1. Introduction
Recently metal oxides have attracted great attention due to their remarkable optical, physical, chemical, and electronic properties [1, 2]. Among the metal oxides, titanium oxide (TiO2) has a wide range of advantageous properties, such as chemical stability, photocatalytic activity, photosensitivity, and electrical conductivity and is applicable to electronic devices, chemical sensors, photocatalysts, solar cells, and photoelectrochemical cells [3-6]. These properties strongly depend on crystallite size and shape of the TiO2. TiO2 has three main crystalline structures including anatase, rutile and brookite. Each structure has unique chemical, physical, and electronic properties and leads different applications.
TiO2 thin films have been fabricated with a variety of techniques including sol-gel process, sputtering with different metallic and ceramic targets, ion beam enhanced deposition, chemical vapor deposition, and pulsed laser deposition. Sol-gel process is one of the most important techniques to synthesize various functional materials. It has advantages over conventional other techniques in terms of low temperature process, large area coating, homogeneous and multi-component metal oxide preparation and low equipment cost. Although sol-gel process has such a superior advantages, the final material performance is greatly affected by the process conditions including species of solvent, concentration of TiO2 and heating process.
In this paper, we report the fabrication of a Schottky diode made by mixing TiO2 nanoparticles and TiO2 solgel. Schottky diodes have been made with inorganic semiconducting material, conducting polymers and a combination of both materials [7-10]. The effect of TiO2 nanoparticles in the TiO2 sol-gel for the performance of Schottky diode is investigated in terms of surface field emission scanning electron microscope (FESEM) images, x-ray diffraction (XRD) patterns and current-voltage (I-V) characteristics of the fabricated Schottky diode. Three possible conduction mechanisms are explained to determine dominant conduction process in the device.
2. Experimental procedure
TiO2 nanoparticles (~30 nm) were purchased from Aldrich Co. and used without further purification. The TiO2 sol was fabricated by titanium (IV) isopropoxide (TIP, 97 %), ethanol (99.8 %), HCl (36.4 %) and deionized (DI) water. The sol was prepared as follows: 50 ml of ethanol was charged in the 100 ml of round bottom flask, and 6 g of TIP was added to the solution. Then, HCl was added to the mixture until the solution became transparent with stirring, and the solution was kept under vigorous stirring for 1 day. The aqueous TiO2 nanoparticle solution was directly mixed with TiO2 sol-solution with 1 wt% (TiO-1), 5 wt% (TiO-5), 10 wt% (TiO-10), and 15 wt% (TiO-15) TiO2 nanoparticle concentrations. The various concentrations of TiO2 nanoparticles and TiO2 sol mixtures were spin coated on a silicon wafer with 2000 rpm. The film was then heated at 300℃ for 1 h in a tube furnace under nitrogen gas purging. The silicon wafer was cleaned by a mixture of sulfuric acid and hydrogen peroxide in an ultrasonic cleaner, followed by cleaning and rinsing with de-ionized water. Finally, the wafer was washed with acetone and dried at 100℃ for 30 minutes. The film thickness was approximately 100nm after heat treatment. Al electrode was then vacuum-deposited onto the film. Fig. 1 shows the three-layered Schottky diode structure. The silicon layer was used as an electrode.
Fig. 1.Three-layered Schottky diode structure: TiO2 nanoparticle-TiO2 sol-gel acts as a semiconducting layer.
3. Results and Discussion
Fig. 2 shows surface FESEM images of (a) TiO-1, (b) TiO-5, (c) TiO-10, and (d) TiO-15. Nanoparticles were not observed on the surface of the TiO-1 film. Small individual particles were observed for the TiO-5. As the concentration of TiO2 nanoparticles increased more than 10%, aggregated particles were observed on the surface of the films as shown in Fig. 2 (d). Fig. 2(e) shows the cross sectional FESEM image of TiO-10. The thickness of the TiO2 layer is about 75 nm.
Fig. 2.FESEM surface images: (a) TiO-1; (b) TiO-5; (c) TiO-10; (d) TiO-15 and (e) FESEM cross-sectional image of TiO-10.
