Abstract:Rapidly-growing demand for wearable and flexible devices is boosting the development of flexible lithium ion batteries (LIBs). The exploitation of flexible electrodes with high mechanical properties and superior electrochemical performances has been a key challenge for the rapid practical application of flexible LIBs. Herein, a flexible composite electrode was prepared from the mixed solutions of Li[Li
0.2
Ni
0.13
Co
0.13
Mn
0.54
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“…In recent years, effective energy storage and utilization have attracted much attention for the fast development of electronic devices and the increasing environmental problems (Liu et al, 2010;Zhou et al, 2019a) Among various energy storage strategies, electrochemical energy storage usually plays a key role in the individual electrical and electronic devices with the requirement of stable power supplement (Mathis et al, 2019;Wang et al, 2020) As an important part of electrochemical energy storage device, the electrode should match various requirements for effective energy storage and power supplement, such as high conductivity, high power and energy density, long cycle stability, facile synthesis, high utilization, low cost and environmental friendliness. In different electrochemical energy storage devices, the metallic compounds (usually hydroxide or oxide) with high energy densities and capacities but poor conductivity are used as the electrodes (Nguyen and Montemor 2017;Li et al, 2019) To increase the power density and active the batteries materials, the electrodes with high conductivity are necessary (Chen et al, 2019;Kim and Moon 2020) In commercialized electrodes, the simple mixing of electrochemical active materials and the conductive fillers is a common method. However, the conductive additive unavoidably sacrifices overall energy storage capacity and the mixture with low ratio of conductive fillers could not ensure the stable conductive network in the electrodes, which limits the performance of the electrodes (Farzaneh and Hadi, 2019) To enhance the construction of the conductive network in the electrodes, direct growth of electrochemical active materials on the as-prepared conductive network is an effective approach.…”
In this work, the Co-Ni basic carbonate nanowires were in-situ grown on carbon nanotube (CNT) network through a facile chemical bath deposition method, which could be further converted into active hydroxide via cyclic voltammetry strategy. A series of carbonate nanowire/nanotube with different Co/Ni ratio revealed the different growth status of the nanowires on CNT network. The nanostructures of the as-synthesized samples were examined via powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) techniques. The Co/Ni ratio of the carbonate largely affected the size of the nanowires, that the low Co/Ni ratio was beneficial for thin nanowire formation and the nanowires loading on CNT network. Subsequently, the electrochemical performance of the Co-Ni basic hydroxides was studied in a three-electrode test system. The nanowires with low Co/Ni ratio 1/2 can form nanowire array on individual CNTs, which exhibited better electrochemical capacitive performance than the composite network with high Co/Ni ratio nanowires after electrochemical activation. The addition of Co enhanced the rate performance of the hydroxide/CNT, especially improved the long cycle stability largely compared to the rate performance of pure Ni converted hydroxide/CNT composite film reported by our previous research. This result is valuable for the design of inorganic electrochemical active composites based on conductive networks for energy conversion/storage applications.
“…In recent years, effective energy storage and utilization have attracted much attention for the fast development of electronic devices and the increasing environmental problems (Liu et al, 2010;Zhou et al, 2019a) Among various energy storage strategies, electrochemical energy storage usually plays a key role in the individual electrical and electronic devices with the requirement of stable power supplement (Mathis et al, 2019;Wang et al, 2020) As an important part of electrochemical energy storage device, the electrode should match various requirements for effective energy storage and power supplement, such as high conductivity, high power and energy density, long cycle stability, facile synthesis, high utilization, low cost and environmental friendliness. In different electrochemical energy storage devices, the metallic compounds (usually hydroxide or oxide) with high energy densities and capacities but poor conductivity are used as the electrodes (Nguyen and Montemor 2017;Li et al, 2019) To increase the power density and active the batteries materials, the electrodes with high conductivity are necessary (Chen et al, 2019;Kim and Moon 2020) In commercialized electrodes, the simple mixing of electrochemical active materials and the conductive fillers is a common method. However, the conductive additive unavoidably sacrifices overall energy storage capacity and the mixture with low ratio of conductive fillers could not ensure the stable conductive network in the electrodes, which limits the performance of the electrodes (Farzaneh and Hadi, 2019) To enhance the construction of the conductive network in the electrodes, direct growth of electrochemical active materials on the as-prepared conductive network is an effective approach.…”
In this work, the Co-Ni basic carbonate nanowires were in-situ grown on carbon nanotube (CNT) network through a facile chemical bath deposition method, which could be further converted into active hydroxide via cyclic voltammetry strategy. A series of carbonate nanowire/nanotube with different Co/Ni ratio revealed the different growth status of the nanowires on CNT network. The nanostructures of the as-synthesized samples were examined via powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) techniques. The Co/Ni ratio of the carbonate largely affected the size of the nanowires, that the low Co/Ni ratio was beneficial for thin nanowire formation and the nanowires loading on CNT network. Subsequently, the electrochemical performance of the Co-Ni basic hydroxides was studied in a three-electrode test system. The nanowires with low Co/Ni ratio 1/2 can form nanowire array on individual CNTs, which exhibited better electrochemical capacitive performance than the composite network with high Co/Ni ratio nanowires after electrochemical activation. The addition of Co enhanced the rate performance of the hydroxide/CNT, especially improved the long cycle stability largely compared to the rate performance of pure Ni converted hydroxide/CNT composite film reported by our previous research. This result is valuable for the design of inorganic electrochemical active composites based on conductive networks for energy conversion/storage applications.
