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Sensors 2013, 13(11), 14764-14776; doi:10.3390/s131114764
Published: 30 October 2013
Abstract: The detection of partial discharge and analysis of SF6 gas components in gas-insulated switchgear (GIS) is important for the diagnosis and operating state assessment of power equipment. The use of a Pt-doped TiO2 nanotube arrays sensor for detecting sulfur hexafluoride (SF6) decomposition products is proposed in this paper. The electrochemical pulse deposition method is employed to prepare the sensor array. The sensor's response to the main characteristic gaseous decomposition products of SF6 is evaluated. The gas sensing characteristic curves of the Pt-doped TiO2 nanotube sensor and intrinsic TiO2 nanotube arrays sensor are compared. The mechanism of the sensitive response is discussed. Test results showed that the Pt-doped nanoparticles not only change the gas sensing selectivity of the TiO2 nanotube arrays sensor with respect to the main characteristic SF6 decomposition products, but also reduce the operating temperature of the sensor.
The excellent insulating and arc extinguishing properties of sulfur hexafluoride (SF6) gas greatly improve the dielectric strength when used as an insulating medium. SF6 has been widely utilized in gas-insulated switchgear (GIS) [1–4]. The reliability of GIS equipment is very high, however, its inevitable intrinsic defects continue to cause varying degrees of partial discharge (PD). Active gas produced by discharge accelerates insulation aging and corrosion of metal surfaces and may eventually lead to equipment failure. Many studies have shown that when a GIS insulation error occurs, the energy generated by discharge causes the SF6 gas to decompose and generate SF4, SF3, SF2, and various low-fluorine sulfides. These low-fluoride sulfides react with trace moisture and the oxygen present in the SF6 gas and generate SOF4, SOF2, SO2F2, SO2, HF, and other compounds [5,6]. The common methods used at present to detect and analyze SF6 partial discharge decomposition products include gas chromatography and infrared absorption spectrometry, but all these methods are offline laboratory detection methods, and on-site detection with these methods is difficult to implement.
Titanium dioxide nanotube arrays (TiO2NTs) are typical 3D nanomaterials that have numerous interesting physical and chemical properties. These materials are inexpensive and can thus be employed in numerous applications . Studies have shown that compared with other nanostructure forms TiO2NTs have a large specific surface area and produce interesting nano-sized effects. TiO2NTs are utilized in photocatalysis, sensors, solar cells, etc. and exhibit a huge potential for development, having become one of the major topics in international nanomaterial research . Miniature gas sensors prepared with TiO2NTs exhibit a fast response and high sensitivity. Several scholars have made great progress in this area in recent years, and TiO2NTs sensors are utilized to test for O2, NO2, H2, ethanol gas, etc. as sensitive materials [9–11].
A Pt-doped TiO2NTs gas sensor prepared through a pulsed electrochemical deposition method based on intrinsic TiO2NTs is developed in this study. The sensor's capability to sense the major decomposition products of SF6 is evaluated. Compared with the gas sensing properties of intrinsic TiO2NTs sensors, the Pt-doped nanoparticles change the gas sensing selectivity of the TiO2NTs sensor towards the main characteristic SF6 decomposition products.
2. Experimental Section
2.1. Preparation of Pt-Doped TiO2NTs
The preparation of the Pt-doped TiO2NTs was based on electrochemical deposition on intrinsic TiO2NTs. The TiO2NTs were prepared by anodic oxidation . With a conventional three-electrode system, Pt-doped nanoparticles were deposited onto TiO2NTs by pulsed electrodeposition. In the three-electrode system, the prepared intrinsic TiO2NTs is the working electrode (geometric area of 4.0 cm2). A Ag/AgCl electrode is the reference electrode, and a platinum electrode is the counter electrode. Electronic pulse signals were provided by an Autolab PGSAT32 instrument (manufacturer, city, state abbrev if US, country) in potential (constant) control mode. The current–time curve of the Pt-doped TiO2NTs preparation is shown in Figure 1. The electrolytes were prepared with pH = 4.4 aqueous H2PtCl6·6H2O (1 g/L) and H3BO3 (20 g/L) at 50 °C. The deposition time of the sample was set to 90 s to obtain moderately-sized Pt nanoparticles. Linear sweep voltammetry was employed at a current density of 5 mA/cm2 and continuous negative pulse for 10 ms. After each negative pulse, a short positive pulse (current density of 5 mA/cm2, continued for 2 ms) is discharged to the barrier layer capacitance. Then toff = 100 ms time was used to restore the concentration of metal ions on the deposition surface.
