Journal of Nanomaterials

Volume 2013 (2013), Article ID 173415, 8 pages

http://dx.doi.org/10.1155/2013/173415

Research Article

Effects of Carbon Nanotubes Acid Treated or Annealed and Manganese Nitrate Thermally Decomposed on Capacitive Characteristics of Electrochemical Capacitors

Chuen-Chang Lin and Chung-Lun Kuo

Department of Chemical & Materials Engineering, National Yunlin University of Science and Technology, 123 University Road, Section 3, Douliu, Yunlin 64002, Taiwan

Received 3 July 2013; Accepted 8 September 2013

Academic Editor: Yun Suk Huh

Copyright © 2013 Chuen-Chang Lin and Chung-Lun Kuo. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Carbon nanotubes (CNTs) directly grown on aluminum foil or nanoporous alumina templates by chemical vapor deposition are treated with acid for different times or annealed at different temperatures. Then, the CNTs are immersed into a manganese nitrate aqueous solution and then manganese oxides are formed by thermally decomposing the manganese nitrate at different temperatures. The longer the time that the CNTs are treated with the acid, the slower the decreasing rate of the specific capacitance. Also, the higher the annealing temperature of the CNTs, the slower the decreasing rate of the specific capacitance. Furthermore, the electrochemical stability for thermally decomposing manganese nitrate at 400°C is better than that at 200 or 300°C and the operational stability with nanoporous alumina templates as a substrate is better than that with Al foil as a substrate.

1. Introduction

Electrochemical capacitors are charge-storage devices which possess higher power density/longer cycle life than batteries [1, 2] and higher energy density than conventional capacitors [3]. Their applications include hybrid power sources, backup power sources, starting power for fuel cells, and burst-power generation in electronic devices [4–8]. Electrochemical capacitors are classified into two types: electric double layer capacitors (EDLC) and pseudocapacitors according to the energy-storage mechanisms. The capacitance of an EDLC arises from the separation of charge at the interface between the electrode and the electrolyte. However, pseudocapacitance arises from redox reactions of electroactive materials with several oxidation states [1, 9–13].

In our previous study [14], carbon nanotubes (CNTs) which were directly grown on nanoporous alumina templates by chemical vapor deposition were modified by radio frequency nitrogen-plasma for different durations. Other methods for the modification of the physical and chemical properties of carbon materials include acid treatment [15, 16] and annealing [16, 17]. In this study, in order to reduce costs, a simpler physicochemical method of acid-treatment or annealing was substituted for the nitrogen-plasma in the modification of CNTs and for improving their organized carbon and hydrophilic nature. The tips of multiwalled CNTs were opened by boiling in 69 wt.% nitric acid for durations of 15 to 45 min and then the multiwalled CNTs were annealed in CO₂ at 525°C for 60 to 100 min in order to eliminate the disordered carbon arising from the tips destruction [18]. CNTs were refluxed in 16 M nitric acid for 3 h and then the CNTs were annealed in nitrogen or hydrogen for 3 h at 450°C or 950°C [19]. CNTs were firstly oxidized by H₂O₂ for opening tube ends as well as shortening the CNT’s length, then treated by HCl for removing the residual oxidized catalyst particles as well as other carbonaceous materials, and finally annealed in air at 450°C for 45 min for maximizing the CNT tip destruction as well as further reducing the amorphous carbon [20]. Single-walled CNTs were annealed in air at increasing temperatures in the range from 300 to 550°C for 1 h [17].

In another previous study [21], manganese-cobalt-zinc oxide films were deposited on graphite foils by radio frequency sputtering with different substrate treatment temperatures and bias potential. In this study, in order to reduce cost, a simple wet method of immersion as well as thermal decomposition was used instead of sputtering and manganese oxides were covered on the surface of the CNT matrix by immersion as well as thermally decomposing Mn(NO₃)₂. In another of our previous studies [22], manganese oxide was coated on a graphite electrode by immersion and durations for immersion were varied to control the amount of manganese oxide coated onto the electrode surface. A definite amount of 50 wt.% Mn(NO₃)₂ aqueous solutions was dripped onto the surface of the CNT electrode by a microsyringe and manganese oxides were formed by thermally decomposing Mn(NO₃)₂ in air at 250°C for 2 h [23]. A mixed aqueous solution of 2 M Ni(NO₃)₂ and 1 M Co(NO₃)₂ was added to the surface of the CNT/graphite electrode by a microsyringe and nickel-cobalt oxides were formed by thermally decomposing nickel as well as cobalt nitrates in air at 250°C for 2 h [24].

