Ultrasonic modification of carbon materials for electrochemical capacitors
The paper is devoted to study the ultrasonic impact on the biomass of natural raw materials, which were used for the creation a nanoporous carbon material (NCM), which was used as electrode material for electrochemical capacitors (EC). The dry shells of apricot seeds were a feedstock, which were modified by the chemical treatment in the phosphoric acid and part of them were impacted by ultrasonic waves for 25 minutes. The NCM, which were obtained by carbonization at 550 °C, were modified by chemical treatment in the nitric acid. Thus, the different of modification NCM was obtained to compare their capacitance characteristics for EC. From experimental data we can do a conclusion, that ultrasonic modification and chemical treatment in nitric acidare improvecapacitance characteristics of NCM for EC.
KeywordsUltrasonic modification Nanoporous carbon material Electrochemical capacitor Chemical treatment Capacity
Nanoporous carbon material
PACS81.05.Uw 82.45.Gj 82.47.Uv 88.80.Fh
The capacity of electrochemical capacitors are mainly determined by high surface are of electrode material and by appropriate pore size distribution [1, 2]. But even for optimal pore size it is not enough to create electrical double-layer (EDL), because notmore than 50% of surface area are taken part in charge/discharge processes .
The reasons, which prevent to create EDL are theavailability of graphite inclusions on the pore surface, which is not wetted with electrolyte, functional groups which are responsible for chemical interaction with the electrolyte, the viscosityof the electrolyte and etc. it means that in general energy barriers appears, which were overcome by ions for creation of EDL on the pore surface.
Obviously, there are another external factors, which have influence on the surface area, electrical and energetic states, and can stimulate the creation of additional EDL surface. Ultrasonic, laser radiation, electromagnetic field can belike external factors, which can be used on the first stage of carbon obtaining and modification or when it is used in EC [4, 5].
There are some papers, where only some aspects are mentioned in this problem, they bring only a fragmented information and do not show us real image of how this factors influence on charge/discharge processes in EC [6, 7]. This paper is devoted to study the mechanisms of EDL creation by ultrasonic modification.
The methods from paper  were used to get NCM, where the main precursor was phosphoric acid. We receive series of samples which half were modified by ultrasonic waves for 25 minutes using a dispersant UZDN-A (operating frequency 22 ± 1,68 kHz) at maximum capacity. Then, all samples were dried at 90 °C to constant weight and the carbonization of feedstock was carried at 550 °C. The part of them were modified by chemical treatment in nitric acid by stirring in a magnetic mixer for 3 hours. All samples were washed to a neutral pH and were dried to constant weight.
Series 1 – processing in the phosphoric acid;
Series 2 – processing in the phosphoric acid with ultrasonic modification for 25 minutes;
Series 3 – processing in the phosphoric and nitric acid;
Series 4 - processing in the phosphoric acid with ultrasonic modification for 25 minutesfollowed by processing in nitric acid;
The electrodes of the investigated EC were formed in the form of lamel from the mixture of:<NCM>:<CA > = < 3>:<1>, where CA is conductive additive. The resulting symmetrical electrodes were seeped by electrolyte, were separated by sealant and placed into the 2-electrodes cell with typical size “2525”, where after it was sealed. The 33% KOH was used as an electrolyte.
The research of electrochemical properties of EC were done by galvanostatic and potentiodynamic cycling. The measurement was made on the complex AUTOLAB PGSTAT12 of the company “ECO CHEMIE” (Netherlands) and stocked with firmware GPES and FRA-2. The galvanostatic measurement was made in the voltage range 0 – 1 V and current of charge/discharge was changed from 10 to 200 mA in increments of 10 mA.
The capacitance was calculated by the equation: C = 2I · t d /[(U m -ΔU) · m], where I is current of charge/discharge, t d is a time of discharge, U m is a maximum voltage, ΔU is a voltages drop of short circuit of discharge circuit, m is a weigh.
Specifications of NCM porous structure (it means surface area and pores total volume) was determined on the basis of analysis of adsorption/desorption isotherms of nitrogen at temperature of its ebullition (-196 °C), received from QuantachromeAutosorbNova2200e.
Results and discussion
In particular, as shown in Fig. 1, even at high currents charge/discharge it shows that samples with ultrasonic modification (series 2 and series 4) have more stable and straight curves, and the smallest decline is observed with increasing current capacity from 10 to 200 mA. This may be due to the fact that under the ultrasonic modification the phosphoric acid filled structural pore in the natural material and the carbonization formed carbon material with appropriate porous microstructure, which provides these properties.
The capacity is greatest for series 4. The decrease of capacity value is with each increase of current charge/discharge, and its average value for series 4 is C = 175 F/g throughout the period of the period of the current charge/discharge 10-200 mA (the maximum value is C = 202 F/g at I = 10 mA).
As shown in Fig. 2, the discharge time was 1 minute at a constant discharge current at 200 mA, which is quite high for this type of electrochemical capacitor  and provides an opportunity to conduct research at a sufficiently high current values.
The results indicate that at the ultrasonic modification with chemical treatment in phosphoric acid of natural material (shells of apricot seeds) and processes in nitric acid of NCM we have an effective electrode material for EC. This allows you to enhance energetic properties of NCM and to increase EC capacity.
The chemical treatment in nitric acid cleans the porous structure of NCM from natural resins and that how it increases the number of effective pore, which are involved in the creation of electrical double-layer (EDL).
