A one-dimensional (1D) nanorod (NR) may be regarded as an ideal single crystal with superior photoelectric performance. Merging NRs into light-emitting diodes (LEDs) can effectively improve device performance , , , . ZnO is a third-generation semiconductor that is a potential building block for short-wavelength LEDs , , , . In particular, 1D ZnO NR arrays have exhibited excellent performance in the field of light-emitting devices , , , , , , , . Recently, Chongxin Shan’s research groups used 1D ZnO micro-nano heterostructures for electrically pumped Fabry-Perot micro-lasers and electrically driven ultraviolet (UV) plasmonic lasers at room temperature , . However, an increased surface-to-volume ratio deteriorates the efficiency and stability of ZnO NR LEDs. Thus, an important challenge is to overcome these surface-mediated non-radiative and deep-level recombination channels in order to improve device performance.
Surface plasmons (SPs) are electron oscillations that have attracted intense interest as a means to increase luminescence efficiency , , , . Recently, graphitic carbon materials have exhibited a resonant SP effect attributed to an induced oscillation behavior of π and π+σ electrons with Dirac-cone-like energy bands , , , , , , . Two-dimensional (2D) graphene, a layered structure of sp2-hybridized carbon atoms with a unique honeycomb lattice structure, has been of considerable interest because of the ability to engineer its band gap and the Fermi energy via electrical gating and carrier doping , . As early as 2008, Nair et al.  reported for the first time that the unexpected absorption was attributed to the excitation of spectrally broadened surface plasmonic modes in graphene and the breakdown of the Dirac-fermion model, caused by triangular warping and non-linearity of energy bands far from the Dirac energy. Next, Dawlaty et al.  presented experimental results on the optical absorption spectra of epitaxial graphene from UV to the visible frequency range. Subsequently, Hwang et al.  also observed that the graphene showed an abnormally increased absorption in the violet-frequency region. They demonstrated that the resonant excitation of graphene plasmon is responsible for such absorption and eventually contributes to enhanced photoemission from structures of graphene/ZnO films when the corrugation of the ZnO surface modulates photons emitted from ZnO to fulfill the dispersion relation of graphene plasmon. Meanwhile, Koppens et al.  expounded a light-matter interaction process and optical field confinement induced by graphene. These important findings have unquestionably confirmed that graphene can show an abnormal absorption in the UV region, which indicated a probable SP effect. Furthermore, compared with metal SPs, graphene-like SPs are conveniently tunable in a wide spectral range and generally have lower optical loss, greater confinement, and better flexibility , . These favorable factors promise greater resonant coupling and should stimulate the development of new optoelectronic devices. Therefore, graphene is now regarded as a more promising plasmonic material than metals. Additionally, versatile 2D graphene nano-materials have many advantages and unique characteristics, such as mechanical, electrical, and thermal stability; higher quantum efficiency; and strong non-linear optical processes. They have been used in plasmonic devices, information storage devices, and LEDs , . Hence, there are significant scientific value and economic benefits in developing graphene-based LEDs with SP modulation. Resonant enhancement induced by graphene SPs and an increased ZnO luminescence have been demonstrated for the graphene/ZnO system. However, most reports focused on enhanced photoluminescence (PL) , , , , , , , ,  rather than greater UV electroluminescence (EL) , .
Here, a hybrid 3D structure of 1D ZnO NR vertical arrays and a 2D graphene plasmon layer was fabricated on a commercial p-GaN substrate. By some effective means, the graphene plasmon layer was directly inserted into the active region between the NR arrays and the substrate, optimizing the SP-enhanced LED luminescence. Compared with the primitive ZnO/GaN heterostructure, the graphene-embedded device demonstrated an approximately 4-fold improvement in near-UV EL intensity. The enhancement mechanism was revealed according to time-resolved spectroscopy and temperature-dependent PL (TD-PL). The internal quantum efficiency (IQE) was estimated to be approximately 53%, which is among the highest reported for ZnO nanostructures. In our current study, by introducing a graphene plasmon layer, improved UV EL behavior was observed. To the best of our knowledge, this contribution may be the first to report on graphene-based SP-improved ZnO UV LEDs.
