Skorjanc Tina, Kamal Khaja Mohaideen, Alkhoori Ayesha, Mali Gregor, Mohammed Abdul Khayum, Asfari Zouhair, Polychronopoulou Kyriaki, Likozar Blaž, Trabolsi Ali, Shetty Dinesh
Science Division, New York University Abu Dhabi, Saadiyat Island, Abu Dhabi, United Arab Emirates.
Materials Research Laboratory, University of Nova Gorica, Vipavska 11c, 5270 Ajdovscina, Slovenia.
ACS Appl Mater Interfaces. 2022 Jul 13;14(27):30796-30801. doi: 10.1021/acsami.2c05606. Epub 2022 Jun 17.
Metal nanoparticles are potent reaction catalysts, but they tend to aggregate, thereby limiting their catalytic efficiency. Their coordination with specific functional groups within a porous structure prevents their aggregation and facilitates the mass flow of catalytic starting materials and products. Herein, we use a thiacalix[4]arene-based polymer as a porous support with abundant docking sites for Au nanoparticles. The sulfur atoms bridging the phenolic subunits of thiacalix[4]arene serve as Lewis basic sites that coordinate Au atoms. Therefore, this approach takes advantage of the functional groups inherent in the monomer and avoids laborious postsynthetic modifications of the polymer. The presented system was tested for visible-light-driven photocatalytic CO reduction, where it showed adequate ability to generate 6.74 μmol g CO over the course of 4 h, while producing small amounts of the CH product. This study aims to stimulate interest in the design and development of synthetically simpler porous polymer supports for various metal nanoparticles in catalytic and other applications.
金属纳米颗粒是高效的反应催化剂,但它们容易聚集,从而限制了其催化效率。它们与多孔结构内的特定官能团配位可防止其聚集,并促进催化原料和产物的质量流动。在此,我们使用基于硫杂杯[4]芳烃的聚合物作为具有丰富金纳米颗粒对接位点的多孔载体。连接硫杂杯[4]芳烃酚亚基的硫原子作为与金原子配位的路易斯碱位点。因此,这种方法利用了单体中固有的官能团,避免了聚合物繁琐的合成后修饰。所展示的体系针对可见光驱动的光催化CO还原进行了测试,在4小时的过程中,它显示出产生6.74 μmol g CO的足够能力,同时产生少量的CH产物。本研究旨在激发人们对设计和开发用于催化及其他应用中各种金属纳米颗粒的合成更简单的多孔聚合物载体的兴趣。