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Journal of applied research and technology

On-line version ISSN 2448-6736Print version ISSN 1665-6423

J. appl. res. technol vol.16 n.1 Ciudad de México Feb. 2018

 

Articles

Effect of oxygen addition on the formation of anatase TiO2 nano-coatings obtained by spray pyrolysis technique

Zineb Benzaita  b  * 

Demet Tatara 

Mehmet Ertugrula 

aNanoscience and Nanoengineering Department, Atatürk University, Erzurum 2540, Turkey

bNanoscience and Nanoengineering Department, Istanbul Technical University, Istanbul 34469, Turkey


Abstract:

High-quality anatase phased titanium dioxide thin films were prepared in this work using an easy, simple and cost-effective method. Normal, partially and highly oxygen-enriched atmospheres were provided during the spray pyrolysis deposition of titania in order to study the oxygen effect on the structure and morphology of the films prepared. High crystalline anatase nano-coatings stable at high temperature (700°C) could be obtained through the delaying of anatase-to-rutile transformation due to the filling of oxygen vacancies by the oxygen added to the spraying atmosphere. These nano-coatings constitute promising materials for different applications such as hydroxyapatite coated metal implanting, rechargeable lithium ion batteries fabrication, gas sensing and photocatalytic applications.

Keywords: Titanium Dioxide; Anatase; Nano-coatings; Thin Films; Spray Pyrolysis Technique

1.INTRODUCCIÓN

Titanium dioxide, one of the most extensively investigated semiconductor oxides, finds extensive applications in the área of solar cells (El Kass et al., 2017: Giordano et al., 2016), photocatalysts (Singh et al., 2017), gas sensors (Park, Kim, Rana, Jamwal, & Katoch, 2017), water-splitting (Ziegler et al., 2016), cáncer therapy (Na & Park, 2016), and self-cleaning materials (Vodisek, Ramanujachary, Brezová, & Lavrencic Stangar, 2017: Chen & Mao, 2007).

TiO2 is also considered as a promising material for the fabrication of safe anodes of rechargeable lithium ion batteries (Bai et al., 2016; Li et al., 2012). Among existing TiO2 nanostructures (anatase, rutile, brookite), anatase presents the most interesting electrochemical properties (Deng, Kim, Lee, & Cho, 2009); its good stability, low volume expansión (3-4%), high operating voltage (1.5-1.8 V vs Li/Li+) and low cost make it a great potential alternative material to graphite based anodes . Furthermore, anatase TiO2 possesses the best photocatalytic activity because of its large band gap (3.2 eV) and strong oxidizing power (Lv, Chen, Liu, Wang, & Meng, 2015a; Periyat, Naufal, & Ullattil, 2016) which make it highly useful in photocatalytic applications.

High crystalline anatase TiO2 has also been reported to improve the osteogenic activity and enhance the hydroxyapatite (HA) formation on metallic implants due to lattice match and superposition of hydrogen-bonding groups in anatase crystals comparing to rutile crystals (Lv. Li, Xie, Cao, & Zheng, 2017; Uchida, Kim, Kokubo, Fujibayashi, & Nakamura, 2003; Xia, Lindahl, Lausmaa. & Engqvist, 2011).

Although high thermal treatment improves the crystallinity of TiO2, it leads to undesirable anatase-rutile phase transformation which occurs generally below 600°C (Pillai et al., 2007). Various attempts have been made to improve the crystallinity of anatase TiO2 while inhibiting its transformation to rutile such as metal or/and nonmetal doping, surface modification with metal oxides (i.e., AI2O3, NiO, and ZnO) (Lv, Chen, Liu, Wang, & Meng, 2015b). However, the formation of secondary impurities (e.g. AI2TiO5, NiTiOa, CeTi4024, Ce2Ti207, etc.) at high-temperature and the consequent decrease in photocatalytic activity make this technique disadvantageous (Lv, Yu, Huang, Liu, & Feng, 2009: Periyat et al, 2016; Pillai et al, 2007). Therefore, it is necessary to develop an effective method for the synthesis of stable anatase phased nanostructures without having such major drawbacks. In this article, we report an easy and economical route to prepare TiO2 nano-coatings with delaying the anatase-to-rutile transformation by adding oxygen to the atmosphere of spray pyrolysis deposition.

