Abstract

Metal–organic frameworks (MOFs) are promising materials for hydrogen storage due to their high specific surface area and structural tunability. In this study, we provide the first demonstration of enhanced hydrogen storage performance in a CuBTC (also known as HKUST-1) MOF by incorporating nickel and magnesium through a combination of in situ and postmodification solvent-free mechanochemical ball milling. A comprehensive combination of structural and adsorption–desorption characterization is employed to examine and understand the impact of Ni2+ and Mg2+ divalent metal ions through in situ and postmodification methods. In general, the post-Ni-modification method achieved higher hydrogen storage capacities than in situ-Ni-modification routes. The post-Ni-modified CuBTC with 30 min milling time exhibited the highest hydrogen storage capacity of 4.2 wt % at 20 bar and 77 K, which is 31% higher than the pristine CuBTC. The substitution of Cu2+ by Ni2+ during the postmodification process increased the active metal sites and Cu+ content, thus contributing to enhanced hydrogen storage capacity. Our findings indicate that modification via a solvent-free mechanochemical route is an effective novel strategy for improving the hydrogen storage performance of MOF materials.
Original languageEnglish
Pages (from-to)68703-68716
Number of pages14
JournalACS applied materials & interfaces
Volume17
Issue number50
Early online date8 Dec 2025
DOIs
Publication statusPublished - 17 Dec 2025

Funding

This work was supported by the Royal Society [IEC\NSFC\211452 and RGS\R1\231093]; the Royal Society of Chemistry [E21–0260978386]; EPSRC [EP/X035069/1, EP/Y007778/1, EP/Y023994/1, EP/X038963/1]; and China Scholarship Council─Exeter PhD Programme [202108430012].

Keywords

  • ball milling
  • hydrogen storage
  • mechanochemical synthesis
  • metal−organic frameworks (MOFs)
  • modification of MOFs

ASJC Scopus subject areas

  • General Materials Science

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