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Article

Micro/Nano Energy Storage Devices Based on Composite Electrode Materials

by
Yanqi Niu
1,2,3,*,
Deyong Shang
1,2,3 and
Zhanping Li
1,2,3
1
School of Mechanical, Electronic & Information Engineering, China University of Mining and Technology (Beijing), Beijing 100083, China
2
Institute of Intelligent Mining & Robotics, China University of Mining and Technology (Beijing), Beijing 100083, China
3
Key Laboratory of Intelligent Mining and Robotics, Ministry of Emergency Management, Beijing 100083, China
*
Author to whom correspondence should be addressed.
Nanomaterials 2022, 12(13), 2202; https://doi.org/10.3390/nano12132202
Submission received: 1 June 2022 / Revised: 23 June 2022 / Accepted: 24 June 2022 / Published: 27 June 2022
(This article belongs to the Special Issue Nanostructured Electrodes for High-Performance Supercapacitors and Batteries)
Browse Figures
Versions Notes

Abstract

:
It is vital to improve the electrochemical performance of negative materials for energy storage devices. The synergistic effect between the composites can improve the total performance. In this work, we prepare α-Fe2O3@MnO2 on carbon cloth through hydrothermal strategies and subsequent electrochemical deposition. The α-Fe2O3@MnO2 hybrid structure benefits electron transfer efficiency and avoids the rapid decay of capacitance caused by volume expansion. The specific capacitance of the as-obtained product is 615 mF cm−2 at 2 mA cm−2. Moreover, a flexible supercapacitor presents an energy density of 0.102 mWh cm−3 at 4.2 W cm−2. Bending tests of the device at different angles show excellent mechanical flexibility.

1. Introduction

Supercapacitors (SCs) have attracted much attention from researchers as an innovative type of energy storage device [1,2,3,4]. Compared with traditional capacitors, SCs shows the advantages of superior cycle stability, outstanding power density and fast charging/discharging [5,6,7]. Recently, electronic devices have progressively high requirements for long-term endurance. However, SCs is severely limited with low energy density [8,9,10]. According to the present research results, one of the most valid ways to settle this issue is to increase the specific capacity of electrode [11]. Therefore, designing electrodes with high specific capacitance is the primary task to broaden the application range of SCs.
Currently, the research on positive and negative materials is unevenly developed and research on negative electrodes is relatively little, which makes it difficult to increase the energy density of SCs. Commonly used negative materials are carbon (AC, CNTs and rGO), transition metal oxides (such as Fe3O4, α-Fe2O3, MoO3 and Mn3O4) and a small amount of metal nitride [12,13,14,15,16,17]. Among them, α-Fe2O3 is considered to have the highest potential and is the most widely used anode material, because of its high redox activity, large theoretical specific capacitance and environmental protection [18]. Nonetheless, the weak conductivity of α-Fe2O3 electrodes leads low practical specific capacitance and poor electrochemical stability [19,20]. Manganese dioxide (MnO2) has gained extensive attention in the construction of supercapacitors due to its high oxidation activity [21]. At present, preparing nanocomposite materials utilizing the synergistic effect of two materials not only promotes redox reactions, but also enhance device energy density [22]. Co3O4@MnO2, SnO2@MnO2, ZnO@MnO2, CuO@MnO2 and α-Fe2O3@MnO2 nanostructures were compounded to achieve both excellent cyclic stability and high capacitance [23,24,25,26].
Seol et al. prepared two types of SCs (EDLC and PC) using activated carbon and graphene/Mn3O4 nanocomposite. The performance degradation of EDLC was negligible after 100,000 cycles, while PC was less than 10% after 25,000 cycles [27]. Both devices demonstrate excellent cyclic stability and durability. Sarkar et al. fabricated α-Fe2O3/MnO2 nano-heterostructure with a specific capacitance of 750 mFcm−2 at 2 mV s−1 [28]. However, in practice, these composites, because of loose contact, might impact their electrochemical performance. Thus, it is necessary to construction α-Fe2O3-based materials with unique nanostructures and excellent electrochemical performance. By combining two materials with high oxidative activity, the synthesis of ordered nanostructures will help to construct electrode materials with excellent specific capacitance. The main objective of our research is that by compounding nanomaterials, the advantages of both can be fully exploited and the electrochemical performance can be effectively enhanced.
Herein, we synthesized α-Fe2O3 nanorods structures through a hydrothermal route. Then, a MnO2 film is coated on α-Fe2O3 surface by subsequent electrochemical deposition. When utilized as negative material for SCs, α-Fe2O3@MnO2 electrode shows a specific capacitance of 615 mF cm−2 at 2 mA cm−2. After 10,000 cycles, it maintains 92.3% of the initial capacitance. Finally, a flexible supercapacitor possesses the maximum energy density is 0.102 mWh cm−3 at 4.2 W cm−2. The results under different angles bending tests demonstrated that the device possesses excellent mechanical flexibility.