2.2. Pt-Doped TiO2NTs Sensor Production
The TiO2NTs gas sensor is different from traditional gas sensors. TiO2NTs grow directly on the surface of a metal titanium plate and are not coated on a traditional Si substrate or an A12O3 base. Therefore, high-temperature conductive silver glue was applied directly to the Pt-doped TiO2NTs surface to prepare the electrical contacts. The electrodes were closely pasted onto the TiO2NTs. Finally, the wires were connected to measure the surface resistance signal of the sensor. A sketch of the Pt-doped TiO2NTs sensor is shown in Figure 2.
2.3. Gas Sensing Test Device and Method for the TiO2NTs Sensor
Figure 3 presents a schematic of the device utilized to measure the TiO2NTs sensor's response to the SF6 gas decomposition products. In the experiment, the calibration gases of the SF6 decomposition products were injected through the air intake. The gas flow meter controls and detects the flow rate of the measured gas, and the ceramic heater chip and thermal resistance probe control and measure the surface sensor temperature. The TiO2NTs sensor was then placed in a sealed quartz glass tube. The resistance characteristics of the sensor were determined with an impedance analyzer, and the resistance value of the entire process was recorded. The relative changes in the TiO2NTs sensor's resistance (i.e., sensitivity) was calculated with the formula:where R is the sensor resistance value after injecting the detected gas, and R0 is the stable resistance in N2. The response time of the sensor is the time when the sensor's resistance reached 90% of the maximum value.
The adsorption of the TiO2NTs, air oxygen, and water vapor was considered. Dynamic measurements were performed in the experimental method to exclude the impact of these factors . The concrete steps are as follows: prior to the gas sensing response experiment, high-purity N2 was injected at a flow rate of 0.1 L/min. The power supply of the heating sheet was turned on simultaneously. The regulator knob was adjusted to control the temperature of the sensor surface (to maintain the desired temperature) until the TiO2NTs sensor resistance value stabilized. The value was recorded as R0. Next, one of the gaseeous SF6 decomposition products, namely, SO2, was injected. The gas flow rate in the device should be consistent with the injection rate for N2. The sensor's resistance changed distinctly and achieved stability quickly (fluctuation near one resistance). The resistance value in this process was recorded as R. Lastly, high-purity N2 was injected at a flow rate of 0.1 L/min when the resistance of the sensor was stable; this procedure was performed until the resistance of the sensor gradually stabilized at a certain value. The value was recorded as R0.
3. Results and Discussion
3.1. Morphology of the Pt-Doped TiO2NTs Obtained through Characterization and Analysis
A JEOL JSM-7000 field emission scanning electron microscope (SEM, JEOL, Japan) with an accelerating voltage of 10 kV was used to observe the sample. Figure 4 shows the SEM images of the intrinsic and Pt-doped TiO2NTs prepared by anodic oxidation and the proposed experimental method, respectively. Figure 4a shows the intrinsic TiO2NTs, and Figure 4b shows the Pt-doped TiO2NTs. The nanoparticles loaded between the tube and pipe in the Pt-doped TiO2NTs are Pt nanoparticles. The SEM images show that TiO2NTs prepared by the proposed experimental method are moderately sized and evenly distributed, thereby achieving the desired effect.
Figure 5 shows that a strong anatase (101) crystal plane peak exists at 2θ = 25.3° (A in the figure) in the intrinsic and Pt-doped TiO2NTs. In the XRD pattern of the Pt-doped TiO2NTs, a Pt (111) and a Pt (200) crystal surface peak exist at 2θ = 40.5° and 2θ = 46°, respectively. The XRD pattern of the intrinsic TiO2NTs did not have this peak. This result shows that pulsed electrodeposition is useful when Pt-doped nanoparticles are utilized with intrinsic TiO2NTs.
