Research Article | Open Access
Sadia Mehmood, Naveed Kausar Janjua, Farhat Saira, Hicham Fenniri, "AuCu@Pt Nanoalloys for Catalytic Application in Reduction of 4-Nitrophenol", Journal of Spectroscopy, vol. 2016, Article ID 6210794, 8 pages, 2016. https://doi.org/10.1155/2016/6210794
AuCu@Pt Nanoalloys for Catalytic Application in Reduction of 4-Nitrophenol
To enhance and optimize nanocatalyst ability for nitrophenol (4-NP) reduction reaction we look beyond Au-metal nanoparticles and describe a new class of Au nanoalloys with controlled composition for core of AuCu-metals and Pt-metal shell. The reduction of 4-NP was investigated in aqueous media spectroscopically on 7.8 nm Au nanospheres (AuNSs), 8.3 nm AuCuNSs, and 9.1 nm AuCu@Pt core-shell NSs in diameter. The rate constants of the catalyzed reaction at room temperature, activation energies, and entropies of activation of reactions catalyzed by the AuCu@Pt core-shell NSs are found to have different values to those of the pure metal NSs. The results strongly support the proposal that catalysis by nanoparticles is taking place efficiently on the surface of NSs. These core-shell nanocatalysts exhibited stability throughout the reduction reaction and proved that heterogonous type mechanisms are most likely to be dominant in nanoalloy based catalysis if the surface of the NSs is not defected upon shell incorporation.
Dedicated to Professor Dr. Mathias Brust
Versatile optical, chemical, and electronic properties of Au nanoparticles (AuNPs) have made them an attractive candidate in the field of sensing, biomedicine, electronics, imaging, and last but not least catalysis [1–5]. As a catalyst, the unique properties of nanomaterials catalyze different reaction types at much faster rates due to higher surface energies (because of unsaturated valencies of surface atoms of NPs) as compared to their respective bulk partners [6–10]. The key factors controlling the catalytic efficiency of the nanomaterials are shape, size, concentration, and temperature which have attracted intense attention over the past few years [6–9]. Reduction of 4-nitrophenol to 4-aminophenol in the presence of sodium borohydride (BH) on the surface of nanoparticles as catalyst is one of the model catalytic reactions [11–14]. This model reaction has also been investigated on bimetallic nanoparticles during the last decade by many researchers due to additional degrees of freedom and versatility of compositions in bimetallic NPs [15–18].
Reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) was first identified by Pradhan et al. in the presence of catalyst . 4-NP is an organic pollutant, found in industrial waste water, while 4-AP is a potent intermediate in the synthesis of many analgesics and fever reducing drugs, for example, phenacetin and paracetamol, are also used in industry as photographic developer, hair dyeing agent, and corrosion inhibitor [20, 21]. Reduction of 4-NP by sodium borohydride (BH) is thermodynamically feasible but without catalyst this reaction is not favorable . This reaction proceeds in aqueous solution in the presence of either immobilized or free nanoparticles. UV-vis spectroscopy easily monitors the reduction of this organic pollutant by the strong absorption of 4-nitrophenolate anion at 400 nm. Spectrophotometric data also allows the calculation of the rate constant, activation energies, frequency factors, and entropy of activation for this reaction .
Reduction of 4-nitrophenol (4-NP) by BH is used as a model reaction for the catalytic evaluation of the synthesized nanomaterials [21, 22]. Many reports have come forward regarding the adsorption of 4-NP and BH on the surface of the AuNPs, following a simple Langmuir-Hinshelwood model [20, 21]. In the present study as well, it was observed that BH adsorbs on the surface of AuNPs and Au alloys. This was monitored by a corresponding blue shift in the SPR (surface plasmon resonance) of AuNPs from 4 to 9 nm, depending upon the BH concentration used [22, 23]. The higher the BH concentration is, the more the SPR shift will be and the greater the conversion of 4-NP to 4-AP will be.
Gathering all the information mentioned above, there is a need for a kinetic model to explain the important findings for this reaction. The kinetic data was found to be best analyzed in terms of the Langmuir-Hinshelwood model . Both the reactants BH and 4-NP get adsorbed on the surface of nanoparticles during the course of reaction producing a Langmuir isotherm [25–30]. In the final step, the 4-AP is removed during the fast reaction.
2. Materials and Methods
Tetrachloroaurate trihydrate (HAuCl4·3H2O, 99.9%), oleylamine (technical grade, 70%), methanol (98%), and hexane (99%) were purchased from Sigma Aldrich and used without any further purification. Sodium borohydride and 4-nitrophenol were purchased from Fluka. Double distilled water was used in all experiments.
