Persistent deNOx Ability of CaAl2O4:(Eu, Nd)/TiO2-xN y Luminescent Photocatalyst
© Li et al. 2010
Received: 3 July 2010
Accepted: 6 August 2010
Published: 20 August 2010
CaAl2O4:(Eu, Nd)/TiO2-xN y composite luminescent photocatalyst was successfully synthesized by a simple planetary ball milling process. Improvement of photocatalytic deNOx ability of TiO2-xN y , together with the persistent photocatalytic activity for the decomposition of NO after turning off the light were realized, by coupling TiO2-xN y with long afterglow phosphor, CaAl2O4:(Eu, Nd). The novel persistent photocatalytic behavior was related to the overlap between the absorption wavelength of TiO2-xN y and the emission wavelength of the CaAl2O4:(Eu, Nd). It was found that CaAl2O4:(Eu, Nd)/TiO2-xN y composites provided the luminescence to persist photocatalytic reaction for more than 3 h after turning off the light.
CaAl2O4:(Eu, Nd)/TiO2-xN y composite luminescent photocatalyst with persistent deNOx activity after turningoff the light was successfully synthesized by a simple planetary ball milling process. Thenovel persistent photocatalytic behavior was related to the overlap between the absorptionwavelength of TiO2-xN y and the emission wavelengthof the CaAl2O4:(Eu, Nd).
KeywordsLuminescent photocatalyst deNOx Composite
Hot photocatalytic research attention has been focused on titania (TiO2), because of its chemical stability , excellent photocatalytic activity  and low cost. However, since titania has large band gap energy of about 3.2 eV corresponding to the wavelength of 387.5 nm, it is active under irradiation of only UV light less than 400 nm of wavelength. Since the content of UV light in sun light is less than 5% , the development of high performance visible light responsive photocatalyst which can use main part of sunlight or indoor light is highly desired [4–7]. Various modifications have been devoted to TiO2 in extending the absorption edge into visible light and enhancing the photocatalytic activity [8–13], and one of them is doping TiO2 with nitrogen because the band gap of titania could be narrowed by doping with nitrogen ion since the valence band of N2p band locates above O2p band .
The aluminate long afterglow phosphor (CaAl2O4:(Eu, Nd)) has characteristics of high luminescent brightness around 440 nm of wavelength, long afterglow time, good chemical stability and low toxicity [15, 16]. Therefore, the coupling of TiO2 with CaAl2O4:(Eu, Nd) was expected to prolong the photocatalytic activity even after turning off the light by using the persistent emitting luminescence of the long afterglow phosphor as a light source of TiO2 photocatalyst. However, TiO2 possessing a large bandgap energy ca. 3.2 eV can not be effectively excited by the visible light luminescence of 440 nm from CaAl2O4:(Eu, Nd). Recently, the combinations of TiO2 photocatalyst with other long afterglow materials such as BaAl2O4:(Eu, Dy)  and Sr4Al14O25:(Nd, Eu)  were also reported. However, the emission wavelengths of these phosphors around 495 nm  and 488 nm, respectively, are also too long to excite TiO2 photocatalyst. Actually, it was reported that BaAl2O4:(Eu, Dy)/TiO2 and Sr4Al14O25:(Nd, Eu)/TiO2 coupled compounds showed photocatalytic performance for the oxidation of gaseous benzene and RhB solution, respectively, under UV light irradiation, but no noticeable degradation was observed after turning off the light .
In the present research, we firstly provided a direct evidence for such persistent photocatalytic deNOx system, by the coupling of long afterglow phosphor CaAl2O4:(Eu, Nd) with brookite type nitrogen-doped titania (TiO2-xN y ), which was produced by a hydrothermal reaction [20, 21]. Brookite phase nitrogen-doped titania possessed band gap of ca. 2.34 eV and showed excellent photocatalytic deNOx ability even under visible light irradiation of wavelength >510 nm . In comparison with anatase and rutile phase nitrogen-doped titania, brookite phase nitrogen-doped titania photocatalyst has seldom been reported, however, it is expected to be a potential novel photocatalyst.
CaAl2O4:(Eu, Nd) powders with the particle size of 13.9 μm (D50) were purchased from Nemoto Co. Ltd. Other chemicals were purchased from Kanto Chem. Co. Inc. Japan and were used as received without further purification. TiO2-xN y nanoparticles with brookite phase were synthesized by hydrothermal reaction using TiCl3 as titanium source and HMT (hexamethylenetetramine) as nitrogen source at pH 7 and 190°C for 2 h . Brookite phase TiO2-xN y nanoparticles were mixed with desired amounts of CaAl2O4:(Eu, Nd) powders followed by planetary ball milling at 200 rpm for 20 min. The mass ratio of CaAl2O4:(Eu, Nd):TiO2-xN y or P25 TiO2 was kept at 3/2. For comparison, undoped titania (Degussa P25) was also coupled with CaAl2O4:(Eu, Nd) by the completely same manner. The UV–vis diffuse reflectance spectra were obtained using a UV–vis spectrophotometer (Shimadazu, UV-2450). The time dependence of photoluminescence spectra and intensity were measured by a spectrofluorophotometer (Shimadzu RF-5300P).
