{
    "title": "Scalable production of ultrafine polyaniline fibres for tactile organic electrochemical transistors",
    "pre_title": "Scalable production of ultrafine polyaniline fibres for tactile organic electrochemical transistors",
    "journal": "Nature Communications",
    "published": "19 April 2022",
    "supplementary_0": [
        {
            "label": "Supplementary Information",
            "link": "https://static-content.springer.com/esm/art%3A10.1038%2Fs41467-022-29773-9/MediaObjects/41467_2022_29773_MOESM1_ESM.pdf"
        },
        {
            "label": "Peer Review File",
            "link": "https://static-content.springer.com/esm/art%3A10.1038%2Fs41467-022-29773-9/MediaObjects/41467_2022_29773_MOESM2_ESM.pdf"
        }
    ],
    "supplementary_1": NaN,
    "supplementary_2": NaN,
    "source_data": [],
    "code": [],
    "subject": [
        "Chemical engineering",
        "Electronic devices"
    ],
    "license": "http://creativecommons.org/licenses/by/4.0/",
    "preprint_pdf": "https://www.researchsquare.com/article/rs-1126903/v1.pdf?c=1650379781000",
    "research_square_link": "https://www.researchsquare.com//article/rs-1126903/v1",
    "nature_pdf": "https://www.nature.com/articles/s41467-022-29773-9.pdf",
    "preprint_posted": "08 Dec, 2021",
    "research_square_content": [
        {
            "section_name": "Abstract",
            "section_text": "The development of continuous conducting polymer fibres is essential for applications ranging from advanced fibrous devices to frontier fabric electronics. The use of continuous conducting polymer fibres requires a small diameter to maximize their electroactive surfaces, microstructural orientations, and mechanical strengths. However, regularly used wet spinning techniques have rarely achieved this goal due primarily to the insufficient slenderization of rapidly solidified conducting polymer molecules in poor solvents. Here we report a good solvent exchange strategy to wet spin the ultrafine polyaniline fibres at the large scale. The slow diffusion between good solvents distinctly decreases the viscosity of gel protofibers, which undergo an impressive drawing ratio. The continuously collected polyaniline fibres have a previously unattained diameter below 5 \u00b5m, high energy and charge storage capacities, and favorable mechanical performance. We demonstrated an ultrathin all-solid organic electrochemical transistor based on ultrafine polyaniline fibres, which substantially amplified microampere drain-source electrical signals with less one volt driving voltage and effectively operated as a tactile sensor detecting pressure and friction forces at different levels. The aggressive electronical and electrochemical merits of ultrafine polyaniline fibres and their great potentials to prepare on industrial scale offer new opportunities for high-performance soft electronics and large-area electronic textiles.",
            "section_image": []
        },
        {
            "section_name": "Additional Declarations",
            "section_text": "There is NO Competing Interest.",
            "section_image": []
        },
        {
            "section_name": "Supplementary Files",
            "section_text": "Supplementaryinformation1130.pdf",
            "section_image": []
        }
    ],
    "nature_content": [
        {
            "section_name": "Abstract",
            "section_text": "The development of continuous conducting polymer fibres is essential for applications ranging from advanced fibrous devices to frontier fabric electronics. The use of continuous conducting polymer fibres requires a small diameter to maximize their electroactive surface, microstructural orientation, and mechanical strength. However, regularly used wet spinning techniques have rarely achieved this goal due primarily to the insufficient slenderization of rapidly solidified conducting polymer molecules in poor solvents. Here we report a good solvent exchange strategy to wet spin the ultrafine polyaniline fibres. The slow diffusion between good solvents distinctly decreases the viscosity of protofibers, which undergo an impressive drawing ratio. The continuously collected polyaniline fibres have a previously unattained diameter below 5\u2009\u00b5m, high energy and charge storage capacities, and favorable mechanical performance. We demonstrated an ultrathin all-solid organic electrochemical transistor based on ultrafine polyaniline fibres, which operated as a tactile sensor detecting pressure and friction forces at different levels.",
            "section_image": []
        },
        {
            "section_name": "Introduction",
            "section_text": "The extended conjugated and easily doped \u03c0-system along the backbone enables conducting polymers to possess intriguing transport, optical, and electrochemical properties, which have rarely been found in conventional polymers and metal conductors1,2,3. Processing conducting polymers into macroscopically fibrous materials makes it possible to translate their nano-object features to human-friendly products in a continuous manner. The combined merits, including but not limited to mechanical flexibility, intrinsic conductivity, and electrochemical activity, of conducting polymer fibers (CPFs) have introduced an era of \u201celectronic textiles\u201d4. For instance, highly conductive and electrochemically active poly(3-methylthiophene) fibers have been achieved by in situ electrochemical oxidation of monomers5. Fast ion transport between CPFs and ionic liquids has given birth to long-term operation actuators, electrochromic windows, and numeric displays6. In recent studies, the wet-spun poly (3,4-ethylene dioxythiophene) (PEDOT) fibers have been widely used in various frontier fields, such as flexible energy storage electrodes, implantable bioelectronics, and organic transistors7,8.