Abstract
Hydrogen energy plays an important strategic role as a sustainable and clean energy source for the future, and the use and efficient design of hydrogen storage and transportation materials are essential. Exploration into the usage and efficient design of hydrogen energy storage and transportation materials is necessary. However, a state of confusion and uncertainty exists regarding the similar operational mechanisms and details of hydrogen storage materials. This article focuses on the study of Zr-, Co-, In-, and Cu-based gas adsorption materials represented by metal organic framework (MOF)-derived structures. In this work, the basic unit planning and configuration design of metal coordination were analyzed and compared separately; the summarized working mode and rules of organic linking agents, represented by benzene-1,4-dicarboxylic acid (BDC) and its longitudinal chain derivatives, were concluded; based on experimental references, the adsorption relationship of samples under non adiabatic conditions was processed and evaluated, and the dynamic evolution process of sample gas adsorption was elucidated. Through the deployment of specific functions and non-adiabatic environment orchestration, we found that both the structural design and samples met the expected actual values, and some structural samples exceeded the theoretical level of the normal UIO-66 and MOF-74 series. This work analyzes and advocates for a potential benign hydrogen adsorption scheme using a MOF morphology, provides potential adsorption materials that can improve environmental tolerance, and reveals their adsorption response laws. Ultimately and fortunately, these materials could become strong competitors in the field of hydrogen storage functional materials.