富氮氮化碳的庚嗪相受热解温度控制,可用于光催化还原六价铀

IF 2 3区 化学 Q4 CHEMISTRY, PHYSICAL Chemical Physics Pub Date : 2024-08-13 DOI:10.1016/j.chemphys.2024.112421
Zhenhua Dang , Gao Weijie , Chu Yanyang , Pang Bopeng , Zhang Lin
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引用次数: 0

摘要

光催化工艺是一种新型高效技术,在还原六价铬过程中具有巨大潜力。氮在高温下易挥发,因此其合成反应受热解温度的影响很大。本文通过将热解温度从 450 °C 改为 650 °C,制备了一系列氮含量不同、催化性质不同的富氮氮化碳。随着热解温度的升高,氮含量不断降低,低温热解产生的三嗪环、四嗪环和偶氮键逐渐被七嗪环和氮单键取代。在 550 °C 下合成的富氮氮化碳对 U(VI) 的还原活性最好,这归功于其良好的空腔结构、窄光吸收带隙和高电子传输通道。这些结果可为调节富氮氮化碳的电子传输结构以提高光催化活性提供指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Nitrogen-rich carbon nitride with heptazine phase controlled by pyrolysis temperature towards photocatalytic U(VI) reduction

Photocatalytic process is a new and efficient technology, which has great potential in the U(VI) reduction process. Nitrogen is volatile at high temperatures, so its synthesis reaction is significantly influenced by pyrolysis temperature. Herein, a series of nitrogen-rich carbon nitride with different nitrogen content and different catalytic properties were prepared by changing the pyrolysis temperature from 450 °C to 650 °C. With the increase of pyrolysis temperature, the nitrogen content decreases continuously, and the triazine ring, tetrazine ring and azo bond generated by low temperature pyrolysis are gradually replaced by heptazine ring and nitrogen single bond. The nitrogen-rich carbon nitride synthesized at 550 °C has the best reducing activity for U(VI) reduction, which is attributed to the good cavity structure, narrow light absorption band gap and high electron transport channel. These results can provide guidance for regulating the electron transport structure of the nitrogen-rich carbon nitride to achieve enhanced photocatalytic activity.

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来源期刊
Chemical Physics
Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
4.60
自引率
4.30%
发文量
278
审稿时长
39 days
期刊介绍: Chemical Physics publishes experimental and theoretical papers on all aspects of chemical physics. In this journal, experiments are related to theory, and in turn theoretical papers are related to present or future experiments. Subjects covered include: spectroscopy and molecular structure, interacting systems, relaxation phenomena, biological systems, materials, fundamental problems in molecular reactivity, molecular quantum theory and statistical mechanics. Computational chemistry studies of routine character are not appropriate for this journal.
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