2D/0D graphene hybrids for visible-blind flexible UV photodetectors.

Nitrogen-functionalized graphene quantum dots (NGQDs) are attractive building blocks for optoelectronic devices because of their exceptional tunable optical absorption and fluorescence properties. Here, we developed a high-performance flexible NGQD/graphene field-effect transistor (NGQD@GFET) hybrid ultraviolet (UV) photodetector, using dimethylamine-functionalized GQDs (NMe2-GQDs) with a large bandgap of ca. 3.3 eV. The NMe2-GQD@GFET photodetector exhibits high photoresponsivity and detectivity of ca. 1.5 × 104 A W-1 and ca. 5.5 × 1011 Jones, respectively, in the deep-UV region as short as 255 nm without application of a backgate voltage. The feasibility of these flexible UV photodetectors for practical application in flame alarms is also demonstrated.

Introduction

Graphene has important potential for use in highly efficient photodetectors becn class="Chemical">ause of its combination of broadband optical absorption and high carrier mobility[1]. However, the use of pristine graphene in photodetectors, for which spectral colour selectivity is desired, is hindered by its gapless nature, and by its weak and flat light absorption over a broad wavelength range. To overcome this shortcoming, the fabrication of hybrid photodetectors that can combine the advantages of graphene and a semiconductor material with a tunable bandgap presents the most promising approach. Hybrid graphene photodetectors with various photo-absorbing media have been studied for detection of ultraviolet (UV), visible, and near-infrared (NIR) light. An NIR photodetector with a photoresponsivity as high as ca. 106 A W−1 has been fabricated by hybridizing graphene with PbS nanocrystals[2]. Integration of plasmonic Au nanorods has also provided NIR light detection with photoresponsivity of 4 × 104 A W−1 at 1,310 nm via the hot carrier injection effect[3]. Visible light detection with photoresponsivity of 180 A W−1 at 400–800 nm was achieved by the combination of graphene with organometallic halide perovskites[4]. More recently, a hybrid photodetector that exhibits a full-colour optical bandwidth was produced through immobilization of rhodamine-based organic dye molecules with red, green, or blue light absorption profiles onto graphene, whereby photoresponsivity of 103 A W−1 was obtained[5]. Such photodetectors’ performance for visible and NIR light detection compares favourably with that of the conventional compound semiconductor-based photodetectors[6-9]. In contrast to visible and NIR light detection, no efficient visible-blind UV detection photodetector has yet been developed. For instance, hybrid structures that use wide-bandgap semiconductors (ZnO nanocrystals or TiO2 nanowires) enable UV light detection[10, 11]. However, the ZnO/graphene hybrid photodetectors were not visible-blind. The TiO2/graphene hybrid photodetectors possessed low photoresponsivity of ca. 0.5 A W−1. Their performance is inferior to those of pristine wide-bandgap semiconductor-based visible-blind UV photodetectors[12, 13].

We have also recently produced a high-performance hybrid photodetector with photoresponsivity of 4 × 104 A W−1 in the deep-UV to n class="Chemical">NIR wavelength region that uses a 2D/0D graphene hybrid consisting of graphene and nitrogen-functionalized graphene quantum dots (NGQDs) with tunable bandgaps[14, 15]. The high photoresponsivity was a consequence of strong light absorption and long-life photogenerated carriers in the NGQDs[16, 17]. In addition to strong light absorption, NGQDs have bandgap tunability that covers a range of absorption from deep-UV to IR. They can thereby be extended to exploit visible-blind UV photodetection. This report describes the performance of a graphene/NGQD hybrid photodetector for visible-blind flexible UV photodetectors. Dimethylamine-functionalized graphene quantum dots (NMe2-GQDs) with a large bandgap of ca. 3.3 eV were used for the NGQD layer to enable visible-blind UV light detection. The photosensitivity and detectivity of the NMe2-GQD@GFET (graphene field-effect transistor) was investigated. The feasibility of these flexible photodetectors for practical application for flame detection was demonstrated.