2. Experimental Section

Material Preparation

The α-Fe2O3 sample was synthesized via a hydrothermal method. In total, 0.808 g Fe(NO3)3·9H2O, 0.2841 g Na2SO4 and 0.5 g PVP were dissolved into 45 mL deionized water. Then, a clean carbon cloth (2.5 × 2.5 cm2) and the above mixed solution was transferred into an 80 mL autoclave and kept 110 °C for 9 h. Finally, the as-synthesized samples were annealed at 350 °C for 2 h (2 °C min−1). An α-Fe2O3@MnO2 sample was prepared by subsequent electrochemical deposition. In total, 2.4509 g C4H6MnO4·4H2O and 1.4204 g Na2SO4 was used as electrolyte. The α-Fe2O3 product was used as the working electrode, Ag/AgCl as the reference electrode and Pt foil as the counter one, with deposition at 1 V constant potential for 30 s. The NiCo2S4 sample was prepared from a homogeneous solution of 0.4 g Ni(NO3)2·6H2O, 1 g Co(NO3)2·6H2O, 0.5 g urea, 0.1 g NH4F and 60 mL deionized water, heated with nickel foam at 140 °C for 12 h. It was then combined with 0.5 g Na2S·9H2O and 60 mL deionized water at 140 °C for 6 h. α-Fe2O3, α-Fe2O3@MnO2 and NiCo2S4 mass loading is 2, 2.3 and 1.2 mg cm−2, respectively.
A supercapacitor was assembled with PVA-KOH gel as the electrolyte, NiCo2S4 as the positive electrode and α-Fe2O3@MnO2 as the negative electrode. The preparation process of PVA-KOH gel electrolyte is as follows: stir 2 g KOH with 2 mL distilled water, mix well and set aside for later use. In a 20 mL beaker, add 2 g polyvinyl alcohol (PVA) and 20 mL deionized water, and stir at 80 °C until transparent. Finally, drop the KOH solution into the PVA solution at a constant speed, and stir at a constant temperature until it becomes a clear and transparent gel.
The crystal structure and the elemental compositions of the products were investigated by an X-ray diffractometer (XRD, Shimadzu-7000, Kyoto, Japan, CuKα, 40 kV) and X-ray photoelectron spectrometer (XPS, Amsterdam, Holland,). The morphology and microstructure of the sample is characterized by scanning electron microscope (SEM, Gemini 300-71-31, Berlin, Germany).
In a three-electrode system, the as-prepared electrode was measured through an electrochemical workstation (Shanghai Chenhua). Electrochemical performance methods include cyclic voltammetry (CV), galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS). The as-synthesized materials were used as the working electrode, Pt foil as the counter electrode and Ag/AgCl as the reference electrode.