3.2. Influence of Operating Temperature on the Gas Sensitivity Characteristics of the Pt-Doped TiO2NTs Sensor
The performance of the metal oxide semiconductor gas-sensitive material is greatly influenced by the operating temperature. Metal or non-metal doping has a significant impact on the temperature characteristics of the metal oxide semiconductor material, therefore, examining the gas sensing response of Pt-doped TiO2NTs sensors to the SF6 partial discharge decomposition products (SOF2, SO2F2, SO2 gas) is necessary in determining the optimum operating temperature of the sensor. The prepared Pt-doped TiO2NTs sensor was placed in the test device described earlier (Figure 3). The surface of the sensor was then heated, and the temperature of the surface was controlled with the temperature control device. The gas sensing characteristics of the Pt-doped TiO2NTs sensor were tested in 50 ppm SOF2 and SO2F2 gas whose surface temperature changes from 20 °C to 240 °C. The result is shown in Figure 6.
Figure 6 shows the curve of the change in the resistance of the Pt-doped and intrinsic TiO2NTs gas sensors in response to the SF6 decomposition component gases SOF2 and SO2F2. The figure shows that the gas response value of the intrinsic TiO2NTs sensor to the SF6 decomposition product gases (i.e., resistance change rate; R%) increases with the increase in the sensor surface temperature. The saturation temperature is approximately 200 °C, which is thus the intrinsic TiO2NTs sensor's optimum operating temperature. The R% of the Pt-doped TiO2NTs sensor also increases with the increase in the sensor surface temperature. The largest response value is generated when the temperature reaches 140 °C to 160 °C. As the temperature continuously increases the sensor response values begin to decline sharply. The response value becomes small when the temperature reaches 240 °C. This result indicates that the optimum operating temperature for the intrinsic TiO2NTs sensor is approximately 150 °C. This finding indicates that the Pt-doped nanoparticles not only reduces the optimal operating temperature of the sensor, but also changes the temperature characteristic curve significantly. Because the Pt doped sensor and SF6 decomposition products undergo redox reactions the sensor resistance decreases and the response values are negative. A detailed explanation can be found below in Section 3.4. When the intrinsic TiO2NTs sensor has reached the optimum operating temperature, the response remains unchanged even with a continuous increase in temperature, possibly because the gas sensor surface adsorption and desorption rates reach a dynamic equilibrium and thus, the sensor response remains unchanged.
The sensor surface microstructure and charge distribution is changed after the Pt nanoparticles are doped on it . When the surface temperature of the TiO2NTs is higher than the optimum operating temperature, the Pt-doped nanoparticles improve the chemical desorption rate of the sensor surface. This phenomenon causes the desorption rate of the chemical adsorption of oxygen to be greater than its adsorption rate; the surface oxygen chemical adsorption density decreases, causing the response value of the sensor to decrease rapidly.
3.3. Response of the Gas-Sensitive Characteristics of the Pt-Doped TiO2NTs Sensor to SF6 Decomposition Component Gas
The sensor operating temperature was 150 °C. The gas-sensitive response curve of the Pt-doped TiO2NTs sensor was tested with SO2, SOF2, and SO2F2 gases at 30, 50, 70, and 100 ppm. The change rate in the sensor's resistance at various concentrations, i.e., gas sensing response values, was calculated. The linear relationship between the change rate in the sensor's resistance and the gas concentration was investigated by the linear fitting based on the results. The concentration of the measured gas was also estimated by curve fitting based on the response value of the sensor.
Response of the gas-sensing characteristics of the Pt-doped TiO2NTs gas sensor to SF6 partial discharge decomposition component SO2.
Figure 7 shows that the resistance of the Pt-doped TiO2NTs sensor to 30, 50, 70, and 100 ppm of SO2 gas is 5.31%, 8.38%, 15.18%, and 24.07%, respectively. The linear fit function between R% and SO2 gas concentration is y = 0.276x + 4.045, and linear correlation coefficient R2 is 0.984.
Response of the gas sensing characteristics of the Pt-doped TiO2NTs gas sensors to SF6 partial discharge decomposition component SOF2
Figure 8 shows the Pt-doped TiO2NTs gas sensor's gas-sensing response curve to 30, 50, 70, and 100 ppm of SOF2 at 150 °C. Figure 8a shows that the resistance change rate with increasing concentration is 3.23%, 6.11%, 12.92%, and 23.75% at different tested concentrations of SOF2. The fitting curve is shown in Figure 8b. The linear fit function is y = 0.301x + 7.333, and linear correlation coefficient R2 is 0.974. This result shows that at a certain concentration range, a linear relationship exists between R% and SOF2 gas concentration.
Response of the gas-sensing characteristics of the Pt-doped TiO2NTs gas sensor to SF6 partial discharge decomposition component SO2F2.
