- Nano Express
- Open Access
Enhanced Optoelectronic Conversion Efficiency of CdSe/ZnS Quantum Dot/Graphene/Silver Nanowire Hybrid Thin Films
© The Author(s). 2016
- Received: 21 April 2016
- Accepted: 31 August 2016
- Published: 6 September 2016
In this study, we prepared the reduced graphene oxide (rGO)-CdSe/ZnS quantum dots (QDs) hybrid films on a three-layer scaffold that the QD layer was sandwiched between the two rGO layers. The photocurrent was induced by virtue of the facts that the rGO quenched the photoluminescence of QDs and transferred the excited energy. The quenching mechanism was attributed to the surface energy transfer, supported in our experimental results. We found that the optoelectronic conversion efficiency of the hybrid films can be significantly improved by incorporating the silver nanowires (AgNWs) into the QD layer. Upon increasing AgNW content, the photocurrent density increased from 22.1 to 80.3 μA cm−2, reaching a near 3.6-fold enhancement compared to the pristine rGO-QD hybrid films. According to the analyses of photoluminescence spectra, shape effect, and electrochemical impedance spectra, the enhancement on the optoelectronic conversion efficiency arise mainly from the strong quenching ability of silver and the rapid electron transfer of AgNWs.
- Quantum dot
- Silver nanowire
Due to the confinement of the charge carriers in three spatial dimensions, quantum dots (QDs) display extraordinarily optoelectronic properties and tunable band gap. Over the past decade, QDs have been widely studied on the application of solar cells [1, 2], sensors , light emitters [4, 5], and bioassays . Recently, many studies revealed that the excited energy of QDs could be transfer effectively to graphene because of the high conductivity and luminescence quenching ability of graphene [7–11]. In general, the quenching possible mechanism can be ascribed to the following routes: Forster resonance energy transfer, surface energy transfer, and photo-induced electron transfer . Some studies have shown experimentally that the quenching of QDs by graphene was assigned to surface energy transfer [10, 12]. The rate of surface energy transfer and the rate of Forster resonance energy transfer are inversely proportional to the fourth and sixth power of the distance between donors and acceptors, respectively. Therefore, the surface energy transfer occurs in a larger range than the Forster resonance energy transfer. At a relatively long distance, the surface energy transfer is more efficient than the Forster resonance energy transfer. The highly effective charge transfer can avoid the recombination of excited electrons and holes and is in favor of the optoelectronic conversion. Therefore, the QD-graphene system has been applied to improve pollution detection [13, 14], light-harvesting devices [15–19], QD-sensitized solar cells [20–22], bioassays , etc.
In fact, the photoluminescence (PL) suppression of QDs also occurs in the presence of metals due to the Forster resonance energy transfer . Unlike graphene, the metal nanostructural surfaces, nanoparticles, or nano-holes not only quench but also enhance the PL of QDs through the excitation of localized surface plasmon resonance (LSPR) of metal nanostructures, which amplifies the local electric field to alter the optical properties of QDs [25–31]. As a result, both the PL quenching and enhancement are observed after the excitons of QDs coupling with LSPR of metal nanostructures. Because the Forster energy transfer is a shorter range effect than the enhanced electromagnetic field, the PL quenching will be weakened with distance and much faster than the LSPR enhancement. At longer distance, the PL enhancement decrease gradually [32–35]. The distance of the QDs from metal nanostructural surfaces affects the competition between enhancement and quenching. Moreover, the LSPR absorption characteristic depends strongly on the size, shape, and coupling of metal nanoparticles and the dielectric properties of their surrounding medium [36–38]. As a result, the effect of nanometals on optoelectronic conversion of QDs is complicated and undetermined.
In this study, we used reduced graphene oxides (rGOs) and CdSe/ZnS QDs to fabricate rGO-QD-rGO sandwich-structure films. The sandwich structure is willing to alleviate the deterioration of QDs in surroundings by virtue of the covering of graphene. We found that the optoelectronic conversion efficiency of the QD-graphene system was significantly improved by incorporating silver nanowires (AgNWs) into the QD layer. The optimal composition for the hybrid films was analyzed and discussed. The incorporation of silver nanoparticles (AgNPs) and silver nanorods (AgNRs) was also done in order to realize the mechanism of enhancement of AgNWs.
Preparation of Water-Soluble CdSe/ZnS Core-Shell QDs
Water-soluble CdSe/ZnS core-shell QDs were synthesized as reported previously . Briefly, solvent-based CdSe/ZnS QDs dispersed in chloroform were synthesized by the solvothermal methods: CdSe core and ZnS shell were prepared at 290 °C for 5 min and at 220 °C for 1 min, respectively. Excess 3-mercaptopropionic acid (MPA; Sigma-Aldrich) was added into 10 wt.% KOH methanol solution, and the mixture was violently stirred. The as-prepared CdSe/ZnS chloroform solution was added into the MPA solution in the volume ratio of 2:1. After 5-min mixing, the QDs in the suspension were precipitated with the addition of acetone. The QDs were purified through centrifugation (9000 rpm, 10 min), decanting the supernatant, and redispersing the precipitate with methanol. Finally, the precipitate was redispersed in water, resulting in MPA-capped CdSe/ZnS QD aqueous solution.
Preparation of AgNPs, AgNRs, and AgNWs
A 0.17 g of AgNO3 (Showa) and 0.17 g of polyvinylpyrrolidone (PVP, Acros) were mixed in 10 mL of water. A 0.028 g of NaBH4 (Alfa Aesar) was then added rapidly into the AgNO3 aqueous solution. After 10 min, the resulting solution was precipitated by acetone and then redispersed with water several times, resulting in the AgNPs.
