Facile Synthesis of CoSe/Co₃O₄-CNTs/NF Composite Electrode for High-Performance Asymmetric Supercapacitor

Abstract

Electrode materials are key factors for supercapacitors to endow them with excellent electrochemical properties. Here, a novel hybrid structure of a CoSe/Co₃O₄-CNTs binder free composite electrode on nickel foam was prepared via a facile flame method, followed by an electrodeposition process. Benefitting from the synergetic effects of the multicomponent (with low resistances of 1.542 Ω cm² and a moderate mesoporous size of 3.12 nm) and the enlarged specific surface area of the composite material (77.4 m² g⁻¹), the CoSe/Co₃O₄-CNTs composite electrode delivers a high specific capacitance of 2906 F g⁻¹ at 5 mV s⁻¹ with an excellent rate stability. The fabricated CoSe/Co3O4-CNTs/NF//AC ASC exhibits a high energy density of 43.4 Wh kg⁻¹ at 0.8 kW kg⁻¹ and a long cycle life (92.7% capacitance retention after 10,000 cycles).

1. Introduction

Highly efficient energy storage devices are one of the important means to satisfy the increasing energy demand. As an important piece of equipment for electrochemical energy storage, supercapacitors (SCs) have been a wide concern in the field of hybrid vehicles, consumer electronics, and industrial power management, because of their long maintenance-free lifetime, high power density, environmental protection, safety and reliability [1,2,3].

Depending on their various energy storage mechanisms, SCs can be compartmentalized into electric double layer capacitors (electrostatic storage charge), pseudocapacitors (reversible faradaic redox reaction storage charge) and asymmetric supercapacitors (ASCs). ASCs especially usually combine advantages of the two different types of electrodes, which can provide a high capacitance and a long cycle life [4]. As a main component of SCs, various electro-active materials have been explored, such as carbonaceous materials (carbon nanotubes [5,6,7] (CNTs), graphene [8,9] and active carbon [10]), transition metal-based materials (RuO₂ [11], MnO₂ [12], NiO [13], Co₃O₄ [14]), sulfides [15], metal selenides [16] and conducting polymers (PANI [17], PPy [18], PEDOT [19]).

Among them, transition metal selenides have been shown to possess higher electronic conductivity than oxides and sulfides and relatively high theoretical specific capacities, implying that transition metal selenides have great potential to be used as advanced electro-active materials for SCs [20,21]. However, the addition of binders usually decreases the electronic conductivity of the electrode, resulting in the deterioration of electrochemical performance. To solve this issue, some 3D porous metallic, such as Cu foam and nickel foam (NF), have been used as substrates to direct growth of electro-active materials to effectively promote the conductivity and electrochemical properties of the electrodes [22,23]. Meanwhile, the electrochemical properties of electro-active materials can be efficiently improved through fabrication of composite (hybrid) materials due to the complementary properties and unique synergistic effects of their multicomponent. For instance, hybrid structure CNT decorated NiSe₂ nanosheets (NiSe₂@CNT) [24], dual S, N-doped CoFe₂O₄@CNTs [25] and graphene nanosheet supported NiSe [26] have been proven to possess excellent electrochemical performance for supercapacitors. Recently, Zhu et al. [27] constructed a porous CNTs@NiCo-LDH nut-shell nanotube arrays for supercapacitor applications, which exhibited an improved mass transfer of ions and enhanced specific capacity.

Herein, we design a novel hybrid structure of CoSe/Co₃O₄-CNTs on NF via facile flame synthesis and followed by electrodeposition as a binder free electrode for SCs. Assisting with the synergetic effects of the multicomponent and low resistance, the as-obtained CoSe/Co₃O₄-CNTs/NF hybrid structure shows high specific capacitance (2906 F g⁻¹, at 5 mV s⁻¹) and rate performance (1362.8 F g⁻¹, at 50 mV s⁻¹). Furthermore, the constructed CoSe/Co₃O₄-CNTs/NF//AC ASC device delivers a high energy density of 43.4 W h kg⁻¹ at 0.8 kW kg⁻¹ with 92.7% capacitance retention after 10,000 cycles.

2. Experimental Section

2.1. Materials

Cobalt(III) acetylacetonate (Co(acac)₃, Co(C₅H₇O₂)₃) was purchased from Alfa Aesar. Cobalt(II) chloride hexahydrate (CoCl₂•6H₂O, ≥99%) and lithium chloride monohydrate (LiCl•H₂O, ≥95%) were obtained from Kelong Chemical Reagent Co. Ltd. (Chengdu, China) Selenium dioxide (SeO₂, ≥99%) was acquired from Shanghai Macklin Biochemical Co., Ltd. (Shanghai, China). All chemical reagents were used directly.

