石墨氮化碳
共晶体系
三聚氰胺
深共晶溶剂
材料科学
碳纤维
溶剂
光催化
硫氰酸盐
化学工程
光化学
无机化学
化学
复合材料
有机化学
合金
催化作用
工程类
复合数
作者
Xiang Yu,Tingting Fan,Wenwen Chen,Zhou Chen,Yunyun Dong,Hong-Qiang Fan,Weiping Fang,Xiaodong Yi
出处
期刊:Carbon
[Elsevier BV]
日期:2019-04-01
卷期号:144: 649-658
被引量:32
标识
DOI:10.1016/j.carbon.2018.12.104
摘要
The room temperature deep eutectic solvent (DES) is demonstrated as an ideal precursor to prepare self-hybridized graphitic carbon nitride (g-C3N4) for the first time, for its special components, randomly reorganized molecules and extensive hydrogen bonds. In this work, by adjusting the proportion of urea and ammonium thiocyanate in the precursor DES, the self-hybridized coralloid g-C3N4, stacked by a mass of double-layer g-C3N4/g-C3N4 nanocages, were prepared without any templates. Compared to conventional g-C3N4 prepared using melamine, urea and AT as precursors, the improved charge transfer between the interfaces of the self-hybridized g-C3N4 has been demonstrated, which is attributed to the well-matched electronic band structures of the two g-C3N4 species, the abundant 2D/2D interfacial contact and increased photocatalytic active sites. As expected, it exhibits highly enhanced photocatalytic activity, which is among the best g-C3N4 photocatalysts without doping any other elements.
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