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首页> 外文期刊>Catalysis science & technology >Enhanced charge separation and photoactivity in heterostructured g-C3N4: a synergistic interaction in environmental friendly CaO/g-C3N4
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Enhanced charge separation and photoactivity in heterostructured g-C3N4: a synergistic interaction in environmental friendly CaO/g-C3N4

机译:增强的电荷分离和感光用g-C3N4:协同曹/ g-C3N4交互环境友好

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摘要

Directional charge transfer across interfaces resulting in a depressed recombination rate is often assumed to explain the enhanced photoactivity of heterostructured g-C3N4, without proof. A novel and eco-friendly CaO/g-C3N4 composite exhibiting good activity is prepared to unravel the microscopic mechanism for enhanced charge separation. X-and Q-band EPR revealed no evidence for electron transfer. A strong agreement between photocatalytic activities and EPR intensities demonstrates that the main driving force for the photoactivity is the electron trapped in the g-C3N4 C-2p state. Light-off EPR tracking showed that more C-2p trapped electrons survived on CaO/g-C3N4 than on g-C3N4 surface, which accounts for the enhanced charge separation. Parallels between EPR and DFT demonstrate that fusion with CaO increases the C-2p character for self-trapping photoexcited electrons, but at the expense of decreasing exciton dissociation efficiency. A synergistic interplay must be balanced for optimal performances of the heterostructured g-C3N4.
机译:定向跨界面电荷转移导致抑郁重组率通常认为解释增强用的光敏g-C3N4,没有证明。复合材料表现出良好的活动准备瓦解增强的微观机理电荷分离。电子转移的证据。光催化活动和之间的法律协议EPR强度主要演示了光敏是驱动力电子被困在g-C3N4 C-2p状态。C-2p点火EPR跟踪显示,更多被困在曹/ g-C3N4比电子幸存下来g-C3N4表面,占增强电荷分离。证明与曹增加了融合C-2p自已诱捕光激的性格电子,但减少为代价的激子分离效率。相互作用必须是最佳的平衡表演用的g-C3N4。

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