AgNRs (to be more exact, the nanorods are Au-Ag core-shell structure.) were synthesized using the seed-mediated growth method as reported by Zhou et al. . Briefly, 0.4 mL of AgNO3 (0.01 M), 10 mL of HAuCl4 (Fluka, 0.01 M) and 10 mL of cetyltrimethylammonium bromide (C16TAB, Sigma-Aldrich, 0.1 M) were mixed. Then, 0.32 mL of ascorbic acid (AA; Sigma-Aldrich, 0.1 M), 0.8 mL of HCl (1 M), and 96 μL of the seed solution were added into the mixture sequentially. The mixture was stirred rigorously for 1 min and then undisturbed for 6 h. A 2 mL of the mixture was washed three times with cetyltrimethylammonium chloride (CTAC; Sigma-Aldrich, 0.1 M) through centrifugation and then re-dispersed in 10 mL of CTAC (80 mM). The resultant solution was reacted with 0.5 mL of AA (100 mM) and 0.17 mL of AgNO3 (0.01 M) at 60 °C for 3 h, resulting in the AgNRs.
AgNWs were synthesized as reported previously . Briefly, 20 μL of AgNO3 (1 M) was added into the mixture of 36 mL of PVP (0.3 M) and 80 μL of NaCl (0.2 M) at 160 °C. A 4 mL of AgNO3 (1 M) was then added slowly into the mixture using a peristaltic pump. The solvent of all the above-mentioned solutions is ethylene glycol (EG). When the color of the mixture turned into a misty auburn, all of the residual AgNO3 solution was poured into the mixture at once. After the color of the solution turned into silver-whitish, the products were washed three times with ethanol through centrifugation, resulting in the AgNWs.
Preparation of the rGO-QD, rGO-QD/AgNW, rGO-QD/AgNR, and rGO-QD/AgNP Sandwich Structures
Indium tin oxide (ITO) glass was rinsed with acetone and de-ionized water through ultrasonication. The cleaned ITO glass was immersed into 10 wt.% 3-aminopropyltrimethoxysilane (APTS) aqueous solution and then dried at 70 °C. Various amounts (100, 300, 500, and 700 μL) of GO solution (4 mg/mL), fabricated by the modified Hummers method as reported in the previous work , were diluted to 2 mL. A 100 μL of CdSe/ZnS QD solution was diluted to 800 μL. GO, QD, and GO was sequentially spin-coated on the APTS-treated ITO glass substrates (2 × 2 cm). The hybrid film was annealed under N2 atmosphere at 200 °C for 15 min and then immersed in 10 wt.% hydrazine solution at 80 °C for 30 min, resulting in the rGOx-QD hybrid film, where x denotes x00-μL GO solution was added. The rGOx-QD/AgNWy hybrid films were prepared as that of the rGOx-QD ones, except that various amount of AgNW solution (100, 300, 500, and 700 μL) were mixed with the QD solution, where y indicates y00-μL AgNW solution was added. To realize the effect of silver shape on the enhancement of optoelectronic conversion efficiency of rGO-QD hybrid films, the AgNWs were replaced by AgNRs and AgNPs individually on the same amount to prepare the hybrid films, denoting as rGOx-QD/AgNR and rGOx-QD/AgNP, respectively.
Particle size and morphology of the as-prepared CdSe/ZnS QDs, AgNPs, and AgNRs were examined using a field-emission scanning-electron microscope (SEM; JSM-7401F, JEOL) and a high-resolution transmission electron microscope (TEM; JEM-2010, JEOL). The absorption spectra of CdSe/ZnS QDs and hybrid films were measured using a UV-Vis spectrophotometer (Lambda 850, PerkinElmer). PL spectra of CdSe/ZnS QDs and their hybrid films were measured using fluorescence spectrophotometer (LS-55/45, PerkinElmer). The size and morphology of the GO and AgNWs were characterized using optical microscopy (OM; M835, M&T Optics). Optoelectronic conversion of the hybrid films was measured through a photoelectrochemical bath: the electrolyte solution was Na2SO3 (0.35 M) and Na2S (0.24 M) in water, and the hybrid film (2 × 2 cm), a Pt wire, and a Ag/AgCl electrode were used as the working, counter, and reference electrodes, respectively. The photocurrent of the working electrode and the electrochemical impedance spectra (EIS) over the frequency range of 50 mHz–100 kHz with a potential perturbation of 10 mV were measured using an electrochemical workstation (Zennium, Zahner) under irradiation of a 75-W halogen lamp with 2-cm interval between the lamp and the working electrode.
The rGO-CdSe/ZnS QD hybrid thin films have been fabricated on a sandwich scaffold. The optoelectronic conversion efficiency of the hybrid film was significantly enhanced by incorporating AgNWs into the QD layer. However, too low or high rGO or AgNW addition decreased the enhanced performance. Compared to AgNPs and AgNRs, the AgNWs displayed superior improvement on optoelectronic conversion. The optimal AgNW incorporation can result in a near 3.6-fold enhancement on the photocurrent density in comparison with the pristine rGO-QD hybrid film. We infer that the enhancement on the optoelectronic conversion efficiency may arise from the strong quenching ability of silver and the rapid electron transfer of AgNWs.
This work was financially supported by the Minister of Science and Technology, the Republic of China (MOST 103-221-E224-074).
BTL planned the study, analyzed data, and wrote the paper. KHW carried out the experiments. RHL helped to improve the data. All authors approved the manuscript.
The authors declare that they have no competing interests.
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