Synthesis of CdxZn1−xS@MIL-101(Cr) Composite Catalysts for the Photodegradation of Methylene Blue

Nanoparticles of the semiconductor catalyst CdxZn 1 − x S were embedded into the metal organic framework MIL-101(Cr) to obtain CdxZn 1 − x S@MIL-101(Cr) nanocomposites. These materials not only possess high surface areas and mesopores but also show good utilization of light energy. The ultraviolet-v...

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Published inNano : brief reports and reviews Vol. 13; no. 10; pp. 60 - 76
Main Authors Yang, Shipeng, Peng, Siwei, Zhang, Chunhui, He, Xuwen, Cai, Yaqi
Format Journal Article
LanguageEnglish
Published Singapore World Scientific Publishing Company 01.10.2018
World Scientific Publishing Co. Pte., Ltd
성균나노과학기술원
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ISSN1793-2920
1793-7094
DOI10.1142/S1793292018501187

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Abstract Nanoparticles of the semiconductor catalyst CdxZn 1 − x S were embedded into the metal organic framework MIL-101(Cr) to obtain CdxZn 1 − x S@MIL-101(Cr) nanocomposites. These materials not only possess high surface areas and mesopores but also show good utilization of light energy. The ultraviolet-visible diffuse reflectance patterns of CdxZn 1 − x S@MIL-101(Cr) nanocomposites showed that Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) possessed good visible light response ability among the synthesized nanocomposites. The photocatalytic performance of the CdxZn 1 − x S@MIL-101(Cr) nanocomposites were tested via degradation and mineralization of methylene blue in neutral water solution under light irradiation using a 300W xenon lamp. As a result, using Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) as a catalyst, 99.2% of methylene blue was mineralized within 30 min. Due to the synergistic effect of adsorption by the MIL-101(Cr) component and photocatalytic degradation provided by the Cd 0 . 8 Zn 0 . 2 S component, the Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) catalyst displayed superior photocatalytic performance relative to Cd 0 . 8 Zn 0 . 2 S and MIL-101(Cr). Furthermore, Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) possessed excellent stability during photodegradation and exhibited good reusability. The remarkable photocatalytic performance of Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) is likely due to the effective transfer of electrons and holes at the heterojunction interfaces. The combination of CdxZn1–xS and MIL-101(Cr) can effectively inhibit the dissolution of heavy metals and improve the material's ability to resist light corrosion. Moreover, it can make the synergistic effect of photocatalysis and adsorption be utilized to increase the mineralization efficiency of the material to the organic matter.
AbstractList Nanoparticles of the semiconductor catalyst CdxZn1−xS were embedded into the metal organic framework MIL-101(Cr) to obtain CdxZn1−xS@MIL-101(Cr) nanocomposites. These materials not only possess high surface areas and mesopores but also show good utilization of light energy. The ultraviolet-visible diffuse reflectance patterns of CdxZn1−xS@MIL-101(Cr) nanocomposites showed that Cd0.8Zn0.2S@MIL-101(Cr) possessed good visible light response ability among the synthesized nanocomposites. The photocatalytic performance of the CdxZn1−xS@MIL-101(Cr) nanocomposites were tested via degradation and mineralization of methylene blue in neutral water solution under light irradiation using a 300W xenon lamp. As a result, using Cd0.8Zn0.2S@MIL-101(Cr) as a catalyst, 99.2% of methylene blue was mineralized within 30min. Due to the synergistic effect of adsorption by the MIL-101(Cr) component and photocatalytic degradation provided by the Cd0.8Zn0.2S component, the Cd0.8Zn0.2S@MIL-101(Cr) catalyst displayed superior photocatalytic performance relative to Cd0.8Zn0.2S and MIL-101(Cr). Furthermore, Cd0.8Zn0.2S@MIL-101(Cr) possessed excellent stability during photodegradation and exhibited good reusability. The remarkable photocatalytic performance of Cd0.8Zn0.2S@MIL-101(Cr) is likely due to the effective transfer of electrons and holes at the heterojunction interfaces.
