scholarly journals Preparation and Characterization of(I2)nSensitized NanoporousTiO2with Enhanced Photocatalytic Activity under Visible-Light Irradiation

2012 ◽  
Vol 2012 ◽  
pp. 1-8
Author(s):  
Juzheng Zhang ◽  
Xin Liu ◽  
Shanmin Gao ◽  
Quanwen Liu ◽  
Baibiao Huang ◽  
...  

A yellow/brown powder of(I2)nsensitized nanoporous TiO2was obtained via an hydrolysis with TiCl4and iodine hydrosol as raw material. I2nanoparticles in the hydrosol were used as seeds to initiate the nucleation of a precursory TiO2shell. The hybridized jumbles were further calcinated at different temperatures. The structure, crystallinity, morphology, and other physical-chemical properties of the samples are characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), N2adsorption-desorption isotherms measurements, and UV-vis diffuse reflectance spectroscopy (DRS). The formation mechanism of these(I2)nsensitized nanoporous TiO2is discussed. Methylene blue solutions were used as model wastewater to evaluate the visible light photocatalytic activity of the samples. The results indicate that iodine can exist even in high-temperature calcination for iodine being encapsulated in the nanocavities inside TiO2. The degradation of methylene blue (MB) accorded with the first-order reaction model.

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Wang Ling-Li ◽  
Ma Wan-Hong ◽  
Wang Shu-Lian ◽  
Zhang Yu ◽  
Jia Man-Ke ◽  
...  

BiOBr nanoplates, marked asα-BiOBr andβ-BiOBr, were synthesized via hydrothermal method using cetylpyridinium bromide (CPB) and NaBr as reactants, respectively. X-Ray Diffraction (XRD), transmission electron microscope (TEM), N2adsorption/desorption, UV-visible diffuse reflectance spectroscopy (UV-Vis DRS), and cyclic voltammetry (CV) were employed to characterize the obtained BiOBr. The results showed thatα-BiOBr andβ-BiOBr can absorb visible light and both the band gaps of them were about 2.76 eV. Under visible light irradiation, the photodegradation of organic dye sulforhodamine (SRB) and salicylic acid (SA) usingα-BiOBr andβ-BiOBr as the catalysts was carried out. The reaction kinetic constants of the degradation of SRB byα-BiOBr andβ-BiOBr were 0.00602 min−1and 0.0047 min−1, respectively, which indicated that the photocatalytic activity ofα-BiOBr was higher than that ofβ-BiOBr. The UV-Vis DRS and total organic carbon (TOC) were also monitored, and the TOC removal rate ofα-BiOBr andβ-BiOBr was 86% and 48%, respectively. At the same time, hydrogen peroxide (H2O2) and active radicals were measured and analyzed, which showed that the main active species wasOH∙during the photocatalytic reaction.


2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Weicheng Xu ◽  
Guangyin Zhou ◽  
Jianzhang Fang ◽  
Zhang Liu ◽  
YunFang Chen ◽  
...  

Praseodymium doped Bi2Sn2O7(BSO), as a visible-light responsive photocatalyst, was prepared by a hydrothermal method with different dopant contents. The as-prepared photocatalysts were investigated by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), N2adsorption-desorption isotherm, X-ray photoelectron spectroscopy analysis (XPS), and UV-Vis diffuse reflectance spectroscopy (DRS). The photocatalytic activity of prepared catalysts was evaluated by the degradation of Rhodamine Bextra (RhB) and 2,4-dichlorophenol (2,4-DCP) in aqueous solution under visible light irradiation. It was found that Pr doping inhibited the growth of crystalline size and the as-prepared materials were small in size (10–20 nm). In our experiments, Pr-doped BSO samples exhibited enhanced visible-light photocatalytic activity compared to the undoped BSO, and the optimal dopant amount of Pr was 1.0 mol% for the best photocatalytic activity. On the basis of the calculated PL spectra, the mechanism of enhanced photocatalytic activity has been discussed.


