- Nano Express
- Open Access
Hybrid Nanomaterials Based on Graphene and Gold Nanoclusters for Efficient Electrocatalytic Reduction of Oxygen
© The Author(s). 2016
Received: 4 June 2016
Accepted: 7 July 2016
Published: 19 July 2016
Nanocomposites based on gold nanoclusters (AuNCs) with polyvinyl pyrrolidone as ligand and reduced graphene oxide (RGO) have been prepared and employed as efficient electrocatalysts for oxygen reduction reaction (ORR). AuNCs were synthesized through a wet chemical approach and then loaded onto the RGO. The as-prepared hybrid materials were pyrolyzed to remove the organic ligands. The composites were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) as well as other techniques. Electrochemical tests demonstrated that the hybrid materials exhibited effective ORR activity in alkaline media. Among a series of samples tested, the pyrolyzed sample with 50 % AuNCs mass loading exhibited the best activity, superior than AuNCs alone, RGO alone, and the others, in terms of onset potential and kinetic current density as well as durability. The method here may provide a generic approach to prepare supported noble metal nanoclusters with excellent reactivity and robust stability for ORR.
Low-temperature fuel cells, an efficient energy conversion device, are expected to tackling the global energy crisis and environmental issues [1–3]. However, their massive commercialization and development have been significantly hindered by the oxygen reduction reaction (ORR), mainly due to the sluggish reaction kinetics and complicated reaction pathways of ORR [4, 5]. Currently, the most extensively employed catalyst for ORR is Pt-based materials [6–9], but the high price and scarcity of Pt as well as low poison resistance significantly retard their widespread commercialization. Therefore, it is urgent to develop cost-effective ORR catalyst with sufficient reactivity and high earth abundance as well as long-term stability [10–12].
Gold nanoclusters (AuNCs), owing to their excellent optical properties, and rich electrochemical behaviors as well as ultrasmall sizes imparted large surface area, have been attracting increasing research attentions in catalytic regime in the past decade . Recent studies have demonstrated that AuNCs possess excellent catalytic activity toward a series of reaction including CO oxidation , selective hydrogenation , and oxidation  of small organic molecules as well as ORR . Unfortunately, when employing AuNCs alone as catalyst, the stability became an inevitable issue, e.g., they can easily dissolve, aggregate, decompose, or sinter in the electrochemical catalytic process . Consequently, a variety of substrates have been developed to support and stabilize these clusters, and the most widely used substrate is porous carbon materials including mesoporous carbon , carbon nanosheets , and carbon nanodots . Graphene, although discovered only recently in 2004 , has already become an extremely promising material as a catalyst support . Graphene-based materials (e.g., graphene, graphene oxide, reduced graphene oxide) possesses a two-dimensional sheet structure with sp2 hybridized carbon, which enables it with large surface area and excellent electric conductivity as well as great chemical stability in acidic or alkaline electrolytes [23, 24]. Notably, the sheet films made of reduced graphene have showed fast electron-transfer kinetics and remarkable electrocatalytic activity for a variety of electroactive species . Molybdenum-doped mesoporous graphene composites have been prepared by Dong et al., and such composites exhibited excellent ORR activity through a four-electron dominant reaction pathway . Surfactant-free Au clusters grown on reduced graphene oxide (RGO) sheets have been fabricated by the in situ approach, and such hybrid materials possessed a nearly close onset potential value with Pt/C in ORR . Chen’s group reported a novel technique for the simultaneous synthesis of Au nanoparticle/RGO hybrid materials with enhanced ORR activity recently . Despite the great success have been achieved, the most facile and straightforward method (mechanical mixing and calcination) have been ignored. Polyvinyl pyrrolidone (PVP) has been widely employed as a ligand or protecting agent to prepare monodisperse noble metal clusters with ultrasmall dimensions and narrow size distributions [29, 30]. The integration of PVP Au clusters and RGO by a simple and straightforward approach (mixing and calcination) might offer a promising alternative as ORR catalyst, and this is the primary motivation of our current study.
In this study, nanocomposites based on AuNCs with PVP as ligand and RGO have been prepared and employed as efficient electrocatalysts for ORR. Monodisperse AuNCs were prepared by a wet chemical approach and loaded onto RGO. The composites were calcined, and PVP ligands were removed. With low loading of AuNCs, the intimate interaction of RGO and AuNCs could prevent the agglomeration of AuNCs during pyrolysis, leading to the formation of uniform materials. At higher loading of AuNCs, obvious agglomeration was observed which resulted in diminished activity. All the hybrid materials demonstrated effective activity toward ORR. Among a series of samples tested, the sample with 50 % mass loading of AuNCs demonstrated best activity with a performance comparable with Pt/C, superior than AuNCs alone and RGO alone as well as other samples.