Simple p-n heterostructure ZnO NR arrays were epitaxially prepared, as described previously , on commercial p-GaN substrates using a hydrothermal synthesis method. Catalysts and seed layers were not required, and zinc acetate and hexamethylenetetramine were used as precursors. The device structure and preparation were modified to investigate the effect of the embedded graphene plasmon layer on ZnO luminescence. Because the layer had to be near the active region to enhance the luminescence, it was transferred to the p-GaN substrate before growth of the ZnO NR arrays, as reported previously , . Initially, polymethyl methacrylate (PMMA) was dissolved in acetone solution at a 4% mass fraction and spin-coated as a protective layer (3600 r/min, 30 s) on a graphene sheet supported on a Cu substrate. The sample was then placed on a 110°C heating plate for 15 min, followed by immersion in an FeCl3 solution to remove the Cu substrate. The graphene/PMMA layer was then transferred onto a p-GaN substrate by a lift-up process and dried in air for 12 h. The sample was again heated at 130°C for 30 min, and then placed in a 50°C acetone solution for 10 min to dissolve and remove the residual PMMA. Thus, a precise and controllable graphene plasmon layer transfer process was accomplished. Because of the graphene dangling bonds and the lattice mismatch with ZnO, plasma processing technology was performed. Specifically, the graphene plasmon layer was placed in 100 Pa oxygen plasma for 1 min at an input power of 40 W to form dangling bonds and nucleation sites favorable to ZnO NR growth. This created oxygen-containing functional groups or defect sites on the surface of graphene for nucleation and growth of oxides, similar to the nitrogen plasma etching used for inorganic nitride growth (e.g. AlN and GaN) on graphene monolayers. High-performance blue LEDs were fabricated with these graphene-buffered nitride emissive layers , , , . ZnO NR arrays were then synthesized on the graphene plasmon layer via the hydrothermal method noted above. A schematic of the fabrication procedure is shown in Figure 1. A primitive reference ZnO NR array/p-GaN LED without graphene plasmon layer decoration was also fabricated for comparison. Au/Ni and In contact electrodes were thermally evaporated on p-GaN and ZnO NR, respectively. PL and EL spectra were recorded and collected from one side of the cathode and detected in the same way for direct comparison.
3 Results and discussion
ZnO NR arrays were synthesized on the commercial p-GaN chip or the graphene/p-GaN substrate was imaged with a scanning electron microscope (SEM), as shown in Figure 2A and B. The NRs were vertically aligned on the p-GaN substrates in a highly ordered distribution. The average NR diameter was approximately 150 nm and the average length was approximately 2 μm. The inset of Figure 2A is a high-magnification SEM image of a single ZnO NR having a flat and smooth side surface. After inserting the oxygen-plasma-processed graphene plasmon layer, the mass and morphology of the ZnO NR arrays did not degrade significantly and the surface density slightly decreased. In Figure 2C and D, the microstructure of a single ZnO NR was imaged with high-resolution transmission electron microscope (HRTEM) and selected-area electron diffraction (SAED). The SAED pattern was along the [011̅0] zone axis, indicating a single-crystal wurtzite structure with a  growth direction. Interplanar spacings of 0.26 and 0.16 nm, corresponding to the orthogonal (0002) and (21̅1̅0) planes of wurtzite ZnO, were clearly observed. Furthermore, superimposed electronic images and energy dispersive X-ray (EDX) mapping of a single ZnO NR on graphene-covered p-GaN (inset of Figure 2A) are shown in Figure 2E–J. They verified the uniform distributions of elemental Zn, O, Ga, N, and C.
