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Article

MnCo2O4/NiCo2O4/rGO as a Catalyst Based on Binary Transition Metal Oxide for the Methanol Oxidation Reaction

by
Mohammad Bagher Askari
1,*,
Sadegh Azizi
2,
Mohammad Taghi Tourchi Moghadam
2,
Majid Seifi
2,
Seyed Mohammad Rozati
2 and
Antonio Di Bartolomeo
3,*
1
Department of Semiconductor, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman 7631818356, Iran
2
Department of Physics, Faculty of Science, University of Guilan, Rasht 413351914, Iran
3
Department of Physics “E. R. Caianiello”, University of Salerno, 84084 Fisciano, SA, Italy
*
Authors to whom correspondence should be addressed.
Nanomaterials 2022, 12(22), 4072; https://doi.org/10.3390/nano12224072
Submission received: 22 October 2022 / Revised: 9 November 2022 / Accepted: 17 November 2022 / Published: 18 November 2022
(This article belongs to the Special Issue Synthesis of Nanocomposites and Catalysis Applications II)
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Abstract

:
The demands for alternative energy have led researchers to find effective electrocatalysts in fuel cells and increase the efficiency of existing materials. This study presents new nanocatalysts based on two binary transition metal oxides (BTMOs) and their hybrid with reduced graphene oxide for methanol oxidation. Characterization of the introduced three-component composite, including cobalt manganese oxide (MnCo2O4), nickel cobalt oxide (NiCo2O4), and reduced graphene oxide (rGO) in the form of MnCo2O4/NiCo2O4/rGO (MNR), was investigated by X-ray diffraction (XRD), scanning electron microscope (SEM), and energy-dispersive X-ray (EDX) analyses. The alcohol oxidation capability of MnCo2O4/NiCo2O4 (MN) and MNR was evaluated in the methanol oxidation reaction (MOR) process. The crucial role of rGO in improving the electrocatalytic properties of catalysts stems from its large active surface area and high electrical conductivity. The alcohol oxidation tests of MN and MNR showed an adequate ability to oxidize methanol. The better performance of MNR was due to the synergistic effect of MnCo2O4/NiCo2O4 and rGO. MN and MNR nanocatalysts, with a maximum current density of 14.58 and 24.76 mA/cm2 and overvoltage of 0.6 and 0.58 V, as well as cyclic stability of 98.3% and 99.7% (at optimal methanol concentration/scan rate of 20 mV/S), respectively, can be promising and inexpensive options in the field of efficient nanocatalysts for use in methanol fuel cell anodes.

