Polyaniline-Based Ink for Inkjet Printing for Supercapacitors, Sensors, and Electrochromic Devices

: In recent years, there has been a huge surge in interest in improving the efﬁciency of smart electronic and optoelectronic devices via the development of novel materials and printing technologies. Inkjet printing, known to deposit ‘ink on demand’, helps to reduce the consumption of materials. Printing inks on various substrates like paper, glass, and fabric is possible, generating ﬂexible devices that include supercapacitors, sensors, and electrochromic devices. Newer inks being tested and used include formulations of carbon nanoparticles, photochromic dyes, conducting polymers, etc. Among the conducting polymers, PANI has been well researched. It can be synthesized and doped easily and allows for the easy formation of composite conductive inks. Doping and the addition of additives like metal salts, oxidants, and halide ions tune its electrical properties. PANI has a large speciﬁc capacitance and has been researched for its applications in supercapacitors. It has been used as a sensor for pH and humidity as well as a biosensor for sweat, blood, etc. The response is generated by a change in its electrical conductivity. This review paper presents an overview of the investigations on the formulation of the inks based on conductive polymers, mainly centered around PANI, and inkjet printing of its formulations for a variety of devices, including supercapacitors, sensors, electrochromic devices, and patterning on ﬂexible substrates. It covers their performance characteristics and also presents a future perspective on inkjet printing technology for advanced electronic, optoelectronic, and other conductive-polymer-based devices. We believe this review provides a new direction for next-generation conductive-polymer-based devices for various applications


Introduction
Advances in materials science, material engineering, and printing technologies for smart electronic, optoelectronic, and other devices are paving the way for the development of extremely efficient devices that are improving quality of life rapidly [1][2][3][4][5][6][7][8][9][10][11].Materials and processes that improve the quality and enhance the performance of the devices while reducing the cost are most desirable.Inkjet printing, one such technology, will continue to expand, driven by the demand for smart devices, lightweight flexible materials, and environmentally sustainable technologies.Over the past years, this technology has advanced from developing simple printable electronic elements like pressure and temperature sensors to state-ofthe-art applications including medical diagnostics, analytical applications, and the development of optoelectronic systems.Inks used for printing have a wide array of properties ranging from electrically conducting and semi-conducting properties to thermal conductivity, electroluminescence, etc. Functionality combined with easy processability are necessary to fabricate tailor-made devices.Novel functional inks include but are not limited to carbon nanoparticles [12], redox-responsive organometallic polymers like poly(ferrocenylsilane) (PFS) [13], photochromic dyes based on organic spiro compounds [14], polysiloxanebased water-repellent microemulsions [15], conductive polymer polyaniline (PANI) and its composite-based inks [16], p-doped poly (3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) [17,18], and n-type poly(benzimidazobenzophenanthroline):poly (ethyleneimine) (BBL:PEI) electrically conductive polymers [19].
Inkjet printing offers rapid, reproducible, and low-cost ways to pattern conductive polymers on substrates and is an excellent tool for printing conductive-polymer-based completely functional products, which include supercapacitors, sensors for different compounds, and energy-storing electrochromic devices on different substrates.Its advantages over other enabling technologies include scalability (small as well as large surface areas), high precision, simultaneous deposition of multicomponent layers [20,21], printing of delicate membranes without fear of contamination (non-contact printing where the substrate and the print head never come in contact) [22], and printing from aqueous solutions, making it well suited for biological species [23].An inkjet printer has an ink chamber to store ink and a channel that connects this chamber to the nozzle.Two types of inkjet printers based on thermal and piezoelectric effects dominate drop-on-demand technologies.Piezoelectric print heads are advantageous, as the risk of thermal degradation of the ink is minimized [24].
Since their accidental discovery by H. Shirakawa et al., conjugated conductive polymers have been well researched due to their distinctive electronic properties [25,26].These conductive polymers with C=C conjugated double bonds forming the backbone display interesting electrical properties, which include low-energy optical transitions, low ionization potentials, and high electron affinities.These polymers can be oxidized and reduced, thereby converting them into p-and n-doped materials with increased conductivity [27].Among the conjugated conductive polymers, polyaniline, poly(phenylenevinyelene), polypyrrole, and PSS have attracted much interest [28].Conductive polymers fall in the class of smart polymer materials with dynamic electroactive structures and have been explored for use in electrochromic devices, electrophotocatalytic materials, sensors for pH and humidity, smart clothes and coatings, soft matter applications, and solar cells, to name a few [29][30][31][32][33]. Electrically conductive membranes are being studied as alternatives to conventional membranes with enhanced performance for water filtration and wastewater treatment [34].Conductive-polymer-based thermoelectric devices exhibit flexibility, are inexpensive, and are potential candidates to convert waste heat to power [35].Conductive polymers are also being researched as electromagnetic radiation shields.Electromagnetic radiation is not only a health hazard but also interferes with the functioning of electronic equipment.Nanohybrids prepared by graft polymerization of aniline on graphene oxide substrate [36] and 3D epoxy nanocomposites based on 3D P-PANI@f-Cu show promise as electromagnetic interference (EMI) shielders [37].Similarly, epoxy-graphene hybrid nanocomposites show an increase in EMI shielding as the amount of PANI increases [38], while polyaniline and vanadium pentoxide nanocomposites not only exhibit good electromagnetic interference shielding but are also great corrosion inhibitors [39].Various nanomaterials in the PVA-PEDOT matrix have microwave-absorbing properties [40], and the polyamide 6/carbon fiber (PA6/CF) composite also exhibits good EMI shielding properties [41].An interesting application of conductive polymers is their use in the preparation of Janus fibers, which are multifunctional.Janus fibers with PANI as a component have been proposed to be useful for drug delivery and electromagnetic shielding [42].
Energies 2023, 16, 6716 3 of 24 Microfabrication, which is now necessary for several applications like microelectronics [43], microanalytical systems [44,45], micro-optics, potable biomedical devices [46,47], and microfluidics [48,49], is facilitated by inkjet printing.As discussed above, due to the excellent electronic and processability features of conductive polymers, growing efforts are devoted to ink formulation and fabrication of devices with conductive polymers via inkjet printing technologies.
One of the most useful conductive polymers is PANI.Electrochemical polymerization, chemical polymerization, vapor-phase polymerization (VPP), photochemically initiated polymerization, enzyme-catalyzed polymerization, and polymerization employing electron acceptors are used for synthesizing PANI.The electrical conductivity of PANI can be modified easily [50].Three structures are well established for PANI based on the oxidation states.They include the leucoemeraldine base (LEB) form, which is the completely reduced state and appears white in color; the emeraldine base (EB) form, which is the semi-oxidized state and appears blue in color; the salt form appears green; and the pernigraniline base (PAB), the totally oxidized form, appears blue to violet in color [50,51].The emeraldine state can be converted to the conductive polymer form by either acid or oxidative doping, as shown in Figure 1.
erties [41].An interesting application of conductive polymers is their use in the preparation of Janus fibers, which are multifunctional.Janus fibers with PANI as a component have been proposed to be useful for drug delivery and electromagnetic shielding [42].
Microfabrication, which is now necessary for several applications like microelectronics [43], microanalytical systems [44,45], micro-optics, potable biomedical devices [46,47], and microfluidics [48,49], is facilitated by inkjet printing.As discussed above, due to the excellent electronic and processability features of conductive polymers, growing efforts are devoted to ink formulation and fabrication of devices with conductive polymers via inkjet printing technologies.
One of the most useful conductive polymers is PANI.Electrochemical polymerization, chemical polymerization, vapor-phase polymerization (VPP), photochemically initiated polymerization, enzyme-catalyzed polymerization, and polymerization employing electron acceptors are used for synthesizing PANI.The electrical conductivity of PANI can be modified easily [50].Three structures are well established for PANI based on the oxidation states.They include the leucoemeraldine base (LEB) form, which is the completely reduced state and appears white in color; the emeraldine base (EB) form, which is the semi-oxidized state and appears blue in color; the salt form appears green; and the pernigraniline base (PAB), the totally oxidized form, appears blue to violet in color [50,51].The emeraldine state can be converted to the conductive polymer form by either acid or oxidative doping, as shown in Figure 1.In this review, we focus on the formulation of the conductive polymer PANI-based inks, their inkjet printing onto substrates, and the fabrication of devices, with special reference to tailor-made supercapacitors, sensors, electrochromic devices, and the patterning of conductive polymers on flexible substrates.Many of the devices fabricated until re- In this review, we focus on the formulation of the conductive polymer PANI-based inks, their inkjet printing onto substrates, and the fabrication of devices, with special reference to tailor-made supercapacitors, sensors, electrochromic devices, and the patterning of conductive polymers on flexible substrates.Many of the devices fabricated until recently were rigid with a fixed architecture, but inkjet printing, falling under additive manufac-turing technologies, allows deposition on flexible substrates.For proper deposition of the conductive material, the inks should be non-viscous with a viscosity lower than 100 mPa.The limited solubility of some conducting polymers in solvent-or water-based formulations may pose a hindrance [24].Sequential deposition and centrifugation techniques allow for control of viscosity.