2.2. The Synthesis of Co₃O₄-CNTs/NF

NF (with the thickness of 1.0 mm, surface density = 34.2 mg cm⁻², pore per inch = 110) was immersed into a 3 M HCl solution for 1 min to remove the oxides and impurities on the surface firstly, then the precleaned NF was washed with acetone, ethanol, and DI water under the assistance of ultrasound. Finally, it was dried in a vacuum oven at 60 °C overnight.

Co₃O₄-CNTs loaded on the skeleton of NF was prepared via a facile flame method. Concisely, an ethanol solution of Co(acac)³ (with a concentration of 10 mg/mL) was prepared. Then, a piece of NF (with the area of 1 × 1 cm²) was immersed into the above solution for about 5 s to make the solution attach onto the skeleton of NF. After that, the NF was ignited and burned under ambient condition to gain the NF decorated by Co₃O₄-CNTs. To increase the mass loading of Co₃O₄-CNTs, the immersing and flaming process could be executed for more times. In our research, the mass of Co₃O₄-CNTs loaded on NF were about 0.1, 0.2, 0.4, 0.9, 1.5 mg, corresponding to the various immersing and flaming times (1, 2, 5, 10, 15).

2.3. The Synthesis of CoSe

CoSe particles were deposited on Co₃O₄-CNTs via electrodeposition process. The bath for electrodeposition consists of 25 mL DI water, 0.2 mmol CoCl₂•6H₂O, 0.2 mmol SeO₂ and 200 mg LiCl•H₂O. After being stirred evenly, a homogeneous pink solution was obtained. Through a typical three-electrode system on an electrochemical workstation (CHI 660C) (CH Instruments, Inc., Shanghai, China), the constant current electrodeposition procedure was realized by using Co₃O₄-CNTs/NF as working electrode, Pt foil and saturated calomel electrode (SCE) as the counter electrode and the reference electrode, respectively. The electrodeposition was conducted at 15 mA cm⁻² for 1200 s. Pure CoSe nanoparticles were also deposited on NF without the flame process for comparison. The mass of CoSe/Co₃O₄-CNTs, Co₃O₄-CNTs and CoSe loaded on NF were 0.7, 0.4 and 1 mg, respectively.

2.4. Characterization

A Rigaku Miniflex600 X-ray diffraction (XRD) system (Rigaku, Tokyo, Japan) with Cu K_α irradiation was applied to analyze the crystal structures of samples. The chemical state of the synthetic elements was determined by X-ray photoelectron spectrometer (Thermo Scientific K-Alpha+) (Thermo Fisher Scientific, Waltham, MA, USA). A FEI Verios 460 scanning electron microscopy (SEM) was used to observe the morphologies and microstructures. The Brunauer–Emmett–Teller (BET) (Kubo X1000) analysis (Beijing Builder Electronic Technology Co., Ltd., Beijing, China) was used to study the specific surface area and pore size distribution of the sample. Raman spectra were obtained with an excitation wavelength of 514 nm, using a Horiba Scientific LabRAM HR Evolution. (HORIBA Scientific, Kyoto, Japan).

2.5. Electrochemical Measurements

The three-electrode system in 3 M KOH was introduced to investigate the electrochemical properties of the as-synthesized materials on NF, where an Hg/HgO electrode and a Pt-wire were used as the reference electrode and the counter electrode, respectively. Cyclic voltammetry (CV) measurements were tested, ranging from 0 to 0.6 V at different sweep rates (5–100 mV s⁻¹), while galvanostatic charge–discharge (GCD) was measured within the potential window of 0–0.5 V at different current densities (1–10 A g⁻¹). Electrochemical impedance spectroscopy (EIS) measurement was performed at a frequency between 0.01 and 100 kHz, where the amplitude was set to be 5 mV. The ASCs were assembled in 3 M KOH with the CoSe/Co₃O₄-CNTs/NF (or CoSe/NF) electrode as the positive electrode and the AC electrode as the negative electrode. The cycling stability was investigated by a Neware battery test instrument (BST-3008) (Neware Technology Limited, Shenzhen, China) in a voltage range of 0–1.6 V at 2 A g⁻¹.