1. Introduction

Due to the high dependence of the modern world on electricity, the energy supply is a major concern for many countries. The severe reduction in fossil fuel sources and the harmful effects of excessive use of these fuels on the environment has led the world to use clean and renewable fuel sources. Energy storage and energy production from these renewable sources are two important topics that have attracted the attention of many researchers in various fields [1,2].
Supercapacitors and electrochemical batteries as energy storage equipment [3,4] and solar cells, wind turbines, and fuel cells as energy production–conversion types of equipment [5] have attracted the attention of researchers [6]. Among fuel cells, alcoholic fuel cells have specific properties such as lower operating temperature [7], ease of use, and portability [8]. Moreover, in alcoholic fuel cells, the problems caused by the storage and conversion of hydrogen in fuel cells have been solved. Therefore, due to these characteristics, alcoholic fuel cells have been considered by researchers more than other fuel cells [9].
In a direct methanol fuel cell, methanol oxidation and oxygen reduction occur at the anode and cathode [10], and a Nafion is placed between the anode and cathode as a membrane capable of proton exchange [11]. Among alcohol fuel cells, methanol fuel cells have become popular due to the simple structure of methanol as a fuel in them [12].
The best and most efficient catalysts for the MOR process in alcoholic fuel cells are platinum-based catalysts and other rare and expensive metals [13,14,15]. Considering that these materials are unrivaled and have attracted the attention of researchers in the field of methanol oxidation [16], their high cost is an obstacle to the industrialization of these catalysts. Studies have shown that doping [17], hybridizing [18], and combining [19] these materials with low-cost materials such as metal–organic frameworks (MOFs) [20], types of carbon [21,22,23], or other materials [24,25,26,27,28] is an attractive way to introduce cost-effective catalysts [29]. However, the introduction of a catalyst with no presence of rare metals can still be a bright prospect for researchers in the field of materials and catalysts. Among the proposed materials as catalysts for alcohol oxidation, sulfides and oxidized metals are considered more than other materials [30]. The simple synthesis of these materials, the low cost of their precursors compared to platinum, and their excellent cyclic stability are their advantages over platinum-based composites. Although none of the proposed materials in the alcohol oxidation process can compete with platinum, they can be promising options for advancing energy production from low-cost materials. Typical materials proposed as catalysts for alcoholic fuel cells are Zn1−xMnxCo2O4/rGO [31], Co3O4-Ni3S4-rGO [32], Fe3O4@MoS2/RGO [33], PSS/MnO2/rGO [34], Ni/NiO/MWCNT [35], NiCo2O4/rGO [36], RuO2-MnCo2O4/rGO [37], MoS2/Ni3S2/rGO [38], and ZnO-MWCNT @ Fe3O4 [39]. Most researchers believe that the main disadvantage of metal oxides and sulfides for use as catalysts is their low electrical conductivity [40].
To increase the contact between reactants and the catalyst, the structure of the electrode must be porous, and the high porosity provides a large, involved surface area with reactants, which allows them to reach active sites easily [41].
Metal oxides, in many cases, do not have a significant active site on their surfaces; however, the active surface can be controlled by various synthesis methods [42]. Furthermore, the main challenge related to low electrical conductivity can be solved by composting these materials with conductive materials or doping conductive metals in their structure [43].
One of the attractive options for introducing low-cost catalysts is applying a variety of carbonaceous materials, including carbon nanotubes, reduced graphene oxide, or biomass carbon in the structure of metal oxide-based catalysts. Thus, by using carbon as the most abundant and available element in nature, we have improved the electrical conductivity of catalysts [44,45].
In this study, MN and MNR nanocatalysts coated on nickel foam (NF) were synthesized by a one-step hydrothermal method to investigate their methanol oxidation ability. Considering the fact that few studies have been conducted to investigate the capability of two BTMOs as catalysts in the MOR process, the main novelty and importance of our research is to introduce a new catalyst that includes two BTMOs as well as an easy synthesis process. The role of rGO, as a promoter component in the oxidation process, was considered, and the presented results show that rGO plays an important role in improving the catalyst performance in the methanol oxidation process.

2. Materials and Methods

All precursors used in this study, including manganese nitrate, cobalt nitrate, nickel nitrate, urea, potassium hydroxide, and methanol, were purchased with purity of more than 99% from Merck. X-ray diffraction analysis was performed by EQUINOX INEL3000, and SEM imaging was provided by Phenom Prox. Potentiostat/Galvanostat AUTOLAB3202N device and related electrode systems were used for the electrochemical studies.

2.1. Synthesis and Characterization

2.1.1. Synthesis of MnCo on a Nickel Foam Substrate

Firstly, nickel foam was washed through the three-time sonication process with 0.5 M hydrochloric acid and deionized water (DI) for 10 min. Then, 234 mg of Mn (NO3) 2 with 464 mg of Co (NO3)2⋅6H2O, 150 mg of urea, and 28 mg of NH4F in a solution containing 60 mL of DI water and 10 mL of ethanol were stirred and dissolved for 30 min. Finally, the cleaned nickel foam (1 × 1 cm2) was placed in an autoclave containing the prepared solution and maintained for 12 h at 140 °C. The autoclave cooled, and the electrode was washed several times with DI water and ethanol and dried for 4 h at 45 °C.