Applications of Inkjet Printer Conducting Polymers
Conductive polymers are explored for various applications, including supercapacitors, sensors, and electrochromic devices, owing to their excellent mechanical and electrical properties, flexibility, and low cost of production [33,[52][53][54][55]. DuPont, Sigma-Aldrich, and Pedotinks are some of the leading manufacturers of conductive-polymer-based inks.Companies like Xaar, FUJIFILM Dimatix, and Global Inkjet Systems Ltd.provide functional material printing for various applications.This section reviews conducting polymers for supercapacitors, sensors, and electrochromic devices, including the formulation of the ink, the inkjet printing process, and the performance highlights.In addition, the patterning of conductive polymers on flexible substrates is reviewed in this section.

Conductive Polymer for Supercapacitors
An excellent choice as a sustainable device for energy storage, the supercapacitor has two electrodes, an electrolyte, and a separator, with the electrochemical material being of utmost importance.Supercapacitors are classified as electrochemical doublelayer capacitors (EDLCs), pseudocapacitors, or hybrids formed by a combination of both types [56].The EDLCs based on large-surface-area carbon materials like carbon nanotubes, activated carbon, etc., are non-Faradaic in nature, storing electrical energy via nanoscale charge separation at the electrode-electrolyte interface and forming electrical double layers.The pseudocapacitors based on metal oxide, metal-doped carbon, and conductive polymers are Faradaic in nature, based on a reversible and quick surface redox reaction between the electrode and electrolyte.They provide a much higher energy density in comparison to EDLCs.Polyaniline (PANI), polypyrrole (PPy), polythiophene (PTh), and poly 3,4ethylenedioxythiophene (PEDOT) are being extensively researched for pseudocapacitive applications because of their large specific capacitance.
Inkjet printing, known to deposit ink on demand, helps greatly economize the consumption of material while also allowing printing of the material on various substrates like paper, glass, and fabric of different designs and patterns, helping make flexible supercapacitors.Thin paper-like electrode materials as well as free-standing electrode materials, which have the advantage of being free of insulating binders, conductive agents, current collectors, and solvents, are best suited for flexible and lightweight devices of the future.The development of a variety of methods by which polyaniline (PANI) can be synthesized has led to it being extensively researched for inkjet-printed supercapacitors.A nanohybrid freestanding electrode based on GP (graphene paper) and GH-PANI (graphene hydrogel-PANI) π−π stacking interactions has been developed via inkjet printing.The steps involved in the fabrication of GP (graphene paper)-and GH-PANI (graphene hydrogel-PANI)-based supercapacitors are illustrated in Figure 2. The asymmetric supercapacitor device demonstrated good mechanical, electrochemical, and capacitive properties, with a tolerable energy density of 24.02 Wh kg −1 at a power density of 400.33 W kg −1 [57].
PANI production has traditionally been achieved by polymerizing the monomer aniline.A benign method where the aniline dimer (DANI) in an organic solvent is added to the oxidative solution of ammonium persulfate in an aqueous medium has been used to prepare the emeraldine PANI (PANI-EB) as a fast reaction, eliminating hazardous and toxic aniline monomer usage directly.Inks with extremely good jettability and geometric realization have been obtained by dedoping this salt doped with chloride ions to obtain PANI doped with trifluorosulphonic acid and camporsulphonic acid as counterions, thereby increasing the conductivity of the resultant inks for producing inkjetprinted tracks of diverse geometry [58].These inks are also of interest as they demonstrate Energies 2023, 16, 6716 5 of 24 that counterion displacement induced by the measurement signal leads to negative resistance/capacitance and supercapacitance (−2.3 mF @ 30 Hz, which corresponds to a mass capacity of −799 F g −1 ), ideal for application in low-frequency-range devices.An ink based on PANI nanoparticles covalently attached to the graphene oxide, i.e., (GO) @ PANI composites, was synthesized by first synthesizing GO and PANI separately, followed by mixing EDC/NHS (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) and N-hydroxysulfosuccinimide (NHS)) activated GO and PANI in the ratio 9:1 to prepare the composite, which was inkjet printed on a gold-coated polymer substrate (PET) and reduced by hypophosphorous acid to fabricate the desired electrodes [59].Sandwiched and interdigitated supercapacitors were assembled (Figure 3).Volumetric supercapacitance for both the sandwiched (258.5 F cm −3 at 1 mV s −1 ) and interdigitated supercapacitors (554 F cm −3 at 1 mV s −1 ) was high, with an excellent cycling retention of over 90% after 2000 cycles of charging and discharging.PANI production has traditionally been achieved by polymerizing the monomer aniline.A benign method where the aniline dimer (DANI) in an organic solvent is added to the oxidative solution of ammonium persulfate in an aqueous medium has been used to prepare the emeraldine PANI (PANI-EB) as a fast reaction, eliminating hazardous and toxic aniline monomer usage directly.Inks with extremely good jettability and geometric The fabrication of the GH-PANI supercapacitor involves graphene oxide (GO) self-assembly into 3D graphene hydrogels (3D GHs), followed by in situ polymerization of PANI on GH.The GH-PANI ink is obtained via ball milling and ultrasonic treatment of the 3D GH-PANI composite formed in the previous step.The ink is printed on the paper substrate, giving GOP, followed by overprinting as represented in step VI.Soaking the fabricated GH-PANI/GOP in the HI solution results in reduction by HI, and removal by peeling from the substrate results in freestanding GH-PANI/GP.Fabrication the occurs of a flexible SC device based on the GH-PANI/GP electrode and gel electrolyte.Reproduced with permission from [57].
Xu and co-workers formulated nanographene/polyaniline (NPG/PANI) inks of appropriate viscosity, surface tension, and conductivity.These inks can be deposited as thin films on substrates using inkjet printing (Figure 4) [60].Two NGP/PANI ink-printed electrodes with carbon fabric as the substrate were sandwiched together using a separator, forming an electrochemical capacitor, and studied using a 1 M H 2 SO 4 electrolyte.They show a maximum specific capacitance of 82 F g −1 , a power density of 124 kW kg −1 , a cycle life of 1000 cycles, and an energy density of 2.4 Wh kg −1 with a scan rate of 20 mVs −1 (Figure 4).On macro-porous graphene foam (ultrathin graphene sheets), a thin film of PANI was deposited via electrochemical deposition (polyaniline-coated graphene).The pores were filled with aniline, phytic acid, and ammonium persulfate by inkjet printing to allow oxidative polymerization.This resulted in PANI-filled graphene foams.The PANI-filled macro-porous graphene used as an electrode for supercapacitors exhibited a high areal capacitance of over 1700 mF cm −2 , more than two times the capacitance achievable with pure graphene, metal oxide, or conductive polymer thin-layer coated graphene [61].Various conducting polymers, such as PANI, PPy, and PTh, have been widely used for the fabrication of supercapacitors via inkjet printing.Some reported supercapacitors based on conductive polymers are tabulated in Table 1.In the case of supercapacitors, improvement in mechanical robustness, structural complexity, convenient fabrication, and device configuration is still a critical task.For example, although conductive polymers have an almost 10-fold stretchability capacity, final devices do not have this ability due to the presence of other device components that are not stretchable.and N-hydroxysulfosuccinimide (NHS)) activated GO and PANI in the ratio 9:1 to prepare the composite, which was inkjet printed on a gold-coated polymer substrate (PET) and reduced by hypophosphorous acid to fabricate the desired electrodes [59].Sandwiched and interdigitated supercapacitors were assembled (Figure 3).Volumetric supercapacitance for both the sandwiched (258.5 F cm −3 at 1 mV s −1 ) and interdigitated supercapacitors (554 F cm −3 at 1 mV s −1 ) was high, with an excellent cycling retention of over 90% after 2000 cycles of charging and discharging.Xu and co-workers formulated nanographene/polyaniline (NPG/PANI) inks of appropriate viscosity, surface tension, and conductivity.These inks can be deposited as thin films on substrates using inkjet printing (Figure 4) [60].Two NGP/PANI ink-printed electrodes with carbon fabric as the substrate were sandwiched together using a separator, forming an electrochemical capacitor, and studied using a 1 M H2SO4 electrolyte.They show a maximum specific capacitance of 82 F g −1 , a power density of 124 kW kg −1 , a cycle life of 1000 cycles, and an energy density of 2.4 Wh kg −1 with a scan rate of 20 mVs −1 (Figure 4).On macro-porous graphene foam (ultrathin graphene sheets), a thin film of PANI was deposited via electrochemical deposition (polyaniline-coated graphene).The pores were filled with aniline, phytic acid, and ammonium persulfate by inkjet printing to allow oxi- conductive polymers are tabulated in Table 1.In the case of supercapacitors, improvement in mechanical robustness, structural complexity, convenient fabrication, and device configuration is still a critical task.For example, although conductive polymers have an almost 10-fold stretchability capacity, final devices do not have this ability due to the presence of other device components that are not stretchable.

