A visible-light-driven core-shell like Ag2S@Ag2CO3 composite photocatalyst with high performance in pollutants degradation. (August 2016)
- Record Type:
- Journal Article
- Title:
- A visible-light-driven core-shell like Ag2S@Ag2CO3 composite photocatalyst with high performance in pollutants degradation. (August 2016)
- Main Title:
- A visible-light-driven core-shell like Ag2S@Ag2CO3 composite photocatalyst with high performance in pollutants degradation
- Authors:
- Yu, Changlin
Wei, Longfu
Zhou, Wanqin
Dionysiou, Dionysios D.
Zhu, Lihua
Shu, Qing
Liu, Hong - Abstract:
- Abstract: A series of Ag2 S-Ag2 CO3 (4%, 8%, 16%, 32% and 40% Ag2 S), Ag2 CO3 @Ag2 S (32%Ag2 S) and Ag2 S@Ag2 CO3 (32%Ag2 S) composite photocatalysts were fabricated by coprecipitation or successive precipitation reaction. The obtained catalysts were analyzed by N2 physical adsorption, powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, UV–vis diffuse reflectance spectroscopy and photocurrent test. Under visible light irradiation, the influences of Ag2 S content and core-shell property on photocatalytic activity and stability were evaluated in studies focused on the degradation of methyl orange (MO) dye, phenol, and bisphenol A. Results showed that excellent photocatalytic performance was obtained over Ag2 S/Ag2 CO3 composite photocatalysts with respect to Ag2 S and Ag2 CO3 . With optimal content of Ag2 S (32 wt%), the Ag2 S-Ag2 CO3 showed the highest photocatalytic degradation efficiency. Moreover, the structured property of Ag2 S/Ag2 CO3 greatly influenced the activity. Compared with Ag2 S-Ag2 CO3 and Ag2 CO3 @Ag2 S, core-shell like Ag2 S@Ag2 CO3 demonstrated the highest activity and stability. The main reason for the boosting of photocatalytic performance was due to the formation of Ag2 S/Ag2 CO3 well contacted interface and unique electron structures. Ag2 S/Ag2 CO3 interface could significantly increase the separation efficiency of theAbstract: A series of Ag2 S-Ag2 CO3 (4%, 8%, 16%, 32% and 40% Ag2 S), Ag2 CO3 @Ag2 S (32%Ag2 S) and Ag2 S@Ag2 CO3 (32%Ag2 S) composite photocatalysts were fabricated by coprecipitation or successive precipitation reaction. The obtained catalysts were analyzed by N2 physical adsorption, powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, UV–vis diffuse reflectance spectroscopy and photocurrent test. Under visible light irradiation, the influences of Ag2 S content and core-shell property on photocatalytic activity and stability were evaluated in studies focused on the degradation of methyl orange (MO) dye, phenol, and bisphenol A. Results showed that excellent photocatalytic performance was obtained over Ag2 S/Ag2 CO3 composite photocatalysts with respect to Ag2 S and Ag2 CO3 . With optimal content of Ag2 S (32 wt%), the Ag2 S-Ag2 CO3 showed the highest photocatalytic degradation efficiency. Moreover, the structured property of Ag2 S/Ag2 CO3 greatly influenced the activity. Compared with Ag2 S-Ag2 CO3 and Ag2 CO3 @Ag2 S, core-shell like Ag2 S@Ag2 CO3 demonstrated the highest activity and stability. The main reason for the boosting of photocatalytic performance was due to the formation of Ag2 S/Ag2 CO3 well contacted interface and unique electron structures. Ag2 S/Ag2 CO3 interface could significantly increase the separation efficiency of the photo-generated electrons (e − ) and holes (h + ), and production of OH radicals. More importantly, the low solubility of Ag2 S shell could effectively protect the core of Ag2 CO3, which further guarantees the stability of Ag2 CO3 . Graphical abstract: Highlights: High visible-light-driven photocatalytic performance in pollutants degradation. Ag2 S content and core-shell property distinct influence activity and stability. Unique Ag2 S/Ag2 CO3 interface largely boosts e − /h + pairs separation and OH radicals production. Ag2 S shell prevents the dissolution of Ag2 CO3 core. … (more)
- Is Part Of:
- Chemosphere. Volume 157(2016)
- Journal:
- Chemosphere
- Issue:
- Volume 157(2016)
- Issue Display:
- Volume 157, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 157
- Issue:
- 2016
- Issue Sort Value:
- 2016-0157-2016-0000
- Page Start:
- 250
- Page End:
- 261
- Publication Date:
- 2016-08
- Subjects:
- Ag2S -- Ag2CO3 -- Core-shell -- Water pollutants -- Photocatalytic degradation
Pollution -- Periodicals
Pollution -- Physiological effect -- Periodicals
Environmental sciences -- Periodicals
Atmospheric chemistry -- Periodicals
551.511 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00456535/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.chemosphere.2016.05.021 ↗
- Languages:
- English
- ISSNs:
- 0045-6535
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.280000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2037.xml