Synthesis of g-C3N4/Bi5O7I microspheres with enhanced photocatalytic activity under visible light
- 1. National Special Superfine Powder Engineering Center, Nanjing University of Science and Technology, Nanjing 210094 (China)
- 2. School of Management, Chengdu University of Information Technology, Chengdu 610225 (China)
- 3. State Key Laboratory of Advanced Technology for Float Glass, Bengbu 233000 (China)
Description
Highlights: • The method for preparing the efficient g-C3N4/Bi5O7I photocatalyst is simple. • Microspheres with unique composition and structure can improve its performance. • The g-C3N4/Bi5O7I has the characteristic of Z-scheme type photocatalyst. Novel g-C3N4/Bi5O7I heterojunction microspheres having excellent photocatalytic activity were successfully prepared by a one-pot ethylene glycol (EG)-assisted hydrothermal method followed by calcination in air. Bi5O7I microspheres grafted with g-C3N4 nano-sheets were formed and studied by electron microscopy. The morphological effects on g-C3N4/Bi5O7I photocatalytic capability with varied g-C3N4 contents were investigated and discussed. The g-C3N4/Bi5O7I microspheres exhibited much improved photocatalytic degradation performance under visible light irradiation compared with bare Bi5O7I and g-C3N4. The preparation conditions of g-C3N4/Bi5O7I microspheres with optimal photocatalytic ability for degrading methyl orange (MO) and rhodamine (RhB) were established. Analyses by both photoluminescence (PL) and photocurrent independently confirmed that photo-induced electron-hole pairs in the g-C3N4/Bi5O7I composite have been effectively created which was responsible for the observed photocatalysis. Based on the analysis of the experiment results, a Z-Scheme heterojunction photocatalytic mechanism was proposed. The excellent photocatalytic performance could be attributed to the effective charge separation at the interface between g-C3N4 and Bi5O7I and the enhanced visible light absorption. In addition, the photocatalytic mechanism was discussed on the basis of the relative band positions of these two semiconductor materials.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apsusc.2018.08.080Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2018.08.080;
- PII
- S0169433218322165;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 462
- Journal Page Range
- p. 18-28
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 52110474
- Subject category
- S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- ABSORPTION; BISMUTH COMPOUNDS; CALCINATION; CARBON NITRIDES; COMPARATIVE EVALUATIONS; EFFECTIVE CHARGE; ELECTRON MICROSCOPY; ETHYLENE GLYCOLS; EXPERIMENT RESULTS; HETEROJUNCTIONS; HYDROTHERMAL SYNTHESIS; METHYL ORANGE; MICROSPHERES; OXYIODIDES; PHOTOCATALYSIS; PHOTOCURRENTS; PHOTOLUMINESCENCE; RHODAMINES; VISIBLE RADIATION
- Descriptors DEC
- ALCOHOLS; AMINES; AZO COMPOUNDS; AZO DYES; CARBON COMPOUNDS; CARBOXYLIC ACIDS; CATALYSIS; CHEMICAL REACTIONS; CURRENTS; DECOMPOSITION; DYES; ELECTRIC CURRENTS; ELECTROMAGNETIC RADIATION; EMISSION; EVALUATION; GLYCOLS; HALOGEN COMPOUNDS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; HYDROXY COMPOUNDS; INDICATORS; IODINE COMPOUNDS; LUMINESCENCE; MICROSCOPY; NITRIDES; NITROGEN COMPOUNDS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; ORGANIC SULFUR COMPOUNDS; OXYGEN COMPOUNDS; OXYHALIDES; PHOTON EMISSION; PNICTIDES; PYROLYSIS; RADIATIONS; REAGENTS; SEMICONDUCTOR JUNCTIONS; SORPTION; SULFONIC ACIDS; SYNTHESIS; THERMOCHEMICAL PROCESSES
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier B.V. All rights reserved.