State Key Laboratory of Fine Chemicals, DUT-KTH Joint Education and Research Center on Molecular Devices, Dalian University of Technology, Dalian, 116024, China.
Chem Commun (Camb). 2019 Dec 5;55(98):14773-14776. doi: 10.1039/c9cc07433c.
Metal-organic frameworks (MOFs) are promising catalysts for electrochemical reactions. Herein, self-supported NiFe-MOF nanoplates grown on Ni foam (NF) were prepared with iron carbonate hydroxide nanosheets (FeCH NSs) as a semisacrificial template and evaluated for the electrocatalytic oxygen evolution reaction (OER). In this approach, the porous FeCH NSs not only serve as the iron source of NiFe-MOF, but also slow down the leaching of Ni ions from the substrate, thus playing a unique role in regulating the morphology of NiFe-MOF with reduced thickness and sizes, enabling rapid electron transfer and mass transport. The resultant NiFe-MOF/FeCH-NF electrode showed higher activity than FeCH template-free electrodes and superior OER performance over other MOF based binder-free OER electrodes. A current density of 10 mA cm-2 was obtained at a low overpotential of 200 mV with excellent durability in alkaline solution. Raman and TEM measurements reveal the partial transformation of NiFe-MOF to hydroxide during water oxidation.
金属-有机骨架(MOFs)是电化学反应有前途的催化剂。本文以碳酸亚铁纳米片(FeCH NSs)为半牺牲模板,制备了自支撑的生长在泡沫镍(NF)上的 NiFe-MOF 纳米片,并将其用于电催化析氧反应(OER)。在这种方法中,多孔 FeCH NSs 不仅充当 NiFe-MOF 的铁源,而且还减缓了 Ni 离子从基底中的浸出,从而在调节厚度和尺寸减小的 NiFe-MOF 的形态方面发挥独特的作用,实现了快速的电子转移和质量传输。所得的 NiFe-MOF/FeCH-NF 电极比没有 FeCH 模板的电极具有更高的活性,并且在其他基于 MOF 的无粘结剂 OER 电极中具有更好的 OER 性能。在碱性溶液中具有出色的耐久性,在低过电势 200 mV 时即可获得 10 mA cm-2 的电流密度。拉曼和 TEM 测量表明,在水氧化过程中 NiFe-MOF 部分转化为氢氧化物。