Polyaniline
Two distinct doped PANI inks were prepared by dissolving the emeraldine salt of PANI in dimethylsuphoxide, followed by the addition of trifluorosulphonic acid and camporsulphonic acid.
Materials with negative capacitance in the low-frequency range can be used in devices working in nominal grid conditions (50-60 Hz) and up to short-wave radio frequencies.
Negative capacitance is reported.The highest negative supercapacitance achieved is −2.3 mF at 30 Hz, corresponding to a specific mass capacity of −799 F g −1 . [58]

Polyaniline
Electrodes were fabricated by printing GO @ PANI composites on gold-coated polymer substrates and then reducing them.Sandwiched and interdigitated supercapacitors were developed.
This method allows the end users to precisely deposit active materials according to their designs for miniature and wearable electronics.
Devices fabricated have high volumetric capacities of 258.5 F cm −3 at 1 mV s −1 for sandwich structures and 554 F cm −3 at 1 mV s −1 for interdigitated ones.Even after 2000 cycles of charging and discharging, over 90% capacitance retention could be achieved. [59]

Polyaniline
Graphene polyaniline (NGP/PANI) inks of appropriate surface tension and viscosity were formulated and then inkjet printed to produce thin-film supercapacitor electrodes.
This preparation method allowed good control over pattern geometry and location in thin films.A major application is manufacturing energy storage devices in printable electronics.
In 1 M H 2 SO 4 solution as the electrolyte, a maximum specific capacitance of 82 Fg −1 , a power density of 124 kW kg −1 , and an energy density of 2.4 Wh kg −1 were observed when a scan rate of 20 mV s −1 was applied.
A long life cycle of over 1000 cycles. [60]

Polyaniline
Graphene foam is made up of a few layers of graphene electrodeposited with a thin layer of PANI, with subsequent filling of the submillimeter-sized pores with PANI by using inkjet printing.
Good option for high-performance supercapacitors.
The synergistic effect of graphene and PANI provides a large areal capacitance of over 1700 mF cm −2 . [61]

