Abstract
Electrode materials having high capacitance with outstanding stability are the critical issues for the development of flexible supercapacitors (SCs), which have recently received increasing attention. To meet these demands, coating of CeO2 nanoparticles have been performed onto MWCNTs by using facile chemical bath deposition (CBD) method. The formed CeO2/MWCNTs nanocomposite exhibits excellent electrochemical specific capacitance of 1215.7 F/g with 92.3% remarkable cyclic stability at 10000 cycles. Light-weight flexible symmetric solid-state supercapacitor (FSSC) device have been engineered by sandwiching PVA-LiClO4 gel between two CeO2/MWCNTs electrodes which exhibit an excellent supercapacitive performance owing to the integration of pseudocapacitive CeO2 nanoparticles onto electrochemical double layer capacitance (EDLC) behaved MWCNTs complex web-like structure. Remarkable specific capacitance of 486.5 F/g with much higher energy density of 85.7 Wh/kg shows the inherent potential of the fabricated device. Moreover, the low internal resistance adds exceptional stability along with unperturbed behavior even under high mechanical stress which can explore its applicability towards high-performance flexible supercapacitor for advanced portable electronic devices.
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Introduction
Significant research on supercapacitors (SCs) is targeted at accumulative power and energy density; however, recently attention is also focused at lowering manufacture costs and using environmental friendly materials too. To fulfill these requirements, the electrode materials should have high surface area and narrow pore size distribution while providing easy access of electrolyte ions to exhibit high energy storage capacity and good stability. To fabricate such electrode for electrochemical SCs, the electroactive materials should offer efficient mass transport, highly accessible electrochemical surface area and good electron conductivity which cannot be supplied solely by the individual electroactive material1.
To address the above mentioned activities, carbonaceous materials (such as activated carbon, carbon nanotube, graphite oxide, and reduced graphite oxide) have been drawn much attention with good electrode conductivity but limited to higher specific capacitance. In fact, hierarchically structured carbon-based composites with faradaic pseudo-capacitive system could be better candidates for SCs offering larger energy density and higher power density. Such composites combine an electric double layer capacitive (EDLC) and a faradaic pseudo-capacitive systems through nanoarchitecturing. This approach takes advantages as both utilize the fast and reversible faradaic capacitance coming from the electroactive pseudocapacitive species and the indefinitely reversible double-layer capacitance at the electrode-electrolyte interfaces. Carbon nanotube (CNT) has a unique set of properties including high mechanical properties, namely tensile strength and elastic modulus, and still remarkable flexibility, excellent thermal and electric conductivities (102−105 S/cm)2, low percolation threshold through loading weight at which a sharp drop in resistivity occurs and high aspect ratios through length to diameter ratio (L/D). Besides being responsible for high conductivity, the delocalized π-electrons of carbon nanotubes could be utilized to promote adsorption of various moieties on the CNT surface via π–π stacking interactions3. Although highly desirable, it is a great challenge to design and synthesize unique carbon based composites with hierarchical nanostructures in a controllable and much simpler manner, which can tailor the physical and chemical properties of the electroactive materials to meet the basic requirements for the supercapacitor applications.
In this feature article, we have designed and fabricated flexible symmetric solid-state supercapacitor (FSSC) device using CeO2/MWCNTs electrodes sandwiched by PVA-LiClO4. Initially, CeO2 nanoparticles were deposited on MWCNTs surface to form composite nanostructure using simple, low-cost and environment-friendly chemical bath deposition (CBD) method (Fig. 1). There are a few literatures available regarding the supercapacitive performance of CeO2-MWCNTs composite electrodes. Kalubarme et al. prepared carbon nanotube (CNT)/cerium oxide composite and gained specific capacitance of 289 F/g4. Deng et al. reported a specific capacitance of 455.6 F/g at specific current of 1 A/g for CeO2/MWCNTs nanocomposite5. Luo et al. synthesized CeO2/CNTs hybrid electrode through hydrothermal method to achieve a maximum specific capacitance of 818 F/g at scan rate of 1 mV/s6. Nanostructured CeO2 can improve the transport and redox properties along with improved surface to volume ratio compared to other bulk and nanostructured materials. By considering nanocryatalline electroctive metal oxides, the energetics may be substantially reduced due to defects and increases the nonstoichiometry levels and electronic carrier generation7. The fluorite-structured cerium oxide forms a close packed structure array of atoms with four coordinate O2− and eight coordinate Ce4+. As inexpensive and environmentally abundant rare earth element, CeO2 draws most attention with a ground state valance of 4f15d16s2 and hence, it not only forms steady Ce3+ by losing one 5d and two 6s electrons but stable Ce4+ by losing one extra 4f electron8. The oxidation state can be easily changed between Ce3+ and Ce4+, making CeO2 as an outstanding redox material as required for supercapacitor application. The efficient characteristics such as structural defects depending upon the partial pressure of oxygen and high mobility of oxygen vacancies can show the potential in energy-related application9. Hence, the assembly in combination with MWCNTs and nanostructured CeO2 opens new perspectives for the development of electrode material towards high-performance SCs including the following options: (i) exhibits sufficient electrical conductivity; (ii) increases the contact surface area between the electrode and the electrolyte; (iii) protects the electrolyte from decomposition by catalytic reactions with the electrodes; (iv) decreases the transport path length for both electrons and ions by using functionalized MWCNTs as structuring agent while maintaining its conductive nature.
Results and Discussion
Structural analysis
The structural investigation was performed by XRD and results are depicted in Fig. 2a. Both CeO2 and CeO2/MWCNTs films show three intense reflections at the 2θ values of 28.5°, 33.1° and 47.5° corresponding to the (111), (200) and (220) planes of cubic CeO2 (JCPDS card no. 81-0792). The relatively weak and broader reflection at 2θ = 25.8° observed in both the bare MWCNTs and the CeO2/MWCNTs thin films corresponds to amorphous carbon10.
