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]
日期:2021-03-01
卷期号:60 (6): 4034-4046
被引量:57
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI