Asian Journal of atmospheric environment
[ Review Article ]
Asian Journal of Atmospheric Environment - Vol. 14, No. 2, pp.85-104
ISSN: 1976-6912 (Print) 2287-1160 (Online)
Print publication date 30 Jun 2020
Received 27 Feb 2020 Revised 12 Mar 2020 Accepted 27 Mar 2020

Conducting Polymer Nanofibers based Sensors for Organic and Inorganic Gaseous Compounds

Ali Mirzaei1), ; Vanish Kumar2), ; Maryam Bonyani3) ; Sanjit Manohar Majhi4), 5) ; Jae Hoon Bang6) ; Jin-Young Kim5) ; Hyoun Woo Kim4), 6), * ; Sang Sub Kim5), * ; Ki-Hyun Kim7), *
1)Department of Materials Science and Engineering, Shiraz University of Technology, Shiraz 71557-13876, Iran
2)National Agri-Food Biotechnology Institute (NABI), S.A.S. Nagar, Punjab, 140306, India
3)Department of Materials Science and Engineering, Shiraz University, Shiraz 71454, Iran
4)The Research Institute of Industrial Science, Hanyang University, Seoul 04763, Republic of Korea
5)Department of Materials Science and Engineering, Inha University, Incheon 22212, Republic of Korea
6)Division of Materials Science and Engineering, Hanyang University, Seoul 04763, Republic of Korea
7)Department of Civil and Environmental Engineering, Hanyang University, 222 Wangsimni-ro, Seoul, 04763, Republic of Korea

Correspondence to: *E-mail: E-mail: E-mail: These two authors contributed equally to this work as co-first authors.

Copyright © 2020 by Asian Association for Atmospheric Environment
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Resistive-based gas sensors built through the combination of semiconducting metal oxides and conducting polymers (CPs) are widely used for the detection of diverse gaseous components. In light of the great potential of each of these components, electrospun CPs produced by a facile electrospinning method can offer unique opportunities for the fabrication of sensitive gas sensors for diverse gaseous compounds due to their large surface area and favorable nanomorphologies. This review focuses on the progress achieved in gas sensing technology based on electrospun CPs. We offer numerous examples of CPs as gas sensors and discuss the parameters affecting their sensitivity, selectivity, and sensing mechanism. This review paper is expected to offer useful insights into potential applications of CPs as gas sensing systems.


Conductive polymer, Nanofibers, Electrospinning, Gas sensor, Sensing mechanism


To eliminate the ongoing environmental problems affecting our livelihood activities, gas sensors are regarded as effective tools to monitor and quantify air pollutants in ambient air and industrial effluetns in various application fields such as medical diagnosis, analytical laboratories, military applications, mines and indoor environments (Mirzaei et al., 2016; Korotcenkov, 2007; Yamazoe, 2005; Azad et al., 1992). The successful commercialization of gas sensors was possible after the pioneering works on metal oxide semiconductor (MOS)-based chemiresistive gas sensors in the 1960s (Seiyama et al., 1962; Taguchi, 1962). Today, MO-based chemiresistive gas sensors are highly popular due to their various advantages such as high sensitivity, simple fabrication, high stability, small size (portability), and low cost (Mirzaei et al., 2016; Wang et al., 2010; Korotcenkov, 2007; Yamazoe, 2005; Azad et al., 1992). In MO-based resistive sensors, the types and concentrations of gases affect the electrical resistance of the sensor (Lin et al., 2017). Response to a target gas, selectivity, stability, sensing temperature, and response time/recovery time are very important features of a gas sensor (Baharuddin et al., 2019; Lin et al., 2017; Miller et al., 2014; Wang et al., 2010). Among them, sensing temperature is a key parameter that controls the overall consumption of power for the operation of gas sensors. Unfortunately, as the sensing temperatures of most of resistive-based gas sensors are high (up to 450°C), it can increase in power consumption while shortening the sensor lifespan (Miller et al., 2014).

Conducting polymers (CPs) can be used for sensing studies to deal with the high sensing temperature of MO-based gas sensors (Patil et al., 2012). These structures are the organic materials with intrinsic electrical conductivity (Gerard et al., 2002). In general, the presence of π-electron backbone is the main reason for their extraordinary electrical properties, low ionization potential, low energy optical transitions, and high electron affinity. These unique characteristics of CPs have tremendous potential toward sensing applications for diverse gases. CPs have the ability to achieve good sensing characteristics at low or room temperature and to tune their physical and chemical properties to improve the sensing properties (Fratoddi et al., 2015). Furthermore, they have other advantages such as low-temperature synthesis, high flexibility, the possibility of large-scale synthesis, and low costs (Janata and Josowicz, 2003). In particular, CPs can be easily synthesized and their molecular chain structure can be easily improved by controlling synthesis parameters (Talwar et al., 2014; Jung et al., 2008; Bartlett and Ling-Chung, 1989). These advantageous attributes have spurred interest in further study of CP-based chemiresistive gas sensors. Accordingly, some CPs such as polyaniline (PANI), polythiophene, polypyrrole (PPy) and their derivatives have been studied as gas sensing materials since the 1980s (Nylander et al., 1983). The sensing performance of a gas sensor relies on its morphology, microstructure and size (Shimizu and Egashira, 1999; Yamazoe, 1991). Hence, synthesizing nano-scale based CPs for sensing applications would be beneficial for sensing studies. Among different nanostructures, one-dimensional (1D) nanomaterials, such as nanowires, nanorods, nanotubes and nanofibers (NFs), are considered to be very interesting for sensing applications (Arafat et al., 2012). The advantages of 1D nanomaterials are large surface area, high charge carrier collection and transport in the axial orientation and the possibility of surface modification (Chinnappan et al., 2017).

Among these 1D nanostructures, the electrospun NFs offer high surface area, which is suitable for the adsorption of target gases and allows rapid diffusion of gases species, thus increasing the sensor response (Chinnappan et al., 2017). Furthermore, since the diameters of electrospun CP NFs are in the nanoscale range, they offer many interesting properties such as excellent flexibility in surface functionality and better mechanical properties relative to their micro scale counterparts (Yanılmaz and Sarac, 2014). In addition to gas sensing applications, CPs NFs are promising candidates for many other practical applications (Kelly et al., 2013; Moon et al., 2013; Zhao et al., 2013; Sowmiya et al., 2012; Bejbouji et al., 2010; Dhand et al., 2010; Huang et al., 2003). However, in this survey, we only focused on the gas sensing applications of electrospun CPs. Several reviews have already been published on CPs and their derivatives for gas sensing applications (Park et al., 2017; Pandey, 2016; Hangarter et al., 2013; Bai and Shi, 2007; Shirakawa et al., 1977). However, to the best of our knowledge, CPs synthesized by electrospinning method such as NF-based CPs have not been reviewed yet. Herein, we have focused on the CPs-based chemoresistive gas sensors. The major focus of this review is to cover the materials developed through electrospinning processes. However, in a few cases, we also covered CP-based materials prepared by other methods for comparison purpose. In this review, we provided a general introduction about CPs (Section 2) and electrospinning process (Section 3). In section 4, we have discussed the CPs-based gas sensors and their mechanism of gas sensing. In the last section, we drew a conclusion of the present work with future suggestions.


