Boosted photocatalytic removal of tetracycline on S-scheme Bi12O17Cl2/α-Bi2O3 heterojunctions with rich oxygen vacancies

[Display omitted] •Ultrathin Bi12O17Cl2 nanosheets were assembled on α-Bi2O3.•Construction of heterojunctions improve the concentration of OVs.•Bi12O17Cl2/α-Bi2O3 heterojunctions possess superior photocatalytic activity.•Bi12O17Cl2/α-Bi2O3 is an S-scheme heterojunction. Construction of heterojunctio...

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Published inApplied surface science Vol. 563; p. 150246
Main Authors Chen, Jiufu, Zhong, Junbo, Li, Jianzhang, Qiu, Kehui
Format Journal Article
LanguageEnglish
Published Elsevier B.V 15.10.2021
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Abstract [Display omitted] •Ultrathin Bi12O17Cl2 nanosheets were assembled on α-Bi2O3.•Construction of heterojunctions improve the concentration of OVs.•Bi12O17Cl2/α-Bi2O3 heterojunctions possess superior photocatalytic activity.•Bi12O17Cl2/α-Bi2O3 is an S-scheme heterojunction. Construction of heterojunctions and introduction of oxygen vacancies (OVs) have been regarded as well-accepted strategies to enhance photocatalytic activity. In this demonstration, novel Bi12O17Cl2/ α-Bi2O3 S-scheme heterojunctions with rich OVs were successfully constructed by a facile chlorinating-calcining route. The characterization results confirm that the concentration of OVs was significantly enhanced after ultrathin Bi12O17Cl2 nanoflakes were anchored on the surface of α-Bi2O3. The experimental results exhibit that Bi12O17Cl2/α-Bi2O3 heterojunctions prepared by 2.33 g α-Bi2O3 and 2.5 mL of 0.01 M HCl solution possess the highest photocatalytic activity in photocatalytic removal of tetracycline (TC). The enhanced photocatalytic performance of Bi12O17Cl2/α-Bi2O3 heterojunctions originates from the excellent separation and migration mobility of photoinduced carriers induced by the interaction between the interfacial electric fields and abundant OVs. Furthermore, the recycling experiments suggest that Bi12O17Cl2/α-Bi2O3 S-scheme heterojunctions have exceptional stability in TC removal. Detailed studies have shown that the photogenerated charge pairs in Bi12O17Cl2/α-Bi2O3 heterojunctions conform to an S-scheme mechanism. This work presents a deep insight into designing S-scheme photocatalysts with rich OVs to effectively treat water pollution.
AbstractList [Display omitted] •Ultrathin Bi12O17Cl2 nanosheets were assembled on α-Bi2O3.•Construction of heterojunctions improve the concentration of OVs.•Bi12O17Cl2/α-Bi2O3 heterojunctions possess superior photocatalytic activity.•Bi12O17Cl2/α-Bi2O3 is an S-scheme heterojunction. Construction of heterojunctions and introduction of oxygen vacancies (OVs) have been regarded as well-accepted strategies to enhance photocatalytic activity. In this demonstration, novel Bi12O17Cl2/ α-Bi2O3 S-scheme heterojunctions with rich OVs were successfully constructed by a facile chlorinating-calcining route. The characterization results confirm that the concentration of OVs was significantly enhanced after ultrathin Bi12O17Cl2 nanoflakes were anchored on the surface of α-Bi2O3. The experimental results exhibit that Bi12O17Cl2/α-Bi2O3 heterojunctions prepared by 2.33 g α-Bi2O3 and 2.5 mL of 0.01 M HCl solution possess the highest photocatalytic activity in photocatalytic removal of tetracycline (TC). The enhanced photocatalytic performance of Bi12O17Cl2/α-Bi2O3 heterojunctions originates from the excellent separation and migration mobility of photoinduced carriers induced by the interaction between the interfacial electric fields and abundant OVs. Furthermore, the recycling experiments suggest that Bi12O17Cl2/α-Bi2O3 S-scheme heterojunctions have exceptional stability in TC removal. Detailed studies have shown that the photogenerated charge pairs in Bi12O17Cl2/α-Bi2O3 heterojunctions conform to an S-scheme mechanism. This work presents a deep insight into designing S-scheme photocatalysts with rich OVs to effectively treat water pollution.
ArticleNumber 150246
Author Chen, Jiufu
Li, Jianzhang
Qiu, Kehui
Zhong, Junbo
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  givenname: Junbo
  surname: Zhong
  fullname: Zhong, Junbo
  email: junbozhong@suse.edu.cn
  organization: Key Laboratory of Green Catalysis of Higher Education Institutes of Sichuan, College of Chemistry and Environmental Engineering, Sichuan University of Science and Engineering, Zigong 643000, PR China
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  givenname: Jianzhang
  surname: Li
  fullname: Li, Jianzhang
  organization: Key Laboratory of Green Catalysis of Higher Education Institutes of Sichuan, College of Chemistry and Environmental Engineering, Sichuan University of Science and Engineering, Zigong 643000, PR China
– sequence: 4
  givenname: Kehui
  surname: Qiu
  fullname: Qiu, Kehui
  email: qkh2188@163.com
  organization: College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu 610059, PR China
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Keywords Oxygen vacancies
S-scheme heterojunctions
α-Bi2O3
Ultrathin Bi12O17Cl2 nanosheets
Tetracycline
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Snippet [Display omitted] •Ultrathin Bi12O17Cl2 nanosheets were assembled on α-Bi2O3.•Construction of heterojunctions improve the concentration of...
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StartPage 150246
SubjectTerms Oxygen vacancies
S-scheme heterojunctions
Tetracycline
Ultrathin Bi12O17Cl2 nanosheets
α-Bi2O3
Title Boosted photocatalytic removal of tetracycline on S-scheme Bi12O17Cl2/α-Bi2O3 heterojunctions with rich oxygen vacancies
URI https://dx.doi.org/10.1016/j.apsusc.2021.150246
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