Carbon Nanotube Based Fiber Supercapacitor as Wearable Energy Storage
- 1School of Fashion Engineering, Shanghai University of Engineering Science, Shanghai, China
- 2Faculty of Engineering and Information Sciences, School of Electrical, Computer and Telecommunications Engineering, University of Wollongong, Wollongong, NSW, Australia
- 3School of Textile Engineering, Zhongyuan University of Technology, Zhengzhou, China
- 4Intelligent Polymer Research Institute, Australian Institute for Innovative Materials, University of Wollongong, Wollongong, NSW, Australia
Energy storage is a key requirement for the emerging wearable technologies. Recent progress in this direction includes the development of fiber based batteries and capacitors and even some examples of such fibers incorporated into prototype textiles. Herein we discuss the advantages of using the wet-spinning process to create nanostructured carbon based materials as wearable energy storage. The ability to control the physical, mechanical, electrical, and electrochemical properties of carbon nanotube based fibers holds great promise to develop smart polymeric structure as an energy storing materials including fibers and textiles. This is the first comprehensive review to discuss effect of nanostructured energy materials on the electrochemical properties of carbon nanotube based fibers which covers the various compositions, spinning and fabrication conditions on the performance of wearable energy storage.
Today's “wearable technologies” mostly consist of electronic devices like wrist bands for fitness and health monitoring. However, it is predicted that in the coming years the fastest growing industry sector will be smart garments, where electronics are incorporated into the fabrics. Recently, leading fashion house Ralph Lauren released a health monitoring sports shirt that incorporates a fabric strain sensor. While functional, the shirt also required a separate and bulky Bluetooth communications module and battery pack for power. The growth projections for smart garments are based around seamless and invisible integration of the electronic functionality into the garments, without losing their aesthetic appeal and comfort (i.e., “fashion”). A particularly high priority is to develop wearable energy storage systems as these are the critical component of future wearable electronics. Consequently, the study of wearable energy storage devices has been under-taken by researchers around the world in recent decades in a quest to meet growing demands in the field of biomedical devices as well as communication and entertainment systems. To develop wearable energy storage, fiber-based or wire-shaped device can be easily integrated into stretchable yarns or fabrics to fulfill a more practical demand of wearable energy storage, conversation or transition in our daily life. Therefore, stretchable and bendable supercapacitors or batteries are two typical energy storage devices used in practical applications while composition and structure of materials used are critical in determining stretchability.
Supercapacitor as one of the most promising energy storage technologies, with relatively high charge-discharge speed and power density has been widely researched. Fiber-based supercapacitors can seamlessly be incorporated in smart garments owing to the softness, knittability, or weavability of the fiber electrodes. The selection of materials is important to manufacture a fiber electrode, which can influence the electrochemical properties of the device (Dalton et al., 2003; Zhang et al., 2010). From one-dimensional fibers and yarns to two- or three-dimensional fabrics, numerous raw materials including natural and synthetic substances can be used as electrode materials for flexible supercapacitors in wearable devices. The development of electrode materials for fiber-based supercapacitors can reflect its practical application value in the following three aspects: (1) the diversity of fiber materials, which can be utilized to develop supercapacitors with different characteristics to compensate for the differences between materials; (2) The structural advantages of the fiber can realize the flexibility in three-dimensional direction to adapt to a variety of product designs, and can also be manufactured into fabrics with good wearability by traditional textile technology; (3) based on existing textile technologies, the mass production of fiber can primely promote the industrialization of flexible energy storage devices. Carbon nanotube fibers, acted as a conductor and substrate, have been demonstrated with supreme flexibility and stiffness as well as the easy post-treatment to combine with active materials comparing with the metal wires (Huang et al., 2015, 2016). Here, we will mainly discuss the processes and novel methods used to fabricate fibers composed of carbon nanotubes and the additional nanostructured energy materials for fabrication of the fiber-based supercapacitor.
Carbon Nanotube Fiber-based Supercapacitor
Synthesis of Carbon Nanotube
Carbon nanotubes (CNT) were discovered by Iijima in 1990s (Iijima, 1991), and have been utilized in a variety of applications such as actuators, artificial muscles, and lightweight electromagnetic shields (Foroughi et al., 2011, 2016; Haines et al., 2014; Sun et al., 2015). The preparation methods of carbon nanotubes basically use energy to decompose the carbon source into atomic or ionic forms, and then condense into a one-dimensional structure of carbon. At present, three most popular fabrication methods have been utilized to obtain large-scale carbon nanotubes, which are, Arc Discharge method (Chhowalla and Unalan, 2011), Laser Ablation method (Danilov et al., 2014) and Chemical Vapor Deposition (CVD) method (Kumar and Ando, 2010). CNT prepared by different methods significantly vary with respect to their structure and properties. Generally, carbon nanotubes prepared by arc discharge method and laser ablation method have high crystallinity and straightness, but these methods suffer from low yield. CVD has achieved industrial production of carbon nanotubes. However, due to the low growth temperature, the prepared carbon nanotubes have a poor degree of graphitization with many defects on ends and surfaces. In the preparation process, catalyst particles are often introduced, which are difficult to be removed and affect the properties and further applications of carbon nanotubes.
Arc Discharge Method
In arc discharge method, a vacuum reaction chamber is filled with an inert gas or hydrogen, two graphite rods act as a cathode and an anode, respectively, and a DC voltage is applied to the graphite electrode resulting in a strong electric arc (as shown in Figure 1). During the arc discharge, the graphite rod of the anode is continuously evaporated at high temperature generated by the arc, and the product containing carbon nanotubes is subsequently deposited on the cathode. Generally, the purity and yield of multi-walled carbon nanotubes (MWNTs) are susceptible to the inside pressure of the reaction vessel (Ebbesen and Ajayan, 1992). Shimotani et al. (2001) found that the yield of MWNTs increased with the increasing gas pressure in the reaction vessel ranged from 150 to 400 Torr for all organic gases. In addition to DC arc discharge, pulsed arcs can also be utilized to prepare MWNTs in the atmosphere (Parkansky et al., 2004). Moreover, some reports shown that high-purity MWNTs can be prepared on a large scale in liquid gases such as liquid nitrogen (Jung et al., 2003).
Figure 1. Schematic progress of CNT formation by arc-discharge method (Journet and Bernier, 1998).
The preparation of SWNTs by arc discharge method usually requires a transition metal catalyst, and the anode generally is made of a composite material, such as graphite composited with a commercial metal like Ni, Fe, Co, Ag, Pt, or a composite of two metals, such as Co-Ni, Fe-Ni, Fe-No, Co-Cu, Ni-Cu, etc. (Ando et al., 2004). In order to ensure the high efficiency of production, it is necessary to guarantee a stable current density and anode consumption rate during the reaction process so that a constant spacing between the electrodes should be maintained. Although the production of carbon nanotubes by arc discharge method has gradually become more and more mature by adjusting the preparation conditions in terms of catalyst, electrode size, electrodes spacing, and types of raw materials, the yield of carbon nanotubes produced by such method is relatively low due to the difficulties in arc control and high cost of fabrication (Pillai et al., 2008).
Laser Ablation Method
High-quality and high-purity SWNTs can be prepared using laser ablation, which was first proposed by Smalley's team in 1995 (Guo et al., 1995; schematically shown in Figure 2). With the similar principle and mechanism of arc discharge method, carbon nanotubes produced by laser ablation method exhibit a relatively high crystallinity and straightness. In this method the energy is generated by hitting a graphite target containing catalytic materials (such as nickel and cobalt) with a specific wavelength of laser (Guo et al., 1992). Transition metals such as Fe, Co, and Ni are firstly doped as a catalyst into the graphite target and placed in the reactor. The surface of the target is bombarded with a laser when the reaction temperature reaches 2,000°C under the protection of an inert gas (such as He; Thess et al., 1996). The formed gaseous carbon and catalyst particles are then brought from the high temperature zone to the low temperature zone by the gas flow, at which time the gaseous carbons are collided with each other to form carbon nanotubes in the carrier gas under the action of the catalyst.
