Spherical α-MnO₂ Supported on N-KB as Efficient Electrocatalyst for Oxygen Reduction in Al-Air Battery.

Traditional noble metal platinum (Pt) is regarded as a bifunctional oxygen catalyst due to its highly catalytic efficiency, but its commercial availability and application is often restricted by high cost. Herein, a cheap and effective catalyst mixed with α-MnO₂ and nitrogen-doped Ketjenblack (N-KB) (denoted as MnO₂-SM150-0.5) is examined as a potential electrocatalyst in oxygen reduction reactions (ORR) and oxygen evolution reactions (OER). This α-MnO₂ is prepared by redox reaction between K₂S₂O₈ and MnSO₄ in acid conditions with a facile hydrothermal process (named the SM method). As a result, MnO₂-SM150-0.5 exhibits a good catalytic performance for ORR in alkaline solution, and this result is comparable to a Pt/C catalyst. Moreover, this catalyst also shows superior durability and methanol tolerance compared with a Pt/C catalyst. It also displays a discharge voltage (~1.28 V) at a discharge density of 50 mA cm-2 in homemade Al-air batteries that is higher than commercial 20% Pt/C (~1.19 V). The superior electrocatalytic performance of MnO₂-SM150-0.5 could be attributed to its higher Mn3+/Mn4+ ratio and the synergistic effect between MnO₂ and the nitrogen-doped KB. This study provides a novel strategy for the preparation of an MnO₂-based composite electrocatalyst.

1. Introduction

The efficiency of oxygen reduction reactions (ORR) and n class="Chemical">oxygen evolution reactions (OER) are critical to the energy conversion efficiency of metal air batteries because of their sluggish reaction kinetics [1]. In recent years, Pt-based materials have been developed as typical catalysts for ORR/OER with high catalytic activity [2,3,4]. However, their widespread application in commerce is seriously hindered, because the noble metal Pt is very expensive, and its reserves in earth are scarce. Therefore, in recent years, non-precious metal-based materials were extensively studied for developing a comparable candidate for Pt-based catalysts. Especially, a manganese-based material (such as manganese oxide) with satisfying catalytic activity has been developed recently, because it possesses a lot of advantages, including cheapness, abundance, environmental friendliness, structural flexibility, and bifunctional catalytic activity for ORR/OER [5,6,7,8,9]. Nevertheless, many factors have been found to play important roles in improving the catalytic activity of manganese dioxide for ORR. Firstly, the crystalline phase of manganese dioxide is critical. It has been reported that α-MnO2 exhibits better catalytic activity than other crystalline phases, because of its abundant di-μ-oxo bridges [10,11,12]. Secondly, micromorphology also has a great influence on its performance. Previous studies had shown that metal oxides with nanostructures exhibited good electrocatalytic performance because of their relatively large surface area and big pore volume, which exposes more active sites and facilitates full contact with electrolyte [13,14,15,16]. Thirdly, Mn3+ is believed to favor ORR/OER due to the single electron occupation in σ*-orbital (eg). Therefore, more content of Mn3+ in MnO2 could promote its electrocatalytic performance [17,18].

Although n class="Chemical">manganese-based materials have good electrocatalytic performance as reported, the superiority of synergic catalysts cannot be neglected. Recently, the research emphasis of manganese oxide has focused on ion doping and its composition with other materials, and results indicate that it has better catalytic property than bare manganese oxide. For example, Fe (or Co) ion-doped MnO2 nanosheets (MONSs) grown on the internal surface of macroporous carbon showed improved ORR catalytic activity compared with the un-doped one, because of the co-electrocatalytic function of MnO2 and Fe (or Co ion) [19]. Moreover, the catalyst of Mn2O3-doped MnO supported by reduced grapheme oxide (rGO) was proved to have a better ORR catalytic performance and stronger stability than that of pure MnO. It was believed that the coexisted metal oxide with different valences and rGO had promoted the catalytic performance [20]. In addition, carbon is one of the most important materials for electron transfer, and it could improve the catalytic activity. The coupling of MnO2 with carbon materials may improve its catalytic activities.