Some recent works have reported the preparation of TiO2 thin films using several methods such as atomic layer deposition (Piercy, Leng, & Losego, 2017), chemical vapor deposition (Rahim, Sahdan, Bakri, Yunus, & Lias, 2016), pulsed láser deposition (Wang et al., 2017) and sputtering (Ben Jemaa, Chaabouni, & Abaab, 2017; Singh et al., 2017). Although they produce high-quality semiconductor thin films, these systems involve very high vacuum or/and temperature, are not suitable for large-area substrates, have low throughput and complex operating conditions, furthermore, they are high-cost equipment and production techniques (Domínguez & Orduña-Diaz, 2017; Jameel, 2015). By contrast, solution-based deposition processes offer cost-effectiveness, simplicity, compatibility with large-area substrates, moreover, possibility of scaling up to industrial level (Song, 2016; You, 2015). Among these solution-process techniques, sol-gel route (Aminirastabi. Weng, Xiong, Ji, & Xue, 2017; Parveen, Mahmood-ul-Hassan, Khalid, Riaz, & Naseem, 2017), chemical bath deposition (Dhandayuthapani, Sivakumar, & Ilangovan. 2016; Govindasamy, Murugasen, Sagadevan, 2016) and spray pyrolysis technique (Chandrashekara, Angadi, Ravikiran, et al., 2016; have been recently used in TiO2 thin film production.

In the present work, spray pyrolysis technique (SPT) has been chosen due to the simplicity of its apparatus and operation, its ability to produce low-cost and high crystalline oxide layers with high quality adherence and uniform thickness, its ability of coating large and complex geometries, in addition to the possibility of scaling it up for industrial applications (Chourashiya, 2013; Filipovic et al., 2013; Shinde, 2012).

2. EXPERIMENTAL METHODS AND MATERIALS

Specimens of stainless steel with dimensions of (lcm*lcm*0,127cm), used as substrates, were ultrasonically cleaned in methanol, acetone and deionized water for 10 minutes each time then dried. Precursor solution containing 6 vol. % titanium (IV) isopropoxide (TTIP) and ethanol, provided by Sigma-Aldrich, was prepared. Acetylacetone (AcAc) provided from Merck Schuchardt OHG was added as a stabilizer in a molar ratio of TTIP:AcAc = 1:2.

To synthesize TiO2 nanostructured thin films, a home-made spray pyrolysis equipment illustrated in the next schematic diagram was used (Figure 1): a pneumatic nozzle sprays fine droplets of the precursor solution using compressed air as a carrier gas, while a rotating píate carries the substrate specimens is heated by halogen lamps controlled using a temperature regulator system.

Fig. 1 Schematic diagram of the home-made SPT equipment used. 

First of all, in order to find the optimum SPT process conditions, the substrate temperature was varied from 320 to 420°C when keeping the other parameters constant (solution concentration (6%), spraying solution quantity (100 mi), distance (35 cm)). Secondly, the experiments were performed at the optimum temperature, with and without an additional flow of oxygen directed to the substrates to study the O2 addition effect. It is worth noting that a post-heat treatment of all the prepared films was carried out at 700°C for one hour in normal atmosphere using a 3 zone-tube furnace (PZE 12/50/500, Protherm Furnace, Turkey).

The evaluation of crystallinity and composition of the prepared TiO2 thin films was carried out using an X-Ray diffractometer (Cu Ka radiation (ƛ=0.154 nm), GNR APD 2000 PRO, Ataturk University) (ƛ=0.154 nm). Morphology and cross-section of the coatings were examined by a high-resolution field emission scanning electrón microscope (Quenta 450 FEG FE-SEM; Erzincan University). Elemental analysis was carried out by energy dispersive X-ray spectroscopy (EDS) detector connected with FE-SEM.

3. RESULTS AND DISCUSSIONS

For the purpose of optimizing the most important SPT parameter, the effect of substrate temperature was first studied. Figure 2 illustrates the XRD patterns of films deposited under 02-enriched atmosphere at different temperaturas. According to the standard JCPDS card no: 71-1166, in all the films except that deposited at 320°C, TiO2 anatase crystalline phase was formed and its main peak at 25,3°, corresponding to (101) diffraction plañe, was clearly detected. Intensities of (101) peak and the other minor peaks increased progressively with the substrate temperature which illustrates the improvement of films crystallinity. These results can be explained by elucidating the different processes that take place by virtue of temperature (Filipovic, et al., 2013; Nakaruk & Sorrell, 2010):

Fig. 2 XRD patterns of TiO2 thin films deposited at different temperatures, after annealing at 700°C. 