The performance of CNTs prepared by laser ablation is mainly affected by the following parameters: laser parameters (energy fluence, peak power, continuous wave and pulse wave, repetition rate, oscillation wavelength), pressure and material composition of the combustion chamber, structure and chemical composition of the target material, flow and pressure of the buffer gas, spacing between target material and matrix, and the temperature of matrix and ambient (Ikegami et al., 2004).
Chemical Vapor Deposition Method
The CVD method has attracted significant interest by researchers. This method mainly uses a hydrocarbon substance as a carbon source to be cleaved into carbon clusters on the surface of the catalyst particles and then regrouped when the carbon source gas is in contact with the catalyst in the quartz tube at a suitable temperature (shown in Figure 3; Ando et al., 2004). A transition metal such as iron, cobalt, nickel, molybdenum, niobium, and tantalum is generally used as a catalyst. The experimental results show that the size of the metal catalyst particles predominantly determines the inner and outer diameter of the carbon nanotubes. Therefore, carbon nanotubes with higher purity and uniform size distribution can be grown by selectively controlling the type and particle size of the catalyst (Steiner et al., 2009).
Compared with other methods, CVD method has the advantages of easy-control of reaction process, simple and convenient preparation apparatus, relatively low growth temperature and high purity, low cost, strong adaptability, and large-scale production. The method also has the ability to align carbon nanotubes arrays by controlling the application of catalysts and increase the density of the array by liquid-induced process (Yao et al., 2007; Zhang K. et al., 2017), which has been widely used in the preparation of carbon nanotubes (Prasek et al., 2011; Das et al., 2016).
Carbon Nanotube Based Fibers
Carbon nanotubes have been widely utilized as electrode materials owing to their extraordinary physical and chemical properties, and assemblies of CNTs in fiber format have been shown to be a viable platform to take these properties from the nanoworld to macroscopic scale (Jarosz et al., 2011, 2012; Lu et al., 2017). As the electrode materials, the conductivity and strength of CNT fibers should be satisfied with the requirement of supercapacitor. The formation of carbon nanotube based fiber can be divided into wet-spun method and solid-state spun method.
Wet-Spun CNT Fibers
Wet-spinning as one of the conventional fiber fabricating methods, and can enlarge the yield of fibers. A 60 wt% carbon nanotube (prepared by arc discharged method) contained fiber was firstly developed by Vigolo and co-workers, in which the fiber were prepared by extruding the surfactant-stabilized single-walled carbon nanotube (SWNT) solution into a PolyVinyl Alcohol (PVA) coagulation bath (Vigolo et al., 2000). In previous researches, dispersing CNTs with polymers or surfactant could form a stable spinning solution, the composite fibers were prepared by following extrusion into coagulation bath and extension (Vigolo et al., 2002; Dalton et al., 2003; Miaudet et al., 2005). With the existence of polymers, large-molecule surfactant, the electrical, and thermal conductivity of the fiber was extremely poor although the mechanical properties were reasonable owing to the enhancement of CNTs. Using this technology, the existing polymer can only be completely removed by thermal annealing that causes pyrolysis of the polymer, which will degrade the mechanical properties of the fibers by decreasing strength and modulus and making them rather brittle (Badaire et al., 2004; Munoz et al., 2004; Miaudet et al., 2005). Polymer-free carbon nanotube fibers can alternatively be achieved by utilizing a small molecule coagulation bath system (Steinmetz et al., 2005), pH adjusting flocculation-based process (Kozlov et al., 2005), super acid based wet-spun fabrication (Ericson et al., 2004; Ramesh et al., 2004; Davis et al., 2009; Parra-Vasquez et al., 2010; Behabtu et al., 2013; Ma et al., 2013; Bucossi et al., 2015). The spinning parameters can also draw an important role in the preparation, including the diameter and shape of needle or spinneret, extruding speed and rotating speed in rotate spinning method, which will affect the morphologies and performances of the obtained fibers (Kozlov et al., 2005).
Solid-State Spun CNT Fibers
CNT fibers prepared by solid-state spinning can be expanded with following methods: directly spinning from a CVD grown CNT aerogel; spinning from a vertical grown CNT arrays; twisting/rolling from “cotton” like CNT bundles or a CNT film. The carbon nanotubes can be self-assembled into fiber due to the van der Waals interactions, by which CNTs hold together to form aligned bundles.
Floating CVD was initially utilized to grow CNTs, Li et al. (2004) then developed a method to draw a fiber from the CNT aerogel formed in a vertical furnace with a purity of 85–95 wt% of MWNTs inside, as well as a good electrical conductivity of 8.3 × 105 S/m. This direct spinning method can be used to obtain a variety of products including nanotube fibers, ribbons, and coatings. On this basis, Li and co-workers (Jang et al., 2009) improved the process and successfully achieved a few kilometers of CNT fiber, meanwhile the strength reached more than 1 GPa.
The key to directly spinning from carbon nanotube arrays is to prepare arrays that are uniform and enough material for continuous spinning (Zhang et al., 2004). Jiang et al. (2002) firstly drew a ultra-long CNT fiber from a spinnable CNT arrays with extraordinary electrical property. Twisted CNT sheets have been proved to enhance the strength of fibers, the height of the grown CNT arrays can also influence the mechanical performance of the fiber (Zhang et al., 2006; Ci et al., 2007). It is mainly due to the defects, which are the density of the end points on the grown ultra-long carbon nanotubes, are relatively low, so that the contact area of the adjacent carbon nanotubes is large to prevent the slipping of the bundles. Zhang et al. (2007) reported a strong, stiff, and lightweight CNT fiber, which was spun from a ultra-high (1 mm) individual CNTs forest. In addition, the density, diameter, number of walls, and the content of amorphous carbon of the carbon nanotubes in the array will affect the forming process of fibers and ultimately determine the properties of the CNT fibers (Zhang et al., 2008).
By using the ancient spinning approach, a CNT “cotton” was twisted into a fiber, regarding as the CNT assembles were readily transferred to fiber format (Zheng et al., 2007). The film-like CNTs similarly can be rolled or twisted into a fiber, which has been demonstrated by Ma et al. (2009). As followed by Feng et al. (2010), they developed another method by rolling a synthesized double-layered carbon nanotube (DWNT) film into a fiber, which had a superior electrical conductivity of 8.0 × 104 S/m.
Generally, the length, diameter, defects, and post-treatment of the prepared carbon nanotubes predominately affect the dispersion of CNT in aqueous or super-acid system to form continuous and uniform CNT fibers in the followed procedure. Besides, the strength, stiffness, and flexibility of the formed CNT fibers also determined by these characteristics of the prepared CNTs by utilizing the wet spinning method. Due to the specific fabrication approach of solid-spun CNT fibers, carbon nanotubes that are grown by CVD have been demonstrated as the major method to obtain the desired fibers. The fibers fabricated by wet spinning technology exhibit a higher electrical conductivity and lower mechanical properties compared to those of solid-state spun fiber, which can be illustrated in Table 1.
