Boosting the Activation of Molecular Oxygen and the Degradation of Rhodamine B in Polar-Functional-Group-Modified g-C3N4
Molecular oxygen activation often suffers from high energy consumption and low efficiency. Developing eco-friendly and effective photocatalysts remains a key challenge for advancing green molecular oxygen activation. Herein, graphitic carbon nitride (g-C3N4) with abundant hydroxyl groups (HCN) was s...
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Published in | Molecules (Basel, Switzerland) Vol. 29; no. 16; p. 3836 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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13.08.2024
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Online Access | Get full text |
ISSN | 1420-3049 1420-3049 |
DOI | 10.3390/molecules29163836 |
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Abstract | Molecular oxygen activation often suffers from high energy consumption and low efficiency. Developing eco-friendly and effective photocatalysts remains a key challenge for advancing green molecular oxygen activation. Herein, graphitic carbon nitride (g-C3N4) with abundant hydroxyl groups (HCN) was synthesized to investigate the relationship between these polar groups and molecular oxygen activation. The advantage of the hydroxyl group modification of g-C3N4 included narrower interlayer distances, a larger specific surface area and improved hydrophilicity. Various photoelectronic measurements revealed that the introduced hydroxyl groups reduced the charge transfer resistance of HCN, resulting in accelerated charge separation and migration kinetics. Therefore, the optimal HCN-90 showed the highest activity for Rhodamine B photodegradation with a reaction time of 30 min and an apparent rate constant of 0.125 min−1, surpassing most other g-C3N4 composites. This enhanced activity was attributed to the adjusted band structure achieved through polar functional group modification. The modification of polar functional groups could alter the energy band structure of photocatalysts, narrow band gap, enhance visible-light absorption, and improve photogenerated carrier separation efficiency. This work highlights the significant potential of polar functional groups in tuning the structure of g-C3N4 to enhance efficient molecular oxygen activation. |
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AbstractList | Molecular oxygen activation often suffers from high energy consumption and low efficiency. Developing eco-friendly and effective photocatalysts remains a key challenge for advancing green molecular oxygen activation. Herein, graphitic carbon nitride (g-C3N4) with abundant hydroxyl groups (HCN) was synthesized to investigate the relationship between these polar groups and molecular oxygen activation. The advantage of the hydroxyl group modification of g-C3N4 included narrower interlayer distances, a larger specific surface area and improved hydrophilicity. Various photoelectronic measurements revealed that the introduced hydroxyl groups reduced the charge transfer resistance of HCN, resulting in accelerated charge separation and migration kinetics. Therefore, the optimal HCN-90 showed the highest activity for Rhodamine B photodegradation with a reaction time of 30 min and an apparent rate constant of 0.125 min−1, surpassing most other g-C3N4 composites. This enhanced activity was attributed to the adjusted band structure achieved through polar functional group modification. The modification of polar functional groups could alter the energy band structure of photocatalysts, narrow band gap, enhance visible-light absorption, and improve photogenerated carrier separation efficiency. This work highlights the significant potential of polar functional groups in tuning the structure of g-C3N4 to enhance efficient molecular oxygen activation. Molecular oxygen activation often suffers from high energy consumption and low efficiency. Developing eco-friendly and effective photocatalysts remains a key challenge for advancing green molecular oxygen activation. Herein, graphitic carbon nitride (g-C 3 N 4 ) with abundant hydroxyl groups (HCN) was synthesized to investigate the relationship between these polar groups and molecular oxygen activation. The advantage of the hydroxyl group modification of g-C 3 N 4 included narrower interlayer distances, a larger specific surface area and improved hydrophilicity. Various photoelectronic measurements revealed that the introduced hydroxyl groups reduced the charge transfer resistance of HCN, resulting in accelerated charge separation and migration kinetics. Therefore, the optimal HCN-90 showed the highest activity for Rhodamine B photodegradation with a reaction time of 30 min and an apparent rate constant of 0.125 min −1 , surpassing most other g-C 3 N 4 composites. This enhanced activity was attributed to the adjusted band structure achieved through polar functional group modification. The modification of polar functional groups could alter the energy band structure of photocatalysts, narrow band gap, enhance visible-light absorption, and improve photogenerated carrier separation efficiency. This work highlights the significant potential of polar functional groups in tuning the structure of g-C 3 N 4 to enhance efficient