Fabrication and characterization of uniform ti o2 nanotube arrays by sol gel template method
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The document summarizes the fabrication and characterization of uniform TiO2 nanotube arrays synthesized using a sol-gel template method with an alumina membrane. Scanning electron microscopy images showed the TiO2 nanotubes were ordered and uniform, with diameters controlled by the alumina pore size. Transmission electron microscopy confirmed the hollow, open-ended structure of individual nanotubes. X-ray diffraction and Raman spectroscopy demonstrated the nanotubes had an anatase crystal phase. UV-vis absorption spectroscopy exhibited a blue shift in the TiO2 nanotubes compared to bulk TiO2, attributed to quantum size effects.
![706 T Maiyalagan, B Viswanathan and U V Varadaraju
2. Experimental 2.3 Characterization methods
2.1 Materials The scanning electron micrographs were obtained after
the removal of alumina template using a JEOL JSM-840
All the chemicals used were of analytical grade. Titanium model, working at 15 keV. For transmission electron micro-
isopropoxide (Aldrich), 2-propanol (Merck) and Degussa scopic studies, the nanotubes dispersed in ethanol were
P-25 titanium dioxide (Germany) were used as received placed on the copper grid and the images were obtained
(BET surface area, 50 m2/g and anatase : rutile ratio, 80 : 20). using Phillips 420 model, operating at 120 keV. The UV-
Anodisc alumina membranes with a pore size of 200 nm vis absorption spectra were obtained on a Cary 5E spec-
and thickness of 60 µm were purchased from Whatman trophotometer. The X-ray diffraction patterns were obtai-
(catalog no. 6809-6022; Maidstone, UK). ned on a Philips PW 1820 diffractometer with CuKα
(1⋅54178 Å) radiation. Micro-Raman scattering experi-
2.2 Synthesis of TiO2 nanotubes ments were performed on a Bruker FRA106 FT-Raman at
room temperature in a quasi-backscattering geometry
Titanium isopropoxide (5 ml) was added to 25 ml of 2- with parallel polarization incident light. The excitation
propanol (mole ratio [Ti4+]/[2-propanol] = 1 : 20). The source used was an Argon ion laser operating at 514⋅5 nm
solution was stirred for 3 h at room temperature (298 K). with an output power of 20 mW.
The alumina template membrane was dipped into this
solution for 2 min. After removal from the solution, vacuum
was applied to the bottom of the membrane until the entire 3. Results and discussion
volume of the solution was pulled through the membrane.
The membrane was then air-dried for 60 min at 303 K The scanning electron microscopic (SEM) image of the
and then placed in a furnace (in air) with a temperature TiO2 nanotubes obtained after dissolving the 200 nm alu-
ramp of 2°C min –1 to 873 K for 2 h. The temperature was mina template membranes is shown in figure 1a. It can be
then decreased at a ramp rate of 2°C min –1 to room tem- seen that an ordered array of nanotubes with uniform
perature (303 K). The ordered TiO2 nanotube arrays were diameter and length is formed. The individual TiO2 nano-
obtained by dissolving the alumina template in 3 M aqueous tubes were characterized by TEM after dissolving the
NaOH for several minutes. TiO2 nanotubes thus formed alumina membrane template. The open end and the hollow
were then washed several times with distilled water to nature of the TiO2 nanotubes have also been confirmed
remove the dissolved anodic alumina membrane and re- by transmission electron microscopic (TEM) image as
maining NaOH solution. shown in figure 1b. The TEM image shows that the single
Figure 1. SEM image (a) and TEM image (b) of TiO2 nanotubes obtained by sol–gel method calcined
at 650°C for 2 h.](https://image.slidesharecdn.com/fabricationandcharacterizationofuniformtio2nanotubearraysbysol-geltemplatemethod-120523135258-phpapp01/85/Fabrication-and-characterization-of-uniform-ti-o2-nanotube-arrays-by-sol-gel-template-method-2-320.jpg)
Fabrication and characterization of uniform ti o2 nanotube arrays by sol gel template method
- 1. Bull. Mater. Sci., Vol. 29, No. 7, December 2006, pp. 705–708. © Indian Academy of Sciences. Fabrication and characterization of uniform TiO2 nanotube arrays by sol–gel template method T MAIYALAGAN, B VISWANATHAN* and U V VARADARAJU Department of Chemistry, Indian Institute of Technology Madras, Chennai 600 036, India MS received 11 October 2005; revised 18 September 2006 Abstract. TiO 2 nanotubes have been synthesized by sol–gel template method using alumina membrane. