Journal of Nanomaterials
Volume 2016 (2016), Article ID 3145912, 8 pages
http://dx.doi.org/10.1155/2016/3145912

Research Article

The Effect of Calcination Temperature on Structure and Photocatalytic Properties of WO₃/TiO₂ Nanocomposites

Joanna Mioduska, Anna Zielińska-Jurek, Marcin Janczarek, and Jan Hupka

Department of Chemical Technology, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk, Poland

Received 5 April 2016; Revised 16 June 2016; Accepted 5 July 2016

Academic Editor: Jim Low

Copyright © 2016 Joanna Mioduska 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.

Abstract.

Series of WO₃/TiO₂ nanocomposites were obtained by hydrothermal method followed by calcination in the temperature range from 400°C to 900°C. The characteristics of photocatalysts by X-ray diffractometry (XRD), scanning electron microscope (SEM), and diffuse reflectance spectroscopy (DRS) showed that increasing the calcination temperature from 400 to 900°C resulted in change of photocatalytic activity under UV-Vis light. Moreover, the amount of WO₃ crystalline phase and amorphous phase in WO₃/TiO₂ aggregates, as revealed by XRD analysis, was dependent on the calcination temperature. The WO₃/TiO₂ samples with 8 mol% load of WO₃ in respect to TiO₂ calcinated at 500 and 800°C possess the highest photocatalytic activity in reaction of phenol degradation, which is about 1.2 and 1.5 times that with calcination at 400°C. The increase in calcination temperature above 400°C resulted in increase of WO₃ crystallinity and reduction of the amount of amorphous phase in the nanocomposite structure. Moreover, the annealing of nanocomposites above 700°C decreases the value of optical band gap energies of obtained WO₃/TiO₂ nanomaterials.

1. Introduction

Photocatalytic reactions at the surface of titanium(IV) oxide have been used for degradation of hydrocarbons, pesticides and dyes from aquatic systems [1, 2], volatile organic compounds [3] and deactivating bacteria in air [4]. However, the application of TiO₂ for degradation of emerging pollutants from gas and aqueous phases still needs to tackle a variety of scientific problems.

Photocatalytic efficiency of TiO₂ is limited by fast recombination of electron-hole pairs. Additionally, for TiO₂ the band gap is equal to 3.2 eV and 3.0 eV in the anatase and rutile crystalline phase, respectively. It corresponds to a radiation wavelength of 388 nm, which lies in the UVA spectrum of 300 to 388 nm. Therefore, the range of radiation required for excitation of TiO₂-based photocatalysts limits the large-scale application of photocatalysis, because solar spectrum contains only a small part (3–5%) of UV radiation. This is the main force for the development of the second generation of photocatalysts, with photocatalytic activity under the visible range ( nm) and reduced recombination rate between electrons and holes [5].

Photocatalysts can be sensitized for visible light by either doping or chemical surface modification by metals, metal ions, or nonmetals [6–8]. However, research on the second generation has revealed several problems regarding practical aspects of photocatalysis. The first issue is that sensitization of photocatalysts to visible light not always results in an increase of photoactivity and selectivity. Moreover, it even can decrease the photoactivity and selectivity. Photosensitizing TiO₂ with suitable dyes leads to its self-destruction, while nonmetal or metal ion dopants may act as recombination centers of and h⁺.

Regarding Emeline et al. [5] the third-generation photoactive materials are based on reducing the band gap of TiO₂ by coupling two different semiconductors which could transfer electrons from an excited band gap semiconductor into another attached one assuming proper conduction band potentials [5]. Such conformation favors separation of photoinduced electrons and holes and improves photocatalytic efficiency of the semiconductor heterostructure.