The aim of the research described herein is to identify the effects of different substrates, carbon nanotubes acid treated or annealed, and manganese nitrate thermally decomposed on the specific capacitance and operational stability of electrochemical capacitors. Thus, to reduce costs and facilitate scaling up production, the CNTs were modified by the simple physicochemical method of acid treatment for different times or different annealing temperatures and then manganese oxides were deposited on the surface of the CNT matrix by the wet method (immersion) as well as thermally decomposing the Mn(NO₃)₂ at different temperatures in this study.

2. Materials and Methods

Aluminum foil (10 cm × 5 cm × 0.001 cm, purity 99.98%) was degreased in acetone for 5 min. In order to remove the oxide layer from its surface, it was then immersed in 1 M aqueous NaOH for 2 min and subsequently rinsed with deionized water. Next, it was rinsed ultrasonically with alcohol for 15 min.

In order to fabricate well-ordered nanoporous AAO templates through a two-step anodization process, the pretreated aluminum foil was electropolished in a solution of sulfuric acid : phosphoric acid : deionized water in ratios of 2 : 2 : 3. Next, for the first anodization of the aluminum foil, 25 V was applied for 30 min in a 0.5 M sulfuric acid solution at 5°C. Etching of the anodized film followed in a mixture of chromic acid (1.8 wt.%) and phosphoric acid (6 wt.%) for 40 min at 60°C. Then, the second anodization was performed under the same conditions as the first anodization except for a duration of 210 sec. At the end of the second anodization, the previous value of the current density was halved and then the sample was reanodized until reaching a stable potential. This process was repeated eight times until reaching almost 0 V potential. Finally, the pores of AAO templates were further widened after the second anodization by etching in phosphoric acid (5 wt.%) for 20 min. This was in order to completely remove the aluminum oxide (barrier layer) on the pore bottom tips of the AAO templates and then electrochemically deposit catalyst particles at the pore bottom tips of AAO templates.

Before carbon nanotube growth, the cobalt (Co) catalyst particles were electrochemically deposited on the pretreated aluminum foil or at the pore bottom tips of AAO templates in an electrolyte of CoSO₄·7H₂O (5 wt.%) and H₃BO₃ (2 wt.%) by applying an alternating current voltage of 10.5 V (frequency: 60 Hz) for 60 sec. Next, CNTs were grown on the Co-coated aluminum foil or the Co-coated nanoporous alumina templates using thermal CVD with the gas mixture (C₂H₂ = 50 sccm and Ar = 100 sccm) at 600°C for 60 min.

The CNT electrodes were immersed in 61 wt.% HNO₃ aqueous solution for different durations (0, 5, 10, and 15 min) or annealed at different temperatures (300, 350, and 400°C) in air for 1 h.

After being acid treated or annealed in air, the CNTs were immersed into a 50 wt.% Mn(NO₃)₂ aqueous solution for 5 min. Then, manganese oxides were formed by thermally decomposing Mn(NO₃)₂ in air for 2 h at different temperatures (200, 300, and 400°C).

Electrochemical measurements for the prepared manganese oxide/CNT/Al foil composite electrodes or the prepared manganese oxide/CNT/nanoporous alumina templates composite electrodes were performed using an electrochemical analyzer (CH Instruments CHI 608B, USA). The three-electrode cell consisted of Ag/AgCl as the reference electrode, Pt as the counter electrode, and the prepared electrode as the working electrode. The electrolytes were degassed with purified nitrogen gas before voltammetric analysis and nitrogen was passed over the solution during all the measurements. The solution temperature was maintained at 25°C by means of a circulating water thermostat (HAAKE DC3 and K20, Germany). Cyclic voltammetry (CV) in the range of 0-1 V was taken with a 0.5 M aqueous electrolyte (Na₂SO₄) for the prepared electrode. A CV scan rate of 100 mV s⁻¹ was used in all measurements unless otherwise stated. Geometric specific capacitance (mF cm⁻²) was utilized unless otherwise stated.

