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Abstract and Applied Analysis
Volume 2014 (2014), Article ID 297632, 6 pages
Development of La3+ Doped CeO2 Thick Film Humidity Sensors
1College of Engineering, Bohai University, Jinzhou 121013, China
2Department of Engineering, Faculty of Engineering and Science, The University of Agder, 4898 Grimstad, Norway
Received 2 January 2014; Accepted 18 January 2014; Published 3 March 2014
Academic Editor: Ming Liu
Copyright © 2014 Chunjie Wang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The humidity sensitive characteristics of the sensor fabricated from 10 mol% La2O3 doped CeO2 nanopowders with particle size 17.26 nm synthesized via hydrothermal method were investigated at different frequencies. It was found that the sensor shows high humidity sensitivity, rapid response-recovery characteristics, and narrow hysteresis loop at 100 Hz in the relative humidity range from 11% to 95%. The impedance of the sensor decreases by about five orders of magnitude as relative humidity increases. The maximum humidity hysteresis is about 6% RH, and the response and recovery time is 12 and 13 s, respectively. These results indicate that the nanosized La2O3 doped CeO2 powder has potential application as high-performance humidity sensor.
Due to the recognized importance of vapor concentration, humidity sensors as an important chemical sensor have been widely used in medicine, agriculture, and environment monitoring [1, 2]. The suitable humidity sensing materials should possess some characteristics including high sensitivity, good chemical and physical stability, rapid response and recovery time, and low hysteresis [3, 4]. In the past few years, humidity sensors are developed towards miniaturization and integration with the development of technology. To improve the performance of the humidity sensor, it is quite essential to improve the sensing materials with high sensitivity and reliability.
Generally, the materials for humidity sensors are mainly organic polymer films and porous ceramic films. In the case of organic polymers, however, the main disadvantages are the low operation temperature, poor physical and chemical stability, and weak mechanical strength. For porous ceramic humidity sensors with porous structured films, the major problems are the dull response and recovery time. Among the various candidate materials of sensors, CeO2 becomes heatedly discussed topic in recent years, which can be attributed to its large diffusion coefficient for oxygen vacancy and good corrosion resistance to corrosive gases (Cl2, SO2, and NO) . Due to the longer response and recovery time, however, the sensor fabricated from pure CeO2 cannot meet the increasing requirements.
Owing to the remarkable physicochemical activity, rare earth materials have been widely used to improve the performance of the functional materials. In the past decade, considerable efforts have been paid to the investigation of rare earth doped sensing materials. Li et al. studied La3+/Ce3+ doped TiO2-SnO2 thin films as humidity sensors . Shimizu et al. devoted their work to the phase separation and leaching techniques of La2O3-TiO2 porous thick film . Anbia and Fard reported the humidity sensing properties of Ce-doped ZnO thin film, which shows high humidity sensitivity, repaid response and recovery, good repeatability, and narrow hysteresis loop . Unfortunately, to the best of our knowledge, the performance of humidity sensors based on La3+ doped with CeO2 has not been reported. In our previous work, the nanosized La2Ce2O7 powders have been synthesized via hydrothermal method, the products show higher specific surface area, smaller particle size for nanoparticles, and a porous networking microstructure for calcined compacted body, which have a potential application as sensors .
To obtain fine nanopowders, various methods have been proposed in recent years. Due to the advantages which related to the homogeneous nucleation processes and fine grain size, hydrothermal method is considered as one of the most promising techniques for the manufacture of nanopowders.
In this paper, nanosized 10 mol% La3+ doped CeO2 powders were prepared by hydrothermal method; the humidity sensing properties, response and recovery time, and hysteresis characteristic of the corresponding sensor were investigated in the relative humidity range from 11% to 95% with various frequencies at room temperature. The main purpose of this study is expected to enhance the humidity sensing performance of the composite films and broaden the database of sensor materials.
Nanopowders of 10 mol% La2O3 doped CeO2 were synthesized via the conventional hydrothermal method. La2O3 and Ce(NO3)36H2O (99.99%, Shanghai Chemicals Ltd.) were used as the starting materials. Firstly, appropriate amounts of La2O3 were dissolved in concentrated nitric acid and then mixed with a stoichiometric Ce(NO3)36H2O aqueous solution under vigorous stirring. The final molar concentration of the solution is 0.1 M. A certain amount of PEG (2 wt.%, Shanghai Chemicals Ltd.) as surfactant was then added into the mixed solution. The pH value of the solution was adjusted to 7 by NaOH (2 M). The nanopowders were obtained by hydrothermal treatment for the suspension at 180°C for 24 h in a Teflon autoclave. The precipitates were then filtered and washed with distilled water and ethanol six times and dried at 70°C for 12 h.
