Unleashing the potential of Ru/FeCo-MOF in water splitting and supercapacitors through Morphology and electronic structure control

Rational design and structural regulation of nanomaterials play a vital role in advancing clean energy and energy storage technologies. Metal-organic frameworks (MOFs) are highly regarded as ideal bi-functional electro-catalytic materials for overall water splitting and supercapacitors applications. However, the utilization of MOF materials in practical applications still presents significant challenges due to their inherent limitations in electrical conductivity and morphology control. In this study, we successfully synthesized FeCo-MOF material and effectively regulated its morphology and electronic structure by varying the amount of RuCl3. and its active surface area was increased. The results show that the addition of Ru can not only introduce new metal active sites, but also shorten the path of ion diffusion. Furthermore, it can establish electronic coupling with the Fe and Co active sites interface, thereby tuning their electronic structures. The optimized 0.04 Ru/FeCo-MOF catalyst displayed remarkably low overpotential and high activity in both oxygen evolution reaction (OER) (eta 50 = 309 mV) and hydrogen evolution reaction (HER) (eta 10 = 180 mV). In a two-electrode system, the 0.04 Ru/FeCo-MOF|| 0.04 Ru/FeCo-MOF drived 10 mA cm-2 current density only need low voltage of 1.498 V. Moreover, this material also exhibits a high specific capacitance of 8600 mF cm-2 and excellent cycle stability in supercapacitor applications (88.9%). This synthesis strategy encompassing the regulation of both morphology and electronic structure presents a distinctive perspective for MOF design.