Recent studies on next generation photocatalysts focused on the coupling of titanium(IV) oxide with tungsten(VI) oxide, a semiconductor with band gap equal to 2.8 eV [9, 10]. The valence and conduction bands of tungsten(VI) oxide are correspondingly lower than in the case of titanium(IV) oxide and the energy band gap is also lower [11, 12]. The combination of these two semiconductors results in enhanced photocatalytic and photochromic potential and accelerates electron transfer from WO₃ to TiO₂. Akurati et al. have observed that the introduction of tungsten to the structure of anatase results in efficient separation of electron-hole pairs, which are formed during irradiation of titanium(IV) oxide [13]. Additionally, combination of these two semiconductors gives the opportunity to obtain a photocatalyst with extended range of optical absorption spectrum [14–16]. However, most of the investigations focused on degradation of dyes in the aqueous phase using WO₃/TiO₂ nanocomposites, but few pertain to the degradation of organic pollutants in the gas phase and aqueous phases.

Recent studies focused on the effect of the particle size and crystallinity on the photocatalytic properties of WO₃/TiO₂ nanocomposites [17, 18]. Crystallinity is one of the critical parameters that influences the photocatalytic performance of photocatalyst. Ohtani et al. reported that amorphous titania plays a role as a recombination center, and it exhibits negligible reactivity in several photocatalytic reactions [19]. However, there is no report in literature concerning the influence of the amorphous fraction of the WO₃/TiO₂ nanocomposites on their photocatalytic activity.

Therefore, the aim of the present paper is systematic study of surface properties of coupled WO₃/TiO₂ nanocomposites and their photocatalytic activity in reaction of phenol degradation under UV-Vis irradiation. Phenol was chosen as a model degradation molecule as it is one of the major pollutants discharged in the wastewater from the various industries that can accumulate in the environment [20]. The influence of calcination temperature in range from 400°C to 900°C on crystallinity, amorphous phase content, and photoactivity for WO₃/TiO₂ nanomaterials is for the first time reported in this paper. Additionally, the effect of precursor and the amount of tungsten(VI) oxide on the photodegradation efficiency was also investigated.

2. Experimental

2.1. Materials and Instruments

All applied reagents were of analytical grade and used without further purification. Titanium(IV) butoxide (≥97%) was supplied by Fluka and used as titanium source for the preparation of TiO₂ nanoparticles. Ammonium metatungstate hydrate was provided by Sigma-Aldrich and used as the starting material for the preparation of tungsten(VI) oxide nanoparticles. Commercial WO₃ nanoparticles were supplied from Sigma-Aldrich and also used for coupling with TiO₂ after hydrolysis unit process.

The crystal structures of the WO₃/TiO₂ nanoparticles were determined from XRD pattern measured in the range of = 20–80° using X-ray diffractometer (X’Pert PRO-MPD, Philips) with Cu target ( Å). The crystallite size was estimated by Scherrer equation using the corrected full width (line-broadening by Cu-Kα2 radiation and emanation in the optical path of a diffractometer) at half maximum (FWHM) of the most intense XRD peaks of anatase, rutile, and WO₃ at ca. 25.3° and 27.4° and 23.1° or 24.3°, respectively. A constant of 0.891 in the Scherrer equation was used.

Amorphous content of photocatalysts was calculated by the internal standard method, in which highly crystalline nickel oxide (NiO, Alfa Aesar) was used as the standard, by mixing photocatalyst (80 wt%) and NiO (20 wt%) samples.

Jasco V-670 spectrophotometer equipped with PIN-757 integrating sphere where the baseline was recorded using BaSO₄ as a reference was used for characterization of light absorption properties of modified photocatalysts. UV/Vis diffuse reflectance (DR) spectra were recorded, and the data were converted to obtain absorption spectra.

Quanta FEG 250 scanning electron microscope (SEM) was used in the investigation of surface morphologies of WO₃/TiO₂ nanocomposites. Photocatalyst samples were coated with a thin layer of gold using a Leica EM SCD500 coater. EDX analyses were performed for selected representative sample areas.

2.2. Preparation of WO₃/TiO₂ Photocatalysts

The WO₃/TiO₂ photocatalysts were obtained by hydrothermal method, as presented in Figure 1. TiO₂ nanoparticles were prepared by hydrolysis of titanium(IV) butoxide (TBT), which was added dropwise to water and stirred for 30 min. Uniformly mixed commercial WO₃ nanoparticles or ammonium metatungstate (AmT) hydrate was added at room temperature to TiO₂ sol and thoroughly mixed. The hydrothermal reaction took place in a Teflon autoclave at 110°C for 24 h. Precipitated WO₃/TiO₂ particles were centrifuged (3000 rpm), dried at 80°C to dry mass, and calcinated at 400–900°C for 2 h.