The EDX patterns (Figure 3A) collected from the surface of the microstructure also indicated the formation of a heterostructure. The X-ray diffraction pattern depicted in Figure 3B, which included (100), (002), (101), (102), (110), (103), (200), and (004) planes, matched well with Joint Committee on Powder Diffraction Standard card no. 36-1451. The sample prepared on graphene-covered p-GaN had a higher-intensity (002) peak, which implied a vertical alignment consistent with the SEM images in Figure 2A and B. A Raman spectrum of transferred graphene (red line in Figure 3C) had two vibrations at 1580 and 2700 cm−1 attributed to the G and 2D bands, respectively. The 2D/G intensity ratio was 2.4, which indicated good-quality layered graphene , . Raman spectroscopy of the sample after oxygen plasma treatment (blue line in Figure 3C) exhibited a stronger D peak (ID) and a weaker G peak (IG), enhancing the ID/IG ratio and indicating that the perfect graphene structure was degraded. This indirectly verified changes in the defect density (point-like defects and nucleation sites) to enable growth of ZnO NR arrays . Cancado et al. and Lucchese et al. carried out theoretical quantitative analysis and proposed that the defect density was closely related to ID/IG. The relationship can be represented by , :
The length scales of rA and rS indicated the region around D band scattering, where rS is the radius of a disordered area, rA is the radius of a point defective area, and LD is the distance between point-like defects. Studies have shown that ID/IG is dependent on the activated area, which is weighted by the parameter CA, and a defective area weighted by the parameter CS . Herein, we chose CS=0 and in terms of approximation and boundary conditions, where EL is the energy of excitation source (488 nm or approximately 2.54 eV) . The fitting coefficient yielded A=(160±48) eV4, by fixing B=4, which was in accordance with Refs.  and . Thus, Eq. (1) could be transformed into
By replacing rA=3.1 nm, rS=1 nm, Eq. (2) can be rewritten as
According to the wavelength of the laser excitation λL, we obtain
Finally, according to Eqs. (3) and (4), the expression for the defect density is
From the Raman spectra of the graphene plasmon layer before and after oxygen plasma treatment, the values of ID/IG (before), (after), nD (before), and (after) were estimated to be 0.17, 1.35, 6.9×1010 cm−2, and 5.5×1011 cm−2, respectively. Hence, the defect density of the graphene plasmon layer was increased by the oxygen plasma. Room-temperature PL spectra of the ZnO NR array/p-GaN heterojunction with and without the graphene plasmon layer were acquired (Figure 3D). With 325-nm lasing excitation, the spectrum of primitive structure consisted of excitonic luminescence centered at approximately 377 nm and weaker broad-band ZnO emission at approximately 525 nm. With the graphene plasmon layer, the PL peak positions and line shapes were not distinctly changed. However, the intensity greatly increased, which suggested a coupling between ZnO excitons and graphene SPs.
Figure 4A displays a structural diagram of the graphene-inserted ZnO NR array/p-GaN heterojunction LED. As described in Section 2 the graphene plasmon layer was introduced without affecting the original heterostructure. A primitive ZnO NR array/p-GaN LED was also constructed, and the performances of both LEDs were characterized. As shown in Figure 4B, the current-versus-voltage (I–V) curves of both junctions exhibited good rectification behavior, which indicated that the graphene plasmon layer did not significantly degrade longitudinal electrical transport. More important, the inserted graphene device had lower forward-injection and reverse-leakage currents at the same voltage, which resulted from the increased series resistance. Additionally, the ohmic contact between the positive electrode (Au/Ni) and p-GaN was acceptable, as shown by the linear I–V curve in the inset of Figure 4B (orange triangles). Negative electrode In easily formed an ideal ohmic contact with ZnO, which was also demonstrated by a linear I–V curve (green squares in the inset). We considered that this graphene plasmon layer also has other advantages during device operation. For example, it has a good heat dissipation layer that allows the heat to spread from the ZnO NR arrays to the p-GaN, reducing the junction temperature. It may promote the radiative recombination of ZnO excitons and probably leads to higher UV emission. Moreover, the oxygen-plasma-processed graphene plasmon layer is a less-conductive semi-insulating blocking layer that slows down the diffusion of electrons from the ZnO NR arrays to p-GaN, which enables ZnO UV luminescence. Overall, introducing the graphene plasmon layer is likely to produce better device performance.