Anatase and rutile crystallite phases are the main structures of TiO2, which have band-gap energies of 3.2 and 3.0 eV, respectively [11, 12]. Anatase TiO2 has excellent photocatalytic activity, long-term stability and nontoxicity [13]. Sol-gel spin-coating process is a promising technique over the other conventional techniques. The prepared films are mostly amorphous phase structures [14]. Fig. 3(a) shows the XRD patterns for the TiO-1, TiO-5, TiO-10 and TiO-15. There is no clear anatase or rutile diffraction peak for the TiO-1 and TiO-5. However, very weak major anatase (101) and rutile (110) diffraction peaks were observed for the TiO-10 and TiO-15. Fig. 3(b) shows XRD pattern for the TiO2 nanoparticles. Strong anatase (101) and rutile (110) peaks are located at 25.4° and 27.5° respectively. The relative intensities of the anatase and rutile diffraction peaks are 54.7 and 45.3 %, respectively. It is clear that the TiO2 nanoparticles are composed of anatase and rutile crystal structures.
Fig. 3.XRD patterns: (a) TiO-1; TiO-5, TiO-10, and TiO- 15. (b) TiO2 nanoparticles.
Schottky diodes fabricated with mixture of TiO2 sol-gel and TiO2 nanoparticles with different concentrations were characterized by measuring their I-V characteristics. The work function of Al is low (approximately 4.1 eV) compared with TiO2 (5.1 eV for anatase structure and 4.9 eV for rutile structure) [11]. Therefore, the Al and TiO2 nanoparticles and TiO2 sol contact might be a Schottky junction due to a big difference in the work functions. Furthermore, due to the similar work function of Si (4.52 eV) and TiO2, the Si and TiO2 nanoparticles and TiO2 sol junction could be an Ohmic contact. Fig. 4 shows the result. The forward bias current was approximately 30 μA for the Schottky diode fabricated with pure TiO2 sol-gel without TiO2 nanoparticles. The forward current for the TiO-1 is approximately 130 μA, which is 4 times higher than the pure sol-gel Schottky diode. As the amount of TiO2 nanoparticles increased, the forward current drastically increased up to 10 wt. % and decreased thereafter. The maximum forward current of 2.7 mA was achieved at 10 wt. % of TiO2 nanoparticles. The improved forward current is due to the high quality crystallite nanoparticles of TiO2, which drastically increase the surface area of the active material. The reduction of the forward current for the TiO-15 might be due to the aggregation of the TiO2 nanoparticles as shown in Fig. 2 (d).
Fig. 4.I-V characteristics of Schottky diodes.
To distinguish the major conduction mechanism, various plots were employed based on the theoretical equation of each conduction mechanism. Three conduction models were employed by plotting Ln(J) versus Ln(V), Ln(J) versus E1/2 and Ln(J/V) versus E1/2 for the space charge limited conduction (SCLC), Schottky conduction (SC) and Poole-Frenkel conduction (PFC) models, respectively. Fig. 5 (a), (b) and (c) represent the plots based on the SCLC, SC and PFC models, respectively. Table 1 shows beta values of SC and PFC mechanisms in linear regime. For both cases, beta values are too big compared with the theoretical values (3.03×10-5 eV/ (V/m)1/2 for SC and 6.06×10-5 eV/(V/m)1/2 for PFC) to match these mechanisms at low electric field [15]. The plot of SCLC model shown in Fig. 5(c) shows best linear fit in the experimental range. Therefore, SCLC process could be a major conduction mechanism [16].
Fig. 5.The plots of three conduction mechanisms: (a) Ln (J) vs Ln(V) for SCLC. (b) Ln(J) vs E1/2 for SC and (c) Ln(J/V) vs E1/2 for PFC.
Table 1.Beta values of TiO2 nanoparticle doped TiO2 solgel Schottky diodes of Schottky emission and Poole-Frenkel emission. Unit: ×10-5 eV/ (V/m)1/2
4. Conclusion
The mixtures of TiO2 sol-gel and TiO2 nanoparticles with different concentrations of TiO2 nanoparticles were used as a semiconducting material for a Schottky diode fabrication. Although TiO2 nanoparticles show strong anatase and rutile XRD peaks, the mixtures of TiO2 sol-gel and TiO2 nanoparticles exhibit no characteristic anatase and rutile diffraction peak. The forward current drastically increased as the concentration of TiO2 nanoparticles increased until 10 wt. %. The forward current decreased as the TiO2 concentration further increased. SCLC mechanism might be dominant for the linear regime.
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