2016 ◽  
Vol 69 (1) ◽  
pp. 119 ◽  
Author(s):  
Li Lin ◽  
Ya Wang ◽  
Manhong Huang ◽  
Donghui Chen

Three-dimensional (3D) BiOBr/BiOI hierarchical microspheres were successfully fabricated on the surface of fly ash cenospheres (FACs) via a facile one-pot solvothermal method for the first time. The as-prepared samples were characterized by XRD, SEM, energy-dispersive X-ray spectroscopy, UV–visible diffuse reflectance spectroscopy, and high-resolution transmission electron microscopy. The results indicated that the loaded hierarchical microspheres exhibited a uniform distribution, and some aggregation was observed. These well-dispersed hierarchical microspheres were composed of 2D nanosheets, which possess heterojunction structures. Based on the photodegradation tests examining the removal of rhodamine B from water under visible light irradiation (λ > 420 nm), the photocatalytic activity of BiOB/BiOI/FACs was superior to that of BiOBr/FACs and BiOI/FACs. A proposed mechanism for the enhanced photocatalytic activity displayed by BiOB/BiOI/FACs is discussed.


2011 ◽  
Vol 335-336 ◽  
pp. 1385-1390 ◽  
Author(s):  
Shuo Wiei Zhao ◽  
Hui Xu ◽  
Hua Ming Li ◽  
Yuan Guo Xu

In order to improve the photocatalytic activity, Co was successfully loaded into Ag3VO4 by using impregnation process. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS) and diffuse reflectance spectroscopy (DRS). The XRD and SEM–EDS analyses revealed that Co ion was dispersed on Ag3VO4. The DRS results indicated that the absorption edge of the Co–Ag3VO4 catalyst shifted to longer wavelength. The enhanced photocatalytic activity of Co–Ag3VO4 for Methylene Blue(MB) dye degradation under visible light irradiation was due to its wider absorption edge and higher separation rate of photo-generated electron and holes. In the experimental conditions, it is demonstrated that the MB was effectively degraded by more than 95% within 40 min when the Co–Ag3VO4 catalyst was calcined at 300°C with 1 wt.% Co content.


2013 ◽  
Vol 448-453 ◽  
pp. 169-173
Author(s):  
Chun Yan Yan ◽  
Wen Tao Yi

Pure and F, Fe-codoped TiO2 were prepared by sol-hydrothermal process, in which titanium (IV) n-butoxide, Fe (NO3)2·6H2O and NH4F were used as precursors. And the samples were characterized by X-ray diffraction (XRD), UV-vis diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), and N2 adsorption-desorption method. The results showed that the F, Fe-codoped samples were principally single-phase anatase structures, and the particles possessed higher BET area than that of pure TiO2. The photocatalytic activity and reusability of the catalysts under UV light (365nm) was investigated with neutral red as the model compound. The results showed that F (2.0%), Fe (4.0%) codoped TiO2 had the highest photocatalytic activity among all as-prepared samples. The kinetic study showed that this photocatalytic process coincided with the Langmuir-Hinshelwood (L-H) pseudo first order reaction model.


2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
Jing Yan ◽  
Xiaojuan Li ◽  
Bo Jin ◽  
Min Zeng ◽  
Rufang Peng

A series of TiO2, TiO2/Pd, and TiO2/PdO hollow sphere photocatalysts was successfully prepared via a combination of hydrothermal, sol-immobilization, and calcination methods. The structure and optical properties of the as-prepared samples were characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Telleranalysis, Barrett-Joyner-Halenda measurement, and UV-Vis diffuse reflectance spectroscopy. The photocatalysis efficiencies of all samples were evaluated through the photocatalytic degradation of rhodamine B under visible light irradiation. Results indicated that TiO2/PdO demonstrated a higher photocatalytic activity (the photocatalytic degradation efficiency could reach up to 100% within 40 min) than the other samples and could maintain a stable photocatalytic degradation efficiency for at least four cycles. Finally, after using different scavengers, superoxide and hydroxyl radicals were identified as the primary active species for the effectiveness of the TiO2/PdO photocatalyst.