\n\nUnfortunately, due primarily to the large diameters, the performance and expectations of most achieved continuous CPFs have been limited by their insufficient electroactive surfaces and weak breaking strengths. Electrospinning and wet spinning are two mainstream strategies to produce continuous CPFs. In the case of electrospinning, the fairly rigid backbone due to the high aromaticity results in an insufficient elasticity of conducting polymer solutions, which fails to be solely electrospun into fine fibers9. Although a two-fluid electrospinning technique has been proposed by coating a soluble and electrospinnable fluid on the conducting polymer cores, the complex procedures involving the addition and removal of second components defy the mass production of electrospun CPFs10,11. In the case of conventional wet spinning, conducting polymer dopes tend to occur a transient solidification in poor solvents, induced by the strong interactions of conducting polymer chains. The rapidly hardened gels suppress the post-stretching and slenderizing procedures, and cause the wet-spun CPFs to show a large diameter, generally beyond 10\u2009\u00b5m12,13,14. The large diameters largely discount the mechanical properties and electrochemical activities of CPFs4,15. Thus, there is an urgent need to realize the mass production of ultrafine CPFs, which remains challenging. In this work, we report a good solvent exchange strategy in a modified wet spinning technique to prepare the ultrafine polyaniline (PAni) fibers (UFPFs) at a large scale. Beyond conventional wet spinning protocol, we replaced poor solvents by good solvents as the coagulation bath to decrease the viscosity of gel protofibres, which were subject to an ultrahigh drawing ratio and reduced to an ultrafine morphology. The obtained UFPFs own a small diameter below 5\u2009\u00b5m, an unprecedented mechanical strength of 1080\u2009\u00b1\u200971\u2009MPa, a high area capacitance beyond 1008\u2009mF\u2009cm\u22122, and an enormous charge storage capacity of 5.25 \u00d7 104\u2009mC\u2009cm\u22122. Based on the structural and electrochemical merits of UFPFs, we demonstrated an ultrathin all-solid organic electrochemical transistor (OECT) with less than 1\u2009V driving voltage, which substantially amplified drain-source electrical signals with low power consumption and responded to vertical pressure and horizontal friction forces at different levels. Our work opens an avenue to prepare continuous ultrafine CPFs and high-performance soft electronics.",
            "section_image": []
        },
        {
            "section_name": "Results",
            "section_text": "In the modified one-step wet spinning process, we used good solvents as the coagulation bath to realize the mass production of UFPFs (Fig.\u00a01a, b and Supplementary Fig.\u00a01). After doping PAni powder (emeraldine base) with camphor sulfonic acid (CSA) at a molar ratio of 2:1, we dispersed fully doped PAni into m-cresol as the raw spinning dopes (see the Methods section)16. Significantly, the direct use of doped PAni solutions as the dopes saves the trouble of conventional post-doping procedures, and further permits the uniform charge distribution throughout the fiber length17. A good solvent, dimethyl formamide (DMF), of PAni operated as the coagulation bath. A slow solvent exchange between m-cresol and DMF facilitated the formation of PAni gel protofibres with a quite low viscosity below 3000\u2009cP. Subsequently, we observed a sharp decrease of diameter from ~0.1\u2009mm to ~4.7\u2009\u00b5m when stretching the gel fibers in the bath (Fig.\u00a01c\u2013f), which, to our knowledge, is a record small value in the achieved wet-spun CPFs4. The ultrafine fiber shows a smooth surface (Fig.\u00a01f and Supplementary Fig.\u00a02), highly crystallized microstructures (Supplementary Fig.\u00a03), and uniform electrical properties (Supplementary Fig.\u00a04). Moreover, such an impressive drawing ratio enables a very high production efficiency of UFPFs beyond 40 m/min. For example, we prepared a 5.4-kilometers-long UFPF in 2 h (Fig.\u00a01g).\n\na Schematic of the good solvent exchange strategy to prepare UFPFs in a modified wet spinning protocol. In the case of poor solvent exchange (light orange region, upper panel), PAni molecules are rapidly solidified into thick gels and protofibres with rough crystallized particles. In the case of good solvent exchange (light blue region, lower panel), the formed gels with low viscosity occur an impressive gel extension and are slenderized into ultrafine fibers. b Schematic of the modified wet spinning process. c Scanning electron microscope (SEM) image of the marked region in (b), showing the sharp necking behavior of gel PAni fibers. The close observation of region 1 (d), region 2 (e), and region 3 (f) in the marked zone of (c), illustrating the sharply necking process of PAni gels. g Photograph of a 5.4-kilometers-long UFPF collected in two hours. Scale bars: c 20\u2009\u00b5m, d 2\u2009\u00b5m, e 10\u2009\u00b5m, g 150\u2009mm.\n\nThe sharp necking behaviors of gel protofibres are highly related to the use of good solvents as coagulation bath. In a good solvent, interactions between PAni chains and solvent molecules are energetically favorable, and will cause PAni chains to expand and disperse well. In a poor solvent, the chain interactions are preferred and suppress the dispersion of PAni molecules. We recorded the evolution of surface morphologies of PAni fibers collected from different solvating species. As shown in Fig.\u00a02a, the obtained fibers in poor solvating species, i.e., water, ethanol, ethyl acetate (EA), and acetone, generally present coarse surfaces and large diameters around 20\u2009\u00b5m. By comparison, we clearly observed a necking phenomenon in both cases of good solvents, i.e., N-methyl-2-pyrrolidone (NMP) and DMF. Such necking effects promoted the finally produced fibers to behave ultrafine morphologies, which assists PAni fibers to behave a higher degree of orientation and crystallization (see the X-ray diffraction analysis in Supplementary Fig.