2.2. Synthesis of Au Nanospheres (AuNSs)
Oleylamine (OAm) stabilized gold nanoparticles (AuNPs) of nm diameters were synthesized using previously reported method . According to this method, 50 mmol HAuCl4 was dissolved in 4.6 mL oleylamine (70%); N2 was blown for 10 min over reaction mixture to remove O2. Solution was heated to 160°C; after 15 min of the reaction solution changed from orange to deep red indicating the reduction of Au3+ ions under stirring. Reaction was completed in 60 min indicated by change of UV-vis profile for Au3+ to Au0. The solution was removed from stirring and cooled to room temperature without stopping the stirring and precipitated by adding methanol (Figure 1(a)).
2.3. Synthesis of AuCu Nanospheres (AuCuNSs)
The synthesized AuNSs were used as seeds for fabrication of AuCuNSs alloy. A solution of 0.23 mM C10H14CuO4 (Cu(acac)2) in OAm was mixed with AuNSs solution in OAm and heated at 280°C for 30 min under nitrogen flow and rapid magnetic stirring. After cooling the AuCu sol to room temperature, methanol addition precipitated out the AuCuNSs. These NPs are dispersible in nonpolar solvent, like hexane. The atomic ratio of Au/Cu was set as 1 : 4 by using precursors of appropriate molarity; hence the synthesized NSs were termed as AuCu4 (Table 1). Then all synthesized nanomaterials were phase transferred from organic to aqueous phase by utilizing protocol adopted by Gao et al. .
2.4. Synthesis of Core-Shell AuCu@Pt Nanospheres (AuCu@PtNSs)
For already synthesized AuCu alloy, Pt shell was formed by adding 14.85 mg of C10H14PtO4 dissolved in OAm and keeping temperature at 240°C under nitrogen flow with continuous stirring for 1 hr. The color of solution turned dark black in tone after 5 min of reaction under nitrogen flow. After 1 hr, the sol was cooled down to room temperature to precipitate AuCu@Pt nanoalloys by adding methanol (Figure 1(b)).
Before each catalytic experiment, these NSs were ultrasonicated for 15 min. In a standard quartz cuvette 100 μL of 10 nM AuNPs was added followed by the addition of 100 μL of 1 mM 4-NP solution. The total volume was adjusted to 3.5 mL with water and at the end a freshly prepared ice-cold NaBH4 (100 μL of 100 mM) was added to the mixture of 4-nitrophenol and NSs. The light yellow color of the 4-nitrophenol became immediately yellowish green due to the formation of 4-nitrophenolate ion. The time-dependent reduction was elucidated from the absorbance spectra which were recorded with a time interval of 1 to 5 min. It was observed that the rate constant was increased with the amount of Au nanocatalyst, BH concentration, and temperature. Furthermore, the Au nanocatalyst was found to be quite stable with excellent catalytic ability.
2.5. Characterization of NSs
TEM analyses were done using high resolution Hitachi S-4800 cold field emission SEM. All the catalytic and stability experiments were carried out on an Agilent 8453 UV-visible spectrophotometer at a wavelength range of 190–1100 nm.
3. Results and Discussion
3.1. Catalytic Reduction of 4-Nitrophenol in the Presence of Au, AuCu, and AuCu@Pt Nanospheres (NSs)
OAm stabilized AuNPs and Au alloys were prepared by Yang et al. method  and were further used for catalytic reduction of 4-NP. The stability and the extent of the catalytic activity of AuNPs were investigated in detail under several different chemical and physical conditions. Graphical abstract is the scheme of the AuNPs catalyzed reduction of 4-NP. SPR is highly sensitive to the chemical environment of the species surrounding the AuNPs; hence, activity of AuNPs was studied in terms of the SPR. There was no shift in SPR after adding 4-NP alone, but 4-NP immediately converts to 4-nitrophenolate ion and shifted from 315 nm to 400 nm in the presence of AuNPs (Figure 2(a)). Thus, it is the 4-nitrophenolate ion that reduces to form aminophenol. This can be taken as an evidence that 4-NP has been adsorbed on the surface of the AuNPs.