Herein, MnO2 spheres are synthesized by the redox reactions between n class="Chemical">K2S2O8 and MnSO4 in acid conditions (denoted as the SM method). These MnO2 spheres mixed with nitrogen-doped Ketjenblack (N-KB) are used as a catalyst for ORR/OER application. This study examines the morphology, structure, and electrochemical properties of MnO2 samples by scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and electrochemical testing. The relationships between the synthesized conditions and electrocatalytic activity of these MnO2-N-KB catalysts are also discussed. Finally, the proposed enhanced catalytic mechanism of these composited catalysts is investigated by controlling the Mn3+ content in MnO2. This work offers a new strategy for the scalable preparation of more efficient MnO2 bifunctional oxygen catalysts for ORR and OER.

2. Experiment

2.1. Preparation of MnO2

First, 1.69 g of manganese sulfate monohydrate, 1.74 g of n class="Chemical">potassium sulfate, and 2.71 g of potassium persulfate were dissolved into 80 mL of deionized water, agitating at least 5 min to form a homogenous aqueous solution. Then, 4 mL of 37% hydrochloric acid was added into the aqueous solution. After agitating another 5 min, the resulting solution was transferred into a 100-mL Teflon lined stainless steel shell autoclave, heated to 120 °C in an oven, and kept at the temperature for 12 h. After it was cooled to room temperature naturally, the as-obtained product was filtrated under vacuum with a membrane of 0.15-μm pore diameter and dried overnight at 80 °C. The obtained product was denoted as MnO2-SM120-12 (S: potassium persulfate; M: manganese sulfate).

For comparison, the n class="Chemical">control samples, such as MnO2-SM150-0.5 and MnO2-SM120-0.5, were also prepared. For the samples of MnO2-SM150-0.5, the synthesis process was the same with that of the MnO2-SM120-12, but the reaction temperature and reaction time were 150 °C and 30 min, respectively. For the samples of MnO2-SM120-0.5, the synthesis process was the same with that of the MnO2-SM120-12, but the reaction temperature and reaction time were 120 °C and 30 min, respectively.

2.2. Preparation of N-KB

First, 0.2 g of ketjenblack (KB) and 1.2 g of melamin were dispersed in 80 mL of deionized n class="Chemical">water by ultrasonic treatment for 30 min. Then, the resulting solution was enclosed into a 100-mL Teflon lined stainless steel shell autoclave, heated to 120 °C in an oven, and kept at the temperature for 24 h. After it was cooled down to room temperature naturally, the as-obtained product was filtrated under vacuum with a membrane of 0.15-μm pore diameter, and dried overnight at 80 °C. After being ground by agate mortar for more than 10 min, the resulting powder was transferred to a piece of porcelain boat, which was then covered with another piece of porcelain boat, and further wrapped by copper foil. The treated porcelain boat was placed into a tube furnace, and then heated to 650 °C for 2 h at a heating rate of 5 °C min−1 in argon flow. After that, it was naturally cooled down to room temperature, and the as-prepared sample was denoted as N-KB.

2.3. Characterization

The morphologies of the as-prepared catn class="Chemical">alysts were characterized by using the scanning electron microscope (FIB 600i, FEI, Hillsboro, OR, USA). The structures of these samples were carried out by X-ray diffraction (XRD, Rigaku D/Max 2550, Tokyo, Japan) with Cu-Kα radiation (λ = 1.5406 Å). The elemental and valence state analysis were characterized by X-ray photoelectron spectroscopy (XPS, K-Alpha1063 spectrometer, Thermo Scientific Co., Waltham, MA, USA).

2.4. Electrochemical Measurements

For electrochemical men class="Chemical">asurements, 2 mg of as-prepared MnO2 and 4 mg of N-KB were dispersed in 950 μL of anhydrous ethanol by sonication for 20 min. Then, 50 μL of Nafion solution (5 wt %) was added and sonicated for another 20 min to get a homogeneous catalytic ink. Then, 8 μL of the ink was loaded onto the surface of glassy carbon disk (the diameter is 5 mm, homemade electrode), and the catalyst loading amount was 0.0815 mg cm−2 (calculated by the mass of MnO2). For comparison, the commercial 20 wt % Pt/C (Johnson Matthey, Royston, UK) was also prepared with the same method.

