A Lightweight Beryllium Metal–Organic Framework for Combined Physical and Chemical Hydrogen Storage
In this work, we report the synthesis and structural characterization of the beryllium-based metal-organic framework of general formula [Be<sub>4</sub>O-(BDC-NH<sub>2</sub>)<sub>2.5</sub>(OAc)] (<b>Be_BDC_NH</b> <sub><b>2</b></sub> ), designed for combined physical and chemical hydrogen storage applications. The material was extensively characterized through a plethora of solid-state techniques (including less conventional <sup>9</sup>Be NMR-MAS spectroscopy). Structural analysis by X-ray powder diffraction confirmed the formation of a crystalline porous framework of <b>fcu</b> topology isostructural to MOF-5 and to MOF-5-(Be), while thermogravimetric studies revealed remarkable thermal stability up to 830 K. Nitrogen adsorption measurements demonstrated a high specific surface area (2264 m<sup>2</sup>/g after removal of residual acetic acid), confirming the accessible porosity of the material. Hydrogen adsorption experiments (physical hydrogen storage) performed at cryogenic temperatures showed fast, fully reversible physisorption with a gravimetric H<sub>2</sub> density of 8.0 wt % H<sub>2</sub> (<i>T</i> = 77 K, <i>p</i> <sub>H<sub>2</sub></sub> = 80 bar) and a H<sub>2</sub> isosteric heat of adsorption of 2.7 kJ/mol (at 0.1 wt % H<sub>2</sub> coverage), consistent with weak, noncovalent interactions between the hydrogen molecules and the framework. To enable chemical hydrogen storage, ammonia borane (NH<sub>3</sub>·BH<sub>3</sub>, AB, 19.6 wt % H) was successfully impregnated into the MOF pores by suspending it on concentrated methanol solutions of AB. Solid-state multinuclear (<sup>11</sup>B, <sup>15</sup>N) NMR spectroscopy revealed the presence of several boron-containing species, indicating partial chemical transformations of ammonia borane within the framework triggered by the formation of an initial B-H···H-N dihydrogen bonding interaction with the amino dangling group on the MOF linker. <sup>11</sup>B NMR quantification determined a maximum hydride loading of 2.1 AB molecules per formula unit. To our knowledge, this is the first example of a beryllium MOF able to host either physisorbed molecular hydrogen or chemically bound hydrogen in the form of BN-based lightweight inorganic hydrides, highlighting its potential as a multifunctional material for advanced hydrogen storage strategies.
Authors
- Cinzia Giannini (ORCID: https://orcid.org/0000-0003-0983-2885)
- Andrea Rossin (ORCID: https://orcid.org/0000-0002-1283-2803)
- Giulia Tuci (ORCID: https://orcid.org/0000-0002-3411-989X)
- Giacomo Provinciali (ORCID: https://orcid.org/0000-0002-6500-4630)
- Anna Moliterni (ORCID: https://orcid.org/0000-0001-6786-6982)
- Rolando Pedicini (ORCID: https://orcid.org/0000-0003-0867-714X)
- M. Innocenti (ORCID: https://orcid.org/0009-0005-5367-699X)
- Rocco Caliandro (ORCID: https://orcid.org/0000-0002-0368-4925)
- Giuliano Giambastiani (ORCID: https://orcid.org/0000-0002-0315-3286)
- Moreno Lelli (ORCID: https://orcid.org/0000-0002-7042-2335)
- Naomi Anna Consoli
- Heryson Tresmann
Institutions
- Institute for the Chemistry of OrganoMetallic Compounds (IT)
- Interuniversity Consortium for Magnetic Resonance (IT)
- Institute for Advanced Energy Technologies (IT)
- National Interuniversity Consortium of Materials Science and Technology (IT)
- Institute of Crystallography (IT)
- University of Florence (IT)
Publication Details
- Journal
- ACS Applied Energy Materials
- Published
- 2025-10-31
- DOI
- https://doi.org/10.1021/acsaem.5c02864
- Primary Topic
- Hydrogen Storage and Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00