Nanostructured Energy Materials in Fibers
Although the stability and high power density of double-layered capacitance materials like carbon nanotube are demonstrated and well-known, the limitation of the energy density has been drew a wide attention to improve. Combing high electrochemical capacitance materials, such as graphene, active carbon (Ma et al., 2016), metal oxide, transition sulfide (Sun et al., 2014a, 2015), and conducting polymer, with prepared carbon nanotube based fibers can extremely enhance the specific capacitance of original fibers and maintain the cyclical properties meanwhile (Wang et al., 2013; Yao et al., 2015). In this part, we will mainly discuss the nanostructured energy materials used in fiber-based supercapacitor from the perspective of compositing approaches. We have summarized the different methods used for fiber electrode fabrication in Table 2 for easy comparison.
Table 2. Electrochemical performances of CNT fiber-based electrodes and supercapacitors in different fabrication and deposition methods.
With the features of self-stacking and self-assembling during the spinning process of carbon nanotube based fibers, which has been demonstrated to affect the electron exchange between ions and materials in the electrolyte, nanostructured energy materials can simultaneously incorporate with these carbonaceous materials by bonding or simply sticking. It is found that combining carbon nanotubes with two-dimensional sheet-like materials can prevent effective surface area reduction and capacitance loss caused by stacking of materials (Yu and Dai, 2009; Jha et al., 2012).
Peng and co-workers prepared a CNT/Graphene hybrid fiber by dip-coating the GO dispersions on the as-grown MWNT arrays and then spun to be a fiber by the approach as described above (Sun et al., 2014b; shown in Figure 4A). Due to the strong interaction of the π-π bond between the graphene oxide sheet and the carbon nanotube, the transfer efficiency of electrons in the composite fiber is greatly improved, and the graphene oxide sheet can reduce the stacking of the carbon nanotubes and increase the paths of ions. The tensile strength of the chemical-reduced hybrid fiber reached at ~500 MPa compared to that of bare CNT fiber (~630 MPa), meanwhile the electrical conductivity of the hybrid fiber can be achieved as high as 450 ± 20 S/cm. The calculated specific capacitance of the hybrid fiber could be reached at ~31.5 F/g compared with ~5.83 F/g of the bare CNT fiber. Depending on the similar principle, Foroughi et al. (2014) explored a novel type of conductive carbon nanotube-graphene composite fiber by the electro-spinning of a chemical-reduced graphene within and cover the surface of MWNT fiber during the drawing procedure (Figure 4B). The electrical conductivity of prepared hybrid fiber could be reached at 900 ± 50 S/cm, while the tensile strength, modulus and elongation at break of the fiber were about 140 MPa, 2.58 GPa, and 6%, respectively. The specific capacitance was dramatically improved to 111 F/g at a scan rate of 2 mV/s.
Figure 4. Schematic illustration of (A) solid-spun carbon nanotube fiber with internal graphene sheets (Sun et al., 2014b). (B) Co-spinning of CNT/graphene hybrid fiber with solid-spun and electrospinning methods (Foroughi et al., 2014). (C) Hydrothermal procedures of rGO/SWNT composite fiber (Yu et al., 2014a). (D) Super-acid exfoliated graphene sheets co-spun with carbon nanotubes (Lu et al., 2018).
A wet-spinning process was proposed by Ma and co-workers to fabricate a CNT-rGO fiber (Ma et al., 2015). The pure few-walled carbon nanotubes (FWNTs) with 3–5 walls were first dispersed in water with the assistance of ultrasonication, and then mixed with a GO solution that was synthesized from expanded graphite. The mixture was extruded into a chitosan/acetic acid coagulation bath to form a fiber with followed washing and drying. The interaction of FWNT and rGO sheets can dramatically increase the stress strength from 193.3 to 385.7 MPa and electrical conductivity from 53.3 to 210.7 S/cm compared to pristine rGO fiber by using the similar method, while the fiber based supercapacitor illustrated a specific capacitance of 38.8 F/cm3.
As a good surfactant to disperse nitric-acid-treated SWNTs, GO dispersion, can homogenously be mixed with SWNTs as a aqueous suspension for composite fiber spinning. Yu et al. (2014a) proposed such suspension to be fed into home-made silica column and heated in an oven with optimal parameters (Figure 4C). The composite SWNT/rGO fiber was self-assembled by hydrothermal method and successively pushed into water by gas flow and further dried in air. The fiber enjoyed a tensile strength of 88 MPa, and the electrical conductivity was ~100 S/cm compared to that of SWNT fiber and rGO fiber, which are 50–150 MPa and ~12.5 S/cm, respectively. The assembled hybrid fiber supercapacitor expressed a ultra-high volumetric specific capacitance of ~45.0 F/cm3.
Recently, we used the violent exothermic reaction of chlorosulfonic acid and hydrogen peroxide to exfoliate the graphite powder to form graphene with a small number of layers, and mixed the prepared graphene and carbon nanotubes with the chlorosulfonic acid as a spinning solution. The graphene/carbon nanotube composite fiber was prepared by wet-spun technology with a three-dimensional structure, as shown in Figure 4D. It can be shown that electron channels were formed when the two-dimensional graphene sheets stacked and upheld by the carbon nanotube bundles, leading to a good electrical and ionic conductivity. The specific surface area of the fiber cross section was greatly increased, and the specific capacitance of the composite fiber was thus increased by about 38% compared with the carbon nanotube fibers prepared by us previously (Lu et al., 2018).
With the assistance of nanoparticles or nanosheets, the co-spun CNT based fiber can also increase the integral electrochemical performances compared with the bare CNT fiber. Ren et al. (2013a) creatively painted a suspension of ordered microporous carbon (OMG) on 10 layers of aligned CNT sheets that drawn from a spinnable CNT array and rolled the combined sheets into a hybrid fiber as one electrode. The electrochemical performances of the OMC/CNT hybrid fiber were investigated in a three-electrode system, which indicated a rectangular shaped CV curve even at a scan rate of 200 mV/s. The prepared negative electrode enjoyed a specific volumetric capacitance up to 121.4 F/cm3 (or 116.3 F/g) at 0.43 A/cm3, which was controlled by the content of OMC particles in the hybrid fiber (~76 wt%).
Choi and co-workers also developed a novel method that biscrolled CNT sheets with drop casting of MnO2 dispersion into a fiber (shown in Figure 5; Choi et al., 2016). The strategy of biscrolling can dramatically expand the loading mass of active nanoparticles as high as 99 wt% without any influences on the mechanical properties of fiber. The biscrolled MnO2/CNT fiber was able to achieve a areal specific capacitance of 889 mF/cm2 (or 155 F/cm3) and possessed an energy density of 35.8 μWh/cm2 (or 5.41 mWh/cm3).
Figure 5. Schematic showing the (a) preparation and structure of biscrolled CNT/MnO2 hybrid fiber, SEM morphologies of (b,c) as-spun biscrolled hybrid fiber and (d,e) two-ply coiled yarn integrated in a fabric (Choi et al., 2016).
Sun et al. (2015) pre-coated the MoS2 nanosheets, which are dispersed in DMF, on the carbon nanotubes arrays during the spinning process. The prepared composite fibers had significantly improved the volumetric specific capacitance. Li et al. also illustrated a cathode active material (V2O5) enhanced CNT fiber by wet-spinning method, which shown a maximum energy density of 1.95 mWh/cm3 at a power density of 7.5 mWR/cm3, although the PVA based coagulation bath relatively influenced the conductivity of the fiber (Li et al., 2017). Recently, Chen's Group prepared a MnO2/CNT fiber by mixing the nanosheet structured MnO2 with SWNT dispersion to form a spinning solution for wet spinning. The fabricated fibers had a content of active substance with more than 75% (Li et al., 2018).