Linear sweep voltammetry (LSV) and cyclic voltammetry (CV) ORR were performed using a RDE (rotating disk electrode) as working electrode, a double fluid boundary Ag/AgCl electrode n class="Chemical">as the reference electrode, and a platinum wire as the counter electrode in 0.1-M of KOH solution saturated with oxygen on a CHI760E electrochemical workstation. All of the potentials were finally converted to the values versus reversible hydrogen electrode. The ORR catalytic stabilities were evaluated by half-wave potential decay (ΔE1/2) before and after the accelerated durability test (ADT). The ADT was performed by using these catalysts in ORR for 5000 cycles. These experiments were carried out in O2-saturated 0.1 M of KOH solution at room temperature, and the voltage was selected from 0.57 V to 0.82 V (versus (Reversible Hydrogen Electrode) RHE) with a scan rate of 100 mV s−1. Methanol tolerance testing of catalysts was carried out in O2-saturated 0.1 M of KOH and 1.0 M of CH3OH-mixed electrolyte [21].

To further verify the ORR mechanism, the RRDE (rotating ring disk electrode) technique was used, and the n class="Chemical">peroxide percentage and the electron transfer number were calculated based on the equations, which were given as follows [22]: where I represents the disk current, I represents the ring current, N represents the current collection efficiency of the Pt ring (0.37), and n means the electron transfer number [22,23].

The OER activities of the as-prepared samples were n class="Chemical">also carried out by RDE experiments at a scan rate of 10 mV s−1 with a rotation speed of 1600 rpm. The current density was operated from 0 to 16.5 mA cm−2. The long-term durability OER measurements of the catalysts were performed by using chronopotentiometry. The tests were conducted at a current density of 10 mA cm−2, and the test time was 8000 s. Finally, the EIS testes were scanned in the frequency range of 105–0.1 Hz at 1.665 V (versus RHE) with the amplitude of 5 mV in 0.1 M of KOH solution [24].

2.5. Electrochemical Test of Al–Air Batteries

For an Al–air full batteries test, a polished n class="Chemical">aluminum stripe was used as anode, and 6 mol L−1 of a KOH solution containing 0.01 mol L−1 of Na2SnO3, 0.0075 mol L−1 of ZnO, and 0.0005 mol L−1 of In(OH)3 was used as electrolyte. The air electrodes were composed of a gas diffusion layer, a foam nickel current collector, and a catalytic layer. The catalytic layer was fabricated as follows. The as-prepared catalysts (10 mg), N-KB (30 mg), and the 60 wt % polytetrafluoroethylene (PTFE) aqueous solution (~50 mg) were mixed and agitated continuously until a paste appeared. Then, this paste was rolled with a glass rod until it turned into a 2 cm × 2 cm film. In the end, the film and the gas diffusion layer were pressed onto the two sides of nickel foam under the pressure of 10 MPa, and dried at 60 °C overnight. For comparison, the air electrode using commercial 20 wt % Pt/C catalyst was also fabricated with the same method. The full battery performance was measured with a Neware Battery Testing System (Shenzhen, China). A homemade electrochemical cell was used for Al–air battery measurements, with the net volume size of 50 mm × 32 mm × 50 mm, and an air hole with a diameter of 10 mm was used for the test [22,25].

3. Results and Discussion

3.1. Micromorphological and Microstructural Properties

The micromorphology of the synthesized samples was characterized by SEM. Figure 1 shows the SEM images of n class="Chemical">MnO2-SM120-12 (a–c), MnO2-SM120-0.5 (d–f), and MnO2-SM150-0.5 (g–i). As we can see from these images, all three samples display spherical morphology. The average size of the MnO2-SM120-12 sample was ~5.0 μm, and these spheres were composed of nanorods with average diameters of 50 nm. The average diameter of the MnO2-SM150-0.5 spherical particles was ~4.2 μm, and are composed of nanorods with an average diameter of 27 nm. The spherical MnO2-SM120-0.5 sample shows an average diameter of ~2.9 μm, and is composed with nanorods (whose average diameter is about 20 nm). The MnO2-SM150-0.5 shows a smaller size than MnO2-SM120-12, which is mainly because of the higher hydrothermal reaction temperature and shorter hydrothermal reaction time. Although the manganese dioxide formed at a higher reaction speed during the production process, the samples with a smaller particle size could be produced in less reaction time [10]. However, the MnO2-SM150-0.5 sample shows a larger size than MnO2-SM120-0.5; this should be attributed to the effect of the higher reacting temperature, which causes a quicker reaction speed, and the quicker speed leads to a bigger size in the same reaction time.

Figure 1

The SEM images of MnO2-SM120-12 (a–c); MnO2-SM120-0.5 (d–f); and MnO2-SM150-0.5 (g–i).