\u00a03). Further, the higher degree of crystallization keeps the doping bonding in PAni chains from the attack of ambientes at the molecular level, and is conducive to a better structure and performance stability. We used Raman spectra to evaluate their structural evolution after placing fibers in air for four weeks. As shown in Fig.\u00a02b, we did not find obvious de-doping signals in Raman spectra of the PAni fibers from good solvents, whereas various de-doping peaks (1223 and 1462\u2009cm\u22121) appeared in the cases of poor solvents, which inflects the dissociation of proton-polymer interactions18,19,20.\n\na SEM images of the PAni fibers produced in different solvating species. Specifically, the upper four panels show the fibers prepared from poor solvents, and the lower two panels show the fibers fabricated from good solvents. b Raman spectra of PAni fibers after placing in air for four weeks. c The diffusivity from PAni dispersions (in m-cresol) to various solvating species. d The viscosity of PAni gels formed in various solvating species. e Mechanics simulation results of extension behaviors of PAni gel fibers at different interfacial pressure. Comparing to the blue regions, the elements in blue regions are subject to larger stress. f Typical tensile stress-strain curves of UFPFs. g Ashby plot comparing the mechanical strength of UFPFs to previously reported CPFs. Scale bars in a: Water, Ethanol, EA, Acetone 20\u2009\u00b5m (left) 10\u2009\u00b5m (right); NMP 20\u2009\u00b5m (left) 5\u2009\u00b5m (right), DMF 20\u2009\u00b5m (left) 2\u2009\u00b5m (right).\n\nWe speculate that this sharp necking phenomenon may be caused by two factors: diffusion difference and interfacial pressure. In the conventional wet spinning protocol, the diffusion from good solvents to poor solvents occurs quickly to solidify dope fluids into gel fibers21,22. The rapid diffusion could be aggravated in the system of conducting polymers due to the strong interactions of rigid chains. Thus, PAni molecules tend to bond into irregularly crystallized particles prior to undergoing extensive drawing, as present in the upper panels of Fig.\u00a01a. In previous reports using poor solvents as coagulation bath, although CPFs with a smooth surface could be collected by enhanced shear flow and strong stretching12,14, diameters are unable to be decreased to the ideal level due to the insufficient stretching slenderization of solidified gels. In contrast, the diffusion from dope fluids to good solvents is quite slow. Such slow diffusion allows the formation of fibrous gels with a low viscosity and the following high drawing ratios. Note that most conventional polymers are incapable of gelling in good solvents due to the poor chain interactions23,24.\n\nWe calculated the diffusivities between various solvents and measured the viscosity of corresponding formed gels to support our explanations. The diffusivity from A molecules to B molecules, \\({D}_{{AB}}^{0}\\) (cm2 s\u22121), is determined by Eq. (1):\n\nwhere \\({\\mu }_{B}\\) (cP) is the solvent viscosity, T (K) is the temperature, and \\({V}_{b}\\) (cm3\u2009g\u22121\u2009mol\u22121) is the molar volume of solvent at its normal boiling temperature25. As displayed in Fig.\u00a02c, the diffusivities from m-cresol to DMF (7.5 \u00d7 10\u22126\u2009cm2\u2009s\u22121) and NMP (7.71 \u00d7 10\u22126\u2009cm2\u2009s\u22121) are generally lower than that of poor solvents. Diffusion in bath further dominates the viscosity of protofibres. To monitor the viscosity of gel fibers in practical conditions, we conducted the viscometer tests at a low revolution (e.g., 10 Rev.). As summarized in Fig.\u00a02d, the formed PAni gels in good solvents show a viscosity below 3000\u2009cP, much lower than that of poor solvents (>4000\u2009cP). The established solvating specie-diffusivity-viscosity formula accords well with our proposed explanations.\n\nInterfacial pressure during the solvent exchange is another major factor relating to the necking behavior of PAni protofibres. In a two-fluid system, the interfacial pressure between two kinds of solvents is inclined to decrease with the improved solvent diffusion26. Based on the slow diffusion from m-cresol to good solvents (Fig.\u00a02c), the interfacial pressure between gel fibers and the coagulation bath is considerable, which further induces the necking of protofibres. To understand this, we conducted a mechanic simulation of the stretching behavior of gel fibers at different interfacial pressures (see the progressive results in Supplementary Fig. 5 and \u201cMethod\u201d section). According to the simulation results in Fig.\u00a02e, the higher interfacial pressure drives gel fibers to occur the sharper necking and thinning effects at a given tensile stress. This probably explains the formation of UFPFs in DMF bath.\n\nUFPFs show impressive mechanical performance. Different from that of conventional polymer fibers, the typical linear strain\u2013stress curves of UFPFs demonstrate a brittle fracture behavior with a small tensile strain of 3.67\u2009\u00b1\u20090.64% (Fig.\u00a02f). It is reasonable if considering the rigid backbone of PAni chains, which likely gather and condense into fragile fibrous assemblies after undergoing strong shear flow in spinning microtubes. According to classical Griffith theory on brittle fracture, fibers\u2019 strength generally improves with the decrease of diameter due to the depressed structural defects27. We compared the mechanical performance of UFPFs with previously reported CPFs.\n\nDerived from the strain-stress curves, we concluded that UFPFs have a modulus of 29.89\u2009\u00b1\u20095.6\u2009GPa, and strength of 1080\u2009\u00b1\u200971\u2009MPa, at least one order of magnitude higher than that of CPFs with larger diameters (Fig.\u00a02g), mainly including PEDOT fibers (<450\u2009MPa)7,28,29,30,31,32 and PAni fibers (<400\u2009MPa)12,33,34,35.\n\nUltrafine morphology optimizes the electroactive surfaces, which enables UFPFs to exhibit superb energy and charge storage capacities. To evaluate the electrochemical activity of UFPFs, we constructed a micro capacitor using polyvinyl alcohol (PVA)-H3PO4 gel electrolyte and two UFPF electrodes (Fig.