron energy band of PANi. With the increase of the forward biasing voltage, more electrons in the conduction band of ZnO are driven to move towards the PANi, and more holes in the valence band of PANi will move towards ZnO. Thus, a larger number of protons can be produced by the recombination of the carriers. Also, peak splitting in the blue region can be observed, which is not well understood. However, it is possible to be caused by the diffraction when the light transmits through hexagonal ZnO NWs. Third, the defect related visible light emission band is broadened, and the peak center is red shifted compared with that in the PL spectra. This may be caused by the redistribution of the deep level defects in the ZnO NWs during the device fabrication process.

4. Conclusions

In this paper, an inorganic/organic heterostructure LED device based on vertically aligned ZnO NW arrays and PANi conducting polymer was reported. A blue light emission peak at around 400 nm as well as a broad defect related emission was observed in the EL spectra of the device. The turn-on voltage of the LED device is around 3 V, favoring the low power consumption of the LED device. Also the NWs/PANi composite appears sufficiently robust to absorb large mechanical strain, which is also a fundamental issue in the practical use of organic/inorganic LEDs. Overall, this study demonstrates the possibility of using ZnO NWs/PANi heterojunction for blue light emission. We believe that the performance of such LED can be further improved through adjusting the thickness, carrier densities, and metal contact of the PANi layers.


The authors acknowledge the financial support of the NSFC (51072119), Innovation Program of Shanghai Municipal Education Commission (12ZZ139), and the Key Project of Chinese Ministry of Education (12057).