在Pd纳米集群和合体功能化的层状酸盐之间进行催化协同作用,以改善酸脱
Esmail Doustkhah1, Muhammed Yusufoğlu2,3,4, Hamza El-Hosainy4,5
1Chemistry Department, Faculty of Engineering and Natural Sciences, Istinye University, Sariyer, Istanbul 34396, Türkiye.
ACS applied materials & interfaces
|November 19, 2024
概括
为 (Pd) 纳米集群合成选择正确的配体是催化过程的关键. 氨基烯基连接剂在酸支上增加了27倍的酸脱活性,而烯基连接剂在酸支上增加了27倍.
科学领域:
- 材料科学 材料科学 材料科学
- 催化剂是一种催化剂.
- 纳米技术 纳米技术
背景情况:
- 在支上合成和稳定具有最佳催化活性的 (Pd) 纳米集群是具有挑战性的.
- 用连接体进行表面功能化提供了解决方案,但涉及反应产量和催化剂稳定性之间的权衡.
研究的目的:
- 为了研究不同连接体对Pd纳米集群合成,稳定和催化活性的影响.
- 为了比较aminopropyl和thiopropyl功能化酸盐支持Pd纳米集群催化物的性能.
主要方法:
- 用烯和乙醇进行分层酸盐中间层的功能化.
- 在功能化的支上合成和描述Pd纳米集群.
- 对于酸脱的催化试验.
- 密度函数理论 (DFT) 计算来分析Pd-连接体相互作用.
主要成果:
- 氨基基组上的Pd纳米集群在70°C时表现出酸脱的约27倍高的催化活性,与基组上的纳米集群相比.
- 据DFT计算,Pd-N债券较弱,共价较少,而Pd-S债券较强,共价较多.
- 醇功能化的表面导致Pd13集群的严重结构变形,减少了表面积和催化稳定性.
结论:
- 酸盐支持的aminopropyl功能化增强了Pd纳米集团用于甲酸脱的催化活性.
- 虽然 thiopropyl 配体提供更好的 Pd-S 键稳定性,但它们会诱导 Pd 纳米集群的有害结构变化,从而损害整体的催化性能.
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