Figure 2b shows the Raman spectra of the bare MWCNTs, CeO2, CeO2/MWCNTs samples. The strongest peak appearing at 457 cm−1 in the spectra of CeO2 and CeO2/MWCNTs corresponds to the Raman F2g mode related to the stretching vibrations of oxygen5. The small hump around 600 cm−1 is assigned to the oxygen defective CeO2 layers11. Moreover, the typical internal vibration of nitrates are associated with the peaks arisen at about 740 and 1049 cm−1, respectively12.
The Raman spectrum of CeO2/MWCNTs also shows the characteristic D band (1346 cm−1) and G band (1578 cm−1), respectively arising from defects and the sp2 hybridized carbon atoms in MWCNTs walls13. The significant G′ (2D) peak (2691 cm−1) is observed due to phonon scattering in MWCNTs; indication of a dense uniform distribution of MWCNTs in the sample14. The peak intensities of D and G bands for CeO2/MWCNTs are enhanced as compared to bare MWCNTs due to the surface enhanced Raman scattering (SERS) effect associated with the CeO2 nanoparticles, which affect the local electromagnetic field15. The relative intensity ratio shows the information about graphitic and disordered carbon. An ID/IG ratio of 0.88 for composite corresponds to the enhanced electronic conductivity of the electrode.
The oxidation states of constituent elements were analyzed by XPS analysis (Fig. 3a). To determine the peak position, the featured survey and core spectra were fitted by nonlinear least-square fitting (NLLSF) method associated with Gaussian–Lorentz distribution function after Shirley integrated background subtraction. The survey spectrum is similar with previous literatures16,17. KLL and MNN are the Auger groups for O and Ce, respectively18.
The main peaks such as Ce4+ 3d3/2 and Ce4+ 3d5/2 related Ce 3d core spectrum can be clearly shown at binding energies of 916.77 and 898.38 eV, respectively (Fig. 3b). Moreover, the Ce3+ 3d3/2 and Ce3+ 3d5/2 peaks are assigned at 900.97 and 882.50 eV, individually. Two additional ‘shake-up’ satellite lines specified by SU1 and SU2 are revealed at 905.63 and 886.49 eV, separately. This Ce 3d spectrum is well consistent with previously reported literatures19. The existence of Ce3+ is a consequence of oxygen vacancies which is superior in nanoparticles. Since, greater number of the atoms are on the surface, the surface atoms will reduce coordination because of reduced particle size5. The oxygen vacancies lead to the transformation between Ce4+ and Ce3+ which is the main factor for enhanced electrochemical reactions on electrode. It is clear that CeO2/MWCNTs composite has a good oxygen release and storage capacity through the reversible redox reactions between Ce3+ and Ce4+ under reducing and oxidizing conditions, respectively.
As shown in Fig. 3c, the peak of C 1s spectrum at 284.14 eV specifies the non-oxygenated C–C bonds whereas the other peaks are due to the oxygenated functional groups present in MWCNTs. The component peak at 284.72 eV is associated with the C atoms directly bonded to hydroxyl group (C–OH). The peak related to carbonyl group (C=O) is indicated at 285.98 eV and the peak at 288.57 eV is due to the carboxyl group (O=C–OH)20.
Three Gaussian components in O 1s spectrum (Fig. 3d) at 529.46, 531.80 and 532.78 eV correspond to the phenolic, carboxylate C–OH and C=O groups, respectively21,22. It is noticeable that the peak assigned at 531.80 eV indicates a greater contribution than from C–OH and C=O bonds. The analyzed results of O 1s spectrum clearly support the details defined by C 1s spectrum.
Morphological analysis
As shown in Fig. 4a, the surface of the stainless steel (SS) substrate is well covered by a complex MWCNT network, while the hierarchical nanoparticle morphology of CeO2 onto SS substrate (as reference) offers plenty of electroactive surface to the electrolyte ions (see Fig. 4b). FESEM images of the CeO2/MWCNTs composite (Fig. 4c,d) reveal that the CeO2 nanoparticles are well encapsulated on the outer surface of MWCNTs. It is well noted that the CeO2/MWCNTs nanostructured material providing high surface area (Supplementary Information S1) with enough space not only opens well-established conductive network for electrolyte diffusion and electron transport but also offers sufficient electroactive sites for electrochemical redox reactions. The cross-linked and intertwisted network of the porous MWCNTs film greatly supports the conductive pathway between oxide layer and the metal substrate, and hence, significantly reduces the charge transfer resistance with increase in the utilization rate of the active materials and consequently, results in the outstanding capacitance value.
The detailed structure is revealed by HRTEM images depicted in Fig. 5a,b. The images depict the anchoring of CeO2 onto MWCNTs to form nanocomposite which is in well agreement with the FESEM images, confirming the successful synthesis of the CeO2/MWCNTs composite with hierarchical structure. The anchoring of CeO2 with the surface attached carboxyl groups of the MWCNTs prevents agglomeration among CeO2 nanoparticles resulting in the higher dispersion23.
Figure 5b displays the lattice fringes with interplanar spacing of 0.31, 0.27, and 0.19 nm, corresponding to the (111), (200), and (220) planes of CeO2 respectively. A set of concentric rings appeared in SAED pattern (Fig. 5c) denote the same (111), (200), and (220) planes of the cubic structured CeO2. Both these results are supportive to the data obtained through XRD studies. EDS elemental mapping analysis of elements C, Ce, and O (shown in Fig. 6b–d, respectively) from a selected area of the hybrid nanostructure (Fig. 6a) confirms the coating of CeO2 nanostructures on MWCNTs.