2.1.2. Synthesis of MnCo2O4/NiCo2O4

To synthesize MnCo2O4/NiCo2O4, 3 mmol Co (NO3)2⋅6H2O with 1.5 mmol Ni (NO3)2⋅6H2O and 18 mmol urea were dissolved in a solution with 30 mL of distilled water and 20 mL of pure ethanol and stirred for 45 min. Then, the nickel foam coated with MnCo was placed in an autoclave containing the solution at 145 °C for 11 h. Finally, after washing and drying at 40 °C, the electrode was annealed at 400 °C.

2.1.3. Synthesis of MnCo2O4/NiCo2O4/rGO

To synthesize MnCo2O4/NiCo2O4/rGO, 3 mg of rGO was prepared by the Hummers method and was added gradually to the solution that was previously prepared for MnCo2O4/NiCo2O4.

3. Results and Discussion

3.1. Characterizations

To investigate the crystal structure of the synthesized nanomaterials, XRD analysis was performed using a 3000 EQUINOX INEL device with a CuKα lamp at room temperature. The corresponding peaks were observed at angles 2θ from 10° to 80°. Figure 1 shows the XRD pattern for MnCo2O4/NiCo2O4. As can be seen, the index peaks at 18.3°, 36.1°, 37.8°, 43.6°, and 57.9° correspond to the Miller indices (111), (311), (222), (400), and (511), respectively, in agreement with the reference data (JCPDS card: 23-1237) [46], which confirms the spinel structure of MnCo2O4; moreover, the index peaks 31.3°, 36.8°, 59.2°, and 64.9° confirm the presence of NiCo2O4 spinel with the Miller indices (220), (311), (511), and (440), conforming to the reference data (JCPDS card 20-0781) [47]. The NiCo2O4 index peaks are visible at some angles of reflection with the MnCo2O4 index peaks, so the XRD results confirm the presence of both NiCo2O4 and MnCo2O4 spinel.
SEM analysis was used to investigate the surface morphology of the MN and MNR nanocomposites. For this purpose, SEM images were prepared using a SEM microscope device (Phenom Prox, Waltham, MA, USA) at different magnifications. Figure 2a,b shows the MnCo2O4/NiCo2O4 SEM images at different scales. Regarding the SEM images, the obtained morphology may provide the appropriate contacting surface between the catalyst and methanol, which can be a positive factor to facilitate the methanol oxidation process. Considering the MNR, Figure 2c,d also clearly shows the MnCo2O4/NiCo2O4 hybrid placed on the surface of rGO nanosheets. The uniform dispersion of the MN catalyst on the surface of the rGO is also clearly visible, and rGO has been marked in Figure 2d.
The EDX mapping analysis is an appropriate way to investigate the presence of manganese, nickel, cobalt, and oxygen. In this system, the number of X-rays emitted is counted against their energy. The amount of energy of each X-ray determines the characteristic of the element from which the beam is emitted. Therefore, by obtaining the energy spectrum against the counted X-rays, the quantitative and qualitative estimates of the elements in the sample are examined. Figure 3 also shows the EDX diagram, which confirms the presence of the elements Mn, Co, O, and Ni on the nickel foam substrate.

3.2. Electrochemical Studies

3.2.1. Electrode Preparation

The electrochemical properties of the catalysts were studied on a Potentiostat/Galvanostat (AUTOLAB3202N, Wuhan, China) device with a typical three-electrode set-up, involving MnCo2O4/NiCo2O4 and MnCo2O4/NiCo2O4/rGO coated on NF as working electrodes, Ag/AgCl as the reference electrode, and 0.5 mm diameter platinum wire as the auxiliary electrode.

