Yin Zhao, Liang Jin, Zhang ZiYi, Luo Hang, Zhou Jun
Hunan Province Key Laboratory of Materials Surface & Interface Science and Technology, Changsha 410004, PR China; College of Material Science and Engineering, Central South University of Forestry and Technology, Changsha 410004, PR China.
Hunan Province Key Laboratory of Materials Surface & Interface Science and Technology, Changsha 410004, PR China; College of Material Science and Engineering, Central South University of Forestry and Technology, Changsha 410004, PR China.
J Colloid Interface Sci. 2022 Oct;623:405-416. doi: 10.1016/j.jcis.2022.05.057. Epub 2022 May 13.
Metal-organic frameworks (MOFs) display promising potential due to their exquisite structural advantages. Carboxylate-based MOFs, such as MIL-53 structures, attract a lot of attention among MOF families because of their remarkable stability in water and even alkaline condition. Hence, the delicate hierarchical microstructure is constructed by introducing MoO into NH-MIL-53(NiFe) using a straightforward solvothermal strategy. The NiFeMo-MOF/NF electrode manifests a superior OER performance, producing an overpotential of 239 mV at 50 mA cm and a decent Tafel slope of 87.0 mV dec. Furthermore, in a typical electrodeposition equipment, NiFeMo-MOF/NF is applied as the working electrode and the composite electrode named as (M) Ni-NiOOH/NF is generated by electrodeposition and electrooxidation process to assess HER performance, producing an overpotential of 119 mV at 50 mA cm and a decent Tafel slope of 58.3 mV dec. The integrated electrolysis device delivers an extraordinarily low cell voltage of 1.50 V at 10 mA cm while applying NiFeMo-MOF/NF as the anode, (M)Ni-NiOOH/NF as the cathode for overall water splitting, exceeding the noble RuO/NF||Pt-C/NF (1.60 V@10 mA cm). This study provides a promising design strategy for future electrolysis catalysts.
金属有机框架材料(MOFs)因其精妙的结构优势而展现出广阔的应用潜力。基于羧酸盐的MOFs,如MIL-53结构,因其在水甚至碱性条件下具有卓越的稳定性,在MOF家族中备受关注。因此,采用简单的溶剂热法将MoO引入NH-MIL-53(NiFe)中,构建了精细的分级微观结构。NiFeMo-MOF/NF电极表现出优异的析氧反应(OER)性能,在50 mA cm时过电位为239 mV,塔菲尔斜率为87.0 mV dec。此外,在典型的电沉积设备中,将NiFeMo-MOF/NF用作工作电极,通过电沉积和电氧化过程生成名为(M)Ni-NiOOH/NF的复合电极,以评估其析氢反应(HER)性能,在50 mA cm时过电位为119 mV,塔菲尔斜率为58.3 mV dec。在以NiFeMo-MOF/NF为阳极、(M)Ni-NiOOH/NF为阴极进行全水解时,集成电解装置在10 mA cm时的电池电压低至1.50 V,超过了贵金属RuO/NF||Pt-C/NF(1.60 V@10 mA cm)。该研究为未来的电解催化剂提供了一种有前景的设计策略。