“…Small particle size can decrease the migration distance of lithium ions from the interior to the surface and increase the diffusion rate (Lim et al, 2008;Hai et al, 2019;Li et al, 2019;Xiao et al, 2019). Various techniques, including solid-state reaction (Zheng et al, 2008), sol-gel (Zhang et al, 2011) hydrothermal (Kiyoshi et al, 2008;Chang et al, 2014), co-precipitation (Park et al, 2003;Wang et al, 2013), and microwave heating (Wang et al, 2007;Beninati et al, 2008;Guo et al, 2010), are adopted to control particle size.…”
In this study, micro/nanoscale LiFePO 4 /graphene composites are synthesized successfully using a one-step microwave heating method. One-step microwave heating can simplify the reduction step of graphene oxide and provide a convenient, economical, and effective method of preparing graphene composites. The structural analysis shows that LiFePO 4 /graphene has high phase purity and crystallinity. The morphological analysis shows that LiFePO 4 /graphene microspheres and micron blocks are composed of densely aggregated nanoparticles; the nanoparticle size can shorten the diffusion path of lithium ions and thus increase the lithium-ion diffusion rate. Additionally, the graphene sheets can provide a rapid transport path for electrons, thus increasing the electronic conductivity of the material. Furthermore, the nanoparticles being packed into the micron graphene sheets can ensure stability in the electrolyte during charging and discharging. Raman analysis reveals that the graphene has a high degree of graphitization. Electrochemical analysis shows that the LiFePO 4 /graphene has an excellent capacity, high rate performance, and cycle stability. The discharge capacities are 166.3, 156.1, 143.0, 132.4, and 120.9 mAh g −1 at rates of 0.1, 1, 3, 5, and 10 C, respectively. The superior electrochemical performance can be ascribed to the synergy of the shorter lithium-ion diffusion path achieved by LiFePO 4 nanoparticles and the conductive networks of graphene.
“…The development of new materials with excellent performance and low cost is of great significance for improving battery performance and reducing battery cost. Therefore, research on LIBs should mainly focus on the three aspects of battery cost, battery capacity, and new electrode materials (Lv et al, 2018a(Lv et al, ,b, 2019An et al, 2019;Li Y. et al, 2019;Wu et al, 2019;Yuan et al, 2019). With the development of anode materials for LIBs, the defects and advantages of various new materials are highlighted.…”
In this study, silicon/carbon composite nanofibers (Si@CNFs) were prepared as electrode materials for lithium-ion batteries via a simple electrospinning method and then subjected to heat treatment. The morphology and structure of these materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The results show that the structure provides good electrical conductivity and affords sufficient space to accommodate volume expansion during charging/discharging. Furtherly, electrochemical performance tests show that the optimized Si@CNFs have an initial reversible capacity of 1,820 mAh g −1 at a current density of 400 mA g −1 and capacity retention of 80.7% after 100 cycles at a current density of 800 mA g −1. Interestingly, the optimized Si@CNFs have a superior capacity of 1,000 mAh g −1 (400 mA g −1) than others, which is attributed to the carbon substrate nanofiber being able to accommodate the volume expansion of Si. The SEI resistance generated by the Si@CNFs samples is smaller than that of the Si nanoparticles, which confirms that SEI film generated from the Si@CNFs is much thinner than that from the Si nanoparticles. In addition, the connected carbon substrate nanofiber can form a fiber network to enhance the electronic conductivity.
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