Tunning the Zeolitic Imidazole Framework (ZIF8) through the Wet Chemical Route for the Hydrogen Evolution Reaction

Nanomaterials (Basel). 2023 May 11;13(10):1610. doi: 10.3390/nano13101610.

Abstract

Utilizing zeolitic imidazolate frameworks (ZIFs) poses a significant challenge that demands a facile synthesis method to produce uniform and nanometer-scale materials with high surface areas while achieving high yields. Herein, we demonstrate a facile and cost-effective strategy to systematically produce ZIF8 nanocrystals. Typically, ZIF8 nanocrystal synthesis involves a wet chemical route. As the reaction time decreased (150, 120, and 90 min), the size of the ZIF8 crystals decreased with uniform morphology, and productivity reached as high as 89%. The composition of the product was confirmed through XRD, FE-SEM, TEM, EDS, and Raman spectroscopy. The ZIF8 synthesized with different reaction time was finally employed for catalyzing the electrochemical hydrogen evaluation reaction (HER). The optimized ZIF8-3 obtained at 90 min of reaction time exhibited a superior catalytic action on the HER in alkaline medium, along with a remarkably long-term stability for 24 h compared with the other ZIF8 nanocrystals obtained at different reaction times. Specifically, the optimized ZIF8-3 sample revealed an HER overpotential of 172 mV and a Tafel slope of 104.15 mV·dec-1. This finding, thus, demonstrates ZIF8 as a promising electrocatalyst for the production of high-value-added green and sustainable hydrogen energy.

Keywords: HER; ZIF8; nanocrystals; water splitting.

Grants and funding

This study was partly supported by the Korea Institute of Energy Technology Evaluation and Planning (KETEP; 20212050100010), the Technology Innovation Program (20017464) funded by the Ministry of Trade, Industry, and Energy (MOTIE, Korea), and the National of Korea (NRF) grant (No. 2019R1F1A1063622) funded by the Korea government (MSIT). The authors also acknowledge the National Research Foundation (NRF) of Korea for their financial support (grant no. 2018R1D1A1B07049046). H. Im acknowledges support from the Dongguk University research fund. This work was also supported by the faculty research fund of Sejong University in 2023.