- Nano Express
- Open Access
Formation of Monodisperse Carbon Spheres with Tunable Size via Triblock Copolymer-Assisted Synthesis and Their Capacitor Properties
Nanoscale Research Letters volume 14, Article number: 124 (2019)
A facile hydrothermal polymerization method has been developed for the preparation of monodisperse carbon spheres (MCSs) using the triblock copolymer F108 as surfactant. The synthesis is based on the ammonia-catalyzed polymerization reaction between phenol and formaldehyde (PF). The resultant MCSs have a perfect spherical morphology, smooth surface, and high dispersity. The particle sizes can be tuned in a wide range of 500~2400 nm by adjusting the dosage of the PF precursor. The activated MCSs with suitable heteroatoms (N and O) doped and a large specific surface area (960 m2 g−1) were obtained. A high-performance electrode of electrical double-layer capacitors fabricated by those active material have an excellent specific capacitance (310 F g−1 at 0.5 A g−1) and outstanding cycling stability (92% capacitance retention after 10,000 cycles). This work provides a new opportunity for the fabrication of MCSs with potential applications.
Over the past few decades, porous carbon materials have been widely used in the fields of gas storage , catalyst supports , supercapacitors , lithium-ion batteries , solar cells , and electronic devices  due to their advantages like the high-specific surface area, good electrical conductivity, and high chemical stability. From the perspective of materials chemistry, porous carbon materials with different morphology and structure such as carbon aerogels , fibers , nanotubes , nanospheres , and activated carbon  have been synthesized successfully. Recently, monodisperse carbon spheres (MCSs) have gained considerable investigation into functional electrode materials for energy storage and conversion devices because of the unique properties such as high stack density, inherent short ion diffusion path way, and good structural stability [12, 13]. The precise control over the morphology, dispersity, smooth surface, and particle size of the MCSs has been the key to meet the requirement for some special practical applications .
The carbonization of pre-synthesized phenolic resin polymer spheres with excellent thermal stability has been demonstrated to be a favored approach for the preparation of MCSs. Zhao group reported a low-concentration hydrothermal route to synthesize highly uniform ordered mesoporous carbon spheres with a tunable size from 20 to 140 nm by using phenolic resol as the carbon precursor . By smartly associating the hydrolysis polymerization reaction mechanism of resorcinol-formaldehyde resins with the classical Stöber silica spheres, Liu and co-researchers successfully developed an extension of the Stöber method for the synthesis of MCSs with a uniform and controllable size on the submicrometer scale . Based on benzoxazine chemistry, Lu and co-workers established a new way to synthesize high dispersity MCSs with tailored sizes in the range of 95~225 nm under precisely programmed reaction temperatures . After these groundbreaking works, tremendous attention has been paid to the design and synthesis of MCSs [18,19,20,21]. However, most of those approaches either require tedious hydrothermal treatment processes, or cannot prepare a wide tunable particle size with smooth surface and narrow size distribution. Therefore, the synthesis of wide tunable sized, highly uniform, and morphological clearly defined MCSs still remains a grand challenge.
In this work, we propose a facile hydrothermal method for the preparation of MCSs using triblock copolymer Pluronic F108 as a surfactant based on the ammonia-catalyzed polymerization reaction of phenol and formaldehyde (PF). The detailed formation mechanism of MCSs has been discussed. The as-prepared MCSs have a perfect spherical morphology and smooth surface and are highly uniform. The particle sizes of MCSs can be tuned in a wide range of 500~2400 nm depending on the concentration of the PF precursor. When used as electrode materials for supercapacitors, the activated MCSs exhibit an excellent electrochemical performance due to the nitrogen and oxygen co-doping and high specific surface.
Synthesis of MCSs
In a typical synthesis, 0.5 mL ammonia aqueous (25 wt%) was mixed with 30 mL ethanol and 50 mL deionized water (H2O). Then, 10 mg Triblock copolymer Pluronic F108 (Mw = 14,600, PEO132-PPO50-PEO132) was dissolved in the mixture solution. Next, 0.2 mL phenol and 0.2 mL formaldehyde (37 wt%) were added respectively, with gentle stirring for 30 min. Finally, the resulting solution was transferred to a 100-mL Teflon-lined autoclave and hydrothermal reaction was regulated at 160 °C for 3 h. The resulting PF resin polymer spheres were obtained by washing with H2O and ethanol for several times. Then, MCSs-x were obtained by annealing the PF resin spheres under N2 atmosphere at 600 °C for 3 h, “x” denotes the phenol and formaldehyde dosage used (for example 0.2, 0.4, 0.6, and 0.8 refer to 0.2, 0.4 ,0.6, and 0.8 mL of phenol and formaldehyde, respectively). The MCSs-x were further chemically activated by KOH (in a mass ratio of 1:2) at 700 °C for 1 h in a N2 atmosphere to prepare the aMCSs-x.