As shown in Fig. 4, the NCM, which was modified by chemical treatment in nitric acid (series 3 and series 4), have a greater specific volume of micro and mesopores in the range of diameters from 1 … 4 nm. This suggests that the chemical processing allows us to obtain highly porous material and taking into account the results of galvanostatic research, it improves their capacitance characteristics for use in the EC. We can also note the presence of micropores with diameter of 0.6 … 2 nm in these samples (series 3 and series 4), which probably also plays a role in improving EDL properties for EC.
The ultrasonic modification makes minimal changes in formation of NCM that has an effect in enhancing the capacitance of EC.
The increasing of surface area is observed for samples that were chemically modified in nitric acid, and vast area are occupied by micropores. The ultrasonic modification provides only to expand the range of average diameters of micro- and mesopores.
Calculated surface area S BET by BET theory, the total pore volume V total and average pore diameter d (nm) for different series
S BET , m2/g
V total , cm3/g
According to the analysis of the data in the Table 1, we can conclude that ultrasonic and chemical modification in nitric acid gives an opportunity to get the average values pore diameter values of the smaller values and thus to enhance capacitance characteristics of EC. Also it shows that the chemical treatment in nitric acid makes it possible to increase surface area of 2 times (series 3 and series 4). The ultrasonic modification gives us the same result for samples, which were processed in nitric acid, where the surface surface area of the series 4 is greaterthan series 3up to 200 m2/g, and the average pore diameter is about the same. The highest energy performance was showed by EC, which based on the series 4, where the combination of ultrasonicand chemical modification in nitric acid, we see that the surface area has 2 times greater value from the original series 1, the specific pore volume is greater and the presence of average pore diameter is ≈ 3 nm. It can be concluded that the optimal energy properties forNCM are with a high specific pores volume (V total , cm3/g), surface area (SBET, m2/g) and the small value of the average pore diameterd (nm).
As a result, we can say that ultrasonic modification in phosphoric acid of natural raw materials and chemical treatment in nitric acid enhance energy properties of NCM for EC. Such an approach in the creation of new methods of modification is important for research and allows to get better capacitance characteristics of EC.
The chemical treatment of natural materials (shells of apricot seeds) in phosphoric acid allows us to get the optimal NCM electrode material for EC, which can be operated at high speeds of charge/discharge current at 150-200 mA.
The ultrasonic modification in phosphoric acid at frequency of 22 kHz for 25 minutes provides significant performance improvements of EC about 25%. Also worth noting that chemical treatment of stirring in nitric acid for 3 minutes gave us a significant improvement of NCM capacitance. It gives us to upgrade the EC in 1,5-2 times. Such methods of processing materials for EC electrodes are environmentally safe and easy to use, which is especially cost-effective.
BIR has obtained nanoporous carbon material with ultrasonic modification in phosphoric acid, performed its chemical modification in nitric acid and wrote the paper. MON has calculated the parameters of the porous structure of carbon materials, conducted potentiodynamic researches and analyzed the experimental data. IMB has defined the methods and subjects of investigation and took a part in data analysis and data interpretation. AIK has conducted galvanostatic researches. All read and approved the final manuscript.
BIR is a doctoral at the Physics and Technology Department, Vasyl Stefanyk PreCarpathian National University, Ivano-Frankivsk, Ukraine. IMB is a professor at the Physics and Technology Department, Vasyl Stefanyk PreCarpathian National University, Ivano-Frankivsk, Ukraine. MON is PhD student at the Physics and Technology Department, Vasyl Stefanyk PreCarpathian National University, Ivano-Frankivsk, Ukraine. AIK is PhD student at the Physics and Technology Department, Vasyl Stefanyk PreCarpathian National University, Ivano-Frankivsk, Ukraine.
The authors declare that they have no competing interests.
- 1.Conway BE (1999) Electrochemical supercapacitors: scientific fundamentals and technological applications. Kluwer Academic Plenum Publishers, New YorkGoogle Scholar
- 2.Malyetin Yu, Strizhakova N, Zielinski A, Gozhenko B, Strelko V (2011) Supercapasitors - storage of electrical energy using nanoscale carbon materials. Visn NAS of Ukraine 12:23–29Google Scholar
- 3.Volfkovych YM, Serdyuk TN (2002) Electrochemical capacitors. Elektrokhimiya 38(9):1043-1068Google Scholar
- 4.Budzulyak IM, Rachiy BI, Vaschynskyy VM, Bereschuk MV (2015) Specific capacitance characteristics of carbon activated potassium hydroxide. Phys Chem Solid 16(1):98-103Google Scholar
- 5.Perez-Maqueda L, Duran A, Perez-Rodriguez J (2005) Preparation of submicrontal particles by sonication. Applied Clay Sci 28:245-255Google Scholar
- 6.Zobov EM, Zobov ME, Gabibov FS, Kamilov IK, Manyakhin FI, Naimi EK (2008) Influence of ultrasonic treatment on photoelectric and luminescent properties of crystals ZnSe. Semiconductors 42(3):277–280Google Scholar
- 7.Balaban OV (2014) Ultrasonic modification of electrode materials supercapacitors. Phys Surf Eng 12:163-168 Google Scholar
- 8.Ostafiychuk BK, Budzulyak IM, Rachiy BI, Kuzyshyn MN, Vaschynskyy VN, Mykyteychuk PM, Ivanichok NJ, Merena RI (2014) Adsorption properties of carbon activated with orthophosphoric acid. Chem, Phys Technol Surf 5(2):204–209Google Scholar
- 9.AipingYu, Chabot V, Zhang J (2013) Electrochemical supercapacitors for energy storage and delivery. CRC Press Taylor and Francis GroupGoogle Scholar
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