1. Introduction
In recent years, graphene-based gas or vapor sensors have attracted much attention due to their unique sensing performance, room-temperature operating conditions, a variety of feasible designs, and tremendous application perspectives. Over the past few decades, the rapid development of graphene-based sensors for various applications has been observed. Humidity measurement is one of the most significant issues in the fields of medical diagnostics, environmental protection, industrial manufacture, agriculture, etc. Graphene demonstrates great potential for application in resistive humidity sensors [
1]. The sensitivity of a sensor prepared from chemical vapor deposition (CVD) grown graphene is normal rather than moderate (resistance change <2%) [
2,
3]. A transition to bi-graphene or multi-graphene increases the sensitivity of the sensor up to ~10%–30% and, in some cases, even up to ~90% depending on the defect inventory of the material since defects act as the centers of water adsorption on the sensor surface [
4,
5,
6,
7].
One of the organic polymers, poly (3,4-ethylenedioxythiophene) doped with poly (styrene sulfonate) (PEDOT: PSS), is a material most often used in humidity-sensor applications [
8]. PEDOT: PSS is a polymer exhibiting the highest conductivity among other organic materials [
9]. Resistive humidity sensors based on PEDOT: PSS demonstrate a high sensitivity (of 430% at humidity changes ranging from 40% to 90%) and a linear dependence of their response on humidity. However, at a high humidity of more than 80% such sensors lose their functional properties due to the saturation of the film with water or due to the formation of a water layer on the surface of the film at humidity exceeding 80%, with the latter process leading to a decrease of resistance and to the necessity of a long recovery of the sensor [
8]. Therefore, PEDOT: PSS is widely used in various composites in combination with other organic materials such as polyvinyl alcohol [
10], ZnSnO
3 or Fe
2O
3 nanoparticles [
11,
12], graphene quantum dots, and silver nanowires [
13]. The use of composite materials allows one to achieve high sensitivity (up to ~100%) of the sensors; however, the nonlinearity of characteristics substantially restricts the area of their application.
Particular interest in humidity sensors based on graphene and PEDOT: PSS is due to the possibility of using those materials in flexible, stretchable, and wearable electronics as well as in the printing technology for creating device structures based on such sensors. For an instant, printed PEDOT: PSS electrodes showed good flexibility in several types of flexibility tests, including outer/inner bending, twisting, and stretching [
14]. The high-performance silver grid/ PEDOT: PSS hybrid transparent films exhibit promising features for various emerging flexible electronics and optoelectronic devices. [
15]. Smart textiles or woven electronics and optoelectronics, attained by intertwined fibers with complementary functions, are the emerging and most ambitious technological and scientific frontier which attained for intertwined fibers with complementary functions due to graphene covering [
16]. The fabric-enabled pixels for displays and position sensitive functions are a gateway for novel electronic skin, wearable electronic, and smart textile applications [
16,
17].
In the present study, we examined the properties of films prepared from the G: PEDOT: PSS composite versus the composition of the material and as dependent on the solid and flexible substrates used. A composition ensuring the maximum sensitivity of the film to water adsorption was identified. It was found that the use of flexible substrates, due to their capability to quickly absorb the liquid components of the solution, leads to a more porous structure of the films, thus making the response of such a humidity sensor increase substantially. An analysis of the properties of such films under deformation proved the films show promise for use in flexible electronics.
2. Preparation of Composite Films and Test Device Structures
A graphene suspension with a graphene content of ~1 mg/ml was used as the starting material in the present study. The suspension was obtained by electrochemical exfoliation of highly oriented pyrolytic graphite, followed by the sonication, centrifugation, and filtration of obtained particles on a track membrane with a pore diameter of 1.2 μm [
18]. The second component of the composite material was a 1% aqueous solution of PEDOT: PSS. The data on the used compositions of the composite are summarized in
Table 1. In obtaining the films and device structures, the screen printing was used. For suppressing the coffee-ring effect during printing, ethylene glycol was added to the final composition. As a result, two types of structures were fabricated: (1) strips 1.5 mm wide whose thickness varied from 300 nm to 7 μm and (2) zigzag test structures about 3 μm thick with line widths of 0.3 and 1 mm (see the insets in Figure 5). Since identical suspension volumes were used to create a series of structures, the thickness of the resulting films in the structures was approximately the same within one series of specimens or it changed in accordance with the suspension volume used. The film thicknesses determined using SEM, AFM, and optical microscopy measurements are indicated in
Table 1. In preparation of the samples, SiO
2/Si wafers, Kapton polyimide films, polyethylene terephthalate (PET) with additional hydrophilic adhesion layer on the surface, and ordinary paper were used as the substrates.
3. Results
3.1. The Structure of the Graphene: PEDOT: PSS Composite Films
Figure 1 shows SEM images of the surface of the films printed from a suspension of graphene, PEDOT: PSS, and C1a1 composite on the surface of SiO
2/Si substrates. In the case of PEDOT: PSS films, the removal of part of the substrate has allowed us to obtain an image of a free film. Raman spectra of the films are shown in
Figure 1d. In the case of the composite, the spectra present the sum of peaks characteristic of graphene and PEDOT: PSS.