3. Results and Discussion

Figure 1 presents the growth process of α-Fe2O3@MnO2 products on carbon cloth. Firstly, α-Fe2O3 nanorods are obtained via a facile hydrothermal approach. Afterwards, a layer of MnO2 film is deposited by subsequent electrochemical deposition on the nanorod-shaped α-Fe2O3 surface.
First, the crystal structure of the obtained product is studied by XRD. Figure 2a shows the XRD patterns of α-Fe2O3 and α-Fe2O3@MnO2 composites. A typical peak of the carbon cloth can be clearly observed. The peaks at 2θ values of 33.4°, 35.8°, 49.7°, 54.4°, 64.3° and 72.4° can be indexed to (104), (110), (024), (116), (300) and (1010) planes of α-Fe2O3 phases, respectively (PDF No. 84-0308). Those at 28.7°, 37.6°, 41.1°, 47.2° and 72.6° match well with (310), (121), (420), (510) and (631) planes of MnO2 (PDF No. 72-1982). The shape and sharpness of the diffraction peaks in figure reveal that the products possess high crystallinity.
Then, XPS is used to investigate the α-Fe2O3@MnO2 materials surface element composition. In Fe 2p spectra, the characteristic peaks of Fe 2p3/2 and Fe 2p1/2 at 711.2 eV and 724.8 eV, respectively (Figure 2b). Additionally, two shake-up satellite peaks (Sat.) at 716 eV and 732.9 eV are determined. This indicates that Fe3+ exists in composite product [29]. Figure 2c depicts the two main peaks of O 1s spectra located at 529.9 eV and 532 eV [30]. Binding energies at 529.9 eV, labeled as O1, denote metal oxygen [31]. Another O2 peak located at 532 eV is due to some degree of hydrolysis on the product surface [32]. For Mn 2p spectra (Figure 2d), four peaks at 642.2 eV, 645.8 eV, 653.9 eV and 658.1 eV are from Mn 2p3/2, Sat., Mn 2p1/2 and Sat., respectively [33].
Figure 3a indicates that α-Fe2O3 shows a short rod-like structure. In addition, it can be found that many nanorods homogeneously grown on carbon cloth with uniform size and shape, and the cross-section of nanorods is rough. The high magnification image (Figure 3b) shows the as-synthesized products average length is 100 nm. Figure 3c presents a thin MnO2 film covers α-Fe2O3, and still maintains the shape of nanorods. From Figure 3d, the cross-section of α-Fe2O3@MnO2 nanorods becomes smooth.
Next, we analyzed several as-obtained electrode electrochemical performances by CV, GCD and EIS. Figure 4a shows CV curves of α-Fe2O3, MnO2 and α-Fe2O3@MnO2 materials. Evidently, α-Fe2O3@MnO2 delivers a large CV area in −1–0 V, reflecting its good energy storage effect in this range. At 8 mA cm−2 (Figure 4b), the GCD curves obvious that α-Fe2O3@MnO2 product with long discharge times, which can be correlative to the synergistic effect between α-Fe2O3 and MnO2 materials. Figure 4c presents CV curves of α-Fe2O3@MnO2 from 5 to 40 mV s−1. The shape of CV curves almost the same as the scan rate increased, indicating excellent reversibility of electrode. In Figure 4d, the GCD curves of α-Fe2O3@MnO2 materials are measured from 2 to 10 mA cm−2. Areal capacitance (Ca) is obtained by GCD, and the equation is shown below:
Ca = I∫Vdt/V
In Equation (1), I is current density, ∫ Vdt stands for the integral area of discharge curve and V is the constant discharge voltage range (V). The α-Fe2O3@MnO2 electrode delivers 615 mF cm−2 specific capacitance at 2 mA cm−2