  • For films deposited at 320°C which is considered low, the thermal gradient was not sufficient to miniaturize the droplets, which approached the substrate in their big form and precipitated in its surface as an amorphous salt (Ti[OH]4) (Process A).

  • For the films deposited at 350° and 380°C, the droplets were greatly evaporated, and the generated aerosols precipitated before arriving at the surface, then the formed precipitates oxidized partially when arriving at the substrate surface (Process B). Consequently, 350°-380°C temperatures are considered intermedíate and henee not suitable to establish a perfect deposition process.

  • For the films deposited at 400° and most importantly at 420°C, the thermal gradient was adequate to diminish the size of the droplets, to evapórate them extensively, and to cause an early precipitation of their aerosols. The obtained precipitates sublimed immediately just before attending the substrate. When this sublímate carne into collision with the surface, it subsequently oxidized then got adsorbed chemically (CVD-like process, process C in Figure 3). In conclusión, substrate temperature nearly equal to 420°C is necessary to carry out the most desired CVD-like mechanism which provides the synthesis of well crystallized TiO2 films.

    Fig. 3 Effect of substrate temperature on SPT 

After determining the optimum temperature, new experiments were carried-out at 420 °C to study the effect of oxygen addition to the spray environment on the titania films crystallinity and morphology.

Figure 4 of the obtained XRD patterns demonstrates that oxygen has a great influence in the films crystalline phase: Films deposited under a high oxygen pressure exhibit XRD peaks correspond to a puré TiO2 anatase phase according to the Standard JCPDS card no:71-1166. In contrast, films obtained without adding an oxygen flow in the SPT process exhibit TiO2 rutile peaks as it is given by JCPDS card no:76-0649. Whereas coatings deposited under low-pressure 02-enriched atmosphere exhibit peaks of both phases with a remarked drop in their intensities which means that these coatings are composed of a mixture of anatase and rutile.

Fig. 4 XRD patterns of TiO2 films obtained with high-pressure, low pressure and zero pressure O2 addition to the spraying atmosphere, after annealing at 700°C. 

To understand the phenomena behind these results, as-deposited films were also characterized. All the as-deposited films consist of puré anatase phase whatever is the degree of oxygen-enrichment (Figure 5). Since the surface Gibbs free energy of anatase is lower than that of rutile phase, TiO2 initially prefers to nucleate into anatase phase rather than into rutile phase (Choudhury & Choudhury, 2013).

Fig. 5 XRD patterns of the as-deposited TiO2 films obtained with high-pressure, low pressure and zero pressure 0-> addition to the spraying atmosphere. 

Per contra, after being annealed at 700°C, coatings synthesized in normal atmosphere exhibit new rutile phase (Figure 4) which signifies that a phase transformation occurred due to heat treatment. Some other writers reported similar results for films obtained without adding oxygen (Castañeda et al., 2003; Nakaruk, Ragazzon, & Sorrell, 2010; Oja, Mere, Krunks, Solterbeck, & Es-Souni. 2004).

Theoretically, puré anatase begins to transform to rutile in air below 600°C, however, it may vary with different factors such as the number of oxygen vacancies which cause positive strain in anatase lattice. These crystalline defects can be removed by heat treatment which provides the activation energy necessary to relax the lattice and rearrange it to the rutile state (Choudhury & Choudhury, 2013; Hanaor & Sorrell, 2011). Filling those vacancies by 02 molecules can partially or completely inhibit the transformation to rutile, which is the case of our films deposited under low or high pressure O2-enriched atmosphere. The above explanation of the obtained results can be confirmed by two previous studies:

- Thin films of Co-TiO2 were deposited using pulsed láser deposition (PLD) technique at various oxygen partial pressures. At higher oxygen partial pressure, the dominant phase was anatase inhibited to be transformed to rutile (Ali, Rumaiz, Ozbay, Nowak, & Ismat Shah, 2009).

- High-temperature stable anatase phased nanocrystalline titania was synthesized by a reaction of amorphous titanium dioxide with hydrogen peroxide (H202 - TiO2) followed by a calcination process. In this route, in-situ generation of oxygen through thermal decomposition of peroxo-titania complex prevented the phase transformation of the produced nano-powder from anatase to rutile (Etacheri, Seery, Hinder, k Pillai, 2011).

In our study, anatase phase was conserved and prevented from being transformed to rutile because the low or high amount of oxygen provided in spraying process was absorbed, and oxygen vacancies were -respectively-partially or completely filled.

