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Optical and NH3 Gas Sensing Properties of Hole-Transport Layers Based on PEDOT: PSS Incorporated with Nano-TiO2

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DOI: 10.4236/msa.2017.89047    132 Downloads   259 Views  

ABSTRACT

Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) incorporated with nanocrystalline TiO2 powder (PEDOT:PSS+nc-TiO2) films were prepared by spin-coating technique. SEM surface morphology, UV-Vis spectra and NH3 gas sensing of were studied. Results showed that the PEDOT:PSS+nc-TiO2 film with a content of 9.0 wt% of TiO2 is most suitable for both the hole transport layer and the NH3 sensing. The responding time of the sensor made from this composite film reached a value as fast as 20 s. The rapid responsiveness to NH3 gas was attributed to the efficient movement of holes as the major charge carriers in PEDOT:PSS+nc-TiO2 composite films. Useful applications in organic electronic devices like light emitting diodes and gas thin film sensors can be envisaged.

1. Introduction

Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is a con- jugate polymer that can be easily prepared in thin film form. PEDOT:PSS films have a high transmission in the visible region, a high conductivity of 80 S/cm [1] [2] [3] , and a particularly good thermal stability [4] that is why PEDOT:PSS is used as the hole transport layer in many optoelectronic devices such as organic light emitting diodes (OLED), organic solar cell (OSC), electrochromic windows, etc. [5] [6] [7] [8] . PEDOT:PSS possesses also a highly valuable property: when adsorbed by various gases, its electrical conductivity changes considerably. Thus PEDOT:PSS can be used for the functional materials in the gases sensors [9] . Recently, Olenych et al. [10] used hybrid composites based on PEDOT: PSS- porous silicon-CNT for preparation and characterization of humidity sensors. Various nanocomposite films consisting of conducting polymers mixed with carbon nanotubes (CNTs) as an active material have been prepared for application in gas thin film sensors for detecting the adsorption of gas molecules such as CO [11] , NH3 [12] and vapors of organic solvents or water [13] [14] . Xing et al. [15] reported that the formation of a nanometer-scale chemically responsive junction (CRJ) within a silver nanowire (AgNW) strongly affected the sensing properties of nanocomposites. The proposed mechanism of the resistance response for a CRJ, supported by temperature-dependent measurements of the conductivity for CRJs and density functional theory calculations, is that semiconducting p-type AgxO is formed within the CRJ and the binding of molecules to this AgxO modulates its electrical resistance. We have shown by our experients that with embedding nanocrystalline TiO2 (nc-TiO2) particles in PEDOT:PSS, the performance parameters of some electronic devices like OLED and OSC were considerably improved [16] . The improvement was attributed to the presence of the heterojunctions of PEDOT:PSS/MEH-PPV (for OLEDs) and PEDOT:PSS/P3HT (for P3HT) in the devices.

Thus in the hope to enhance the sensitivity of the NH3 sensor, PEDOT:PSS + nc-TiO2 composite films were prepared and characterized using UV-Vis and current-voltage measurements. The NH3 gas sensing vs. nc-TiO2 concentration embedded in PEDOT:PSS has been also studied.