In order to investigate the structure of the products, the powders were calcined at different temperatures for 5 h with a heating rate of 5°Cmin−1 and then cooled down naturally. The crystalline phases of nanocrystalline powders were identified by powder X-ray diffraction (XRD, Bruker D8 Focus powder X-ray diffractometer) using Cu Kα radiation ( 1.5406 Å) with a scanning rate of 5°Cmin−1. The operation voltage and current were maintained at 40 kV and 40 mA, respectively.
The mean particle size of powders was determined by Scherrer’s equation : where is the wavelength of the X-ray radiation, is the diffraction angle, is a constant (0.89), and is the corrected full-width half maximum (FWHM). The Gaussian-Gaussian relationship was also used for the correction of the instrument : where FWHM of the sample is represented by and is for the standard width of reference silicon sample.
FT-Raman spectra were recorded on a Thermo Nicolet 960 instrument with an excitation wavelength of 1064 nm, and the wave number range is from 100 to 900 cm−1. The specific surface area () was determined by Brunauer-Emmet-Teller (BET) equation [11, 12] with a Micromeritics ASAP2020 instrument. The morphology and the particle size of the sample were investigated by a field emission scanning electron microscope (SEM, Hitachi S-4800) and a Philips TF-F20 electron transmission microscope (TEM).
Figure 1 is the schematic diagram of the humidity sensor. In order to fabricate the humidity sensor, the as-synthesized nanopowders were dispersed in ethanol with magnetic stirring for 30 min. The mixed solution was then dropped onto a ceramic substrate (6 cm 3 cm, 0.5 cm in thick) to form a film with a thickness of about 10 μm. Furthermore, the humidity sensors were annealed at 180°C for 1 h and then dried naturally. The characteristic curves of humidity sensitivity were obtained from a ZL-5 model LCR analyzer (Shanghai, China). In our study, the voltage was fixed at 1 V, and the frequencies were varied from 20 Hz to 100 KHz. The humidity of laboratory atmosphere was 25% RH controlled by an automatic drier. The humidity environments were obtained by LiCl, MgCl2, Mg(NO3)3, NaCl, KCl, and KNO3 saturated salt solutions, and the corresponding RH values were 11, 33, 54, 75, 85, and 95% RH, respectively.
3. Results and Discussion
The crystal structure of the as-obtained and sintered powders of 10 mol% La2O3 doped CeO2 (10 LC) was examined by XRD, as shown in Figure 2(a). It can be noted that all XRD patterns match well with the standard cubic fluorite phase of CeO2 [JCPDS 43-1002]. The diffraction peaks at about 28.1°, 32.6°, 46.8°, and 55.7° can be indexed to the (111), (200), (220), and (311) reflections of cubic fluorite structure, respectively. The diffraction peaks become sharper and narrower with the increasing temperature which can be attributed to the growth of crystal. In addition, the average crystallite size and specific surface area were also investigated. The average crystallite size and the specific surface area of as-synthesized 10 LC are 17.26 nm and 126.54 m2g−1, respectively. The crystal size was calculated by Scherrer’s equation as mentioned in Experimental section.
Raman scattering was also utilized to carefully identify the phase structure in the wave number range of 100900 cm−1. Figure 2(b) represents the Raman spectra of as-synthesized 10 mol% La2O3 doped CeO2 and pure CeO2 nanocrystal. Careful investigation of the spectra revealed a detailed structure of cubic type. For both samples, the main peak at about 464 cm−1 corresponds to the Raman band of a cubic fluorite structure. Obviously, for 10 LC, this band is broader and more asymmetric than that of pure CeO2, which is the common feature of the effect of rare earth-doping on the band [13, 14]. Moreover, a small shoulder appeared at about 600 cm−1 which can be assigned as a longitudinal optical mode arises .
The morphology and particle size of the synthesized materials were further investigated by SEM and TEM. Figure 3 is the typical SEM image of as-prepared 10 LC nanopowders. It is easy to find that the mean particle sizes are in the range of 1520 nm. The agglomerates of nanopowders may be due to the uncontrolled coagulation during the process of preparation . Typical TEM and SAED images of as-synthesis 10 LC are shown in Figure 4. From the figure, it can be clearly noted that the as-synthesized powders are mainly composed of monodispersed square particles with an average particle size of 17.63 nm. The determined mean particle size is the average value of 20 particles selected randomly. The average particle size obtained from TEM pattern is consistent with that calculated from Scherrer’s equation. Furthermore, the individual bright diffraction spots (inset in Figure 4) indicate that the particles are polycrystals.