Supercapacitor properties of the electrodes
The electrochemical properties of the as-grown hierarchical CeO2 nanostructures on the MWCNTs surface were explored at a scan rate of 100 mV/s in 0.5 M NaOH electrolyte within a potential window of −0.5 to −1.1 V (Supplementary Information S2). As reference, CeO2 and MWCNTs nanostructures were also assessed and shown in Fig. 7a. The CV curve of MWCNTs displays a distinct capacitive behavior which is consistent with previous reports24. Both the CeO2 and CeO2/MWCNTs composite electrodes exhibit well-defined oxidation-reduction peaks. Additionally, the CeO2/MWCNTs electrode exhibits the highest current responses, with approximately similar areas in the anodic and cathodic regions, resulting superior capacitance value (inset, Fig. 7a). The scan rate dependent CV curves are shown in Fig. 7b. The CeO2/MWCNTs electrode exhibits a much superior capacitance of 1215.7 F/g at scan rate of 2 mV/s (Fig. 7c). The origin of the peaks is associated to the following reversible redox reaction25:
The CV curve of CeO2/MWCNTs composite electrode principally retains faradaic peaks even at scan rates up to 100 mV/s, which is symptomatic of a fast charge transport, i.e., pseudocapacitance, in the electrode. Both the magnitudes of the current and the potential peak separation increase with the rise in scan rate, and the oxidation and reduction peaks shift towards more positive and negative values, respectively, mainly due to polarization and ohmic resistance appeared during the faradaic processes26.
The cyclic stability of the electrode was executed at 100 mV/s scan rate within the same potential window. The unperturbed CV curves even at 10000 cycles are depicted in the inset of Fig. 7d. Notably, the composite electrode exhibits very high capacitance retention, maintaining 92.3% of its initial capacitance at 10000 cycles (Fig. 7d). These remarkable results prove that CeO2/MWCNTs is chemically stable in NaOH electrolyte with very low degradation, constantly delivering power upon long-term cycling with good reversibility in spite of its pseudocapacitive behavior. In fact, MWCNTs supports the prevention of the degradation of electroactive material to electrolyte solution by strong synergy during electrochemical reaction process.
The effect of the current density on the specific capacitance of MWCNTs, CeO2, and CeO2/MWCNTs electrodes was investigated by galvanostatic charge/discharge (CD) studies. Figure 8a demonstrates the CD curves of the supercapacitors at a CD current density of 1.5 mA/cm2. The MWCNTs electrode shows electric double layer capacitance (EDLC), exhibiting the typical triangular CD plot. However, both the CeO2 and the CeO2/MWCNTs electrodes show pseudocapacitive characteristics27. Moreover, the CeO2/MWCNTs composite electrode shows the greatest discharge time at a same current density of 1.5 mA/cm2, exhibiting greater capacitance as shown in inset of Fig. 8a. The discharge curve includes two stages in the voltage ranges between −0.5 to −0.8 and −0.8 to −1.1 V. The first stage, with a comparatively smaller duration is attributed to EDLC; whereas, the second stage, with a much longer discharge duration, involves the combination of EDLC and faradaic capacitance originating from MWCNTs and CeO2, respectively28. Furthermore, CD curves for composite were analyzed with different current densities ranging from 1.5 to 3 mA/cm2 and depicted in Fig. 8b. Utilizing both the charge storage mechanisms, the CeO2/MWCNTs electrode yields a maximum specific capacitance of 1044.2 F/g at a current density of 1.5 mA/cm2, decreasing to 573.5 F/g at 3 mA/cm2 (Fig. 8c). A little iR drop at the starting of every discharge curves is observed due to the presence of internal resistance29.
Non-intrusive and highly sensitive EIS measurements were performed in the 0.1 Hz to 100 kHz frequency range. As shown in Nyquist plots in Fig. 8d, a semicircle in the high frequency region is observed, resulting from the charge-transfer resistance (RCT) associated to the faradaic reactions. The equivalent series resistance (RS) constituted by the electrolyte resistance, the contact resistance between the active material and the current collector, and the intrinsic resistance of the electro-active material is obtained from the high frequency intersect of the impedance curve30. The electrode shows low values of RS (1.87 Ω/cm2) and RCT (1.06 Ω/cm2), these obtained low values are of great importance as they affect the power and energy performance, but also reduce undesired heat dissipation throughout the charge–discharge processes31. The reason behind the optimal behavior is that the MWCNTs can effectively transport the current to and from the active material (Supplementary Information S3). Additionally, they prevent the agglomeration of the CeO2 nanoparticles, facilitating the contact between the active material (CeO2) and the electrolyte, which in turns lead to the improved utilization of the active material (i.e., to high capacitance). Moreover, the fitted equivalent circuit of the Nyquist plot is presented in the inset of Fig. 8d. The constant phase element (CPE) represents the double layer capacitance occurring at the interface between the electroactive material and the electrolyte32. The impedance due to the diffusion of OH− ions within pores of the CeO2 electrode is represented by the Warburg element, and is dependent upon the frequency whereas RL represents the leakage resistance during the electrochemical activities33.
Figure 9a shows the Bode plots of the real (C′) and imaginary (C″) components of the capacitance against the frequency. The variation of C″ with the frequency shows a maxima at the characteristic frequency (f0 = 20.6 Hz), defining the relaxation time as \({{\rm{\tau }}}_{0}=\frac{1}{{{\rm{f}}}_{0}}\). The time \({{\rm{\tau }}}_{0}\) is a measure of the rate capability of the supercapacitor as it is normally associated with the swiftness of the capacitive discharge. The relaxation time is the minimum time required to deliver the stored energy with an efficiency greater than 50% of its maximum value and redirects the shift among the resistive and capacitive activities of the supercapacitor34. The small relaxation time constant of 48.5 ms suggests the excellent charge-discharge rate performance of the electrode material. The experimental impedance data has been converted to imaginary capacitance (C″) using the following equation.
