Cobalt oxide coupled with graphitic carbon nitride composite heterojunction for efficient Z-scheme photocatalytic environmental pollutants degradation performance

被引:8
|
作者
Suganthi, Sanjeevamuthu [1 ]
Vignesh, Shanmugam [2 ]
Sundar, Jeyaperumal Kalyana [2 ]
Alqarni, Sondos Abdullah [3 ]
Pandiaraj, Saravanan [4 ]
Oh, Tae Hwan [1 ]
机构
[1] Yeungnam Univ, Sch Chem Engn, Gyongsan 38541, South Korea
[2] Periyar Univ, Dept Phys, Mat Sci Res Lab, Salem 636011, Tamil Nadu, India
[3] King Khalid Univ, Dept Elect Engn, Abha, Saudi Arabia
[4] King Saud Univ, Dept Selfdev Skills, POB 2455, Riyadh 11451, Saudi Arabia
关键词
Photocatalytic degradation; Various pollutant; Recycling stability; Z-scheme; Co3O4; g-C3N4; WASTE-WATER TREATMENT; LIGHT; G-C3N4; FABRICATION; HYBRIDS; CATALYSTS; DYE;
D O I
10.1016/j.envres.2023.116574
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Co3O4/g-C3N4 Z-scheme composite heterojunction has been effectively built in a facile sonication-assisted hydrothermal manner. The as-synthesized optimal 0.2 M Co3O4/g-C3N4 (GCO2) composite photocatalysts (PCs) revealed admirable degradation efficiency towards methyl orange (MO, 65.1%) and methylene blue (MB, 87.9%) organic pollutant compared with bare g-C3N4 within 210 min under light irradiation. Besides, the features of investigating structural, morphological and optical properties have evidence that the unique decoration effect of Co3O4 nanoparticles (NPs) on the g-C3N4 structure with intimate interface heterojunction of wellmatched band structures noticeably facilitates the photo-generated charge transport/separation efficiency, reduces the recombination rates and widens the visible-light fascination which could advantageous to upgrading photocatalytic action with superior redox ability. Especially, the probable Z-scheme photocatalytic mechanism pathway is also elucidated in detail based on the quenching results. Hence, this work delivers a facile and hopeful candidate for contaminated water remediation via visible-light photocatalysis over the efficient g-C3N4-based catalysts.
引用
收藏
页数:12
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