Figure 9 shows that the resistance of the Pt-doped TiO2NTs sensor to 30, 50, 70, and 100 ppm of SO2F2 gas is 8.65%, 17.91%, 27.86%, and 38.02%, respectively. The fitting curve is shown in Figure 8b. The linear fit function is y = 0.422x + 3.285, and linear correlation coefficient R2 is 0.992.
3.4. Discussion on the Mechanism of the TiO2NTs Sensor's Gas Response Sensitivity
Figure 10 provides a comparison of the gas response of the intrinsic and Pt-doped TiO2NTs gas sensors to 50 ppm of the three SF6 decomposition productt gases (SO2, SOF2, SO2F2) at the optimal operating temperature. The gas response of the intrinsic TiO2NTs sensor to the three decomposition gases is discussed in Reference . We find that the R% response value of the intrinsic and Pt-doped TiO2NTs to the three SF6 decomposition component gases is negative. This finding indicates that after the three gases were injected separately, the resistance of the intrinsic and Pt-doped TiO2NTs decreased, however, the three response values are different in size.
TiO2 is an N-type semiconductor and has many oxygen vacancies, thus, its gas sensitive effect is obvious and is generally considered a surface adsorption-controlled mechanism. Its response to the measured gas is caused by the chemisorption reaction between oxygen in the air and the TiO2NTs sensor surface. Oxygen ions exist in the grain boundaries between grains, thereby causing the grain boundary barrier to become higher, thus, the resistance of the TiO2NTs sensor increases, blocking the transfer of the carriers. When meeting the reducing gas or the electron supply gas, an oxidation reduction occurs between the surface adsorbed oxygen ions and the reducing gas. The number of adsorbed oxygen ions decreases sharply, the sensor surface potential barrier is reduced, carrier shifting is promoted, TiO2 resistance is reduced, and the gas sensing response is finally achieved.
Figure 10 shows that the R% response values of the intrinsic and Pt-doped TiO2NTs to the three SF6 decomposition component gases are negative. This result means that the resistance of the intrinsic and Pt-doped TiO2NTs decreased. The response mechanism shows that the three measured gases function as a reducing gas or an electron-donating gas. The reaction occurs as follows:where R is one of SF6 decomposition component gases, and Oads− pertains to the oxygen ions adsorbed by the sensor surface.
The gas-sensing responses of the intrinsic TiO2NTs to the three tested gas are SO2 (74.6%) > SOF2 (7.82%) > SO2F2 (5.52%). This finding shows that the decreasing electron supply of SO2 gas is the strongest in the above-mentioned micro-oxidation reduction reaction (i.e., the most likely to lose electrons), and the supply of SOF2 and SO2F2 gas is the weakest. The selectivity of the sensor is best for SO2 gas. The gas-sensing response of the Pt-doped TiO2NTs to the three tested gases is SO2F2 (17.91%) > SO2 (8.38%) > SOF2 (6.11%). The Pt-doped TiO2NTs sensor's response (i.e., the selectivity of the sensor changes) to the three SF6 decomposition component gases (SO2, SOF2, SO2F2) changes significantly.
When the metal catalyst is doped, Pt functions as an oxygen storage point, such that it constantly provides Oads− to the TiO2NTs sensor surface. Noble metal doping decreases the O2 + e− → 2 Oads− activation energy, thus, the optimum operating temperature point also decreases, and the reaction rate and gas sensitive effects are enhanced. As the catalyst particles on the surface of TiO2 sensitive body have a significant affinity interaction with the gas to be measured, the gas is attached firmly to the sensor's surface at a low temperature. The gas will “migrate” from the catalyst particles to the surface of the sensitive body and react with the adsorbed oxygen ions. Ultimately, the sensitivity of the gas sensor increases, and the sensor response rate is accelerated .
The three sulfide gases tested were SO2, SOF2, and SO2F2. Sulfides have a specific degree of toxicity to a noble metal catalyst, and the level of toxicity is related to sulfide valence and molecular structure. The toxicity of the three experimental gases from the strongest to the weakest is SO2 > SOF2 > SO2F2. S6+ within a certain range is non-toxic . When the toxicity of SO2 passes through, the Pt-doped TiO2NTs sensor is poisoned. The specific process is as follows: First, SO2 is physical adsorbed on the active center of the catalyst; Second, a redox reaction occurs in the SO2 with the active ingredient; Third, the reaction produces the corresponding alkylene sulfide and sulfides, which block the active sites. The catalyst activity decreases in this complex series of processes . The sensitivity of the almost non-toxic SO2F2 is greatly improved. The sensitivity of SOF2 is almost unchanged .