Conductive Polymers for Sensors
Nanostructured conductive polymers are good candidates for sensor and biosensor design.A response is generated when the electrical conductivity is modified via redox reactions or protonation.The polymers can be deposited on various surfaces with good thermal and chemical stability at a low cost, making them ideal for many applications.In addition, the conductivity can be tuned by doping or combining the conductive polymer with various additives, including oxidants like ammonium persulfate and ammonium peroxy disulfate, aqueous copper (II) and iron (III) salts, and halogen electron acceptors like bromine and iodine.Inkjet printing a solution or suspension containing the conductive polymer offers a simple and cost-effective method for preparing varied sensors for environmental sensing, food testing, and clinical applications.Among various sensors, pH sensors have received much attention in the food and healthcare industries, especially for foodborne pathogen detection and as personal wearable biochemical sensors to monitor sweat, blood, and tumors as a complement to lab-based equipment.
Energies 2023, 16, 6716 9 of 24 A paper-based colorimetric sensor using Polyaniline-Pectin nanoparticles (PANI-PEC NPs) printed on Whatman filter paper grade 4 has been used for sensing the presence of E. coli.both qualitatively and quantitatively in milk and milk products.The acid metabolites produced by the bacterium (succinates, lactates, acetates, malates, etc.) convert the blue emeraldine base form of PANI to a green-colored emeraldine salt form with increased conductivity.With a sensitivity of 0.52 ± 0.17 log CFU/mL E. coli within 10: 21 h, it represents a practical system with good applicability and efficiency [62].
Aqueous-based PANI ink formulations with acrylic resin additives as binders were used to print pH-sensitive electrodes by Bilbao and coworkers.The working electrode is a screen-printed carbon ink layer on Valox ® (polybutylene terephthalate), modified by inkjet-printed PANI ink.Its performance was compared with the electrodes prepared by electropolymerization of PANI on carbon paste electrodes and found to be better.The response of these electrodes fabricated by inkjet printing PANI inks and acrylic resins onto screen-printed carbon electrodes for synthetic sweat showed good sensitivity of up to 69.1 mV/pH [63].
PANI has long been used as a sensor for toxic ammonia gas.It deprotonates the emeraldine salt and converts it to the emeraldine base form, with a corresponding drop in conductivity.Toxic ammonia gas can be sensed by piezoelectric inkjet printing of polyaniline nanoparticle films on interdigitized silver electrode arrays (Ag IDAs) on a PET substrate.The sensor is further attached to polyimide-based flexible heating foils to facilitate operation at different temperatures.It has a stable logarithmic response of 1-100 ppm to ammonia with a t 50 value of 15 s at room temperature, with better performance at 80 • C [64].The response was also found to be largely independent of the relative humidity range of 35 to 98%.
Sensors for gaseous ammonia developed by Duy Dam Le and co-workers gave promising results.Silver inkjet printed on Si/SiO 2 substrates was drop-coated with a blend film of the emeraldine salt form of PANI and ethylene glycol (EG) to sense NH 3. It showed good sensitivity as well as a linear response to ammonia concentration at a relative humidity of 3-70% [65].The sensor could be regenerated for use by heat treatment at 60 • C in about 15 min.Inkjet-printed layers (Dimatix material printer) of polyaniline and copper (II) chloride on a screen-printed silver interdigitated electrode (IDE) on a flexible PET substrate function as a chemiresistor for hydrogen sulfide with a sensitivity of 2.5 ppm by volume [66].A linear relationship between measured current and concentration is observed in the 10-100 ppmv region.The variation in current in the circuit is due to the protonation of PANI to the emeraldine salt by H 2 S, as opposed to the protonation of ammonia by PANI in ammonia sensors.A class of CuCl 2 /PANI chemiresistor sensors with inkjet-printed silver electrodes on kaolin-coated paper substrates has also been studied for sensing H 2 S. Exposure to H 2 S resulted in the formation of copper sulfide and the acid HCl, which protonates the EB PANI, resulting in an increase in conductivity.Concentrations as low as 10 ppm H 2 S could be sensed [67].
Inkjet printing provides a low-consumption, cost-effective method of preparing disposable diagnostic tools for medical applications.A disposable paper-based electrochemical sensor for the detection of ascorbic acid has a good sensitivity of 17.7 µA/mM, with the limit of detection for ascorbic acid being 30 ± 3 µM in a concentration range of 30-270 µM.The assembly consists of screen-printed conductive carbon graphite paste on Whatman Grade No. 1 filter paper as the reference electrode and counter electrode, and five-layer PANI inkjet printed onto the screen-printed carbon electrodes as the working electrode in acetate buffer at a pH of 5 [68].
The conducting emeraldine salt phase of PANI ink prepared by ammonium persulfate oxidation used for the printing of interdigitated patterns on the flexible untreated polymer substrate using an HP inkjet printer exhibited a change in resistance with a change in relative humidity.The sensor exhibited a short response time of 5 s under low humidity conditions (6% RH); on exposure for 50 s, the electrical resistance exhibited an apparent increase; and when the sensor was exposed to high humidity conditions (97.3% RH), the resistance started decreasing [69].The sensor has applications as low-cost RFID tags, polymer photovoltaic cells, and printed flexible electronics devices.
Multiplexed detection of various metabolites is useful for early and easy detection of diseases.It is a challenge to deposit electroactive materials and enzymes on selective electrodes in a precise fashion.By using a 'drop on demand' selective inkjet printing process, an assembly of a working electrode layer specific to each metabolite, a microfluidic channel layer, and a top cover has been fabricated (Figure 5).It has been tested for analyzing biomolecules like triglycerides, glucose, and lactates in phosphate-buffered saline as well as human serum samples [70].The sensitivity with respect to triglycerides was found to be 7.49 µA/mM −1 cm −2 between 0.1 mM and 6 mM, while that of lactate was 3.94 µAmM −1 cm −2 between 0.08 mM and 5 mM.The glucose sensitivity exhibited by the sensor was 5.03 µAmM −1 cm −2 between 1 mM and 25 mM.
The conducting emeraldine salt phase of PANI ink prepared by ammonium persulfate oxidation used for the printing of interdigitated patterns on the flexible untreated polymer substrate using an HP inkjet printer exhibited a change in resistance with a change in relative humidity.The sensor exhibited a short response time of 5 seconds under low humidity conditions (6% RH); on exposure for 50 seconds, the electrical resistance exhibited an apparent increase; and when the sensor was exposed to high humidity conditions (97.3% RH), the resistance started decreasing [69].The sensor has applications as low-cost RFID tags, polymer photovoltaic cells, and printed flexible electronics devices.
Multiplexed detection of various metabolites is useful for early and easy detection of diseases.It is a challenge to deposit electroactive materials and enzymes on selective electrodes in a precise fashion.By using a 'drop on demand' selective inkjet printing process, an assembly of a working electrode layer specific to each metabolite, a microfluidic channel layer, and a top cover has been fabricated (Figure 5).It has been tested for analyzing biomolecules like triglycerides, glucose, and lactates in phosphate-buffered saline as well as human serum samples [70].The sensitivity with respect to triglycerides was found to be 7.49 µA/mM −1 cm −2 between 0.1 mM and 6 mM, while that of lactate was 3.94 µAmM −1 cm −2 between 0.08 mM and 5 mM.The glucose sensitivity exhibited by the sensor was 5.03 µAmM −1 cm −2 between 1 mM and 25 mM.Urea has long been known to function as an indicator of human kidney health.With the aim of developing a cheap disposable biosensor for urea, inkjet-printed assemblies have been tried.Carbon paste electrodes were screen printed onto pre-shrunk PET plates.This was followed by sequential inkjet printing of PANI nanoparticles, urease enzyme solution containing glycerol (0.1%, v/v), and then Triton X-100 (0.01%, v/v) in a phosphate Urea has long been known to function as an indicator of human kidney health.With the aim of developing a cheap disposable biosensor for urea, inkjet-printed assemblies