Nanoparticles of the semiconductor catalyst CdxZn1-xS were embedded into the metal organic framework MIL-101(Cr) to obtain CdxZn1-xS@MIL-101(Cr) nanocomposites. These materials not only possess high surface areas and mesopores but also show good utilization of light energy. The ultraviolet-visible diffuse reflectance patterns of CdxZn1-xS@MIL-101(Cr) nanocomposites showed that Cd0.8Zn0.2S@MIL-101(Cr) possessed good visible light response ability among the synthesized nanocomposites. The photocatalytic performance of the CdxZn1-xS@MIL-101(Cr) nanocomposites were tested via degradation and mineralization of methylene blue in neutral water solution under light irradiation using a 300W xenon lamp. As a result, using Cd0.8Zn0.2S@MIL-101(Cr) as a catalyst, 99.2% of methylene blue was mineralized within 30 min. Due to the synergistic effect of adsorption by the MIL-101(Cr) component and photocatalytic degradation provided by the Cd0.8Zn0.2S component, the Cd0.8Zn0.2S@MIL-101(Cr) catalyst displayed superior photocatalytic performance relative to Cd0.8Zn0.2S and MIL-101(Cr). Furthermore, Cd0.8Zn0.2S@MIL-101(Cr) possessed excellent stability during photo-degradation and exhibited good reusability. The remarkable photocatalytic performance of Cd0.8Zn0.2S@MIL-101(Cr) is likely due to the effective transfer of electrons and holes at the heterojunction interfaces. KCI Citation Count: 0
Nanoparticles of the semiconductor catalyst CdxZn 1 − x S were embedded into the metal organic framework MIL-101(Cr) to obtain CdxZn 1 − x S@MIL-101(Cr) nanocomposites. These materials not only possess high surface areas and mesopores but also show good utilization of light energy. The ultraviolet-visible diffuse reflectance patterns of CdxZn 1 − x S@MIL-101(Cr) nanocomposites showed that Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) possessed good visible light response ability among the synthesized nanocomposites. The photocatalytic performance of the CdxZn 1 − x S@MIL-101(Cr) nanocomposites were tested via degradation and mineralization of methylene blue in neutral water solution under light irradiation using a 300W xenon lamp. As a result, using Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) as a catalyst, 99.2% of methylene blue was mineralized within 30 min. Due to the synergistic effect of adsorption by the MIL-101(Cr) component and photocatalytic degradation provided by the Cd 0 . 8 Zn 0 . 2 S component, the Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) catalyst displayed superior photocatalytic performance relative to Cd 0 . 8 Zn 0 . 2 S and MIL-101(Cr). Furthermore, Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) possessed excellent stability during photodegradation and exhibited good reusability. The remarkable photocatalytic performance of Cd 0 . 8 Zn 0 . 2 S@MIL-101(Cr) is likely due to the effective transfer of electrons and holes at the heterojunction interfaces. The combination of CdxZn1–xS and MIL-101(Cr) can effectively inhibit the dissolution of heavy metals and improve the material's ability to resist light corrosion. Moreover, it can make the synergistic effect of photocatalysis and adsorption be utilized to increase the mineralization efficiency of the material to the organic matter.
Author He, Xuwen
Peng, Siwei
Cai, Yaqi
Zhang, Chunhui
Yang, Shipeng
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CdxZn
photodegradation
S@MIL-101(Cr)
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Nanoparticles of the semiconductor catalyst CdxZn1−xS were embedded into the metal organic framework MIL-101(Cr) to obtain CdxZn1−xS@MIL-101(Cr)...
Nanoparticles of the semiconductor catalyst CdxZn1-xS were embedded into the metal organic framework MIL-101(Cr) to obtain CdxZn1-xS@MIL-101(Cr)...
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SubjectTerms Catalysis
Catalysts
Chemical synthesis
Chromium
Heterojunctions
Light irradiation
Metal-organic frameworks
Methylene blue
Mineralization
Nanocomposites
Nanoparticles
Photocatalysis
Photodegradation
Reflectance
Synergistic effect
Ultraviolet reflection
Xenon lamps
자연과학
Title Synthesis of CdxZn1−xS@MIL-101(Cr) Composite Catalysts for the Photodegradation of Methylene Blue
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