School of Chemical Engineering , The University of Queensland , Brisbane , Queensland 4072 , Australia.
Centre for Future Materials , University of Southern Queensland , Springfield Central , Queensland 4300 , Australia.
ACS Appl Mater Interfaces. 2019 Nov 27;11(47):44300-44307. doi: 10.1021/acsami.9b15794. Epub 2019 Nov 13.
Metal-organic frameworks (MOFs) have recently emerged as promising electrocatalysts because of their atomically dispersed metal sites and porous structures. The active sites of MOF catalysts largely exist as coordinatively unsaturated metal sites (CUMSs). In this study, facile microwave-induced plasma engraving is applied to fine-tune the CUMSs of cobalt-based MOF (Co-MOF-74) without destroying its phase integrity by controlling the plasma-engraving species, intensity, and duration. The electrochemical activity of the engraved MOF is found to be quantitatively correlated to the coordination geometry of the metal centers corresponding to CUMSs. Specifically, the hydrogen plasma-engraved Co-MOF-74 shows an enhanced catalytic activity of oxygen evolution reaction, which exhibits a low overpotential (337 mV at 15 mA cm), high turnover frequency (0.0219 s), and large mass activity (54.3 A g). The developed CUMS control strategy and the revealed CUMSs activity correlation can inspire the further microstructure tuning of MOFs for various applications.
金属-有机骨架(MOFs)由于其原子分散的金属位点和多孔结构,最近作为有前途的电催化剂出现。MOF 催化剂的活性位点主要存在于配位不饱和金属位点(CUMS)中。在这项研究中,通过控制等离子体刻蚀的种类、强度和持续时间,采用简便的微波诱导等离子体刻蚀方法,在不破坏其相完整性的情况下,对基于钴的 MOF(Co-MOF-74)的 CUMS 进行微调。刻蚀 MOF 的电化学活性被发现与对应 CUMS 的金属中心的配位几何形状定量相关。具体而言,氢等离子体刻蚀的 Co-MOF-74 显示出增强的析氧反应催化活性,其表现出低过电势(在 15 mA cm 时为 337 mV)、高周转频率(0.0219 s)和大质量活性(54.3 A g)。所开发的 CUMS 控制策略和揭示的 CUMS 活性相关性可以激发 MOFs 在各种应用中的进一步微观结构调整。