在高效光催化剂的共价有机框架中对堆叠配置进行精确的溶剂驱动控制
Yixue Xu1,2, Fan Qiu1,2, Yubin Fu3,4
1Research Center for Nano Photoelectrochemistry and Devices, School of Chemistry and Chemical Engineering, Southeast University, Nanjing, 211189, China.
Angewandte Chemie (International ed. in English)
|August 30, 2025
概括
研究人员开发了一种新方法来控制二维COF的堆叠,以实现更好的光催化. 与AA相比,ABC堆叠的COF-TD-ABC显示出显著更高的进化率.
科学领域:
- 材料科学
- 催化剂
- 纳米技术
背景情况:
- 由于它们的大面积和可调性特性,二维共价有机框架 (2D COF) 显示出作为光催化剂的巨大潜力.
- 控制二维COF中的层间堆叠对于优化电荷传输和催化效率至关重要,但仍然是一个重大挑战.
研究的目的:
- 开发一种以溶剂为导向的策略,以精确控制金属嵌入的二维COF中的层间堆叠配置.
- 调查不同堆叠配置 (AA阴影与ABC分层) 对光催化性能的影响,特别是对的进化.
主要方法:
- 使用1-butanol的溶剂驱动策略用于调节协调相互作用,并在金属内置的2D COF中实现特定的AA (COF-TD-AA) 和ABC (COF-TD-ABC) 堆叠配置.
- 对COF-TD-AA和COF-TD-ABC以及Pt辅助催化剂进行了测量.
主要成果:
- 与COF-TD-AA相比,ABC堆叠的COF-TD-ABC显示了增强的光吸收和更高的电荷迁移/分离效率.
- COF-TD-ABC 的高演变率为 10. 92 mmol g-1 h-1,大约是 COF-TD-AA 的 3.5 倍 (3. 12 mmol g-1 h-1).
结论:
- 精确控制二维COF中的层间堆叠,显著影响其光催化活性.
- 开发的溶剂驱动策略为设计高性能COF光催化剂提供了一条途径,通过调整堆叠配置以改善充电动力学.
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