Hydrothermal synthesis of oxygen functionalized S–P codoped g-C3N4 nanorods with outstanding visible light activity under anoxic conditions

2015 ◽  
Vol 44 (48) ◽  
pp. 20889-20897 ◽  
Author(s):  
Shaozheng Hu ◽  
Lin Ma ◽  
Ying Xie ◽  
Fayun Li ◽  
Zhiping Fan ◽  
...  

S–P codoping and oxygen functionalization influence the physical property, structural property, optical property and band gap energy of g-C3N4, which increases the anoxic RhB photo-degradation constant by ∼13 times.

Chemosphere ◽  
2018 ◽  
Vol 213 ◽  
pp. 481-497 ◽  
Author(s):  
Carlos Alberto Huerta-Aguilar ◽  
Viviana Palos-Barba ◽  
Pandiyan Thangarasu ◽  
Ranjit T. Koodali

2015 ◽  
Vol 1131 ◽  
pp. 237-241 ◽  
Author(s):  
Akkarat Wongkaew ◽  
Chanida Soontornkallapaki ◽  
Naritsara Amhae ◽  
Wichet Lamai

This work aims to study the effect of ZnO containing in TiO2/SiO2 film on the superhydrophilic property after exposed to different types of light. The metal solutions were prepared by sol-gel technique and the film was deposited on glass slides by dip coating method. The parameter studied was the amount of ZnO in the TiO2/SiO2 film. The contents of ZnO were 5-20% weight (increased by 5%). The amount of TiO2 was constant at 30% weight. The obtained films were analyzed for their roughness. The results indicated that film roughness changed according to the ZnO contents. With 5%ZnO in the thin film, the roughness was 0.726 nm while 20%ZnO obtained the roughness of 2.128 nm. UV-Vis spectrophotometer was used for measuring of transmittance of films. At wavelength of 550 nm, the transmittances of each film were greater than 90%. Band gap energy of each film was calculated from the transmittance data. It was found that the average band gap energy of the films was 2.47 eV. Then, the films contained various amount of ZnO were grouped into 2 sets. The first set was exposed to visible light while the other set was exposed to UV. The duration of exposure was 5 hr. Both sets of films after exposed to any light were kept in a black box controlled relative humidity of 85%. Each film was measured contact angle every day. It was found that the 30%TiO2/5%Zn/SiO2 film exposed to visible light showed the best superhydrophilic property. The contact angle was about 0-5° within 3 days. This may due to the reduction of band gap energy in the presence of ZnO in TiO2/SiO2 films to 2.41 eV and the roughness of the film.


2015 ◽  
Vol 68 (7) ◽  
pp. 1129 ◽  
Author(s):  
Pei Wen Koh ◽  
Leny Yuliati ◽  
Hendrik O. Lintang ◽  
Siew Ling Lee

The amount of rutile phase in chromium-doped titania photocatalyst was controlled by varying stirring time (0.5–2.0 h) at room temperature during a sol–gel synthesis process. The percentage of rutile phase increased from 15.1 % to 28.6 % when stirring time was prolonged from 0.5 to 1.5 h. Further increases in the stirring time had negligible effect on the rutile phase amount. As evidenced by analyses using diffuse reflectance ultraviolet–visible spectroscopy and X-ray photoelectron spectroscopy, a sufficient stirring time was important for more substitution of Cr3+ for Ti4+ in the lattice, resulting in anatase-to-rutile phase transformation. The formation of more rutile phase in Cr-doped TiO2 not only reduced the band gap energy, but also induced surface defects that retarded electron–hole recombination. It has been demonstrated that the Cr-doped TiO2 prepared with a stirring time of 1.5 h possessed the lowest band gap energy of 1.89 eV, and hence it achieved the highest photodegradation of methylene blue under visible light irradiation.


2012 ◽  
Vol 622-623 ◽  
pp. 883-888
Author(s):  
Natkritta Boonprakob ◽  
Natda Wetchakun ◽  
Sukon Phanichphant ◽  
Jun Chen ◽  
Burapat Inceesungvorn

Nitrogen-loaded TiO2(N-loaded TiO2), a visible-light driven catalyst, was successfully synthesized by the modified sol-gel method. Physical characterizations of the as-prepared catalysts have been performed by using X-ray diffraction (XRD), Diffuse reflectance UVvisspectroscopy(DRUVvis), Raman spectroscopyand BETspecific surface areain order to obtain structure-activity relationship. Results from Raman spectroscopy clearly suggested that N atoms were incorporated into the TiO2crystal lattice as evidenced by the vibrational peak of TiN in TiO2-xNx.DR UVvis results also suggested that the nitrogen dopant might be responsible for narrowing the TiO2band gap energy, thus resulting in a shift towards the visiblelight region. Photocatalytic activity of N-loaded TiO2evaluated through the degradation of methyl orange (MO)under visible light irradiation (l> 400 nm) indicated that all N-loaded photocatalysts exhibited significantly higher activities than the unloaded TiO2and Degussa P25 TiO2. According to the results from DR UV-vis, XRD and BET studies, the enhanced photoactivity observed from N-loaded samples might be due to a decrease in TiO2band gap energy and/or changes in chemical and physical properties of the materials upon loading with nitrogen.