\u00a03a). The electrochemical properties were checked by cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) measurements. At different scan rates, the nearly rectangular shape of CV curves and instantaneous current response to voltage reversal at each end potential suggest the good electrochemical activity of UFPFs36 (Fig.\u00a03b). The nearly triangular shape of GCD curves at different current densities illustrates the formation of efficient electric double layers and charge propagation across the UFPF electrodes37 (Fig.\u00a03c). According to the GCD results, we determined the electrochemical properties of UFPFs. Among them, the area capacitance, CA, is between 1008 and 1666 mF cm\u22122 at the current densities between 0.32 and 3.18\u2009mA\u2009cm\u22122, outperforming previously reported thick CPFs27 and other electrodes, such as carbon nanomaterials34,38, metal oxides39 and conducting polymers40,41,42,43, and approaching to that of PAni nanowires44 (Fig.\u00a03d). The volumetric capacitance, power density, and energy density reached 83.8\u2009F\u2009cm\u22123, 0.96\u2009W\u2009cm\u22123, and 4.19\u2009mWh\u2009cm\u22123, respectively (Supplementary Fig.\u00a06). In lifetime tests of UFPF-based capacitors, both the potential and capacitance continued without a significant decrease for 120 charge/discharge cycles at a low current density of 1.59\u2009mA\u2009cm\u22122, indicating the reliable electrochemical performance stability of UFPFs (Fig.\u00a03e).\n\na Schematic of a micro capacitor constructed using two UFPF electrodes on a substrate. b Cyclic voltammetry curves with the increasing scan rates from 10 to 20, 50, 80, and 100\u2009mV\u2009s\u22121. c Galvanostatic charge/discharge curves at various current densities increasing from 0.32 to 0.63, 1.59, and 3.18\u2009mA\u2009cm\u22122. d The area capacitance of UFPFs compared to previously reported electrodes. e Cycle galvanostatic charge/discharge curves during 120 cycles between 0 and 0.6\u2009V at 1.59\u2009mA\u2009cm\u22122. f The relationship between current and voltage at a slow rate of 10\u2009mV\u2009s\u22121. g The charge storage capacity of UFPFs comparing to other charge storage materials.\n\nWe were able to confirm the amount of transported charge per unit area to UFPF during the charge/discharge cycle. The charge during a triangular wave potential between \u22120.9\u2009V and 1.0\u2009V (water window, see Supplementary Fig.\u00a07) was calculated by integrating the measured current with respect to the time of period at a low scan rate of 10\u2009mV\u2009s\u22121 (Fig.\u00a03f)6. We determined that the charge storage capacity of UFPF was 5.25 \u00d7 104\u2009mC\u2009cm\u22122, a value at least two orders of magnitude higher than that of noble metals45, carbon bulk46,47,48 and previously reported conducting polymers49 (Fig.\u00a03g). This value decreases slightly to 2.015 \u00d7 104\u2009mC\u2009cm\u22122 at a tenfold scan rate of 100\u2009mV\u2009s\u22121 (Supplementary Fig.\u00a08).\n\nBenefitting from the favorable energy and charge storage performance of UFPFs, we demonstrated a high-performance all-solid OECT. OECT amplifies drain-source current intensities at low operating voltages by ion penetration into the organic mixed ionic-electronic conductors, i.e., conducting polymers50,51. This process is controlled by the gate bias, and, to date, has generally conducted in aqueous electrolytes. To preclude the interference of the external environment, we promoted the working conditions of OECT from aqueous environments to all-solid state by using gel electrolytes as the ion matrix. As shown in Fig.\u00a04a, b, our OECT is mainly constructed by three polymer layers. The upper layer is the cured polyurethane (PU) working as the dielectric coating and protecting the device from the invasion of external action52. A fibrous silver gate electrode with a diameter of 7\u2009\u00b5m is fixed in PU. Since UFPFs have demonstrated reliable electrochemical activities in PVA-H3PO4 gel, we used PVA-H3PO4 gel as the middle layer to inject ions to or uptake ions from the drain-source channel materials. A UFPF right below the silver gate is fused in the ion gel, and operates as the channel material. The bottom layer is also pure PU acting as the supporter of the whole device. Along the gate bias direction, the gate bias is mainly distributed in the gate/electrolyte interface and electrolyte/channel interface due to the almost insulating gel electrolyte (with a resistance beyond 10\u2009M\u03a9). Due to the remarkable flexibility and transparency of PVA and PU, the all-solid OECT is very soft, and shows a transmittance beyond 80% in the region of visible light (Fig.\u00a04c), and a small thickness below 300\u2009\u00b5m.\n\na Schematic of the all-solid OECT composed of three polymer layers, one silver wire as the gate electrode, and one UFPF as the drain-source channel. b Cross-section SEM image and schematic of OECT. The yellow break lines direct the charge flow along the fiber chains (green solid lines). c Transmittance of the OECT in the region of visible light. A typical output curve (d), transfer curve (e), and power consumption in operation (f) of OECT. Scale bars: b 20\u2009\u00b5m.\n\nDespite the long channel length (~0.48\u2009cm), much larger than that of a conventional micrometer-scale device, the all-solid OECT showed favorable amplification performance with a high on-off current ratio (>103, Fig.\u00a04e) at low voltages (<1\u2009V, Fig.\u00a04d). The relatively fair transconductance (gm, < 60 \u00b5S) is probably ascribed to the small cross-sectional area, which dramatically magnifies the resistance of fibrillar channel. The comparison of electrical properties with previously reported fiber-based OECTs is listed in Supplementary Tab.\u00a01. Note that the all-solid OECT is an energy-saving device with extremely low power consumption. For example, at a given drain-source voltage of 0.6\u2009V, the consumed power is below 18\u2009\u00b5W (Fig.\u00a04f).