2021 ◽  
Vol 11 (1) ◽  
pp. xx-xx
Author(s):  
Nga Phan To ◽  
Lien Nguyen Hong ◽  
Tuyen Le Van ◽  
Nhan Phan Chi ◽  
Huyen Phan Thanh

Porous LaFeO3 were synthesised by nanocasting method using mesoporous silica (SBA-15) as a hard template and used as a visible-light-driven photocatalyst. The as-synthesised LaFeO3 photocatalyst were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray Diffraction (XRD), N2 adsorption-desorption, and Ultraviolet–Visible Diffuse Reflectance Spectroscopy (UV-vis DRS). The photo-Fenton catalytic activities of porous LaFeO3 were investigated for the degradation of oily-containing wastewater. The results showed that porous LaFeO3 had better photo-Fenton catalytic activity under visilbe light irradiation than pure LaFeO3. The remarkable improvement photo-Fenton catalytic activity of porous LaFeO3 material could be attributed to the synergistic effect of adsorption and visible light photo-Fenton processes thanks to its porous structure.


2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Qianzhi Xu ◽  
Xiuying Wang ◽  
Xiaoli Dong ◽  
Chun Ma ◽  
Xiufang Zhang ◽  
...  

S/Zn codoped TiO2nanomaterials were synthesized by a sol-gel method. X-ray diffraction, UV-vis diffuse reflectance spectroscopy, transmission electron microscopy, photoluminescence spectroscopy, and X-ray photoelectron spectroscopy were used to characterize the morphology, structure, and optical properties of the prepared samples. The introduction of Zn and S resulted in significant red shift of absorption edge for TiO2-based nanomaterials. The photocatalytic activity was evaluated by degrading reactive brilliant red X-3B solution under simulated sunlight irradiation. The results showed S/Zn codoped TiO2exhibited higher photocatalytic activity than pure TiO2and commercial P25, due to the photosynergistic effect of obvious visible light absorption, efficient separation of photoinduced charge carriers, and large surface area. Moreover, the content of Zn and S in the composites played important roles in photocatalytic activity of TiO2-based nanomaterials.


2011 ◽  
Vol 197-198 ◽  
pp. 786-789 ◽  
Author(s):  
Rui Liu ◽  
Wein Duo Yang ◽  
Hui Ju Chueng

TiO2 nanotubes were synthesized using TiO2 powder as raw material from a hydrothermal method. It was observed that the sample prepared at 130°C and calcined at 450°C only anatase formed, but the sample calcined at 800°C, both anatase and rutile formed. The obtained TiO2 nanotubes prepared at a hydrothermal temperature of 130°C and calcined at 450°C have a greater surface area of 356.8m2/g. Moreover, the TiO2 nanotubes demonstrate the photocatalytic degradation of methylene blue solution effectively by exposing the nanotubes in aqueous solution under visible light.


2013 ◽  
Vol 699 ◽  
pp. 708-711 ◽  
Author(s):  
Ling Xiang Jia ◽  
Jun Yue Zhu ◽  
Ting Ting Lin ◽  
Zhen Jiang ◽  
Chao Wan Tang ◽  
...  

Using Yb(NO3)3•6H2O and Fe(NO3)3•9H2O as raw material, the YbFeO3 nanoparticles were synthesized by microwave assisted method. The YbFeO3 nanoparticles were characterized by thermogravimetry and differential thermal analysis (TG-DTA), powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and UV-visible diffuse reflectance spectroscopy (DRS). It was found that the prepared YbFeO3 show an average grain size of 80 nm in diameter, and strong visible-light absorption with absorption onset of 608 nm, indicating a narrow optical band gap of 2.04eV. Consequently, the YbFeO3 nanoparticles show high photocatalytic activity for decomposition of methylene blue under visible-light irradiation.


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