2. Experiment

For preparing an initial solution of PEDOT:PSS, the pure PEDOT powder was dissolved in a largely diluted PSS by a volume ratio of PEDOT:PSS equal to 1:10. To get nanocomposite of PEDOT:PSS with nanocrystalline TiO2 (nc-TiO2), TiO2 nanopowder with average size of 5 nm was embedded in this solution according to a weight ratio TiO2/PEDOT-PSS of 0.05 to 0.07, 0.09 and 0.11 (or 5.0 to 7.0, 9.0 and 11.0 wt%), further referred to as PECT-1, PECT-2, PECT-3 and PECT-4 sample, respectively. To obtain a homogenous dispersion of nc-TiO2 in polymer, the solutions were mixed for 8 hours by using magnetic stirring. These liquid composites were then used for spin-coating. The conditions for spin-coating were as follows: a delay time of 90 s, a rest time of 20 s, a spin speed of 1500 rpm, an acceleration of 500 rpm and finally a drying time of 3 min. The Corning-247 glass pieces with 2 cm ´ 3 cm in size was used as substrates for optical characterization, and ITO-coated glass substrates were used for the anode in OLEDs. Both the glass and ITO-coated glass substrates used for spincoating nanocomposite films were ultrasonically cleaned in distilled water, followed by cleaning in ethanol and acetone. Preparation of OLEDs for density current-voltage (J-V) measurements was carried-out following the process that was described in [16] , herein the conjugate polymer of poly [2-methoxy-5-(2'-ethyl-hexyloxy)-1,4- phenylene vinylene] (MEH-PPV) was used as the electroluminescent layer, PECT films―as the hole transport layer (HTL) and aluminum coating―as the cathode. For preparing thin film sensors, the PEDOT:PSS+nc-TiO2 solutions were spin-coated onto glass substrates which were coated by two silver planar electrode arrays with a square of 5 × 5 mm in size. The two electrodes were separated from each other by a distance of 5 mm. To dry the films, the samples were put in a flow of dried gaseous nitrogen for 8 hours. For the solidification without involving solvents, the film samples were annealed at 120˚C for 8h in a “SPT-200” vacuum drier. The thickness of the PECT films was controlled at an average value of 450 nm. All the samples were put in a fore vacuum box until the measurements.

The surface morphology of samples was characterized by using a NT-MDT Atomic Force Microscope operating in a tunnel current mode. The compositional characterization of the PEDOT-PSS films was done through Fourier Transform Infrared Spectroscopy (FTIR) on a BRUKER TENSOR-27 spectrometer. Ultraviolet-Visible absorption spectra (UV-Vis) were carried-out by using a JASCO V570 spectrophotometer and J-V characteristics were measured on an Auto-Lab Potentiostat PGS-30.

3. Results and Discussion

The surface of nanocomposite samples was examined by AFM techniques. Figure 1 shows AFM images of a pure PEDOT:PSS and a PECT with an embedding of 9.0 wt% nc-TiO2. In the PEDOT:PSS sample there is a lot nanopores, whereas in the composite sample considered, a distribution of completely dispersive TiO2 nanoparticles can be seen. Moreover, in the composite film the nanopores did not appear, instead nc-TiO2 particles were formed (as seen in Figure 1 for examples, pores 1 and 2 (Figure 1(a)) were replaced by particles 1’ and 2’ (Figure 1(b))). This AFM micrograph also shows that the PEDOT:PSS+nc-TiO2 composite film contained numerous TiO2/PEDOT-PSS nano-heterojunctions.

Figure 2 shows the FTIR spectra obtained for a PEDOT:PSS film sample. Signals from 1527 to 1368 cm−1 are associated with the C=C bonds, peaks at 985, 844, and 688 cm−1 can be attributed to the C-S interaction in the thiophene ring, and peaks 1228 through 1051 cm−1 correspond to the ethylenedioxy group. There are 10 characteristic peaks signed with a red star belong to PEDOT:PSS as reported in [17] . Figure 3 shows the optical absorption spectra (UV-Vis) of the PEDOT:PSS and PECT films. The absorbance of the films decreased with increasing TiO2 content embedded in the polymer. The decrease in absorption spectra can be explained due to i) a large bandgap of nc-TiO2 and ii) a stronger scattering effect of the light illuminating to the composite films.

The UV-Vis data in Figure 3 can be used to estimate the energy band gap, Eg, of the samples by using the following expression [18] .

(a) (b)

Figure 1. AFM images of a pure PEDOT:PSS (a) and a PEDOT:PSS+nc-TiO2 (9.0 wt%) composite film (b).

Figure 2. FTIR spectrum of a PEDOT:PSS film.

