Influence of solvothermal synthesis on the photocatalytic degradation activity of carbon nitride under visible light irradiation

2017 ◽  
Vol 167 ◽  
pp. 1-9 ◽  
Author(s):  
Che-Chia Hu ◽  
Mao-Sheng Wang ◽  
Wei-Zeng Hung
RSC Advances ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 6383-6394 ◽  
Author(s):  
Haishuai Li ◽  
Linlin Cai ◽  
Xin Wang ◽  
Huixian Shi

A noval ternary nanocomposite AgCl/Ag3PO4/g-C3N4 was successfully synthesized for photocatalytic degradation of methylene blue, methylparaben and inactivation of E. coli under visible light irradiation, showing excellent photocatalytic degradation performance and stability.


RSC Advances ◽  
2014 ◽  
Vol 4 (88) ◽  
pp. 47615-47624 ◽  
Author(s):  
Ping Li ◽  
Chunbo Liu ◽  
Guoling Wu ◽  
Yang Heng ◽  
Shuang Lin ◽  
...  

In this paper, Fe-doped SrTiO3 (FSTO) photocatalysts were successfully prepared via a facile solvothermal method, and their photocatalytic activities for degrading tetracycline (TC) under visible light irradiation were examined.


2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Shuo Xu ◽  
Xiaoya Gao ◽  
Wenfeng Xu ◽  
Pengfei Jin ◽  
Yongmei Kuang

A series of ultrathin BiOCl 2D nanosheet photocatalysts were prepared by the TBAOH-assisted hydrolysis method in water. The effects of tetrabutylammonium hydroxide (TBAOH) dosages, chlorine source, preparation pH value, ultrasonic treatment, and magnetic stirring on the photocatalytic degradation dynamics of carbamazepine were examined under visible-light irradiation to optimize the preparation parameters. It was found that ultrathin BiOCl prepared with TBAOH dosages of 1 mmol and chlorine source of NaCl in the pH of 2 upon magnetic stirring of 6 h displayed the highest photocatalytic degradation rate constant (0.0038 min−1) of carbamazepine, which is 7.6 times higher than that with the ordinary BiOCl (without TBAOH). To clarify the mechanism on the outstanding photocatalytic activity of ultrathin BiOCl, the elemental composition/state, micromorphology, and separation efficiency of photogenerated electron-hole pairs were investigated by X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), and photoluminescence (PL). Results showed that the presence of oxygen vacancy, ultrathin nanosheet structure, and improved separation efficiency of photogenerated electron-hole pairs contributed to the excellent photocatalytic degradation activity of ultrathin BiOCl. The obtained result provides a novel method to fabricate ultrathin BiOCl with excellent photocatalytic degradation activity of carbamazepine under visible-light irradiation.


2014 ◽  
Vol 807 ◽  
pp. 101-113 ◽  
Author(s):  
J. Theerthagiri ◽  
R.A. Senthil ◽  
J. Madhavan ◽  
B. Neppolian

The graphitic carbon nitride (g-C3N4) materials have been synthesized from nitrogen rich precursors such as urea and thiourea by directly heating at 520 °C for 2 h. The as-synthesized carbon nitride samples were characterized by x-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible (UV-vis) absorption spectroscopy, photoluminescence (PL) and particle size analysis. The photoelectrochemical measurements were performed using several on-off cycles under visible-light irradiation. The x-ray diffraction peak is broader which indicates the fine powder nature of the synthesized materials. The estimated crystallite size of carbon nitrides synthesized from urea (U-CN) and thiourea (T-CN) are 4.0 and 4.4 nm respectively. The particle size of U-CN and T-CN were analysed by particle size analyser and were found to be 57.3 and 273.3 nm respectively. The photocatalytic activity for the degradation of the textile dye namely, direct red-81 (DR81) using these carbon nitrides were carried out under visible light irradiation. In the present investigation, a comparison study on the carbon nitrides synthesized from cheap precursors such as urea and thiourea for the degradation of DR81 has been carried out. The results inferred that U-CN exhibited higher photocatalytic activity than T-CN. The photoelectrochemical studies confirmed that the (e--h+) charge carrier separation is more efficient in U-CN than that of T-CN and therefore showed high photocatalytic degradation. Further, the smaller particle size of U-CN is also responsible for the observed degradation trend.


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