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      Synthesis of Ta3N5/Bi2MoO6 core–shell fiber-shaped heterojunctions as efficient and easily recyclable photocatalysts

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          Abstract

          Ta 3N 5/Bi 2MoO 6 core–shell fiber-shaped heterojunctions have been prepared, and they can be used as efficient and easily recyclable photocatalysts for environmental remediation.

          Abstract

          Developing efficient and easily recyclable photocatalysts has drawn much attention. Herein, we report the design and synthesis of Ta 3N 5/Bi 2MoO 6 core–shell fiber-shaped heterojunctions as a kind of efficient and easily recyclable photocatalyst. Ta 3N 5 nanofibers have been prepared by an electrospinning–calcination–nitridation method, and then in situ growth of Bi 2MoO 6 on their surfaces is realized by a solvothermal method. The resulting Ta 3N 5/Bi 2MoO 6 heterojunctions are composed of porous Ta 3N 5 nanofibers (diameter: ∼200 nm) whose surfaces are decorated with Bi 2MoO 6 nanosheets (length: 100–200 nm; thickness: ∼15 nm). They exhibit remarkably enhanced photocatalytic activities for the degradation of rhodamine B (RhB) and para-chlorophenol (4-CP) under visible light, compared with pure Bi 2MoO 6 or Ta 3N 5. In particular, the heterojunction with a Ta 3N 5/Bi 2MoO 6 molar ratio of 1/1 achieves the highest photodegradation efficiency of RhB (99.5%), which is about 1.85 times that (53.7%) of Bi 2MoO 6 and 1.66 times that (60.1%) of the mechanical mixture (49.8 wt% Bi 2MoO 6 + 50.2 wt% Ta 3N 5). The superior photocatalytic properties can be attributed to the efficient separation of photo-induced electron–hole pairs and the high BET surface area. The dominant active species are determined to be superoxide and the photogenerated holes. More importantly, the Ta 3N 5/Bi 2MoO 6 heterojunction can be easily recycled by simple sedimentation while maintaining good stability. This work offers more valuable insights into the design of efficient and easily recyclable photocatalysts for environmental remediation.

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          TiO2 photocatalysis: Design and applications

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            Graphitic Carbon Nitride Polymers toward Sustainable Photoredox Catalysis.

            As a promising two-dimensional conjugated polymer, graphitic carbon nitride (g-C3 N4 ) has been utilized as a low-cost, robust, metal-free, and visible-light-active photocatalyst in the field of solar energy conversion. This Review mainly describes the latest advances in g-C3 N4 photocatalysts for water splitting. Their application in CO2 conversion, organosynthesis, and environmental purification is also briefly discussed. The methods to modify the electronic structure, nanostructure, crystal structure, and heterostructure of g-C3 N4 , together with correlations between its structure and performance are illustrated. Perspectives on the challenges and opportunities for the future exploration of g-C3 N4 photocatalysts are provided. This Review will promote the utilization of g-C3 N4 materials in the fields of photocatalysis, energy conversion, environmental remediation, and sensors.
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              Two-dimensional covalent carbon nitride nanosheets: synthesis, functionalization, and applications

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                Author and article information

                Journal
                ESNNA4
                Environmental Science: Nano
                Environ. Sci.: Nano
                Royal Society of Chemistry (RSC)
                2051-8153
                2051-8161
                2017
                2017
                : 4
                : 5
                : 1155-1167
                Affiliations
                [1 ]Innovation & Application Institute
                [2 ]Zhejiang Ocean University
                [3 ]Zhoushan
                [4 ]China
                [5 ]State Environmental Protection Engineering Center for Pollution Treatment and Control in Textile Industry
                [6 ]College of Environmental Science and Engineering
                [7 ]Donghua University
                [8 ]Shanghai 201620
                Article
                10.1039/C6EN00706F
                4a40b021-ac04-4001-9c7c-4e3341c4b546
                © 2017
                History

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