3.2.2. Electrochemical Investigation of Catalysts for Methanol Oxidation

According to many studies, metal oxide-based nanocatalysts are more efficient in the oxidation process of alcohols in alkaline media. Therefore, we investigated the capability of MN and MNR nanocatalysts in the methanol oxidation process. In the initial part, the cyclic voltammetric analysis of the nanocatalysts was performed in a 2 M KOH solution at a scan rate of 20 mV/s.
As can be seen in Figure 4a, both nanocatalysts have capacitive behavior, in that these materials are used as supercapacitor electrodes for electrochemical energy storage devices. Based on the CV analysis of catalysts in KOH, the MNR catalyst has a higher current density than the MN catalyst. The electrochemical impedance spectroscopy (EIS) analysis was performed to further study the electrical properties of catalysts. According to Figure 4b, the EIS analysis was accomplished at open circuit potential (OCP) over the frequency range of 0.01 Hz–100 kHz in a 2 M KOH aqueous solution. The charge transfer resistance (RCT) for MN and MNR in an alkaline medium obtained 9 and 6 ohms, respectively.
The ability of catalysts for MOR was evaluated by performing CV analysis in 2 M KOH solution in the presence of 0.5 M methanol in the potential range of 0 to 0.8 mV.
Figure 4c shows that both nanocatalysts have a methanol oxidation peak in their CV analysis, which confirms the efficiency of the catalysts in the oxidation of methanol. It can also be seen that the oxidation peaks observed in MNR are much higher than in MN. Two important points can be concluded from Figure 4a–c: both nanocatalysts have the ability for MOR and can be used in the anode of methanol fuel cells, and the performance of MNR is better than MN in the methanol oxidation reaction. The MNR nanocatalyst has lower charge transfer resistance than MN and has a higher oxidation current density. This advantage can be related to the presence of rGO in the structure of the catalyst, which improved the performance of the catalyst by increasing the electrical conductivity [48] as well as by increasing the electrochemically active surface area [49,50,51]. In the following, we examine the influence of various parameters such as methanol concentration, scan rates, and temperature in MOR by MNR and MN, and we optimize these parameters for two nanocatalysts.

The Effect of Methanol Concentration on MOR Process by MN and MNR

To study the effect of methanol concentration on the MOR process of MN and MNR nanocatalysts, the CV analysis was performed in the constant concentration of 2 M KOH with different concentrations of methanol (0.3, 0.5, 0.7, 1, 1.5, 2, 2.5, and 3 M) at a scan rate of 20 mV/s.
According to Figure 5a, for the MN catalyst, the oxidation peak has an upward behavior up to 1 M methanol, and then at 1.5 and 2 M methanol concentrations, the peak oxidation current density decreases. In the same behavior, the MNR catalyst showed an upward trend in methanol oxidation activity up to 2 M methanol, and then from 2.5 M methanol, the oxidation current density trend decreased (Figure 5b). It appears that at concentrations higher than the critical concentration of methanol, the surface of the catalyst is saturated and the methanol oxidation process is disrupted.

Investigation of the Effect of Scan Rates on MOR Process by MN and MNR

By choosing one and two molar concentrations of methanol as the optimal concentrations for the two nanocatalysts, MN and MNR, in the process of MOR at different scan rates (20, 40, 60, 80, 100, and 120 mV/s), we investigate the behavior of nanocatalysts by increasing the scan rate. Figure 6a,b shows the CV analysis of MN and MNR at an optimal concentration of methanol in the presence of a 2 M alkaline solution of KOH at different scan rates. As seen in the behavior of both nanocatalysts, capacitive and faradic currents increase with the increasing scan rate. The square root of the scan rate is plotted in terms of the maximum current density for two catalysts in Figure 3c. The linear relationship between these two parameters, with R2 = 0.998 and 0.997 for the two catalysts, indicates the diffusion control mechanism in the methanol oxidation process.
The proposed mechanism of methanol oxidation by nanocatalysts can be proposed in the form of a six-electron mechanism, as follows:
Catalyst   + CH 3 OH → Catalyst   − CH 3 OH ads
Catalyst   − CH 3 OH ads + 4 OH ¯ → Catalyst   − ( CO ) ads + 4 H 2 O + 4 e ¯
Catalyst   + OH ¯ → Catalyst   − OH ads +   e ¯
Catalyst   − CO ads + Catalyst   − OH ads   + OH ¯   → Catalyst   + CO 2 + H 2 O + e ¯