EIS is a significant factor in assessing the electrochemical kinetics of products. The sample is tested over a frequency range of 0.01 Hz to 100 kHz (Figure 4e). In the low frequency region, the slope of the straight line shows the ion diffusion resistance. Among the three samples, α-Fe2O3@MnO2 sample presents the largest slope, which expresses fast diffusion of ions in electrolyte [34]. The intersection with the real axis represents the equivalent resistance (Rs) [35]. α-Fe2O3, MnO2 and α-Fe2O3@MnO2 electrodes Rs value is 5.1 Ω, 4.1 Ω and 3.3 Ω, respectively. According to above analysis, α-Fe2O3@MnO2 shows the largest slope and smallest Rs, so the conductivity of composite material is better than α-Fe2O3 and MnO2.
At the end, the cyclic stability is investigated at 4 mA cm−2. Figure 4f indicates that the capacitance of α-Fe2O3@MnO2 is only reduced by 7.7% after 10,000 cycles, while α-Fe2O3 and MnO2 products present only 71.4% and 75% of the initial capacitance. This phenomenon is due to the MnO2 film covering the α-Fe2O3 nanorods, which can help alleviate the volume expansion during long cycle measurements. Similarly, the positive NiCo2S4 is also studied by the same methods. Figure 4g presents the CV curves of NiCo2S4 sample. Redox peaks and shapes, confirming its pseudocapacitive material. Five symmetrical GCD curves shows an obvious platform (Figure 4h), which indicates their Faradaic redox behavior [36]. At 2 mA cm−2, the specific capacitance is 720.8 mF cm−2. Nyquist plots of NiCo2S4 products are shown in Figure 4i; the value of Rs is 0.9 Ω.
To further explore the α-Fe2O3@MnO2 electrodes for practical applications, a flexible supercapacitor is assembled. From Figure 5a, the voltage windows of α-Fe2O3@MnO2 and NiCo2S4 are −1–0 V and 0–0.6 V, respectively. Figure 5b shows CV curves from 1.1 V to 1.5 V with a sweep rate of 100 mV s−1, demonstrating the device can maintain operate stably within 1.5 V. It can be seen that with the decrease of voltage, the area becomes small. Figure 5c depicts all CV curves at different scan rates keep similar shapes, revealing outstanding rate performance of device. GCD curves from 1 to 8 mA cm−2 possess the same charging and discharging time (Figure 5d). The specific capacitance of the device at 1 mA cm−2 is 37.8 mF cm−2 and it still delivers 15.6 mF cm−2 at 8 mA cm−2. The equivalent resistance value of the device is 1.9 Ω, as shown in Figure 5e.
At present, electronic devices are developing towards wearable, which puts forward higher requirements for the mechanical flexibility of supercapacitors [37]. We twisted the device and then examined it by cyclic voltammetry (Figure 5f). While device is folded at 15°, 45°, 90° and 135°, the shape sustains virtually unchanged, demonstrating its superior mechanical stability. Figure 5g illustrates that the device maintains 88.9% capacitance retention after 6000 cycles. Figure 5h is the Ragone diagram of α-Fe2O3@MnO2//NiCo2S4. The capacitor values of energy density (E) and power density (P) can be derived based on the Equations (2) and (3):
E = 1/2 × Ca × V2
P = 3600 × E/Δt
where Ca stands for the areal capacitance of the capacitor, V represent the discharge voltage and Δt is the discharge time. At 1 mA cm−2, the energy density of device is 0.102 mWh cm−3 at 4.2 W cm−2. This is better than some previously reported materials [38,39,40,41] (Table 1).
α-Fe2O3@MnO2 delivers excellent performance, which can be explained by the following reasons: (a) Nanostructure uniformly covered on the carbon cloth, which provides outstanding electrical conductivity and flexibility; (b) With α-Fe2O3 as a strong mechanical support and MnO2 as an outer layer, this structure not only protects the morphological structure, but also provides many active sites; (c) The composite utilizes the synergistic effect of α-Fe2O3 and MnO2, so that electrode processes high capacitance and low resistance.