3. Results and Discussion

3.1. Characterization of Materials

Scheme 1 illustrates the fabrication process of the CoSe/Co₃O₄-CNTs/NF electrode. The forming mechanism of Co₃O₄-CNTs is that the hydrocarbon of cobalt acetylacetonate are catalytic-decomposed to Co + C (Co₂C, Co₃C) over NF, then cobalt nanoparticles combined with oxygen atoms (air atmosphere) and Co₃O₄-CNTs is the final product [28,29,30]. Cobalt nanoparticles act as the catalyst for in situ formation of CNTs and oxidized to finally form Co₃O₄. The effect of different loading amounts on the morphology and properties of Co₃O₄-CNTs is shown in Figures S1 and S2. The SEM image with five flame cycles show the appropriate load amount. In Figure S2, the NF electrodes have a lower performance and almost no contribution to electrochemical performance. The Co₃O₄-CNTs electrodes with different flame cycles show extremely low capacitance (180 F g⁻¹). After consideration, the Co₃O₄-CNTs/NF-0.4 (0.4 stans for the loading amount of 0.4 mg cm⁻²) was used for the next electrodeposition. In the process of cathodic current reduction, the SeO₂ will be reduced stepwise to Se²⁻ and then reacted with the metal ions to form metal selenides. The electrodeposition mechanism can be interpreted by the following chemical equations [31,32]:

$${\mathrm{SeO}}_2+4{\mathrm{H}}^{+}+4{\mathrm{e}}^{-}\to \mathrm{Se}+2{\mathrm{H}}_2\mathrm{O}$$

(1)

$$\mathrm{Se}+2{\mathrm{H}}^{+}+2{\mathrm{e}}^{-}\to {\mathrm{H}}_2\mathrm{Se}$$

(2)

$${\mathrm{SeO}}_2+6{\mathrm{H}}^{+}+6{\mathrm{e}}^{-}\to {\mathrm{H}}_2\mathrm{Se}+2{\mathrm{H}}_2\mathrm{O}$$

(3)

$${\mathrm{Co}}^{2+}+{ \mathrm{Se}}^{2-}\to \mathrm{CoS}\mathrm{e}$$

(4)

Figure 1 shows the SEM image of CoSe/NF, Co₃O₄-CNTs/NF and CoSe/Co₃O₄-CNTs/NF. The morphology of CoSe/NF with a homologous nanoparticle architecture with less pores is shown in Figure 1a,b, showing the typical SEM image of the Co₃O₄-CNTs/NF sample, indicating that Co₃O₄-CNTs coated on the surface of NF shows a loose structure with abundant micro-voids. This superhydrophilic architecture with excellent conductivity is believed to provide more nucleation sites for the subsequent electrodeposition to expand the specific surface area of composites, which is beneficial to promote the electrochemical properties of the electro-active materials [33,34]. XRD pattern of Co₃O₄-CNTs is shown in Figure S3. Three diffraction peaks of NF substrate (JCPDS no. 04-0850), which are located at 44.7°, 52.1° and 76.6°, can be seen clearly. The other four weak diffraction peaks at 31.4°, 36.9°, 59.6°, and 65.4° are assigned to Co₃O₄ (JCPDS no.74-1657). However, no diffraction peaks of CNTs are observed, which maybe imply the poor crystallinity of CNTs. The Raman spectrum in Figure S4 further indicated the relatively good graphitization of Co₃O₄-CNTs. The I_D/I_G of about 0.96 suggests this carbon material possesses rich defects [35]. The TEM image (Figure S5) indicates the diameter of the CNTs is about 18 nm, and Co₃O₄(2–4 nm) nanoparticles adhere on the surface of CNTs and encapsulate at the tip. Figure 1c shows the SEM micrographs of the CoSe/Co₃O₄-CNTs/NF sample, which reveals a uniform nanoparticle-like architecture with plenty of pores on its surface. As mentioned above, this porous structure is beneficial for the infiltration of electrolyte and the improvement of electrochemical properties of CoSe. N₂ adsorption–desorption technique was employed to analyze the characteristics of pores quantitatively. The specific surface area (SSA) and the pore diameter distribution of Co₃O₄-CNTs/NF, CoSe/NF and CoSe/Co₃O₄-CNTs/NF are displayed in Figure S6. As can be seen, all of them show type IV curves with mesoporous feature. The SSA of CoSe/Co₃O₄-CNTs/NF (77.4 m² g⁻¹) is much larger than that of CoSe/NF (17.1 m² g⁻¹) and Co₃O₄-CNTs/NF (21.5 m² g⁻¹). The insert patterns display Barrett–Joyner–Halenda (BJH) pore size distribution curves. Among them, CoSe/Co₃O₄-CNTs/NF displays the main pores of 3.21 nm in a range of 1–100 nm. The larger SSA and moderate mesoporous size feature contribute to the fast ion migration/diffusion during redox reaction [36]. Actually, double-layer capacitance (CDL) or Gaussian fitting of the SEM or TEM images method can also be used to analyze the pore diameter distributions, which were more convenient [37,38].