Investigation of the Effect of Temperature on the MOR Process by MN and MNR

As mentioned in the introduction, one of the most important features of methanol fuel cells is the performance of these cells at relatively lower temperatures than other fuel cells. So, to investigate the behavior of MN and MNR catalysts at various temperatures, a series of CV analyses were performed at optimal concentrations and scan rates of 20 mV/s for two nanocatalysts at different temperatures (ambient temperature, 30, 40, and 50 °C). It can be seen from Figure 7a,b that the oxidation current increases with increasing peak temperature. This increase in the current density can be related to the increase in temperature to facilitate OH− adsorption by the catalyst [38]. Moreover, the rising temperature can affect the activation energy of reactants and provide sufficient energy to break chemical bonds of the methanol in the methanol oxidation reaction. Therefore, it can be said that with increasing temperature, the oxidation process of methanol is facilitated by two nanocatalysts. The linear relationship between the temperature rise and maximum oxidation peak current density is shown in the inset of Figure 7a,b.

MN and MNR Stability Evaluation in MOR Process at Optimal Scan Rate and Concentration

To evaluate the stability of nanocatalysts in the methanol oxidation process, 500 consecutive CV cycles of MN and MNR were performed in an alkaline solution at an optimal concentration and scan rate of 60 mV/s. As can be seen, the MNR is almost 99.7% stable after this number of cycles and there is no decrease in its oxidation current density peak (Figure 8a), and this stability rate for MN is about 98.3% (Figure 8b). In order to check the stability of the synthesized nanocatalysts in the MOR process, chronoamperometry analysis was performed at a potential of 0.6 V for a duration of 4000 s. As seen in Figure 8c, MNR and MN have 89.8% and 75.9% stability in current density, respectively. Although both nanocatalysts have adequate stability in the MOR process, the superiority of MNR over MN can also be related to its higher electrical conductivity and higher electrochemical active surface area, which is due to the presence of rGO in the structure of the nanocatalyst.
The performance of the MNR catalyst in the process of methanol oxidation is compared with other reported studies in Table 1. Examining Table 1 shows that the proposed catalyst is competitive with other research in terms of overvoltage and current density.

4. Conclusions

In this study, we introduced nanocatalysts based on transition metal oxides. In this regard, we synthesized the MN and MNR nanocatalysts deposited on the surface of NF by a simple hydrothermal method. After the physical characterization of the nanocatalysts, we studied the capability of nanocatalysts in the MOR process. Although both nanocatalysts performed relatively well in methanol oxidation, the MNR catalyst is more efficient in the MOR process due to the presence of rGO as a two-dimensional material with suitable conductivity and an active surface area. The two proposed nanocatalysts, MN and MNR, with a current density of 14.58 and 24.76 mA/cm2 and 98.3% and 99.7% cyclic stability, respectively, after 500 consecutive CV cycles in the MOR process, can be inexpensive and attractive candidates for use in the anode of methanol fuel cells.

Author Contributions

Conceptualization, M.B.A. and A.D.B.; Data curation, M.B.A., S.A., M.T.T.M., M.S. and S.M.R.; Formal analysis, M.B.A., M.T.T.M. and M.S.; Funding acquisition, A.D.B.; Investigation, S.A., M.T.T.M. and M.S.; Methodology, M.B.A., S.A., S.M.R. and A.D.B.; Resources, S.M.R.; Software, S.A., M.T.T.M. and S.M.R.; Supervision, S.M.R. and A.D.B.; Validation, M.B.A. and A.D.B.; Visualization, M.S.; Writing—original draft, M.B.A.; Writing—review and editing, A.D.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by University of Salerno, grant numbers ORSA218189 and ORSA223384. The APC was funded by A.D.B.