AFM images of the surface of the films obtained using a suspension of graphene and PEDOT: PSS, and AFM images of the surface of the C1a1 and C1c structures with one and the same film composition yet printed on different substrates are shown in
Figure 2. Evidently, the PEDOT: PSS film is more porous. It is the property that ensures a high response of such films to absorb water molecules. It is important that, with the same film composition, the structure of the films, as it turned out, could change fundamentally depending on the substrate used. In the case of paper, the film proved to be much more porous (compare
Figure 2c,d).
3.2. The Response of the Humidity Sensors
Figure 3a shows the relative change in the resistance of a G: PEDOT: PSS composite film as a function of time during a 30% to 90% change of air humidity in the measurement chamber. It is seen that in the case of pure PEDOT: PSS (composition 0:1), there occurs almost no recovery of resistance due to the saturation of the material with water molecules (this circumstance makes the relaxation process long). In the case of an increased graphene content, the rate of recovery increases, and for the composition of graphene: PEDOT: PSS 1:(1–2), it attains a maximum possible value. Later, the rate of increase/decrease in humidity is limited by the inertia of the chamber.
The response of the structures with different compositions observed on the humidity change to 90% is shown in
Figure 3b. It is seen that the dependence of the response on the composition of the suspension from which the film was formed demonstrates a maximum. That maximum refers to the composition of 35%–50% of graphene. Yet, the most important consequence of the data shown in
Figure 3b is a strong effect due to the substrates on which the film was printed. Evidently, the transition to flexible substrates, capable of absorbing part or all the liquid applied onto the printed layer, drastically changes the film structure. In our case, it is the paper and the PET with an additional hydrophilic adhesive layer on the surface. This feature of flexible substrates may significantly affect the sensitivity of the sensors. In the case of paper used as the substrate, the absorption of the liquid component occurred most rapidly; this, as it follows from the data of
Figure 2, led to the formation of a porous film structure yielding a maximum response to moisture.
No less important parameters for the response to moisture is the film thickness. Among the structures fabricated on SiO2/Si substrates, the C1a2 structure with a minimum film thickness of 300 nm exhibited a maximum response of 27%–60%, and at a film thickness of 3.5 μm, and that response dropped to 15%–35%. In the case of relatively thick G: PEDOT: PSS composite films formed on paper (6.5 to 7.5 μm thick), the film thickness was no longer an obstacle for reaching a pronounced response due to the porosity of the film formed on paper. Moreover, a decrease in film thickness to 3 μm led to a decrease in response to 72%.
Figure 4 shows the curves of the resistance of the samples obtained from suspensions with the same composition (1:1) on different substrates; those curves were recorded during a two-sided sweep of humidity. Despite the micron thicknesses of the sensing layer, due to its porosity, not only high response but, also, almost linear dependences of the resistance on the humidity and the absence of hysteresis were obtained. The relatively weak hysteresis observed for the structure on paper was most likely associated with the capability of the substrate to absorb moisture and then give it back.
In general, it should be noted that the rate of change of the resistance is determined, first of all, by the inertia of the measurement chamber. The inset in
Figure 4a shows the changes in the resistance and humidity due to a sharp opening and closing of the chamber. Both composite sensors and, also, the HIH4000 industrial capacitive sensor, with the fast operation, displayed this event on the same time scale.
3.3. Testing of the Functional Properties of the Humidity Sensors under Mechanical Deformations
The study of the changes in the resistance of the structures during deformation was carried out by applying bending deformations to these structures. Depending on the bending direction, tensile (positive) or compressive (negative) strains could be generated. The strain estimated from the bending radius
r at the substrate thickness
t = 100 μm and film thickness
d amounts to
=(t + d)/2r [
18]. On a change of the bending radius to 3 mm, the strain in the structures on PET films increased to 1.5%.
Figure 5 shows the resistance changes for a strip printed on PET from a G: PEDOT: PSS suspension and one of the fabricated zigzag test structures. In the first case, a relatively weak increase in resistance under tensile deformations and an almost unchanged resistance under compressive deformations were observed. The scatter of resistance values during repeated measurements was most likely associated with a poor reproducibility of the position of the sample when the sample was mounted in the holder; this circumstance could lead to a change in the current paths in the film and to a scatter of resistance values [
19,
20]. In the case of measuring the zigzag test structure (
Figure 5b), the resistance during deformation and during repeated measurements remained almost unchanged. The effect due to the shape of the tested structure on the maximum possible deformations is well known [
21,
22,
23,
24] but, in our case, the creation of a test structure with a zigzag shape led to a profound reduction in the scatter of resistance values.
Figure 6 shows the results of measurements of the test structures of humidity sensors in the deformed state. It is seen that the bending of structures in the chamber during exposing them to moisture practically did not change at the implemented bending radii (the minimum bending radius was 3 cm, which value corresponds to a tensile strain of 1.5%).
