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Metal-organic framework derived iron-nickel sulfide nanorods for oxygen evolution reaction

机译:金属 - 有机框架衍生铁镍硫化物纳米杆,用于氧气进化反应

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Highly efficient oxygen evolution reaction (OER) on noble metal-free catalysts is a major challenge for green hydrogen production. We report herein a rational preparation strategy for MOF-derived chalcogenide electrocatalysts. The optimal sulfuration time is 12 h under the conditions of the theoretical Fe/Ni ratio of 1:1 and treatment temperature at 120 degrees C. In this case, the pyrite Fe0.75Ni0.25S2 nanorods combining with amorphous FeNiOOH formed in situ exhibit a low overpotential of 247 mV with a small Tafel slope of 47.6 mV dec(-1) at a current density of 10 mA cm(-2) in alkaline media along with high electrochemical stability for OER. The enhanced performance is derived from the synergistic effect between FeNi sulfide with favorable electrical conductivity and generated (oxy)hydroxides with high intrinsic activity. More importantly, the more active sites and appropriate mesoporous structure further facilitate electrocatalytic activity due to improved mass transfer. This facile synthesis method is a potential pathway for MOF derived highly efficient electrocatalysis for sustainable hydrogen product. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:高效的无金属催化剂上的高效氧气进化反应(OER)是绿色氢生产的主要挑战。我们在此报告了MOF衍生的硫属化物电催化剂的合理制备策略。在理论为Fe / Ni比率为1:1的条件下,最佳硫化时间为12小时,并且在这种情况下,处理温度为120℃。在这种情况下,与原位形成的无定形FenioOH组合的吡啶矿石Fe0.75Ni0.5S2纳米棒247 mV的低过电位,具有47.6 mV DEC(-1)的小TAFEL斜率,在碱性介质中的电流密度为10 mA cm(-2),具有高电化学稳定性的OER。增强的性能来自Feni硫化物与具有良好导电性的协同效应,并且具有高固有活性的(氧)氢氧化物产生(氧基)。更重要的是,由于改善的传质导致,更活跃的部位和适当的介孔结构进一步促进了电催化活性。该容易合成方法是用于可持续氢产物的MOF衍生的高效电常见的潜在途径。 (c)2021氢能出版物LLC。 elsevier有限公司出版。保留所有权利。

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