Figure 3. UV-Vis absorption spectra of the PECT thin films incorporated with nc-TiO2: 5.0 wt% (curve “1”), 7.0 wt% (curve “2”), 9.0 wt% (curve “3”) and 11.0 wt% (curve “4”) of nc-TiO2.

(1)

where h is Planck’s constant, ν is the frequency of the incident UV-Vis radiation, A is a constant and n is 1/2 for direct band semiconductors and 2 for indirect band gap semiconductors. As expected, best fits were obtained for n = 2 (indirect band).

A graph is plotted between the square of (ahn) and hn (as abscissa), and a straight line is obtained. From the extrapolation of the straight line to (ahn)1/2 = 0 axis, one can determine the bandgap of the investigated sample. Thus from our experiments, the energy gap (Eg) of two samples (namely PECT-1 and PECT-3) were found to be of approximately 2.50 eV and 2.57 eV, respectively (Figure 4). For PECT-2 and PECT-4 similar results were obtained, and their Eg values were found to be of 2.52 and 2.54 eV, respectively. The value of the bandgap of nanocomposites is a little larger than that for the pure PEDOT-PSS film prepared by electrochemical polymerization [19] . In addition, the effect of widening in the bandgap (or blue shift) of PEDOT-PSS vs. nc-TiO2 content was demonstrated as shown in Table 1. This is quite similar to the reported blue shift that was observed for MEH-PPV+nc-TiO2 [20] or for PPV+nc-SiO2, where the blue shift was explained by a reduction in the polymer conjugation chain length due to the presence of inorganic nanoparticles in polymers [21] .

Figure 4. Plots of (ahn)1/2 dependence on photon energy (hn) for determining Eg of the PECT-1 and PECT-3 samples.

Table 1. The widening in Eg of conjugate polymer (PEDOT:PSS) vs. TiO2 content.

It is known that PEDOT:PSS can be considered as a p-type organic semiconductor [22] , where holes play the role of major charge carriers. This is why PEDOT:PSS thin film is often used for hole transport layer (HTL) in OLEDs [23] [24] [25] [26] . To better understand the effect of hole transport in nanocomposite films, we measured the J-V characteristics of the devices made from different layers, such as ITO/MEH-PPV/PECT-1/Al, ITO/MEH-PPV/PECT-2/Al, ITO/ MEH-PPV/PECT-3/Al and ITO/MEH-PPV/PECT-4/Al, abbreviated as DMP-1, DMP-2, DMP-3 and DMP-4, respectively. The measurement data for J-V characteristics of these devices were plotted as shown in Figure 5.

From Figure 5 one can notice the following: i) TiO2 nanoparticles embedded in PEDOT:PSS used as HTL favors the hole injection from ITO into the organic layer deposited on the HTL, resulting in an enhancement of the J-V characteristics. Thus the turn-on voltage decreased from 1.80 to 1.42, 1.32 and 1.10 V, respectively for devices DMP-1, DMP-2, DMP-4 and DMP-3, where J-V characteristic of DMP-3 device (with nc-TiO2 content of 9.0 wt%) exhibits the best one; ii) The effect of the HTL on the enhancement of the J-V characteristics was well demonstrated, associated with the equalization process of injection rates of holes and electrons [27] . The reason why the nanoparticles can improve the device performance was recently discussed, when we reported the role of the surface morphology of the HTL layer in the composites [23] . With spinning process in the spin-coating technique, the nanopores can be filled-up by strong electrostatic forces, consequently eliminating the pores acting as big traps for charge carriers in polymers, thus more charge carriers (i.e. holes and electrons) can reach the anode and the cathode of the devices.