Results and Discussion

Figure 1a portrays a schematic diagram of the top-contact graphene/n class="Chemical">NGQD hybrid UV photodetector. The carrier transport channel was graphene on top of the 188-μm-thick polyethylene naphthalate (PEN) substrate. The photon-absorbing layer comprised NMe2-GQDs with an energy gap of 3.3 eV, which enables visible-blind UV light detection. HRTEM observations indicated that the NMe2-GQDs had diameters of ca. 5 nm (Fig. S1a). AFM observations revealed most of the NMe2-GQDs as ca. 1.0 nm thick, which corresponds to 1–2 layers of functionalized GQDs (Fig. S1b and c). The high-resolution N 1 s XPS spectrum of the NMe2-GQDs revealed that nitrogen atoms were predominantly engaged in C–N bonding (400.1 eV), which is characteristic of primary dimethyl amines bonded to graphene (Fig. S1d). The band alignment at the graphene/NMe2-GQD interface under light irradiation is illustrated schematically in Fig. 1b. The lowest unoccupied molecular orbital (LUMO) level of NMe2-GQDs was estimated by subtracting the band gap (Fig. S1e) from the highest occupied molecular orbital (HOMO) level. The HOMO level was measured using ultraviolet photoelectron yield spectroscopy (Fig. S1f). Incident photons excite the ground-state electrons of the NMe2-GQDs into excited states. Electron-hole pairs are then generated. The photoexcited carriers are separated at the NMe2-GQD/graphene interface because of the internal built-in electric field. Only the electrons are swept into the graphene layer driving efficient charge separation and transfer, whereas the photoexcited holes remain in the NMe2-GQD layer.

Figure 1

(a) Schematic representation of the NMe2-GQD@GFET hybrid photodetector. (b) Schematic diagram of the energy level alignment for the photodoping effect under illumination. Photoexcited electrons in the NMe2-GQDs are transferred to the graphene layer. (c) Spectral response (left axis) from the NMe2-GQD@GFET photodetector (V SD = 0.1 V, V G = 0 V, 0.06 μW cm−2). The solid orange spectrum (right axis) corresponds to the UV-vis absorption spectrum of a NMe2-GQD solution.

(a) Schematic representation of the NMe2-GQD@GFET hybrid photodetector. (b) Schematic diagram of the energy level alignment for the photodoping effect under illumination. Photoexcited electrons in the n class="Gene">NMe2-GQDs are transferred to the graphene layer. (c) Spectral response (left axis) from the NMe2-GQD@GFET photodetector (V SD = 0.1 V, V G = 0 V, 0.06 μW cm−2). The solid orange spectrum (right axis) corresponds to the UV-vis absorption spectrum of a NMe2-GQD solution.

The spectral response was measured. It corresponded well with typical absorbance behaviour for NMe2-GQDs, i.e., a steep rin class="Chemical">sing edge positioned at ca. 420 nm. Figure 1c shows that the photodetector is exclusively sensitive to UV light. It is almost blind to visible light, although the NMe2-GQDs have an absorption tail in the visible light range (>450 nm), presumably because the localized edge states or surface states in the NMe2-GQDs. The edge states or surface states that contribute to light absorption of NMe2-GQDs in the longer wavelength range have little contribution to the photocurrent because the carriers on these states are highly localised. Moreover, they recombine shortly after generation. In contrast, the shorter wavelength light offers sufficient energy to excite the carriers to the LUMO energy level of the NMe2-GQDs, generating an efficient photocurrent[18]. A response cut-off wavelength was ca. 430 nm. The UV-to-visible rejection ratio (ΔI370/ΔI450 nm, where ΔI (=I light − I dark) is the photocurrent)[12, 13] of the photodetector is over two orders of magnitude (>5 × 102), as shown in the response spectrum, which indicates that the photodetector exhibits a high signal-to-noise ratio. In fact, a negative value of ΔI was detected, as discussed below.