The photocatalytic activity for nitrogen monoxide destruction was determined by measuring the concentration of NO gas at the outlet of the reactor (373 cm3 of internal volume) during the photo-irradiation of a constantly flowing 1 ppm NO/50 vol% air mixed (balance N2) gas (200 cm3min-1). 0.16 g of CaAl2O4:(Eu, Nd)/TiO2-xN y , TiO2-xN y or CaAl2O4:(Eu, Nd)/P25 photocatalyst material was placed in the same area of a hollow of 40 × 30 × 0.5 mm on a glass holder plate and set in the bottom center of the reactor. A 450 W high-pressure mercury lamp was used as the light source, where the inner cell had water flowing through a Pyrex jacket between the mercury lamp and the reactor. The light of λ < 290 nm wavelength was cut off by Pyrex glass [20–22]. Before light irradiation, the NO gas was continuously flowed through the reactor for 10 min to achieve adsorption balance. Then, the light was irradiated for 30 min to realize the steady status of the photocatalytic NO degradation and let long afterglow phosphor CaAl2O4:(Eu, Nd) absorb enough exciting energy. After that, the light was switched off, while the NO gas was flowed further for 3 h.
Results and Discussion
The characterization system used in the present research was similar to that of the Japanese Industrial Standard which was established at the beginning of 2004 . In this JIS standard, it is recommended that the photocatalytic activity of photocatalyst should be characterized by measuring the decrease in the concentration of NO at the outlet of a continuous reactor. One ppm of NO gas with a flow rate of 3.0 dm3/min is introduced to a reactor then irradiated by a lamp with light wavelength of 300–400 nm. The mechanism of photocatalytic deNOx had been researched carefully by M.Anpo . During the deNOx photocatalytic reaction, the nitrogen monoxide reacts with these reactive oxygen radicals, molecular oxygen, and very small amount of water in air to produce HNO2 or HNO3. It was confirmed that about 20% of nitrogen monoxide was decomposed to nitrogen and oxygen directly  Because a continuous reaction system was utilized in the deNOx characterization [20, 21], after turning off the light, it took about 10 min (total 50 min from the start of the characterization) to achieve diffusion balance and return to the initial NO concentration.
The degree of NO destruction by TiO2-xN y and CaAl2O4:(Eu, Nd)/undoped TiO2 (P25) immediately decreased after turning off the light, however, as-expected, CaAl2O4:(Eu, Nd)/TiO2-xN y retained the NO destruction ability for about 3 h. Since the decay profile of the NO destruction degree of CaAl2O4:(Eu, Nd)/TiO2-xN y was similar to the emission decay profile shown in Figure 2, it might be concluded that the emission by CaAl2O4:(Eu, Nd) was used as a light source to excite TiO2-xN y photocatalyst. It was also confirmed that CaAl2O4:(Eu, Nd)/TiO2-xN y composite consisted of 40% brookite TiO2-xN y (mass ratio of CaAl2O4:(Eu, Nd)/TiO2-xN y = 3/2) possessed the best performance after turning off the light.
Present results indicate that the combination of CaAl2O4:(Eu, Nd) and TiO2-xN y is a key point to realize the persistent catalytic activity even after turning off the light. In addition, it is well known that the combination of the two different band structure compounds may cause the charge transfer on the photocatalyst surface to depress the recombination of photo-induced electrons and holes, which is helpful for the improvement of photocatalytic activity [27, 28]. This novel system provides a possibility of atmosphere purification not only in day time, but also in night time. A promising strategy involves coupling of visible light induced photocatalyst with long afterglow phosphor might be established. It is a new concept for the photocatalyst synthesis and applications.
A novel CaAl2O4:(Eu, Nd)/TiO2-xN y composite luminescent photocatalyst was successfully synthesized. Not only the UV-light induced photocatalytic activity, but also the persistent catalytic ability after turning off the light was realized successfully. The CaAl2O4:(Eu, Nd)/TiO2-xN y composite photocatalyst provided enough luminescence intensity for the photocatalytic reaction for more than 3 h after turning off the light source.
This research was carried out as one of the projects under the Special Education and Research Expenses on "Post-Silicon Materials and Devices Research Alliance", supported by Grant-in-Aid for Science Research (No. 20360293 & No. 22651022).