4. Conclusions

In this manuscript, α-Fe2O3@MnO2 nanorods are synthesized through a hydrothermal route and subsequent electrochemical deposition. By combining two oxides of α-Fe2O3 and MnO2, it is favorable to accelerate the electron transport and the oxidation reaction. The synergistic effect between two materials improves electrochemical performance for negative electrode. MnO2 film, after electrodeposition, affects the performance of the electrode material, and the full use of the active area of the film increases, which increases the capacitance of the electrode material. XPS results show that the material processes abundant redox valence states. α-Fe2O3@MnO2 sample presents high specific capacitance and excellent cycling stability. Furthermore, the as-assembled capacitors still show outstanding electrochemical performance and mechanical stability. Therefore, it provides an alternative method for constructing supercapacitor negative materials with higher specific capacitance.

Author Contributions

Conceptualization, Y.N and D.S.; methodology, Y.N.; software, Z.L; validation, Y.N, D.S. and Z.L.; formal analysis, D.S.; investigation, Z.L.; resources, Y.N.; data curation, Y.N.; writing—original draft preparation, D.S.; writing—review and editing, Y.N.; visualization, D.S.; supervision, Y.N.; project administration, Y.N.; funding acquisition, Y.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Ye, S.; Ding, C.M.; Liu, M.Y.; Wang, A.Q.; Huang, Q.G.; Li, C. Water oxidation catalysts for artificial photosynthesis. Adv. Mater. 2019, 31, 1902069. [Google Scholar] [CrossRef] [PubMed]
  2. Liu, Y.; Wu, X. Hydrogen and sodium ions co-intercalated vanadium dioxide electrode materials with enhanced zinc ion storage capacity. Nano Energy 2021, 86, 106124. [Google Scholar] [CrossRef]
  3. Cao, X.H.; Tan, C.L.; Zhang, X.; Zhao, W.; Zhang, H. Solution-processed two-dimensional metal dichalcogenide-based nanomaterials for energy storage and conversion. Adv. Mater. 2016, 28, 6167. [Google Scholar] [CrossRef] [PubMed]
  4. Dai, M.Z.; Zhao, D.P.; Wu, X. Research progress on transition metal oxide based electrode materials for asymmetric hybrid capacitors. Chin. Chem. Lett. 2020, 31, 2177–2188. [Google Scholar] [CrossRef]
  5. Rakibuddin, M.; Shinde, M.A.; Kim, H. Sol-gel fabrication of NiO and NiO/WO3 based electrochromic device on ITO and flexible substrate. Ceram. Int. 2020, 46, 8631–8639. [Google Scholar] [CrossRef]
  6. Zheng, X.; Han, Z.C.; Yao, S.Y.; Xiao, H.H.; Chai, F.; Qu, F.Y.; Wu, X. Spinous α-Fe2O3 hierarchical nanostructures anchored on Ni foam for supercapacitors electrodes and visible light driven photocatalysts. Dalton Trans. 2016, 45, 7094–7103. [Google Scholar] [CrossRef]
  7. Zhao, D.P.; Zhang, R.; Dai, M.Z.; Liu, H.Q.; Jian, W.; Bai, F.Q.; Wu, X. Constructing high efficient CoZnxMn2-xO4 electrocatalyst by regulating the electronic structure and surface reconstruction. Small 2022, 18, 107268. [Google Scholar] [CrossRef]
  8. Liu, H.Q.; Zhao, D.P.; Hu, P.F.; Chen, K.F.; Wu, X.; Xue, D.F. Design strategies toward achieving high performance [email protected] electrode materials, Mater. Today Phys. 2020, 13, 100197. [Google Scholar]
  9. Rakibuddin, M.; Shinde, M.A.; Kim, H. Facile solegel fabrication of MoS2 bulk, flake and quantum dot for electrochromic device and their enhanced performance with WO3. Electrochim. Acta 2020, 349, 136403. [Google Scholar] [CrossRef]
  10. Ahmad, K.; Ahmad, M.A.; Song, G.; Kim, H. Design and fabrication of MoSe2/WO3 thin films for the construction of electrochromic devices on indium tin oxide based glass and flexible substrates. Ceram. Int. 2021, 47, 34297–34306. [Google Scholar] [CrossRef]
