Pyrene-Based Multicomponent Metallacages for Highly Efficient Adsorption and Photocatalytic Degradation of Perfluorooctanoic Acid
Source abstract
Abstract
The remediation of perfluorooctanoic acid (PFOA) remains a critical challenge due to its exceptional chemical stability and bioaccumulation risks. Here, we present two pyrene-based multicomponent metallacages that synergistically integrate high-capacity adsorption and photocatalytic degradation of PFOA. The 4,4'-bipyridine tetracarboxylate-derived metallacage demonstrates a high PFOA adsorption capacity of 1223 mg/g, facilitated by multivalent electrostatic interactions and hydrogen bonds. Subsequent photocatalytic treatment of the preconcentrated PFOA achieves 91% defluorination within 6 h through a superoxide radical-mediated chain-shortening mechanism, as verified by electron paramagnetic resonance and intermediate analyses. A practical immobilized system fabricated by anchoring metallacages onto molecular sieves retains over 80% of its initial activity over six consecutive cycles. This work establishes the molecular-level integration of adsorption and photocatalysis in supramolecular architectures, providing a highly efficient approach to address persistent organic pollutants.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Per- and polyfluoroalkyl substances research · Luminescence and Fluorescent Materials · Porphyrin and Phthalocyanine Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry and Chemical Engineering
Xi’an University of Architecture and Technology
State Key Laboratory of Porous Metal Materials, Shaanxi International Research Center for Soft Matter
School of Materials Science and Engineering, Xi’an Jiaotong University
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry
Jilin University
Funding
National Natural Science Foundation of China · Shaanxi Province · Shaanxi Province for Science and Technology Innovation Team
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