光催化
石墨氮化碳
过氧化氢
钾
制氢
氮化碳
化学
兴奋剂
无机化学
碳纤维
氮化物
氢
材料科学
催化作用
有机化学
复合数
光电子学
复合材料
图层(电子)
作者
Shengyu Jing,Qingyuan Xu,Haoran Wang,Palanisamy Kannan,Huagen Liang,Angeliki Brouzgou,Ruiyu Wang,Panagiotis Tsiakaras
标识
DOI:10.1016/j.jcis.2025.137675
摘要
Hydrogen peroxide (H2O2) has long been recognized as an important green cleaning chemical. Due to its narrow bandgap and nitrogen-rich structure, graphitic carbon nitride (g-C3N5) is considered a promising photocatalyst for H2O2 generation. However, the limited visible light harvesting capacity and weak charge separation ability of bulk g-C3N5 limit its photocatalytic activity. Herein, to address the low photogenerated carrier mobility of g-C3N5, we successfully synthesized a series of K-ion-doped g-C3N5 (KCN) by co-calcination of 3-amino-1,2,4-triazole with potassium salt. The effects of different potassium salts (potassium oxalate-K2C2O4, potassium nitrate-KNO3, and potassium hydroxide-KOH) and different additions on the photocatalytic ability of g-C3N5 were compared and systematically analyzed. The results showed that the KCN sample synthesized with KOH as dopant exhibits the highest H2O2 yield up to 1546.7 µmol L-1h-1, seven times more than that of pure g-C3N5. The excellent photocatalytic H2O2 evolution efficiency is confirmed by DFT calculations to be mainly attributed to the rational design of g-C3N5, which produces more pronounced cyano groups under high-temperature calcination and alkaline environment while promoting the formation of N vacancies. This design effectively promotes the separation of electron-hole pairs and the optimization of carrier transport capacity, and as a result, KOH doping exhibits better photocatalytic performance. The current work provides a more favorable modification strategy for future solar energy conversion.
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