The structural characterization of n class="Chemical">MnO2-SM120-12 (green line), MnO2-SM120-0.5 (blue line), and MnO2-SM150-0.5 (orange line), were carried out and compared by XRD. As shown in these XRD patterns (Figure 2), the diffraction peaks located at the 12.8, 18.1, 25.8, 28.8, 37.5, 42.0, 49.9, 56.9, 60.3, 65.1, 69.7 and 72.7 positions in all three samples belonged to the (110), (200), (220), (310), (211), (301), (411), (431), (521), (002), (541) and (312) facets, respectively. These sharp peaks indicated the good crystallization property of the samples, and there no other diffraction peaks were observed in these patterns, further indicating the good crystallization property of these samples. The standard card of α-MnO2 (PDF#44-0141) was presented for comparison, and these diffraction peaks matched well with this standard card. It revealed that these as-synthesized MnO2 particles are α-MnO2 particles. Obviously, the diffraction peaks intensity of MnO2-SM150-0.5 (orange line) were inferior to those of the other two samples; this is probably because more defects existed in this sample, which could improve its catalytic activities. Moreover, it has been generally accepted that α-MnO2 exhibits better catalytic activity than other crystalline phases because of its abundant di-μ-oxo bridges [11]. Thus, the α-MnO2 particles prepared here could be used for high-performance catalytic application.

Figure 2

XRD patterns of MnO2-SM120-12 (green line), MnO2-SM120-0.5 (blue line), and MnO2-SM150-0.5 (orange line), the standard PDF card of MnO2 (PDF#44-0141) is carried out for comparison.

XPS spectra were carried out for further elemental and vn class="Chemical">alence state analysis of MnO2-SM120-12, MnO2-SM120-0.5, and MnO2-SM150-0.5 samples. As shown in Figure 3, the high-resolution XPS spectra of Mn 2p for MnO2-SM120-12 (Figure 3a), MnO2-SM120-0.5 (Figure 3b), and MnO2-SM150-0.5 (Figure 3c) are presented, and four peaks located at 642.30, 643.25, 653.80, and 654.80 eV were obtained by peak-differentiating technique. These peaks were assigned to the Mn3+ (2p3/2), Mn4+ (2p3/2), Mn3+ (2p1/2), and Mn4+ (2p1/2) species, respectively [6,26,27]. Moreover, based on the XPS results, the perk areas of Mn3+ and Mn4+ in each sample are presented in Table 1, and the ratio values of Mn3+/Mn4+ (Figure 3d) for MnO2-SM120-12, MnO2-SM120-0.5, and MnO2-SM150-0.5 were calculated as 0.813, 0.512 and 0.965, respectively. As shown in Figure 3d, obviously, the Mn3+/Mn4+ ratio in MnO2-SM150-0.5 (0.965) was higher than that in MnO2-SM120-12 (0.813), which should be ascribed to the higher reacting temperature that causes the faster reaction rate. It is believed that the faster reaction rate could cause more Mn3+ content in MnO2. A higher content of Mn3+ in MnO2 can lead to a better electrocatalytic performance, due to the single electron occupation in the σ*-orbital (eg) of Mn3+ [17,18,28]. In addition, a shorter reacting time could produce MnO2-SM150-0.5 with a smaller size (Figure 1), which would impact its electrocatalytic performance. The Mn3+/Mn4+ ratio in MnO2-SM150-0.5 (0.965) was also higher than that in MnO2-SM120-0.5 (0.512), which should be because the faster reaction rate could cause more Mn3+ content in MnO2 [10].

Figure 3

XPS spectra of Mn 2p for MnO2-SM120-12 (a); MnO2-SM120-0.5 (b); MnO2-SM150-0.5 (c); and the Mn3+/Mn4+ values of the three samples (d).

Table 1

The XPS dates of Mn 2p for MnO2-SM120-12; MnO2-SM120-0.5; MnO2-SM150-0.5; and the corresponding perk areas and Mn3+/Mn4+ values.

