Electrospun Fe-Incorporated ZIF-67 Nanofibers for Effective Electrocatalytic Water Splitting

化学 塔菲尔方程 过电位 析氧 X射线光电子能谱 静电纺丝 分解水 化学工程 贵金属 阳极 金属有机骨架 沸石咪唑盐骨架 阴极 咪唑酯 纳米技术 无机化学 催化作用 电化学 电极 有机化学 物理化学 聚合物 光催化 吸附 工程类 材料科学
作者
Selvasundarasekar Sam Sankar,G Keerthana,Karthikeyan Manjula,Jeyashankararaj Hirithya Sharad,Subrata Kundu
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:60 (6): 4034-4046 被引量:59
标识
DOI:10.1021/acs.inorgchem.1c00097
摘要

The explorations of earth-abundant, noble metal-free, highly efficient electrocatalysts for water-splitting reactions have been considered as highly significant for imperishable energy production. Though the metal organic framework (MOF)-based materials are highly promising candidates in the area of material chemistry, the combined properties associated with MOFs and the one-dimensional (1D) fibrous matrix, which can lead to better electrocatalytic performance, have been less explored. Herein, we ascertain a fabrication method for ZIF-67 (zeolite imidazolate framework) nanofibers (NFs), Fe-ZIF NFs, and Fe-ZIF-67 NFs via the wet chemical combined electrospinning (ES) approach. The as-synthesized catalysts were utilized for the electrochemical reaction, which showed a high efficiency toward the oxygen evolution reaction (OER). Compared to other catalysts, the Fe-ZIF-67 NF catalyst showed a very less overpotential of 278 mV at a fixed current density of 10 mA cm–2. The obtained Tafel slope and Rct values are 77 mV dec–1 and 1.2 Ω, respectively. The post-X-ray photoelectron spectroscopy (XPS) analysis revealed the transformation of FeOOH during the OER study along with Co3+ states in mixed Fe-ZIF-67 NFs. In an alkaline electrolyzer, Fe-ZIF-67 NFs were utilized as the anode and a Pt wire as the cathode in 1 M KOH solution, which required a cell voltage of 1.68 V at 10 mA cm–2 current density with astonishing stability. Hence, this work should open a new path for the exploration of efficient non-noble metal catalysts for energy-related applications.
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