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy, UV ab- sorption spectrum and X-ray diffraction techniques have been used to investigate the structure, morphology and optical properties of TiO 2 nanotubes. SEM image showed that TiO 2 nanotubes obtained were ordered and uniform. The diameter and length of the nanotubes were decided by the pore size and thickness of alumina template. Raman and XRD measurements confirmed the crystallinity and anatase phase of the TiO 2 nano- tubes. The optical absorption measurement of TiO 2 nanotubes exhibits a blue shift with respect to that of the bulk TiO 2 owing to the quantum size effect. Keywords. TiO 2 nanotubes; Raman spectra; template synthesis; alumina template. 1. Introduction Many approaches such as template-assisted method (Sander et al 2004), electrochemical anodic oxidation of Titanium dioxide (TiO2 ) has been widely investigated as pure titanium sheet (Gong et al 2001; Macak et al 2005), a key material for applications in photovoltaic cells, batteries, and methods involving chemical treatment of fine titania chemical sensing (Varghese et al 2003), optical emissions, particles (Kasuga et al 1998; Du et al 2001) have been photonic crystals, catalysis, photocatalysis (Livraghi et al reported to fabricate TiO2 nanotubes. There are respective 2005) and environmental purification (Homyara et al advantages and limitations in each of the above-men- 2001). Anatase TiO2 electrodes are used in solar cells, tioned methods. However, technical problems may arise lithium batteries and electrochromic devices (Hagfeldt from the difficulties in achieving uniform inner diameter and Gratzel 1995; Kavan et al 2000; Gratzel 2001). of titanium oxide nanotubes. In addition, oriented nano- Nanocrystalline form of anatase TiO2 is a promising ele- structures of the TiO2 nanotubes are often more desirable ctrode material for Li-ion batteries, owing to its good Li- for applications in photovoltaic cells, sensing, catalysis storage capacity, cycling-stability and safety against and photocatalysis. Template-synthesis method has been overcharging (Huang et al 1995). Non-toxicity, environ- used to prepare nanotubes or fibrils of electronically con- mental compatibility and low price are other practical ductive polymers (Martin et al 1993), metals (Martin advantages of TiO2 . As a catalyst and/or catalyst support, 1996), semiconductors (Lakshmi et al 1997) and carbon it is employed in the processes of photo degradation of nanotubes (Maiyalagan and Viswanathan 2005). This chlorine hydrocarbons. Recently, efforts have been directed method entails synthesis of a desired material within the to obtain nanostructured TiO2-based materials with a large pores of an alumina membrane, which has cylindrical pores specific surface area. The energy band structure becomes with monodisperse diameters. The tubule of the desired discrete for titanium dioxide of nanometer scale, and its material is obtained within each pore. This template approach photophysical, photochemical, and surface properties are is proving to be a versatile method for synthesizing quite different from those of the bulk ones due to the nanomaterials because the aspect ratio of the nanostructu- quantum size effect. TiO2 -based nanotubes have attracted res prepared via this method can be controlled. wide attention owing to their potential for application in In this article, we report the sol–gel template synthesis highly efficient photocatalysis (Adachi et al 2000), lithium of ordered TiO2 nanotube of uniform diameter using alumina ion batteries (Zhou et al 2003), photovoltaic cells membrane as a template. The composition and crystalli- (Poulios et al 1998; Adachi et al 2002; Uchida et al nity of these structures were determined by transmission 2002) and environmental applications (Quan et al 2005). electron microscopy (TEM), scanning electron microscopy (SEM), Raman spectroscopy and powder X-ray diffrac- tion (XRD). The optical absorption spectra of these ordered *Author for correspondence (bvnathan@iitm.ac.in) TiO2 nanotube arrays have also been investigated. 705
- 2. 706 T Maiyalagan, B Viswanathan and U V Varadaraju 2. Experimental 2.3 Characterization methods 2.1 Materials The scanning electron micrographs were obtained after the removal of alumina template using a JEOL JSM-840 All the chemicals used were of analytical grade. Titanium model, working at 15 keV. For transmission electron micro- isopropoxide (Aldrich), 2-propanol (Merck) and Degussa scopic studies, the nanotubes dispersed in ethanol were P-25 titanium dioxide (Germany) were used as received placed on the copper grid and the images were obtained (BET surface area, 50 m2/g and anatase : rutile ratio, 80 : 20). using Phillips 420 model, operating at 120 keV. The UV- Anodisc alumina membranes with a pore size of 200 nm vis absorption spectra were obtained on a Cary 5E spec- and thickness of 60 µm were purchased from Whatman trophotometer. The X-ray diffraction patterns were obtai- (catalog no. 6809-6022; Maidstone, UK). ned on a Philips PW 1820 diffractometer with CuKα (1⋅54178 Å) radiation. Micro-Raman scattering experi- 2.2 Synthesis