材料科学
化学工程
带隙
剥脱关节
光催化
降级(电信)
热稳定性
石墨氮化碳
质子化
纳米技术
氮化碳
晶体结构
热处理
无定形固体
可见光谱
溶剂热合成
导带
氮化物
纳米颗粒
磷
化学
纳米晶
晶格常数
反应速率常数
作者
Wenyi Zhu,Nianwei Yang,Ruixue Fan,Funing Zhang,Yunqing Liu,Hai Lin
标识
DOI:10.1016/j.rineng.2026.109406
摘要
Phosphorus‑doped graphitic carbon nitride nanosheets (P-CN-4.2) were synthesized via a synergistic strategy combining phosphoric‑acid‑mediated protonation and thermal exfoliation. Under visible light, P-CN-4.2 exhibits optimal performance, achieving 99% degradation of levofloxacin within 45 min, with a photocatalytic rate constant 3.8 times that of pristine g‑C3N4. The enhanced activity originates from the combined effects of exfoliation‑induced morphological engineering and electronic structure tailoring by phosphorus doping. XRD, TEM, and UV‑Vis DRS characterizations confirm the transformation of bulk layered aggregates into ultrathin nanosheets while preserving the crystalline heptazine skeleton. Concurrently, lattice P‑N bonding narrows the bandgap from 2.76 eV to 2.66 eV, shifts the conduction band upward by 0.17 eV, prolongs carrier lifetime, and enhances visible‑light absorption. Furthermore, P-CN-4.2 retains >90% activity after seven consecutive cycles without detectable phosphorus leaching, underscoring its excellent stability and reusability. This work establishes a scalable synthesis of high‑efficiency metal‑free photocatalysts and delivers in‑depth mechanistic insights for the remediation of antibiotic‑contaminated water.
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