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Updated: May 12, 2026

Synthesis and Characterization of Functionalized Metal-organic Frameworks
Published on: September 5, 2014
Complexity in Order: High-Porosity Multicomponent Metal-Organic Frameworks for Clean Energy Gas Storage
Yuanlong Zhong1,2, Puhao Fang1,2, Mengyang Zhai1,2
1Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang Key Laboratory of Excited-State Energy Conversion and Energy Storage, State Key Laboratory of Silicon and Advanced Semiconductor Materials, Zhejiang University, Hangzhou 310058, P. R. China.
Abstract:
The development of high-performance adsorbent materials offers a promising method for the efficient storage of clean energy gas to achieve a carbon-neutral energy cycle. Herein, we report reticular synthesis of high-porosity and structurally robust metal-organic frameworks (MOFs)─tsn-MOF-1 with the (3,6,9)-connected tsn net─from the precise assembly of 9-connected metal μ3-oxo-centered trinuclear nodes, 6-connected trigonal prismatic peripherally extended triptycene carboxylate ligands, and 3-connected triangular pyridine-based ligands in a geometry- and size-matching manner. The tsn-MOF-1-Fe3 maintains high porosity under common solvent activation conditions, exhibiting a high apparent Brunauer-Emmett-Teller surface area of 5100 m2 g-1 and an experimental pore volume of 2.11 cm3 g-1. As a result, this MOF displays a good methane working capacity of 365.4 cm3 cm-3 (0.688 g g-1) under a combined temperature and pressure swing condition (159 K/6 bar → 298 K/5 bar) and shows respectable potential for low-temperature methane storage. Moreover, the tsn-MOF-1-Fe3 shows a hydrogen-deliverable capacity of 48.6 g L-1 (11.3 wt %) under a related swing condition (77 K/100 bar → 159 K/5 bar). This geometry-directed strategy allows the precise design and synthesis of high-connectivity and high-porosity multicomponent reticular structures with robust pore structures for the storage of clean energy gases.
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