Samples	Species	Peak Position (eV)	Peak Area	Mn3+/Mn4+
MnO2-SM150-0.5	2p 3/2 Mn3+	642.60	36429.72	0.965
	2p 3/2 Mn4+	643.60	33877.38
	2p 1/2 Mn3+	654.00	18763.28
	2p 1/2 Mn4+	654.90	23322.43
MnO2-SM120-0.5	2p 3/2 Mn3+	642.30	20298.63	0.512
	2p 3/2 Mn4+	643.25	44859.42
	2p 1/2 Mn3+	653.80	14298.36
	2p 1/2 Mn4+	654.80	22753.79
MnO2-SM120-12	2p 3/2 Mn3+	642.30	29778.53	0.813
	2p 3/2 Mn4+	643.25	45449.07
	2p 1/2 Mn3+	653.80	23045.48
	2p 1/2 Mn4+	654.80	19499.66

3.2. ORR Activity and Stability

The LSV curves for the ORR of MnO2-SM120-12, n class="Chemical">MnO2-SM120-0.5, and MnO2-SM150-0.5 are shown in Figure 4a; these measurements were carried out in 0.1 M of KOH solution at a rotating speed of 1600 rpm. The MnO2-SM150-0.5 sample showed a better ORR catalytic performance than MnO2-SM120-12 at the same test conditions, because the size of the particles in the MnO2-SM150-0.5 sample was smaller, and it contained more Mn3+ in comparison with the MnO2-SM120-12 sample [28,29]. It is clear that MnO2-SM150-0.5 also exhibited a better ORR catalytic performance than the MnO2-SM120-0.5 samples, mainly because of the higher Mn3+ content. As shown in Figure 4b, MnO2-SM150-0.5 (supported on N-KB) exhibited a much better ORR catalytic performance than bare N-KB, with a half-wave potential of 0.76 V and a limiting current density of 6.0 mA cm−2. This phenomenon should be attributed to the synergetic catalytic activity of α-MnO2 and N-KB. It is believed that the intrinsically abundant di-μ-oxo bridges in α-MnO2 could facilitate the ORR process [7,12,19,28]. As observed, the limiting current density (6.0 mA cm−2) of MnO2-SM150-0.5 (supported on N-KB) was higher than Pt/C (~5.0 mA cm−2), despite its lower half-wave potential (0.76 V) compared with Pt/C (~8.2 V). As shown in Figure 4c, the average n value of MnO2-SM150-0.5 was 3.85 (from 3.78 to 3.95), confirming a four-electron (4e−) oxygen reduction mechanism.

Figure 4

(a) Oxygen reduction reaction (ORR) linear sweep voltammetries (LSVs) of MnO2-SM120-12, MnO2-SM120-0.5, and MnO2-SM150-0.5 in 0.1 M of KOH solution at a scan rate of 10 mV s−1 with a rotation speed of 1600 rpm; (b) ORR LSVs of MnO2-SM120-0.5, N-KB, and 20% JM. Platinum (Pt)/C in 0.1 M of KOH solution at a scan rate of 10 mV s−1 with a rotation speed of 1600 rpm; (c) Percentage of peroxide () and the electron transfer number (n) of MnO2-SM150-0.5.

The catalytic stabilities of the n class="Chemical">MnO2-SM150-0.5 and Pt/C samples in ORR were evaluated by the half-wave potential decay (ΔE1/2) before and after the accelerated durability test (ADT) [30]. The ADT was performed by using these catalyst in an ORR for 5000 cycles. These experiments were carried out in an O2-saturated 0.1 M of KOH solution at room temperature, and the voltage was selected from 0.57 V to 0.82 V (versus RHE) with a scan rate of 100 mV s−1. As shown in Figure 5a, the half-wave potential of the MnO2-SM150-0.5 sample (supported on N-KB) exhibited a negative shift of ~33 mV after 5000 cycles; this result is slightly higher than that of Pt/C (~22 mV, Figure 5b), which is probably because of the inferior electroconductibility of MnO2 compared with the noble metal Pt.

Figure 5

LSV curves of MnO2-SM150-0.5 (a) and Pt/C (b) before and after the accelerated durability test (ADT). The ADT was performed by subjecting the catalyst to 5000 circles from 0.57 V to 0.82 V (vs. RHE) in an O2-saturated 0.1 M of KOH solution at room temperature at a scan rate of 100 mV s−1.

