Photochargeable Mn-Based Metal-Organic Framework and Decoupled Photocatalysis.
Shufan WuPhilip M StanleySimon N DegerMian Zahid HussainAndreas JentysJulien WarnanPublished in: Angewandte Chemie (International ed. in English) (2024)
Designing multifunctional materials that mimic the light-dark decoupling of natural photosynthesis is a key challenge in the field of energy conversion. Herein, we introduce MnBr-253, a precious metal-free metal-organic framework (MOF) built on Al nodes, bipyridine linkers and MnBr(CO) 3 (bipyridine) complexes. Upon irradiation, MnBr-253 colloids demonstrate an electron photocharging capacity of ~42 C ⋅ g -1 MOF , with state-of-the-art photocharging rate (1.28 C ⋅ s -1 ⋅ g -1 MOF ) and incident photon-to-electron conversion efficiency of ~9.4 % at 450 nm. Spectroscopic and computational studies support effective electron accumulation at the Mn complex while high porosity and Mn loading account for the notable electron storage performance. The charged MnBr-253 powders were successfully applied for hydrogen evolution under dark conditions thus emulating the light-decoupled reactivity of photosynthesis.