have been tried.Carbon paste electrodes were screen printed onto pre-shrunk PET plates.This was followed by sequential inkjet printing of PANI nanoparticles, urease enzyme solution containing glycerol (0.1%, v/v), and then Triton X-100 (0.01%, v/v) in a phosphate buffer of pH 7.12 (0.1 M) on the working electrodes.The decomposition of urea was measured chronocoulometrically via the doping of ammonium at the polyaniline-modified, i.e., urease/nanoPANI biosensor electrode surface at −0.3 V vs. Ag/AgCl [71].The sensor successfully measured ammonia in the 0.1-100 mM range and urea in the 2-12 mM range (r 2 = 0.98).Inkjet printing was used to fabricate a three-electrode configuration on a coated paper substrate.An assembly of inkjet-printed gold nanoparticle-based working and counter electrodes, along with a quasi-reference inkjet-printed silver nanoparticle electrode with an electrochemically deposited layer of Ag/AgCl, was devised and studied as sensors after various modifications.The formation of self-assembled monolayers (SAMs) of alkanethiols on the gold electrode surface was studied as a possible sensor for materials where terminally substituted thio groups are used.Electropolymerization of the working electrode with polyaniline (PANI) conductive polymer for pH-sensing applications, and glucose oxidase (Gox)-entrapped poly-3,4-ethylenedioxythiophene (PEDOT) films (PEDOT-Gox) with the possibility of forming amperometric glucose sensors, were also explored [72].Morrin and coworkers investigated PANI nanoparticles in an enzyme biosensing application.Aqueous nanoparticles of PANI along with horseradish peroxidase (HRP) enzyme were cast simultaneously using a drop coating method onto the surface of the screen-printed carbon working electrode, the disadvantage being the inherent thickness of the film, which affected its potential [73].Oxidant patterning by inkjet printing on polyethylene terephthalate films, followed by deposition of the emeraldine salt form of PANI patterns and immobilization of the RGD peptide over it via covalent linkages, were used for the detection of biomolecules from live cells (Figure 6).Rat pheochromocytoma PC12 cells were cultured on the RGD-immobilized PANI pattern, and real-time electrical signal detection to track biomolecular release was studied [74].To study inkjet printing for printable chemical sensors, low-sheet-resistance electrodes of multiwalled carbon nanotubes were inkjet printed on a transparent film.This was followed by the printing of randomly oriented PANI nanowires dispersed in an aqueous medium, giving a fully printed sensor assembly.The sensor was capable of detecting changes in pH as PANI changed the resistivity with pH; furthermore, a H2O2 sensor was To study inkjet printing for printable chemical sensors, low-sheet-resistance electrodes of multiwalled carbon nanotubes were inkjet printed on a transparent film.This was followed by the printing of randomly oriented PANI nanowires dispersed in an aqueous medium, giving a fully printed sensor assembly.The sensor was capable of detecting changes in pH as PANI changed the resistivity with pH; furthermore, a H 2 O 2 sensor was fabricated by depositing silver nanoparticles (which catalyze the decomposition of H 2 O 2 to produce OH − ) over the PANI layer [75].To explore the superior sensing of nanotubes and nanoparticles, carbon nanotubes as electrodes and chemiresistive polyaniline nanowire sensors were inkjet printed sequentially on the PET film to prepare a chemiresistive glucose sensor.The glucose oxidase and platinum nanoparticle catalysts were placed between the CNT layers.The glucose oxidase enzyme catalyzes glucose oxidation to produce gluconolactone and hydrogen peroxide; H 2 O 2 is further catalyzed by platinum nanoparticles to produce OH − ; the local change in pH is sensed by the PANI layer, which changes resistivity [76].A paper-based sensor was fabricated as a DNA biosensor and used for the determination of high-risk HPV type 16 by inkjet printing graphene polyaniline (G-PANI) conductive ink onto the screen-printed carbon ink working electrode.The AQ-PNA (anthraquinone-labeled pyrrolidinyl peptide nucleic acid (acpcPNA)) probe was immobilized on this electrode and modified to introduce negative charges, which facilitated coulombic immobilization on the positively charged G-PANI electrode.It showed a linear response range of 10-200 nM, and the HPV type 16 DNA detection limit of 2.3 nM was reported.The sensor was successfully tested for its ability to detect the PCR-amplified DNA from HPV type 16 positive SiHa cells, successfully demonstrating that it functions as a highly sensitive ePAD DNA biosensor for the diagnostic screening and detection of cervical cancer [77].
Soft photomasks were printed on different substrates.Desired design patterns were inkjet printed onto a transparent hybrid composite inorganic oxide film (biaxially oriented polypropylene coated with silica oxide (BOPP-SiOx)) [78].The inkjet-printed soft photomasks were further used for depositing organic polymers (PANI) and inorganic materials on polymer films and photografting organic polymer materials like PAA onto polymer films and non-planar substrates.Inkjet printing was used by Zea et al. to create a printed pH sensor made of polyaniline, polypyrrole, and polyelectrolyte poly (sodium 4-styrenesulphonate) (PSS) based on PANI: PSS/PPy: PSS inks, which were deposited on a gold microelectrode printed on a flexible substrate (Figure 7).The gold ink functionalized with pthalocyanin as the substrate enhanced the conductivity by improving the electron mobility between the conductive polymer chain and gold nanoparticles.A linear super-Nernstian response (81.2 0.5 mV/pH unit) over a wide pH range (pH 3-10) makes it a promising sensor for various applications [79].Furthermore, various inkjet-printed conducting polymers used in sensing applications are summarized in Table 2.In spite of the excellent potential of inkjet-printable conductive polymers, PANI conductive-polymerbased sensors have some issues such as cross-selectivity, short sensor lifetime, speed, and instability, which is a major drawback for conductive-polymer-based sensor technology.The durability and sensitivity of sensors are highly dependent upon conducting polymer nanocomposites and the interaction between organic and inorganic materials.linear response range of 10-200 nM, and the HPV type 16 DNA detection limit of 2.3 nM was reported.The sensor was successfully tested for its ability to detect the PCR-amplified DNA from HPV type 16 positive SiHa cells, successfully demonstrating that it functions as a highly sensitive ePAD DNA biosensor for the diagnostic screening and detection of cervical cancer [77].Soft photomasks were printed on different substrates.Desired design patterns were inkjet printed onto a transparent hybrid composite inorganic oxide film (biaxially oriented polypropylene coated with silica oxide (BOPP-SiOx)) [78].The inkjet-printed soft photomasks were further used for depositing organic polymers (PANI) and inorganic materials on polymer films and photografting organic polymer materials like PAA onto polymer films and non-planar substrates.Inkjet printing was used by Zea et al. to create a printed pH sensor made of polyaniline, polypyrrole, and polyelectrolyte poly (sodium 4-styrenesulphonate) (PSS) based on PANI: PSS/PPy: PSS inks, which were deposited on a gold microelectrode printed on a flexible substrate (Figure 7).The gold ink functionalized with pthalocyanin as the substrate enhanced the conductivity by improving the electron mobility between the conductive polymer chain and gold nanoparticles.A linear super-Nernstian response (81.2 0.5 mV/pH unit) over a wide pH range (pH 3-10) makes it a promising sensor for various applications [79].Furthermore, various inkjet-printed conducting polymers used in sensing applications are summarized in Table 2.In spite of the excellent potential of inkjet-printable conductive polymers, PANI conductive-polymer-based sensors have some issues such as cross-selectivity, short sensor lifetime, speed, and instability, which is a major drawback for conductive-polymer-based sensor technology.The durability and sensitivity of sensors are highly dependent upon conducting polymer nanocomposites and the interaction between organic and inorganic materials.and (c) the inkjet printing process: (i) printing of Ag RE, tracks, and pads, followed by a drying step; (ii) printing of the Au IE, followed by a drying step and thermal sintering of both metallic Au and Ag layers; (iii) printing of the dielectric SU-8, drying, and UV cross-linking; and (iv) printing of CP inks, followed by a drying step.Reproduced with permission from [79].