Figure 2a depicts the representative XRD pattern of CoSe/Co₃O₄-CNTs/NF. As presented, three diffraction peaks at 44.7°, 52.1° and 76.5° can be assigned to the NF, while no other diffraction peaks can be observed, implying that the CoSe grown on the Co₃O₄-CNTs/NF mainly exists in amorphous form. The composition and chemical valence of the CoSe/Co₃O₄-CNTs/NF sample was further investigated by using XPS analysis (as shown in Figure S7). The full XPS survey spectrum of CoSe/Co₃O₄-CNTs/NF represents the co-existence of Co and Se elements (Figure S7a). Two major peaks at 795.92 and 780.48 eV in the high-resolution XPS spectrum of Co 2p (Figure S7b) correspond to the Co 2p_1/2 and 2p_3/2, with two satellites at 802.51 and 784.73 eV, respectively [34,39,40,41,42,43], which suggests the presence of Co²⁺. Figure S7c shows the detailed analysis of Se 3d high-resolution XPS spectra at a lower energy. Although there is interference on the Co 3p line on 59.1 eV, the emerged peaks at 55.8 and 54.8 eV can be appointed to the Se 3d_3/2 and 3d_5/2 [41,44], suggesting that the Se elemental mainly exists in Se²⁻. XPS results verify the successful formation of CoSe on the Co₃O₄-CNTs/NF substrate. In order to obtain the detailed morphology of samples, CoSe was stripped from the substrate via ultrasonic vibration slightly to avoid structural damage. The TEM image in Figure 2b shows that the CoSe displays a connected nanosheet-like structure construction with ultrathin thickness and a rough surface. Furthermore, no clear lattice fringes are observed in the corresponding high-resolution TEM pattern (Figure 2c), which means that the as-synthesized CoSe possesses a low-crystalline characteristic. This result is consistent with the result of XRD. Active materials with higher SSA and low-crystalline have been proven to be beneficial to provide more active sites and withstand the distortion of structure during the charge/discharge process [45], resulting in a higher specific capacitance and longer cycling stability. Therefore, we deduced that the as-synthesized CoSe/Co₃O₄-CNTs/NF will exhibit excellent electrochemical properties.

3.2. Electrochemical Performances of CoSe/Co₃O₄-CNTs/NF

Electrochemical performances of the CoSe/Co₃O₄-CNTs/NF electrodes are shown in Figure 3. For the CV curves in Figure 3a, a pair of redox peaks clearly show the faradaic pseudocapacitive characteristics of the battery-like electrode, corresponding to the following redox reactions [46,47]:

$${\mathrm{Co}}_3{\mathrm{O}}_4+{\mathrm{OH}}^{-}+{\mathrm{H}}_2\mathrm{O}\leftrightarrow 3\mathrm{CoOOH}+{\mathrm{e}}^{-}$$

(5)

$$2\mathrm{CoS}\mathrm{e}+2{\mathrm{H}}_2\mathrm{O}+{\mathrm{O}}_2 \leftrightarrow 2\mathrm{Co}{\left(\mathrm{OH}\right)}_2+2\mathrm{Se}$$

(6)

$$3\mathrm{Se}+6{\mathrm{OH}}^{-}\leftrightarrow 2{\mathrm{Se}}^{2-}+{\mathrm{SeO}}_3^{2-}+3{\mathrm{H}}_2\mathrm{O}$$

(7)

$$\mathrm{Co}{\left(\mathrm{OH}\right)}_2+{\mathrm{OH}}^{-} \leftrightarrow \mathrm{CoOOH}+{\mathrm{H}}_2\mathrm{O}+{\mathrm{e}}^{-}$$

(8)

$$\mathrm{CoOOH}+{\mathrm{OH}}^{-} \leftrightarrow { \mathrm{CoO}}_2+{\mathrm{H}}_2\mathrm{O}+{\mathrm{e}}^{-}$$