4. Discussion
The obtained experimental results can be summarized as follows.
(a) The content of the composite was identified at which the response of the sensor to humidity was maximum. This is a composite in which a suspension of graphene and PEDOT: PSS is in a proportion of 1:(1–2). It is shown that the response of the system is unambiguous, the resistance increases by increasing the humidity up to 95%. Film recovery occurs on the same time scales in the entire range of humidity. Estimations of the 1:1 G: PEDOT: PSS film weight content after drying of printed layer gives the value of 10% addition of PEDOT: PSS to graphene and 5% in the case of 1:2. In our paper [
7] we have demonstrated that edge defects determine the graphene sensor response. Addition of the relatively small mass value of PEDOT: PSS to graphene creates better conditions for humidity sensitivity due to better access to individual flakes and their edges in comparison with a monolithic film formed from graphene. Good water absorption by PEDOT: PSS also leads to a higher response.
(b) The use of flexible substrates capable of absorbing the liquid ink component permits the formation of sensor elements with high porosity. As a result, the relatively large thickness of such films does not lead to a loss of layer sensitivity.
(c) As it could be expected, in the case of using a rigid SiO2/Si substrate a maximum sensor response was observed for the thinnest film.
The used G: PEDOT: PSS composites and test structures possess properties promising for the use of such humidity sensors in flexible and printed electronics: When the structures are bent to a bending radius of 3 mm (1.5% deformation), their properties remain almost unchanged. A pronounced reduction of the scatter of resistance values was obtained for zigzag-shaped test structures.
The bending-induced effects in flexible electronics have emerged as a relatively new experimental and theoretical research area. The optimum device design for flexible electronics requires a comprehensive understanding and accurate modeling of strain-induced effects in sensor devices [
25]. The shape of the substrate, its parameters, and the resultant distribution of strain during bending can be expected to exert an influence on the responses of the devices formed on flexible substrates. Uniaxial deformation occurs when an applied bending moment deforms the specimen along an in-plane axis. The use of thin substrates can lead to a distortion of the surface because of the various types of occurred deformations such as the tensile, compressive, shearing, and torsional ones. Those deformations can be quantified in terms of stresses and strains having components such as uniaxial, biaxial, and torsion bending deformations. Namely, this type of thin substrates entails a scatter of resistance values shown in the present study in
Figure 5a. A periodic serpentine shape provides a regular contribution of the various components of the deformations, thus reducing the spread of resistance values (
Figure 5b). Generally, the periodic serpentine shape can be engineered to accommodate the enhanced elastic strain along some selected dimensions and to support the biaxial, radial, and other deformation modes. In addition, the choice of topologies ranging from lines to a serpentine shape is capable of tailoring those topologies to particular electronic applications.
5. Conclusions
The properties of graphene: PEDOT: PSS composite films are compared as a material for resistive humidity sensors for moisture range 30%–95% fabricated on flexible and rigid substrates. It is shown that the resistance increases almost linearly depending on the environmental humidity. The composite films G: PEDOT: PSS provide the maximum response (increase in resistance) up to 220% for film content 1:(1–2) (10–5 weight % of PEDOT: PSS in graphene film) when exposed to a humid environment without the restrictions typical of humidity sensors prepared from PEDOT: PSS (80% RH). It is found that the response of the sensor depends not only on the composition of the layer but, also, on its thickness, film structure, and substrate used. Formation of the porous film, for instance, due to the capability of flexible substrates to absorb the liquid component of the ink, used to print the sensing layer, leads to increase the response to humidity. However, in the case of using paper as a substrate, a hysteresis occurs in the resistance value under a two-sided variation of humidity. This hysteresis is associated with the capability of such substrates to absorb water. The measurements of the resistivity of G: PEDOT: PSS films under bending deformation showed that down to a bending radius of 3 mm (1.5% deformation), the resistance of the structures remained almost unchanged. Moreover, the transition from strips to zigzag structures reduces the scatter of resistance values observed during multiple measurements. The response of the test device structures also remained almost unchanged for a tensile bending radius from 3 cm to 3 mm. Thus, used composite material and humidity sensors prepared from it are highly promising for use in flexible and printed electronics.
Author Contributions
Conceptualization, I.V.A.; data curation, S.A.S.; methodology and experiments, V.I.P., I.A.K.; validation, S.A.S.; supervision, I.V.A.; writing-reviewing & editing, I.V.A.
Funding
The grant of the Russian Scientific Foundation (grant N 19-72-10046) and of the Ministry of Education and Science of Russia FSRG-2017-0017.
Acknowledgments
The study in the part of film and structure creation is supported by the Russian Scientific Foundation (grant N 19-72-10046). The results (in sensor measurements) were obtained as part of the implementation of the state task of the Ministry of Education and Science of Russia FSRG-2017-0017. The authors are grateful to Mr. D.M. Akhmerov from NSTU (Novosibirsk) for the help in measurements.
Conflicts of Interest
The authors declare no conflict of interest.
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