The phase angle is −77° (close to 90°) as exhibited in the Bode plot (Fig. 9b), suggesting excellent capacitive response35. As capacitive and resistive impedances are identical at phase angle of −45°, relaxation time constant can be estimated by \({{\rm{\tau }}}_{0}=\frac{1}{{{\rm{f}}}_{0}}\) at that particular phase and found to be 43.6 ms, consistent with the results obtained from the previous result.
Electrochemical performance of flexible symmetric solid-state supercapacitor (FSSC)
Recent literatures suggest that the measurements performed on two-electrode cells are more effective than those made on three-electrode cells to ascertain the performance of the electrode materials (including the synthesis route) and electrolytes for commercial purposes. Considering the fast ionic transport property and high capacitance of the CeO2/MWCNTs composite, a symmetric solid-state supercapacitor device of dimension 3.5 × 3.5 cm2 was assembled using PVA-LiClO4 gel as solid-state electrolyte and separator. As shown in Fig. 10, the resulting device could be bent and twisted easily, which combines additional advantage compared to other SCs.
The fabricated symmetric SC showed the characteristic pseudocapacitive behavior exhibiting oxidation and reduction peaks in the potential up to 1.2 V (Fig. 11a). The scan rate dependent CV curves of the FSSC consist of well-defined and almost symmetric peaks as a result of the reversible redox reactions of CeO2 involving Li+ insertion/release. Till date, many reports are available on high performance solid-state symmetric devices based on excellent electroactive materials. Chen et al. have constructed a symmetric device by using hybrid SWCNTs/RuO2 electrodes with a specific capacitance of 138 F/g36. The specific capacitance of 159.6 F/g was reported by Hou et al. for the symmetric device using layered ZnS/CNTs composite37. Zhao et al. improved electrochemical properties by porous highly flexible and conductive cellulose-Mediated PEDOT:PSS/MWCNT composite assembly that allowed for an enhanced specific capacitance of 380 F/g2. In present case, the specific capacitance of the device calculated on the basis of CV curve is 486.5 F/g at scan rate of 2 mV/s in spite of having a total mass loading of 8.33 mg as depicted in Fig. 11b. The CV curves maintain its original shape with the inclusion of large potential window of 1.2 V even at high scan rate (100 mV/s). Asymmetric device takes account of both the advantages of positive and negative electrodes, and hence exhibiting excellent electrochemical behavior than the symmetric devices. But, our fabricated symmetric device shows greater capacitance than many asymmetric devices reported by Liu et al. for carbon aerogel//Co3O4 (57.4 F/g)38, Wang et al. for NiCo-LDH//carbon nanorods (147.6 F/g)39, Kong et al. for NiCo2O4@PPy//activated carbon (AC) (165.4 F/g)40, Choi et al. for graphene(IL-CMG)//RuO2–IL-CMG (175 F/g)41, and Yan et al. for Ni–Co@Ni–Co LDH//carbon fibers (319 F/g)42.
The charge-discharge (CD) has also been analyzed with different current densities varying from 3 to 6 mA/cm2 and shown in Fig. 11c. The total specific capacitance of the device obtained as 428.3 F/g at a current density of 3 mA/cm2 is quite higher than other solid-state devices reported recently too (inset, Fig. 11c). Though various resistive factors are involved during device fabrication, the discharge curves show small iR drop by referring internal resistance. The Ragone plot relating the energy and power densities is shown in Fig. 11d. The device shows a maximum specific energy of 85.7 Wh/kg with the power density of 2.6 kW/kg. Moreover, the device can deliver energy density of 41.9 Wh/kg with the upsurge in power density of 5.3 kW/kg. The energy density of present device is substantially higher than those of recently reported all-solid-state symmetric SCs with electrode materials such as MoS2/carbon cloth (5.42 Wh/kg)43, GO/PPy (15.1 Wh/kg)44, SWCNTs/RuO2 (18.8 Wh/kg)36, rGO-PEDOT/PSS (2.83 Wh/kg)45, MWCNTs (3.5 Wh/kg)46, N-doped cotton-derived carbon frameworks (NCCF)-rGO (20 Wh/kg)47, MoSe2 (36.2 Wh/kg)48, PEDOT:PSS/MWCNT (13.2 Wh/kg)2, ZnS/CNTs (22.3 Wh/kg)37, ZnCo2O4/rGO (11.44 Wh/kg)49, Pt/n-CNT@PANI (30.22 Wh/kg)50, waste paper fibers-RGO–MnO2 (19.6 Wh/kg)51, and porous carbon (7.22 Wh/kg)52. Due to current collector-free feature, present ultrathin device showed remarkable energy density, a value considerably higher than even solid-state asymmetric devices, such as CNT/polyaniline//CNT/MnO2/GR (24.8 Wh/kg)53, carbon aerogel//Co3O4 (17.9 Wh/kg)38, graphene(IL-CMG)//RuO2–IL-CMG (19.7 Wh/kg)41, TiN@GNSs//Fe2N@GNSs (15.4 Wh/kg)54, NiCo2O4@PPy//activated carbon (AC) (58.8 Wh/kg)40, NiCo2O4/CC//porous graphene papers (PGP) (60.9 Wh/kg)55, γ-MnS//eggplant derived AC (EDAC) (37.6 Wh/kg)56, CoS//AC (5.3 Wh/kg)57, CoMoO4@NiMoO4•xH2O//Fe2O3 (41.8 Wh/kg)58, CuS/3D graphene//3D graphene (5 Wh/kg)59, MnO2@PANI//3D graphene foam (GF) (37 Wh/kg)60, NiCo2S4/polyaniline//AC (54.06 Wh/kg)61, NiCo-LDH//carbon nanorods (59.2 Wh/kg)39, Ni(OH)2/RGO/Ni//RGO aerogel/Ni (24.5 Wh/kg)62, and rGO/CoAl-LDH//rGO (22.6 Wh/kg)63.