(9)

The distinct peaks may be attributed to the redox features of Co²⁺/Co³⁺ and Co³⁺/Co⁴⁺. Additionally, the CoSe/Co₃O₄-CNTs/NF electrode has a much larger integrated area than the CoSe/NF electrode, indicating that the CoSe/Co₃O₄-CNTs/NF electrode will provide a satisfying energy storage ability. Figure 3b displays the compared GCD curves of CoSe/Co₃O₄-CNTs/NF, CoSe/NF and Co₃O₄-CNTs/NF electrodes at 1 A g⁻¹. Apparently, the CoSe/Co₃O₄-CNTs/NF delivered a higher specific capacitance of 2906 F g⁻¹, which was two times larger than that of the CoSe/NF electrode (1440.8 F g⁻¹). Co₃O₄-CNTs/NF has a relatively high surface area (Figure S6), and its capacitance is 180 F g⁻¹ at 1 A g⁻¹.

To evaluate the charge transfer rate of the hybrid electrode, EIS tests were conducted (Figure 3c). The intercepts at the real axis are associated with R_s (contributions of the ionic resistance of the electrolyte, intrinsic resistance, and contact resistance between the active material and the current collector). In addition, the semicircles represent R_ct (charge-transfer resistance) of electrode materials. The slopes of the impedance line in the low-frequency region denote W (Warburg impedance), which indicates the ion diffusion in the interface of electrode material/electrolyte. The corresponded fitting results of Nyquist plots (Table S1) reveal that CoSe/Co₃O₄-CNTs/NF has a lower charge-transfer resistance (R_ct = 0.89 Ω cm²) and solution resistance (R_s = 0.73 Ω cm²), indicating its superior charge mobility. We also calculate the resistances of Co₃O₄-CNTs/NF, CoSe/NF and CoSe/Co₃O₄-CNTs/NF electrodes from the voltage drop in GCD plots at the higher current densities (100 to 500 A g⁻¹) (Figure S8 and Table S2). The electrode of CoSe/Co3O4-CNTs/NF has the lower resistance 1.542 Ω cm². The outstanding impedance characteristics of CoSe/Co₃O₄-CNTs/NF arise from the synergetic effect of Co3O4-CNTs and CoSe materials, in which the Co₃O₄-CNTs winded with each other can provide good conductivity and stability. Meanwhile, the larger SSA and moderate mesoporous size of CoSe/Co₃O₄-CNTs/NF can offer excellent infiltration of the electrolyte [36].

The CV cures of the CoSe/Co₃O₄-CNTs/NF electrode at various scan rates are depicted in Figure S9a. Notably, with the increasing of scan rates, the anodic and cathodic peaks shift to higher and lower voltage, respectively, suggesting the increased internal diffusion resistance of the electrode [48]. Meanwhile, the perfect linear relationship of i and v^1/2 (Figure 3d) indicates the redox reactions between electrolyte and electrode interface at the electrolyte/electrode interface is related to a quasi-reversible and diffusion control process [24].

The specific capacitance and rate capacity of the CoSe/Co₃O₄-CNTs/NF electrode are further investigated by GCD test at different current densities (Figure S9b and Figure 3e). Obviously, each GCD curve shows an apparent charge–discharge platform without obvious voltage drop, indicating the excellent pseudocapacitance properties and electronic conductivity of the CoSe/Co₃O₄-CNTs/NF electrode. Moreover, the CoSe/Co₃O₄-CNTs/NF electrode has a rate capability (46.8% specific capacitance retention from 5 to 50 mV s⁻¹), which is higher than that of CoSe/NF electrode (42.5%) at the same condition (Figure 3e) and other Co_xSe_y-based electrodes, such as core-branch CoSe₂, CoSe₂/C, CoSe₂ nanosheet arrays (Table S3) [34,49,50,51,52,53]. The cycling performance of the CoSe/Co₃O₄-CNTs/NF electrode was further investigated. As shown in Figure 3f, after cycling at 10 A g⁻¹ for 5000 cycles, the CoSe/Co₃O₄-CNTs/NF electrode still retains 97.5% of its initial capacitance, suggesting the CoSe/Co₃O₄-CNTs/NF electrode possesses satisfied long-term cycling stability due to the synergistic effects between the good graphitization of Co₃O₄-CNTs and CoSe.

