Department of Chemistry, CB#3290, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
J Am Chem Soc. 2012 May 2;134(17):7211-4. doi: 10.1021/ja300539p. Epub 2012 Apr 18.
Pt nanoparticles of 2-3 nm and 5-6 nm in diameter were loaded into stable, porous, and phosphorescent metal-organic frameworks (MOFs 1 and 2) built from Ir(ppy)(2)(bpy)-derived dicarboxylate ligands (L(1) and L(2)) and Zr(6)(μ(3)-O)(4)(μ(3)-OH)(4)(carboxylate)(12) secondary building units, via MOF-mediated photoreduction of K(2)PtCl(4). The resulting Pt@MOF assemblies serve as effective photocatalysts for hydrogen evolution by synergistic photoexcitation of the MOF frameworks and electron injection into the Pt nanoparticles. Pt@2 gave a turnover number of 7000, approximately five times the value afforded by the homogeneous control, and could be readily recycled and reused.
将直径为 2-3nm 和 5-6nm 的 Pt 纳米颗粒负载到由[Ir(ppy)(2)(bpy)]衍生的二羧酸配体(L(1)和 L(2))和 Zr(6)(μ(3)-O)(4)(μ(3)-OH)(4)(羧酸)(12)构建的稳定、多孔和磷光金属有机骨架(MOFs 1 和 2)中,通过 MOF 介导的 K(2)PtCl(4)的光还原。所得的 Pt@MOF 组装体作为有效的光催化剂,通过 MOF 框架的协同光激发和电子注入到 Pt 纳米颗粒中,促进了氢的释放。Pt@2 给出了 7000 的周转数,大约是均相对照值的五倍,并且可以容易地回收和再利用。