Conductive Polymers for Electrochromic Devices
Electrochromic devices can change their color reversibly and find use in display systems, smart windows, and camouflage garments [80][81][82].Deformable or flexible electrochromic devices without any deterioration in performance are capable of indicating stored energy levels by visual color variation.Inkjet-printed stretchable transmissive electrochromic energy storage with WO 3 nanoparticles on a transparent electrode was fabricated [83].The silver nanowires were spray coated on a glass slide, and SiO 2 nanoparticles were spin coated on the AgNW/glass slide surface.PDMS (polydimethylsiloxane) was poured over the transparent conductive electrode, cured, and the composite film was removed from the glass slide.The PEDOT:PSS buffer layer was spin coated on to the ST AgNWs/PDMS, followed by inkjet printing of the WO 3 nanoparticles with a fewnanometer thickness (Figure 8).The electrode demonstrated large optical modulation of 40%, fast switching speed (<4.5 s), high coloration efficiency (75.5 cm 2 C −1 ), good stability, and high specific capacity (32.3 mAh g −1 and 44.8 mAh cm −3 ).The electrode demonstrated good functionality when stretched up to 50%, and electrochromic performance was maintained even when stretched further to 80% strain.Devices assembled with WO 3 /PEDOT:PSS/AgNWs/PDMS negative hybrid electrodes, PANI/MWCNT composite positive electrodes, H 2 SO 4 /PVA gel electrolyte, and 3 M VHB tape as a separator showed good performance, making them well suited for wearable devices.
Energies 2023, 16, x FOR PEER REVIEW 17 of 26 energy levels by visual color variation.Inkjet-printed stretchable transmissive electrochromic energy storage with WO3 nanoparticles on a transparent electrode was fabricated [83].The silver nanowires were spray coated on a glass slide, and SiO2 nanoparticles were spin coated on the AgNW/glass slide surface.PDMS (polydimethylsiloxane) was poured over the transparent conductive electrode, cured, and the composite film was removed from the glass slide.The PEDOT:PSS buffer layer was spin coated on to the ST AgNWs/PDMS, followed by inkjet printing of the WO3 nanoparticles with a few-nanometer thickness (Figure 8).The electrode demonstrated large optical modulation of 40%, fast switching speed (<4.5 s), high coloration efficiency (75.5 cm 2 C −1 ), good stability, and high specific capacity (32.3 mAh g −1 and 44.8 mAh cm −3 ).The electrode demonstrated good functionality when stretched up to 50%, and electrochromic performance was maintained even when stretched further to 80% strain.Devices assembled with WO3/PE-DOT:PSS/AgNWs/PDMS negative hybrid electrodes, PANI/MWCNT composite positive electrodes, H2SO4/PVA gel electrolyte, and 3 M VHB tape as a separator showed good performance, making them well suited for wearable devices.Small et al. reported the synthesis and inkjet processing of polyaniline/MWCN water dispersible composite inks.These films allowed for the switching between yellow, green, and blue when printed onto photopaper, PET, Pt-ITO, and Au-PVDF substrates and exhibited excellent optical transparency, sheet resistance, and electrochromic activity.A change in sheet resistance (1000-5000 ohm sq −1 ) and optical transmittance (30-70%) was reported with a change in the nanotube percentage [84].PANI-silica and PEDOT-silica Small et al. reported the synthesis and inkjet processing of polyaniline/MWCN water dispersible composite inks.These films allowed for the switching between yellow, green, and blue when printed onto photopaper, PET, Pt-ITO, and Au-PVDF substrates and exhibited excellent optical transparency, sheet resistance, and electrochromic activity.A change in sheet resistance (1000-5000 ohm sq −1 ) and optical transmittance (30-70%) was reported with a change in the nanotube percentage [84].PANI-silica and PEDOT-silica composites formed by oxidative polymerization of the monomers aniline and ethylenedioxythiophene (EDOT) on 20 nm sized silica sol particles were converted via solvent exchange to intrinsically conductive-polymer inks, which were inkjet printed on indium-tin-oxide-coated poly (ethylene terephthalate) films.PANI-silica or PEDOT-silica/ITO-PET as well as a blend of the two composites were studied as active layers in electrochromic devices fabricated using polyethylene glycol methacrylate (PEGMA)-based polymeric electrolytes.The color of the devices changed with the change in potential.The color could also be tuned by inkjetprinted PANI-silica and PEDOT-silica blended particles as an electrochromic layer [85].The various electronic and optoelectronics devices fabricated via inkjet printing of conductive polymers are summarized in Table 3.The stability and conductivity of conductive polymers are major factors that determine the performance of electrochromic devices.Although conductive-polymer-based electrochromic devices are promising candidates for commercial-scale use, different challenges need to be addressed, such as non-dispersion and uniform morphology and size as comparable to metal oxide electrochromic devices.

