首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Iron-Based Metal-Organic Framework System as an Efficient Bifunctional Electrocatalyst for Oxygen Evolution and Hydrogen Evolution Reactions
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Iron-Based Metal-Organic Framework System as an Efficient Bifunctional Electrocatalyst for Oxygen Evolution and Hydrogen Evolution Reactions

机译:铁基金属有机框架系统作为氧气进化和氢气进化反应的有效双官能电催化剂

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The fabrication of highly efficient and sustainable electrocatalysts used for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is exceedingly challenging and warranted for overall water splitting. In this work, we successfully synthesized a series of metal-organic frameworks (MOFs), namely, as Fe2M-MOF (M = Fe, Co, Ni, Zn, Mn; H4L = 3,3,5,5'-azoxybenzenetetracarboxylic acid) under a simple and mild condition, in which the Fe3 cluster as a basic building unit was replaced by the second kind of metal center; at the same time, a redox-active organic linker was adopted. The Fe2M-MOF system as a multifunctional catalyst realizes great improvement of the OER and HER performances. Among of them, the Fe2Co-MOF catalyst exhibits an extremely low overpotential of 339 mV at a current density of 10 mA cm(-2) and a very small Tafel slope of 36.2 mV dec(-1) in an alkaline electrolyte for OER. This result has far exceeded the commercial catalyst IrO2. Meanwhile, Fe2Zn-MOF manifests excellent HER activity with a small overpotential of 221 mV at 10 mA cm(-2) and a low Tafel slope of 174 mV dec(-1). In addition, the good long-term stability for these catalysts can be evaluated under working conditions. Systematic investigations are used to explain the enhanced electrocatalytic mechanism. In conclusion, we provide a simple and effective strategy for the preparation of multifunctional catalysts for energy conversion applications based on a pristine MOF material with redox-active metal centers and organic linkers.
机译:用于氢气进化反应(她)和氧气进化反应(Oer)的高效和可持续的电催化剂的制备非常具有挑战性,并保证整体水分裂。在这项工作中,我们成功地合成了一系列金属 - 有机骨架(MOF),即作为Fe2M-MOF(M = Fe,Co,Ni,Zn,Mn; H4L = 3,3,5,5'-氮杂苯并苯甲酸羧酸)在简单和温和的条件下,其中FE3集群作为基本建筑单元被第二种金属中心取代;同时,采用氧化还原活性有机接头。 FE2M-MOF系统作为多功能催化剂,实现了Oer和她的表演的巨大改善。其中,Fe 2CO-MOF催化剂在10 mAcm(-2)的电流密度为339mV的极低过电位,以及在oer的碱性电解质中为36.2mV dec(-1)的非常小的Tafel斜率。该结果远远超过商业催化剂IRO2。同时,Fe2ZN-MOF在10 mA cm(-2)下的小型221mV的小型过电位和174mV DEC(-1)的低TAFEL斜率,表现出优异的她的活性。此外,可以在工作条件下评估这些催化剂的良好长期稳定性。系统研究用于解释增强的电催化机制。总之,我们提供了一种简单有效的策略,用于制备基于氧化还原活性金属中心和有机接头的原始MOF材料的能量转化应用的多功能催化剂。

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