Scanning electron microscopy (SEM) was performed on a NovaNanoSEM230 instrument. Transmission electron microscopy (TEM) was conducted on a Tecnai G2 F20 S-TWIX instrument. X-ray diffraction (XRD) patterns were carried out with a SIEMENS D500 diffractometer with Cu Kα radiation (λ = 0.15056 nm). Raman spectroscopy was performed on a LabRAMHR-800 system. X-ray photo-electron spectroscopy (XPS) analysis was conducted on an ESCALAB 250Xi instrument. Nitrogen adsorption-desorption isotherms were measured at 77 K on an ASAP 2020 instrument.
The electrochemical test of cyclic voltammetry (CV), galvanostatic charge/discharge (GCD), and electrochemical impedance spectroscopy (EIS) was conducted on the CHI660E electrochemical workstation with a three-electrode system in 6 M KOH electrolyte solution. The platinum foil and Hg/HgO were used as the counter electrode and reference electrode, respectively. The working electrodes were fabricated by the mixing of the aMCSs-x, polytetrafluoroethylene (60 wt%), and acetylene black with a mass proportion of 8:1:1. The gravimetric-specific capacitance was calculated by the following equation:
where I (A), Δt (s), ΔV (V), and m (g) are the applied current, discharge time, potential window, and the active material mass of the electrodes, respectively.
Results and Discussion
In this study, we present a possible synthesis mechanism of the MCSs in Scheme 1. Step I is the sol-gel process. In path a, the emulsion droplets formed through the hydrogen-bonding interaction between phenol, formaldehyde, ammonia molecule, ethanol, and water . Ammonia molecules catalyze the polymerization of PF which takes place from the inside of the emulsion droplets . In addition, a large number of PF hydroxymethyl substituted units are produced by rapid reaction of phenol and formaldehyde, which are positioned at the outer surface of the emulsion droplets because of the electrostatic interaction with ammonia ions. Simultaneously, path b shows the self-forming process of F108 micelles formed by triblock copolymer F108 monomers, which are the hydrophobic PPO blocks to form the nucleus inside and the hydrophilic PEO segments outside . Then, in path c, abundant emulsion droplets/PF hydroxymethyl-substituted species can interact with the hydrophilic PEO segments of F108 micelles via hydrogen-bonding interaction to form the emulsion colloidal . In step II, under mild hydrothermal treatment conditions, the species are for further cross-linking polymerization and result in uniform PF resin/F108 copolymer spheres. Finally, in step III, the PF resin/F108 copolymer spheres are followed by carbonization at a high temperature to obtain the MCSs.
The SEM images of MCSs prepared at different PF dosages shown in Fig. 1a–d demonstrate that the MCSs have a perfect spherical morphology with a uniform size. TEM images present in Fig. 1e–h further confirm the MCSs have spherical particles, smooth surface, and high dispersity. The average particle diameter increased from 500 to 2400 nm with the increasing dosage of the PF precursor from 0.2 to 0.8 mL, as shown in Fig. 1i–l. This is because the increasing concentration of the PF precursor led to emulsion droplets and colloidal with a larger size and resulted in a larger final MCS diameter. The use of ammonia in this system is critical to the successful synthesis of such highly dispersive MCSs, which can provide the NH4+ to adhere to the surface of PF spheres and inhibit the aggregation. It is noticed that the MCSs were without any obvious surface defect and structure collapse after high-temperature carbonization. This is the main benefit from the high cross-linking reaction between phenol and formaldehyde. In addition, we also investigated the role of triblock copolymer F108 in this system. Additional file 1: Figure S1a presents the SEM image of the carbon spheres obtained in the absence of F108. The products have a non-uniform particle size and encounter agglomeration. Furthermore, the particle size decreases systematically with increasing F108 dosage from 20 to 80 mg, and small particles and flaky substances appear on the surface of carbon spheres and finally encounter great conglutination (Additional file 1: Figure S1b~d). The reason is that when the triblock copolymer F108 is sufficient in the system, the surface tension decreases, stronger cross-linking interaction occurs, and smaller-sized emulsion droplets and carbon spheres are formed. However, appropriate F108 concentration can balance the surface tension and cross-linking interaction forces and obtain the smooth surface and uniformly sized carbon spheres. In addition, the effect of F108 concentration on the electrode properties of the MCSs was also investigated, as shown in Additional file 1: Figure S2. The result reveals that the triblock copolymer F108 played as a surface active agent for the formation of MCSs.