Patterning with Conductive Polymers
Conductive polymers have been patterned using various techniques like templateassisted synthesis, photolithography, softlithography, electrochemical deposition and dippen nanolithography [86].Conductive polymers have also been inkjet printed directly onto substrates, but the method has certain limitations.Conductive polymers like polypyrrole, polyaniline (PANI), and polythiophene and their derivatives are insoluble in common polar solvents, and inks are usually prepared using stabilizers and surfactants to achieve the desired viscosity and surface tension.Vapor deposition polymerization (VDP)-mediated inkjet printing (VDP-IJP) can overcome some of the processability issues.Jang and coworkers suggested a simple method to pattern conductive polymers using vapor deposition polymerization (VDP)-mediated inkjet printing (VDP-IJP), wherein uniform, well-defined patterns of PANI were formed by chemical oxidation polymerization of aniline vapor on oxidant patterns that were previously inkjet printed in the VDP chamber (Figure 9).This process resulted in the formation of densely connected polyaniline nanofibers without the use of surfactants and stabilizers, resulting in patterned PANI being electrically active with low sheet resistance in the range of 10 3 Ωsq −1 on the polymeric substrate [87].

Patterning with Conductive Polymers
Conductive polymers have been patterned using various techniques like templateassisted synthesis, photolithography, softlithography, electrochemical deposition and dip-pen nanolithography [86].Conductive polymers have also been inkjet printed directly onto substrates, but the method has certain limitations.Conductive polymers like polypyrrole, polyaniline (PANI), and polythiophene and their derivatives are insoluble in common polar solvents, and inks are usually prepared using stabilizers and surfactants to achieve the desired viscosity and surface tension.Vapor deposition polymerization (VDP)-mediated inkjet printing (VDP-IJP) can overcome some of the processability issues.Jang and coworkers suggested a simple method to pattern conductive polymers using vapor deposition polymerization (VDP)-mediated inkjet printing (VDP-IJP), wherein uniform, well-defined patterns of PANI were formed by chemical oxidation polymerization of aniline vapor on oxidant patterns that were previously inkjet printed in the VDP chamber (Figure 9).This process resulted in the formation of densely connected polyaniline nanofibers without the use of surfactants and stabilizers, resulting in patterned PANI being electrically active with low sheet resistance in the range of 10 3 Ωsq −1 on the polymeric substrate [87].Reactive inkjet printing can be used to pattern functional organic materials on a solid substrate with a small amount of reagent.A new strategy for the formation of poly(phenylenevinylene) (PPV) patterns on paper by using the reactive inkjet printing (RIJ) method was reported by Jeon and coworkers (Figure 10).Synthesized hydrophilic terephthaldehyde (ink A), bis(triphenylphosphonium salt) (ink B), and potassium t-butoxide (ink C) were printed using an inkjet printer under high humidity conditions in order (A, B, and C) at the same location (overprinting), and an in situ Wittig reaction ensued, resulting in Reactive inkjet printing can be used to pattern functional organic materials on a solid substrate with a small amount of reagent.A new strategy for the formation of poly(phenylenevinylene) (PPV) patterns on paper by using the reactive inkjet printing (RIJ) method was reported by Jeon and coworkers (Figure 10).Synthesized hydrophilic terephthaldehyde (ink A), bis(triphenylphosphonium salt) (ink B), and potassium t-butoxide (ink C) were printed using an inkjet printer under high humidity conditions in order (A, B, and C) at the same location (overprinting), and an in situ Wittig reaction ensued, resulting in the formation of PPV patterns [88].The unreacted reagents and byproducts could be efficiently removed by washing with water and chloroform, as the prepared PPV was found to be insoluble in these solvents.
the formation of PPV patterns [88].The unreacted reagents and byproducts could be efficiently removed by washing with water and chloroform, as the prepared PPV was found to be insoluble in these solvents.Inkjet printing of conductive polymer patterns on the surface of electrospun scaffolds using cell stimulation has been explored.As a part of the investigations, gelatin (Gel) and polycaprolactone (PCL) were modified with calcium phosphate nanoparticles (SG5) and Osteogenon (Osteo) drugs, respectively, and further utilized for the preparation of a bilayer scaffold by accumulating electrospun PCL/Osteo and Gel/SG5 fibers in a common collector [89].Inkjet printing was then used to deposit thin PANI patterns on the surface of the hybrid bilayer scaffold.A bioactive hybrid scaffold system that can provide an electrically conductive environment for cells by bringing together conductive PANI, bioactive particles, and drugs in an electrospun scaffold was prepared.A combination of nanotemplating and inkjet printing was used to prepare nanopatterned thin polymer films.Nanoperforated TiO2 (NP-TiO2) functionalized with hydrophobic perfluorinated phosphate Zonyl FSE (ZFNP-TiO2) fabricated on top of silicon wafers were used as substrates.Biotinylated polythiophene derivative (PBTL) ink, a biosensor material, and dinonylnaphthalene-sulfonic-acid-doped polyaniline (PANI-DNNSA) ink, a pH-and gas-sensing material, were inkjet printed on NP-TiO2 and ZFNP-TiO2 substrates [90].The non-functionalized polymer had higher surface energy and allowed for the deposition of uniform thin films.They have uses in biosensing and electrical devices.Aniline dimer DANI was used to produce PANI via oxidative polymerization in an aqueous medium using polystyrene sulphonate (PSS) as an emulsioning and doping agent.Controlling the amount of the oxidant resulted in mixed leucoemeraldine and emeraldine oxidation states.Solubilized in DMSO, PANI/PSS was suitable as an ink for inkjet printing on flexible substrates and gave interesting negative capacitance effects [16].Inkjet-printed conductive polymers for nanopatterning are summarized in Table 4. Inkjet printing of conductive polymer patterns on the surface of electrospun scaffolds using cell stimulation has been explored.As a part of the investigations, gelatin (Gel) and polycaprolactone (PCL) were modified with calcium phosphate nanoparticles (SG5) and Osteogenon (Osteo) drugs, respectively, and further utilized for the preparation of a bilayer scaffold by accumulating electrospun PCL/Osteo and Gel/SG5 fibers in a common collector [89].Inkjet printing was then used to deposit thin PANI patterns on the surface of the hybrid bilayer scaffold.A bioactive hybrid scaffold system that can provide an electrically conductive environment for cells by bringing together conductive PANI, bioactive particles, and drugs in an electrospun scaffold was prepared.A combination of nanotemplating and inkjet printing was used to prepare nanopatterned thin polymer films.Nanoperforated TiO 2 (NP-TiO 2 ) functionalized with hydrophobic perfluorinated phosphate Zonyl FSE (ZFNP-TiO 2 ) fabricated on top of silicon wafers were used as substrates.Biotinylated polythiophene derivative (PBTL) ink, a biosensor material, and dinonylnaphthalene-sulfonic-acid-doped polyaniline (PANI-DNNSA) ink, a pH-and gas-sensing material, were inkjet printed on NP-TiO 2 and ZFNP-TiO 2 substrates [90].The non-functionalized polymer had higher surface energy and allowed for the deposition of uniform thin films.They have uses in biosensing and electrical devices.Aniline dimer DANI was used to produce PANI via oxidative polymerization in an aqueous medium using polystyrene sulphonate (PSS) as an emulsioning and doping agent.Controlling the amount of the oxidant resulted in mixed leucoemeraldine and emeraldine oxidation states.Solubilized in DMSO, PANI/PSS was suitable as an ink for inkjet printing on flexible substrates and gave interesting negative capacitance effects [16].Inkjet-printed conductive polymers for nanopatterning are summarized in Table 4.

Conclusions and Future Perspectives
In the past years, various inkjet printable conductive polymers such as PANI, PPV, polyaniline, PEDOT, etc., and their composites have been explored for various applications, with a significant improvement in device performance as the conductive and mechanical properties of conductive polymers are tunable.We have primarily reviewed conducting polymer PANI-based inks, and device fabrication using this conductive polymer ink via inkjet printing for a variety of applications such as supercapacitors, sensors, and electrochromic devices.The ink formulations for inkjet printing and the key improvements in devices were summarized in the tables in this article.The inkjet printing of conductive polymer PANI for nanopatterning directly on substrates was also briefly discussed in this review.The properties of conductive polymers need to be further tuned using optimized device configurations for better device performance.
Inkjet printing has proven to be a simple, cost-effective, and green method that saves material and deposits the ink on large areas uniformly, as well as allows accurate patterning.With more research into tuning the properties of conductive polymers like PANI and PANI-based inks, and also with strides in the inkjet printing process, scalable flexible device fabrication with optimum performance is achievable.Improving conducting polymer nanocomposites via modifying the surface and functionalization with inorganic particles and substrates, using inorganic particles with a high aspect ratio, etc., are possible approaches that could be adopted for improving conductive-polymer-based sensors [91].We believe this review provides an overview of recent developments in inkjet-printable conductive polymers for various applications and a new direction for next-generation conductive-polymer-based devices for various applications.The inkjet printing ability of conductive polymers provides an endless number of prospects for designing highly efficient devices with high reproducibility at a low cost, which can be easily scaled up at the commercial level to make technologies commercially viable.With improvements in inks and fabrication technology, scalable, low-cost, single-use, disposable glucose, urea, pH, gas, and enzyme sensors, along with better-performing supercapacitors and electrochromic devices, are achievable.