Figure 1: Schematic diagram of the preparation of WO₃/TiO₂ photocatalysts.

2.3. Evaluation of Photocatalytic Activity

The photocatalytic activity of WO₃/TiO₂ powders in the UV-Vis light irradiation was estimated by measuring the decomposition rate of phenol in an aqueous solution. A 25 cm³ of  M phenol solution containing 0.05 g suspended photocatalyst was stirred using a magnetic stirrer and aerated (5 dm³/h) prior to and during the photocatalytic process. The suspension was irradiated using a Xenon lamp (6271H, Oriel), with UV-Vis emission range. Measured light flux was (in the range from 310 to 380 nm) 24 mW/cm². The photoreactor was equipped with a quartz window and exposure layer thickness was 3 cm. The temperature of the aqueous phase during irradiation was kept at 15°C using water jacket. Aliquots of 1.5 cm³ of the aqueous suspension were collected at regular time periods during irradiation and filtered through syringe filters ( μm) to remove photocatalyst particles. Phenol concentration was estimated by colorimetric method using a UV-Vis spectrophotometer (DU-7, Beckman). Photocatalytic degradation runs were preceded by blind test in the absence of a photocatalyst or illumination for 1 hour. No degradation of phenol was observed in the absence of either the photocatalyst or illumination.

3. Results and Discussion

The effect of tungsten(VI) oxide amount as well as calcination temperature during preparation route on the photocatalytic activity of obtained WO₃/TiO₂ nanocomposites was investigated. The amount of ammonium metatungstate taken for photocatalyst preparation was calculated on the assumption that the content of WO₃ in the photocatalysts after synthesis should be from 3 to 10 mol% of the photocatalyst dry mass.

3.1. Absorption Properties

Modification of titanium(IV) oxide with tungsten(VI) oxide resulted in increased absorption range in the visible light range. The UV-Vis diffuse reflectance spectra of WO₃/TiO₂ samples prepared with different amounts of ammonium metatungstate (AmT) from 3 to 10 mol% are shown in Figure 2(a). Pure TiO₂ showed absorption threshold at 395 nm. Samples of coupled semiconductors WO₃/TiO₂ exhibited two characteristic light absorption edges in DRS curves. The UV region is attributable to the intrinsic band gap of TiO₂ semiconductor and others in the visible region from 410 nm to 500 nm, related to modification of TiO₂ with WO₃. It was observed that increasing AmT amount results in an increase of absorbance in the visible light region.

(a)

(b)

(c)

(d)

Figure 2: The DR/UV-Vis spectra of WO₃/TiO₂ with different amounts of ammonium metatungstate (a), WO₃/TiO₂ calcinated at 400, 500, 600, 700, and 800°C for TiO₂ modified with AmT (b), determination of indirect interband transition energies for TiO₂ modified with commercial WO₃ (c), and the DR/UV-Vis spectra of pure TiO₂ calcinated at 400°C and 800°C and WO₃/TiO₂ powders with the highest intensity of visible light absorption (d).

The effect of the calcination temperature on absorption properties for TiO₂ modified with commercial WO₃ and obtained from precursor (AmT) is shown in Figures 2(b) and 2(c). The red shift in the absorption edge of the WO₃/TiO₂ samples depends on the calcination temperature and the chemical nature of WO₃ (commercial WO₃ particles or WO₃ obtained from AmT precursor). As the calcination temperature increases, the absorption edges of photocatalysts’ red-shifts and the absorption intensity in the visible region increase, especially for samples calcinated at most elevated temperatures, that is, at 800 to 900°C.

The DR/UV-Vis spectra of pure TiO₂ calcinated at 400°C and 800°C as well as WO₃/TiO₂ powders with the highest intensity of visible light absorption are presented in Figure 2(d). The greatest increase in the intensity of the visible light absorption was observed for sample AmT_10%_800 containing 10 mol% of WO₃. The obtained results are in accordance with those obtained by other authors [21, 22] showing that the red shift in the absorption edge of the WO₃/TiO₂ nanoparticles results from the formation of defect energy levels and tungsten impurity energy levels in the structure of nanocomposites.

