Breaking Symmetry of Active Sites in Metal‐Organic Frameworks for Efficient Photocatalytic Valorization of Polyester Plastics

Abstract Chemical upcycling of waste plastics offers a promising way toward achieving a circular economy and alleviating environmental pollution but remains a huge challenge. Inspired by hydrolase enzymes and aiming to overcome their intrinsic limitations, we put forward a design principle for an innovative nanozyme featuring asymmetric metal sites. This nanozyme functions as photocatalyst, enabling sustainable valorization of polyester plastics. As a proof of concept, an asymmetric ligand substitution strategy is developed to construct metal‐organic frameworks (MOFs) that are defective MIL‐101(Fe) (D‐MIL‐101) with asymmetric Fe 3‐δ /Fe 3+ (0< δ <1) sites. The differential electronic configurations inherent to adjacent Fe 3‐δ /Fe 3+ sites endow a high photocatalytic activity for the valorization of polyester plastic. Accordingly, the ester bonds of polyesters can be preferentially cleaved, contributing to the low energy barrier of upcycling plastics. As a result, the D‐MIL‐101 achieves a high monomer yield with terephthalic acid (TPA) of ∼93.9% and ethylene glycol (EG) of ∼87.1% for photocatalytic valorization of poly (ethylene terephthalate) (PET), beyond the efficiency of natural enzymes and state‐of‐the‐art photocatalysts. In addition, such a D‐MIL‐101 is demonstrated to be feasible for the valorization of various real‐world polyester plastic wastes in a flow photocatalysis system.