\n\nWe proved that the all-solid OECT functioned to amplify small electrical signals in gel environments and respond to mechanical deformation as a tactile sensor. As illustrated in Fig.\u00a05a, the applied vertical pressure on the surface of the all-solid OECT adjusted the ion penetration due to the improved gate-source electric field and the redistribution of intrinsic capacitance53. At a VG of \u22120.1\u2009V and a VD of 0.35\u2009V, we observed a stable increase of drain-source current, IDS, with the increasing pressure, up to a 92% amplification from 0 to 40 kPa (Fig.\u00a05b). The sensitivity is at the level of 0.01\u20130.1 kPa\u22121 in this process (dark cyan dots in Fig.\u00a05b). As shown in Fig.\u00a05c, the average rising time and falling time under instantaneous pressure of 17.8 kPa is ~536\u2009ms and ~698\u2009ms, respectively. Such integrated parameters facilitated the all-solid OECT to respond to different pressure levels from 0.92 to 22.2 kPa (Fig.\u00a05d). In addition to the response to pressure in the vertical direction, the all-solid OECT also reacted to friction in the horizontal direction (Fig.\u00a05e and Supplementary Fig.\u00a09). The forward and backward friction of a load on the surface incurred horizontal movement of the PU layer, which drove the displacement of the Ag gate. Further, the real-time distance between the silver gate and the UFPF channel was changed repeatedly, thus producing a bimodal response curve (Fig.\u00a05g). Note that, to enable the enlargement of IDS with the increasing gate-channel distance under the repeated friction, we applied a positive VG of 0.1\u2009V at a VD of 0.55\u2009V. The all-solid OECT responded stably to friction at different magnitudes (Fig.\u00a05f, from 1.84 to 5.55 kPa) and different speeds (Fig.\u00a05h, from 4 to 20\u2009mm\u2009s\u22121) during our cyclic tests. For example, IDS increased ~86% at 5.55 kPa.\n\na Schematic of the mechanism explaining the response to the action of external pressure. b Relative drain-source change (\u0394IDS/IDS0) and sensitivity as a function of pressure. c Response time of the all-solid OECT when pressing (rising edge) and releasing (falling part) under the instantaneous pressure of 17.8 kPa. d Cyclic response at three different pressure levels (0.92, 6.8, and 22.2 kPa). e, Schematic of the working principle of the response to friction. f Cyclic response at three different frictions (1.84, 4.69, and 5.55 kPa). g An enlarged curve of the marked part in (f). h Cyclic response at different friction speeds from 4, 6, 8, 10, 15, to 20\u2009mm\u2009s\u22121.",
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            "section_name": "Discussion",
            "section_text": "The past decades have witnessed great achievements in preparing high-performance CPFs, which made a vast difference to the rapid development of advanced electronics. However, due to the limitations of both technology and strategy, it is still difficult to produce ultrafine CPFs at a large scale. We proposed a good solvents strategy in modified wet spinning technology. With a principle of diffusion-controlled slow gelation of protofibres, the system successfully downsized the diameter of PAni fibers to below 5\u2009\u00b5m, a value smaller than that of most previous work. Furthermore, the ultrafine morphology with highly improved electroactive surfaces promotes UFPFs to behave superb electrochemical activities and mechanical performance.\n\nIt is of great importance to realize the mass production of ultrafine CPFs. We constructed an all-solid OECT to employ the impressive energy and charge storage capacities of UFPFs. A handful of fibers are robust enough to satisfy the operation as the tactile sensor. In view of the ability to produce on the industrial scale, UFPFs are promised to be extended to large-area electronics, such as textile-scale numeric displays, soft electrochromic windows, and wearable energy harvesting systems.",
            "section_image": []
        },
        {
            "section_name": "Methods",
            "section_text": "All the SEM images were collected on a tungsten thermionic emission SEM system (the Tescan VEGA3). XRD spectra were obtained from the XRD system (Rigaku SmartLab) equipped with a 9\u2009kW rotating anode X-ray source (\u03bb\u2009~\u20091.54\u2009\u00c5) coupling with a high-quality semiconductor detector that supports 0D, 1D, or 2D x-ray diffraction measurement. Raman spectra were recorded from Renishaw Micro-Raman Spectroscopy system fully integrated with a confocal microscope spectrometer and a 785\u2009nm laser source. Mechanical tests were conducted on an advanced rheometric expansion system at the Hong Kong University of Science and Technology. All the electrochemical tests were processed on an electrochemical workstation (VersaSTAT3). The measurements of OECT were conducted on a probe station (Micromanipulator) with Keithley 4200A-SCS parameter analyzer. The test of viscosity was conducted by the viscometer (NDJ-5S/9\u2009S/8\u2009S). The probe of viscometer inserted into PAni gels after soaking in solvents, and the viscosity was measured at an increasing shear speed from 10 to 60 Rev.\n\nPAni powder (emeraldine base, purchased from Aladdin, 25233-30-1) was mixed with CSA at a molar ratio of 2:1. After being milled for 15\u2009min, the uniform doped PAni was dispersed in m-cresol (after degassing) at a concentration of 0.05\u2009g\u2009mL\u22121. The dispersions were used as spinning dopes after blending in air for 4\u201324\u2009h, and extruded through a PEEK microtube with an inner diameter of 100\u2009\u00b5m at a rate of 1\u2009mL\u2009min\u22121. A coagulation bath was chosen according to the experimental requirements. PAni fibers were directly drawn out from the bath and collected on a graphite roller continuously.