In the late 1970s, it was demonstrated that polymers having π-conjugated chains have excellent conductivity in partially reduced or oxidized states (Chiang et al., 1978; Shirakawa et al., 1977). In 2000, CP research gained more attention after the Nobel Prize in Chemistry was given for work on CPs. CPs (or simply conjugated polymers) are a special class of polymers containing a sp2 structure with alternating п-bonds that allow delocalized transport of charge carriers (Heeger, 2001). They have the advantages of excellent electronic properties, easy synthesis procedure, tunable properties, flexibility, and environmental stability. As shown in Fig. 1, the most important CPs include polyaniline (PANI), poly(3, 4-ethylenedioxythiophene) (PEDOT), polyacetylene (PA), polythiophene (PTh), polypyrrole (PPy), poly (phenylene vinylene) and poly (p-phenylene) (Heeger, 2001).

Fig. 1.

Structure of the most important CPs. Reproduced from (Heeger, 2001), copyright 2020.

One of the shortcomings of CPs is their low conductivity (<10-5 S cm-1). Hence, a doping process is necessary to extract the electrons from the backbone of the CPs to increase their electrical conductivity. However, the protonation process is only applicable to polyaniline (PANI). CPs containing positive charges in its backbone are considered to be charge carriers, leading to conducting properties (1-105 S cm-1) (Le et al., 2017; Hangarter et al., 2013). Obviously, the resulting conductance is related to the concentration and type of dopants (Abdiryim et al., 2005; Kumar and Sharma, 1998; Chiang et al., 1978). Most CPs, such as PPy and PANI, show p-type semiconducting behavior and are unstable in the un-doped state. The dopants can help maintain charge neutrality and also increase the conductivity (Miasik et al., 1986). The most widely used process for synthesis of CPs is oxidative polymerization of aromatic benzoids (aniline, phenylenevinylene, and diphenylamine) or heterocycles (thiophenes, pyrroles, azines) (Shirakawa et al., 1977). Usually, the monomer is oxidized, and cation radicals are formed. The oxidation can be tracked between two cation radicals by a dimerization reaction. Growth of the chain occurs via the connection of radical ions, as shown in Fig. 2 for pyrrole (Choudhary et al., 2014). The oxidation process could be performed either electrochemically (using anodic polarization on the electrode) or chemically (by adding oxidants). In electrochemical polymerization, the oxidation state can be controlled by the electrode potential, while the chemical route is better for preparing composites or large quantities of polymer (Choudhary et al., 2014).

Fig. 2.

The scheme of pyrrole polymerization mechanism. Reproduced with permission from (Choudhary et al., 2014), copyright 2020.

A protonic acid as oxidant is needed to produce a linear polymer. The most commonly used oxidants are (NH4)2S2O8, (H2O2) and (Ce(SO4))2. Both organic media and aqueous media can be employed for the production of linear polymers. Galvanostatic, potentiostatic, and potentiodynamic methods can be utilized in an electrochemical process. All methods have three-electrodes: a reference electrode, a counter electrode and a working electrode (Bai and Shi, 2007; Skotheim and Reynolds, 2007). Some CPs such as poly (phenylene ethynylene), poly (phenylene vinylene) and their derivatives have been prepared via other chemical methods instead of oxidation polymerization (Jung et al., 2000; Yang et al., 1995; Gilch and Wheelwright, 1966).

Controlling the morphology and conductivity of CPs strongly depends on the synthesis procedure (Skotheim and Reynolds, 2007). In addition to polymerization and electrochemical techniques, chemical, plasma, photochemical and enzymatic methods can be used to prepare polymer chains from the monomer precursors (Liu et al., 1999; Chandler and Pletcher, 1986; Mohammadi et al., 1986). However, the chemical synthesis method is the preferred method according to literature, followed by electrochemical polymerization. Conducting polymers synthesized using chemical methods require initial solubilization of the polymers and then inkjet coating, drop casting or electrospinning techniques for fabrication (Rojas and Pinto, 2008; Kovtyukhova et al., 2002). However, CP NFs synthesized by electrospinning offer a high surface area, which is a big advantage for sensing studies. Therefore, we discuss the principles of the electrospinning technique for preparation of CPs in the following section.


The electrospinning process is a kind of electrospray process introduced by Formhals in 1934 (Formhals, 1934). Electrospinning is an efficient process that can produce long polymeric NFs (NFs) (Long et al., 2011; Huang et al., 2006). The electrical, magnetic, as well as sensing properties of the resulting NF can be tuned by changing the diameter of synthesized NFs (Wong et al., 2008; Cai and Martin, 1989).

An electrospinning instrument consists of three major parts: a syringe equipped with a pump, a high-voltage system and an electrically grounded collector (Fig. 3) (Ramakrishna et al., 2006). During electrospinning, NFs are produced by applying an electric force to polymer solutions kept inside the syringe. The mechanism of fiber formation is due to ‘‘electrostatic attraction” of charges. The solution inside the syringe has a definite surface tension, which is charged by applying a high voltage acting at the tip of the needle. To collect the ejected NFs, the charged collector is placed at a given distance (~10-30 cm) from the tip of the syringe. When a driving voltage (10-30 kV) is applied, the solution in the syringe is ejected by overcoming surface tension and accelerates towards the collector plate, forming a cone-like structure. During this process, the solvent undergoes evaporation and the polymer stretches greatly, leading to the formation of a solid polymer fiber. The produced NFs accumulate on the collector plate and are then collected for further use (Chinnappan et al., 2017; Subbiah et al., 2005).

Fig. 3.

Basic scheme for electrospinning process. Reproduced with permission from Ramakrishna et al. (2006).

