Hydrogen adsorption on Co2+ - and Ni2+- exchanged -US-Y and -ZSM-5. A combined sorption, DR UV-Vis, synchrotron XRD and DFT study

Hydrogen adsorption on Co2+ and Ni2+ exchanged Ultrastable-Y (US-Y) and ZSM-5 are investigated experimentally at 298 K and up to 50 bar as well as theoretically. The experimentally calculated initial isosteric heat of H-2 adsorption values are between -28 and -32 kJ/mol for Ni2+-ZSM-5, -16 kJ/mol for Co2+-ZSM-5, -23 kJ/mol for Ni2+-US-Y and -18 kJ/mol for Co2+-US-Y. Due to the optimum heat of adsorption values observed on Co2+ and Ni2+ exchanged US-Y and ZSM-5, a reversible volumetric H-2 storage capacity of 20 g H-2/L is achieved on Ni2+-ZSM-5 at 298 K and 50 bar. The site information of Co2+ and Ni2+ cations are investigated using diffuse reflectance (DR) UV-Vis spectra, synchrotron powder X-ray Diffraction (XRD) as well as theoretical calculations using both periodic and cluster density functional theory (DFT) models for ZSM-5. Majority of Co2+ and Ni2+ cations are found at beta and gamma-sites in ZSM-5 and at Site III in US-Y. (C) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

Automated summary

Hydrogen adsorption on Co2+ and Ni2+ exchanged US-Y and ZSM-5 was investigated experimentally and theoretically. The results showed that the initial isosteric heat of H-2 adsorption values varied for different systems, and a reversible volumetric H-2 storage capacity was achieved on Ni2+-ZSM-5. The site information of Co2+ and Ni2+ cations was studied using various techniques.