In Figure 5A and B, there are two sets of EL spectra obtained under a forward bias from ZnO NR array/p-GaN heterojunctions without and with graphene plasmon layer decoration. With the injection current ranging from 1 to 10 mA, both EL spectra exhibited a broad near-UV emission band, which may have included several luminescence sources and increased in intensity with injection current. The most striking feature in Figure 5A and B was that the LED with the embedded graphene plasmon layer had much stronger near-UV luminescence centered at approximately 395 nm. The integrated intensities of both heterojunctions as a function of injection current are shown in Figure 5C. The intensities of both LEDs increased with injection current and saturated near 10 mA. The inset of Figure 5C shows a change rule between the enhancement ratio and injection current. The ratio gradually decreased and leveled off at approximately 1.0 when the injection current reached 10 mA. This was most likely because Joule heating became more dominant at higher injection currents and also because of the screening effect of excess carriers induced by higher injection levels for the SP-enhanced LEDs. The above discussion indicated a more appreciable enhancement observed at lower injection levels. Therefore, both EL measurements detected at 1 mA acted as the objects of the study for comparison. In Figure 5D, the main difference was that the intensity of the graphene-inserted heterojunction was more than approximately 4 times that of the primitive ZnO NR array/p-GaN LED device, as reflected in the EL photographs. Moreover, the broad-band near-UV emission peak position experienced no red shift in the EL spectra.
A traditional ZnO/GaN heterojunction can generally produce several luminescence sources, as demonstrated by the broad-band EL spectra. To better analyze and recognize the changes in the spectral lines, both spectra were analyzed with Gaussian deconvolution fits in Figure 6A and B. The applied current was fixed at 1 mA, and defect-related ZnO emissions were very weak. Therefore, the EL broad-band emissions from the two LEDs were split into three independent types of recombination. According to previous reports and the aforementioned PL characterization, these emission peaks were reasonably given to ZnO excitonic radiative recombination, interfacial recombination, and Mg-acceptor dependent emission in p-GaN , , . All spectra from the primitive ZnO NR array/p-GaN LED derived from pronounced ZnO excitonic emission and interfacial recombination, while the p-GaN acceptor emission accounted for a relatively small proportion, as seen in the weight distribution in Figure 6A. However, after inserting the graphene plasmon layer, the components of decomposed sub-peaks greatly improved (Figure 6B) because of the spectral overlap between the near-UV luminescence and the increased abnormal absorption of graphene in the UV region. Additionally, the weight and enhancement of each sub-peak were changed observably, as described in Figure 6C and D. Similar to PL enhancement, the ZnO excitonic emission was effectively enhanced by approximately 4-fold. The increased abnormal absorption of graphene suggested that its SP resonance frequency was mainly situated in the UV region. Therefore, there was a near-UV emission enhancement from the ZnO NR arrays.
As expected from a plasmonic material, graphene SP can also provide an additional radiative recombination route, which can improve the IQE. The energy of some particles, such as electron-hole pairs/excitons in semiconductors, can be coupled to an SP mode and then scattered into free space radiatively. It has been proposed that SP can be generated on the surface of a graphene plasmon layer in a driven heterojunction LED, which has a great effect on luminescence enhancement. To demonstrate this proposal, finite-difference time-domain (FDTD) numerical simulations were performed on the spatial distributions of the electric field intensity at the ZnO NR array/p-GaN interface without and with graphene. The simulation model construction and parameter selections resembled the actual device configuration to ensure reliability. A dipole light source was situated in the junction area, i.e. in accordance with the active region. As presented in Figure 7A and B, the simulations first suggested that the luminescence can be rather confined to the active region and propagate along the NR growth direction, which has been previously confirmed in waveguide-type transmission and light-emitting modes . Further, the SP effect similar to a surface propagation plasmon can be generated on the surface of a graphene plasmon layer, and the graphene enables the energy of light to spread horizontally. Finally, the FDTD results demonstrated that graphene in the active region clearly improved the emitted luminescence intensity of an individual ZnO NR. For ZnO NR array/p-GaN heterojunction, its EL enhancement originates from the collective effect of luminescence improvement of individual ZnO NR. In fact, Chunxiang Xu’s groups have reported some related works on graphene-improved ZnO UV emission , , , , . Especially, some interesting works have been focused on numerical simulation of graphene/ZnO heterostructures , . These works indicated that the graphene SP can be located in the UV frequency region and couple with ZnO excitons to generate ZnO UV luminescence enhancement.