Surface morphologies of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min) composite electrodes with an Al foil as a substrate and with nanoporous alumina templates as a substrate before or after potential cycling were conducted by a field emission scanning electron microscope (FE-SEM, JEOL JSM-6700F, Japan). Furthermore, an X-ray diffractometer (XRD, Bruker AXS SMART APEX CCD, Germany) with low angles of incidence was used to characterize the crystalline structure of the CNT (treated with acid for 5 min)/Al foil electrode and the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at different temperatures)/CNT (treated with acid for 5 min)/Al foil composite electrode. Moreover, the intensity ratios of the C-C stretching mode to the disorder-induced mode of graphite structure for CNTs treated with acid at different times and CNTs annealed at different temperatures were investigated by a microscope Raman spectrometer (inVia, Renishaw, UK). The chemical environment of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min)/Al foil composite electrode before and after potential cycling was explored by X-ray photoemission spectroscopy (XPS, Kratos AXIS Ultra DLD, Japan).

3. Results and Discussion

Figure 1 shows the effects of time of acid treatment for the CNTs and different charge-discharge cycles on the specific capacitance of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT/Al foil composite electrode. For no acid treatment for CNTs (0 min), their performance of the specific capacitance was worse than that of others (5, 10, and 15 min). The reason behind this behavior may be that after the CNTs being treated with acid, the CNTs were transformed from the hydrophobic nature (contact angle of about 154°) to the hydrophilic nature (contact angle of about 3°-4°) which led to an increase in the amount (from 0.005 mg cm⁻² to 1.14–2.52 mg cm⁻²) of manganese oxide (electroactive material) coated on the CNTs, thus leading to an increase in the capacitance. Furthermore, at the 100th cycle of potential cycle, the shorter the acid treatment time, the higher the specific capacitance of the CNTs (see Figure 1) since the shorter the treatment time, the greater the amount of manganese oxide coated on the CNTs (see Table 1), thus leading to an increase in the specific capacitance. Moreover, during the 100–3000 cycles of potential cycling, the longer the time that the CNTs were treated with acid, the slower the decreasing rate of the specific capacitance (see Figure 1) because the longer the time, the higher the intensity ratio of the C-C stretching mode to the disorder-induced mode of graphite structure for carbon products (see Table 1).

Table 1: The amount of immersion/thermal decomposition of manganese oxide and / of the CNTs modified by different methods and conditions.

CNTs modified by different methods and conditions
Amount of immersion/decomposition of manganese oxide, mg cm⁻²
/

CNTs treated with acid for 5 min
2.52
0.936

CNTs treated with acid for 10 min
1.40
1.005

CNTs treated with acid for 15 min
1.14
1.028

CNTs annealed at 300 °C
0.65
0.985

CNTs annealed at 350 °C
1.13
0.991

CNTs annealed at 400 °C
1.64
1.009

Figure 1: The effects of time of acid treatment for the CNTs and different charge-discharge cycles on the specific capacitance of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT/Al foil composite electrode.

Figure 2 shows the effects of annealing temperatures of the CNTs and different charge-discharge cycles on the specific capacitance of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT/Al foil composite electrode. At the 100th cycle of potential cycle, the higher the annealing temperature of the CNTs, the higher the specific capacitance (see Figure 2). The reason behind this behavior may be that the higher the annealing temperature of the CNTs, the more the electroactive manganese oxide deposited on the CNTs annealed (see Table 1), consequently leading to higher capacitance. Furthermore, during the 100–8000 cycles of potential cycling, the higher the annealing temperature, the slower the decreasing rate of the specific capacitance (see Figure 2). This picture may be explained because the higher the annealing temperature of the CNTs, the greater the amount of organized carbon material (see Table 1).

