Photoinduced Coloration and Photobleaching of Titanium Dioxide in TiO2/Polymer Compositions upon UV- and Visible-Light Excitation of Color Centers' Absorption Bands:  Direct Experimental Evidence Negating Band-Gap Narrowing in Anion-/Cation-Doped TiO2s

2007 ◽  
Vol 111 (42) ◽  
pp. 15277-15288 ◽  
Author(s):  
Vyacheslav N. Kuznetsov ◽  
Nick Serpone
Nanoscale ◽  
2013 ◽  
Vol 5 (14) ◽  
pp. 6323 ◽  
Author(s):  
Shafeer Kalathil ◽  
Mohammad Mansoob Khan ◽  
Sajid Ali Ansari ◽  
Jintae Lee ◽  
Moo Hwan Cho

Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 163 ◽  
Author(s):  
Numair Manzoor ◽  
Muhammad Sadiq ◽  
Muhammad Naqvi ◽  
Umair Sikandar ◽  
Salman Raza Naqvi

Ozone layer depletion is a serious threat due to the extensive release of greenhouse gases. The emission of carbon dioxide (CO2) from fossil fuel combustion is a major reason for global warming. Energy demands and climate change are coupled with each other. CO2is a major gas contributing to global warming; hence, the conversion of CO2 into useful products such as methanol, formic acid, formaldehyde, etc., under visible light is an attractive topic. Challenges associated with the current research include synthesizing a photocatalyst that is driven by visible light with a narrow band gap range between 2.5 and 3.0 eV, the separation of a mixed end product, and the two to three times faster recombination rate of an electron–hole pair compared with separation over yield. The purpose of the current research is to convert CO2 into useful fuel i.e., methanol; the current study focuses on the photocatalytic reduction of CO2into a useful product. This research is based on the profound analysis of published work, which allows the selection of appropriate methods and material for this research. In this study, zinc ferrite (ZnFe2O4) is synthesized via the modified sol–gel method and coupled with titanium dioxide (TiO2). Thereafter, the catalyst is characterized by Fourier transform infrared (FTIR), FE-SEM, UV–Vis, and XRD characterization techniques. UV–Vis illustrates that the synthesized catalyst has a low band gap and utilizes a major portion of visible light irradiation. The XRD pattern was confirmed by the formation of the desired catalyst. FE-SEM illustrated that the size of the catalyst ranges from 50 to 500 nm and BET analysis determined the surface area, which was 2.213 and 6.453 m2/g for ZnFe2O4 and ZnFe2O4/TiO2, respectively. The continuous gas flow photoreactor was used to study the activity of the synthesized catalyst, while titanium dioxide (TiO2) has been coupled with zinc ferrite (ZnFe2O4) under visible light in order to obtain the maximum yield of methanol as a single product and simultaneously avoid the conversion of CO2 into multiple products. The performance of ZnFe2O4/TiO2was mainly assessed through methanol yield with a variable amount of TiO2 over ZnFe2O4 (1:1, 1:2, 2:1, 1:3, and 3:1). The synthesized catalyst recycling ability has been tested up to five cycles. Finally, we concluded that the optimum conditions for maximum yield were found to be a calcination temperature of ZnFe2O4at 900 °C, and optimum yield was at a 1:1 w/w coupling ratio of ZnFe2O4/TiO2. It was observed that due to the enhancement in the electron–hole pair lifetime, the methanol yield at 141.22 μmol/gcat·h over ZnFe2O4/TiO2was found to be 7% higher than the earlier reported data.


2002 ◽  
Vol 81 (3) ◽  
pp. 454-456 ◽  
Author(s):  
T. Umebayashi ◽  
T. Yamaki ◽  
H. Itoh ◽  
K. Asai

Nanomaterials ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 1586 ◽  
Author(s):  
Nawaz ◽  
Kait ◽  
Chia ◽  
Isa ◽  
Huei

In this study, we developed a glycerol-mediated safe and facile method to synthesize colored titania nanoparticles (NPs) via solution route. Our method is considerably effective and greener than other options currently available. Colored titania NPs were produced by hydrolyzing TiCl4 precursor in aqueous solution containing different concentrations of glycerol (0.0, 1.163, 3.834, and 5.815 mol/L) and subsequent calcination at 300 °C for 1 h. Our results highlight firstly that glycerol-mediated synthesis is unlikely to affect the anatase crystalline structure of TiO2, and secondly, that it would lead to coloration, band gap narrowing, and a remarkable bathochromic redshift of the optical response of titania. More importantly, the synthesized colored titania have Ti3+ ions, which, at least in terms of our samples, is the major factor responsible for its coloration. These Ti3+ species could induce mid gap states in the band gap, which significantly improve the visible light absorption capability and photocatalytic performance of the colored titania. The photocatalytic experiments showed that the colored TiO2 NPs prepared in 1.163 mol/L aqueous glycerol solution displayed the best photocatalytic performance. Almost 48.17% of phenolic compounds and 62.18% of color were removed from treated palm oil mill effluent (POME) within 180 min of visible light irradiation.


2001 ◽  
Vol 40 (Part 2, No. 6A) ◽  
pp. L561-L563 ◽  
Author(s):  
Takeshi Morikawa ◽  
Ryoji Asahi ◽  
Takeshi Ohwaki ◽  
Koyu Aoki ◽  
Yasunori Taga

2016 ◽  
Vol 15 (10) ◽  
pp. 1289-1298 ◽  
Author(s):  
V. N. Kuznetsov ◽  
N. I. Glazkova ◽  
R. V. Mikhaylov ◽  
N. Serpone

A novel cryostat-type accessory for a UV/Vis/NIR spectrophotometer was used to determine the relative positions of hole and electron traps within the band-gap of the visible-light-active TiO2 rutile.


2011 ◽  
Vol 11 (3) ◽  
pp. 517-520 ◽  
Author(s):  
Yong Cheol Hong ◽  
Taihyeop Lho ◽  
Bong Ju Lee ◽  
Han Sup Uhm ◽  
O-Pil Kwon ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Hsuan-Chung Wu ◽  
Yu-Siang Lin ◽  
Syuan-Wei Lin

We have systematically studied the photocatalytic mechanisms of nitrogen doping in anatase TiO2using first-principles calculations based on density functional theory, employing HubbardU(8.47 eV) on-site correction. The impurity formation energy, charge density, and electronic structure properties of TiO2supercells containing substitutional nitrogen, interstitial nitrogen, or oxygen vacancies were evaluated to clarify the mechanisms under visible light. According to the formation energy, a substitutional N atom is better formed than an interstitial N atom, and the formation of an oxygen vacancy in N-doped TiO2is easier than that in pure TiO2. The calculated results have shown that a significant band gap narrowing may only occur in heavy nitrogen doping. With light nitrogen doping, the photocatalysis under visible light relies on N-isolated impurity states. Oxygen vacancies existence in N-doped TiO2can improve the photocatalysis in visible light because of a band gap narrowing and n-type donor states. These findings provide a reasonable explanation of the mechanisms of visible light photocatalysis in N-doped TiO2.


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