Key Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing, 211816, P.R. China.
X-ray Sciences Division, Argonne National Laboratory, Argonne, IL, 60439, USA.
Adv Mater. 2018 Dec;30(49):e1803263. doi: 10.1002/adma.201803263. Epub 2018 Oct 10.
Nanoparticles@metal-organic frameworks (MOFs) composites have attracted considerable attention in recent years due to the prominent selective catalytic activity. However, it is highly desirable to develop a simple and universal way to settle the trade-off between the catalytic efficiency and selectivity. Herein, by employing the thermal instability of inherent defects, hierarchically porous Pt@UiO-66-NH , Pt@UiO-66, Pt@ZIF-8, and Au@ZIF-8 are successfully constructed after annealing at an appropriate temperature, respectively. The generated mesopores in the MOFs can be located around the external nanoparticle to retain the MOF shell for catalytic selectivity. Finally, when tested in olefin hydrogenation, Pt@UiO-66-NH shows significantly improved catalytic rate and enhanced dynamic selectivity.
纳米颗粒@金属有机骨架(MOFs)复合材料由于其突出的选择性催化活性,近年来引起了广泛关注。然而,开发一种简单而通用的方法来解决催化效率和选择性之间的权衡问题是非常可取的。在此,通过利用固有缺陷的热不稳定性,在适当的温度下退火后,分别成功地构建了分级多孔 Pt@UiO-66-NH 、Pt@UiO-66、Pt@ZIF-8 和 Au@ZIF-8。MOFs 中生成的介孔可以位于外部纳米颗粒周围,以保留 MOF 壳用于催化选择性。最后,在烯烃加氢反应中,Pt@UiO-66-NH 表现出显著提高的催化速率和增强的动态选择性。