of TiO2 nanotubes ments were performed on a Bruker FRA106 FT-Raman at room temperature in a quasi-backscattering geometry Titanium isopropoxide (5 ml) was added to 25 ml of 2- with parallel polarization incident light. The excitation propanol (mole ratio [Ti4+]/[2-propanol] = 1 : 20). The source used was an Argon ion laser operating at 514⋅5 nm solution was stirred for 3 h at room temperature (298 K). with an output power of 20 mW. The alumina template membrane was dipped into this solution for 2 min. After removal from the solution, vacuum was applied to the bottom of the membrane until the entire 3. Results and discussion volume of the solution was pulled through the membrane. The membrane was then air-dried for 60 min at 303 K The scanning electron microscopic (SEM) image of the and then placed in a furnace (in air) with a temperature TiO2 nanotubes obtained after dissolving the 200 nm alu- ramp of 2°C min –1 to 873 K for 2 h. The temperature was mina template membranes is shown in figure 1a. It can be then decreased at a ramp rate of 2°C min –1 to room tem- seen that an ordered array of nanotubes with uniform perature (303 K). The ordered TiO2 nanotube arrays were diameter and length is formed. The individual TiO2 nano- obtained by dissolving the alumina template in 3 M aqueous tubes were characterized by TEM after dissolving the NaOH for several minutes. TiO2 nanotubes thus formed alumina membrane template. The open end and the hollow were then washed several times with distilled water to nature of the TiO2 nanotubes have also been confirmed remove the dissolved anodic alumina membrane and re- by transmission electron microscopic (TEM) image as maining NaOH solution. shown in figure 1b. The TEM image shows that the single Figure 1. SEM image (a) and TEM image (b) of TiO2 nanotubes obtained by sol–gel method calcined at 650°C for 2 h.
- 3. Fabrication and characterization of uniform TiO2 nanotube arrays 707 TiO2 nanotube is straight and dense. The outer diameter the valence band (VB) to the conduction band (CB). An of the nanotube is ca. 200 nm, retaining the size and near absorbance below 370 nm was observed for the TiO2 cylindrical shape of the pores of the aluminium oxide nanotubes, which is ascribed to bulk anatase TiO2 . Here membrane. This indicates that the diameter of the nano- the blue shift of absorption maximum with higher band tube synthesized is controlled by the pore size of aluminium energy of TiO2 nanotubes compared with that of the bulk oxide membrane. This result is in agreement with other Degussa TiO2 can be attributed to the quantum-size effect reports on the sol–gel based template method (Lee et al (Takagahara and Takeda 1992). 2004). The powder XRD was used to investigate the phase of Figure 2 shows the UV-vis absorption spectrum of the TiO2 nanotubes. The X-ray pattern of the TiO2 nanotube anatase TiO2 nanotube compared with that of the Degussa arrays is shown in figure 3(b). The diffraction peaks of TiO2 . The spectral lines for both TiO2 nanotubes and De- (101), (004), (200), (105) and (211) correspond to the gussa TiO2 exhibit only one characteristic absorption anatase TiO2 phase. The peak positions and their relative band, which is assigned to the intrinsic transition from intensities are consistent with the standard powder diffrac- tion pattern of anatase-TiO2 and there is no preferred ori- entation. Figure 3 shows that the crystal phase of TiO2 nanotubes is polycrystalline anatase structure whereas the Degussa P-25 contains a mixture of anatase and rutile phases. Further, no peaks for the amorphous alumina membrane were observed in the TiO 2 nanotubes. The Raman spectra of fabricated anatase TiO2 nano- tubes and Degussa TiO2 are shown in figure 4. The result of XRD analysis is supported by the Raman spectra of TiO2 nanotubes as shown in figure 4(b). The vibration mode symmetries of the anatase are indicated. Raman peaks at 156⋅9, 206, 408⋅48, 529⋅54, 649⋅54 and 801 cm–1 were assigned to E g, E g, B 1g, A 1g, E g and B 1g, respectively. The positions and intensities of the six Raman active modes correspond well with the anatase phase of TiO2 (Bersani and Lottici 1998; Lei et al 2001). A weak overtone scattering (B 1g) at 801 cm –1 was observed in this study. Overtone can be found in both bulk Degussa TiO2 and nanotube, but the intensity of overtone is very less in bulk Degussa TiO2 . This is due to the large intensity ratio of Figure 2. UV-vis absorption spectrum of (a) Degussa TiO2 and (b) anatase TiO2 nanotube. Figure 3. X-ray diffraction patterns of (a) Degussa TiO2 as a Figure 4. Raman spectrum of (a) Degussa TiO2 and (b) fabri- reference and (b) TiO2 nanotubes obtained by sol–gel method cated anatase-TiO2 nanotube (The vibration mode symmetries calcined at 650°C for 2 h anatase phase. of the anatase are indicated).