We further characterized the NMe2-GQD@GFET hybrid photodetector by measuring the transfer curve upon illumination. Figure 2a and b present the transfer characteristics (V SD = 0.5 V) for the n class="Gene">NMe2-GQD@GFET hybrid photodetector and a pristine GFET. The Dirac point (charge neutrality point, V D) from the pristine GFET was observed at ca. 23.5 V, implying unintentional hole doping from contamination, lithography processes, and/or surface oxygen-related adsorbates[19]. After hybridization with the NMe2-GQDs, V D shifted to ca. 4.2 V, which suggests that electrons were transferred from the NMe2-GQDs to graphene. This transferral is consistent with the higher work function of NMe2-GQDs. Upon irradiation (405 nm, 18 μW cm−2) of the NMe2-GQD@GFET hybrid photodetector, V D shifts to a lower voltage, which suggests that photoexcited electrons are transferred to the graphene. From the transfer curves measured in the absence of light, it is estimated that the field-effect mobility for holes is ca. 985 and 1,575 cm2 V−1 s−1, respectively, for the GFET and the NMe2-GQD@GFET. The hole-carrier mobility is increased by the incorporation of NMe2-GQDs, which is contrary to previously observed trends for graphene hybrid phototransistors, which exhibit decreased carrier mobility because of disorder or defects induced by hybridization[2, 10]. The increase in carrier mobility might be attributable to an increase in the density of states near the Fermi level induced by the widely distributed π orbitals of the NMe2-GQDs.

Figure 2

(a) I SD–V curve (V SD = 0.5 V) for the ON (405 nm, 18 μW cm−2) and OFF states of a NMe2-GQD@GFET photodetector. (b) I SD–V curve (V SD = 0.5 V) for a pristine GFET. (c) Photoresponsivity as a function of gate voltage. Insets show the direction of electron transfer from the NMe2-GQDs to graphene for the hole and electron conduction regimes in graphene under illumination (405 nm, 18 μW cm−2). (d) Temporal photocurrent response of the NMe2-GQD@GFET photodetector (V SD = 0.1 V, V G = 0 V, 405 nm, 15 μW cm−2). (e) Transient response dynamics for the NMe2-GQD@GFET photodetector (V SD = 0.1 V, V G = 0 V, 405 nm, 31 μW cm−2).

(a) I SD–V curve (V SD = 0.5 V) for the ON (405 nm, 18 μW cm−2) and OFF states of a n class="Gene">NMe2-GQD@GFET photodetector. (b) I SD–V curve (V SD = 0.5 V) for a pristine GFET. (c) Photoresponsivity as a function of gate voltage. Insets show the direction of electron transfer from the NMe2-GQDs to graphene for the hole and electron conduction regimes in graphene under illumination (405 nm, 18 μW cm−2). (d) Temporal photocurrent response of the NMe2-GQD@GFET photodetector (V SD = 0.1 V, V G = 0 V, 405 nm, 15 μW cm−2). (e) Transient response dynamics for the NMe2-GQD@GFET photodetector (V SD = 0.1 V, V G = 0 V, 405 nm, 31 μW cm−2).

When the NMe2-GQD@GFET is operated at V G = 0 V, the major carriers in the n class="Chemical">graphene layer are holes. The holes are compensated by the transferred electrons, which engenders decreased conductance and a negative ΔI (Fig. 1c). The back-gate dependence of the photoresponsivity (Fig. 2c) is also consistent with this trend. A clear carrier type and concentration dependence of the external photoresponsivity R ext (R ext = ΔI/P light, where P light is the incident optical power density) were observed. R ext (R ext = ΔI/(P light A PD/A light), where A light is the light spot area) was calculated with a scaling factor (A PD/A light) that takes into account that only a fraction of the optical power density impinges on the photodetector. In the hole-conduction region (V G < 4.2 V), the holes are compensated by the photoinduced electron carriers, which engenders decreased conductance and a negative R ext. In contrast, the photoinduced electron carriers raise the electron concentration, which engenders increased conductance and a positive R ext in the electron-conduction region (V G > 4.2 V).

