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首页> 外文期刊>Journal of Colloid and Interface Science >TiO2-on-C3N4 double-shell microtubes: In-situ fabricated heterostructures toward enhanced photocatalytic hydrogen evolution
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TiO2-on-C3N4 double-shell microtubes: In-situ fabricated heterostructures toward enhanced photocatalytic hydrogen evolution

机译:TiO2-ON-C3N4双壳微管:原位制造的异质结构朝向增强的光催化氢气进化

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Structural design, doping, and construction of heterojunctions are effective strategies for producing highly efficient photocatalytic materials. Herein, N-doped TiO2 was formed on hexagonal C3N4 tube through in-situ hydrolysis of a Ti source on a supramolecular precursor, followed by thermal treatment. As a result, a double-shell microtube, C3N4@TiO2 heterostructure was fabricated. It was worth noting that the supramolecular precursor was prepared from melamine and cyanuric acid, which not only served as a template for the double-shell tubular structure, but also provided nitrogen for the doping of TiO2. The photocatalytic efficiency of C3N4 @TiO2 was investigated by conducting hydrogen production experiments. The hydrogen production rate of C3N4@TiO2 was measured to be 10.1 mmol h(-1) g(-1), which is 4 times and 15 times that of C3N4 and TiO2, respectively. The improved photocatalytic activity of C3N4@TiO2 can be ascribed to (1) the tubular structure that provides a large number of reaction sites and enhances mass transport, (2) the heterojunction that is beneficial to charge separation, and (3) doping of TiO2 with nitrogen which extends its optical absorption range to visible light. This work demonstrates a facile method for synthesizing a highly efficient photocatalyst towards hydrogen evolution by modifying its structure and chemical composition as well as forming a heterojunction. (C) 2020 Elsevier Inc. All rights reserved.
机译:杂交功能的结构设计,掺杂和施工是生产高效光催化材料的有效策略。在此,通过在超分子前体上的Ti源的原位水解在六边形C3N4管上形成N-掺杂的TiO 2,然后进行热处理。结果,制造了双壳Microtube,C3N4 @ TiO2异质结构。值得注意的是,超分子前体由三聚氰胺和氰尿酸制备,其不仅用作双壳管状结构的模板,而且还提供了氮气的TiO2掺杂。通过进行氢生产实验研究了C3N4 @ TiO2的光催化效率。测量C3N4 @ TiO 2的氢气产生速率为10.1mmol H(-1)g(-1),分别为C3N4和TiO 2的4倍和15倍。 C3N4 @ TiO 2的改善的光催化活性可以归因于(1)的管状结构,该管状结构提供大量的反应位点并增强质量传输,(2)有利于电荷分离的异质结,以及(3)TiO2的掺杂用氮气将其光学吸收范围延伸到可见光。该工作通过改变其结构和化学组成以及形成异质结来合成高效光催化剂的容纳方法。 (c)2020 Elsevier Inc.保留所有权利。

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