- Li Y, Sun X, Li H, Wang S, Wei Y: Powder Technol. 2009, 194: 149–152. 10.1016/j.powtec.2009.03.041View ArticleGoogle Scholar
- Kim D, Kwak S: Appl Catal A-Gen. 2007, 323: 110–118. 10.1016/j.apcata.2007.02.010View ArticleGoogle Scholar
- Tafen D, Wang J, Wu N, Lewis J: Appl Phys Lett. 2009, 94: 093101. 10.1063/1.3093820View ArticleGoogle Scholar
- Yin S, Zhang Q, Saito F, Sato T: Chem Lett. 2003, 32: 358–359. 10.1246/cl.2003.358View ArticleGoogle Scholar
- Yin S, Yamaki H, Komatsu M, Zhang Q, Wang J, Tang Q, Saito F, Sato T: J Mater Chem. 2003, 13: 2996–3001. 10.1039/b309217hView ArticleGoogle Scholar
- Wang J, Yin S, Zhang Q, Saito F, Sato T: J Mater Chem. 2003, 13: 2348–2352. 10.1039/b303420hView ArticleGoogle Scholar
- Aita Y, Komatsu M, Yin S, Sato T: J Solid State Chem. 2004, 177: 3235–3238. 10.1016/j.jssc.2004.04.048View ArticleGoogle Scholar
- Moon J, Yun C, Chung K, Kang M, Yi J: Catal Today. 2003, 87: 77–86. 10.1016/j.cattod.2003.10.009View ArticleGoogle Scholar
- Cho Y, Kyung H, Choi W: Appl Catal B:Environ. 2004, 52: 23–32. 10.1016/j.apcatb.2004.03.013View ArticleGoogle Scholar
- Kaur S, Singh V: Ultrason Sonochem. 2007, 14: 531–537. 10.1016/j.ultsonch.2006.09.015View ArticleGoogle Scholar
- Liu S, Chen X: J Hazard Mater. 2008, 152: 48–55. 10.1016/j.jhazmat.2007.06.062View ArticleGoogle Scholar
- Chen F, Zou W, Qu W, Zhang J: Catal Commun. 2009, 10: 1510–1513. 10.1016/j.catcom.2009.04.005View ArticleGoogle Scholar
- Jirapat A, Puangrat K, Supapan S: J Hazard Mater. 2009, 168: 253–261. 10.1016/j.jhazmat.2009.02.036View ArticleGoogle Scholar
- Asahi R, Morikawa T, Ohwaki T, Aoki K, Tage Y: Science. 2001, 293: 269–271. 10.1126/science.1061051View ArticleGoogle Scholar
- Chang C, Xu J, Jiang L, Mao D, Ying W: Mater Chem Phys. 2006, 98: 509–513. 10.1016/j.matchemphys.2005.09.069View ArticleGoogle Scholar
- Zhao C, Chen D: Mater Lett. 2007, 61: 3673–3675. 10.1016/j.matlet.2006.12.015View ArticleGoogle Scholar
- Li S, Wang W, Chen Y, Zhang L, Guo J, Gong M: Catal Commun. 2009, 10: 1048–1051. 10.1016/j.catcom.2008.12.064View ArticleGoogle Scholar
- Zhang J, Pan F, Hao W, Ge Q, Wang T: Appl Phys Lett. 2004, 85: 5778–5780. 10.1063/1.1833554View ArticleGoogle Scholar
- Chen X, Ma C, Li X, Shi C, Li X, Lu D: J Phys Chem C. 2009, 113: 2685–2689. 10.1021/jp806375pView ArticleGoogle Scholar
- Yin S, Aita Y, Komatsu M, Wang J, Tang Q, Sato T: J Mater Chem. 2005, 15: 674–682. 10.1039/b413377cView ArticleGoogle Scholar
- Yin S, Hasegawa H, Maeda D, Ishitsuka M, Sato T: J Photoch Photobio A: Chem. 2004, 163: 1–8. 10.1016/S1010-6030(03)00289-2View ArticleGoogle Scholar
- Gateshki M, Yin S, Ren Y, Petkov V: Chem Mater. 2007, 19: 2512–2518. 10.1021/cm0630587View ArticleGoogle Scholar
- Yin S, Zhang P, Liu B, Liu X, Sato T, Xue D, Lee S: Res Chem Intermed. 2010, 36: 69–75. 10.1007/s11164-010-0115-8View ArticleGoogle Scholar
- Yin S, Liu B, Zhang P, Morikawa T, Yamanaka K, Sato T: J Phys Chem C. 2008, 112: 12425–12431. 10.1021/jp803371sView ArticleGoogle Scholar
- Japanese Industrial Standard (JIS R 1701–1:2004(J)), Test method for air purification performance of photocatalytic materials—part 1: removal of nitric oxide, Japanese Standards Association, Established on 20-Jan-2004
- Anpo M: "Recent Development on Visible Light Response Type Photocatalyst". NTS, Tokyo; 2002:9. (ISBN4-86043-009-03)Google Scholar
- Wang J, Xie Y, Zhang Z, Li J, Chen X, Zhang L, Xu R, Zhang X: Sol Energ Mat Sol C. 2009, 93: 355–361. 10.1016/j.solmat.2008.11.017View ArticleGoogle Scholar
- Kamei M, Miyagi T, Ishigaki T: Chem Phys Lett. 2005, 407: 209–212. 10.1016/j.cplett.2005.03.075View ArticleGoogle Scholar
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