We investigated the dynamic performance of the NMe2-GQD@GFET hybrid photodetector by measuring its response time. Figure 2d shows the on/off photocurrent of the photodetector at an incident power denn class="Chemical">sity of 15 μW cm−2 (V G = 0 V, V SD = 0.1 V, 405 nm. The temporal photoresponse was measured at the on/off cycle of 1 s. The photocurrent level is well retained, demonstrating good reliability and reversibility of NMe2-GQD@GFET hybrid photodetector. Figure 2e gives the transient response dynamics. The rise time was ca. 3.7 s (which corresponds to a rise of ca. 90%). The decay trace can be fitted by a double exponential; ΔI DS = ΔI 1[1 − exp(−t/τ 1)] + ΔI 2[1 − exp(−t/τ 2)][10, 20]. Time constants τ 1 and τ 2 are, respectively, 22 s and 77 s. This slow decay is probably associated with the multiplicity of carrier traps in NMe2-GQDs from quantum confinement and different localized states in the π-π* gap[21]. The short relaxation time τ 1 corresponds to the lifetime of the holes trapped in the NMe2-GQDs, whereas the long relaxation time τ 2 represents the time duration for the charge transfer and transportation in NMe2-GQDs layer. The carrier transit time τ transit (τ transit = L 2⁄μ∙V DS) is estimated as 1.3 ns (based on a carrier mobility (μ) of 1,575 cm2 V−1 s−1, a channel length (L) of 10 μm, and a bias (V DS) of 0.5 V), thereby the photoconductive gain G (G = τlife/τtransit)[22] is between 1.7 × 1010 and 5.9 × 1010, respectively using lifetimes of 22 s and 77 s. The high photoconductive gain is attributed to the cooperative effect of long hole-carrier lifetime in the NMe2-GQDs and the high carrier mobility of graphene. Multiple carrier circulation occurs in the graphene channel, depending on the ratio of the photoexcited holes relaxation time in the NMe2-GQDs layer to the carrier transit time in the graphene layer. Because the photogenerated holes remain trapped in the NMe2-GQDs, the positively charged NMe2-GQDs induce negative carriers in the graphene sheet through capacitive coupling. As long as the NMe2-GQDs remain positively charged, negative charges in the graphene sheet are highly recirculated because of their high carrier mobility, resulting in high photoconductive gain[2].

Figure 3a presents the optical power density-den class="Chemical">pendent external photoresponsivity R ext, and the specific detectivity D* of the NMe2-GQD@GFET hybrid photodetector at a fixed bias of 0.1 V under light irradiation at wavelengths of 255, 370, and 405 nm. D* (D* = (∆f A PD)1/2 R ext/i n, where A PD, ∆f and i n respectively stand for the area of the photodetector channel, electrical bandwidth, and noise current)[23, 24] represents the capability of detecting low-level light signals. The noise current of photodetectors is dominated by the shot noise, but the noise current in the shot-noise limit is given as i n = (2eI dark ∆f), where e and I dark respectively denote the electron charge and the dark current[24]. Therefore, D* in the shot-noise limit is calculable by the expression: R ex A PD 1/2/(2eI dark)  [23-25], which has been used to estimate the D* of photodetectors in earlier studies[23, 24, 26, 27]. The NMe2-GQD@GFET hybrid photodetector exhibited high photoresponsivity and detectivity in the deep UV region. R ext and D* respectively reached ca. 1.5 × 104 A W−1 and ca. 5.5 × 1011 Jones at 255 nm. The maximum values of R ext and D* are comparable to those reported for other high performance UV photodetectors (Table S1)[6, 28–37]. The increased R ext and D* toward the shorter wavelength is consistent with the fact that the absorption of the NMe2-GQDs is enhanced at high-energy wavelengths. The photocurrent increases linearly with the source–drain bias. High R ext and D* is achieved when the bias voltage is increased and the incident optical power density is decreased (Fig. 3b). The decrease in R ext and D* with the incident optical power density is explainable by consideration of the following reason. As more photogenerated electrons are injected into the graphene channel, the corresponding holes left in NMe2-GQD layers weaken the original internal field near the NMe2-GQD/graphene interface built by the Fermi-level alignment. The ability in charge separation declines with reduced interfacial electric field, leading to decreased photocurrent as the incident optical power density increases. Therefore, a reduced injection of electrons causes R ext and D* to decrease.