Data Availability Statement

Data are available on request from the authors.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. XRD patterns of MnCo2O4/NiCo2O4.
Figure 1. XRD patterns of MnCo2O4/NiCo2O4.
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Figure 2. SEM images of MN (a,b) and MNR (c,d).
Figure 2. SEM images of MN (a,b) and MNR (c,d).
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Figure 3. EDX mapping analysis of MnCo2O4/NiCo2O4.
Figure 3. EDX mapping analysis of MnCo2O4/NiCo2O4.
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Figure 4. CV curves of MN and MNR (a), EIS plots of MN and MNR in 2M KOH (b), and CV curves of the MN and MNR 2 M KOH and in the presence of 0.5 M methanol (c).
Figure 4. CV curves of MN and MNR (a), EIS plots of MN and MNR in 2M KOH (b), and CV curves of the MN and MNR 2 M KOH and in the presence of 0.5 M methanol (c).
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Figure 5. CV curves of MN (a) and MNR (b) at different concentrations of methanol.
Figure 5. CV curves of MN (a) and MNR (b) at different concentrations of methanol.
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Figure 6. CV curves of MN (a) and MNR (b) at different scan rates and (c) plot of methanol concentration versus maximum current density.
Figure 6. CV curves of MN (a) and MNR (b) at different scan rates and (c) plot of methanol concentration versus maximum current density.
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Figure 7. CV curves of MN (a) and MNR (b) at different temperatures.
Figure 7. CV curves of MN (a) and MNR (b) at different temperatures.
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Figure 8. Cyclic stability of MN (a) and MNR (b) in MOR process after 500 consecutive CV and (c) chronoamperometry analyses of MN and MNR.
Figure 8. Cyclic stability of MN (a) and MNR (b) in MOR process after 500 consecutive CV and (c) chronoamperometry analyses of MN and MNR.
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Table
Table 1. Comparison of electrochemical properties of MNR in MOR with some reported works.
Table 1. Comparison of electrochemical properties of MNR in MOR with some reported works.
Electrode MaterialCurrent CollectorMethanol Concentration (M)Scan Rate (mV s−1)Anodic Potential (V)Peak Current Density (mA cm−2)Ref.
NiCo2O4/rGoGCE0.1 M KOH/0.5 M Methanol500.25616.6[52]
NiO-MOF/rGOGCE1 M NaOH/3 M Methanol500.8275.85[53]
α-CoMoO4 nanoflakesCarbon cloth1 M KOH/0.5 M Methanol500.825[54]
NiCo2O4/carbon xerogelGCE0.5 M NaOH/0.5 M Methanol500.2998[55]
FeO/NiO MOFGCE1 M NaOH/3 M Methanol500.85486.14[56]
NiMoO4/CCarbon paper1 M KOH/2 M Methanol500.4549[57]
Zn1−xMnxCo2O4/rGO with x = 0.4GCE1 M KOH/0.5 M Methanol500.6142.3[58]
Mn3O4-Co3O4-rGOGCE1 M KOH/1 M Methanol1000.4816.5[59]
Mn3O4-CeO2-rGOGCE1 M KOH/0.8 M Methanol900.5117.7[1]
MNRNickel Foam2 M KOH/2 M Methanol200.5824.76This work
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Askari, M.B.; Azizi, S.; Moghadam, M.T.T.; Seifi, M.; Rozati, S.M.; Di Bartolomeo, A. MnCo2O4/NiCo2O4/rGO as a Catalyst Based on Binary Transition Metal Oxide for the Methanol Oxidation Reaction. Nanomaterials 2022, 12, 4072. https://doi.org/10.3390/nano12224072

AMA Style

Askari MB, Azizi S, Moghadam MTT, Seifi M, Rozati SM, Di Bartolomeo A. MnCo2O4/NiCo2O4/rGO as a Catalyst Based on Binary Transition Metal Oxide for the Methanol Oxidation Reaction. Nanomaterials. 2022; 12(22):4072. https://doi.org/10.3390/nano12224072

Chicago/Turabian Style

Askari, Mohammad Bagher, Sadegh Azizi, Mohammad Taghi Tourchi Moghadam, Majid Seifi, Seyed Mohammad Rozati, and Antonio Di Bartolomeo. 2022. "MnCo2O4/NiCo2O4/rGO as a Catalyst Based on Binary Transition Metal Oxide for the Methanol Oxidation Reaction" Nanomaterials 12, no. 22: 4072. https://doi.org/10.3390/nano12224072

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