Figure 5 shows the resistance variation of 10 LC as a function of relative humidity (RH) measured at room temperature with various frequencies. Obviously, the humidity dependences of the impedance of the sensor are influenced by the frequency and remarkably decreased at low frequency range (less than 100 Hz). It can be seen from the figure, at low frequency region, that the impedance of the sensor varied five orders of magnitude with the relative humidity changing from 11% to 95%. As a comparison between the humidity sensitivity of 10 LC at high and low frequencies, the best sensitivity of the impedance versus RH curve appears at 100 Hz which shows higher sensing properties, better linear relation of resistance versus RH, and larger impedance dropping. In the case of high frequencies (10 KHz), however, the situation is just the reverse. In order to gain high RH sensitivity, therefore, the appropriate frequency should be fixed at 100 Hz. This fact can be attributed to the mechanism of depletion type adsorption of semiconductor materials. As the carrier, for pure CeO2 humidity sensor, electrons have a significant role in the conduction process. Based on the Akubuiro study , the addition of low valent cation dopants results in decreasing the concentration of electrons, which implies that conductivity declines and impedance increases.
Response and recovery time are two important features to characterize the performance of humidity sensor. The time taken by a sensor to attain 90% to the total impedance change in the case of adsorption process and desorption process is defined as the response time and recovery time, respectively. Based on the results mentioned above, the response and recovery characteristics of 10 LC at 100 Hz were investigated at room temperature, as shown in Figure 6. The sensor was transferred from laboratory atmosphere (25% RH) to target chamber (95% RH) to test the response time and then transferred back to investigate the recovery characteristic. As shown in Figure 6, the response and recovery time of the humidity sensor is 12 s and 13 s, respectively. Such results indicate that the sensor made from 10 LC has rapid response and recovery characteristics.
The hysteresis loop of the 10 LC for adsorption and desorption behavior was measured in the whole humidity range at 100 Hz and room temperature, as represented in Figure 7. The humidification process is the black squares in the figure which was measured from low to high RH, while the desiccation process is the write squares which was measured in the opposite direction. As can be seen from the figure, the sensor exhibits narrow hysteresis loop in the humidity range from 11% to 95% RH, and the maximum humidity hysteresis is about 6% RH. The narrow hysteresis loop indicates the facility of the humidification and desiccation process of water molecules.
Unfortunately, to the best of our knowledge, data on humidity sensing of La2O3 doping CeO2 is scarce in the literature. To explain the humidity sensitive properties of 10 LC, a possible mechanism was proposed. It is well known that the humidity sensing is closely related to chemisorption and physisorption processes of water molecules . At low humidity, only a few water molecules are adsorbed by chemisorption mechanism, while several serial water layers will be formed at higher humidity by physisorption mechanism [19, 20]. In our case, the great change in conductivity of the 10 LC also relates to the adsorption of water molecules on the surface of 10 LC film. In the case of low humidity, the sensor exhibits higher impedance which can be attributed to adsorption of a few water molecules on the surface of the film. The humid atmosphere on the surface is not continuous, which results in the electrolytic conduction being difficult. Based on [21, 22], the high local charge density and the strong electrostatic field caused by the tip, defects, and contracts of the powders can promote water dissociation to provide charge carriers. On the other hand, for high humidity, more and more water molecules physisorbed to form continuous water layer on the surface of film [23, 24]. A large amount of H+ decomposed from water molecules to be the dominant charged carriers and lead to large decrease of impedance. In addition, as mentioned above, the 10 mol% La2O3 doped CeO2 thin film has nanosized grains and high specific surface area. The nanoscale grain size leads to much more grain boundaries which result in more active sites available for water molecules to react . The specific surface area of the particles also plays an important role in their conduction. The water molecules are easily absorbed on the surface of the sensors due to the large surface of nanomaterials, which can improve the response and recovery characteristics. Furthermore, the properties of humidity sensor which is fabricated by doped CeO2 are better than those of the bare one. This can be explained by two aspects as follows: for doped CeO2, the adsorption capacity of water molecular is larger than that of the undoped one due to the higher content of adsorption oxygen; on the other hand, the electrons will be depleted as the La3+ substitute the site of Ce4+. Thus, the electronic conductivity of the humidity sensor decreases.
Humidity sensing properties of 10 mol% La2O3 doped CeO2 prepared via hydrothermal method were investigated at different frequencies. It was found that the sensor at 100 Hz shows a high sensitivity, narrow hysteresis loop, and rapid response and recovery in the humidity range of 11%95% RH. The maximum humidity hysteresis is about 6% RH, and the response and recovery time of this thin film is 12 and 13 s, respectively. Furthermore, the studies about La2O3 doped CeO2 with different content and different surfactants are in progress, which will be published elsewhere.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
This work was supported by the National Natural Science Foundation of China under Grant no. 11347167.
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