Figure 3

(a) Photoresponsivity and specific detectivity of the NMe2-GQD@GFET hybrid photodetector (V SD = 0.1 V, V G = 0 V) as a function of optical irradiation power density at various wavelengths: blue, 255 nm; green, 370 nm; pink, 405 nm. (b) Source-drain voltage dependence of the photoresponsivity and detectivity for the NMe2-GQD@GFET hybrid photodetector (V G = 0 V, 405 nm, 35 nW cm−2).

(a) Photoresponsivity and specific detectivity of the n class="Gene">NMe2-GQD@GFET hybrid photodetector (V SD = 0.1 V, V G = 0 V) as a function of optical irradiation power density at various wavelengths: blue, 255 nm; green, 370 nm; pink, 405 nm. (b) Source-drain voltage dependence of the photoresponsivity and detectivity for the NMe2-GQD@GFET hybrid photodetector (V G = 0 V, 405 nm, 35 nW cm−2).

Finally, the practical application of the NMe2-GQD@GFET hybrid photodetector to flame detection is demonstrated. Figure 4a presents the temporal change in the photocurrent upon illumination by light from a gas match from a distance of ca. 1 m. A clear change of the photocurrent was observed with switching of the gas match on and off, which confirms that the photodetector is useful for flame detection. Figure 4b depicts digital images of the prototype flame alarm mounted on a front panel conn class="Chemical">sisting of “nanoblocks” in conjunction with the open-source Arduino Uno electronics platform.

Figure 4

(a) Change in the photocurrent under UV light irradiated from a flame (the distance between the photodetector and flame was ca. 1 m. (b) Digital images (snapshots from Movie S1, Supplementary Information) showing the operation of the flame alarm using a NMe2-GQD@GFET hybrid photodetector. (i) Schematic of the prototype flame alarm. (ii) The green-LED of the fire alarm was turned on when the flame was detected.

(a) Change in the photocurrent under UV light irradiated from a flame (the distance between the photodetector and flame was ca. 1 m. (b) Digital images (snapshots from Movie S1, Supplementary Information) showing the operation of the flame alarm using a n class="Gene">NMe2-GQD@GFET hybrid photodetector. (i) Schematic of the prototype flame alarm. (ii) The green-LED of the fire alarm was turned on when the flame was detected.

A movie showing operation of the flame alarm is given in the Supplementary Information (Movie S1). When the photocurrent from the photodetector is increased to the threshold value of the photocurrent set in the program that controls the detectable distance, the green LED is turned on. The flame alarm LED was turned respectively off (Fig. 4b(i)) and on (Fig. 4b(ii)) in the absence and in the presence of a flame. Our flame alarm based on the NMe2-GQD@GFET hybrid photodetector is well operated. These results indicate that the proposed n class="Gene">NMe2-GQD@GFET hybrid photodetector offers great potential for use in practical devices.

In summary, flexible UV photodetectors based on graphene/n class="Chemical">nitrogen-functionalized graphene quantum dot hybrid were produced using dimethylamine-functionalized GQDs with a large bandgap of ca. 3.3 eV. The hybrid photodetector exhibited high photoresponsivity and detectivity in the deep ultraviolet region. Its photoresponsivity and detectivity reached values exceeding 104 A W−1 and 1011 Jones, respectively, at 255 nm. Moreover, the potential application for flame alarms was demonstrated. This hybrid photodetector is promising for use in future graphene-based photonic devices.

Materials and Methods

Materials

Graphite nanoparticles (Gn class="Chemical">NPs; <50 nm; SkySpring Nanomaterials, Inc.) were used as a precursor for preparation of the NGQDs. N,N-dimethylformamide (DMF) as a solvent, and sulfuric acid and nitric acid as oxidizing agents were obtained from Wako Pure Chemical Industries Ltd.