The co-spinning method can be appropriate for solid-state spinning and wet spinning of CNT fibers by mixing or casting active materials dispersed solution with intrinsic spinnable suspension or arrays. CNT fibers have the feasibility to be incorporated with the nanostructured materials during the wet spinning, hydrothermal reactions (with graphene) and assembling process. Consequently, such approach can be considered to apply a various of functional materials into the CNT based fibers (Figures 5d,e).
As we known, the obtained CNT based fibers have a potential to embrace with the nanostructured energy materials. Dip-coating, as one of the most utilized methods to compose different substances, has been frequently reported and relatively effective than co-spinning (Peng et al., 2009; Guo et al., 2012; Li et al., 2012). PEDOT, as a conducting polymer with good film forming properties, high concentration in aqueous solution, accompanied with high stability and conductivity, has attracted a lot of interests recently. The salt doped PEDOT has been proved to be directly spun into a conductive fiber and well film-forming (Jalili et al., 2011, 2012, 2013). Su and Miao (2014b) used the commercial PSS doped PEDOT solution as a doping medium, in which SO3H groups improved the electroactivity of principal conducting polymer in a neutral electrolyte due to the “doping effect” of PSS, and a gamma-irradiated CNT fiber as a current collector to produce a fiber-based supercapacitor (demonstrated in Figure 6). The easy preparation of fiber electrode could be scaled up and the existing of PEDOT and CNT illustrated a rectangular-shape of CV curves as well as remarkable fast charge-discharge properties during electrochemical measurement. The gravimetric specific capacitance of the supercapacitor achieved at 18.5 F/g, which was almost twice compared to that of bare irradiated CNT fiber supercapacitor (9.2 F/g).
Figure 6. (A) Photograph and (B) schematic diagram of the continuous dip-coating process apparatus for hybrid fiber fabrication (Su et al., 2014).
To enhance the adhesion of the applied electrochemical active materials on the fibers, polymer-assisted dispersions are good medium to be further utilized for dipping and coating. Meanwhile, the format of asymmetric fiber supercapacitor can extend the operating potential window and result in much higher energy and power densities of the whole device. Su and Miao (2014a) dispersed a mass of MnO2 nanoparticles in PVA solution by vigorous stirring to form a uniform MnO2-PVA paste. The as-spun CNT fibers were then dip-coated with the prepared paste by a self-designed set-up, and the obtained CNT/MnO2/PVA fiber electrode was twisted with a bare CNT fiber by overall casting of a gel electrolyte to form an asymmetric supercapacitor. This type of supercapacitor expressed a wide operating potential window of 2.0 V and the highest energy and power densities reached 42.0 Wh/kg and 19,250 W/kg, respectively. With the similar method, they synthesized PANI nanowire solution beforehand the fiber spinning, the obtained irradiated CNT fiber was orderly covered with PANI-PVA and PVA gel electrolyte. The composited fiber revealed a gram specific capacitance of 78 F/g (or 43 mF/cm2), which was almost twice comparing to that of a bare CNT/PANI fiber based supercapacitor (Su et al., 2014).
The dip-coating method can not only fill the interspaces in carbon nanotube based fibers, but also enhance the mechanical properties of the original fibers by specifically selecting film-forming solutions. Many active materials are insoluble or reactive in aqueous dispersions by using co-spinning; dip-coating can alternatively be chosen to incorporate such materials with suitable solvent.
In-situ composition is derived from the concepts of in-situ crystallization and in-situ polymerization. The second phase in the material of the composite is formed during the formation of the material or synthesized on a substrate. The in-situ formation may be a phase of metal (Randeniya et al., 2010; Xu et al., 2011; Zhang et al., 2012, 2014; Chen et al., 2013), ceramic or polymer (Cai et al., 2013), which may be presented in the matrix in the form of microstructures such as particles, whiskers, crystal plates or microfibers. For fiber based electrodes, in-situ synthesis and electrochemical deposition have been generally utilized for enhancing the electrochemical performances.
As-spun all-carbon fibers can be regarded as a scaffold to deposit pseudocapacitive materials such as metal oxide (i.e., MnO2, Ni(OH)2, Fe2O3, V2O5), plolypyrrole, and polyaniline in room temperature or using the hydrothermal procedure (Zhang et al., 2018; Li et al., 2019a). The porous CNT or graphene based fibers are hydrophilic, which facilitate the diffusion of deposition ions throughout the fibers. Based on the CNT fiber prepared with CNT aerogel, Xiao et al. (2012) immersed the fiber in ethanol, which was added with KMnO4 aqueous solution. The fiber could reduce aqueous permanganate to obtain MnO2 by the following reaction:
The obtained CNT/MnO2 fibers were designed and applied in a stretchable asymmetric configuration, extending the potential window from 0.8 to 1.5 V with a high linear specific capacitance of ~157.53 μF/cm at 50 mV/s. The calculated energy density reached from 17.26 to 46.59 nWh/cm when the power density varying from 7.63 to 61.55 μW/cm. By using the similar principle, Yu et al. (2014b) compared the MnO2 deposited rGO/SWCNT hybrid fiber with different dipping times, which indicated that the 30 min dipped fiber expressed a highest specific capacitance of 3.3 mF/cm. Zheng et al. (2014) extruded the dispersed GO solution into a rotating coagulation bath with Mn2+ ions and the obtained fiber was further reduced and deposited in KMnO4 solution. MnO2/graphene fiber was assembled with a MWNT/graphene composite fiber that was spun in a similar method to form an asymmetric supercapacitor. The MnO2 was obviously coated on the surface of fiber and the prepared fiber electrode possessed a high specific capacitance of 59.2 mF/cm2 at a current density of 0.1 mA/ cm2. With the contribution of MnO2, the assembled fiber supercapacitor also obtained a large areal specific capacitance around 33.6 mF/cm2.
Yao's group has dramatically increased the capacitance of the as-spun CNT fiber electrode by inducing the cathode materials based active materials in recent years. The dandelion-like molybdenum-nickel-cobalt ternary oxide (MNCO) nanowire arrays were grown on the surface of the as-prepared solid-spun carbon nanotube fiber as the positive electrode and a vanadium nitride (VN)@C coated CNT fiber as negative electrode to form a fiber-shaped asymmetric supercapacitor (Sun et al., 2017). The growth of the crystal was controlled by the hydrothermal method and largely increased the surface area of the fiber electrode, which obviously enhanced the specific capacitance of the supercapacitor. They then improved the volumetric capacitance of the supercapacitor by alternating the positive electrode to the three-dimensionally aligned zinc-nickel-cobalt oxide (ZNCO)@Ni(OH)2 nanowire arrays coated CNT fiber, the capacitance increased from 62.3 to 94.7 F/cm3 (Zhang Q. et al., 2017). Recently, a CoNiO2@Ni(OH)2 grown CNT fiber electrode was demonstrated by them and assembled with a TiN@VN coated CNT fiber, the supercapacitor shown a higher capacitance of 109.4 F/cm3 (Li et al., 2019b).
Conducting polymers like polyaniline (PANI) can also be synthesized by such conventional method, Wang et al. (2013) proposed a novel fiber electrode by immersing an as-spun reduced CNT fiber in a aniline monomer contained solution with ethanol and perchloric acid, and then dropped additional ammonium persulfate for further reaction. The as-prepared thread-like supercapacitor could be woven or knitted into textiles alone or together with other devices for energy supplying. The supercapacitor showed the areal specific capacitance of 38 mF/cm2 compared with 2.3 mF/cm2 of bare CNT fiber.
