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In situ fabrication of I-doped Bi 2 O 2 CO 3 /g-C 3 N 4 heterojunctions for enhanced photodegradation activity under visible light
Iodine-doped Bi O CO /g-C N heterojunctions consisting of graphitic carbon nitride (g-C N ) and iodine-doped bismutite (Bi O CO ) components were successfully in situ synthesized by a one-pot hydrothermal method. Characterizations such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XP...
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Published in: | Journal of hazardous materials 2020-03, Vol.385, p.121622 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | Iodine-doped Bi
O
CO
/g-C
N
heterojunctions consisting of graphitic carbon nitride (g-C
N
) and iodine-doped bismutite (Bi
O
CO
) components were successfully in situ synthesized by a one-pot hydrothermal method. Characterizations such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscope (SEM) demonstrated iodine was favorably doped into the Bi
O
CO
component, of which the {001} facets grew in situ from {002} facets of g-C
N
for the heterostructure construction of I-doped Bi
O
CO
/g-C
N
(IB/CN). The photocatalytic activity of catalysts was evaluated by the degradation efficiency of 1,5-dihydroxynaphthalene under visible light. 1.5-IB/CN with a reasonable iodine doping amount (Bi: I molar ratio = 1.0: 1.5) exhibited the superior photodegradation performance compared to Bi
O
CO
, achieving an 85.5% removal ratio after 100 min illumination. The enhanced activity of 1.5-IB/CN was attributed to both of the heterostructure that promoted the separation of photoinduced carriers and iodine doping that tuned the bandgap for sufficient visible-light harvesting. The degradation intermediates of 1,5-dihydroxynaphthalene in the system were determined and its possible photodegradation pathway was proposed in detail. This study provides a rational approach for enhancing the visible-light catalytic activity of wide-bandgap Bi
O
CO
, and reveals a new perspective on the removal mechanism of organic pollutants. |
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ISSN: | 1873-3336 |