Hydrogen tetrachloroauric acid (III) trihydrate (HAuCl4 · 3H2O, 98 %, Energy Chemicals, Shanghai), polyvinyl pyrrolidone K30 (PVP K30, Boao Biotechnology Co. Ltd, Shanghai), sodium borohydride (NaBH4, 98 %, Aladdin industrial Corporation, Shanghai), Pt/C (20 wt%, Alfa Aesar), graphite powder (99.95 %, Aladdin industrial Corporation, Shanghai), concentrated sulfuric acid (concentrated H2SO4, 98 %, Dingshengxin, Tianjian), sodium nitrate (NaNO3, >99 %, Chemical Reagent Factory, Tianjin), potassium permanganate (KMnO4, >99.5, Aladdin industrial Corporation, Shanghai), hydrogen peroxide (H2O2, 30 %, Dingshengxin, Tianjian), hydrochloric acid (HCl, 36–38 %, Aladdin industrial Corporation, Shanghai), and hydrazine hydrate (H6N2O, >99.7 %, Dingshengxin, Tianjian) were used as received without further purification. Water was supplied by a Barnstead Nanopure Water System (18.3 MΩ cm).
Preparation of PVP Stabilized Au Nanoclusters (PVP-AuNCs)
PVP-AuNCs were synthesized by following a modified procedure in the previous reports [29, 31]. Typically, 555.5 mg PVP was added to the tetrachloroauric acid (III) trihydrate (50 mM, 1 mL) solution and stirred for 30 min in an ice bath. Then, a freshly prepared sodium borohydride aqueous solution (0.1 M, 5 mL) was added under vigorously stirring. The solution color turned from light yellow into dark brown immediately, indicating the formation of PVP-AuNCs. The as-formed AuNCs were dialyzed by a semi-permeable membrane for 3 days to remove all the free ligands.
Preparation of Reduced Graphene Oxide (RGO)
Graphene oxide (GO) was first acquired according to Hummer’s method . Then, RGO was synthesized by following a reported protocol . Briefly, 50 mg GO was dispersed in 50 mL water and sonicated for 1 h to obtain a brown suspension. Then, the dispersion was transferred into a three-neck flask, heated to 80 °C, and 1 mL hydrazine hydrate was added. The solution was kept stirring for 24 h and then filtered. The obtained solid was washed repeatedly with copious methanol and water and fully dried in a vacuum drying oven.
Preparation of RGO Supported PVP-AuNCs
Twenty milligrams of RGO was dispersed in 20-mL water in a round bottom flask. Separately, 20 mg of AuNCs were added into 20-mL water under constant stirring for 20 min. Then, they were mixed with AuNCs-to-RGO mass ratios of 1:2, 1:1, and 2:1, respectively. The mixtures were sonicated for 3 h at room temperature. Subsequently, the solvents were removed by freeze drying, and the residual solids were calcined for 2 h under nitrogen stream at 600 °C to obtain the nanocomposite catalysts of RGO supported AuNCs.
The ultraviolet visible absorption spectrum of AuNCs was tested through a Shimadzu 2600/2700 UV-visible scanning spectrophotometer. For high-resolution transmission electron microscopic (HR-TEM) tests, the samples were dispersed in absolute ethanol and dropcast directly onto a copper grid coated with a holey carbon film. The X-ray diffraction (XRD) were obtained with the Bragg angle (2 θ) changes in the scope of 10°–90° at room temperature by using Bruker D8 diffraction and Cu K alpha radiation (λ = 0.1541 nm). X-ray photoelectron spectroscopy (XPS) analysis was conducted with a VG MultiLab 2000 instrument with a monochromatic Al K X-ray source (Thermo VG Scientific).
The electrochemical tests were performed on an electrochemical workstation with the type of CHI 750E (CH instruments) in 0.1 M KOH solution at room temperature. The platinum wire electrode and Ag/AgCl electrode worked as the counter electrode and the reference electrode, respectively. The working electrode was a glassy carbon (5.61 mm in diameter) rotating ring disk electrode (37 % collection efficiency) from the pine instruments; the working electrode was cleaned with 0.3-um alumina powder on a polishing mica cloth.