Bimetallic nanoparticles are particularly useful due to versatile composition and structural variations that may be adjusted in order to improve catalytic behavior. Bimetallic catalysts frequently display catalytic activity that is higher than either constituent material for reduction of 4-NP [15–17]. Accordingly, the reduction rates can be regarded as being independent of the concentration of NaBH4. After adding NaBH4 into the aqueous solution of 4-NP, the color of the solution changed from light yellow to dark yellow due to the formation of 4-nitrophenolate ion. Then, the color of the 4-nitrophenolate ions faded with time after the addition of AuCuNSs. The progress of the reaction could be monitored by UV-vis spectroscopy. The characteristic peak of 4-NP at 400 nm decreased, while at 315 nm a new peak appeared which was assigned to 4-AP (Figure 2(b)) with the progress of reaction. The reaction was finished within 12 min at 25°C. The reaction did not proceed in this period in the absence of AuCuNSs. In Figure 2(b), decrease in absorbance of 4-NP peak from a value of 2.13 to 0.12 in the presence of AuCuNSs is obvious within 15 min of the reaction time, which shows faster reaction kinetics than in the presence of AuNSs where a decrease in absorbance occurred in 30 min from a value of 2.8 to 0.35.
The catalytic reduction of 4-NP is obvious in the presence of AuCu@PtNSs (Figure 2(c)). In this case, the decreasing trend in the peak value is observed at 400 nm and a new peak at 315 is indicative of 4-AP production as the result of reduction reaction [12–15]. Also the SPR of AuCu@Pt nanospheres in the range of 608–615 nm is present showing the stability of nanocatalyst even after the reaction is completed.
3.2. Kinetics of Reaction
Reaction follows pseudo first-order kinetics. To calculate the rate constants, different experiments by varying the reactant concentrations ratios were performed under pseudo first-order kinetics. The rate constant was evaluated by plotting (where is the absorbance of 4-nitrophenolate ion at any time ) versus time and the slope values of the straight lines estimate the rate constantswhere is absorbance of 4-NP, is time, and is rate constant. Plotting versus time in Figure 3, pseudo first-order rate constant values were obtained [13, 14] (also see Table 2). It was observed that the rate constant for the degradation of 4-NP was greater at higher temperatures, that is, 35°C and 40°C, and also the core-shell AuCu@Pt nanocatalyst offered better values of rate constants owing to the synergistic effects of the core and shell strategy.
Reduction of 4-NP on AuNPs has been demonstrated to follow Langmuir-Hinshelwood mechanism statistics . In this mechanism, both reactant molecules adsorb on the surface of NPs before undergoing the bimolecular reaction. When NaBH4 is in excess, the rate is controlled by the adsorption of 4-NP, only. In the case of bimetallic AuCu nanoalloys, adsorbed molecules may diffuse and desorb from the surface; therefore, at higher temperature rate of desorption of molecules is faster, resulting in a higher value of rate constant as compared to that of pure AuNSs .
Increase in the kinetic data is rapid for 30–35°C temperature range. It can be correlated with the fact that this reaction is most favorable at 30–35°C in the presence of AuCu@Pt nanocatalysts. This kind of result was also obtained in previous experiments for Pd nanoalloys for the same reaction .
The activation energy was calculated using Arrhenius equation :
In this case, (rate constant) were plotted against (Kelvin); the frequency factor and were obtained from intercept and slope of straight line, respectively (Figure 4).
Previously oligomer functionalized AuNPs of almost the same diameter were subjected to 4-NP reduction reaction under the same conditions as the current one . A comparison of resultant data with current experiments has shown that rate constant of 2.32 × 10−3 s−1 with oligomer functionalized AuNPs is increased to 9 × 10−3 s−1 proving higher catalytic activity of currently synthesized Au nanocatalyst.
In this study, the synthesized nanospheres of Au, AuCu, and AuCu@Pt were subjected to catalyzing the reduction reaction of 4-nitrophenol to aminophenol. The catalytic activities of Au, AuCu, and AuCu@PtNSs were compared for their rate of reduction of 4-NP. It was shown that AuCu@PtNSs were the most active catalyst for this reaction. This study has also elucidated a synergistic catalytic effect when AuCu is alloyed with a Pt shell for the reduction of 4-NP. The catalysis is attributed to the dominant behavior of the catalyst surface with bifunctional character with an electronically modified surface . The temperature-dependent rate constant of this catalytic reduction reaction has been studied in the temperature range of 25–40°C and it was found that the rate of reduction was enhanced for AuCu@PtNSs at higher temperature, thus manifesting the stability of core-shell NSs.
It was anticipated that the reduction of 4-NP may have been controlled by the surface properties of the Au and its alloy nanoparticles. The morphological difference of the Au, AuCu, and AuCu@Pt nanospheres may pose different catalytic activities as has been observed for the 4-NP reduction; see the HRSEM shown in Figure 5 which are markedly different. The triangular shape indicates alloy core with a shell of Pt; both of these alloy core and monometallic shells are hence responsible for synergistic enhancement of catalytic reduction reaction (Figure 5).
The authors declare that there are no competing interests regarding the publication of this paper.
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