Xue-Jing Zhao, Ke Zhao, Hao-Han Jiang, Shu-Yuan Li, Jun-Yu Li, Si-Hua Liu, Zhen-Wen Wang, Hong-Wei Ma, Jian-Ke Sun
The development of advanced adsorbents for the selective and efficient recovery of gold from complex aqueous matrices is of paramount importance for sustainable resource recycling. Here, we report a phosphorus-functionalized, quaternized ammonium cages (Phos-QA-Cage-Cl) featuring multiple integrated binding sites, which delivers exceptional Au(III) uptake of up to 2331 mg g- 1. The intrinsically cationic skeleton and Au-affinitive phosphorus sites synergistically capture AuCl4 - through combined electrostatic and coordination interactions. Thermal activation generates persistent radicals within the cage, which further enhance Au uptake by reducing Au(III) to nanoparticles, followed by halide-promoted ripening of the nascent Au species. DFT calculations reveal the cooperative roles of noncovalent interactions, coordination bonding and radical-assisted redox chemistry in driving efficient Au(III) capture. As a result, the cage exhibits rapid adsorption kinetics, high selectivity, and good recyclability in complex aqueous matrices. Leveraging its solution processability, a mixed-matrix membrane based on polyvinylidene fluoride is fabricated, enabling efficient filtration and recovery of Au(III) (up to 95%) from dilute solutions, with a high permeate flux (87 L m- 1 h- 1 bar- 1). This work introduces a new class of functionalized porous cages for precious metal recovery and highlights the potential of integrating molecular design with solution processibility for environmental applications.