The indirect band gap values of WO₃/TiO₂ photocatalysts are listed in Table 1. The undoped TiO₂ has a band gap of 3.1 eV. As it is evident from Figures 2(a)–2(c), there were changes in absorbance wavelength, which can be correlated to a change in the band gaps of prepared particles.

Table 1: Characteristics of WO₃/TiO₂ nanocomposites. The effect of calcination temperature on energy band gap and photocatalytic properties.

Sample label
WO₃ amount (mol%)
Phenol degradation constant rate (min⁻¹) · 10⁻²
Energy band gap (eV)

TiO₂_100%_400
0
0.75
3.15

TiO₂_100%_800
0
0.66
3.0

WO₃_100%_400
100
0.37
2.65

WO₃_100%_800
100
0.26
2.60

AmT_3%_400
3
0.06
2.95

AmT_5%_400
5
0.15
2.95

AmT_8%_400
8
0.12
2.95

AmT_8%_500
8
0.24
2.95

AmT_8%_600
8
0.32
2.85

AmT_8%_700
8
0.32
2.70

AmT_8%_800
8
0.77
2.75

AmT_10%_400
10
0.21
2.95

AmT_10%_500
10
0.32
2.90

AmT_10%_600
10
0.34
2.80

AmT_10%_700
10
0.39
2.75

AmT_10%_800
10
0.87
2.84

WO₃_5%_300
5
0.87
3.05

WO₃_5%_400
5
0.91
3.05

WO₃_5%_500
5
1.21
3.05

WO₃_5%_600
5
0.66
3.05

WO₃_5%_700
5
0.61
2.95

WO₃_5%_800
5
0.95
2.75

WO₃_8%_400
8
0.84
2.95

WO₃_8%_500
8
1.04
2.98

WO₃_8%_600
8
0.81
2.95

WO₃_8%_700
8
0.67
2.95

WO₃_8%_800
8
1.27
2.95

WO₃_8%_900
8
0.8
2.85

WO₃_10%_400
10
0.56
3.0

WO₃_10%_500
10
0.41
3.0

WO₃_10%_600
10
0.67
3.0

WO₃_10%_700
10
0.39
2.95

WO₃_10%_800
10
0.66
2.85

The determined energy band gaps of WO₃/TiO₂ nanocomposites are lower than that of pure TiO₂ nanoparticles; hence coupled semiconductors extend the range of excitation light, which could result in greater photocatalytic activities under visible light. It can also be observed that the band gap () of WO₃/TiO₂ nanocomposites decreases at calcination temperatures above 700°C. Yang et al. [23] reported that formation of defective energy levels decreases the total energy band gap of coupled photocatalysts. The impact of WO₃ contribution to the adjustment energy band gap achieved by coupling TiO₂ nanoparticles with changing percent of WO₃ depends on the source of tungsten in the photocatalyst and its amount [15]. Our observations confirm results presented by Kwon et al. [15]. Moreover, we also found that not only the amount of dopant but also the chosen calcination temperature during preparation procedure influences the energy band gap.

3.2. XRD Analysis

XRD patterns of WO₃/TiO₂ samples of different calcination temperatures are shown in Figure 3(a). The presence of the primary diffraction peaks of TiO₂ at = 25.29, 37.95, 47.97, 54.56, and 62.69 was observed, which can be, respectively, indexed as (101), (103), (200), (105), and (213) planes of anatase phase of titanium(IV) oxide (JCPDS number 21-1272). Pure self-obtained anatase particles transform to rutile at temperature above 700°C. The peaks at   27.5 (110), 36.1 (101), 56.7 (220), and 64.1 (310), were corresponding to rutile and were observed for TiO₂ sample calcinated at 800°C, regarding phase transition from anatase to rutile. For coupled semiconductors the presence of WO₃ in the structure of nanocomposites results in inhibition of anatase/rutile transformation. The increase of the calcination temperature above 700°C led to an increase of proportion of the rutile phase to anatase in WO₃/TiO₂ samples but not full transformation of anatase to rutile. For WO₃/TiO₂ sample calcinated at 900°C, the ratio of anatase to rutile was 2 : 1.