Typically, 1-mg catalyst was dispersed in 0.5 mL of anhydrous ethanol solution, and 5-μL Nafion was added into the mixture and sonicated for at least half an hour. Ten-microliter mixed liquor was applied onto the glassy carbon electrode and dried at room temperature. The loading capacity of all catalyst samples on the electrode surface was 40.4 μg cm–2. In all tests, the Ag/AgCl reference electrode was calibrated with respect to a reversible hydrogen electrode (RHE). The calibration of the working electrode and the counter electrode was carried out in a highly pure H2 (99.999 %) saturated electrolyte using a platinum wire. The cyclic voltammograms (CV) were conducted at a scan rate of 10 mV s–1, and the linear sweep voltammograms (LSV) were operated with the rotation rates ranging from 100 to 2500 rpm. All electrochemical tests were conducted in 0.1 M KOH solution, E RHE = E Ag/AgCl + 0.966 V.
Results and Discussion
in which, I d is the disk current, I r is the ring current, and N is the collection efficiency of RRDE (0.37). As can be seen from Fig. 3c, for nanocomposite of AuNCs:RGO (1:1), in the potential range from 0.2 to 0.55 V, the n value varied from 3.0 to 3.3, while the H2O2 yield changed from 46 to 49 %. The relatively low electron transfer number and high H2O2 yield indicated that the oxygen molecule probably took a partially 4e reduction pathway while some oxygen molecules were reduced to H2O2 but not directly to H2O [12, 17, 37].
Figure 4d presents the RRDE results of oxygen reduction for nanocomposites of AuNCs:RGO (1:1) collected with different rotation rates (from 100 to 2500 rpm) in O2-saturated 0.1 M KOH solution. One can see that the voltammetric current increased with the increasing of the rotation rates of the electrode. The corresponding Koutecky Levich (K-L) curve in Fig. 4e displayed a good linearity within the potential range of 0.3 to 0.56 V, implying a first-order reaction kinetics of ORR with respect to the oxygen concentration in the solution. Figure 4f shows the corresponding tafel curves for nanocomposite of AuNCs:RGO (1:1) (red curve) (60 mV dec−1) and Pt/C (black curve) (58 mV dec−1). Note that the two slopes are quite close, which implies that they exhibit similar reaction mechanism on the catalyst surface, where the rate determining step is probably the first electron transfer to oxygen molecule for both catalysts.
One can notice that the ORR activity of the nanocomposite catalysts was remarkably better than AuNCs or RGO alone, and the sample of AuNCs:RGO = 1:1 outperforms the other two composites. These results can be attributed into the following factors: First, the monodisperse PVP-AuNCs are very small with narrow size distribution, which favors for the activation for molecular oxygen [37–39]. As the AuNC loading increases, more effective catalytic sites are provided; however, overloading can cause agglomeration during pyrolysis, hence, lower the catalytic activity. Secondly, the RGO is probably more than a support but also plays an important role in the electronic interaction with AuNCs, evidenced by Au4f binding energy shift in the XPS results shown in Fig. 2b . With appropriate AuNC loading, such interaction might prevent the migration and/or fusion of AuNCs in the RGO, hence, markedly enhanced the stability of the catalyst.
In this work, the composite catalysts of RGO supported AuNCs were fabricated and employed as efficient catalysts for ORR. The hybrid materials exhibited effective ORR catalytic activity in alkaline media. Among a series of samples, the composite with AuNCs:RGO = 1:1 demonstrated the best reactivity, within the context of onset potential and kinetic current density as well as durability. This work highlights the facile and straightforward approach to fabricate hybrid materials based on ultrasmall noble metal clusters with improved electrocatalytic performance. Further investigation with rational design of supported metal nanoclusters to achieve better electrocatalytic properties is still underway.
This work was supported by the National Natural Science Foundation of China (No. 51306040). Z. H. T. acknowledges financial support from the Fundamental Research Funds for Central Universities (SCUT grant nos. 2015ZM012 and 2015PT026), Project of Public Interest Research and Capacity Building of Guangdong Province (2015A010105009), Guangdong Natural Science Funds for Distinguished Young Scholars (No. 2015A030306006), and Guangdong Provincial Science and Technology project (Grant No. 2014A010106027).
CW designed the experiments. NL prepared the samples and conducted all the characterizations and ORR tests. QW assisted the characterizations and the tests. ZT wrote and revised the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
UV-visible absorbance spectrum of AuNCs, TEM images of AuNCs and RGO, Au4f XPS spectrum, and CV measurements of nanocomposites with different AuNCs loadings.
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