These synthesized MCSs may have some potential applications such as catalysis, adsorption, and electrode materials for supercapacitors and lithium-ion batteries. In order to understand the structure property of the as-prepared material, the aMCSs-0.4 was selected as a sample further used for characterization analysis. As shown in Fig. 2a, the XRD pattern of aMCSs-0.4 displays two obvious broad diffraction peaks at 25° and 43°, corresponding to the (002) and (100) lattice planes of the amorphous carbon material, respectively. It also indicates the PF resin’s complete conversion to carbon material and the almost removal of triblock copolymer F108 after carbonization. The Raman spectrum of the aMCSs-0.4 (Fig. 2b) exhibits two typical peaks at 1337 cm−1 (D band) and 1590 cm−1 (G band), which correspond to the crystal defects and the hexagonal graphitic property of carbon materials, respectively. The intensity ratio (ID/IG) of carbon materials reflects the graphitization degree . The ID/IG value of the aMCSs-0.4 is about 0.88, which also corroborates the amorphous structures.
As shown in Fig. 2c, the XPS survey of the aMCSs-0.4 exhibits three peaks of C 1s (285.2 eV), N 1s (400.1 eV), and O 1s (532.7 eV). The elemental compositions of C, N, and O in aMCSs-0.4 are 92.54 at%, 1.04 at%, and 6.42 at%, respectively. The results suggest that the ammonia can act as a source of nitrogen to introduce the N element into the carbon frameworks. Figure 2d displays the high-resolution N 1s spectrum of aMCSs-0.4. Four type peaks at 398.6 eV, 399.4 eV, 400.6 eV, and 402.4 eV are correlated to pyridinic-N (N-6), pyrrolic-N (N-5), quaternary-N (N-Q), and pyridine-N-oxides (N-X), respectively . Generally, the presence of nitrogen-based functional groups can not only contribute to addition pseudocapacitance but also can improve the surface wettability and electric conductivity of carbon materials, and thus enhance electrochemical performance [3, 26].
The N2 adsorption/desorption measurements were conducted to investigate the specific surface areas and internal pore structure of the prepared materials. As shown in Fig. 2e, the isotherm of aMCSs-0.4 belongs to a typical type I curve with a steep uptake at low relative pressures, and an almost horizontal plateau at higher relative pressures reveals the microporous structure. The BET surface areas and total pore volume of aMCSs-0.4 are determined to be 960 m2 g−1 and 0.51 m3 g−1, respectively. The pore size distribution curve of aMCSs-0.4 is shown in Fig. 2f, which exhibits the micropore structure with diameters of 0.7 nm, 1.1 nm, and 1.4 nm. The high-resolution TEM image (Additional file 1: Figure S3) is also in good agreement with this result. The micropore carbon structures are generated from the decomposition of F108 during carbonization and the chemical activity of KOH [27, 28].
Here, we employ the aMCSs-0.4 as electrode materials for electrical double-layer capacitors (EDLCs) to demonstrate their structural and performance advantages. The CV curves of aMCSs-0.4 electrode exhibit rectangular shapes at different scan rates from 10 to 100 mV s−1 (Fig. 3a), and the GCD curves display typical triangular profiles (Fig. 3b). These reveal that the aMCSs-0.4 materials have a perfect EDLC performance. As shown in Fig. 3c, the aMCSs-0.4 electrode exhibits an excellent specific capacitance of 310 F g−1 at a current density of 0.5 A g−1, which is higher than other similar MCS electrodes [12,13,14]. The high specific capacitance benefits from the large surface areas and heteroatoms doped. In addition, the specific capacitance still maintains 200 F g−1 even at a large current density of 20 A g−1; it exhibits good capacitance retention. The charge transport and transfer kinetic behaviors can be examined by EIS. The Nyquist plot of the aMCSs-0.4 electrode (Fig. 3d) features a small internal resistance (0.45 Ω) and charge transfer resistance (0.12 Ω) revealing the high electron conductivity of the prepared aMCSs-0.4 materials and good electrode/electrolyte contact interface. The nearly vertical line in the low-frequency region suggests the aMCSs-0.4 electrode has an ideal capacitor property and efficient electrolyte ion diffusion. This result was further confirmed by Bode plots (Fig. 3e), which display the phase angle (− 80.5°) close to − 90°. Furthermore, the aMCSs-0.4 electrode shows good cycling stability with 92% retention over 10,000 cycles at a current density of 20 A g−1 (Fig. 3f). Therefore, from above, all results clearly highlight the attractive potential applications of MCSs for electrodes of EDLCs.
