کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6454416 1418817 2017 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Highly active TiO2/g-C3N4/G photocatalyst with extended spectral response towards selective reduction of nitrobenzene
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Highly active TiO2/g-C3N4/G photocatalyst with extended spectral response towards selective reduction of nitrobenzene
چکیده انگلیسی


- TiO2/g-C3N4/G was synthesized by photochemical reduction self-assembly methods.
- Noticeable photocurrent response exhibits during both UV-region and visual-region.
- High photocatalytic activity and selectivity show in the reduction of nitrobenzene.
- Synergistic effect facilitate the separation of photogenerated charges.

A simple self-assembly photochemical reduction method has been proposed to prepare highly photocatalytic TiO2 nanowire/g-C3N4 nanosheet/graphene heterostructures (TiO2/g-C3N4/G). In this hybrid structure, graphene enhances the charge transportation during photocatalytic process, and TiO2 nanowires prevent graphene and g-C3N4 from restacking. Meanwhile, g-C3N4 with a more suitable band gap, extends the adsorption edge of the TiO2/g-C3N4/G composite to visual-region. Benefiting from the positive synergetic effect, 97% of nitrobenzene can be selectively reduced within 4 h by using TiO2/g-C3N4/G as the photocatalyst. The TiO2/g-C3N4/G composite with 3D structure demonstrates a great potential in selective oxidation and reduction of organics for the synthesis of high added-value organic compounds.

241TiO2 nanowire/g-C3N4 nanosheet/graphene heterostructures (TiO2/g-C3N4/G) with highly photocatalytic activity has been prepared via a simple self-assembly photochemical reduction method. Benefiting from the positive synergetic effect, 97% of nitrobenzene can be selectively reduced within 4 h by using TiO2/g-C3N4/G as the photocatalyst.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis B: Environmental - Volume 203, April 2017, Pages 1-8
نویسندگان
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