Guest Polarizability Directed Molecular “Freezing” Within Non‐metal Porous Salt Frameworks
Isoreticular non-metal salt frameworks with permanent porosity have emerged recently as a fantastic platform for molecular separation, but the underlying guest-framework interactions within their charge-separated ionic channels remain to be explored. Here, we report the first case of guest polarizability-directed molecular "freezing" of noble gas occurring within a non-metal porous organic ammonium framework, which bears well-organized, high-density chloride anions as nodes. Notably, the framework exhibits a distinctive, thermally-independent commensurate adsorption toward highly polarizable Xe, while traditional thermodynamic adsorption behaviors are observed for Kr with lower polarizability. A remarkable Xe adsorption capacity of 1.47 mmol g<sup>-1</sup> and a record-high separation factor of 10.2 are thus achieved in dynamic Xe/Kr separation under ambient conditions. The practical potential for realistic Xe/Kr separation from the off-gas of used nuclear fuel (UNF) reprocessing is demonstrated. Theoretical calculations identify the presence of multiple strong Xe⋯Cl interactions as the driving force within the size-matching ionic channels of the salt framework.
Authors
- Qiang Gao (ORCID: https://orcid.org/0000-0001-7571-4903)
- Jianchen Wang (ORCID: https://orcid.org/0000-0002-8425-9129)
- Gang Ye (ORCID: https://orcid.org/0000-0002-7066-940X)
- Banglin Chen (ORCID: https://orcid.org/0000-0001-8707-8115)
- Yi Xie (ORCID: https://orcid.org/0009-0009-2813-4493)
Institutions
- Fujian Normal University (CN)
- Zhejiang Normal University (CN)
- North Minzu University (CN)
- Key Laboratory of Nuclear Radiation and Nuclear Energy Technology (CN)
- Tsinghua University (CN)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2025-05-23
- DOI
- https://doi.org/10.1002/anie.202509905
- Citations
- 4
- Primary Topic
- Metal-Organic Frameworks: Synthesis and Applications
- Type
- article
- Field-Weighted Citation Impact
- 2.15
Funders
- National Natural Science Foundation of China
- Tsinghua University