超薄2D Co-MOF展示了卓越的电催化析氧以及无与伦比的稳定性

IF 2.6 4区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ChemNanoMat Pub Date : 2025-01-27 DOI:10.1002/cnma.202400649
Parul Sood, Harshita Bagdwal,  Krishankant, Arti Joshi, Monika Singh
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引用次数: 0

摘要

析氧反应(OER)通常是利用贵金属和基于金属氧化物的纳米结构进行的。然而,由于其众多的缺点,包括高成本,稳定性差和负面的环境影响;研究人员被驱使去创造新的电活性材料。为此,我们报道了一种超薄2D Co-MOF [Co2(bpe)2.5(NO3)4(ch30)] (Co-MOF),它在水热条件下结晶,在电流密度为10 mA cm - 2时显示出极好的OER活性,过电位为267 mV, Tafel斜率值低至104 mV dec - 1。与3D mof相比,二维mof具有许多优点,例如更好的暴露和活性位点的可访问性。二维mof的分层结构可以提供更大的结构灵活性,有利于适应OER过程中的变化,并在运行条件下保持结构的完整性。Co-MOF的性能超过了市售的OER催化剂RuO2,表现出前所未有的112小时的长稳定性,据我们所知,这是迄今为止观察到的任何原始MOF中最长的稳定性。通过oer后表征,发现原位形成的Co(OH)2和CoOOH是负责析氧的活性位点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ultrathin 2D Co-MOF Showcasing Remarkable Electrocatalytic Oxygen Evolution Coupled with Unparalleled Stability

Ultrathin 2D Co-MOF Showcasing Remarkable Electrocatalytic Oxygen Evolution Coupled with Unparalleled Stability

Oxygen Evolution Reaction (OER) is typically carried out utilizing noble metals and metal oxides based nanostructures. Yet, due to their numerous drawbacks, including high cost, poor stability and negative environmental effects; researchers are driven to create new electro-active materials. To that end, we report an ultrathin 2D Co-MOF [Co2(bpe)2.5(NO3)4(CH3O)] (Co-MOF) that crystallized under hydrothermal conditions, showing a terrific OER activity with an overpotential of 267 mV at the current density of 10 mA cm−2 and the low Tafel slope value of 104 mV dec−1. Two-dimensional MOFs offer numerous advantages over 3D MOFs such as better exposure and accessibility of active sites. The layered structure of 2D MOFs can provide greater structural flexibility, which can be beneficial for accommodating the changes during the OER process and maintaining structural integrity under operating conditions. The performance of Co-MOF surpasses commercially available OER catalyst RuO2, demonstrating an unprecedented prolonged stability of 112 hours, which, to the best of our knowledge, represents the longest stability, observed for any pristine MOF to date. From the post-OER characterization, it was discovered that in situ formed species, Co(OH)2 and CoOOH served as the active sites responsible for oxygen evolution.

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来源期刊
ChemNanoMat
ChemNanoMat Energy-Energy Engineering and Power Technology
CiteScore
6.10
自引率
2.60%
发文量
236
期刊介绍: ChemNanoMat is a new journal published in close cooperation with the teams of Angewandte Chemie and Advanced Materials, and is the new sister journal to Chemistry—An Asian Journal.
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