光催化
石墨氮化碳
可见光谱
双酚A
氮化碳
光化学
催化作用
带隙
兴奋剂
三聚氰胺
材料科学
化学
氧气
无机化学
核化学
有机化学
环氧树脂
光电子学
作者
Ikki Tateishi,Mai Furukawa,Hideyuki Katsumata,Satoshi Kaneco
出处
期刊:Catalysis Today
[Elsevier]
日期:2022-08-18
卷期号:411-412: 113877-113877
被引量:10
标识
DOI:10.1016/j.cattod.2022.08.019
摘要
Oxygen-doped dual precursor carbon nitride (CN-U10.3M1.7 + AF5) with ammonium formate (AF), which has both characteristics of melamine-derived carbon nitride (CN-M) and urea-derived carbon nitride (CN-U) was prepared by simple one-step heat treatment. CN-U10.3M1.7 + AF5 promotes electron-hole pair separation, controls the bandgap energy, and increases the surface area. The bandgap is controlled from 3.0 to 1.5 eV. The separation of photogenerated electron-hole pairs was efficiently promoted. The surface area was controlled from 11.6 to 91.3 m2 / g. The CN-M / CN-U photocatalyst decomposed about 20% of 5 ppm bisphenol A (BPA) in 90 min under visible light (λ ≧ 420 nm). This result is higher than when only CN-M (10%) and CN-U (15%) are used. In addition, oxygen doping significantly improves the photocatalytic activity of CN-M, CN-U, and CN-M / CN-U. The photocatalytic activity of the optimized oxygen-doped CN-M / CN-U showed a degradation efficiency of 75% in 90 min.
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