石墨氮化碳
光催化
煅烧
过氧化氢
材料科学
制氢
碳纤维
产量(工程)
氢
纳米技术
蒽醌
化学
化学工程
无机化学
氯化物
光化学
钾
半导体
降级(电信)
可持续生产
可见光谱
催化作用
作者
Xujing Tantai,Qun Zhou,Lili Shi,Meixuan Wu,Pengfei Sun,Xiaoping Dong
标识
DOI:10.1021/acsanm.5c03533
摘要
The photocatalytic synthesis of hydrogen peroxide (H 2 O 2 ) has emerged as a promising alternative to the energy-intensive anthraquinone process. Among various photocatalysts, graphitic carbon nitride (g-C 3 N 4 ), as a metal-free semiconductor with visible-light responsiveness, has demonstrated exceptional potential for the selective production of H 2 O 2 . In this work, a K-modified g-C 3 N 4 photocatalyst (KCN) was facilely synthesized via a secondary calcination method using potassium chloride (KCl) as the doping precursor. The optimized sample KCN-6 exhibited remarkable H 2 O 2 generation activity, achieving a production rate of 409.4 μmol·g –1 ·h –1 in a 10% ethanol solution, an 8-fold enhancement compared to that of pristine g-C 3 N 4 . Subsequently, a cyclic test was conducted, and its performance remained at 90% after five cycles. At the same time, the H 2 O 2 yield further increased to 818.9 μmol·g –1 ·h –1 under sunlight irradiation, highlighting its practical applicability. The superior performance stems from the synergistic effect of K incorporation and modification of cyano groups, which narrows the band gap, broadens light absorption, and facilitates charge-carrier separation. Based on the detection of active species, a plausible mechanism involving a two-step single-electron-transfer pathway was proposed. This study elucidates that K incorporation can modulate the photophysical properties and charge-transfer dynamics, offering valuable insights for designing high-performance, solar-driven photocatalytic systems for sustainable H 2 O 2 production.
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