The fiber morphology is related to the features of environmental conditions, the solution (system parameters) and process conditions (operational parameters) (Teo and Ramakrishna, 2006). Non-woven or uniaxially aligned NFs can be produced in three-dimensional NFs with a huge specific surface area and high porosity (Lim, 2017). NF structures with desirable physico-chemical and electrical properties can be manufactured by electrospinning, and these structures can have an extraordinary effect on the sensing properties (Sun et al., 2003). Moreover, secondary structures of NFs can be controlled to synthesize NFs with core/shell structures (Starr and Andrew, 2013), NFs with hollow structures and NFs with porous structures (Bhardwaj and Kundu, 2010; Sun et al., 2003).

3. 1 Types of Electrospinning

Different types of electrospinning techniques and instruments are available. However, they differ in the type of collector and spinneret. Some of them use an electrode material as a spinneret, whereas some others are needleless (Afshari, 2016). Co-axial electrospinning, co-electrospinning ( Jiang et al., 2005a), multi-needle electrospinning (Tomaszewski and Szadkowski, 2005) and needleless electrospinning (Wang et al., 2009a) are the main types of electrospinning processes. Multi-needle and needleless electrospinning methods are used to improve the efficiency of the traditional electrospinning method. Co-axial electrospinning is utilized to prepare multi-layer and core-shell composite NFs structures with more functionality and better quality (Zhang et al., 2004). In this technique, two discrete NF building blocks are provided via coaxial narrow channels and are synthesized into core-shell NFs (Lim, 2017). Co-electrospinning is also capable of producing single layer and bilayer NFs (Starr and Andrew, 2013). Multi-layer electrospinning can also be utilized to prepare hierarchical NF morphologies (Kayaci et al., 2014; Li et al., 2014; Tran and Kalra, 2013).

3. 2 Operational Parameters

Structure, porosity, diameter, and surface area play important roles in the final features of the NFs, and fortunately they can be controlled during the electrospinning process (Tan et al., 2005). The parameters involved in the electrospinning method should be carefully optimized to synthesize NFs with better performance in gas sensors. We discuss electrospinning parameters in the following sections. More details can be found in Tan et al. (2005).

3. 2. 1 Solution Parameters

3. 2. 1. 1 Concentration of Solution

The optimum solution concentration should be used for the electrospinning process, otherwise beads are formed instead of fibers. A minimum solution concentration for fiber formation is needed. At low solution concentrations, NFs contain beads, and the bead shapes vary from spherical to spindle-like as the solution concentration increases (Tan et al., 2005). The fabrication of continuous fibers at higher concentrations is forbidden due to the inability to maintain solution flow at the tip of the needle (Sukigara et al., 2003).

3. 2. 1. 2 Molecular Weight of CPs

The quantity of entanglements in the polymer chains is influenced by the polymer molecular weight, which changes the characteristics of NFs. Furthermore, it has a remarkable influence on the electrical and rheological features like surface tension, viscosity and conductivity of CPs (Haghi and Akbari, 2007). Polymers with different molecular weights create fibers with different diameters (Liu et al., 1999). Polymers with optimal molecular weights must be selected for producing continuous and smooth NFs (Tan et al., 2005).

3. 2. 1. 3 Viscosity of Solution

These factors greatly affect the morphology of the resulting NFs and should be optimized. If the solution viscosity is too low, electrospraying may occur. Higher viscosity solutions are very hard to force through the needle, resulting in unstable feed rate control of the solution at the tip (Patil et al., 2017; Sukigara et al., 2003).

3. 2. 1. 4 Surface Tension of Solution

Surface tension, which strongly depends on the solvent composition, plays an essential role in the electrospinning synthesis of polymers. Various solvents have various surface tensions. NFs without beads can be made by decreasing the surface tension of the solution. A high surface tension makes the electrospinning method difficult due to the instability of jets and the production of sprayed droplets (Hohman et al., 2001). However, lower surface tensions help make the electrospinning method easier at a lower electric field (Haghi and Akbari, 2007).

3. 2. 1. 5 Solution Conductivity

Jet formation is highly depended on the charged ions in the polymer solution. The final conductivity of the solution depends on the solvent, polymer, and the availability of ionizable salts. Solutions with high conductivity are unstable in the vicinity of severe electric fields, which results in wide diameter distributions. In contrast, a solution with a low conductivity cannot generate uniform fibers because the electrical force is cannot adequately elongate the fibers (Haghi and Akbari, 2007; Hayati et al., 1987). Electrospun NFs can often be prepared with ultra-small diameters from solutions with high electrical conductivities (Li and Wang, 2013; Huang et al., 2003; Fong et al., 1999).

3. 2. 2 Process Parameters

3. 2. 2. 1 Applied Voltage

The voltage is another key factor during the electrospinning of polymer NFs. Electrostatic interaction forces, due to the applied voltage, will result in the formation of a Taylor cone. When the electrostatic forces are larger than the surface tension force, the ejected Taylor cone is distorted (Kriegel et al., 2008). Electrostatic forces increase as the applied voltage increases, which will result in accelerating the polymer jet. Accordingly, the fiber is stretched, leading to a reduction in the NF diameters (Kriegel et al., 2008; Buchko et al., 1999).

3. 2. 2. 2 Flow Rate

Overall, lower flow rates of the solution favor polarization of the polymer solution. The pore diameter and fiber diameter increase with increasing solution feed rate, and beads appeared on NFs. Flow rates that are too low can increase the overall time of the electrospinning process (Thenmozhi et al., 2017; Chronakis, 2005).

3. 2. 2. 3 Types of Collectors

A conductive substrate is always used as a collector for collecting NFs. Aluminum foil is widely used for the fabrication of collectors due to its low cost, wide availability and ease of modification, which allows the collection of several NFs. Usually collectors in the form of rotating drums are used to create NFs with uniform thickness and excellent reproducibility (Patil et al., 2017). Other occasionally used collectors are conductive cloth, conductive paper, pins (Sundaray et al., 2004), rotating disks (Xu et al., 2004), wire mesh (Wang et al., 2005), and parallel bars (Li et al., 2004).

3. 2. 2. 4 Tip to Collector Distance

One good method to control the morphology and diameter of NFs is to control the tip to collector distance. Generally, there is an optimal distance between the collector and tip that improves the evaporation of NF solutions and accordingly a minimum distance is needed for drying the fiber before it reaches the collector. When the distance is too short or too long, beads can be formed (Xu et al., 2004). Flatter fibers can be generated at closer distances, but rounder fibers form at longer distances (Chronakis, 2005).