Another way to understand this phenomenon is that the light source of energy can be coupled with the excited graphene SP, which indicates the existence of a resonance coupling interaction between graphene SP and ZnO exciton. To verify this proposal, time-resolved PL (TR-PL) was performed with a fluorescence measurement system (Photon Technology International, London, Ontario, Canada), a pulsed laser of nitrogen molecule, and a photomultiplier. ZnO UV emission at 377 nm was monitored. In Figure 7C, fluorescence decay curves with and without the graphene plasmon layer are illustrated. The curves were normalized and fit to bi-exponential functions. The effective PL lifetimes for the graphene-decorated structure and the pure ZnO NR were determined to be approximately 747 and 1876 ps, respectively. The graphene-decorated ZnO NR array/p-GaN exhibited a faster spontaneous radiative recombination rate than that of the primitive heterostructure, indicating exciton-SP resonant coupling and an increased IQE. To further confirm the latter, TD-PL spectra were acquired over the temperature range 85–310 K. Figure 7D displays Arrhenius plots of UV integrated intensity for ZnO NRs without and with graphene decoration. Interestingly, the graphene-inserted structure presented slower temperature quenching than the primitive structure. Thus, its IQE increased from 30% to 53% via exciton-SP resonant coupling. Herein, it is noteworthy that the IQE of graphene SP-decorated ZnO NR array reaches approximately 53%, which is among the highest reported for ZnO nanostructures. In addition, there was an anomalous change in the integrated intensity over the temperature range 170–230 K in both structures. This was because bound excitons in the surface or interface states were thermally dissociated into free excitons, which provide newly created energy for UV luminescence , . More detailed TR-PL and TD-PL characteristics have been previously reported , , . These experimental results verified the origin of the luminescence enhancement.
The spatial distribution of the light output in the light-emitting device is as important as the emission efficiency. The angle-resolved and normalized EL intensities from the LEDs without and with graphene plasmon layer were thus acquired. The inset of Figure 8A shows a structural diagram with respect to the angle-resolved EL configuration used for data acquisition. The primitive LED exhibited high light output directionality because of the waveguide model. The EL had maximum intensity along the growth direction and decayed rapidly with increased angle. In contrast, the LED device with the graphene plasmon layer exhibited a broader angular distribution in Figure 8B. The width of the spatial distribution was extended, and the spatial uniformity was improved. The luminescence from the active region was divergent; however, the excited graphene SPs coupled with photons in the axial direction of the NRs. Hence, wasted photon energy was re-extracted by the SP mode and uniformly scattered into all directions, resulting in increased light extraction.
A near-UV nano-LED was fabricated according to procedures for ZnO NR/p-GaN junctions. When a graphene plasmon layer was introduced into the active region, there was a significant increase in ZnO UV PL and EL relative to the primitive device. This resulted from resonance coupling interaction between graphene SPs and ZnO excitons. The IQE of graphene-decorated ZnO NR array was approximately 53%, which is among the maximum values ever reported for ZnO nanostructures. Although the device structure should be redesigned and optimized, the current consideration of preparing graphene-decorated SP structures provide a novel approach for performance improvement for various LED devices.
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About the article
Published Online: 2019-09-26
Funding Source: National Natural Science Foundation of China
Award identifier / Grant number: 51732003
Award identifier / Grant number: 51872043
Award identifier / Grant number: 61604037
Award identifier / Grant number: 11874104
Funding Source: “111” Project
Award identifier / Grant number: B13013
Funding Source: Jilin Province
Award identifier / Grant number: JJKH20180007KJ
Award identifier / Grant number: JJKH20190274KJ
Funding Source: Central Universities
Award identifier / Grant number: 2412019BJ006
Award identifier / Grant number: 2412019FZ034
Cen Zhang and Yue Qiu contributed equally to this work. This work was supported by the Program of National Natural Science Foundation of China (Funder Id: http://dx.doi.org/10.13039/501100001809, nos. 51732003, 51872043, 61604037, and 11874104), the “111” Project (no. B13013), the Fund from Jilin Province (nos. JJKH20180007KJ and JJKH20190274KJ), and the Fundamental Research Funds for the Central Universities (nos. 2412019BJ006 and 2412019FZ034).
Citation Information: Nanophotonics, 20190228, ISSN (Online) 2192-8614, DOI: https://doi.org/10.1515/nanoph-2019-0228.
©2019 Weizhen Liu and Haiyang Xu et al., published by De Gruyter, Berlin/Boston. This work is licensed under the Creative Commons Attribution 4.0 Public License. BY 4.0