异质结
材料科学
光催化
量子点
环境污染
合理设计
降级(电信)
可见光谱
纳米技术
化学工程
密度泛函理论
电子转移
光电子学
地下水修复
半导体
经济短缺
环境修复
复合数
纳米晶
电子顺磁共振
光化学
罗丹明B
作者
Fengyu Tian,Jiayu Liang,Honglei Zhang,Yifan Wang,Xuemin Yan
标识
DOI:10.1016/j.seppur.2025.135838
摘要
Rational design of dual-functional photocatalysts capable of concurrently driving CO 2 photoreduction and environmental remediation holds significant promise for addressing global energy shortages and environmental pollution challenges. Herein, we successfully fabricated a novel 0D/2D S-doped ZnO quantum dots/g-C 3 N 4 nanosheets (SZ-QDs/CNNS) S-scheme heterojunction through a facile self-sacrificing template approach. Structural characterization reveals that the S-doped ZnO QDs are homogeneously dispersed across the g-C 3 N 4 nanosheets, leading to the enhancement in visible-light harvesting capability of the composite system. Through combined density functional theory calculations and experimental investigations, we elucidated the interfacial charge transfer mechanism, revealing electron transfer from g-C 3 N 4 to S-doped ZnO that establishes an internal electric field (IEF) oriented from g-C 3 N 4 to S-doped ZnO. Electron spin resonance analysis under visible light irradiation confirmed that the IEF effectively drives photoexcited electrons from S-doped ZnO to g-C 3 N 4 , validating the formation of an S-scheme charge transfer pathway that significantly enhances electron-hole pair separation efficiency. The SZ-QDs/CNNS heterojunction demonstrates remarkable photocatalytic performance, achieving a CO evolution rate of 34.5 μmol·g −1 ·h −1 under visible light irradiation, which is 2.4 and 4.8 times higher than pristine g-C 3 N 4 and S-doped ZnO, respectively. Furthermore, the SZ-QDs/CNNS also exhibits outstanding degradation efficiency for NO (56.5 % in 40 min), RhB (100 % in 40 min) and tetracycline (90 % in 180 min) compared to individual components. This work provides valuable insights into the rational design of efficient S-scheme photocatalysts for sustainable energy conversion and environmental applications.
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