HE Zhiqiao, CHEN Jinping, TONG Lili, et al. BiOCl/g-C3N4 heterojunction catalyst for efficient photocatalytic reduction of CO2 under visible light[J]. CIESC Journal, 2016, (11): 4634-4642. DOI: 10.11949/j.issn.0438-1157.20160337.
DOI:
HE Zhiqiao, CHEN Jinping, TONG Lili, et al. BiOCl/g-C3N4 heterojunction catalyst for efficient photocatalytic reduction of CO2 under visible light[J]. CIESC Journal, 2016, (11): 4634-4642. DOI: 10.11949/j.issn.0438-1157.20160337.DOI:
BiOCl/g-C3N4 heterojunction catalyst for efficient photocatalytic reduction of CO2 under visible light
BiOCl/g-C3N4 heterojunction catalyst was synthesized by a hydrothermal method using KCl
Bi(NO3)3 and g-C3N4 as precursors
over which the photocatalytic reduction of CO2 under visible light irradiation was conducted. The catalytic activity and the stability during CO2 photoreduction was studied. Moreover
effects of molar ratio of BiOCl to g-C3N4
usage amount of catalyst and illumination intensity on the photocatalytic reduction of CO2 was investigated. It suggests that the BiOCl/g-C3N4 heterojunction catalysts showed much enhanced photocatalytic activities for the reduction of gaseous CO2 with water vapor in comparison with BiOCl and g-C3N4. The BiOCl/g-C3N4 catalyst with molar ratio of 1:1 exhibited the highest photocatalytic activity for CO2 reduction under the optimal conditions of 0.1 g catalyst and 2.413×10-6 einstein·min-1·cm-2 of illumination intensity. Moreover
the catalyst maintained stable performance even after five cycles of test. Techniques of X-ray diffraction
scanning electron microscopy
transmission electron microscopy
X-ray photoelectron spectroscopy
Brunauer-Emmett-Teller analyses and UV-vis absorption spectroscopy were conducted on the catalyst
and it is speculated that the effective separation of photogenerated electrons and holes due to the formation of p-n heterojunctions between BiOCl and g-C3N4 accounted for the improved photocatalytic activities of BiOCl/g-C3N4.
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