  11. Liu, H.Q.; Zhao, D.P.; Liu, Y.; Tong, Y.L.; Wu, X.; Shen, G.Z. NiMoCo layered double hydroxides for electrocatalyst and supercapacitor electrode. Sci. China Mater. 2021, 64, 581–591. [Google Scholar] [CrossRef]
  12. Xia, T.; Zhao, D.P.; Xia, Q.; Umar, A.; Wu, X. Realizing high performance flexible supercapacitors by electrode modification. RSC Adv. 2021, 11, 39045–39050. [Google Scholar] [CrossRef] [PubMed]
  13. Xia, Q.; Xia, T.; Dai, M.Z.; Wu, X.; Zhao, Y.F. A facile synthetic protocol of α-Fe2O3@FeS2 nanocrystals for advanced electrochemical capacitor. CrystEngComm 2021, 23, 2432–2438. [Google Scholar] [CrossRef]
  14. Xia, Q.; Xia, T.; Wu, X. PPy decorated α-Fe2O3 nanosheets as flexible supercapacitor electrode. Rare Met. 2022, 41, 1195–1201. [Google Scholar] [CrossRef]
  15. Liu, H.; Zhu, J.; Li, Z.; Shi, Z.; Zhu, J.; Mei, H. Fe2O3/N doped rGO anode hybridized with NiCo LDH/Co(OH)2 cathode for battery-like supercapacitor. Chem. Eng. J. 2021, 403, 126325. [Google Scholar] [CrossRef]
  16. Yang, J.; Xiao, X.; Chen, P.; Zhu, K.; Cheng, K.; Ye, K.; Wang, G.L.; Cao, D.X.; Yan, J. Creating oxygen-vacancies in MoO3-x nanobelts toward high volumetric energydensity asymmetric supercapacitors with long lifespan. Nano Energy 2019, 58, 455–465. [Google Scholar] [CrossRef]
  17. Feng, J.X.; Ye, S.H.; Lu, X.F.; Tong, Y.X.; Li, G.R. Asymmetric paper supercapacitor based on amorphous porous Mn3O4 negative electrode and Ni(OH)2 positive Electrode: A novel and high-performance flexible electrochemical energy storage device. ACS Appl. Mater. Inter. 2015, 7, 11444–11451. [Google Scholar] [CrossRef]
  18. Liu, L.; Lang, J.; Zhang, P.; Hu, B.; Yan, X. Facile synthesis of Fe2O3 nano-dots@nitrogen-doped graphene for supercapacitor electrode with ultralong cycle life in KOH electrolyte. ACS Appl. Mater. Inter. 2016, 8, 9335–9344. [Google Scholar] [CrossRef]
  19. Ready, D.W. Mass Transport and Sintering in Impure Ionic Solids. J. Am. Ceram. Soc. 1966, 49, 366. [Google Scholar] [CrossRef]
  20. Liu, T.; Ling, Y.; Yang, Y.; Finn, L.; Collazo, E.; Zhai, T.; Li, Y. Investigation of hematite nanorod–nanoflake morphological transformation and the application of ultrathin nanoflakes for electrochemical devices. Nano Energy 2015, 12, 169–177. [Google Scholar] [CrossRef]
  21. Racik, M.K.; Manikandan, A.; Mahendiran, M.; Madhavan, J.; Raj, M.V.A.; Mohamed, M.G.; Maiyalagan, T. Hydrothermal synthesis and characterization studies of α-Fe2O3/MnO2 nanocomposites for energy storage supercapacitor application. Ceram. Int. 2020, 46, 6222–6233. [Google Scholar] [CrossRef]
  22. Sun, Z.P.; Ai, W.; Liu, J.L.; Qi, X.Y.; Wang, Y.L.; Zhu, J.H.; Zhang, H.; Yu, T. Facile fabrication of hierarchical ZnCo2O4/NiO core/shell nanowire arrays with improved lithium-ion battery performance. Nanoscale 2014, 6, 6563. [Google Scholar] [CrossRef] [PubMed]
  23. Liu, J.P.; Jiang, J.; Cheng, C.W.; Li, H.X.; Zhang, J.X.; Gong, H.; Fan, H.J. Co3O4 nanowire@MnO2 ultrathin nanosheet core/shell arrays: A new class of high-performance pseudocapacitive materials. Adv. Mater. 2011, 23, 2076. [Google Scholar] [CrossRef] [PubMed]
  24. Sun, X.; Li, Q.; Lv, Y.N.; Mao, Y.B. Three-dimensional ZnO@MnO2 core@shell nanostructures for electrochemical energy storage. Chem. Commun. 2013, 49, 4456–4458. [Google Scholar] [CrossRef] [PubMed]
  25. Chen, H.; Zhou, M.; Wang, T.; Li, F.; Zhang, Y.X. Construction of unique cupric oxide-manganese dioxide core-shell arrays on a copper grid for high-performance supercapacitors. J. Mater. Chem. A 2016, 4, 10786. [Google Scholar] [CrossRef]