Figure 3: XRD patterns of WO₃/TiO₂ nanoparticles calcinated from 400 to 900°C.

The signals corresponding to the primary reflections of WO₃ can be observed in the WO₃/TiO₂ samples at = 23.1, 23.7, 24.3, 26.6, 28.7, 33.3, 34.2, and 49.9. These signals can be associated with (001), (020), (200), (120), (111), (021), (220), and (400) planes of the monoclinic phase of WO₃ (JCPDS number 036-0101).

The morphology of WO₃-loaded TiO₂ is strongly influenced by heat treatment procedure. The results presented in Table 2 indicated that below 500°C WO₃/TiO₂ nanocomposites contain a high amorphous phase content (60%) with respect to the crystalline phase content (40%). Further increase in the calcination temperature (from 500 to 900°C) affects the increase in the amount of crystalline phase (80%) and reduction in the amount of amorphous phase (20%) in the nanocomposite structure. This means that for the selected parameters of preparation of WO₃/TiO₂ nanocomposites the calcination is preferably carried out at temperature 500°C, regarding the morphological properties of the nanocomposites. The hydrothermal reaction time and temperature as well as duration of the calcination may affect the further reduction in the amount of amorphous phase in the WO₃/TiO₂ structure. Therefore, the further optimization of the conditions of hydrothermal reaction of WO₃/TiO₂ coupled photocatalysts should be continued and correlated with amorphous and crystalline phase content.

Table 2: The effect of calcination temperature on the content of amorphous and crystalline phases of WO₃/TiO₂ samples.

Sample
Calcination temperature (°C)
Crystalline phase content (%)
Amorphous phase content (%)

WO₃_8% (without heat treatment)
—
42
58

WO₃_8%_400
400
39
60

WO₃_8%_500
500
77
23

WO₃_8%_600
600
76
22

WO₃_8%_700
700
75
25

WO₃_8%_800
800
80
20

WO₃_8%_900
900
82
18

3.3. Microscopic Analysis

Microstructure of obtained nanocomposites and their surface morphology were studied by SEM equipped with EDS. SEM analyses of WO₃/TiO₂ sample containing the same amount of tungsten trioxide but obtained by generating in situ WO₃ particles from WO₃ precursor (AmT) during preparation of nanocomposites (a) and using commercial WO₃ nanoparticles (b) are presented in Figure 4. Both samples have similar spherical particles shape and size in the range from 30 nm to 70 nm. The particles form loose aggregates with a significant porosity. Figures 4(c) and 4(d) show that annealing at 800°C increases the crystallinity of WO₃ nanoparticles compared to WO₃/TiO₂ sample calcined at 400°C. Sample calcinated at 800°C comprises well-developed crystals of WO₃/TiO₂ compared to that calcinated at 400°C with 3-fold lower crystallinity and higher amorphous phase content. Therefore, it can be concluded that the calcination temperature is crucial in the formation of particular morphology of spherical WO₃ nanoparticles. The tungsten content estimated with SEM-EDS for both WO₃_8%_400 and WO₃_8%_800 samples varied between 1 and 2 at.%. For sample WO₃_8%_800 the measured amount of O was 78.6 at.%, Ti was 20 at.%, and W was 1.4 at.%. The atomic percent amounts of the species detected by EDX indicate a W/Ti atomic ratio equal to 0.27, which confirms the W nominal amount assessed in the preparation procedure. These results confirm that tungsten is present at the surface regions of the TiO₂ nanoparticles, although a minor incorporation into the TiO₂ lattice cannot be excluded and suggests the formation of WO₃ microdomains that create a structure in WO₃/TiO₂ rather than producing of TiO₂ doping.

(a)

(b)

(c)

(d)

Figure 4: SEM images for sample AmT_8%_400 (a) and for sample WO₃_8%_400 (b). The effect of calcination temperature on the structure of WO₃_8%_400 (c) and WO₃_8%_800 nanocomposites.