To test the gas sensitivity of the sensors made from PECT composites, the samples were placed in a chamber and device electrodes were connected to elec-

Figure 5. J-V characteristics of the PECT samples with different contents of nc-TiO2 from 5.0 wt% (curve “a”) to 7.0 wt% (curve “b”), 9.0 wt% (curve “c”) and 11.0 wt% (curve “d”).

trical feedthroughs. For example, for monitoring NH3 gas, the best hole transport film (namely sample PECT-3) was put in a testing chamber of 10 dm3 in volume. By using “EPA-2TH” profilometer (USA) a100 ppm (in concentration) NH3gas value was chosen for monitoring. The adsorption process was controlled by insertion of measuring NH3 gas and the desorption process was done by extraction of the gas followed by insertion of dry gaseous Ar. To characterize the sensing performance of the PECT composite films used for the sensors, a sensitivity (h) of the devices was introduced. It is determined by following equation:

(2)

where Ro is the initial resistance of the sensor, and R - the resistance of the sensor after theNH3 gas adsorption.

Typical NH3 gas sensing data for two sensors, namely PEC-1 and PECT-3 are plotted in Figure 6. The sensing curves of the PECT-2 and PECT-4 lay between PEC-1 and PECT-3 curves, but for clear observation they were not inserted in Figure 6. From Figure 6, it is seen that with adsorption of NH3 gas the resistance of the PECT-3 sample increased. The sensitivity of the sensors increased from about 6% (for PECT-1) to 10% (for PECT-3). The responding time of the sensing shortened from 40 s to 32 s, 26 s and 20 s, respectively for PECT-1, PECT-2, PECT-4 and PECT-3 sensors (see gray-marked parts in Figure 6). For the PECT-3 sensor, the resistance of the PECT-3 film quickly recovered to baseline when exposed to air (i.e. desorption of the gas). Indeed, the recovery time of the sensor was estimated as 80s. This would imply that the electrons generated from the NH3 adsorption process in the sensor surface eliminated a part of holes in PEDOT:PSS with results similar to those reported in [9] .

The fast responding time of the sensing can be attributed to the efficient movement of the holes in the nanocomposite-based hole transport layer, which

Figure 6. The sensitivity of the PECT-1 and PECT-3 sensor responding to NH3 gas.

is demonstrated in the J-V characteristics in Figure 5. The PECT-3 sensor showed a quick response and a fast recovery time to NH3 gas. The response is considerably better than the one that was reported as 30 s in [28] and 32 s in [29] where the NH3 gas sensors were made from Ag/PEDOT:PSS and Ag/polypyrrole nano-composites, respectively.

4. Conclusions

Using spin-coating technique, films of PEDOT-PSS embedded with TiO2-na- noparticles were prepared. The surface morphology, UV-Vis spectra and gas sensing of NH3 were characterized. The results obtained showed that 9.0 wt% of nc-TiO2 was the most suitable concentration that was embedded in PEDOT:PSS for hole transport layer as well as for NH3 sensing. The responding time of the sensor made from PEDOT:PSS+nc-TiO2 (with 9.0 wt%) possessed a value as fast as 20s that is much better than the response of the NH3 gas sensor made from Ag/polypyrrole nano-composites. The rapid responsiveness to NH3 gas was attributed to the efficient movement of the holes as major charge carriers in PEDOT:PSS+nc-TiO2 composite films.

The obtained results suggest a useful application in monitoring NH3 gas in a polluted environment with a concentration of less than 100 ppm. For further works, to enhance both the sensitivity and selectivity of the gases in a range of few parts per million, PEDOT:PSS films incorporated with other additives like carbon nanotubes and graphene quantum dots will be synthesised.

Acknowledgements

One of the authors (L. M. Long) expresses his sincere thanks to University of Engineering and Technology (VNU Hanoi) and University of Science, VNU Ho Chi Minh city for the support in sample fabrication and experimental measurements.

Cite this paper

Long, L. , Trung, T. , Truong, V. and Dinh, N. (2017) Optical and NH3 Gas Sensing Properties of Hole-Transport Layers Based on PEDOT: PSS Incorporated with Nano-TiO2. Materials Sciences and Applications, 8, 663-672. doi: 10.4236/msa.2017.89047.

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