Figure 2 .
Figure 2. (Steps I-V):The fabrication of the GH-PANI supercapacitor involves graphene oxide (GO) self-assembly into 3D graphene hydrogels (3D GHs), followed by in situ polymerization of PANI on GH.The GH-PANI ink is obtained via ball milling and ultrasonic treatment of the 3D GH-PANI composite formed in the previous step.The ink is printed on the paper substrate, giving GOP, followed by overprinting as represented in step VI.Soaking the fabricated GH-PANI/GOP in the HI solution results in reduction by HI, and removal by peeling from the substrate results in freestanding GH-PANI/GP.Fabrication the occurs of a flexible SC device based on the GH-PANI/GP electrode and gel electrolyte.Reproduced with permission from[57].

Figure 2 .
Figure 2. (Steps I-V):The fabrication of the GH-PANI supercapacitor involves graphene oxide (GO) self-assembly into 3D graphene hydrogels (3D GHs), followed by in situ polymerization of PANI on GH.The GH-PANI ink is obtained via ball milling and ultrasonic treatment of the 3D GH-PANI composite formed in the previous step.The ink is printed on the paper substrate, giving GOP, followed by overprinting as represented in step VI.Soaking the fabricated GH-PANI/GOP in the HI solution results in reduction by HI, and removal by peeling from the substrate results in freestanding GH-PANI/GP.Fabrication the occurs of a flexible SC device based on the GH-PANI/GP electrode and gel electrolyte.Reproduced with permission from[57].

Figure 4 .
Figure 4. Representative supercapacitor device structure is depicted in (A).(B,C) Comparisons of current voltage (CV) curves of nanographene (NGP) and NGP/PANI electrodes measured at different scan rates, in 1 M H2SO4 electrolyte for a two-electrode system.(D) Comparison of the specific capacitance vs. scan rate plots of nanographene (NGP) and NGP/PANI electrodes in two-electrode system, with 1 M H2SO4 aqueous electrolyte.Specific capacitance as a function of scan rate in twoelectrode system, with 1 M H2SO4 aqueous electrolyte.Reproduced with permission from [60].

Figure 4 .
Figure 4. Representative supercapacitor device structure is depicted in (A).(B,C) Comparisons of current voltage (CV) curves of nanographene (NGP) and NGP/PANI electrodes measured at different scan rates, in 1 M H 2 SO 4 electrolyte for a two-electrode system.(D) Comparison of the specific capacitance vs. scan rate plots of nanographene (NGP) and NGP/PANI electrodes in two-electrode system, with 1 M H 2 SO 4 aqueous electrolyte.Specific capacitance as a function of scan rate in two-electrode system, with 1 M H 2 SO 4 aqueous electrolyte.Reproduced with permission from [60].

Figure 5 .
Figure 5. Inkjet-printed multiplexed biosensor based on PANI conductive hydrogels: (a) Precursor solutions A and B were printed on the predefined areas to form a PANI hydrogel on the working electrode (WE).(b) Subsequent printing of chloroplatinic acid (P) and formic acid (F) solutions generated platinum nanoparticles (PtNPs) on the PANI hydrogel film.(c) This was followed by sequential printing of the enzyme solutions of glucose oxidase, lactic oxidase, and lipase/glycerol kinase/Lα-glycerophosphate oxidase on separate electrodes.(d) The biosensor has three layers: the top layer, the microfluidic channel layer in the middle, and the electrode layer at the bottom.(e) Detection of multiple metabolites in human blood.Reproduced with permission from [70].

Figure 5 .
Figure 5. Inkjet-printed multiplexed biosensor based on PANI conductive hydrogels: (a) Precursor solutions A and B were printed on the predefined areas to form a PANI hydrogel on the working electrode (WE).(b) Subsequent printing of chloroplatinic acid (P) and formic acid (F) solutions generated platinum nanoparticles (PtNPs) on the PANI hydrogel film.(c) This was followed by sequential printing of the enzyme solutions of glucose oxidase, lactic oxidase, and lipase/glycerol kinase/L-α-glycerophosphate oxidase on separate electrodes.(d) The biosensor has three layers: the top layer, the microfluidic channel layer in the middle, and the electrode layer at the bottom.(e) Detection of multiple metabolites in human blood.Reproduced with permission from [70].

26 Figure 6 .
Figure 6.Patterning of the oxidant on the PET substrate via inkjet printing.Formation of PANI conductive polymer patterns via VDP process and subsequent modification of PANI patterns via RGD peptide.Reproduced with permission from [74].

Figure 6 .
Figure 6.Patterning of the oxidant on the PET substrate via inkjet printing.Formation of PANI conductive polymer patterns via VDP process and subsequent modification of PANI patterns via RGD peptide.Reproduced with permission from [74].

Figure 7 .
Figure 7. Schematic depicting the (a) desired design patterns for a pH sensor, (b) microscopic image of the printed electrodes, and (c) the inkjet printing process: (i) printing of Ag RE, tracks, and pads, followed by a drying step; (ii) printing of the Au IE, followed by a drying step and thermal sintering of both metallic Au and Ag layers; (iii) printing of the dielectric SU-8, drying, and UV cross-linking; and (iv) printing of CP inks, followed by a drying step.Reproduced with permission from[79].

Figure 7 .
Figure 7. Schematic depicting the (a) desired design patterns for a pH sensor, (b) microscopic image of the printed electrodes, and (c) the inkjet printing process: (i) printing of Ag RE, tracks, and pads, followed by a drying step; (ii) printing of the Au IE, followed by a drying step and thermal sintering of both metallic Au and Ag layers; (iii) printing of the dielectric SU-8, drying, and UV cross-linking; and (iv) printing of CP inks, followed by a drying step.Reproduced with permission from[79].

Figure 8 .
Figure 8. Schematic illustration of fabrication procedure of the inkjet-printed stretchable WO3 transparent electrode.Reproduced with permission from [83].

Figure 8 .
Figure 8. Schematic illustration of fabrication procedure of the inkjet-printed stretchable WO 3 transparent electrode.Reproduced with permission from [83].

Figure 10 .
Figure 10.Formation of poly(phenylenevinylene) (PPV) patterns on paper by using the reactive inkjet printing (RIJ) method.Inks A, B, and C are inkjet printed at the same location.They react to produce the PPV pattern [88].

Figure 10 .
Figure 10.Formation of poly(phenylenevinylene) (PPV) patterns on paper by using the reactive inkjet printing (RIJ) method.Inks A, B, and C are inkjet printed at the same location.They react to produce the PPV pattern [88].

Table 2 .
Conductive-polymer sensor inks for inkjet printing.

Table 4 .
Conductive-polymer pattern inks for inkjet printing.