3.3. Electrochemical Performances of CoSe/Co₃O₄-CNTs/NF//AC ASC

To further explore the potential of CoSe/Co₃O₄-CNTs/NF composite electrodes for practical application, an ASC (CoSe/Co₃O₄-CNTs/NF//AC) was established in 3 M KOH using CoSe/Co₃O₄-CNTs/NF and AC as positive and negative electrodes, respectively. The mass ratio of AC and CoSe/Co₃O₄-CNTs in CoSe/Co₃O₄-CNTs/NF//AC ASC is 17.4:1, which was calculated by Formula (1) in the supporting information. At 10 mV s⁻¹, the complementary CV curves of CoSe/Co₃O₄-CNTs/NF (2631.9 F g⁻¹) and AC electrode (202.3 F g⁻¹) in the typical three-electrode system were obtained in Figure S10, which inferred that the voltage window of CoSe/Co₃O₄-CNTs/NF//AC ASC can be extend to 1.6 V. Both the CV (Figure 4a) and GCD (Figure 4b) curves of CoSe/Co₃O₄-CNTs/NF//AC ASC at different voltage windows exhibit a good electrochemical stability, indicating that the CoSe/Co₃O₄-CNTs/NF//AC ASC can work stably at a high voltage window of 0 to 1.6 V or a low voltage window of 0 to 1.0 V.

Figure 4c reveals the CV curves of the CoSe/Co₃O₄-CNTs/NF//AC ASC measured at different scanning rates of 5–100 mV s⁻¹. The shape of CV curves performs no obvious deformation with the increment of scan rates, verifying its good reversibility. As shown in Figure 4d, the near symmetry of GCD curves of the CoSe/Co₃O₄-CNTs/NF//AC ASC from 1 to 10 A g⁻¹ confirm the good columbic efficiency (CE) of the device. At the different current density of 1, 2, 3, 4, 5, 6, 8 and 10 A g⁻¹, the specific capacitances of CoSe/Co₃O₄-CNTs/NF//AC ASC are 121.9, 112.3, 105.9, 101, 96.6, 92.3, 85.5 and 76.9 F g⁻¹. Figure S11 displays the compared GCD curves of the CoSe/Co₃O₄-CNTs/NF//AC and CoSe/NF//AC at 2 A g⁻¹. The absolutely longer discharge time of CoSe/Co₃O₄-CNTs/NF//AC indicates its enhanced energy storage capability. In addition, CoSe/Co₃O₄-CNTs/NF//AC exhibit an excellent durableness with 92.7% capacitance retention after 10,000 cycles (Figure 4e), suggesting its practicability in real life time.

Furthermore, the Ragone plot in Figure 4f shows the functional relationship between the energy density and the power density of the ASC device, and the value could be obtained by Formulas (3) and (4) in the supporting information. A high energy density of 43.4 Wh kg⁻¹ was obtained at 800 W kg⁻¹, which is higher than that of CoSe/NF//AC (34.6 Wh kg⁻¹ at 800 W kg⁻¹) and many ASCs reported previous, such as CoSe₂//AC [54], Ni_0.6Co_0.4Se₂//BNPC [34], CoSe₂//AC [49], Co_0.85Se//N-PCNs [42] and CoSe//AC [40]. Additionally, a red LED bulb can be powered brightly by two CoSe/Co₃O₄-CNTs/NF//AC ASC devices in series for 15 min, suggesting the potential application of the ASC in energy storages (Figure 4f).

4. Conclusions

In summary, a free-standing and highly active CoSe/Co₃O₄-CNTs hybrid material was synthesized by electrodepositing CoSe nanoparticles on a forest of density and uniform Co₃O₄-CNTs supported by NF, which was used as a positive electrode of supercapacitor directly. Due to the synergist effects of the multicomponent, nanoporous structure and the enlarged SSA of the CoSe/Co₃O₄-CNTs composite material, the hybrid electrode delivered a high specific capacitance of 2906 F g⁻¹, at 5 mV s⁻¹ and 1362.8 F g⁻¹, at 50 mV s⁻¹. ACS assembled using CoSe/Co₃O₄-CNTs/NF and AC as positive and negative electrodes achieved a high energy density of 43.4 Wh kg⁻¹ at 0.8 kW kg⁻¹ with an excellent capacitance retention of 92.7% after 10,000 cycles. Meanwhile, it is worth noting that, due to the facile fabrication process, the novel hybrid electrode structure can be scaled up by supercapacitor manufacturers easily. This work presents an effective strategy to design a hybrid composite electrode for a high-performance asymmetric supercapacitor.