Electrochemical deposition refers to a technique in which electrons are transferred through anions and cations in an electrolyte solution under an external electric field and a redox reaction of specific ions occurs on the electrode to form a plating layer (Ju et al., 2012). Electrochemical deposition is widely used and can form nanostructure crystals or conductive polymers to greatly improve the capacitive properties of fiber electrodes. Peng's group firstly applied the electrochemical deposited MnO2 nanoparticles on a MWNT fiber spun from an aligned MWNT forest (Ren et al., 2013b). They used Mn(CH3COO)2 and Na2SO4 mixed solution as the sources for growing MnO2 particles at a potential range from −0.2 to 0.8 V. The as prepared composite fibers shown a mass specific capacitance of 13.31 F/g (or 3.01 mF/cm2 or 0.015 mF/cm) when they were in a twisted supercapacitor configuration, and the fibers could further be utilized as a linear Li-battery.
Choi et al. (2014) then utilized the solid-stated spun CNT fiber as a substrate to composite with MnO2 nanoparticles, in which the fiber was immersed in a MnSO4 and Na2SO4 contained solution. By using a three-electrode system and applying constant voltage of 1.3 V, the flower-like MnO2 nanoflakes were uniformly deposited out and inside the porous CNT fiber (Figure 7a). The consequent specific capacitance of the all-solid-stated fiber-based supercapacitor was 25.4 F/cm3, and the average energy density was 3.52 mWh/cm3 when the average power densities were 127 mW/cm3. Based on this principle, we also pioneered a high-performance flexible fiber supercapacitor by using the super-acid spun CNT fiber (shown in Figure 7b; Lu et al., 2017). The as-spun fiber was highly conductive with many micropores, and MnO2 nanoflakes were deposited by electrodeposition. The characterized specific capacitance of the assembled supercapacitor was over 152 F/g (or 156 F/cm3), which was about 500% higher than that of Choi's device at the same scan rate. The measured energy density was 14.1 Wh/kg at a power density of 202 W/kg.
Figure 7. Cross section morphologies of (a) the solid-spun CNT fiber with electrodeposited MnO2 nano-particles (Choi et al., 2014) and (b) EDS of each elements of deposited MnO2 in wet-spun CNT fiber (Lu et al., 2017), (c) schematic fabrication procedures of electrodeposited PANI/CNT textile supercapacitor (Pan et al., 2015), and (d) solid-spun CNT fiber from pre-deposited PPy carbon nanotube film (Xu et al., 2015).
Cathode materials like NiO and Co3O4 have also been electrochemical deposited by Su et al. to relatively enhance the capacitance of the bare solid-spun CNT fibers (Su et al., 2015), the CNT@ Co3O4 yarn-based supercapacitor exhibited a high capacitance of 52.6 mF/cm2 when the CNT@ NiO also enjoyed a capacitance of 15.2 mF/cm2.
Electrochemical deposited conducting polymers were developed by Peng's group, they incorporated polyaniline with aligned MWNT fibers through an electrochemical analyzer system (Cai et al., 2013). The as-spun fiber was first dipped into the electrolyte containing H2SO4 and aniline monomer, and the well-infiltrated fiber was then applied with a potential of 0.75 V. To form an all-solid-state fiber supercapacitor, the gel electrolyte was coated the overall fiber as the separator meanwhile. The assembled supercapacitor was fabricated by twisting two composite fibers with a corresponding gravimetric specific capacitance of 274 F/g (or 263 mF/cm). Furthermore, in their following improvement, two pieces of CNT/PANI composite fiber based textiles was attached together with gel electrolyte to form a thin, lightweight, transparent and flexible supercapacitor (Figure 7c; Pan et al., 2015). The as-prepared supercapacitor displayed a high specific capacitance of 272.2 F/g, which could be further integrated in a garment to store the energy that was converted from solar energy. We also Lu et al. (2018) reported a super-elastic wire-like supercapacitor by springing the polyaniline electrodeposited carbon nanotube/graphene hybrid fiber covered with SEBS rubber. The obtained coiled-like supercapacitor presented a superior stretchability of 800% with a specific capacitance of about 138 F/g at a current density of 1 A/g, which could be further allied in the stretchable textiles to afford the shape deformation of body gesture.
Besides the conducting polyaniline, plolypyrrole (PPy) has also been drawn with a superior pseudocapacitive performance. Xu et al. (2015) electrodeposited a thin layer of PPy on a aligned CNT film by placing the film between two pieces of stainless steel mesh as the working electrode. The deposited films were then coiled into fibers in wet state by two motors with opposite direction (shown in Figure 7d). High specific capacitance (350 F/g) and extreme stability were then exhibited by the as-prepared fiber electrode in cyclic testing even under bending and twisting.
It can be seen from Table 2 method of electrochemical deposition facilitates the composition between double-layer capacitive carbon nanotube based fibers with high capacitive active materials. In some occasions, such approach can extend to the stretchable fibers which are prepared by wrapping the CNT film on a stretched substrate. The stretchable composite fibers like CNT/MnO2 (Choi et al., 2015; Yu et al., 2016), CNT/PANI (Chen et al., 2014; Zhang et al., 2015), CNT/PPy (Shang et al., 2015), CNT/PEDOT fibers (Chen et al., 2015), possessed a reasonable electrochemical performances even under a large elongation, showing a potential to be applied in large deformation devices.
As the excellent electrode materials, carbon nanotube can be widely used as compatible electrochemical active materials, as well as the carrier or substrate integrated in wearable energy storage devices. In this review paper, we first summarize the main methods that synthesize the carbon nanotube, and briefly describe the development of wet spinning and solid-state spinning methods that are presently utilized to form carbon nanotube fibers, with an extension of approaches to manufacture the composite fibers based on them. We subsequently focus on the potential applications of the fibers in energy storage system, and elaborately discuss how to combine the prepared fibers with nanostructured active materials with different compositing approaches to intrinsically enhance their capacitive performances.
Flexible energy storage technology has been regarded as the key supporting technology for smart wearable electronics. The flexible energy storage device assembled from carbon nanotube fiber-based electrodes has the advantages of being bendable, lightweight, and invisible encapsulation, which will be the foundation of the wearable smart textiles and promotes the rapid development of flexible energy storage devices. The relatively low specific capacitance and yield have been the most drawbacks of carbon nanotube based fibers, it is theoretically to overcome these points from the perspective of fiber structure, proper nano-structured active materials and improvement of existing fiber fabrication method. The summarization of appropriable nanostructured energy materials equally enriches the paths to synthesize high-performance fibers and provides a reference for the development of other novel fiber-based electrode materials in the future.
ZL is a lecturer at School of Fashion Engineering, Shanghai University of Engineering Science. He received the B.S. degree in Textile Engineering in 2012 China and the Ph.D degree in Textile Engineering from College of Textiles, Donghua University, China in 2018. He was supported by Chinese Scholarship Council to visit Intelligent Polymer Research Institute, University of Wollongong from 2015 to 2017. He has published more than 5 articles and 1 patent in recent 3 years. His research interests is focus on the fabrication and development of fiber-based wearable devices, nano-structured materials in fibers, and smart textiles.
JF is a Senior Research Fellow at Intelligent Polymer Research Institute, University of Wollongong and a recipient of Australian Research Council DECRA Fellowship. He received the B.S. and MS degree in Engineering (Fibre Science - Textile Chemistry) in 1997 Iran and the Ph.D degree in Material Engineering from School of Mechanical, Materials, Mechatronic and Biomedical Engineering, University of Wollongong, Australia in 2009. He has published more than 150 articles, including one book, five book chapter, 55 journal papers, 1 patent and 68 conference papers in top ranked journals including four papers in the prestigious journal of Science and a growing national and international recognition through various awards and invited presentations. In addition He has supervised 15 Ph.D students. His research focus is now on the development of novel nanomaterials and fibers for use in wearable technologies and biomedical applications.
All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.