  26. Liu, Y.; Jiao, Y.; Yin, B.S.; Zhang, S.W.; Qu, F.Y.; Wu, X. Enhanced electrochemical performance of hybrid SnO2@MOx (M = Ni, Co, Mn) core-shell nanostructures grown on flexible carbon fibers as the supercapacitor electrode materials. J. Mater. Chem. A 2015, 3, 3676. [Google Scholar] [CrossRef]
  27. Seol, M.L.; Nam, I.; Ribeiro, E.L.; Segel, B.; Lee, D.; Palma, T.; Wu, H.L.; Mukherjee, D.; Khomami, B.; Hill, C.; et al. All-Printed in-plane supercapacitors by sequential additive manufacturing process. ACS Appl. Energy Mater. 2020, 3, 4965–4973. [Google Scholar] [CrossRef]
  28. Sarkar, D.; Khan, G.G.; Singh, A.K.; Mandal, K. High-performance pseudocapacitor electrodes based on α-Fe2O3/MnO2 core-shell nanowire eterostructure arrays. J. Phys. Chem. C 2013, 117, 15523. [Google Scholar] [CrossRef]
  29. Zhang, Y.; Zeng, T.; Huang, D.X.; Yan, W.; Zhang, Y.Y.; Wan, Q.J.; Yang, N.J. High-energy-density supercapacitors from dual pseudocapacitive nanoelectrodes. ACS Appl. Energy Mater. 2021, 3, 10685–10694. [Google Scholar] [CrossRef]
  30. Tang, Q.Q.; Wang, W.Q.; Wang, G.C. The perfect matching between the low-cost Fe2O3 nanowire anode and the NiO nanoflake cathode significantly enhances the energy density of asymmetric supercapacitors. J. Mater. Chem. A 2015, 3, 6662–6670. [Google Scholar] [CrossRef]
  31. Zhao, J.; Li, Z.J.; Yuan, X.C.; Yang, Z.; Zhang, M.; Meng, A.; Li, Q.D. A high-energy density asymmetric supercapacitor based on Fe2O3 nanoneedle arrays and NiCo2O4/Ni(OH)2 hybrid nanosheet arrays grown on sic nanowire networks as free-standing advanced electrodes. Adv. Energy Mater. 2018, 8, 1702787. [Google Scholar] [CrossRef]
  32. Zhang, M.; Wu, X.W.; Yang, D.Z.; Qin, L.Y.; Zhang, S.Y.; Xu, T.; Zhao, T.Y.; Yu, Z.Z. Ultraflexible reedlike carbon nanofiber membranes decorated with Ni-Co-S nanosheets and Fe2O3-C coreshell nanoneedle arrays as electrodes of flexible quasisolidstate asymmetric supercapacitors. ACS Appl. Energy Mater. 2021, 4, 1505–1516. [Google Scholar]
  33. Chen, Y.C.; Kang, C.X.; Ma, L.; Fu, L.K.; Li, G.H.; Hu, Q.; Liu, Q.M. MOF-derived Fe2O3 decorated with MnO2 nanosheet arrays as anode for high energy density hybrid supercapacitor. Chem. Eng. J. 2021, 417, 129243. [Google Scholar] [CrossRef]
  34. Hong, X.Y.; Li, J.H.; Zhu, G.S.; Xu, H.R.; Zhang, X.Y.; Zhao, Y.Y.; Zhang, J.; Yan, D.L.; Yu, A.B. Cobalt-nickel sulfide nanosheets modified by nitrogen-doped porous reduced graphene oxide as high-conductivity cathode materials for supercapacitor. Electrochim. Acta 2020, 362, 37156. [Google Scholar] [CrossRef]
  35. Ke, Q.; Guan, C.; Zhang, X.; Zheng, M.; Zhang, Y.; Cai, W.; Zhang, H.; Wang, J. Surface charge-mediated formation of H-TiO2@Ni(OH)2 heterostructures for high-performance supercapacitors. Adv. Mater. 2017, 29, 1604164. [Google Scholar] [CrossRef]
  36. Kong, W.; Lu, C.C.; Zhang, W.; Pu, J.; Wang, Z.H. Homogeneous core–shell NiCo2S4 nanostructures supported on nickel foam for supercapacitors. J. Mater. Chem. A 2015, 3, 12452–12460. [Google Scholar] [CrossRef]
  37. Hu, P.F.; Zhao, D.P.; Liu, H.Q.; Chen, K.F.; Wu, X. Engineering PPy decorated MnCo2O4 urchins for quasi-solid-state hybrid capacitors. CrystEngComm 2019, 21, 1600–1606. [Google Scholar] [CrossRef]
  38. Wang, Y.; Zhang, Y.Z.; Dubbink, D.; Elshof, J.E.T. Inkjet Printing of δ-MnO2 Nanosheets for Flexible Solid-state Microsupercapacitor. Nano Energy 2018, 49, 481–488. [Google Scholar] [CrossRef]
  39. Wang, Y.; Du, Z.X.; Xiao, J.F.; Cen, W.L.; Yuan, S.J. Polypyrrole-encapsulated Fe2O3 nanotube arrays on a carbon cloth support: Achieving synergistic effect for enhanced supercapacitor performance. Electrochim. Acta 2021, 386, 138486. [Google Scholar] [CrossRef]