3. 2. 3 Ambient Conditions

3. 2. 3. 1 Temperature and Humidity

During the electrospinning method, temperature and humidity also play an essential role in the final properties of synthesized NFs. As temperature increases, the final diameters of the NFs decrease because of increased evaporation of solvent, while the higher humidity will result in the formation of more pores on the surface of NFs (Pillay et al., 2013; Casper et al., 2004).


4. 1 Sensor Configuration

In resistive-based gas sensors, the electrical resistance greatly depends on the ambient gases in terms of type and concentration (Mirzaei et al., 2016). Such gas sensors are particularly suitable for detecting different gases and concentration variations (Neri and Donato, 1999). Fabrication of the sensor includes the deposition of a sensing layer (CPs) on an alumina, SiO2/Si or flexible substrate that has interdigitated electrodes (e.g., Au, Pt) for reading the sensor resistance. A heater is also used on the back side of the sensor to heat it to the desired sensing temperature.

The electrospun CP-based gas sensors discussed in this review can be used to detect many toxic, VOC, and flammable gases such as H2, NO2, CO2, triethylamine, methanol, and liquefied petroleum gas (LPG). In Table 1, the main source of emission, hazardous effects, and the threshold limit value (TLV) of the most important gases are presented.

A list of organic compounds detected by resistive CP-based gas sensors.

4. 2 General Sensing Mechanism

The sensing capabilities of CPs are due to interactions of the target gas with the CP sensing materials, which can result in changes in conductivity, the doping level and electron transport in the conjugated backbone. It has been suggested that there are five possible interactions between the CP NF sensing layer and the target gas that can alter the conductance (Neri and Donato, 1999), as shown in Fig. 4. First, such a response may be caused by how the target gas affects the charge transfer between the electrode and CP. Second, this response may be due to direct creation or elimination of the charge carriers, e.g., via oxidation or reduction of the polymer chain. In particular, this interaction may be significant for NH3, although this seems less likely for weakly interacting organic vapors such as alcohols (Wetchakun et al., 2011; Gardner and Bartlett, 2000). Third, the charge carrier mobility in a polymer chain can be altered via interactions between the mobile charge carriers and the target gas across the polymer chains. Fourth, the target gas can interact with counter ions (X-) in the sensing layer, thus altering the mobility of the charge carriers along the polymer chain. Counter ions with relatively low mobility are generally connected in the polymer chains. The target gas diffuses into the polymer film and acts as a solvent for the counter ions, resulting in ionic conduction (Dixit et al., 2005). Finally, the target gas can modulate the resistance of a CP film by affecting the rate of interchain hopping.

Fig. 4.

Possible interaction sites for a target gas on a CPs sensing layer. Reproduced with permission from (Neri and Donato, 1999), copyright 2020.

Electron transfer is the general sensing mechanism in CP-based gas sensors. Gases with an electron acceptor nature like NO2 can eliminate electrons from CPs. It is well-known that at low temperatures (<100°C), O2- is the dominant chemisorbed oxygen type on the surfaces of most sensing materials. First, oxygen gas is adsorbed on the surface of the sensor and then (by taking of electrons from the surfaces of the sensor), it becomes adsorbed in the form of a molecular ion: O2+e → O2-. By exposing CP-based gas sensors to a reducing target gas, the target gas molecules can react with the oxygen species and transfer electrons back to the conduction bands of the sensor. Such electrons transferred in the conduction band can be combined with holes from the valence band, thus leading to higher resistances and lower carrier concentrations for the CP gas sensors. In addition, the resistance decreases for oxidizing gases. However, a signal can appear in both cases. At room temperature, this type of mechanism may contribute less to the sensor signal in CP-based gas sensors, as the concentration of O2- is generally very low at room temperature (Densakulprasert et al., 2005).

Occasionally, a noble metal catalyst like Pd, Au, or Pt is added to the CP film, which allows for the detection of various less reactive gases (Shirsat et al., 2009). Noble metals can catalytically decompose and increase the adsorption of target gases via a spill over process. Furthermore, since the work functions of noble metals and CPs are different, heterojunctions can form between a noble metal and a CP, which can change the resistance of the sensor by modulating the height of the potential barrier formed in the presence of target gases. Hybrid composites of CPs and n-type metal oxides show synergic interactions between the CPs and metal oxides, resulting in the generation of p-n junctions. For example, in a hybrid consisting of PPy (which is a p-type material) and WO3 (which is an n-type material), the p-n junctions formed in the PPy-WO3 p-n heterojunctions can enhance the depletion barrier height, resulting in changes in the sensor response (Sun et al., 2017). Swelling is another mechanism present in CP-based gas sensors (Thenmozhi et al., 2017); as the gas molecules diffuse into the polymer chains, electron hopping becomes difficult because of the increased distance between polymer chains resulting from swelling. Swelling can disrupt conductive pathways in the CP film and increase the sensor resistance when the desired gas is injected, thus enhancing the gas response of the sensor (Guernion et al., 2002).

In the next sections, we analyze how the above gas sensing mechanisms can explain the sensing behavior of CP-based gas sensors. The sensing parameters (e.g., sensing range, sensitivity, DL, response time, and selectivity) of all the covered CPs-based sensors are shown in Table 2.

Sensing parameters of different CPs-based sensors for the sensing of diverse gases.

4. 3 Polyaniline (PANI)-based NF Gas Sensors

Among many CPs, PANI has been the most studied material due to its various characteristics such as reversible doping, dedoping, tunable electrical conductivity, high environmental stability and easy preparation (Sen et al., 2016). PANI can be synthesized using the oxidizing polymerization of aniline from two structural units, i.e., a reduced (B-NH-B-NH) unit and an oxidized (B-N=Q=N-) unit, where B is denoted as a benzenoid and Q is denoted as a quinoid ring.

PANI has the ability to undergo reversible doping under acidic (proton doping) or basic conditions. When PANI is doped with an acid, the imine nitrogen of the polymer backbone is protonated to induce charge carriers. In this situation, the electrical conductivity of PANI increases (σ>1 S cm-1), and this doped form of PANI is known as an emeraldine oxidation state or emeraldine salt (Fig. 5). The un-doped polymer chain is known as an emeraldine base (σ<1×10-10 S cm-1) (Fratoddi et al., 2015; Huang et al., 2004).

Fig. 5.

Repeat unit of the emeraldine oxidation state of polyaniline in the un-doped base form (top) and the fully doped, acid form (bottom). Reproduced with permission from (Huang et al., 2004) from Springer, copyright 2020.