This work has been supported by the Australian Research Council under the Discovery Early Career Researcher Award (JF, DE130100517). The authors also are grateful to the support of Shanghai University of Engineering Science (ZL, 2019-96) and Shanghai Municipality of Science and Technology Commission (ZL, 19YF1417700).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Badaire, S., Pichot, V., Zakri, C., Poulin, P., Launois, P., Vavro, J., et al. (2004). Correlation of properties with preferred orientation in coagulated and stretch-aligned single-wall carbon nanotubes. J. Appl. Phys. 96, 7509–7513. doi: 10.1063/1.1810640
Behabtu, N., Young, C. C., Tsentalovich, D. E., Kleinerman, O., Wang, X., Ma, A. W., et al. (2013). Strong, light, multifunctional fibers of carbon nanotubes with ultrahigh conductivity. Science 339, 182–186. doi: 10.1126/science.1228061
Bucossi, A. R., Cress, C. D., Schauerman, C. M., Rossi, J. E., Puchades, I., Landi, B. J. J., et al. (2015). Enhanced electrical conductivity in extruded single-wall carbon nanotube wires from modified coagulation parameters and mechanical processing. ACS Appl. Mater. Interfaces 7, 27299–27305. doi: 10.1021/acsami.5b08668
Cai, Z., Li, L., Ren, J., Qiu, L., Lin, H., and Peng, H. (2013). Flexible, weavable and efficient microsupercapacitor wires based on polyaniline composite fibers incorporated with aligned carbon nanotubes. J. Mater. Chem. A 1, 258–261. doi: 10.1039/C2TA00274D
Chen, T., Cai, Z., Qiu, L., Li, H., Ren, J., Lin, H., et al. (2013). Synthesis of aligned carbon nanotube composite fibers with high performances by electrochemical deposition. J. Mater. Chem. A 1, 2211–2216. doi: 10.1039/C2TA01039A
Choi, C., Kim, K. M., Kim, K. J., Lepró, X., Spinks, G. M., Baughman, R. H., et al. (2016). Improvement of system capacitance via weavable superelastic biscrolled yarn supercapacitors. Nat. Commun. 7:13811. doi: 10.1038/ncomms13811
Choi, C., Kim, S. H., Sim, H. J., Lee, J. A., Choi, A. Y., Kim, Y. T., et al. (2015). Stretchable, weavable coiled carbon nanotube/MnO2/polymer fiber solid-state supercapacitors. Sci. Rep. 5:9387. doi: 10.1038/srep09387
Choi, C., Lee, J. A., Choi, A. Y., Kim, Y. T., Lepró, X., Lima, M. D., et al. (2014). Flexible supercapacitor made of carbon nanotube yarn with internal pores. Adv. Mater. 26, 2059–2065. doi: 10.1002/adma.201304736
Ci, L., Punbusayakul, N., Wei, J., Vajtai, R., Talapatra, S., and Ajayan, P. M. (2007). Multifunctional macroarchitectures of double-walled carbon nanotube fibers. Adv. Mater. 19, 1719–1723. doi: 10.1002/adma.200602520
Danilov, P. A., Ionin, A. A., Kudryashov, S. I., Makarov, S. V., Mel'nik, N. N., Rudenko, A. A., et al. (2014). Femtosecond laser ablation of single-wall carbon nanotube-based material. Laser Phys. Lett. 11:106101. doi: 10.1088/1612-2011/11/10/106101
Das, R., Shahnavaz, Z., Ali, M. E., Islam, M. M., and Hamid, S. B. A. (2016). Can we optimize arc discharge and laser ablation for well-controlled carbon nanotube synthesis? Nanoscale Res. Lett. 11:510. doi: 10.1186/s11671-016-1730-0
Davis, V. A., Parra-Vasquez, A. N., Green, M. J., Rai, P. K., Behabtu, N., Prieto, V., et al. (2009). True solutions of single-walled carbon nanotubes for assembly into macroscopic materials. Nat. Nanotechnol. 4, 830–834. doi: 10.1038/nnano.2009.302
Feng, J.-M., Wang, R., Li, Y.-L., Zhong, X.-H., Cui, L., Guo, Q.-J., et al. (2010). One-step fabrication of high quality double-walled carbon nanotube thin films by a chemical vapor deposition process. Carbon N. Y. 48, 3817–3824. doi: 10.1016/j.carbon.2010.06.046
Foroughi, J., Spinks, G. M., Antiohos, D., Mirabedini, A., Gambhir, S., Wallace, G. G., et al. (2014). Highly conductive carbon nanotube-graphene hybrid yarn. Adv. Funct. Mater. 24, 5859–5865. doi: 10.1002/adfm.201401412
Foroughi, J., Spinks, G. M., Aziz, S., Mirabedini, A., Jeiranikhameneh, A., Wallace, G. G., et al. (2016). Knitted carbon-nanotube-sheath/spandex-core elastomeric yarns for artificial muscles and strain sensing. ACS Nano 10, 9129–9135. doi: 10.1021/acsnano.6b04125
Guo, T., Nikolaev, P., Thess, A., Colbert, D., and Smalley, R. (1995). Catalytic growth of single-walled manotubes by laser vaporization. Chem. Phys. Lett. 243, 49–54. doi: 10.1016/0009-2614(95)00825-O
Guo, W., Liu, C., Sun, X., Yang, Z., Kia, H. G., and Peng, H. (2012). Aligned carbon nanotube/polymer composite fibers with improved mechanical strength and electrical conductivity. J. Mater. Chem. 22, 903–908. doi: 10.1039/C1JM13769G
Haines, C. S., Lima, M. D., Li, N., Spinks, G. M., Foroughi, J., Madden, J. D., et al. (2014). Artificial muscles from fishing line and sewing thread. Science 343, 868–872. doi: 10.1126/science.1246906
Ikegami, T., Nakanishi, F., Uchiyama, M., and Ebihara, K. (2004). Optical measurement in carbon nanotubes formation by pulsed laser ablation. Thin Solid Films 457, 7–11. doi: 10.1016/j.tsf.2003.12.033
Jalili, R., Razal, J. M., Innis, P. C., and Wallace, G. G. (2011). One-step wet-spinning process of poly (3, 4-ethylenedioxythiophene): poly (styrenesulfonate) fibers and the origin of higher electrical conductivity. Adv. Funct. Mater. 21, 3363–3370. doi: 10.1002/adfm.201100785
Jalili, R., Razal, J. M., and Wallace, G. G. (2012). Exploiting high quality PEDOT: PSS–SWNT composite formulations for wet-spinning multifunctional fibers. J. Mater. Chem. 22, 25174–25182. doi: 10.1039/c2jm35148j
Jalili, R., Razal, J. M., and Wallace, G. G. (2013). Wet-spinning of PEDOT: PSS/functionalized-SWNTs composite: a facile route toward production of strong and highly conducting multifunctional fibers. Sci. Rep. 3:3438. doi: 10.1038/srep03438
Jang, E. Y., Kang, T. J., Im, H., Baek, S. J., Kim, S., Jeong, D. H., et al. (2009). Macroscopic single-walled-carbon-nanotube fiber self-assembled by dip-coating method. Adv. Mater. 21, 4357–4361. doi: 10.1002/adma.200900480
Jarosz, P., Schauerman, C., Alvarenga, J., Moses, B., Mastrangelo, T., Raffaelle, R., et al. (2011). Carbon nanotube wires and cables: near-term applications and future perspectives. Nanoscale 3, 4542–4553. doi: 10.1039/c1nr10814j