Towards stability check, CV was repeated 10000 times for FSSC device and results are shown in Fig. 12a. There was a quick drop of specific capacitance for first 1000 cycles and stabilized after 2000 cycles. At 10000 cycles, it shows an excellent retention of 92.1% which is higher than recently reported solid-state devices (Supplementary Information S4) and strongly favors the commercial use of FSSC device. Continuously, the performance durability of the FSSC device was further tested under harsh mechanical conditions through bending states by bending the assembled symmetric device at various degrees from 0 to 175° where almost no loss in the capacitance (98.2% retention at 175°) is observed Fig. 11b; suggesting its superior mechanical stability under stress environment. This superior performance is attributed to the excellent adhesion of gel electrolyte, good mechanical robustness, electrical conductivity, intimate interfacial contact among multiple components, and well adherence of MWCNTs to the SS substrate. The overlapping of CV curves of all bending angles shows the high rate capability of the electrode material (Fig. 12c).
As practical demo, a series combination of two SC devices was assembled and charged with 2.4 V. The system can easily lighten up a ‘VNIT’ panel consisted of 21 red LEDs with luminous intensity for 120 s duration (Supplementary video) as depicted in Fig. 12d–g which explores the potential ability of the device. The successful attempt to drive commercial LEDs shows that our device has the opportunity to be applied in energy storage and portable/flexible electronics.
As compared with recently reported solid-state devices, present assembled symmetric device shows superior supercapacitive characteristics including excellent energy and power densities which can be described in the following aspects: (i) unique morphology by the hybridization of CeO2 nanoparticles and MWCNTs nanostructures with richer specific surface and porosity, enabling short electron transport paths and high rate of charge propagation which overall improves the electrochemical performance, (ii) use of MWCNTs is not only to encapsulate CeO2 nanostructure with strong synergy but to enhance the conductivity and stability of the prepared composite too, and (iii) combining two symmetric CeO2/MWCNTs electrodes using PVA-LiClO4 gel extends the voltage window up to 1.2 V, ensuing remarkable enhancement in energy density of the device and empower the device to one step closer to hands-on application.
Conclusions
Hierarchical CeO2 nanostructure was successfully anchored onto outer surface of MWCNTs using facile chemical method. Supercapacitor based on hybrid CeO2/MWCNTs nanostructured electrode displays an enhanced capacitive performance in terms of specific capacitance of 1215.7 F/g, cyclic stability of 92.3% at 10000 cycles and low vaues of resistive factors (RS = 1.87 Ω/cm2 and RCT = 1.06 Ω/cm2). The assembled device impressively shows excellent supercapacitive performance with superb electrochemical and mechanical stability. The durability operation was achieved successfully with a wide cell voltage of 1.2 V, giving rise to energy and power densities. Well-integrated interface between the electrodes and the electrolyte enables fast charge storage/release processes at high rates and good cycling performance over 10000 cycles even under harsh mechanical (bent) conditions. These rationally designed symmetric SCs represent a promising pathway to build-up flexible energy storage devices with high-performance to drive wearable and stretchable electronic devices for advance applications.
Experimental
Fabrication of electrodes and devices
Previously reported synthesis procedure to coat MWCNTs onto SS substrate has been adopted64,65. Briefly, 95% pure MWCNTs (length = 5–15 μm and Outward diameter = 20–40 nm) procured from Monad Nanotech Pvt. Ltd. (Maharashtra, India) were refluxed using H2O2 at 90 °C for 48 h in order to anchor oxygenated functional groups by removing amorphous carbon derivatives. The residue was rinsed repeatedly in double distilled water (DDW) followed by drying at 60 °C for 12 h. To obtain well-dispersed solution of MWCNTs, the product was processed through ultra-sonication in 1 wt% Triton X-100 and DDW with the ratio of Tx-100:DDW equal to 0.01. The two-step mechanical process involving immersion of SS substrate into the dispersed MWCNTs solution and dehydration under IR lamp yields uniform and well adherent coating of MWCNTs on SS substrate.
The simple chemical bath deposition (CBD) method was employed to deposit cerium oxide over the pre-coated MWCNTs (Supplementary Information S5). In brief, cerium (III) nitrate (Ce(NO3)3, 6H2O) was used as cationic solution, while hydrogen peroxide (H2O2, 30%) was used as anionic precursor during the process. The precursor solution was prepared by dissolving 0.04 M Ce(NO3)3 in 50 ml DDW under constant stirring to get uniform distribution. Furthermore, 2.5 mL H2O2 was added to the prepared solution under vigorous stirring. After, the MWCNTs coated substrate was immersed in the bath kept at a constant temperature of 60 °C. After 1 h, the yellowish cerium oxide deposited MWCNTs substrate was taken out from the bath and rinsed several times in DDW and dried under infrared (IR) radiation. The as-prepared film was air annealed at 200 °C to remove extra hydroxide. The synthesis involves two steps. Firstly, \({{\rm{Ce}}}^{3+}\) ions in association with H2O2 form complex \({\rm{Ce}}{{({\rm{OH}})}_{2}}^{2+}\) ions as:
In the second reaction step, \({\rm{Ce}}{{({\rm{OH}})}_{2}}^{2+}\) yields CeO2 as thin film form on SS substrate.
The non-oxidized hydroxide originating from reaction, was eliminated via the annealing process as follows:
Further, the PVA-LiClO4 gel electrolyte was obtained by adding 6 g of LiClO4 and 6 g of polyvinyl alcohol (PVA) powder into 60 ml of DDW66. The mixture was heated at 90 °C under stirring until the solution became clear and viscous. Then the composite electrode on the flexible SS substrate was coated with a thin layer of the prepared PVA-LiClO4 gel electrolyte followed by evaporation of the excess water. When the gel electrolyte got solidified, the two electrodes were sandwiched and packaged to assemble flexible symmetric supercapacitor (FSSC) device.
