Enhanced Cocatalyst-Free Visible-Light Activities for Photocatalytic Fuel Production of g‑C3N4 by Trapping Holes and Transferring Electrons
We have successfully synthesized boron-doped g-C3N4 nanosheets (B-CN) and its nanocomposites with nanocrystalline anatase TiO2 (T/B-CN). The as-prepared T/B-CN nanocomposites with the proper amounts of boron and TiO2 exhibit rather high cocatalyst-free photoactivities for producing H2 from CH3OH sol...
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Published in | Journal of physical chemistry. C Vol. 120; no. 1; pp. 98 - 107 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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American Chemical Society
14.01.2016
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Abstract | We have successfully synthesized boron-doped g-C3N4 nanosheets (B-CN) and its nanocomposites with nanocrystalline anatase TiO2 (T/B-CN). The as-prepared T/B-CN nanocomposites with the proper amounts of boron and TiO2 exhibit rather high cocatalyst-free photoactivities for producing H2 from CH3OH solution (∼29× higher) and CH4 from CO2-containing water (∼16× higher) under visible-light irradiation, compared to those of bare g-C3N4. This is attributed to the greatly enhanced photogenerated charge separation after doping boron and subsequent coupling with TiO2, mainly based on the measurements of atmosphere-controlled steady-state surface photovoltage spectra, transient-state surface photovoltage responses, photoluminescence spectra, and fluorescence spectra related to the produced hydroxyl radical amount. It is suggested for the first time that the great charge separation enhancement results from the B-induced surface states near the valence band top to trap holes and the formed heterojunctions to transfer electrons from B-CN to TiO2. Moreover, the created surface states are also responsible for the visible-light extension from 450 nm of g-C3N4 to 500 nm of B-CN (T/B-CN) for solar fuel production. Interestingly, the obtained 6T/6B-CN exhibits much larger quantum efficiencies, which are 3.08% for hydrogen evolution and 1.68% for CH4 production at λ = 420 nm, respectively, with 5.1× and 7.6× enhancement as compared to CN, even superior to other works. This work will provide feasible routes to synthesize g-C3N4-based nanophotocatalysts for efficient solar fuel production. |
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AbstractList | We have successfully synthesized boron-doped g-C3N4 nanosheets (B-CN) and its nanocomposites with nanocrystalline anatase TiO2 (T/B-CN). The as-prepared T/B-CN nanocomposites with the proper amounts of boron and TiO2 exhibit rather high cocatalyst-free photoactivities for producing H2 from CH3OH solution (∼29× higher) and CH4 from CO2-containing water (∼16× higher) under visible-light irradiation, compared to those of bare g-C3N4. This is attributed to the greatly enhanced photogenerated charge separation after doping boron and subsequent coupling with TiO2, mainly based on the measurements of atmosphere-controlled steady-state surface photovoltage spectra, transient-state surface photovoltage responses, photoluminescence spectra, and fluorescence spectra related to the produced hydroxyl radical amount. It is suggested for the first time that the great charge separation enhancement results from the B-induced surface states near the valence band top to trap holes and the formed heterojunctions to transfer electrons from B-CN to TiO2. Moreover, the created surface states are also responsible for the visible-light extension from 450 nm of g-C3N4 to 500 nm of B-CN (T/B-CN) for solar fuel production. Interestingly, the obtained 6T/6B-CN exhibits much larger quantum efficiencies, which are 3.08% for hydrogen evolution and 1.68% for CH4 production at λ = 420 nm, respectively, with 5.1× and 7.6× enhancement as compared to CN, even superior to other works. This work will provide feasible routes to synthesize g-C3N4-based nanophotocatalysts for efficient solar fuel production. We have successfully synthesized boron-doped g-C₃N₄ nanosheets (B-CN) and its nanocomposites with nanocrystalline anatase