Figure 2: The effects of annealing temperatures of the CNTs and different charge-discharge cycles on the specific capacitance of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT/Al foil composite electrode.

Therefore, those CNTs treated with acid for 5 min were chosen as better/superior modification method/condition due to a higher capacitance at the 8000th cycle of potential cycling (see Figures 1 and 2) and the shortest time.

Figure 3 shows the effects of thermal decomposition temperatures of Mn(NO₃)₂ and different charge-discharge cycles on the specific capacitance of the manganese oxide/CNT (treated with acid for 5 min)/Al foil composite electrode. The specific capacitance reached a maximum at the 100th cycle of potential cycle. The reason behind this behavior may be explained as follows. Surface morphologies of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min)/Al foil composite electrode before potential cycling and after potential cycling 10, 100, and 1000 cycles are shown in Figures 4(a), 4(b), 4(c), and 4(d), respectively. The surface of the manganese oxide/CNT/Al foil composite electrode (see Figure 4(a)) revealed that manganese oxides were coated on the surface of CNTs and distributed in the CNT entangled matrix; the surface of the manganese oxide/CNT/Al foil composite electrode at 10 cycles of potential cycling (see Figure 4(b)) revealed a small three-dimensional network of flakes; the surface of the manganese oxide/CNT/Al foil composite electrode at 100 cycles of potential cycling (see Figure 4(c)) revealed a large three-dimensional network of flakes which led to increasing surface area as well as then increasing specific capacitance; and the surface of the manganese oxide/CNT/Al foil composite electrode at 1000 cycles of potential cycling (see Figure 4(d)) revealed that parts of three-dimensional network of flakes were dissolved which led to decreasing surface area as well as finally decreasing specific capacitance. XPS spectral data of Mn 2p3/2, Mn 3s, and O 1s for the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min)/Al foil composite electrode before and after potential cycling (10, 100, and 1000 cycles) are also listed in Table 2. The differences of binding energy between the splitting peaks of Mn 3s in Table 2 changed from 5.2 eV to 4.8 eV and 4.9 eV for manganese oxide following the 100 and 1000 cycles of potential cycling. The difference of binding energy between the splitting peaks of Mn 3s decreases with increasing valence of manganese oxide [25–27], so manganese oxide before CV as well as after 10 cycles of potential cycling mainly consists of Mn³⁺ species; manganese oxide after 100 cycles of potential cycling consists of Mn⁴⁺ species; and manganese oxide after 1000 cycles of potential cycling almost consists of Mn⁴⁺ species. Therefore, the specific capacitance reached a maximum at the 100th cycle of potential cycle since the larger the amount of trivalent manganese oxide, the higher the specific capacitance [28]. From the Mn 3s and O 1s data in Table 2, the difference of binding energy between the splitting peaks of Mn 3s decreased with decreasing the amount of Mn-OH (hydroxide). Similar results have been published in previous reports in the literature [25, 26]. From the O 1s data in Table 2, the greater the number of cycles, the greater the amount of H-O-H (water). The charge-discharge cycles of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min)/Al foil composite electrode were investigated in Figure 5, which shows from the 1st to 300th charge-discharge cycle, the area enclosed by 100th charge-discharge cycle is the largest and then the specific capacitance reached a maximum at the 100th cycle of potential cycle. Furthermore, X-ray diffraction patterns of the CNT (treated with acid for 5 min)/Al foil electrode and the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 200, 300, and 400°C)/CNT (treated with acid for 5 min)/Al foil composite electrode are shown in Figures 6(a), 6(b), 6(c), and 6(d), respectively. The operational stability for thermal decomposition of Mn(NO₃)₂ at 400°C is better than that for thermal decomposition of Mn(NO₃)₂ at 200°C or 300°C since more crystal peaks appeared for thermal decomposition of Mn(NO₃)₂ at 400°C by comparing Figures 6(b), 6(c), and 6(d). However, the thermal decomposition temperature of Mn(NO₃)₂ at 300°C was chosen as the best condition due to a higher capacitance at the 8000th cycle of potential cycling (see Figure 3) and a lower temperature. Moreover, the main chemical reaction for thermal decomposition of manganese nitrate solution is Mn(NO₃)₂ → MnO₂ + 2NO₂; but manganese in manganese nitrate is not being completely oxidized to Mn(IV) during thermal decomposition; instead, Mn(II) and Mn(III) are byproducts of the above reaction [29].