In summary, we have demonstrated a facile surfactant-assisted hydrothermal method to effectively synthesize MCSs. The prepared MCSs have a perfect spherical morphology, uniform size, smooth surface, and tunable particle sizes in a wide range of 500~2400 nm. In particular, this methodology allows the aMCSs-0.4 to have unique structural features with a high surface area (960 m2 g−1) and suitable surface functionality of N and O co-doped. A high-performance electrode of EDLCs has been fabricated by using the aMCSs-0.4 as the active material which delivered an excellent specific capacitance (310 F g−1 at 0.5 A g−1) and outstanding cycling stability (92% capacitance retention after 10,000 cycles). This research provides a new opportunity for the fabrication of MCSs with potential applications.
Electrical double-layer capacitors
Electrochemical impedance spectroscopy
Monodisperse carbon spheres
Phenol and formaldehyde
Ströbel R, Garche J, Moseley PT, Jörissen L, Wolf G (2006) Hydrogen storage by carbon materials. J Power Sources 159(2):781–801
Lam E, Luong JHT (2014) Carbon materials as catalyst supports and catalysts in the transformation of biomass to fuels and chemicals. Acs Catal 4(10):3393–3410
Liu S, Zhao Y, Zhang B, Xia H, Zhou J, Xie W, Li H (2018) Nano-micro carbon spheres anchored on porous carbon derived from dual-biomass as high rate performance supercapacitor electrodes. J Power Sources 381:116–126
Huang Q, Wang S, Zhang Y, Yu B, Hou L, Su G, Ma S, Zou J, Huang H (2016) Hollow carbon nanospheres with extremely small size as anode material in lithium-ion batteries with outstanding cycling stability. J Phys Chem C 120(6):3139–3144
Lin S, Yang B, Qiu X, Yan J, Shi J, Yuan Y, Tan W, Liu X, Huang H, Gao Y, Zhou C (2018) Efficient and stable planar hole-transport-material-free perovskite solar cells using low temperature processed SnO2 as electron transport material. Org Electron 53:235–241
Tong S, Sun J, Yang J (2018) Printed thin-film transistors: research from China. ACS Appl Mater Inter 10(31):25902–25924
Pekala RW, Alviso CT, Kong FM, Hulsey SS (1992) Aerogels derived from multifunctional organic monomers. J Non-Cryst Solids 145:90–98
Yu B, Zhang Q, Hou L, Wang S, Song M, He Y, Huang H, Zou J (2016) Temperature-dependent chemical state of the nickel catalyst for the growth of carbon nanofibers. Carbon 96:904–910
Zhou S, Liu X, Yang K, Zou H (2013) Study of H2 physical adsorption in single-walled carbon nanotube array. AIP Adv 3(8):082119
Liang Z, Liu H, Zeng J, Zhou J, Li H, Xia H (2018) Facile synthesis of nitrogen-doped microporous carbon spheres for high performance symmetric supercapacitors. Nanoscale Res Lett 13:314
Li H, Guo H, Huang K, Liu B, Zhang C, Chen X, Xu X, Yang J (2018) Carbon electrode with conductivity improvement using silver nanowires for high-performance supercapacitor. Appl Phys A 124(11):763
Yang X, Xia H, Liang Z, Li H, Yu H (2017) Monodisperse carbon nanospheres with hierarchical porous structure as electrode material for supercapacitor. Nanoscale Res Lett 12:550
Yu Q, Guan D, Zhuang Z, Li J, Shi C, Luo W, Zhou L, Zhao D, Mai L (2017) Mass production of monodisperse carbon microspheres with size-dependent supercapacitor performance via aqueous self-catalyzed polymerization. ChemPlusChem 82(6):872–878
Tanaka S, Nakao H, Mukai T, Katayama Y, Miyake Y (2012) An experimental investigation of the ion storage/transfer behavior in an electrical double-layer capacitor by using monodisperse carbon spheres with microporous structure. J Phys Chem C 116(51):26791–26799
Fang Y, Gu D, Zou Y, Wu Z, Li F, Che R, Deng Y, Tu B, Zhao D (2010) A low-concentration hydrothermal synthesis of biocompatible ordered mesoporous carbon nanospheres with tunable and uniform size. Angew Chem Inter Ed 49(43):7987–7991