TiO₂ (T/B-CN). The as-prepared T/B-CN nanocomposites with the proper amounts of boron and TiO₂ exhibit rather high cocatalyst-free photoactivities for producing H₂ from CH₃OH solution (∼29× higher) and CH₄ from CO₂-containing water (∼16× higher) under visible-light irradiation, compared to those of bare g-C₃N₄. This is attributed to the greatly enhanced photogenerated charge separation after doping boron and subsequent coupling with TiO₂, mainly based on the measurements of atmosphere-controlled steady-state surface photovoltage spectra, transient-state surface photovoltage responses, photoluminescence spectra, and fluorescence spectra related to the produced hydroxyl radical amount. It is suggested for the first time that the great charge separation enhancement results from the B-induced surface states near the valence band top to trap holes and the formed heterojunctions to transfer electrons from B-CN to TiO₂. Moreover, the created surface states are also responsible for the visible-light extension from 450 nm of g-C₃N₄ to 500 nm of B-CN (T/B-CN) for solar fuel production. Interestingly, the obtained 6T/6B-CN exhibits much larger quantum efficiencies, which are 3.08% for hydrogen evolution and 1.68% for CH₄ production at λ = 420 nm, respectively, with 5.1× and 7.6× enhancement as compared to CN, even superior to other works. This work will provide feasible routes to synthesize g-C₃N₄-based nanophotocatalysts for efficient solar fuel production. |
Author | Wu, Jing Qu, Yang Zada, Amir Humayun, Muhammad Sun, Xiaojun Raziq, Fazal Zhang, Xuliang Yu, Haitao Jing, Liqiang |
AuthorAffiliation | Key Laboratory of Green Chemical Engineering and Technology of College of Heilongjiang Province, College of Chemical and Environmental Engineering National Center for International Research of Catalytic Technology Harbin University of Science and Technology Key Laboratory of Functional Inorganic Material Chemistry (Heilongjiang University), Ministry of Education, School of Chemistry and Materials Science |
AuthorAffiliation_xml | – name: Key Laboratory of Green Chemical Engineering and Technology of College of Heilongjiang Province, College of Chemical and Environmental Engineering – name: Key Laboratory of Functional Inorganic Material Chemistry (Heilongjiang University), Ministry of Education, School of Chemistry and Materials Science – name: National Center for International Research of Catalytic Technology – name: Harbin University of Science and Technology |
Author_xml | – sequence: 1 givenname: Fazal surname: Raziq fullname: Raziq, Fazal – sequence: 2 givenname: Yang surname: Qu fullname: Qu, Yang – sequence: 3 givenname: Xuliang surname: Zhang fullname: Zhang, Xuliang – sequence: 4 givenname: Muhammad surname: Humayun fullname: Humayun, Muhammad – sequence: 5 givenname: Jing surname: Wu fullname: Wu, Jing – sequence: 6 givenname: Amir surname: Zada fullname: Zada, Amir – sequence: 7 givenname: Haitao surname: Yu fullname: Yu, Haitao email: yuhaitao@hlju.edu.cn – sequence: 8 givenname: Xiaojun surname: Sun fullname: Sun, Xiaojun email: sunxiaojun@hrbust.edu.cn – sequence: 9 givenname: Liqiang surname: Jing fullname: Jing, Liqiang email: Jinglq@hlju.edu.cn |
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Snippet | We have successfully synthesized boron-doped g-C3N4 nanosheets (B-CN) and its nanocomposites with nanocrystalline anatase TiO2 (T/B-CN). The as-prepared T/B-CN... We have successfully synthesized boron-doped g-C₃N₄ nanosheets (B-CN) and its nanocomposites with nanocrystalline anatase TiO₂ (T/B-CN). The as-prepared T/B-CN... |
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SubjectTerms | boron carbon nitride fluorescence emission spectroscopy fuel production hydrogen hydrogen production hydroxyl radicals irradiation methane methane production methanol nanocomposites nanocrystals nanosheets photocatalysis photoluminescence physical chemistry solar energy titanium dioxide |
Title | Enhanced Cocatalyst-Free Visible-Light Activities for Photocatalytic Fuel Production of g‑C3N4 by Trapping Holes and Transferring Electrons |
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