- 4. 708 T Maiyalagan, B Viswanathan and U V Varadaraju fundamental peak to overtone one makes it difficult to be Gratzel M 2001 Nature 414 338 observed. While for nanotube, the decreasing ratio makes Gong D, Grimes C A, Varghese O K, Hu W, Singh R S, Chen Z it easy to be observed. No significant broadening and and Dickey E C 2001 J. Mater. Res. 16 3331 shift of Raman spectra were found when one compared Hagfeldt A and Gratzel M 1995 Chem. Rev. 95 49 Homyara H et al 2001 Thin Solid Films 386 173 the obtained anatase-TiO2 nanotube with that of the bulk Huang S Y, Kavan L, Gratzel M and Exnar I 1995 J. Electro- Degussa TiO2 . chem. Soc. 142 142 Kasuga T, Hiramatsu M, Hoson A, Sekino T and Niihara K 4. Conclusions 1998 Langmuir 14 3160 Kavan L, Attia A, Lenzmann F, Elder S H and Gratzel M 2000 J. Electrochem. Soc. 147 2897 In summary, highly ordered TiO2 nanotubes and nano- Lakshmi B B, Patrissi C J and Martin C R 1997 Chem. Mater. 9 fibrils have been synthesized by sol–gel chemical method 2544 within the pores of anodic alumina template membrane. Lee S, Jeon C and Park Y 2004 Chem. Mater. 16 4292 The results of SEM and TEM show that the synthesized Lei Y, Zhang L D and Fan J C 2001 Chem. Phys. Lett. 338 nanotubes have a uniform length, diameter and form a 231 highly ordered array and the XRD measurements confirm Livraghi S, Votta A, Paganini M C and Giamello E 2005 Chem. the presence of polycrystalline anatase phase in the TiO2 Commun. 4 498 nanotubes. This method can be employed for obtaining Macak J M, Tsuchiya H and Schmuki P 2005 Angew. Chem. large surface area TiO2 for use in photocatalysis and as Int. Ed. 44 2100 electrodes in solar cells. Maiyalagan T and Viswanathan B 2005 Mater. Chem. Phys. 93 291 Martin C R 1996 Chem. Mater. 8 1739 Acknowledgements Martin C R, Parthasarathy R and Menon V 1993 Synth. Met. 55 1165 We thank the Council of Scientific and Industrial Research Poulios I, Kositzi M and Kouras A 1998 J. Photochem. Photo- (CSIR), India, for a senior research fellowship to one of biol. A: Chem. 115 175 the authors (TM). Quan X, Yang S, Ruan X and Zhao H 2005 Environ. Sci. Tech- nol. 39 3770 Sander M S, Cote M J, Gu W, Kile B M and Tripp C P 2004 References Adv. Mater. 16 2052 Takagahara T and Takeda K 1992 Phys. Rev. B46 15578 Adachi M, Murata Y and Yoshikawa S 2000 Chem. Lett. 8 942 Uchida S, Chiba R, Tomiha M, Masaki N and Shirai M 2002 Adachi M, Okada I, Ngamsinlapasathian S, Murata Y and Electrochemistry 70 418 Yoshikawa S 2002 Electrochemistry 70 449 Varghese O K, Gong D W, Paulose M, Ong K G, Dickey E C Bersani D and Lottici P P 1998 Appl. Phys. Lett. 72 73 and Grimes C A 2003 Adv. Mater. 15 624 Du G H, Chen Q, Che R C, Yuan Z Y and Peng L M 2001 Appl. Zhou Y, Cao L, Zhang F, He B and Li H 2003 J. Electrochem. Phys. Lett. 79 3702 Soc. 150 A1246