\n\nThe experimental result is verified by a numerical method using commercial software ANSYS. The simulation is performed using workbench 18.0. In the simplified computational model, a geometric model of gel tube is developed, in which the ratio of diameter to length is chosen as 1:18, and the mechanical properties, density, Young\u2019s modulus, and Poisson\u2019s ratio are selected as 300\u2009kg\u2009m\u22123, 1000\u2009Pa and 0.01, respectively. For the boundary conditions, one end of the gel model set as fixed support, and another end applies extended displacement to mimic the stretching effect in the actual situation. Meanwhile, the corresponding pressure is applied on the outer surface of the gel model to account for the function of the impressive interfacial pressure on the surface of gel fibers. To ensure the convergence of the result, a grid independence test is conducted by refining mesh size sequentially, and the finite element mesh with 162641 nodes and 37128 hexahedral elements is adopted finally.\n\nMicro capacitor composed of two UFPF electrodes and the gel electrolyte was constructed on a glass substrate. To prepare the gel electrolyte, PVA power was dispersed into deionized water at a mass ratio of 9:1. PVA was dissolved after being heated for 5\u2009hours at 85\u2009\u00b0C. Then phosphoric acid was added at a mass ratio of 1:10 with deionized water. The mixture cooled at room temperature and was ready for use. Two UFPFs were placed in parallel on the glass slide. The transparent PVA-H3PO4 gel was dropped between UFPFs. Two copper wires connected to the UPPFs with silver paste worked as the conductor lines. After condensing for 10\u2009\u2009min at 40\u2009\u00b0C, the whole device was subject to electrochemical tests.\n\nThe OECT was built from three layers: two PU layers and one ion gel layer. PU dispersion in DMF was cast on a PVDF substrate. After being treated in the oven at 60\u2009\u00b0C, a thin and transparent layer of pure PU was obtained. One drop of PVA-H3PO4 gel electrolyte was added to the surface of solidified PU. A UFPF was immersed in gel. After being dried at 45\u2009\u00b0C for 15\u2009\u2009min, a UFPF channel locked in PVA-H3PO4 gel was obtained. Afterward, another drop of PU was added and a silver wire operation as the gate electrode was put in PU at the liquid state. After being dried at 60\u2009\u00b0C, an all-solid OECT was prepared. Note that all three electrodes were connected to cooper electrodes for the following measurements.",
            "section_image": []
        },
        {
            "section_name": "Data availability",
            "section_text": "The authors declare that the data supporting the findings of this study are available from the corresponding author upon reasonable request.",
            "section_image": []
        },
        {
            "section_name": "References",
            "section_text": "Sariciftci, N. S., Smilowitz, L., Heeger, A. J. & Wudl, F. Photoinduced electron transfer from a conducting polymer to buckminsterfullerene. Science 258, 1474\u20131476 (1992).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nFrommer, J. E. Conducting polymer solutions. Acc. Chem. Res. 19, 2\u20139 (1986).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nShi, G., Jin, S., Xue, G. & Li, C. A conducting polymer film stronger than aluminum. Science 267, 994\u2013996 (1995).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nMirabedini, A., Foroughi, J. & Wallace, G. G. Developments in conducting polymer fibres: from established spinning methods toward advanced applications. RSC Adv. 6, 44687\u201344716 (2016).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nLi, S., Macosko, C. W. & White, H. S. Electrochemical processing of conducting polymer fibers. Science 259, 957\u2013960 (1993).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nLu, W. et al. Use of ionic liquids for \u03c0-conjugated polymer electrochemical devices. Science 297, 983\u2013987 (2002).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nKim, Y. et al. Strain\u2010engineering induced anisotropic crystallite orientation and maximized carrier mobility for high\u2010performance microfiber\u2010based organic bioelectronic devices. Adv. Mater. 33, 2007550 (2021).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nKoizumi, Y. et al. Electropolymerization on wireless electrodes towards conducting polymer microfibre networks. Nat. Commun. 7, 1\u20136 (2016).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nJian, H. Y., Fridrikh, S. V. & Rutledge, G. C. The role of elasticity in the formation of electrospun fibers. Polymer 47, 4789\u20134797 (2006).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nZhang, Y. & Rutledge, G. C. Electrical conductivity of electrospun polyaniline and polyaniline-blend fibers and mats. Macromolecules 45, 4238\u20134246 (2012).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nZhang, Y. et al. Electrospun polyaniline fibers as highly sensitive room temperature chemiresistive sensors for ammonia and nitrogen dioxide gases. Adv. Funct. Mater. 24, 4005\u20134014 (2014).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nHsu, C. H., Cohen, J. D. & Tietz, R. F. Polyaniline spinning solutions and fibers. Synth. Met. 59, 37\u201341 (1993).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nPomfret, S. J., Adams, P. N., Comfort, N. P. & Monkman, A. P. Inherently electrically conductive fibers wet spun from a sulfonic acid-doped polyaniline solution. Adv. Mater. 10, 1351\u20131353 (1998).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nMottaghitalab, V., Xi, B., Spinks, G. M. & Wallace, G. G. Polyaniline fibres containing single walled carbon nanotubes: Enhanced performance artificial muscles. Synth. Met. 156, 796\u2013803 (2006).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nPark, J. H. & Rutledge, G. C. 50th anniversary perspective: advanced polymer fibers: high performance and ultrafine. Macromolecules 50, 5627\u20135642 (2017).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nJiang, H., Geng, Y., Li, J., Jing, X. & Wang, F. Organic acid doped polyaniline derivatives. Synth. Met. 84, 125\u2013126 (1997).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nWang, H. L., Romero, R. J., Mattes, B. R., Zhu, Y. & Winokur, M. J. Effect of processing conditions on the properties of high molecular weight conductive polyaniline fiber. J. Polym. Sci. Pol. Phys. 38, 194\u2013204 (2000).