Journal of Nanomaterials

Journal of Nanomaterials / 2013 / Article
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Low-Dimensional Carbon Nanomaterials 2013

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Research Article | Open Access

Volume 2013 |Article ID 602602 |

Ru Liu, Qingshan Zhao, Yang Li, Guoliang Zhang, Fengbao Zhang, Xiaobin Fan, "Graphene Supported Pt/Ni Nanoparticles as Magnetically Separable Nanocatalysts", Journal of Nanomaterials, vol. 2013, Article ID 602602, 7 pages, 2013.

Graphene Supported Pt/Ni Nanoparticles as Magnetically Separable Nanocatalysts

Academic Editor: Teng Li
Received12 Mar 2013
Accepted10 Sep 2013
Published22 Oct 2013


Efficient recovery of nanocatalysts, especially the graphene supported noble metal catalysts, is a challenge. In this study, we report a simple one-step route to prepare the graphene supported Pt/Ni nanocatalysts with ideal superparamagnetic properties. We demonstrated that they had excellent catalytic activities in the catalytic reduction of aromatic nitro compounds and could be easily separated from the reaction mixtures by applying an external magnetic field.

1. Introduction

Graphene [1], a one-atom-thick planar sheet of hexagonally arrayed sp2 carbon atoms, has attracted tremendous attention in recent years [25]. Especially, graphene has been emerging as a promising supporting in heterogeneous catalytic processes [610] due to its large surface areas [11], impressive mechanical strength [12, 13], chemical inertness, and strong interactions with metal clusters. In recent years, many monometallic and bimetallic catalytic nanoparticles, such as Pd [14], Au [15], Pt [16], Au@Pd [17], and Pt-on-Pd [18], have been successfully dispersed on graphene. The obtained hybrids show impressive catalytic performances in various reactions. However, most of the time, noble metals act as key components of these nanocatalysts, and the efficient recovery of these noble metals from reaction systems remains a challenge. In this respect, a promising solution to solve this problem is the magnetic separation by which the magnetically separable nanoparticles are employed to efficiently separate the catalyst from reaction mixture [19, 20]. In fact, a number of functionalized magnetically separable nanoparticles have been employed in organic reactions as C–C coupling [21], hydrogenation [22], oxidation [23], amination [24], and nitrile hydration [25].

Here, we report a one-step route to prepare the graphene supported Pt/Ni hybrids (Pt/Ni-G) (Scheme 1), which have superparamagnetic properties and show superior catalytic activities in the model reaction of p-nitrophenol (4-NP) reduction.


2. Experimental

2.1. Synthesis of Pt/Ni-G Hybrids

Graphite oxide was prepared by the modified Hummers method [26] and exfoliated into graphene oxide (GO) at a concentration of 0.5 mg/mL by sonication in water [27]. Typically, 100 mL of graphene oxide (GO) was dispersed in 50 mL Tannin (TA) aqueous solution (5 mg/mL) under sonication for 30 min. Then, the excess TA was discarded by centrifugation and the as-prepared TA-functionalized GO was dissolved into 50 mL of water. The concentrations of H2PtCl6 and NiSO4 were adjusted to 4.8 × 10−4 and 1.2 × 10−2 M in the TA-GO solution, respectively; thus, Pt : Ni became 1 : 25. Nitrogen was purged through the solution for 5 min, and then the solution was stirred in airtight conditions. After 30 min of stirring, 0.3 mL of N2H4 H2O (80%) and 2 mL of KOH solution (9.0 M) were injected into the solution. The solution turned black immediately and was kept stirred for 15 min. Finally, the product was washed 8–10 times with ethanol and deionized water for purification purposes.

2.2. Catalytic Reduction of p-Nitrophenol by Pt/Ni-G Hybrids

To investigate the catalytic activity of the as-prepared hybrids, the reduction of p-nitrophenol (4-NP) was tested in a quartz cuvette. In brief, 20 μL of 10−2 M aqueous 4-NP and 40 μL of ultrasonically dispersed Pt/Ni-G solution (0.1 mg/mL) were introduced into 2 mL deionized water, resulting in a constant metal loading of 4.0 μg. Then, 0.3 mL of 10−1 M aqueous NaBH4 was rapidly added. The yellow color of the solution gradually vanished, indicating the formation of p-aminophenol (4-AP) [28]. The time-dependent UV-Vis absorption spectra were recorded in a scanning range of 200–600 nm at 25 ± 1°C.