Characterizations
XRD was performed by Bruker AXS D8 Advance diffractometer using Cu Kα X-ray source. Raman studies were performed with LabRAM HR, 532 nm laser excitation. Energy-dispersive X-ray spectroscopy (EDX) was acquired using a JSM-7610F analyzer connected with a scanning electron microscope (FESEM, JEOL JSM-7610F). The detailed morphological study was performed by high-resolution transmission electron microscopy (HRTEM) using JEOL 2100 with LaB6 source. XPS measurements were carried out in a PHI 5000 VersaProbe II (ULVAC INC, Japan) photoelectron spectrometer under ultrahigh vacuum (UHV) below 5 × 10−10 Torr. XPS system is equipped with the Al Kα X-ray monochromator operated with an anode power of 350 W and the sample surface normal was oriented at 45° to both the X-ray source and photoelectron spectrometer.
Electrochemical characteristics of the as-obtained films were studied on PARSTAT 4000 electrochemical workstation (Princeton Applied Research, USA) using cyclic voltammetry (CV), charge-discharge (CD) and electrochemical impedance test on three-electrode cells. In these, the composite electrode acts as the working electrode, Pt wire as the counter electrode and a saturated Ag/AgCl electrode as the reference electrode.
References
Jun, L. et al. Oriented Nanostructures for Energy Conversion and Storage. ChemSusChem 1, 676–697 (2008).
Zhao, D. et al. Highly Flexible and Conductive Cellulose-Mediated PEDOT:PSS/MWCNT Composite Films for Supercapacitor Electrodes. ACS Appl. Mater. Interfaces 9, 13213–13222 (2017).
Vaisman, L., Wagner, H. D. & Marom, G. The role of surfactants in dispersion of carbon nanotubes. Adv. Colloid Interface Sci. 128–130, 37–46 (2006).
Ramchandra, S. K., Yong-Han, K. & Chan-Jin, P. One step hydrothermal synthesis of a carbon nanotube/cerium oxide nanocomposite and its electrochemical properties. Nanotechnology 24, 365401 (2013).
Deng, D. et al. Cerium oxide nanoparticles/multi-wall carbon nanotubes composites: Facile synthesis and electrochemical performances as supercapacitor electrode materials. Physica E 86, 284–291 (2017).
Luo, Y., Yang, T., Zhao, Q. & Zhang, M. CeO2/CNTs hybrid with high performance as electrode materials for supercapacitor. J. Alloys Compd. 729, 64–70 (2017).
Sun, C., Li, H. & Chen, L. Nanostructured ceria-based materials: synthesis, properties, and applications. Energy Environ. Sci. 5, 8475–8505 (2012).
Zhang, H. et al. Hierarchical porous MnO2/CeO2 with high performance for supercapacitor electrodes. Chem. Eng. J. 286, 139–149 (2016).
Li, Y. & Shen, W. Morphology-dependent nanocatalysts: Rod-shaped oxides. Chem. Soc. Rev. 43, 1543–1574 (2014).
Jadhav, C. D., Pandit, B., Karade, S. S., Sankapal, B. R. & Chavan, P. G. Enhanced field emission properties of V2O5/MWCNTs nanocomposite. Appl. Phys. A 124, 794 (2018).
Hamlaoui, Y., Tifouti, L., Remazeilles, C. & Pedraza, F. Cathodic electrodeposition of cerium based oxides on carbon steel from concentrated cerium nitrate. Part II: Influence of electrodeposition parameters and of the addition of PEG. Mater. Chem. Phys. 120, 172–180 (2010).
Hamlaoui, Y. et al. Cathodic electrodeposition of cerium-based oxides on carbon steel from concentrated cerium nitrate solutions: Part I. Electrochemical and analytical characterisation. Mater. Chem. Phys. 113, 650–657 (2009).
Singh, A. P. et al. Probing the engineered sandwich network of vertically aligned carbon nanotube–reduced graphene oxide composites for high performance electromagnetic interference shielding applications. Carbon 85, 79–88 (2015).
Vinod, S. et al. Synthesis of ultralow density 3D graphene-CNT foams using a two-step method. Nanoscale 8, 15857–15863 (2016).
Pandit, B., Karade, S. S. & Sankapal, B. R. Hexagonal VS2 Anchored MWCNTs: First Approach to Design Flexible Solid-State Symmetric Supercapacitor Device. ACS Appl. Mater. Interfaces 9, 44880–44891 (2017).
Zhang, Y., Hou, F. & Tan, Y. CeO2 nanoplates with a hexagonal structure and their catalytic applications in highly selective hydrogenation of substituted nitroaromatics. Chem. Commun. 48, 2391–2393 (2012).
Li, X. et al. Layer-by-layer synthesis of hollow spherical CeO2 templated by carbon spheres. J. Porous Mater. 17, 297–303 (2010).
Li, S. et al. Study on cerium-doped nano-TiO2 coatings for corrosion protection of 316 L stainless steel. Nanoscale Res. Lett. 7, 227 (2012).
Li, H. et al. Surfactant-assisted synthesis of CeO2 nanoparticles and their application in wastewater treatment. RSC Adv. 2, 12413–12423 (2012).
Zheng, L. et al. Freeze-drying for sustainable synthesis of nitrogen doped porous carbon cryogel with enhanced supercapacitor and lithium ion storage performance. Nanotechnology 26, 374003 (2015).
Rojas, J. V., Toro-Gonzalez, M., Molina-Higgins, M. C. & Castano, C. E. Facile radiolytic synthesis of ruthenium nanoparticles on graphene oxide and carbon nanotubes. Mater. Sci. Eng., B 205, 28–35 (2016).