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nNobrega, M. M., Ceppatelli, M., Temperini, M. L. & Bini, R. Pressure-induced reactivity in the emeraldine salt and base forms of polyaniline probed by FTIR and Raman. J. Phys. Chem. C 118, 27559\u201327566 (2014).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nLouarn, G. et al. Vibrational properties of polyaniline-isotope effects. J. Phys. Chem. 100, 6998\u20137006 (1996).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nGruger, A., Novak, A., Regis, A. & Colomban, P. Infrared and Raman-study of polyaniline 0.2. influence of ortho substituents on hydrogen-bonding and UV/Vis near-Ir electron charge-transfer. J. Mol. Struct. 328, 153\u2013167 (1994).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nFang, B., Peng, L., Xu, Z. & Gao, C. Wet-spinning of continuous montmorillonite-graphene fibers for fire-resistant lightweight conductors. ACS Nano 9, 5214\u20135222 (2015).\n\nArticle\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nPaul, D. R. Diffusion during the coagulation step of wet\u2010spinning. J. Appl. Polym. Sci. 12, 383\u2013402 (1968).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nFang, B., Chang, D., Xu, Z. & Gao, C. A review on graphene fibers: expectations, advances, and prospects. Adv. Mater. 32, 1902664 (2020).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nChang, D. et al. Reversible fusion and fission of graphene oxide-based fibers. Science 372, 614\u2013617 (2021).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nYang, D., Fadeev, A., Adams, P. N. & Mattes, B. R. Controlling macrovoid formation in wet-spun polyaniline fibers. Proc. SPIE 4329, 59\u201371 (2001).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nWijmans, J. G. & Baker, R. W. The solution-diffusion model: a review. J. Membr. Sci. 107, 1\u201321 (1995).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nLajtai, E. Z. A theoretical and experimental evaluation of the Griffith theory of brittle fracture. Tectonophysics 11, 129\u2013156 (1971).\n\nArticle\u00a0\n    ADS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nOkuzaki, H. & Ishihara, M. Spinning and characterization of conducting microfibers. Macromol. Rapid Commun. 24, 261\u2013264 (2003).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nOkuzaki, H., Harashina, Y. & Yan, H. Highly conductive PEDOT/PSS microfibers fabricated by wet-spinning and dip-treatment in ethylene glycol. Eur. Polym. J. 45, 256\u2013261 (2009).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nJalili, R., Razal, J. M., Innis, P. C. & Wallace, G. G. One\u2010step wet\u2010spinning process of poly (3, 4\u2010ethylenedioxythiophene): poly (styrenesulfonate) fibers and the origin of higher electrical conductivity. Adv. Funct. Mater. 21, 3363\u20133370 (2011).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nZhang, J. et al. Fast and scalable wet-spinning of highly conductive PEDOT: PSS fibers enables versatile applications. J. Mater. Chem. A 7, 6401\u20136410 (2019).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nWang, Z. et al. All-in-one fiber for stretchable fiber-shaped tandem supercapacitors. Nano Energy 45, 210\u2013219 (2018).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nAndreatta, A., Cao, Y., Chiang, J. C., Heeger, A. J. & Smith, P. Electrically-conductive fibers of polyaniline spun from solutions in concentrated sulfuric acid. Synth. Met. 26, 383\u2013389 (1988).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nPomfret, S. J., Adams, P. N., Comfort, N. P. & Monkman, A. P. Electrical and mechanical properties of polyaniline fibres produced by a one-step wet spinning process. Polymer 41, 2265\u20132269 (2000).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nPomfret, S. J., Adams, P. N., Comfort, N. P. & Monkman, A. P. Advances in processing routes for conductive polyaniline fibres. Synth. Met. 101, 724\u2013725 (1999).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nKou, L. et al. Coaxial wet-spun yarn supercapacitors for high-energy density and safe wearable electronics. Nat. Commun. 5, 1\u201310 (2014).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nYoo, J. J. et al. Ultrathin planar graphene supercapacitors. Nano Lett. 11, 1423\u20131427 (2011).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nYu, D. et al. Scalable synthesis of hierarchically structured carbon nanotube\u2013graphene fibres for capacitive energy storage. Nat. Nanotechnol. 9, 555\u2013562 (2014).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nLu, X. et al. Oxygen\u2010deficient hematite nanorods as high\u2010performance and novel negative electrodes for flexible asymmetric supercapacitors. Adv. Mater. 26, 3148\u20133155 (2014).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nZheng, Y. et al. Thermally-treated and acid-etched carbon fiber cloth based on pre-oxidized polyacrylonitrile as self-standing and high area-capacitance electrodes for flexible supercapacitors. Chem. Eng. J. 364, 70\u201378 (2019).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nZeng, S. et al. Electrochemical fabrication of carbon nanotube/polyaniline hydrogel film for all-solid-state flexible supercapacitor with high areal capacitance. J. Mater. Chem. A 3, 23864\u201323870 (2015).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nYuan, L. et al. Polypyrrole-coated paper for flexible solid-state energy storage. Energ. Environ. Sci. 6, 470\u2013476 (2013).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nChi, K. et al. Freestanding graphene paper supported three-dimensional porous graphene-polyaniline nanocomposite synthesized by inkjet printing and in flexible all-solid-state supercapacitor. ACS Appl. Mater. Interfaces 6, 16312\u201316319 (2014).\n\nArticle\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nHorng, Y. Y. et al. Flexible supercapacitor based on polyaniline nanowires/carbon cloth with both high gravimetric and area-normalized capacitance. J. Power Sources 195, 4418\u20134422 (2010).