Cobalt and sulfur co-doped TiO2 nanostructures with enhanced photo-response properties for photocatalyst

2017 ◽  
Vol 10 (05) ◽  
pp. 1750061 ◽  
Author(s):  
Qiu Jin ◽  
Chaoyin Nie ◽  
Qianqian Shen ◽  
Yusheng Xu ◽  
Yanzhong Nie

Cobalt (Co) and sulfur (S) co-doped titanium dioxide (TiO2) catalysts were synthesized via sol–gel method. The structure of TiO2was characterized by X-ray diffraction (XRD) and transmission electron microscope (TEM). The valence states of elements were studied by X-ray photoelectron spectroscopy (XPS), and the optical-absorption properties of the catalysts were tested using the ultraviolet–visible (UV–Vis) spectrophotometer. The results showed that the grain sizes of Co and S co-doped TiO2 decreased with the increase of Co and S doping concentration within a certain range, and then the catalysts had obvious red shift on the absorption of visible light. Sample (2%Co–5%S–TiO2) showed excellent light absorption characteristics and the photo-response threshold increased significantly to about 760[Formula: see text]nm. Also, the further degradation test under visible light shows the 2%Co–5%S-TiO2 sample exhibit apparently improved degradation efficiency for Rhodamine B compared to the undoped one.

2021 ◽  
Vol 11 (5) ◽  
pp. 706-716
Author(s):  
Nada D. Al-Khthami ◽  
Tariq Altalhi ◽  
Mohammed Alsawat ◽  
Mohamed S. Amin ◽  
Yousef G. Alghamdi ◽  
...  

Different organic pollutants have been remediated photo catalytically by applying perovskite photocatalysts. Atrazine (ATR) is a pesticide commonly detected as a pollutant in drinking, surface and ground water. Herein, FeYO3@rGO heterojunction was synthesized and applied for photooxidation decomposition of ATR. First, FeYO 3nanoparticles (NPs) were prepared via routine sol-gel. After that, FeYO3 NPs were successfully incorporated with different percentages (5, 10, 15 and 20 wt.%) of reduced graphene oxide (rGO) in the synthesis of novel FeYO3@rGO photocatalyst. Morphological, structural, surface, optoelectrical and optical characteristics of constructed materials were identified via X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Transmission electron microscopy (TEM), adsorption/desorption isotherms, diffusive reflectance (DR) spectra, and photoluminescence response (PL). Furthermore, photocatalytic achievement of the constructed materials was evaluated via photooxidative degradation of ATR. Various investigations affirmed the usefulness of rGO incorporation on the advancement of formed photocatalysts. Actually, novel nanocomposite containing rGO (15 wt.%) possessed diminished bandgap energy, as well as magnified visible light absorption. Furthermore, such nanocomposite presented exceptional photocatalytic achievement when exposed to visible light as ATR was perfectly photooxidized over finite amount (1.6 g · L-1) from the optimized photocatalyst when illuminated for 30 min. The advanced photocatalytic performance of constructed heterojunctions could be accredited mainly to depressed recombination amid induced charges. The constructed FeYO3@rGO nanocomposite is labelled as efficient photocatalyst for remediation of herbicides from aquatic environments.


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.


Nanomaterials ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1671 ◽  
Author(s):  
Weike Zhang ◽  
Yanrong Zhang ◽  
Kai Yang ◽  
Yanqing Yang ◽  
Jia Jia ◽  
...  

A silicon dioxide/carbon nano onions/titanium dioxide (SiO2/CNOs/TiO2) composite was synthesized by a simple sol-gel method and characterized by the methods of X-ray diffraction (XRD), scanning electronic microscope (SEM), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), Fourier transform infrared (FTIR), thermogravimetric analysis (TG), differential scanning calorimeter (DSC) and UV-Vis diffuse reflectance spectra (UV-Vis DRS). In this work, the photocatalytic activity of the SiO2/CNOs/TiO2 photocatalyst was assessed by testing the degradation rate of Rhodamine B (RhB) under visible light. The results indicated that the samples exhibited the best photocatalytic activity when the composite consisted of 3% CNOs and the optimum dosage of SiO2/CNOs/TiO2(3%) was 1.5 g/L as evidenced by the highest RhB degradation rate (96%). The SiO2/CNOs/TiO2 composite greatly improved the quantum efficiency of TiO2. This work provides a new option for the modification of subsequent nanocomposite oxide nanoparticles.