Vanitha, M., Keerthi, Cao, P. & Balasubramanian, N. Ag nanocrystals anchored CeO2/graphene nanocomposite for enhanced supercapacitor applications. J. Alloys Compd. 644, 534–544 (2015).
Yuan, C. Z. et al. Hierarchically structured carbon-based composites: Design, synthesis and their application in electrochemical capacitors. Nanoscale 3, 529–545 (2011).
Pandit, B. & Sankapal, B. R. Highly conductive energy efficient electroless anchored silver nanoparticles on MWCNTs as a supercapacitive electrode. New J. Chem. 41, 10808–10814 (2017).
Arul, N. S., Mangalaraj, D., Ramachandran, R., Grace, A. N. & Han, J. I. Fabrication of CeO2/Fe2O3 composite nanospindles for enhanced visible light driven photocatalysts and supercapacitor electrodes. J. Mater. Chem. A 3, 15248–15258 (2015).
Pendashteh, A., Rahmanifar, M. S., Kaner, R. B. & Mousavi, M. F. Facile synthesis of nanostructured CuCo2O4 as a novel electrode material for high-rate supercapacitors. Chem. Commun. 50, 1972–1975 (2014).
Pandit, B., Dubal, D. P. & Sankapal, B. R. Large scale flexible solid state symmetric supercapacitor through inexpensive solution processed V2O5 complex surface architecture. Electrochim. Acta 242, 382–389 (2017).
Wu, Q., Xu, Y., Yao, Z., Liu, A. & Shi, G. Supercapacitors Based on Flexible Graphene/Polyaniline Nanofiber Composite Films. ACS Nano 4, 1963–1970 (2010).
Pandit, B., Devika, V. S. & Sankapal, B. R. Electroless-deposited Ag nanoparticles for highly stable energy-efficient electrochemical supercapacitor. J. Alloys Compd. 726, 1295–1303 (2017).
Pandit, B., Dhakate, S. R., Singh, B. P. & Sankapal, B. R. Free-standing flexible MWCNTs bucky paper: Extremely stable and energy efficient supercapacitive electrode. Electrochim. Acta 249, 395–403 (2017).
Si, W. et al. On chip, all solid-state and flexible micro-supercapacitors with high performance based on MnOx/Au multilayers. Energy Environ. Sci. 6, 3218–3223 (2013).
Pandit, B., Sharma, G. K. & Sankapal, B. R. Chemically deposited Bi2S3:PbS solid solution thin film as supercapacitive electrode. J. Colloid Interface Sci. 505, 1011–1017 (2017).
Kampouris, D. K., Ji, X., Randviir, E. P. & Banks, C. E. A new approach for the improved interpretation of capacitance measurements for materials utilised in energy storage. RSC Adv. 5, 12782–12791 (2015).
Xu, P. et al. Laminated Ultrathin Chemical Vapor Deposition Graphene Films Based Stretchable and Transparent High-Rate Supercapacitor. ACS Nano 8, 9437–9445 (2014).
Pande, S. A., Pandit, B. & Sankapal, B. R. Electrochemical approach of chemically synthesized HgS nanoparticles as supercapacitor electrode. Mater. Lett. 209, 97–101 (2017).
Chen, P., Chen, H., Qiu, J. & Zhou, C. Inkjet printing of single-walled carbon nanotube/RuO2 nanowire supercapacitors on cloth fabrics and flexible substrates. Nano Res. 3, 594–603 (2010).
Hou, X. et al. Ultrathin ZnS nanosheet/carbon nanotube hybrid electrode for high-performance flexible all-solid-state supercapacitor. Nano Res. 10, 2570–2583 (2017).
Liu, W., Li, X., Zhu, M. & He, X. High-performance all-solid state asymmetric supercapacitor based on Co3O4 nanowires and carbon aerogel. J. Power Sources 282, 179–186 (2015).
Wang, T. et al. 2-Methylimidazole-Derived Ni–Co Layered Double Hydroxide Nanosheets as High Rate Capability and High Energy Density Storage Material in Hybrid Supercapacitors. ACS Appl. Mater. Interfaces 9, 15510–15524 (2017).
Kong, D. et al. Three-Dimensional NiCo2O4@Polypyrrole Coaxial Nanowire Arrays on Carbon Textiles for High-Performance Flexible Asymmetric Solid-State Supercapacitor. ACS Appl. Mater. Interfaces 7, 21334–21346 (2015).
Choi, B. G. et al. High performance of a solid-state flexible asymmetric supercapacitor based on graphene films. Nanoscale 4, 4983–4988 (2012).
Yan, L. et al. Design of Hierarchical Ni-Co@Ni-Co Layered Double Hydroxide Core–Shell Structured Nanotube Array for High‐Performance Flexible All‐Solid‐State Battery‐Type Supercapacitors. Adv. Funct. Mater. 27, 1605307 (2017).
Javed, M. S. et al. High performance solid state flexible supercapacitor based on molybdenum sulfide hierarchical nanospheres. J. Power Sources 285, 63–69 (2015).
Cao, J. et al. Three-dimensional graphene oxide/polypyrrole composite electrodes fabricated by one-step electrodeposition for high performance supercapacitors. J. Mater. Chem. A 3, 14445–14457 (2015).
Liu, Y. et al. High-Performance Flexible All-Solid-State Supercapacitor from Large Free-Standing Graphene-PEDOT/PSS Films. Sci. Rep. 5, 17045 (2015).
Li, S. et al. General Method for Large‐Area Films of Carbon Nanomaterials and Application of a Self‐Assembled Carbon Nanotube Film as a High‐Performance Electrode Material for an All‐Solid‐State Supercapacitor. Adv. Funct. Mater. 27, 1700474 (2017).