Various nanostructures of PANI including NFs, nanotubes, and nanoparticles have been synthesized by numerous of methods (Kumar et al., 2017, 2016; Gu et al., 2014; Ayad et al., 2013; Long et al., 2011; Rahy and Yang, 2008). These morphologies have high exposed surface area (e.g., PANI NFs with 50 nm diameter have 49.3 m2/g surface area), which can facilitate gas molecules adsorption and greater penetration into the pores (Huang et al., 2004). Introducing a secondary component to the primary PANI nanostructures further enhances its sensing properties due to the synergistic effect between both the components. Various materials such as metallic nanoparticles, metal-oxides, carbonbased materials (CNT, Graphene), and polymers have been added to PANI to tune the sensitivity and selectivity properties (Park et al., 2017). In this section, we discuss gas sensors based on PANI NFs as a sensing layer in their pristine or composite form.

For the sensing of H2, PANI NFs were fabricated as a resistive sensor on Pt or Au electrodes (Fowler et al., 2009). The responses (Rg/Ra) of the sensors with Pt and Au electrodes were 1.65 and 1.03, respectively. The reason for the low sensor response on an Au electrode is the interaction between hydrogen and PANI NFs. The high response of the sensor on Pt electrodes is because of interactions with Pt at the PANI-Pt interface. Hydrogen helps to form a Schottky barrier between Pt and PANI via a variation in the work function as Pt was changed to Pt hydride. The formation of a hydride between the PANI NF layer and the platinum electrode resulted in non-ohmic behavior in the Pt-PANI NFs upon exposure to a H2 environment. Pt is introduced to make a platinum hydride in contact with H2 gas.

The mechanism of hydride formation is shown in Fig. 6. The sensor includes a porous mesh of PANI NFs on Pt electrodes (Fig. 6a). When this sensor is in contact with H2, the gas passes through PANI and reaches the Pt surfaces (Fig. 6b-d). However, some of the hydrogen can also react with PANI before reaching the Pt. Platinum hydride (PdHx) is produced at the interface of the PANI NFs and the platinum metal. When the PANI NFs mesh is exposed to oxygen, it reacts with the PdHx surface. Water and Pt metal form due to the elimination of hydride. Because the work function for PANI NFs is between the work functions for Pt and PdHx, H2 results in the formation of a Schottky barrier, which is the main reason for the sensitivity of the Pt-PANI NFs gas sensor. The hydrogen exposure results in large changes in the work function of the Pt contact. Metal hydride cannot form on Au electrodes, and ohmic contacts with the PANI NFs are formed, and only the interaction between PANI NFs and H2 are observed. The small change in resistance is due to binding between H2 and PANI NFs. In fact, platinum hydride forms via the Pt-PANI NF-hydrogen interactions, and Pt hydride formation is the main reason for the improved sensor response.

Fig. 6.

Interaction of PANI-coated platinum-based sensor with the H2 gas. (a) Sensor structure and (b-d) interaction of hydrogen and oxygen on the surface of sensor. (e) Work functions of Pt, Au, PtHx. Reprinted with permission from (Fowler et al., 2009). Copyright (2020) American Chemical Society.

In another work, camphorsulfonic acid (CSA) doped PANI NF thin films were utilized for sensing of hydrogen (Virji et al., 2006). The resistance change of PANI NFs was greater than conventional PANI due to their porous structure backbone that leads to enhanced diffusion of gas into the film. Hydrogen gas sensing studies showed that the response (Ra/Rg) of the gas sensor was 1.03 for 10000 ppm H2 gas. Fig. 7 shows a gas sensing mechanism for the interaction of H2 with PANI. H2 interacts with doped PANI at the charged amine nitrogen sites. Formation of new N-H bonds to the amine nitrogen of the PANI chains lead to dissociation of H2 bonds. This reaction is quite reversible because charge transfer among adjoining amine nitrogen groups brought the PANI back to its doped, polaronic, emeraldine salt state free of H2. This mechanism just occurs in the emeraldine salt form of PANI.

Fig. 7.

Possible mechanism for hydrogen interaction with doped PANI, where A represents the counteranion. Reprinted with permission from (Virji et al., 2006), copyright (2020) American Chemical Society.

The PANI base emeraldine form is electrically insulating. Thus, there is no transfer of charge among the nitrogen units on the PANI chain, hindering the interactions between H2 and the polymer. In other words, the response of dedoped PANI towards hydrogen is negligible since hydrogen cannot dissociate to interact with the dedoped PANI. The presence of water can also significantly decrease the response of a sensor for hydrogen. Since water molecules have a high affinity to bond with the nitrogen atoms of PANI, the available sites for adsorption of hydrogen decrease, resulting in a low response of sensors to hydrogen. The doping and dedoping in PANI is the crucial for the sensing of H2. In a report on conductometric H2 sensor, it was observed that the doped form of PANI displayed higher sensitivity in comparison to the dedoped PANI. Nonetheless, the dedoped PANI-based H2 sensor outperformed doped PANI in terms of repeatability and baseline stability (Sadek et al., 2007). The composite forms of PANI are also found excellent in improving the H2 sensing capabilities of PANI. In particular, the composites of PANI with graphene-materials (e.g., reduced graphene oxide; rGO), metal organic frameworks (MOFs), and SnO2 displayed good performance for the sensing of H2 gas (Mashao et al., 2019; Zou et al., 2016; Sharma et al., 2015; Al-Mashat et al., 2010). The performance of these sensors can be accessed from Table 2.

The conductivity of PANI composites may increase by including metallic particles or acidic or oxidative doping (Ayad and Zaki, 2008). The selectivity of PANI gas sensors may increase by adding different kinds of dopants like protonic acids (Samui et al., 2001), surfactants (Stejskal et al., 2003) and metals (Wong et al., 2019). Mixing PANI with nanosized metal oxides can increase the selectivity and sensitivity of the CPs. The sensors worked at ambient temperature, and the selectivity to different gases could be improved by increasing the concentration of nanosized metal oxides. Nimkar et al. (2015) prepared TiO2 incorporated PANI NFs using the electrospinning technique. The NFs of the PANI/TiO2 nanocomposite showed a good response (Rg/Ra) of~2.68 towards 0.1% CO2 gas at 48°C. Also, the response time of the PANI/TiO2 NFs film for 0.1% CO2 gas was~80 s. When PANI/TiO2 NFs films were exposed to CO2 gas, the gas penetrated into the PANI matrix, and the improved sensitivity of this sensor was related to the formation of a positively charged depletion layer. Electron transfer from TiO2 to PANI occurs at the heterojunction. As a result, the activation energy and enthalpy of physisorbed CO2 gas decreased. The excellent reversibility and the short response time of the PANI/TiO2 NFs layer is due to the surface morphologies of NFs. Specifically, the gas can diffuse in a NF structure more easily, resulting in large exposure regions and high penetration depths for gas molecules. As shown in Table 2, the composites of PANI with other potential structures, e.g., cross-linked bacterial cellulose-amino graphene (CLBC-AmG) and LaFeO3 microsphere (PLFO) are also efficient for the sensing of CO2 (Abdali et al., 2019; Hashemi Karouei and Milani Moghaddam, 2019).