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nLu, Y. et al. Electrodeposited polypyrrole/carbon nanotubes composite films electrodes for neural interfaces. Biomaterials 31, 5169\u20135181 (2010).\n\nArticle\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nGerwig, R. et al. PEDOT-CNT composite microelectrodes for recording and electrostimulation applications: fabrication, morphology, and electrical properties. Front. Neuroeng. 5, 8 (2012).\n\nArticle\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    PubMed Central\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nVitale, F., Summerson, S. R., Aazhang, B., Kemere, C. & Pasquali, M. Neural stimulation and recording with bidirectional, soft carbon nanotube fiber microelectrodes. ACS Nano 9, 4465\u20134474 (2015).\n\nArticle\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nWang, K. et al. High\u2010performance graphene\u2010fiber\u2010based neural recording microelectrodes. Adv. Mater. 31, 1805867 (2019).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nVenkatraman, S. et al. In vitro and in vivo evaluation of PEDOT microelectrodes for neural stimulation and recording. IEEE Trans. Neural Syst. Rehab. 19, 307\u2013316 (2011).\n\nArticle\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nInal, S., Malliaras, G. G. & Rivnay, J. Benchmarking organic mixed conductors for transistors. Nat. Commun. 8, 1\u20137 (2017).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nRivnay, J. et al. Structural control of mixed ionic and electronic transport in conducting polymers. Nat. Commun. 7, 1\u20139 (2016).\n\nArticle\u00a0\n    CAS\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nLee, S. et al. Nanomesh pressure sensor for monitoring finger manipulation without sensory interference. Science 370, 966\u2013970 (2020).\n\nArticle\u00a0\n    ADS\u00a0\n    CAS\u00a0\n    PubMed\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nWang, X. et al. A Sub-1-V, microwatt power-consumption iontronic pressure sensor based on organic electrochemical transistors. IEEE Electron Device Lett. 42, 46\u201349 (2020).\n\nArticle\u00a0\n    ADS\u00a0\n    PubMed\u00a0\n    PubMed Central\u00a0\n    \n                    Google Scholar\u00a0\n                \n\nDownload references",
            "section_image": []
        },
        {
            "section_name": "Acknowledgements",
            "section_text": "The authors are grateful for the financial support of the Research Grants Council of Hong Kong (No. 15201419), Hong Kong Polytechnic University Postdoctoral Fellowship and Endowed Professorship Fund (No. 847A). P.G. and Q.G. acknowledge funding from Shenzhen-Hong Kong Innovation Circle (No. SZSTI20EG14).",
            "section_image": []
        },
        {
            "section_name": "Author information",
            "section_text": "These authors contributed equally: Bo Fang, Jianmin Yan.\n\nResearch Institute for Intelligent Wearable Systems, The Hong Kong Polytechnic University, 999077, Hong Kong, China\n\nBo Fang,\u00a0Jianmin Yan,\u00a0Jinli Piao,\u00a0Kit Ming Ma,\u00a0Yang Chai\u00a0&\u00a0Xiaoming Tao\n\nInstitute of Textiles and Clothing, The Hong Kong Polytechnic University, 999077, Hong Kong, China\n\nBo Fang,\u00a0Jinli Piao,\u00a0Kit Ming Ma\u00a0&\u00a0Xiaoming Tao\n\nDepartment of Applied Physics, The Hong Kong Polytechnic University, 999077, Hong Kong, China\n\nJianmin Yan\u00a0&\u00a0Yang Chai\n\nDepartment of Polymer Science and Engineering, Zhejiang University, 310027, Hangzhou, China\n\nDan Chang\n\nDepartment of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, 999077, Hong Kong, China\n\nQiao Gu\u00a0&\u00a0Ping Gao\n\nAdvanced Materials Thrust, The Hong Kong University of Science and Technology (Guangzhou), 510000, Guangzhou, China\n\nQiao Gu\u00a0&\u00a0Ping Gao\n\nSearch author on:PubMed\u00a0Google Scholar\n\nSearch author on:PubMed\u00a0Google Scholar\n\nSearch author on:PubMed\u00a0Google Scholar\n\nSearch author on:PubMed\u00a0Google Scholar\n\nSearch author on:PubMed\u00a0Google Scholar\n\nSearch author on:PubMed\u00a0Google Scholar\n\nSearch author on:PubMed\u00a0Google Scholar\n\nSearch author on:PubMed\u00a0Google Scholar\n\nSearch author on:PubMed\u00a0Google Scholar\n\nX.T. supervised this study. B.F. designed and conducted the main experiments. J.Y., Y.C., and B.F. constructed and characterized the transistor. D.C. helped to build the wet spinning equipment and discussed the results. J.P. did the mechanic simulations. K.M.M. helped to draw a part of schematics. Q.G. and P.G. helped to conduct the mechanical tests. B.F. and X.T. wrote the manuscript.\n\nCorrespondence to\n                Bo Fang, Yang Chai or Xiaoming Tao.",
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            "section_text": "Fang, B., Yan, J., Chang, D. et al. Scalable production of ultrafine polyaniline fibres for tactile organic electrochemical transistors.\n                    Nat Commun 13, 2101 (2022). https://doi.org/10.1038/s41467-022-29773-9\n\nDownload citation\n\nReceived: 30 November 2021\n\nAccepted: 30 March 2022\n\nPublished: 19 April 2022\n\nVersion of record: 19 April 2022\n\nDOI: https://doi.org/10.1038/s41467-022-29773-9\n\nAnyone you share the following link with will be able to read this content:\n\nSorry, a shareable link is not currently available for this article.\n\n\n\n\n                            Provided by the Springer Nature SharedIt content-sharing initiative\n                        ",
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            ]
        },
        {
            "section_name": "This article is cited by",
            "section_text": "npj Flexible Electronics (2025)\n\nNature Communications (2025)\n\nAdvanced Fiber Materials (2025)\n\nNature (2024)\n\nNature (2024)",
            "section_image": []
        }
    ],
    "supplementary_files": [
        {
            "title": "Supplementaryinformation1130.pdf",
            "link": "https://assets-eu.researchsquare.com/files/rs-1126903/v1/677e92c6f04ecaa50fb44c9e.pdf"
        }
    ]
}