Hongbo Yu, Lixia Wang, Huatong Li, Zuyang Luo, Dr. Tayirjan Taylor Isimjan, Prof.?Dr. Xiulin Yang
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引用次数: 3
摘要
金属有机骨架(MOFs)因其超薄结构、成分可调、高表面积和高孔隙率而被认为是潜在的析氧反应(OER)电催化剂。本文采用简单的两步溶剂热法在泡沫镍(NF)上设计并制备了掺钒镍有机骨架(V1−x−nixof)体系。钒的掺杂显著提高了V1−x−nixof的OER活性,在高电流密度(>400 mA cm−2)下表现出比相应的Ni-MOF、NiV-MOF和RuO2催化剂更好的性能。V0.09−Ni0.91MOF/NF在电流密度为10 mA cm−2时具有235 mV的低过电位和30.3 mV dec−1的小塔菲尔斜率。更重要的是,以Pt/C/NF和V0.09 - Ni0.91MOF/NF作为阴极和阳极组装的水分解装置产生了1.96 V@1000 mA cm−2的电池电压,从而优于最先进的RuO2(+)||Pt/C(−)。我们的工作为制备稳定、高效的OER电催化剂和设计各种mof基材料提供了新的思路。
Improving the Electrocatalytic Activity of a Nickel-Organic Framework toward the Oxygen Evolution Reaction through Vanadium Doping
Metal-organic frameworks (MOFs) have been considered as potential oxygen evolution reaction (OER) electrocatalysts owning to their ultra-thin structure, adjustable composition, high surface area, and high porosity. Here, we designed and fabricated a vanadium-doped nickel organic framework (V1−x−NixMOF) system by using a facile two-step solvothermal method on nickel foam (NF). The doping of vanadium remarkably elevates the OER activity of V1−x−NixMOF, thus demonstrating better performance than the corresponding single metallic Ni-MOF, NiV-MOF and RuO2 catalysts at high current density (>400 mA cm−2). V0.09−Ni0.91MOF/NF provides a low overpotential of 235 mV and a small Tafel slope of 30.3 mV dec−1 at a current density of 10 mA cm−2. More importantly, a water-splitting device assembled with Pt/C/NF and V0.09−Ni0.91MOF/NF as cathode and anode yielded a cell voltage of 1.96 V@1000 mA cm−2, thereby outperforming the-state-of-the-art RuO2(+)||Pt/C(−). Our work sheds new insight on preparing stable, efficient OER electrocatalysts and a promising method for designing various MOF-based materials.
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