Hybridization of CPs and metal oxides can enhance the features of the resulting gas sensor, and newly fabricated materials demonstrate the synergistic results of these two materials. In an interesting study, electrospun D-camphor-10-sulphonic acid (CSA) doped PANI/polyethylene oxide (PANI/PEO) and PANI/ZnO/PEO NFs were synthesized (Patil et al., 2015). A sol-gel method was employed for the synthesis of ZnO NPs. PANI (in the form of emeraldine base) and PANI/ZnO were prepared by chemical oxidative polymerization with CSA to improve conductivity and solubility. These were mixed with PEO solutions to obtain NFs by the electrospinning method. The LPG sensing capabilities of the sensors were tested at 30-90°C, and the optimal sensing temperature was 36°C, which is a safe temperature for LPG detection due to the explosive nature of LPG gas. The LPG gas sensing results showed that PANI/ZnO/PEO sensors had a higher response to LPG relative to PANI/PEO sensors. In particular, the responses (Rg/Ra) to 1000 ppm LPG were 1.087 and 1.073 for the PANI/ZnO/PEO and PANI/PEO gas sensors, respectively. CPs are often doped/undoped by redox reactions. Thus, transferring electrons can change the doping level and alter the resistance and work function of the CPs. The transfer of electrons happens when PANI and PANI/ZnO composite NFs were in contact with LPG gas. Electron acceptors remove electrons from PANI, resulting in an increased doping level and electrical conductivity in p-type CPs. In contrast, when an electro-donating gas such as LPG is used, the doping level of PANI decreases, thus changing the resistance of the sensor. Also, in PANI/ZnO/PEO NFs, p-n heterojunctions lead to additional resistance modulation, resulting in enhanced gas sensing. The other mechanism is the alteration of physical properties of the polymers such as crystallinity and morphology, which alter the electrical resistance via an increase in electron transfer. In such a case, the sensitivity of the sensor in the presence of LPG is related to adsorption on a polymer surface via diffusion to inner domain spaces.

4. 4 Polypyrrole (PPy)-based NF Gas Sensors

After PANI CPs, polypyrrole (PPy) is highly popular due to its easy synthesis via chemical or electrochemical oxidation polymerization, high electrical conductivity and high stability. The material and sensing properties of PPy can be enhanced by combining it with additional inorganic or organic components. Usually a doped PPy behaves like a p-type semiconductor, where a change in conductivity occurs through interactions with a target gas ( Joshi et al., 2011; Kim and Yoo, 2011; Yoon et al., 2006; Penza et al., 1997). Lots of PPy composite materials have been reported for gas sensing applications for a wide range of gases or vapors such as NO2, H2S, water, and VOCs (Su and Shiu, 2011; Geng, 2010; Wang et al., 2009b; Han and Shi, 2007; Geng et al., 2006; Tandon et al., 2006; An et al., 2004; Bhat et al., 2003).

A highly porous core-shell polyacrylonitrile-(Tos doped) PAN-PPy NF mat was fabricated as a methanol sensor through electrospinning and two-step vapor-phase polymerization (Jun et al., 2013). The results demonstrated that very thin (~10 nm) conductive PPy shell layers were deposited on electrospun PAN NFs with a median diameter of 258 nm. The PAN-PPy gas sensor revealed a response (Rg/Ra) of 1.4 to 10000 ppm methanol at room temperature. The resistance increase upon exposure to methanol was explained by the electron donating character of the CH3OH gas and the p-type semiconducting nature of PPy. The interactions between Tos-doped PPy and CH3OH might be described by the redox (dedoping) reaction: PPy+/Tos-+CH3OH (δ-) ↔ [PPy-CH3OH (δ-)]+/Tos-. Likewise, PPy-based materials (e.g., poly (vinyl alcohol) (PVA), silver nanoparticle (Ag NPs), and plastic optical fiber (POF)) are also an effective option to sense other oxygen-containing VOCs, e.g., ethanol and acetone (Table 2) (Adhikari et al., 2020; Liu et al., 2020; Das and Sarkar, 2018; Jiang et al., 2005b).

The transfer of electrons from electron-donating CH3OH to the positively-charged PPy backbone led to the formation of neutral polymer chains, resulting in a reduction in the hole carrier density (i.e., a resistance increase). In another study (Al-Mashat et al., 2008), PPy NFs were prepared through a simple chemical method for the detection of hydrogen at different temperatures. The preparation of PPy NFs was completed using bipyrrole to accelerate the polymerization of pyrrole with iron chloride as the oxidizing agent. The effects of temperature (up to 100°C) on the H2 sensing properties were studied. At higher working temperatures (>70°C), the response was low (Ra/Rg=1.07 for 10000 ppm H2 at 75°C) because a lot of carriers with high energy moved freely in the polymer chain, preventing the polymer from exhibiting its inherent redox reaction behavior. In addition, the nanostructured PPy film was smoother at high temperatures and included a dense NF morphology that had less porosity relative to the film at lower temperatures, which led to improved conductivity due to enhanced charge carrier hopping between localized states in the polymer chains. The high conductivity of the nanostructured PPy layer decreased the response at high temperatures because the gas molecules could not deeply penetrate into the bulk of the sensor. Accordingly, the sensor showed its maximum response (Ra/Rg=1.12 to 10000 ppm H2 gas) at ambient temperature. A dynamic response was produced because of the interactions between the adsorbed hydrogen gas molecules and the polymer film. This interaction led to a heterogeneous charge transfer reaction, and chemical modulation of the polymer doping level, which depends on the Fermi level of the sensing film. This can cause a shift in the work function or electrical conductivity of the organic film. In terms of the work function, the polarity of the response relates to the ability of the diffusing gas to shift charge density with the polymer matrix by reduction or oxidation reactions. Hydrogen behaves as a reducing gas, so the PPy NFs resistance decreased when in contact with H2 gas. However, the large variation in its electrical resistance is due to the redox reaction of PPy. The modification of PPy with Pt and Pd nanoparticles have also been tested for the sensing of H2 gas (Su and Liao, 2016). Out of both types of sensors, the sensor developed using Pd nanoparticles modified with PPy exhibited superior sensing characteristics. Such modification led to the formation of more catalytically active sites for the H2 gas molecules. The performances of PPy-based H2 gas sensors are displayed in Table 2.