2019 ◽  
Vol 12 (04) ◽  
pp. 1950045 ◽  
Author(s):  
Lin Zhao ◽  
Yanzhao Xie ◽  
Qiuyu Lin ◽  
Rongze Zheng ◽  
Yong Diao

A series of composite catalysts of C, N and P co-doped TiO2 were prepared by sol-gel method, using a biomass (soluble starch) dopant. The samples were characterized by field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), fourier transform infrared (FTIR) spectroscopy. The results show that TiO2 is co-doped with C, N and P by one step. The resulting composite exhibited higher specific surface area, wider visible-light absorption band with respect to the pure TiO2. The sample calcined at 400∘C for 2[Formula: see text]h with a doping amount of 6[Formula: see text]g soluble starch showed the best electrochemical performance. The C, N and P co-doped TiO2 was also used for the degradation of methylene blue (MB) and degradation ratio was up to 98% in 80[Formula: see text]min under visible light irradiation.


2017 ◽  
Vol 76 (6) ◽  
pp. 1436-1446 ◽  
Author(s):  
Chenmo Wei ◽  
Jing Zhang ◽  
Yongli Zhang ◽  
Gucheng Zhang ◽  
Peng Zhou ◽  
...  

Sulfate radical-based advanced oxidation processes have had considerable attention due to the highly oxidizing function of sulfate radicals (SO4−·) resulting in acceleration of organic pollutants degradation in aqueous environments. A Co-Ni mixed oxide nanocatalyst, which was prepared by the sol-gel method, was employed to activate peroxymonosulfate (PMS, HSO5−) to produce SO4−· with Acid Orange 7 (AO7) selected as a radical probe. The catalyst was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). The characterization results indicated that the ingredient of the catalyst had been changed and the amount of surface hydroxyl increased significantly with the addition of Ni. Therefore, it proved that Co-NiOx catalyst was more effective than CoOx to activate PMS. Moreover, ultrasound (US) can increase the degradation rate of AO7 and US/Co-NiOx/PMS system. This study also focused on some synthesis parameters and the system reached the maximum efficiency under the condition when [PMS] = 0.4 mM, [catalyst] = 0.28 g/L, Pus = 200 W. The AO7 removal in these systems follows first order kinetics. Last but not least, quenching studies was conducted which indicated that the amount of hydroxyl radicals (·OH) increases with the increase of initial pH and SO4−· was the primary reactive oxidant for AO7 degradation.


2021 ◽  
Author(s):  
Yu Fan ◽  
Yan-ning Yang ◽  
Chen Ding

Abstract The g-C3N4 nanosheet was prepared by calcination method, the MoS2 nanosheet was prepared by hydrothermal method. The g-C3N4/MoS2 composites were prepared by ultrasonic composite in anhydrous ethanol. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible spectroscopy (UV-Vis), and photoluminescence (PL) techniques were used to characterize the materials. The photocatalytic degradation of Rhodamine B (Rh B) by g-C3N4/MoS2 composites with different mass ratios was investigated under visible light. The results show that a small amount of MoS2 combined with g-C3N4 can significantly improve photocatalytic activity. The g-C3N4/MoS2 composite with a mass ratio of 1:8 has the highest photocatalytic activity, and the degradation rate of Rh B increases from 50% to 99.6%. The main reason is that MoS2 and g-C3N4 have a matching band structure. The separation rate of photogenerated electron-hole pairs is enhanced. So the g-C3N4/MoS2 composite can improve the photocatalytic activity. The photocatalytic mechanism was proposed through the active matter capture experiment.


