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Graphitic Carbon Nitride with S and Fe(III) Codoping for Improved Photodegradation Performance

机译:具有S和Fe(III)的石墨碳氮化物,用于改善光降解性能

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摘要

The visible light photocatalytic performance of graphitic carbon nitride (g-C3N4) can be enhanced by tuning its electronic structure and bandgap via metal and nonmetal elements doping. The Fe and S codoped g-C3N4 is synthesized by the polymerization of melamine, iron chloride and trithiocyanuric acid at elevated temperature and characterized as crimped nanosheets with mesoporous structures. The photocatalytic performance of Fe-S codoped g-C3N4 for RhB degradation increases seven times by enhancing visible light adsorption and increasing the mobility of photoinduced electron/hole pair by narrowing its bandgap compared to the pure g-C3N4 nanosheets. The synergetic effect of Fe(III) ion coordinated in the pore centre among three triazine units and S dopant substituted the N in triazine skeleton causes much stronger delocalized HOMO and LUMO and increases the reactive sites, facilitating the migration of photogenerated charge carriers, thus enhances the visible-light driven photocatalytic performance.
机译:通过通过金属和非金属元件掺杂通过调谐电子结构和带隙,可以提高石墨碳氮化物(G-C3N4)的可见光光催化性能。通过在升高的温度下聚酰胺,铁酰氯和三氰脲酸的聚合来合成Fe和S编码G-C3N4,并以培养基结构为卷曲的纳米片。通过增强可见光吸附并增加与纯G-C3N4纳米晶片相比,通过增强可见光吸附并增加光致电子/空穴对的迁移率来增加Fe-S编码G-C3N4的光催化性能增加了七次。在三嗪单位和S掺杂剂中的Fe(III)离子在三嗪单位和S掺杂剂中取代的二嗪骨架中N的协调效应导致较强的划分的冠状型和LumO,并增加反应性位点,促进光生电荷载体的迁移,从而增强可见光驱动的光催化性能。

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