4. 5 PEDOT based NF Gas Sensor

Electrospun NFs of poly(3,4-ethylenedioxythiophene) doped with (polystyrene sulfonic acid)-PEDOT-PSSA were synthesized to sense methanol, ethanol, and 2-propanol vapors (Pinto et al., 2011). Due to the large surface to volume ratio, the sensors had higher sensitivity and faster response times compared to other PEDOT-based alcohol sensors. The sensing mechanisms were related to polymer swelling that increased the inter-chain distance, which reduced the hopping rate. The response times for sensing of methanol, ethanol and 2-propanol were 8, 10 and 20 s, respectively, which are relatively fast for room temperature sensors. Zampetti et al. (2013) prepared PEDOT-PSS/TiO2 NFs for NO2 gas sensing (Fig. 8). The sensor detected 20 ppb NO2 in the presence of 40 RH% at room temperature with a response (Ig/Ia, where Ia and Ig are the electrical current of the sensor in the presence of air (reference current) and NO2 gas, respectively) of 1.045. The sensing mechanism was mainly related to the change in electrical resistance of the sensor at the interface between CP and TiO2, where the NO2 gas is able to easily alter the resistance of the formed p-n heterojunction. Some other PEDOT-based hybrid structures (e.g., Ti3C2Tx/PEDOT : PSS) are also explored for the sensing of methanol (Wang et al., 2019).

Fig. 8.

Scanning electron microscopic images of (a) TiO2 electrospun fibrous on IDE and (b) PEDOT-PSS coated TiO2 fibers. E and g in Figure A represents electrode and gap between electrodes, respectively. Reprinted with permission from Zampetti et al.(2013).

The same group used electrospinning to fabricate sensing materials via a TiO2 NF scaffold to support a CP (PEDOT: PSS), which resulted in a sensitive membrane (Zampetti et al., 2013). It showed a response (Ig/Ia) of 0.5 ppm NO2 gas at ambient temperature. In the presence of 8 RH% it was 1.25. This outcome is related to the competitive nature of absorption/desorption between H2O vapor and NO2 gas, which decreased the available adsorption sites needed for effective adsorption of NO2 gas. The other PEDOT-based materials (e.g., WO3- PEDOT/PSS and PEDOT-graphene) have also tested successfully for the fabrication of NO2 gas sensors (Dunst et al., 2017, 2016; Lin et al., 2015).


Recently, CPs have received much attention for the realization of resistive gas sensors working at low or room temperatures. We discussed the gas sensing performance of electrospun CPs. Electrospun CPs having a high surface area can offer many adsorption sites for effective adsorption of gases. Consequently, they can offer much higher sensitivity to toxic gases compared with thin film sensors. However, because of the room temperature or low-temperature working temperature, the response and recovery times of CP-based gas sensors are generally longer than that of metal oxide-based gas sensors. So, most researchers have explored composites of CPs with metal oxides to enhance the resulting gas sensing properties.

Among different CPs, most studies have focused on the sensing characteristics of PANI, PPy and PEDOT. This is due to their advantages like low price, high stability and high conductivity. However, most PANI-based sensors suffer from resistance drift and poor recovery time. Flexible CP-based gas sensors would be promising for future gas sensing technologies. With further advancements in synthesis procedures and discovery of novel CPs, electrospun CP NFs will become some of the most promising candidates for realizing different kinds of gas sensors. However, the major challenge for electrospinning process is its complexity. A complex set-up is required to generate electrospun NFs. Moreover, high power requirement for the generation of NFs is another factor which make electrospinning process more complex.

The electrospun CPs-based gas sensors should be tested on diverse environmental conditions before final implementation. Moreover, by considering the high potential of CPs, CP-based sensors should also be tested for the possible expansion of their applicabilities to cover other types of analytes, e.g., semi-VOCs and aerosols.


This work was supported by an Inha University Research Grant. KHK acknowledges support provided by a grant from the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (Grant No: 2016R1E1A1A01940995).


The authors declare no conflict of interest, and the sponsors had no role in the design of the study, in the collection, analyses, or interpretation of data, in the writing of the manuscript, or in the decision to publish the results.


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Fig. 1.

Fig. 1.
Structure of the most important CPs. Reproduced from (Heeger, 2001), copyright 2020.

Fig. 2.

Fig. 2.
The scheme of pyrrole polymerization mechanism. Reproduced with permission from (Choudhary et al., 2014), copyright 2020.

Fig. 3.

Fig. 3.
Basic scheme for electrospinning process. Reproduced with permission from Ramakrishna et al. (2006).

Fig. 4.

Fig. 4.
Possible interaction sites for a target gas on a CPs sensing layer. Reproduced with permission from (Neri and Donato, 1999), copyright 2020.

Fig. 5.

Fig. 5.
Repeat unit of the emeraldine oxidation state of polyaniline in the un-doped base form (top) and the fully doped, acid form (bottom). Reproduced with permission from (Huang et al., 2004) from Springer, copyright 2020.

Fig. 6.

Fig. 6.
Interaction of PANI-coated platinum-based sensor with the H2 gas. (a) Sensor structure and (b-d) interaction of hydrogen and oxygen on the surface of sensor. (e) Work functions of Pt, Au, PtHx. Reprinted with permission from (Fowler et al., 2009). Copyright (2020) American Chemical Society.

Fig. 7.

Fig. 7.
Possible mechanism for hydrogen interaction with doped PANI, where A represents the counteranion. Reprinted with permission from (Virji et al., 2006), copyright (2020) American Chemical Society.

Fig. 8.

Fig. 8.
Scanning electron microscopic images of (a) TiO2 electrospun fibrous on IDE and (b) PEDOT-PSS coated TiO2 fibers. E and g in Figure A represents electrode and gap between electrodes, respectively. Reprinted with permission from Zampetti et al.(2013).

Table 1.

A list of organic compounds detected by resistive CP-based gas sensors.