3.5. Recovery Test for the Pt-Doped TiO2NTs Sensor
The recovery of the sensor in one of the SF6 decomposition product gases (SO2) at 150 °C was tested. The test results are shown in Figure 11. The sensor's resistance changed significantly when 50 ppm of SO2 gas was injected. When the sensor's resistance stabilized, pure N2 gas was injected. The sensor's resistance increased gradually, but did not revert to the initial resistance value. The above experimental procedure was repeated when the resistance value of the sensor stabilized again. The sensitivity of the sensor decreased greatly; the resistance value did not revert to the initial value, which indicates that the sensor underwent chemical poisoning. Afterward, irradiation with ultraviolet light was performed, and N2 gas was injected again. The resistance value of the sensor gradually increased and ultimately reverted to the initial value and became stable. When 50 ppm of SO2 gas was injected, the sensitivity of the sensor returned to its level in the first test. Although S4+ is toxic to the Pt-doped TiO2NTs sensor and may affect the initial resistance and sensitivity of the sensor, UV light irradiation resolves this problem by allowing sulfide ion desorption.
The recovery of the sensor in one of the SF6 decomposition product gases (SO2F2) at 150 °C was tested. The test results are shown in Figure 12.
This phenomenon is due to the residual thermal decomposition of SO2F2 molecules fixed in the TiO2 nanotube arrays as the result of chemical adsorption. The adsorption energy of chemical adsorption is much larger than the physical adsorption capacity. Therefore, ultraviolet light is used to desorb SO2F2 molecules attached on the sensor. The forbidden bandwidth of the ultraviolet photon energy is almost the same as that of many metal oxide semiconductors, hence ultraviolet radiation can be absorbed effectively by the TiO2NTs. The surface of the film and the inner portion undergo a range of physical and chemical processes. In the case of gas adsorption, ultraviolet radiation can be absorbed by the TiO2NTs through electron-hole pair excitation, thus increasing the carrier concentration and reducing the grain interface barrier. Through these processes, the TiO2NTs conductivity can be increased, and the resistor reduced. Ultraviolet radiation can be absorbed directly by gas molecules to produce desorption or stimulate chemical reactions between different types of molecules . This method can improve sensor repeatability and reduce sensor chemical poisoning . The recovery curve of SOF2 is very similar to that of SO2F2, so in the paper we do not repeat the corresponding discussion.
A Pt-doped TiO2NTs sensor was prepared by pulse electrodeposition; the sensor is based on an intrinsic TiO2NTs sensor prepared by anodic oxidation. The temperature characteristics of the Pt-doped TiO2NTs sensor were analyzed, and the gas sensing properties of three SF6 decomposition product gases were determined through experiments on their gas sensing properties. The gas sensing characteristics of the Pt-doped TiO2NTs sensor were compared with those of the intrinsic TiO2NTs sensor. The response mechanism was also discussed. The following conclusions were obtained:
Under similar conditions, the Pt-doped TiO2NTs sensor's response to SO2F2 is strong, and its response to SOF2 and SO2 is weak. This result means that the Pt-doped TiO2NTs sensor exhibits good selectivity to SO2F2 gas.
The temperature characteristic curve of the Pt-doped TiO2NTs sensor is different from that of the intrinsic TiO2NTs sensor. The optimum operating temperature of the Pt-doped TiO2NTs sensor is approximately 150 °C. When the temperature increases to 200 °C, the sensitivity response of the sensor declines sharply. When the temperature reaches 240 °C, the response value is very small (essentially zero).
Comparative analysis of the gas sensing properties of the Pt-doped and intrinsic TiO2NTs sensors indicates that the Pt-doped nanoparticles change the gas sensing response of the intrinsic TiO2NTs sensor (i.e., the selectivity of the sensor) to the three SF6 decomposition component gases. A preliminarily discussion of the response mechanism of the Pt-doped TiO2NTs sensor was presented.
We gratefully acknowledge the financial support from China National Natural Science Foundation (51277188), program for China New Century Excellent Talents (NCET-12-0590) and project No. 0213005202042 supported by the Fundamental Research Funds for the Central Universities, in China.
Conflicts of Interest
The authors declare no conflict of interest.
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