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(>300%) without detrimental effects to the conductivity of the electrode. Figures 2.4b exhibited the top‐view and cross‐section SEM (scanning electron microscope) images of the twisted SCs. From the SEM images, we can see that the thickness of PVA/H3PO4 and CNT sheets were 50 and 10 mm, respectively. The electrochemical performances of the fabricated twisted SCs were also carried out, as displayed in Figure 2.4c. The inset is the photos of the twisted devices under various strains ranging from 0% to 370%. The normalized capacitance (a ratio of the capacitance under a specific strain to that at 0 strain) as a function of the tensile strain showed a 13% of increase for the device based on CNT wrapped elastic wire electrodes as the tensile strain increased from 0% to 250%. This can be explained by the strain‐induced enhancement in the contact between the two twisted electrodes upon stretching. When the tensile strength was above 250%, a slight decrease in the capacitance was appeared caused by the imperfect contact between CNT and/or PVA/H3PO4, but it was still 10% higher than the initial capacitance. Moreover, in this paper, the CNT/PEDOT‐PSS (poly (3,4‐ethylenedioxythiophene)‐poly (styrene sulfonate)) based stretchable twisted SCs were also fabricated using the same technology, which depicted an excellent capacitance retention under different stretching state, indicating that it's a feasible method to large‐scale produce different kinds of stretchable twisted SCs.

Schematic illustrations of (a) fabricating twisted SCs by wrapping aligned CNT sheet around a pre-stretched elastic wire. (b) Top-view and cross section SEM images of the fiber SCs. (c) Changes in the normalized capacitance under stretching.

      Source: Reproduced with permission [58]. © 2014, Wiley‐VCH.

      (d) Schematics of the fabrication procedures for stretchable fiber SCs by twisting the devices. (e) Optical microscopy images the fiber devices. (f) Specific capacitance of the fiber SCs under stretching.

      Source: Reproduced with permission [35]. © 2014, Wiley‐VCH.

      Another group of stretchable twisted SC have no ability of stretchability itself, with the whole devices twined around the elastic substrate. For example, Xu et al. proposed a fabrication method by using spandex fiber as the substrate (Figure 2.4d) [35]. Specifically, a fiber‐shaped SC was fabricated by twisting two CNT based fiber electrodes. Then, next, spandex fiber was pre‐stretched to 100% with a PDMS coat to prevent influence from acidic H2SO4‐PVA gel electrolyte. And then the fiber‐shaped SCs were “glued” onto the spandex fiber. When the substrate was released, the SCs with stretchability over 100% were accomplished. Figure 2.4e showed the photography of the serpentiform stretchable SCs. A slightly enlarged of the CV loop areas suggested the enhanced capacitance when the SC was stretched to a large strain of up to 100%. Moreover, the specific capacitance of the fiber SCs under stretching (Figure 2.4f) also surpassed those of the initial unbuckled SCs after 20 cycles of deep stretching. The outstanding stretchability can contribute to the buckled structures formed after releasing the strain. This fabrication method could make most of the twisted SCs stretchable, but the devices and the stretchable substrate are two separate parts, which is unfavorable to keeping the electrochemical performances under repeated deformation. Nevertheless, more advanced technologies for solving the above‐mentioned problems are demanded imminently to realize its practical application in wearable electronics.

      2.2.1.3 Fabrication of Stretchable Coaxial SCs

Schematic illustrations of the fabrication procedures for coaxial SCs and corresponding electrochemical performances at different tensile strains. (a, b) Pre–stretching substrate and electrode.

      Source: Reproduced with permission [36]. © 2013, Wiley‐VCH.

      (c, d) Over‐twisting the SCs device into a helical structure. (e) Areal specific capacitance variations with scan rates.

      Source: Reproduced with permission [60]. © 2016, Wiley‐VCH.

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