Fan, Y.-M., Song, W.-L., Li, X. & Fan, L.-Z. Assembly of graphene aerogels into the 3D biomass-derived carbon frameworks on conductive substrates for flexible supercapacitors. Carbon 111, 658–666 (2017).
Qiu, Y. et al. Flexible full-solid-state supercapacitors based on self-assembly of mesoporous MoSe2 nanomaterials. Inorg. Chem. Front. 4, 675–682 (2017).
Kyu, M. I., Seonno, Y. & Jungwoo, O. Three‐Dimensional Hierarchically Mesoporous ZnCo2O4 Nanowires Grown on Graphene/Sponge Foam for High‐Performance, Flexible, All‐Solid‐State Supercapacitors. Chem. Eur. J. 23, 597–604 (2017).
Wu, Y., Wang, Q., Li, T. & Zhang, D. & Miao, M. Fiber-shaped Supercapacitor and Electrocatalyst Containing of Multiple Carbon Nanotube Yarns and One Platinum Wire. Electrochim. Acta 245, 69–78 (2017).
Su, H. et al. Waste to wealth: A sustainable and flexible supercapacitor based on office waste paper electrodes. J. Electroanal. Chem. 786, 28–34 (2017).
Li, X. et al. Hierarchical porous carbon from hazardous waste oily sludge for all-solid-state flexible supercapacitor. Electrochim. Acta 240, 43–52 (2017).
Jin, Y., Chen, H., Chen, M., Liu, N. & Li, Q. Graphene-Patched CNT/MnO2 Nanocomposite Papers for the Electrode of High-Performance Flexible Asymmetric Supercapacitors. ACS Appl. Mater. Interfaces 5, 3408–3416 (2013).
Changrong, Z. et al. All Metal Nitrides Solid‐State Asymmetric Supercapacitors. Adv. Mater. 27, 4566–4571 (2015).
Gao, Z., Yang, W., Wang, J., Song, N. & Li, X. Flexible all-solid-state hierarchical NiCo2O4/porous graphene paper asymmetric supercapacitors with an exceptional combination of electrochemical properties. Nano Energy 13, 306–317 (2015).
Chen, T. et al. All-solid-state high performance asymmetric supercapacitors based on novel MnS nanocrystal and activated carbon materials. Sci. Rep. 6, 23289 (2016).
Subramani, K., Sudhan, N., Divya, R. & Sathish, M. All-solid-state asymmetric supercapacitors based on cobalt hexacyanoferrate-derived CoS and activated carbon. RSC Adv. 7, 6648–6659 (2017).
Wang, J. et al. Assembly of flexible CoMoO4@NiMoO4·xH2O and Fe2O3 electrodes for solid-state asymmetric supercapacitors. Sci. Rep. 7, 41088 (2017).
Tian, Z., Dou, H., Zhang, B., Fan, W. & Wang, X. Three-dimensional graphene combined with hierarchical CuS for the design of flexible solid-state supercapacitors. Electrochim. Acta 237, 109–118 (2017).
Ghosh, K., Yue, C. Y., Sk, M. M. & Jena, R. K. Development of 3D Urchin-Shaped Coaxial Manganese Dioxide@Polyaniline (MnO2@PANI) Composite and Self-Assembled 3D Pillared Graphene Foam for Asymmetric All-Solid-State Flexible Supercapacitor Application. ACS Appl. Mater. Interfaces 9, 15350–15363 (2017).
He, X. et al. High-performance all-solid-state asymmetrical supercapacitors based on petal-like NiCo2S4/Polyaniline nanosheets. Chem. Eng. J. 325, 134–143 (2017).
Lu, K. et al. Interfacial Deposition of Three-Dimensional Nickel Hydroxide Nanosheet-Graphene Aerogel on Ni Wire for Flexible Fiber Asymmetric Supercapacitors. ACS Sustain. Chem. Eng. 5, 821–827 (2017).
Zhang, R. et al. Mesoporous graphene-layered double hydroxides free-standing films for enhanced flexible supercapacitors. Chem. Eng. J. 289, 85–92 (2016).
Pandit, B., Dubal, D. P., Gómez-Romero, P., Kale, B. B. & Sankapal, B. R. V2O5 encapsulated MWCNTs in 2D surface architecture: Complete solid-state bendable highly stabilized energy efficient supercapacitor device. Sci. Rep. 7, 43430 (2017).
Pande, S. A., Pandit, B. & Sankapal, B. R. Facile chemical route for multiwalled carbon nanotube/mercury sulfide nanocomposite: High performance supercapacitive electrode. J. Colloid Interface Sci. 514, 740–749 (2018).
Pandit, B., Bommineedi, L. K. & Sankapal, B. R. Electrochemical engineering approach of high performance solid-state flexible supercapacitor device based on chemically synthesized VS2 nanoregime structure. J. Energy Chem. 31, 79–88 (2019).
Acknowledgements
B.R.S. acknowledges DST/TMD/MES/2k16/09 project, Government of India. The authors sincerely acknowledge the cooperation and facilities provided by Prof. Akihiro Furube, Department of Optical Science, Tokushima University, Japan. The authors gratefully acknowledge technical staff Mr. Tomoyuki Ueki from Tokushima University for XPS measurements.
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B.P. performed the experiments, electrochemical characterizations, data analysis and wrote the manuscript. B.P., B.R.S., and P.M.K. reviewed the data and manuscript. To the preparation of manuscript, all authors contributed equally.
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Pandit, B., Sankapal, B.R. & Koinkar, P.M. Novel chemical route for CeO2/MWCNTs composite towards highly bendable solid-state supercapacitor device. Sci Rep 9, 5892 (2019). https://doi.org/10.1038/s41598-019-42301-y
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DOI: https://doi.org/10.1038/s41598-019-42301-y
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