To the best of our knowledge, there are no systematic studies that reported the synthesis of high-temperature stable anatase TiO2 thin film by spray pyrolysis technique without using any dopants. Thus, we report in this work a new, easy and economical route to synthesize stable and high crystalline anatase nano-coating deposited under O2-enriched atmosphere by SPT.

Average sizes of the obtained thin films crystallites were determined using the famous Scherrer's formula:

D=Kλβcosθ (1)

D is the mean grain size of nanoparticles, K=0.9, the diffractometer used is with CuKa radiation thus the wavelength ƛ = 1,5406 Ǻ, ϴ is Bragg's angle and β is the full width at half of the peak máximum (FWHM) correspond to the main peak A(101) for anatase phase and R(110) peak for rutile phase.

The amount of anatase phase in bi-phased films was determined using Spurr equation:

FA=11+1,26(IrIa) (2)

FA is the anatase amount in the anatase-rutile mixture, Ia and Ir are the intensities of anatase and rutile main peak, ie (101) and (110) respectively.

Qualitative assessment reveáis that the film deposited under high-pressure O2-enriched atmosphere is composed of anatase crystallites with ~33 nm in size. Oppositely, the film deposited under normal atmosphere consists of rutile phase which its grains size is about 52 nm. This film was first composed of anatase, however, after being annealed at 700°C it was completely transformed to rutile with bigger crystallite size. In contrast, the film deposited under low-pressure O2-enriched atmosphere shows a mixture of 56% anatase and 44% rutile crystallites with sizes of 42 nm and 45 nm respectively. In this film, a partial transformation of anatase to rutile occurred and was accompanied by grain growth, this resulted in a nano-coating constituted of large rutile grains and small anatase grains. These calculations were confirmed by scanning electrón microscopy images reported in Figure 6.

Fig. 6 Representative FE-SEM images of the films deposited at 420°C under (a) under high-pressure O2-enriched atmosphere, (b) low-pressure O2-enriched atmosphere, and (c) normal atmosphere. 

Figure 6a shows the morphology of the film deposited in an environment rich in O2. This film is fully dense, composed of aggregates which are primary small particles. In contrast, the film deposited without enriching the deposition atmosphere with oxygen (Figure 6c) consists largely of square-based pyramidal individual grains with narrow size distribution. These grains size is relatively large comparing to those of the film shown in Figure 6 a.

Deposition of Titania in a partially O2-enriched atmosphere results in the film presented in Figure 6 b . The structure of this film exhibits a mixture of individual grains and agglomerated small particles. These results confirm those obtained by XRD: rutile grains which constitute the film shown in Figure 6c are bigger than the anatase ones which constitute the film shown in Figure 6 a , and the film illustrated in Figure 6b is a mixture of both phases with near grain sizes according to SEM morphology, exactly as it was concluded from XRD patterns.

The cross-section of a representative TiO2 thin film is presented in Figure 7. It is clearly observed that the nano-coatings prepared in this work using SPT method are very thin, continuous and smooth with a uniform thickness of approximately 414 nm.

Fig. 7 Cross-section of a typical prepared TiO2 

The EDS patterns of the previous films (Figure 8) confirm again the effect of oxygen addition to the deposition environment. O2 addition allows the formation of interstitial oxygen in anatase TiO2 thin films. On the other hand, the absence of oxygen leads to thin films with lower composition of O2 (Ti/O=1,54 w/w, TiOi,94 which comply with the rutile formula TiO2-X)-

Fig. 8 EDS of the films deposited under (a) under higth-pressure O2-enriched atmosphere, (b) low-pressure O2-enriched atmosphere, and (c) normal atmosphere. 

4. CONCLUSIONS

High crystalline and continuous anatase and rutile nano-coatings have been successfully prepared using spray pyrolysis technique. High-temperature stable anatase TiO2 thin films with ~33nm sized-crystallites have been synthesized using a simple and cost-effective CVD-like process under high-pressure oxygen-enriched atmosphere.

These films constitute promising materials used in hydroxyapatite coated metal implants, rechargeable lithium ion batteries, gas sensors and photocatalytic solar panels.

CONFLICT OF INTEREST

The autors have no conflicts of interest to declare.

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Corresponding author. e-mail address:zincb@itu.edu.tr(Zincb Benzait). Peer Review under the responsibility of Universidad Nacional Autónoma de México. http://

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