Synthesis of NMe2-GQDs

NMe2-GQDs were selected for the n class="Chemical">NGQD layer because their large energy gap (3.3 eV) enables visible-blind UV light detection. The NMe2-GQDs were prepared as follows. Oxidized GNPs (oGNPs) were obtained by refluxing GNPs in a 2:1 solution of concentrated H2SO4 and HNO3. 5 mg of the oGNPs were dispersed in 5 mL of DMF. The mixture was refluxed at 154.5 °C for 5 h. After cooling to room temperature, the suspension was dried using an evaporation system (Soltramini; Techno Sigma Corp.). The dried powder (NMe2-GQDs) was re-dispersed in water and was dialyzed for 3 days. After drying, the NMe2-GQD powder was re-dispersed in DMF.

Photodetector device fabrication

Monolayer graphene sheets formed by chemical vapour depon class="Chemical">sition (CVD) onto a PEN substrate (188 μm) were obtained from Graphene Platform Corp. Gold source and drain electrodes (100 nm) were fabricated directly on the top of the graphene/PEN substrate using sputter deposition through a metal shadow mask. These devices had effective channel length L of 80 μm and a channel width W of 200 μm. NMe2-GQD dispersions were subsequently dropped directly onto the top of the graphene layer.

Measurements of the gate-voltage dependence on the photoresponn class="Chemical">sivity were taken using photodetectors fabricated by replacement of the PEN substrate with a Si substrate. The gate contact was deposited onto the back side of the Si wafer substrate. Monolayer graphene sheets formed by CVD onto a p-doped Si wafer (525 μm, 0.002 cm, 90 nm SiO2 layer) were obtained from Graphene Platform Corp. The source and drain electrodes were patterned directly on the top of the graphene/Si wafer using a conventional photolithography process with a poly(methyl methacrylate) resist. The contacts were formed with titanium and gold (15 nm/100 nm) using a sputtering deposition method, followed by a lift-off process. These devices were fabricated with L = 10 μm and W = 10 μm. After the gate contact was deposited onto the back side of the Si wafer, the device was diced into 1 × 1 cm substrates. The NMe2-GQD dispersions were dropped directly onto the top of the graphene layer.

Photoresponse measurements

A light source was guided into the photodetector through a circular aperture with area A. Light-emitting diodes (LEDs) with different wavelengths were used as light sources to provide light with wavelengths of 255, 370, and 405 nm. A fibre probe, coupled to a monochromator with a deuterium lamp, was used for spectral response measurements. The optical power denn class="Chemical">sity through the aperture (P opt) was measured using a silicon photodetector (S130VC; Thorlabs, Inc.). The incident (P inc) power density was then calculated using the relation: P inc = (A det × P opt)/A, where A det is the active area of the photodetector. Electrical measurements were taken using a system source meter (2602 A; Keithley Instruments Inc.) in conjunction with LabVIEW software. All measurements were conducted at room temperature in the ambient atmosphere.

Instrumentation

X-ray photoelectron spectroscopy (XPS; Quantera SXM; Ulvac-Phi Inc.) measurements were performed using a monochromated Al Kα radiation source (100 μm spot diameter) of 1486.6 eV under high-vacuum conditions. Scans were acquired in the fixed analyzer transmisn class="Chemical">sion mode with pass energy of 26 eV and a surface/detector takeoff angle of 45°. High-resolution transmission electron microscopy (HRTEM; EX-2000; Hitachi Ltd.) was used with accelerating voltage of 200 kV. Optical transmittance and reflectance in the visible/NIR region of the samples was recorded using a spectrophotometer (UV-3600; Shimadzu Corp.). Reflectance was measured at an incident angle of 5° using an additional attachment. Measurements of work function and shallow energy levels were taken using a photoelectron spectrometer (AC-2; Riken Keiki Co. Ltd.). Atomic force microscopy (AFM; NanoscopeV D3100; Veeco Instruments) was used to investigate the height profile.

Data Availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request and with permisn class="Chemical">sion of Toyota Central R&D Laboratories, Inc.