Gas Source of emission or application Toxicity/Hazardous effects TLV
OSHA: The Occupational and Safety Health Administration; ACGIH: American Conference of Government Industrial Hygienists.
Widely used as solvent Nausea, blurred vision, headaches,
eye irritation dizziness drowsiness,
dermatitis and scaling.
Mirzaei et al., 2016
Widely used in catalysts, organic solvents,
high energy fuels, preservatives, and
Explosive and flammable gas that
irritates skin and causes asthma,
visual disturbances, headaches
Xie et al., 2013;
Song et al., 2017
LPG Widely used as a fuel in homes,
vehicles and industries
Highly flammable and explosive 100
Patil et al., 2015;
Yang et al., 2018
Widely used as industrial solvent Mild irritation to the nose and eyes.
Ingestion causes drowsiness,
dizziness and nausea.
Kumar et al., 2014;
Mirzaei et al., 2016

Table 2.

Sensing parameters of different CPs-based sensors for the sensing of diverse gases.

Type of CP Analyte gas Sensing range Sensing mechanism DL Sensitivity Response time Selectivity Ref
1 PANI NFs H2 10 ppm Formation of hydride
with the platinum
10 ppm 2.5%
for 10 ppm H2
Fowler et al., 2009
2 CSA-doped
PANI NF thin films
H2 0.1%-1% Doping-dedoping in PANI 1.03 for
10000 ppm of H2
Virji et al., 2006
3 HCl-doped PANI H2 0.06%-1% Protonation of PANI 1.11 for 1% H2 32 s Sadek et al., 2007
4 Dedoped PANI H2 0.06%-1% Protonation of PANI 1.07 for 1% H2 28 s Sadek et al., 2007
SnO2/Polyaniline H2 1000 and 2000 ppm Interaction of H2 molecules
with depletion region and
act as a dielectric between
the PANI and SnO2 border
4.5 for
2000 ppm H2
3 s Sharma et al., 2015
5 Graphene/PANI H2 0.06%-1% Depletion of holes from
the valence band of graphene
and formation of N-H bonds
16.57% for 1% H2 Al-Mashat et al., 2010
6 Pd-PANI-rGO H2 0.01-2 vol% Increase in resistance
in presence of H2
0.01 vol% 25 for 1 vol% H2 20 s Selective over
and H2S
Zou et al., 2016
7 PANI/Zinc-based
zeolitic benzimidazolate
H2 0.6-3.0×10-3 M Protonation and
de-protonation in PANI
5.27 μM 11.9 μA mM H2 4 s Mashao et al., 2019
8 PANI/TiO2 NFs CO2 1000 ppm p-n junction based reduction
in activation energy for CO2
Not provided 80 s Not tested Nimkar et al., 2015
9 CLBC-AmG/PANI CO2 50 to 2000 ppm p-n junction based ~26.55 ppm 20 s Selective in
presence of 550 ppm
NH3, H2, and CO
Abdali et al., 2019
10 PANI/PLFO CO2 5000-20000 ppm Protonation and
44.9 for
20000 ppm CO2
101.37 s Hashemi Karouei and Milani Moghaddam, 2019
11 PANI/PEO LPG 1000 ppm Transfer of electrons
from PANI to LPG
Not provided 7.33% 110 s Not tested Patil et al., 2015
12 PANI/ZnO/PEO LPG 1000 ppm Transfer of electrons
from PANI to LPG
Not provided 8.73% 100 s Not tested Patil et al., 2015
1 PAN/Tos-PPy CH3OH 0.7-6.5% Dedoping reaction between
methanol and Tos-Ppy
7.5% for
3.4% methanol
20 s Jun et al., 2013
2 PPy/PVA CH3OH 49-1059 ppm Donation of electron
from alcohol to p-type Ppy
2.6% for 49 ppm 304 s Jiang et al., 2005b
3 PPy/PVA Ethanol 100 ppm Formation of
N-H partial bond
72% for 100 ppm ethanol 42 s Selective over
100 ppm of
ammonia, toluene,
chloroform, and
acetone vapors
Das and Sarkar, 2018
4 Ag NPs deposited
rod-like Ppy
Acetone 195-580 ppm Doping-dedoping in PPy 25 ppm 280 s Selective over
propanol, water, and
Adhikari et al., 2020
5 PPy H2 1.12 for
10000 ppm H2 gas
Al-Mashat et al., 2008
6 Pd nanoparticles
modified PPy films
H2 100 to 5000 ppm Catalytic properties of
Pd nanoparticles and
increase in the number of
delocalized charge carriers
on Ppy
42 for
20 ppm H2 gas
6.5 s Selective over
20 ppm of NH3,
200 ppm of CO,
and 5 ppm NO2 gas
Su and Liao, 2016
1 PEDOT-PSSA Methanol,
NH3, HCl,
and NO2 gas
1.28×105 ppm
for methanol,
6×104 ppm
for ethanol,
1.3×104 ppm
for 2-propanol,
1.5×105 ppm
for NH3,
2.47×105 ppm
for HCl,
and 1×103 ppm
for NO2
Polymer swelling
for methanol, ethanol,
and 2-propanol
De-dpoing/doping for
NH3, HCl, and NO2
Not provided 8 s for methanol,
10 s for ethanol,
20 s for 2-propanol,
13 s for NH3,
95 s for HCl,
and 120 s for NO2
Not tested Pinto et al., 2011
2 Ti3C2Tx/PEDOT/PSS CH3OH 180-500 ppm Donation of electron by
analyte gas to sensing
1.6 for 500 ppm
Selective over
acetone and ethanol
Wang et al., 2019
3 PEDOT NO2 10-100 ppm Oxidation of PEDOT
by NO2 gas
22% for
100 ppm NO2
60 min Selective over
100 ppm of NH3,
H2S and SO2
Dunst et al., 2017
4 PEDOT-PSS/TiO2 Oxidized NO 10-130 ppb Reduction in the
depletion region of
p-n junction
1 ppb 2.9±0.1×103 ppb−1 5-17 min In presence of H2O,
CO2, and O2
Zampetti et al., 2013
5 WO3-PEDOT : PSS NO2 50-200 ppb Interaction of NO2 gas
with the p-n junction
30 ppb ~1.2 for
50 ppb NO2
45.1 s Selective over
NH3, H2,
ethanol, methanol,
and acetone
Lin et al., 2015
6 PEDOT-graphene NO2 5-100 ppm Increase in number of charge
carriers in rGO and PEDOT
due to NO2 interaction
3 min Displayed much
higher response
in comparison to
100 ppm of NH3,
H2S and SO2
Dunst et al., 2016