3.3. OER Activity and Stability

In addition, the OER activities of three as-prepared samples (n class="Chemical">MnO2-SM120-12, MnO2-SM120-0.5, and MnO2-SM150-0.5) were carried out for further comparing their electrocatalytic performances, and they were tested by RDE experiments at the scan rate of 10 mV s−1 with a rotation speed of 1600 rpm. Generally, OER activities are judged by the potential at the current density from 0 mA cm−2 to 16.5 mA cm−2 [31]. As presented in Figure 6a, MnO2-150-0.5 showed a more negative shift than the MnO2-120-12 and MnO2-SM120-0.5 samples when the current density increased from 0 mA cm−2 to 16.5 mA cm−2, which means that the MnO2-15-0.5 could catalyze OER at a lower overpotential than the MnO2-120-12 and MnO2-SM120-0.5 samples. In other words, the MnO2-150-0.5 sample exhibited much better OER kinetic behavior than the MnO2-120-12 and MnO2-SM120-0.5 samples. Similar to the ORR, the higher content of Mn3+ and smaller size of the α-MnO2 nanorods also played a vital role on the OER. Moreover, the stability tests of the OER activity of the MnO2-SM150-0.5 and Pt/C samples are presented. The long-term durability measurements of the catalysts were performed by using chronopotentiometry. The tests were conducted at a current density of 10 mA cm−2, and the test time was 8000 s. As presented in Figure 6b, after reaction for 8000 s, MnO2-SM150-0.5 showed a good stability in OER, but slightly not as good as Pt/C, indicating that the practical catalytic performance of MnO2-SM150-0.5 needs further improvement to replace the Pt/C.

Figure 6

The oxygen evolution reaction (OER) performances of MnO2-150-0.5 and MnO2-120/12 are evaluated by LSVs in 0.1 M of KOH solution at a scan rate of 10 mV s−1 with a rotation speed of 1600 rpm (a); the stability test of OER activity of MnO2-SM150-0.5 and Pt/C samples in 1.0 M of KOH solution at a current density of 10 mA cm−2 for 8000 s (b).

3.4. EIS Performance

The charge transfer efficiency of the catn class="Chemical">alyst plays an important role in the OER process, as the high electron transfer efficiency could indicate the high catalytic activity. The electrochemical impedance spectroscopy (EIS) is a good method for understanding charge transfer efficiency, because the arc radius size of the EIS curve could indicate the value of electrical resistance. The lower resistance of the sample implies the high electroconductibility. Thus, the EIS method is used for deep insights into the OER process. The EIS tests were scanned in the frequency range of 105–0.1 Hz at 1.665 V (versus RHE) with the amplitude of 5 mV in 0.1 M of KOH solution [17,32]. The Nyquist plots are shown in Figure 7, in which the EIS data (Figure 7 left) have been fitted according to the equivalent circuit (Figure 7 right). The equivalent circuit consisted of Rs, Rf, Rct, C, and CPE, representing the uncompensated solution resistance, intrinsic resistance of the catalyst, charge transfer resistance, capacitance of catalyts, and constant phase element of the double layer, respectively. All of the fitting parameters are listed in Table 2. The Rs relating to the uncompensated solution of the MnO2-120-0.5, MnO2-120-12, and MnO2-150-0.5 samples are 55.72 Ω, 61.75 Ω, and 62.01 Ω, respectively. The Rct relates to the reaction kinetics; MnO2-150-0.5 exhibited a lower charge transfer resistance (146.4 Ω) than those of the MnO2-120-12 (257.1 Ω) and MnO2-120-0.5 (313.5 Ω) samples. Note that it is in good accordance with the OER performance.

Figure 7

Nyquist plots of MnO2-120-0.5, MnO2-120-12, and MnO2-150-0.5 samples obtained from electrochemical impedance spectroscopy (EIS) measurements in 0.1 M of KOH solution at 1.665 V (vs. RHE) and the inserted is the corresponding equivalent circuit.

Table 2

Component values of fitted equivalent circuit based on the Nyquist plots.