molecular oxygen activation. Molecular oxygen activation often suffers from high energy consumption and low efficiency. Developing eco-friendly and effective photocatalysts remains a key challenge for advancing green molecular oxygen activation. Herein, graphitic carbon nitride (g-C3N4) with abundant hydroxyl groups (HCN) was synthesized to investigate the relationship between these polar groups and molecular oxygen activation. The advantage of the hydroxyl group modification of g-C3N4 included narrower interlayer distances, a larger specific surface area and improved hydrophilicity. Various photoelectronic measurements revealed that the introduced hydroxyl groups reduced the charge transfer resistance of HCN, resulting in accelerated charge separation and migration kinetics. Therefore, the optimal HCN-90 showed the highest activity for Rhodamine B photodegradation with a reaction time of 30 min and an apparent rate constant of 0.125 min-1, surpassing most other g-C3N4 composites. This enhanced activity was attributed to the adjusted band structure achieved through polar functional group modification. The modification of polar functional groups could alter the energy band structure of photocatalysts, narrow band gap, enhance visible-light absorption, and improve photogenerated carrier separation efficiency. This work highlights the significant potential of polar functional groups in tuning the structure of g-C3N4 to enhance efficient molecular oxygen activation.Molecular oxygen activation often suffers from high energy consumption and low efficiency. Developing eco-friendly and effective photocatalysts remains a key challenge for advancing green molecular oxygen activation. Herein, graphitic carbon nitride (g-C3N4) with abundant hydroxyl groups (HCN) was synthesized to investigate the relationship between these polar groups and molecular oxygen activation. The advantage of the hydroxyl group modification of g-C3N4 included narrower interlayer distances, a larger specific surface area and improved hydrophilicity. Various photoelectronic measurements revealed that the introduced hydroxyl groups reduced the charge transfer resistance of HCN, resulting in accelerated charge separation and migration kinetics. Therefore, the optimal HCN-90 showed the highest activity for Rhodamine B photodegradation with a reaction time of 30 min and an apparent rate constant of 0.125 min-1, surpassing most other g-C3N4 composites. This enhanced activity was attributed to the adjusted band structure achieved through polar functional group modification. The modification of polar functional groups could alter the energy band structure of photocatalysts, narrow band gap, enhance visible-light absorption, and improve photogenerated carrier separation efficiency. This work highlights the significant potential of polar functional groups in tuning the structure of g-C3N4 to enhance efficient molecular oxygen activation. |
Author | Liu, Zhenguo Chen, Yuxin Yu, Ruohan Yang, Minghua Ji, Yujie Zhang, Hongjiao Chen, Jing |
AuthorAffiliation | 4 School of Flexible Electronics and Henan Institute of Flexible Electronics, Henan University, Zhengzhou 450046, China 1 Key Laboratory of Flexible Electronics of Zhejiang Province, Ningbo Institute of Northwestern Polytechnical University, Ningbo 315103, China 3 Department of Chemistry, Lishui University, 1 Xueyuan Road, Lishui 323000, China; chenyuxin@lsu.edu.cn (Y.C.); jiyujie@lsu.edu.cn (Y.J.); yuruohan@lsu.edu.cn (R.Y.) 2 Department of Chemical and Material Engineering, Quzhou College of Technology, Quzhou 324002, China; yangmh@qzct.edu.cn (M.Y.); zhanghongjiao@qzct.edu.cn (H.Z.) |
AuthorAffiliation_xml | – name: 3 Department of Chemistry, Lishui University, 1 Xueyuan Road, Lishui 323000, China; chenyuxin@lsu.edu.cn (Y.C.); jiyujie@lsu.edu.cn (Y.J.); yuruohan@lsu.edu.cn (R.Y.) – name: 1 Key Laboratory of Flexible Electronics of Zhejiang Province, Ningbo Institute of Northwestern Polytechnical University, Ningbo 315103, China – name: 2 Department of Chemical and Material Engineering, Quzhou College of Technology, Quzhou 324002, China; yangmh@qzct.edu.cn (M.Y.); zhanghongjiao@qzct.edu.cn (H.Z.) – name: 4 School of Flexible Electronics and Henan Institute of Flexible Electronics, Henan University, Zhengzhou 450046, China |
Author_xml | – sequence: 1 givenname: Jing surname: Chen fullname: Chen, Jing – sequence: 2 givenname: Minghua orcidid: 0009-0007-9734-4780 surname: Yang fullname: Yang, Minghua – sequence: 3 givenname: Hongjiao surname: Zhang fullname: Zhang, Hongjiao – sequence: 4 givenname: Yuxin surname: Chen fullname: Chen, Yuxin – sequence: 5 givenname: Yujie surname: Ji fullname: Ji, Yujie – sequence: 6 givenname: Ruohan surname: Yu fullname: Yu, Ruohan – sequence: 7 givenname: Zhenguo surname: Liu fullname: Liu, Zhenguo |
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SubjectTerms | Adsorption Contact angle degradation Efficiency Energy consumption g-C3N4 Oxidation Photocatalysis polar functional group Pollutants Spectrum analysis visible-light photocatalysis |
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Title | Boosting the Activation of Molecular Oxygen and the Degradation of Rhodamine B in Polar-Functional-Group-Modified g-C3N4 |
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