Enhanced Photocatalytic Hydrogen Peroxide Synthesis Performance of Polymeric Carbon Nitrides with a Controllable Carbonization Strategy

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL
Ziqi Wang, Runjie Zhao, Xinyu Chen, Jiahui Xie, Qihua Yang, Xiaobo Li
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引用次数: 0

Abstract

Polymeric carbon nitrides have gained significant interest in photocatalysis owing to their tunable electronic and structural diversity. However, traditional polymeric carbon nitrides, regardless of their structural motifs, have shown limited or no effectiveness in producing H2O2 through photocatalysis. This study introduces a controllable carbonization technique assisted by post molten salt treatment, as demonstrated across three structurally distinct polymeric carbon nitrides: melon and two ionic variants. Through the molten salt treatment, the photoactivities for H2O2 synthesis were significantly enhanced on all three carbon nitride variants. The enhanced activity is attributed to the precise control of the carbonization process, resulting in the formation of a composite material comprising carbon and carbon nitride. The formation of this composite material not only improves charge separation but also imparts hydrophobic properties to the material, thereby preventing the decomposition of H2O2 synthesized under photocatalytic conditions.

Abstract Image

利用可控碳化策略提高聚合物氮化碳的光催化过氧化氢合成性能
聚合碳氮化物因其可调的电子和结构多样性而在光催化领域备受关注。然而,传统的聚合碳氮化物,无论其结构模式如何,在通过光催化产生 H2O2 方面的效果都很有限,甚至没有效果。本研究介绍了一种通过熔盐后处理辅助的可控碳化技术,并在三种结构不同的聚合碳氮化物(甜瓜和两种离子变体)中进行了演示。通过熔盐处理,所有三种氮化碳变体合成 H2O2 的光活性都显著增强。活性的增强归功于对碳化过程的精确控制,从而形成了一种由碳和氮化碳组成的复合材料。这种复合材料的形成不仅改善了电荷分离,还赋予了材料疏水特性,从而防止了在光催化条件下合成的 H2O2 的分解。
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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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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