Table 2: Mn 2p3/2, Mn 3s, and O 1s of XPS for manganese oxide before and after potential cycling.

Sample

Mn 2p3/2
Mn 3s
Band
O 1s

Eb, eV
Eb(1), eV
Eb(2), eV
, eV
Eb, eV
Area, %

Before CV
641.4
83.1
88.3
5.2
Mn–O–Mn
529.13
67.58

Mn–OH
530.49
24.86

H–O–H
531.85
7.29

10 cycles
641.7
83.4
88.6
5.2
Mn–O–Mn
529.14
47.14

Mn–OH
530.44
24.19

H–O–H
531.43
28.67

100 cycles
641.7
83.6
88.4
4.8
Mn–O–Mn
529.13
47.62

Mn–OH
530.18
16.69

H–O–H
531.32
30.31

1000 cycles
641.8
83.9
88.8
4.9
Mn–O–Mn
529.42
29.99

Mn–OH
530.65
20.52

H–O–H
531.6
49.49

Figure 3: The effects of thermal decomposition temperatures of Mn(NO₃)₂ and different charge-discharge cycles on the specific capacitance of the manganese oxide/CNT (treated with acid for 5 min)/Al foil composite electrode.

(a)

(b)

(c)

(d)

Figure 4: Surface morphologies of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min)/Al foil composite electrode (a) before potential cycling and after potential cycling, (b) at 10 cycles, (c) at 100 cycles, and (d) at 1000 cycles.

Figure 5: The charge-discharge cycles of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min)/Al foil composite electrode.

(a)

(b)

(c)

(d)

Figure 6: X-ray diffraction patterns of (a) the CNT (treated with acid for 5 min)/Al foil electrode and the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at (b) 200°C, (c) 300°C, and (d) 400°C)/CNT (treated with acid for 5 min)/Al foil composite electrode.

Figure 7 shows the effects of different charge-discharge cycles on the specific capacitance of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min) composite electrodes with an Al foil as a substrate and with nanoporous alumina templates as a substrate. At the 100th cycle of potential cycle, the capacitance with an Al foil as a substrate was higher than that with nanoporous alumina templates as a substrate because of the rigid structure of the CNTs grown on nanoporous alumina templates. However, the operational stability with nanoporous alumina templates as a substrate was better than that with an Al foil as a substrate since the surface of the manganese oxide/CNT composite electrode with nanoporous alumina templates as a substrate maintained more three-dimensional network of flakes compared with the surface of the manganese oxide/CNT composite electrode with an Al foil as a substrate at 8000 cycles of potential cycling (see Figure 8).

Figure 7: The effects of different charge-discharge cycles on the specific capacitance of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min) composite electrodes with an Al foil as a substrate and with nanoporous alumina templates as a substrate.

(a)

(b)

Figure 8: Surface morphologies of the manganese oxide (formed by thermally decomposing Mn(NO₃)₂ at 300°C)/CNT (treated with acid for 5 min) composite electrodes (a) with an Al foil as a substrate and (b) with nanoporous alumina templates as a substrate at 8000 cycles of potential cycling.

4. Conclusions

The specific capacitance reached a maximum at the 100th cycle of potential cycle. At the 100th cycle of potential cycling, the shorter the duration that the CNTs were treated with acid, the higher the specific capacitance and the higher the annealing temperature of the CNTs, the higher the specific capacitance. Furthermore, the CNTs treated with acid for 5 min were adopted as a better modification method as well as providing a superior condition and a thermal decomposition temperature of Mn(NO₃)₂ at 300°C was chosen as the best.

Acknowledgment

Financial support by the National Science Council China (under Grant no. NSC 100-2221-E-224-036) is gratefully acknowledged.

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