  40. Yang, P.H.; Xiao, X.; Li, Y.Z.; Ding, Y.; Qiang, P.F.; Tan, X.H.; Mai, W.J.; Lin, Z.Y.; Wu, W.Z.; Li, T.Q.; et al. Hydrogenated ZnO Core-Shell Nanocables for Flexible Supercapacitors and Self-Powered Systems. ACS Nano 2013, 7, 2617–2626. [Google Scholar] [CrossRef]
  41. Wu, X.H.; Chen, Y.H.; Liang, K.J.; Yu, X.A.; Zhuang, Q.Q.; Yang, Q.; Liu, S.F.; Liao, S.; Lia, N.; Zhang, H.Y. Fe2O3 nanowire arrays on Ni-coated yarns as excellent electrodes for high performance wearable yarn-supercapacitor. J. Alloys Compd. 2021, 886, 158156. [Google Scholar] [CrossRef]
Nanomaterials 12 02202 g001 550
Figure 1. Synthesis schematic of the products.
Figure 1. Synthesis schematic of the products.
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Figure 2. Structural characterization using (a) XRD patterns and (b–d) XPS spectra.
Figure 2. Structural characterization using (a) XRD patterns and (b–d) XPS spectra.
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Figure 3. SEM images of the samples. (a,c) single materials (b,d) conposite materials.
Figure 3. SEM images of the samples. (a,c) single materials (b,d) conposite materials.
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Figure 4. Electrochemical performance. (a) CV curves. (b) GCD curves. (c) CV curves of α-Fe2O3@MnO2. (d) GCD curves of α-Fe2O3@MnO2. (e) Nyquist plots. (f) Cycling performance at 4 mA cm−2. (g) NiCo2S4 CV curves. (h) NiCo2S4 GCD curves. (i) NiCo2S4 Nyquist plots.
Figure 4. Electrochemical performance. (a) CV curves. (b) GCD curves. (c) CV curves of α-Fe2O3@MnO2. (d) GCD curves of α-Fe2O3@MnO2. (e) Nyquist plots. (f) Cycling performance at 4 mA cm−2. (g) NiCo2S4 CV curves. (h) NiCo2S4 GCD curves. (i) NiCo2S4 Nyquist plots.
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Figure 5. (a) CV curves of the α-Fe2O3@MnO2 and NiCo2S4 electrode at 40 mV s−1. (b) CV curves in different potential windows at 50 mV s−1. (c) CV curves. (d) GCD curves. (e) EIS. (f) CV curves at different bending angles. (g) cycling performance at 2 mA cm−2. (h) Ragone plot.
Figure 5. (a) CV curves of the α-Fe2O3@MnO2 and NiCo2S4 electrode at 40 mV s−1. (b) CV curves in different potential windows at 50 mV s−1. (c) CV curves. (d) GCD curves. (e) EIS. (f) CV curves at different bending angles. (g) cycling performance at 2 mA cm−2. (h) Ragone plot.
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Table
Table 1. Electrochemical performance of various devices.
Table 1. Electrochemical performance of various devices.
SupercapacitorCapacitanceEnergy Density
(mWh cm−3)		Power Density
(W cm−2)		Capacitance RetentionRef.
PEDOT: PSS/δ-MnO22.4 F cm−30.0180.01888%[38]
Fe2O3NTs@PPy//MnO2-0.0594192%[39]
ZnO@MnO226 mF cm−20.042.4487.5%[40]
Fe2O3//Ni/Yarns0.67 F cm−30.0863.8787.1%[41]
α-Fe2O3@MnO2//NiCo2S437.8 mF cm−20.1024.288.9%this work
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Niu, Y.; Shang, D.; Li, Z. Micro/Nano Energy Storage Devices Based on Composite Electrode Materials. Nanomaterials 2022, 12, 2202. https://doi.org/10.3390/nano12132202

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Niu Y, Shang D, Li Z. Micro/Nano Energy Storage Devices Based on Composite Electrode Materials. Nanomaterials. 2022; 12(13):2202. https://doi.org/10.3390/nano12132202

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Niu, Yanqi, Deyong Shang, and Zhanping Li. 2022. "Micro/Nano Energy Storage Devices Based on Composite Electrode Materials" Nanomaterials 12, no. 13: 2202. https://doi.org/10.3390/nano12132202

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