Jarosz, P. R., Shaukat, A., Schauerman, C. M., Cress, C. D., Kladitis, P. E., Ridgley, R. D., et al. (2012). High-performance, lightweight coaxial cable from carbon nanotube conductors. ACS Appl. Mater. Interfaces 4, 1103–1109. doi: 10.1021/am201729g
Jha, N., Ramesh, P., Bekyarova, E., Itkis, M. E., and Haddon, R. C. (2012). High energy density supercapacitor based on a hybrid carbon nanotube–reduced graphite oxide architecture. Adv. Energy Mater. 2, 438–444. doi: 10.1002/aenm.201100697
Ju, H., Lee, J. K., Lee, J., and Lee, J. (2012). Fast and selective Cu2O nanorod growth into anodic alumina templates via electrodeposition. Curr. Appl. Phys .12, 60–64. doi: 10.1016/j.cap.2011.04.042
Jung, S.-H., Kim, M.-R., Jeong, S.-H., Kim, S.-U., Lee, O.-J., Lee, K.-H., et al. (2003). High-yield synthesis of multi-walled carbon nanotubes by arc discharge in liquid nitrogen. Appl. Phys. A 76, 285–286. doi: 10.1007/s00339-002-1718-8
Kozlov, M. E., Capps, R. C., Sampson, W. M., Ebron, V. H., Ferraris, J. P., and Baughman, R. H. (2005). Spinning solid and hollow polymer-free carbon nanotube fibers. Adv. Mater. 17, 614–617. doi: 10.1002/adma.200401130
Li, G.-X., Hou, P.-X., Luan, J., Li, J.-C., Li, X., Wang, H., et al. (2018). A MnO2 nanosheet/single-wall carbon nanotube hybrid fiber for wearable solid-state supercapacitors. Carbon N. Y. 140, 634–643. doi: 10.1016/j.carbon.2018.09.011
Li, Q., Zhang, Q., Liu, C., Sun, J., Guo, J., Zhang, J., et al. (2019a). Flexible all-solid-state fiber-shaped Ni–Fe batteries with high electrochemical performance. J. Mater. Chem. A 7, 520–530. doi: 10.1039/C8TA09822K
Li, Q., Zhang, Q., Sun, J., Liu, C., Guo, J., He, B., et al. (2019b). All hierarchical core–shell heterostructures as novel binder-free electrode materials for ultrahigh-energy-density wearable asymmetric supercapacitors. Adv. Sci. 6:1801379. doi: 10.1002/advs.201801379
Li, S., Zhang, X., Zhao, J., Meng, F., Xu, G., Yong, Z., et al. (2012). Enhancement of carbon nanotube fibres using different solvents and polymers. Compos. Sci. Technol. 72, 1402–1407. doi: 10.1016/j.compscitech.2012.05.013
Ma, A. W., Nam, J., Behabtu, N., Mirri, F., Young, C. C., Dan, B., et al. (2013). Scalable formation of carbon nanotube films containing highly aligned whiskerlike crystallites. Ind. Eng. Chem. Res. 52, 8705–8713. doi: 10.1021/ie303042x
Ma, W., Chen, S., Yang, S., Chen, W., Weng, W., and Zhu, M. (2016). Bottom-up fabrication of activated carbon fiber for all-solid-state supercapacitor with excellent electrochemical performance. ACS Appl. Mater. Interfaces 8, 14622–14627. doi: 10.1021/acsami.6b04026
Ma, W., Liu, L., Yang, R., Zhang, T., Zhang, Z., Song, L., et al. (2009). Monitoring a micromechanical process in macroscale carbon nanotube films and fibers. Adv. Mater. 21, 603–608. doi: 10.1002/adma.200801335
Ma, Y., Li, P., Sedloff, J. W., Zhang, X., Zhang, H., and Liu, J. (2015). Conductive graphene fibers for wire-shaped supercapacitors strengthened by unfunctionalized few-walled carbon nanotubes. ACS Nano 9, 1352–1359. doi: 10.1021/nn505412v
Miaudet, P., Badaire, S., Maugey, M., Derre, A., Pichot, V., Launois, P., et al. (2005). Hot-drawing of single and multiwall carbon nanotube fibers for high toughness and alignment. Nano Lett. 5, 2212–2215. doi: 10.1021/nl051419w
Pan, S., Lin, H., Deng, J., Chen, P., Chen, X., Yang, Z., et al. (2015). Novel wearable energy devices based on aligned carbon nanotube fiber textiles. Adv. Energy Mater. 5:1401438. doi: 10.1002/aenm.201401438
Parkansky, N., Boxman, R., Alterkop, B., Zontag, I., Lereah, Y., and Barkay, Z. (2004). Single-pulse arc production of carbon nanotubes in ambient air. J. Phys. D Appl. Phys. 37:2715. doi: 10.1088/0022-3727/37/19/015
Parra-Vasquez, A. N. G., Behabtu, N., Green, M. J., Pint, C. L., Young, C. C., Schmidt, J., et al. (2010). Spontaneous dissolution of ultralong single-and multiwalled carbon nanotubes. ACS Nano 4, 3969–3978. doi: 10.1021/nn100864v
Peng, H., Sun, X., Cai, F., Chen, X., Zhu, Y., Liao, G., et al. (2009). Electrochromatic carbon nanotube/polydiacetylene nanocomposite fibres. Nat. Nanotechnol. 4, 738–741. doi: 10.1038/nnano.2009.264
Pillai, S. K., Augustyn, W. G., Rossouw, M. H., and McCrindle, R. I. (2008). The effect of calcination on multi-walled carbon nanotubes produced by Dc-Arc discharge. J. Nanosci. Nanotechnol. 8, 3539–3544. doi: 10.1166/jnn.2008.115
Ramesh, S., Ericson, L. M., Davis, V. A., Saini, R. K., Kittrell, C., Pasquali, M., et al. (2004). Dissolution of pristine single walled carbon nanotubes in superacids by direct protonation. J. Phys. Chem. B 108, 8794–8798. doi: 10.1021/jp036971t
Randeniya, L. K., Bendavid, A., Martin, P. J., and Tran, C. D. (2010). Composite yarns of multiwalled carbon nanotubes with metallic electrical conductivity. Small 6, 1806–1811. doi: 10.1002/smll.201000493
Ren, J., Li, L., Chen, C., Chen, X., Cai, Z., Qiu, L., et al. (2013b). Twisting carbon nanotube fibers for both wire-shaped micro-supercapacitor and micro-battery. Adv. Mater. 25, 1155–1159. doi: 10.1002/adma.201203445
Shang, Y., Wang, C., He, X., Li, J., Peng, Q., Shi, E., et al. (2015). Self-stretchable, helical carbon nanotube yarn supercapacitors with stable performance under extreme deformation conditions. Nano Energy 12, 401–409. doi: 10.1016/j.nanoen.2014.11.048
Shimotani, K., Anazawa, K., Watanabe, H., and Shimizu, M. (2001). New synthesis of multi-walled carbon nanotubes using an arc discharge technique under organic molecular atmospheres. Appl. Phys. A 73, 451–454. doi: 10.1007/s003390100821
Steiner, S. A. III., Baumann, T. F., Bayer, B. C., Blume, R., Worsley, M. A., Moberlychan, W. J., et al. (2009). Nanoscale zirconia as a nonmetallic catalyst for graphitization of carbon and growth of single-and multiwall carbon nanotubes. J. Am. Chem. Soc. 131, 12144–12154. doi: 10.1021/ja902913r
Steinmetz, J., Glerup, M., Paillet, M., Bernier, P., and Holzinger, M. (2005). Production of pure nanotube fibers using a modified wet-spinning method. Carbon N. Y. 43, 2397–2400. doi: 10.1016/j.carbon.2005.03.047