3.4. Photocatalytic Activity of WO₃/TiO₂ Nanocomposites

The kinetics of phenol photodegradation in the presence of obtained WO₃/TiO₂ nanoparticles are shown in Figure 5 and the determined rate constants are also included in Table 1. The apparent rate constants of the first-order kinetics of phenol photodegradation increased from  min⁻¹ to  min⁻¹ for AmT_3%_400 and WO₃_8%_800, respectively. An increase in tungsten(VI) oxide content from 3 to 10 mol% for samples obtained using ammonium metatungstate (AmT) as WO₃ precursor resulted in enhancement of the photocatalytic activity under UV-Vis light irradiation. Moreover, as shown in Figure 5(a), the photocatalytic activity strongly depends on WO₃ source and calcination temperature. Phenol degradation rate constant for the most active sample WO₃_8%_800 increased about 1.6 times reaching  min⁻¹ compared to the sample AmT_8%_800 with the highest activity among WO₃/TiO₂ photocatalysts containing 8 mol% nominal value of tungsten(VI) oxide.

(a)

(b)

Figure 5: Kinetics of phenol degradation for samples AmT_8%, AmT_10%, WO₃_10%, and WO₃_8% under UV-Vis light. Experimental conditions: light source: Xe lamp, irradiation flux 24 mW/cm², phenol initial concentration: 0.2 mM, (TiO₂) = 0.05 g, and °C. The effect of calcination temperature for the most active samples WO₃_8%, WO₃_5%, and AmT_10% (b).

As shown in Figure 5(b), an increase of the calcination temperature from 400°C to 500°C resulted in an increase in photoactivity of the most active samples WO₃_8%, WO₃_5%, and AmT_10% and then decreased for the WO₃/TiO₂ nanocomposites obtained using commercial WO₃ particles (WO₃_5% and WO₃_8% series) and calcinated at 600°C and 700°C. The increase of photoactivity for those samples calcinated above 400°C can be correlated with 3-fold lower amount of amorphous phase in the structure of photocatalyst. Ohtani et al. reported the results of photocatalytic activity of anatase and amorphous TiO₂ and stated that amorphous titania contains imperfections, for example, impurities, dangling bonds, or microvoids, which lead to electronic states in the band gap, and acts as a recombination of charge carriers. Therefore, the photocatalytic activity of anatase crystallites is improved further by the heat treatment [19].

After annealing at 600°C samples with predominantly anatase structures were produced in which the contribution of the rutile phase can become more dominant by further increasing the annealing temperature. However, the highest photoactivity was observed for the sample containing 8 mol% of WO₃ calcined at 800°C (namely, 8%_WO₃_800). Further increase in annealing temperature to 900°C resulted in a drop of photoactivity from  min⁻¹ to  min⁻¹ for the sample WO₃_8% calcinated at 800°C and 900°C, respectively. The decrease of photoactivity above the optimal calcination temperature results from an increase in number of defects in the oxide structure, acting as charge carriers recombination centers [24].

4. Conclusions

The effect of annealing temperature is confirmed by the XRD, microscopy, and photocatalytic analysis. Increase in the calcination temperature resulted in increased clearly crystallite WO₃ content in the WO₃/TiO₂ nanocomposites structure, as well as decrease of WO₃/TiO₂ optical band gap energies due to incorporation of tungsten(VI) oxide into the structure of TiO₂. Moreover, an increase in the calcination temperature affects the increase in the amount of crystalline phase and reduction in the amount of amorphous phase in the nanocomposite structure. Therefore, taking into account the morphological properties of as-prepared WO₃/TiO₂ nanocomposites the calcination should proceed at 500°C. The annealing of WO₃/TiO₂ nanocomposites above 400°C increases the crystallinity of WO₃ nanoparticles and improves photoinduced charge carriers separation. The best photocatalytic activity revealed samples containing 5 mol% and 8 mol% of WO₃ and calcinated at temperature 500°C and 800°C. The results of photodecomposition of phenol in aqueous solution using WO₃/TiO₂ nanocomposites under UV-Vis light irradiation indicated effect of tungsten(VI) oxide source and amount as well as the calcination temperature of the photocatalyst on the process efficiency.

Competing Interests

The authors declare that they have no competing interests.

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