Liu J, Qiao SZ, Liu H, Chen J, Orpe A, Zhao D, Lu GQ (2011) Extension of the Stöber method to the preparation of monodisperse resorcinol–formaldehyde resin polymer and carbon spheres. Angew Chem Inter Ed 50(26):5947–5951
Wang S, Li W-C, Hao G-P, Hao Y, Sun Q, Zhang X-Q, Lu A-H (2011) Temperature-programmed precise control over the sizes of carbon nanospheres based on benzoxazine chemistry. J Am Chem Soc 133(39):15304–15307
Pol VG, Shrestha LK, Ariga K (2014) Tunable, functional carbon spheres derived from rapid synthesis of resorcinol-formaldehyde resins. ACS Appl Mater Inter 6(13):10649–10655
Zhao J, Niu W, Zhang L, Cai H, Han M, Yuan Y, Majeed S, Anjum S, Xu G (2013) A template-free and surfactant-free method for high-yield synthesis of highly monodisperse 3-aminophenol–formaldehyde resin and carbon nano/microspheres. Macromolecules 46(1):140–145
Wang S, Li W-C, Zhang L, Jin Z-Y, Lu A-H (2014) Polybenzoxazine-based monodisperse carbon spheres with low-thermal shrinkage and their CO2 adsorption properties. J Mater Chem A 2(12):4406–4412
Wu Y, Li Y, Qin L, Yang F, Wu D (2013) Monodispersed or narrow-dispersed melamine formaldehyde resin polymer colloidal spheres: preparation, size-control, modification, bioconjugation and particle formation mechanism. J Mater Chem B 1(2):204–212
Lu A-H, Hao G-P, Sun Q (2011) Can carbon spheres be created through the Stöber method? Angew Chem Inter Ed 50(39):9023–9025
Liang C, Dai S (2006) Synthesis of mesoporous carbon materials via enhanced hydrogen-bonding interaction. J Am Chem Soc 128(16):5316–5317
Meng Y, Gu D, Zhang F, Shi Y, Cheng L, Feng D, Wu Z, Chen Z, Wan Y, Stein A, Zhao D (2006) A family of highly ordered mesoporous polymer resin and carbon structures from organic−organic self-assembly. Chem Mater 18(18):4447–4464
Miao L, Zhu D, Liu M, Duan H, Wang Z, Lv Y, Xiong W, Zhu Q, Li L, Chai X, Gan L (2018) Cooking carbon with protic salt: nitrogen and sulfur self-doped porous carbon nanosheets for supercapacitors. Chem Eng J 347:233–242
Zhu D, Jiang J, Sun D, Qian X, Wang Y, Li L, Wang Z, Chai X, Gan L, Liu M (2018) A general strategy to synthesize high-level N-doped porous carbons via Schiff-base chemistry for supercapacitors. J Mater Chem A 6(26):12334–12343
Liu C, Li L, Song H, Chen X (2007) Facile synthesis of ordered mesoporous carbons from F108/resorcinol-formaldehyde composites obtained in basic media. Chem Commun 7:757–759
Liu M, Qian J, Zhao Y, Zhu D, Gan L, Chen L (2015) Core-shell ultramicroporous@microporous carbon nanospheres as advanced supercapacitor electrodes. J Mater Chem A 3(21):11517–11526
This work was supported by the Graduate Independent Exploration and Innovation Project of Central South University (No.2018zzts008).
Availability of Data and Materials
All data and materials are fully available without restriction.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Figure S1. SEM images of MCSs prepared at different dosage of F108: (a) 0 mg, (b) 20 mg, (c) 40 mg and (d) 80 mg. Figure S2. The electrochemical characteristics of the aMCSs-0.4 electrode: (a) GCD curves with current density of 1 A/g at different F108 dosage, (b) Specific capacitance as a function of F108 dosage. Figure S3. The high-resolution TEM image of aMCSs-0.4. (DOCX 1965 kb)
About this article
Cite this article
Liang, Z., Zhang, L., Liu, H. et al. Formation of Monodisperse Carbon Spheres with Tunable Size via Triblock Copolymer-Assisted Synthesis and Their Capacitor Properties. Nanoscale Res Lett 14, 124 (2019). https://doi.org/10.1186/s11671-019-2952-8
- Triblock Copolymer F108
- Monodisperse carbon spheres
- Energy storage and conversion