2.3. Characterization

The as-prepared Pt/Ni-graphene hybrids were characterized by high-resolution transmission electron microscopy (HRTEM) (Philips Tecnai G2 F20), scanning electron microscopy (SEM) (Hitachi S-4800), energy dispersive X-ray spectroscopy (EDX) (Philips Tecnai G2 F20 & Hitachi S-4800), and X-ray photoelectron spectroscopy (XPS) (PerkinElmer, PHI 1600 spectrometer). The X-ray diffraction (XRD) was conducted on a Bruker-Nonius D8 FOCUS diffractometer. The catalytic activity of Pt/Ni-G hybrids was measured by UV absorption spectra on a UV-2802H system with a temperature controller.

3. Results and Discussion

3.1. Synthesis of Pt/Ni-G Hybrids

The XRD diffraction pattern of the Pt/Ni-graphene hybrids was recorded to identify the product (Figure 1). The main diffraction peaks show the face-centered cubic (fcc) structure of both metallic nickel and nickel oxide [29]. Corresponding XPS pattern has authenticated this result. No peaks of Pt are observed because of the pretty low proportion of Pt : Ni, but the of Ni (111) peak shifts to a lower angle compared to that of nickel nanoparticles, indicating the alloy formation where the lattice expansion occurred due to the substitution of nickel atoms by larger platinum atoms [30]. Based on the Ni (111) peak, the crystallite size diameter ( ) of supported nanoparticles is calculated to be about 14.7 nm by Debye-Scherrer equation.

Further evidence for the chemical state and composition of the hybrids was obtained by X-ray photoelectron spectra (XPS). Compared with GO (Figure 2(a)), the full range XPS spectra of the obtained hybrids (Figure 2(b)) show an obvious decrease of O : C atomic ratio. This result should be attributed to the partial removal of the oxide functional groups from GO during the reduction procedure (Figures 2(c) and 2(d)). In addition, clear evidence for the existence of Pt and Ni in the hybrids is readily observed. The Pt 4f spectrum (Figure 2(e)) consists of two peaks for metallic platinum at 71.3 (Pt 4f7/2) and 74.2 eV (Pt 4f5/2), without the peaks for Pt2+ and Pt4+ at 72.8 and 74.6 eV, respectively [31]. This result indicates that Pt is present in the zero-valent metallic state in the alloy nanoparticles. In contrast, the Ni 2p3/2 spectrum (Figure 2(f)) shows a complex structure with intense satellite signals of high binding energy adjacent to the main peaks, which may be ascribed to a multielectron excitation (shake-up peaks) [32]. After these shake-up peaks are considered, the Ni 2p3/2 spectrum has been deconvoluted into two peaks; the first small one located at 852.6 eV corresponds to metallic nickel, and the main one located at 854.0 is assigned to NiO [33]. From the intensities of the deconvoluted XPS signal of Ni, it is obvious that the surface of the nanoparticles is predominately NiO.

The surface morphological study was carried out by using TEM. As shown in Figure 3(a), spherical nanoparticles were homogeneously dispersed on the surfaces of graphene. The sizes of nanoparticles are in the range of 12–19 nm, with a mean size of 15.4 nm. This value is in close agreement with the diameter of 14.7 nm obtained from XRD.

Interestingly, it is easy to find that the graphene supported nanoparticles show a dark core and a comparatively pale shell under the HRTEM image of Pt/Ni-G (Figure 3(b)), indicating the core-shell structure. The lattice spacing in the core of the graphene supported Pt/Ni nanoparticles (marked as “a,” Figure 3(b)) is 0.207 nm, whereas those of pure Pt (111) and Ni (111) are 0.23 and 0.203 nm, respectively. The supported Pt/Ni nanoparticles also show NiO lattice fringes on the particle surface (marked as “b”), with the d-spacing of 0.24 nm corresponding to the NiO (200) planes [34, 35]. These results suggest the alloy formation of Pt and Ni, and the particles would be covered by a NiO layer that was formed by the surface oxidation.

These results are further supported by line scanning analysis. As shown in Figure 3(c), Pt is primarily in the 8 nm core while Ni uniformly is distributed on the whole surface of the Pt/Ni nanoparticle.