2013 ◽  
Vol 745-746 ◽  
pp. 685-689
Author(s):  
Jun Yan Wu ◽  
Fei Chen ◽  
Qiang Shen ◽  
Lian Meng Zhang

Antimony-doped tin oxide (ATO) nanoparticles with controlled doping level were prepared by a nonaqueous solution route, using alcohol as the solvent, citric acid as an agent, tin (IV) tetrachloride as tin source and antimony (III) chlorideas as antimony sources. As-synthesized samples were characterized by Thermogravimetric analysis (TGA), powder X-ray diffraction (XRD), transmission electron micrographs (TEM), N2 adsorption-desorption isotherms, and X-ray photoelectron spectroscopy (XPS). The results showed that the content of citric acid was the most important processing parameter which was largely governing the reaction course and the complete incorporation of Sb. When the citric acid to metal mol ratio was 2, the particles were the highly crystallized ATO nanoparticles of about 20nm and the Sb atoms were indeed incorporated into the SnO2 crystal structure (cassiterite SnO2).


2011 ◽  
Vol 55-57 ◽  
pp. 1506-1510 ◽  
Author(s):  
Jing Wei ◽  
Xin Tan ◽  
Tao Yu ◽  
Lin Zhao

A series of Y/TiO2nanoparticles (NPs) were synthesized via sol-gel method. The crystal structures, morphologies and chemical properties were characterized using X-ray diffraction (XRD), high resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS). We investigated the effects of different doping amounts of Y on the reaction of CO2photoreduction. The results shown that 0.1 wt.%Y/TiO2(0.1YT) performed the highest photocatalytic activity, which yielded 384.62 µmol/g∙cat. formaldehyde after 6 h of UV illumination.


Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 355
Author(s):  
Ksenia O. Potapenko ◽  
Anna Yu. Kurenkova ◽  
Andrey V. Bukhtiyarov ◽  
Evgeny Yu. Gerasimov ◽  
Svetlana V. Cherepanova ◽  
...  

A series of solid solutions of cadmium and manganese sulfides, Cd1−xMnxS (x = 0–0.35), and composite photocatalysts, CdS-β-Mn3O4-MnOOH, were synthesized by precipitation with sodium sulfide from soluble cadmium and manganese salts with further hydrothermal treatment at 120 °C. The obtained photocatalysts were studied by the X-ray diffraction method (XRD), UV-vis diffuse reflectance spectroscopy, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and N2 low temperature adsorption. The photocatalysts were tested in hydrogen production using a Na2S/Na2SO3 aqueous solution under visible light (λ = 450 nm). It was shown for the first time that both kinds of photocatalysts possess high activity in hydrogen evolution under visible light. The solid solution Cd0.65Mn0.35S has an enhanced photocatalytic activity due to its valence and conduction band position tuning, whereas the CdS-β-Mn3O4-MnOOH (40–60 at% Mn) samples were active due to ternary heterojunction formation. Further, the composite CdS-β-Mn3O4-MnOOH photocatalyst had much higher stability in comparison to the Cd0.65Mn0.35S solid solution. The highest activity was 600 mmol g−1 h−1, and apparent quantum efficiency of 2.9% (λ = 450 nm) was possessed by the sample of CdS-β-Mn3O4-MnOOH (40 at% Mn).


2013 ◽  
Vol 690-693 ◽  
pp. 511-517 ◽  
Author(s):  
Xi Kang ◽  
Jing Qi ◽  
Long Ye ◽  
Hong You ◽  
Li Jiang Hu

Ag⁄N co–doped TiO2 nanotube arrays (TNTs) were prepared by anodic oxidation, a certain amount of Ag deposited on the surface of TNTs by photodeposition and annealing post-treatment. The doped TNTs were characterized by field-emission scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV–vis diffusion reflection spectroscopy (UV–vis DRS). The photocatalytic activities of the prepared TiO2 were evaluated by degrading rhodamine B (RhB) under visible light irradiation (≤ 420 nm). The photocatalytic degradation efficiency of the Ag/N-TNTs obtained for the degradation of RhB are 0.32 times, 0.6 times and 1.86 times higher than that of TNTs, N–TNTs, AgTNTs, respectively.


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