Su, F., Lv, X., and Miao, M. (2015). High-performance two-ply yarn supercapacitors based on carbon nanotube yarns dotted with Co3O4 and NiO nanoparticles. Small 11, 854–861. doi: 10.1002/smll.201401862
Su, F., and Miao, M. (2014b). Flexible, high performance two-ply yarn supercapacitors based on irradiated carbon nanotube yarn and PEDOT/PSS. Electrochim. Acta 127, 433–438. doi: 10.1016/j.electacta.2014.02.064
Su, F., Miao, M., Niu, H., and Wei, Z. (2014). Gamma-irradiated carbon nanotube yarn as substrate for high-performance fiber supercapacitors. ACS Appl. Mater. Interfaces 6, 2553–2560. doi: 10.1021/am404967x
Sun, G., Liu, J., Zhang, X., Wang, X., Li, H., Yu, Y., et al. (2014a). Fabrication of ultralong hybrid microfibers from nanosheets of reduced graphene oxide and transition-metal dichalcogenides and their application as supercapacitors. Angew. Chem. Int. Ed. 126, 12784–12788. doi: 10.1002/ange.201405325
Sun, G., Zhang, X., Lin, R., Yang, J., Zhang, H., and Chen, P. (2015). Hybrid fibers made of molybdenum disulfide, reduced graphene oxide, and multi-walled carbon nanotubes for solid-state, flexible, asymmetric supercapacitors. Angew. Chem. Int. Ed. 54, 4651–4656. doi: 10.1002/anie.201411533
Sun, H., You, X., Deng, J., Chen, X., Yang, Z., Ren, J., et al. (2014b). Novel graphene/carbon nanotube composite fibers for efficient wire-shaped miniature energy devices. Adv. Mater. 26, 2868–2873. doi: 10.1002/adma.201305188
Sun, J., Zhang, Q., Wang, X., Zhao, J., Guo, J., Zhou, Z., et al. (2017). Constructing hierarchical dandelion-like molybdenum–nickel–cobalt ternary oxide nanowire arrays on carbon nanotube fiber for high-performance wearable fiber-shaped asymmetric supercapacitors. J. Mater. Chem. A 5, 21153–21160. doi: 10.1039/C7TA06353A
Vigolo, B., Pénicaud, A., Coulon, C., Sauder, C., Pailler, R., Journet, C., et al. (2000). Macroscopic fibers and ribbons of oriented carbon nanotubes. Science 290, 1331–1334. doi: 10.1126/science.290.5495.1331
Vigolo, B., Poulin, P., Lucas, M., Launois, P., and Bernier, P. (2002). Improved structure and properties of single-wall carbon nanotube spun fibers. Appl. Phys. Lett. 81, 1210–1212. doi: 10.1063/1.1497706
Wang, K., Meng, Q., Zhang, Y., Wei, Z., and Miao, M. (2013). High-performance two-ply yarn supercapacitors based on carbon nanotubes and polyaniline nanowire arrays. Adv. Mater. 25, 1494–1498. doi: 10.1002/adma.201204598
Xu, G., Zhao, J., Li, S., Zhang, X., Yong, Z., and Li, Q. (2011). Continuous electrodeposition for lightweight, highly conducting and strong carbon nanotube-copper composite fibers. Nanoscale 3, 4215–4219. doi: 10.1039/c1nr10571j
Xu, R., Wei, J., Guo, F., Cui, X., Zhang, T., Zhu, H., et al. (2015). Highly conductive, twistable and bendable polypyrrole–carbon nanotube fiber for efficient supercapacitor electrodes. RSC Adv. 5, 22015–22021. doi: 10.1039/C5RA01917F
Yao, F., Pham, D. T., and Lee, Y. H. (2015). Carbon-based materials for lithium-ion batteries, electrochemical capacitors, and their hybrid devices. ChemSusChem 8, 2284–2311. doi: 10.1002/cssc.201403490
Yao, Y., Li, Q., Zhang, J., Liu, R., Jiao, L., Zhu, Y. T., et al. (2007). Temperature-mediated growth of single-walled carbon-nanotube intramolecular junctions. Nat. Mater. 6:283. doi: 10.1038/nmat1865
Yu, D., Goh, K., Wang, H., Wei, L., Jiang, W., Zhang, Q., et al. (2014a). Scalable synthesis of hierarchically structured carbon nanotube-graphene fibres for capacitive energy storage. Nat. Nanotechnol. 9, 555–562. doi: 10.1038/nnano.2014.93
Yu, D., Goh, K., Zhang, Q., Wei, L., Wang, H., Jiang, W., et al. (2014b). Controlled functionalization of carbonaceous fibers for asymmetric solid-state micro-supercapacitors with high volumetric energy density. Adv. Mater. 26, 6790–6797. doi: 10.1002/adma.201403061
Yu, J., Lu, W., Smith, J. P., Booksh, K. S., Meng, L., Huang, Y., et al. (2016). A high performance stretchable asymmetric fiber-shaped supercapacitor with a core-sheath helical structure. Adv. Energy Mater. 7:1600976. doi: 10.1002/aenm.201600976
Zhang, K., Li, T., Ling, L., Lu, H., Tang, L., Li, C., et al. (2017). Facile synthesis of high density carbon nanotube array by a deposition-growth-densification process. Carbon N. Y. 114, 435–440. doi: 10.1016/j.carbon.2016.12.047
Zhang, Q., Xu, W., Sun, J., Pan, Z., Zhao, J., Wang, X., et al. (2017). Constructing ultrahigh-capacity zinc–nickel–cobalt oxide@ Ni (OH) 2 core–shell nanowire arrays for high-performance coaxial fiber-shaped asymmetric supercapacitors. Nano Lett. 17, 7552–7560. doi: 10.1021/acs.nanolett.7b03507
Zhang, Q., Zhou, Z., Pan, Z., Sun, J., He, B., Li, Q., et al. (2018). All-metal-organic framework-derived battery materials on carbon nanotube fibers for wearable energy-storage device. Adv. Sci. 5:1801462. doi: 10.1002/advs.201801462
Zhang, S., Ji, C., Bian, Z., Yu, P., Zhang, L., Liu, D., et al. (2012). Porous, platinum nanoparticle-adsorbed carbon nanotube yarns for efficient fiber solar cells. ACS Nano 6, 7191–7198. doi: 10.1021/nn3022553
Zhang, S., Zhu, L., Minus, M. L., Chae, H. G., Jagannathan, S., Wong, C.-P., et al. (2008). Solid-state spun fibers and yarns from 1-mm long carbon nanotube forests synthesized by water-assisted chemical vapor deposition. J. Mater. Sci. 43, 4356–4362. doi: 10.1007/s10853-008-2558-5
Zhang, X., Jiang, K., Feng, C., Liu, P., Zhang, L., Kong, J., et al. (2006). Spinning and processing continuous yarns from 4-inch wafer scale super-aligned carbon nanotube arrays. Adv. Mater. 18, 1505–1510. doi: 10.1002/adma.200502528
Keywords: carbon nanotubes, energy storage, wearable technologies, supercapacitor, fiber spinning
Citation: Lu Z, Raad R, Safaei F, Xi J, Liu Z and Foroughi J (2019) Carbon Nanotube Based Fiber Supercapacitor as Wearable Energy Storage. Front. Mater. 6:138. doi: 10.3389/fmats.2019.00138
Received: 16 April 2019; Accepted: 29 May 2019;
Published: 18 June 2019.
Edited by:Chunyi Zhi, City University of Hong Kong, Hong Kong
Copyright © 2019 Lu, Raad, Safaei, Xi, Liu and Foroughi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Javad Foroughi, email@example.com