Interestingly, quantitative analysis by EDX (Figure 3(d)) suggests that the Pt : Ni atomic ratio is 1 : 26, a value close to the stoichiometric ratio (1 : 25) of the metal precursors. But the surface Pt : Ni atomic ratio measured by XPS is only 1 : 57 (Figure 2(b)). Given that XPS can only penetrate several nanometers of the surface, this result strongly supports the formation of a NiO layer out of the supported Pt/Ni alloy. Quantitative energy dispersive X-ray spectroscopy (EDS) mapping confirms that both Pt and Ni are homogeneously distributed on the whole surface of graphene, shown in Figure 4.

3.2. Magnetic Characterization

Figure 5(a) shows the magnetization versus field plots ( versus hysteresis loops) of Pt/Ni-G hybrids by Quantum Design SQUID-VSM magnetometer under −10 to 10 KOe at room temperature. The saturation magnetization ( ) for the sample is 11.6 emu/g. And the curve does not exhibit hysteresis, indicating that Pt/Ni-G hybrids at room temperature show superparamagnetic behavior. Previous studies on magnetic nanoparticles have demonstrated that when the size of the magnetic particles decreases they change from multidomain to single domain [36]. Therefore, when particles become small enough (typically below 35 nm [37]), the magnetic moment in the domain fluctuates in direction, leading to superparamagnetism (SPM).

3.3. Catalytic Reaction

To probe the catalytic performances of the obtained hybrids, reduction of p-nitrophenol (4-NP) to its corresponding amino derivative was used as the model reaction. In brief, the catalytic reduction of 4-NP by excessive NaBH4 was carried out at room temperature under solvent free condition by using as-synthesized Pt/Ni-G hybrids catalysts. The reaction process was monitored by the UV-Vis spectrophotometry and conducted in the absence of catalysts first. It was observed that the yellow color of the solution deepened after the addition of NaBH4, and a red shift of the peak from 317 to 400 nm occurred. This phenomenon was caused by the formation of p-nitrophenolate ions in alkaline condition [38]. The intensity of the absorbance remained unchanged at 400 nm even after several days, indicating that no reduction of 4-NP occurred. However, in the presence of the Pt/Ni-G hybrids, quick reduction of 4-NP to p-aminophenol (4-AP) by NaBH4 was observed (Figure 5(b)). The absorption of 4-NP at 400 nm completely vanished within 2.5 minutes, accompanied by the fast appearance of the new peaks of 4-AP at 300 nm [39].

The excellent catalytic activity of the Pt/Ni-G hybrids can be attributed to the alloy nature of the supported Pt/Ni nanoparticles, which usually show superior catalytic performance than their monometallic counterparts [40]. In addition, by dispersing on the two-dimensional graphene sheets with large surface areas, the Pt/Ni nanoparticles can prevent aggregation that shields their active catalytic sites. Therefore, 4-NP molecules readily access the catalytic Pt/Ni nanoparticles from two sides of the graphene sheets with limited mass transfer hindrance. Importantly, the Pt/Ni-G hybrids can be easily recycled by using an external magnetic field after the reaction and reused without observable decrease in their catalytic activities.

4. Conclusions

In summary, we developed a simple one-step route to prepare the graphene supported Pt/Ni nanoparticles (Pt/Ni-G). The supported Pt/Ni nanoparticles had a mean diameter of 15 nm and showed superparamagnetic behavior. Catalytic investigation revealed the excellent catalytic activity of the obtained hybrids in the catalytic reduction of aromatic nitro compounds. Notably, the Pt/Ni-G hybrids could be easily separated from the reaction mixtures by applying an external magnetic field. Given their excellent catalytic performances, as well as their magnetically separable nature, these Pt/Ni-G hybrids are ideal recoverable nanocatalysts and may find potential applications in a variety of reactions.


This study was supported by the National Natural Science Funds for Excellent Young Scholars (no. 21222608), Research Fund of the National Natural Science Foundation of China (no. 21106099), Foundation for the Author of National Excellent Doctoral Dissertation of China (no. 201251), the Tianjin Natural Science Foundation (no. 11JCYBJC01700), and the Programme of Introducing Talents of Discipline to Universities (no. B06006).


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