氮化碳
同质结
氮化物
材料科学
三嗪
无机化学
三聚氰胺
纳米技术
光化学
化学工程
化学
光电子学
兴奋剂
催化作用
光催化
有机化学
复合材料
图层(电子)
高分子化学
工程类
作者
Zhengliang Zhao,Zhu Shu,Jun Zhou,Tiantian Li,Kai Wang,Jingyang Song
标识
DOI:10.1016/j.jallcom.2022.168484
摘要
LiCl-based molten salts have been widely used to induce the polymerization of melamine-derived monomer or intermediate into triazine-based or heptazine-based crystalline carbon nitride. Nevertheless, the role of LiCl beyond lowering melting point has not been fully revealed, and pure LiCl was exclusively reported to induce the formation of triazine-based crystalline counterpart. Herein, we firstly found that single LiCl can promote the deep deamination of melon-based pristine carbon nitride (PCN) to heptazine-based crystalline counterpart. As a result, a heptazine-/triazine-based crystalline carbon nitride homojunction was in situ formed by single LiCl-induced deamination and phase transition of PCN. It exhibits a favorable photocatalytic H2 evolution reaction rate 18.3 times higher than PCN, which benefits from the promoted charges separation between heptazine and triazine units in phase homojunction. This work emphasizes that single LiCl can realize diverse modulation of carbon nitride framework with advanced photocatalytic activity.
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