Sample	Rs (Ω)	Rf (Ω)	Rct (Ω)	C (F)	CPE-T	CPE-P
MnO2-SM150-0.5	55.72	4.77	146.4	0.001010	0.002368	0.842
MnO2-SM120-12	61.75	8.89	257.1	0.005600	0.003926	0.692
MnO2-SM120-0.5	62.01	9.69	313.5	0.000031	0.002031	0.895

3.5. Methanol Tolerance Performance

The methanol tolerance of the catn class="Chemical">alysts is usually used to evaluate the performance of ORR catalysts in DMFCs (direct methanol fuel cells). The LSV and CV experimental groups (by using the MnO2-SM150-0.5 sample (supported on N-KB) and Pt/C samples as catalysts) and control group were carried out in an O2-saturated 0.1 M of KOH electrolyte for testing the methanol tolerance. These results are presented in Figure 8. As we can see in Figure 8a, when the ORR process was carried out in an O2-saturated 0.1 M of KOH electrolyte with 1.0 M of methanol, the MnO2-SM150-0.5 catalyst exhibited excellent methanol tolerance properties, because there was no negative shift of onset potential and no oxidation currents of methanol, but rather only a slight decrease of the limiting current density (~0.25 mA cm−2) (Figure 8b). However, a strong oxidation current of methanol is shown in Figure 8d with the Pt/C sample by comparison with the background line. Moreover, a larger negative shift of onset potential for ORR (from ~1.0 V to ~0.52 V) is observed in Figure 8c, indicating the poor methanol tolerance of the Pt/C sample in comparison with the MnO2-SM150-0.5 catalyst [9].

Figure 8

LSV curves of MnO2-SM150-0.5 (a) and Pt/C (c) in an O2-saturated 0.1 M of KOH electrolyte with (purple line) and without (blue line) 1.0 M methanol; cyclic voltammetry (CV) curves of MnO2-SM150-0.5 (b) and Pt/C (d) at 20 mV s−1 in an O2-saturated 0.1 M of KOH electrolyte with (red line) and without (black line) 1.0 M methanol.

3.6. Application in Al-Air Battery

For further evaluating the practicn class="Chemical">al catalytic performance of the MnO2-SM150-0.5 sample in an Al–air battery, cell voltages at various current densities and constant current discharge tests were carried out. The commercial Pt/C sample was also investigated for comparison. As the results show in Figure 9a, overall, the cell polarization curve with the MnO2-SM150-0.5 sample was better than that of Pt/C. Specifically, when the discharge current density was lower than 150 mA cm−2, the cell voltages of MnO2-SM150-0.5 were higher than those of the Pt/C sample. However, the cell voltages of the MnO2-SM150-0.5 sample were almost equal to those of Pt/C at the range of 150 mA cm−2–180 mA cm−2. As shown in Figure 9b, MnO2-SM150-0.5 showed a discharge voltage platform of ~1.24 V, which was slightly higher than that of Pt/C (~1.19 V) at the end of the discharge test with a constant current density of 50 mA cm−2 in homemade Al–air batteries. However, it can be observed that the MnO2-SM150-0.5 sample took about 2 h to achieve the smoothing discharge voltage platform, which was longer than that of Pt/C (less than 1 h), indicating that the practical catalytic performance of MnO2-SM150-0.5 needs further improvement to replace the Pt/C.

Figure 9

(a) Polarization curves of Al–air batteries and (b) discharge curves at a constant current density of 50 mA cm−2.

4. Conclusions

In this work, three kinds of α-MnO2 microspheres n class="Chemical">composed with nanorods were synthesized in acid conditions using K2S2O8 and MnSO4 as raw materials by a facile hydrothermal process. The influences of Mn3+ content on the electrocatalytic activity of ORR/OER were also studied. These results demonstrated that catalysts with more Mn3+ content play an important role in electrocatalytic application. Especially, the MnO2-SM150-0.5 sample with higher Mn3+ content showed a better electrocatalytic performance than the MnO2-SM120-0.5 and MnO2-SM120-12 samples. The half-wave potential (E1/2) of the MnO2-SM150-0.5/N-KB sample was 0.76 V (versus RHE), and the limiting current density was about 6.0 mA cm−2. This result could be comparable to those of Pt/C (0.82 V and ~5.0 mA cm−2, respectively). Moreover, the MnO2-SM150-0.5 sample showed an excellent methanol tolerance compared to the Pt/C sample. In addition, the MnO2-SM150-0.5 sample exhibited good ORR catalytic stability; as its half-wave potential only negatively shifted ~33 mV after 5000 cycles. Besides, the MnO2-SM150-0.5 sample exhibited a higher discharge voltage (1.28 V) at a density of 50 mA cm−2 than the Pt/C catalyst (1.19 V) when used in homemade Al–air batteries as cathode catalysts. Thus, this strategy for the preparation of α-MnO2 could provide a scalable preparation method for significant ORR/OER application.