2020 ◽  
Vol 15 (2) ◽  
pp. 257-263 ◽  
Author(s):  
Yipin Wang ◽  
Rongfang Zhang ◽  
Genliang Han ◽  
Xiaoping Gao

The weak transport charge efficiency and great band gap energy of layered MoS2 hamper its further commercial application. To overcome these deficiencies, we report a simple, controlled and handy hydrothermal process for realizing 2H MoS2 to 1T MoS2 transition with P source. Due to the more conductive ability and larger surface area, P-doped 1T@2H MoS2 nanosheets show an outstanding catalytic activity. Noticeably, P-doped 1T@2H MoS2 nanosheets with narrowed bandgap exhibits a remarkable optical photochemical performance. It fully eliminates 50 ml of 20 mg L–1 RhB in 70 minutes with outstanding recycling and structural stability by using 10 mg catalyst.


2014 ◽  
Vol 925 ◽  
pp. 200-204
Author(s):  
Leny Yuliati ◽  
Melody Kimi ◽  
Mustaffa Shamsuddin

Zinc sulfide (ZnS) has been reported to act as a photocatalyts to reduce water to hydrogen. However, ZnS could not work under visible light irradiation due to its large band gap energy. In order to improve the performance of ZnS, Ga and Sn were doped to ZnS. The series of Ga (0.1),Sn (x)-ZnS with various amounts of Sn (x) was prepared by hydrothermal method. XRD patterns suggested that the addition of Ga might reduce the crystallinity of ZnS, suggesting that Ga might inhibit the crystal growth or agglomeration of ZnS. On the other hand addition of Sn did not much affect the structure of the Ga (0.1)-ZnS. The DR UU-visible spectra confirmed the red shift of the absorption edge with the addition of Ga due to the reduced band gap energy, while the addition of Sn did not much shift the absorption edge of the Ga (0.1)-ZnS to longer wavelength. FESEM images showed that all the prepared samples have sphere-shaped particles and no remarkable change was observed with the addition of Ga or Sn. The photocatalytic hydrogen production from water was carried out at room temperature in the presence of sacrificial agent under visible light irradiation. While ZnS did not show activity under visible light, all the prepared Ga (0.1)-ZnS and Ga (0.1),Sn (x)-ZnS samples exhibited photocatalytic activity for hydrogen production. The highest hydrogen production was achieved on Ga (0.1),Sn (0.01)-ZnS, which activity was ca. three times higher than that of the single doped Ga (0.1)-ZnS. This study clearly showed that Sn acted as a good co-dopant to increase the photocatalytic activity of Ga (0.1)-ZnS for hydrogen production from water under visible light irradiation.


Catalysts ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1445
Author(s):  
Maryam Saadati ◽  
Omid Akhavan ◽  
Hossein Fazli

Single-layer MoS2-MoO3-x heterojunction nanosheets with visible-light-sensitive band gap energy and average lateral dimensions of ~70 nm were synthesized by using a two-step combined exfoliation method. The exfoliation was initiated from pristine MoS2, while some sulfur sites in expanded MoS2 sheets during exfoliating were substituted by ambient non-thermal oxygen, resulting in formation of α-MoO3-x crystalline domains. The morphological features, crystalline structure, phase formation, number of layers, and optical properties of the MoS2-MoO3-x nanosheets were determined by atomic force microscopy; X-ray diffraction; field emission electron microscopy; transmission electron microscopy; and Raman, UV–visible–NIR, diffuse transmittance, and photoluminescence spectroscopies. The produced α-MoO3-x domains displayed a narrower indirect band gap energy (~1.95 eV) than that of stoichiometric MoO3 (~3 eV), and a broad light absorption range from visible to near-infrared region can act as a plasmonic material facilitating the separation of the photoinduced carriers and enhancing the photocatalytic activity of the MoS2 domain, having ~1.75(2.16) eV indirect (direct) band gap energy. In this regard, the MoS2-MoO3-x heterojunction nanosheets showed single-layer-based excitation-dependent luminescence emissions and visible-light-induced photocatalytic features, at the same time. This study can contribute to promising applications of sheet-like nanomaterials for purposes requiring simultaneous photoluminescence and photocatalytic features, such as in-vivo monitoring and targeting


2019 ◽  
Author(s):  
Pejman Monazzam ◽  
azadeh ebrahimian pirbazari ◽  
Behnam Fakhari Kisomi ◽  
Ziba Khodaee

In this work, we focused on improvement of rutile-type TiO2 degradation efficiency by cobalt doping and decorating on carbon nanotubes walls (CNTs) (Co-TiO2/CNTs). X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), field emission scanning electron microscopy (FESEM), diffuse reflectance spectroscopy (DRS), and nitrogen physisorption were used to characterize the prepared samples. The XRD results indicated after cobalt doping, we obtained rutile phase as the major phase for cobalt containing samples. The band gap energy of the synthesized samples were calculated by Kubelka-Munk equation using diffuse reflectance spectra. The surface area of the samples was obtained by BET model and average pore diameter and pore volume of the samples were extracted from desorption branch of BJH model. The effectiveness of the samples was examined through degradation of 2,4-dichlorophenol (2,4-DCP) as a model of organic pollutants under visible light. We achieved 27% and 50% visible light degradation of 2,4-DCP in the presence of pure TiO2 and Co-TiO2/CNTs after 180 min irradiation, respectively. The high visible light activity of Co-TiO2/CNTs sample can be approved that the presence of cobalt and CNTs reduce the band gap energy and sensitize TiO2 surface to visible light respectively. The mechanism for degradation of 2,4-DCP by Co-TiO2/CNTs photocatalyst under visible light is proposed.


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