Boosting HER performance of ZIF-67 via optimizing synthesis parameters in alkaline medium

被引:6
|
作者
Amirpoor, S. [1 ]
Dolati, A. [1 ]
机构
[1] Sharif Univ Technol, Dept Mat Sci & Engn, Azadi Ave,POB 11155-9466, Tehran, Iran
关键词
Electrochemical water splitting; Hydrogen evolution reaction; Metal-organic framework; ZIF-67; Electrocatalytic activity; ZEOLITIC IMIDAZOLATE FRAMEWORKS; HYDROGEN EVOLUTION REACTION; LAYERED DOUBLE HYDROXIDE; CARBON; EFFICIENT; METAL; ELECTROCATALYSTS; ADSORPTION; NANOSHEETS; REDUCTION;
D O I
10.1016/j.ijhydene.2024.07.434
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrochemical water splitting offers a promising route to sustainable hydrogen production. Metal-Organic Frameworks (MOFs) have emerged as potential electrocatalysts due to their tunable structure and composition. We investigated the electrocatalytic activity of ZIF-67 for the hydrogen evolution reaction (HER) in alkaline media. Synthesis parameters, including temperature, reaction time, acidity, molar ratio of 2-methylimidazole (2MIM) to cobalt source, cobalt source type, addition method of 2-MIM, and solvent type, were systematically varied to optimize the electrocatalytic properties of ZIF-67. The synthesized ZIF-67 electrocatalysts were characterized using BET, FESEM, EDS, TEM, XRD, FTIR, and UV-vis spectroscopy. The electrocatalytic properties were evaluated by cyclic voltammetry (CV), linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS), and chronoamperometry methods. The optimized ZIF-67 electrocatalyst exhibited remarkable performance, with a low overpotential of 171 mV, a small Tafel slope of 82 mV.dec- 1, a low charge transfer resistance of 97 Omega, a high double-layer capacitance of 13.5 mF cm- 2, and high stability for 15 h at the current density of 10 mA cm- 2. The enhanced electrocatalytic activity of the optimized ZIF-67 was attributed to its high surface area, tunable pore structure, and the presence of active cobalt sites.
引用
收藏
页码:14 / 27
页数:14
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