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Accelerated confined mass transfer in piezoelectric semiconducting metal-organic frameworks for H<sub>2</sub>O<sub>2</sub> piezo-photosynthesis.


ABSTRACT: The piezo-photocatalytic O2 reduction reaction offers a promising pathway towards H2O2 synthesis. However, in addition to rapid recombination of photogenerated electrons and holes, this gas-consuming reaction is inherently limited by O2 dissolution and mass transfer dynamics. Here, energy band structures and dipole moments of piezoelectric semiconducting UiO-66 metal-organic frameworks (MOFs) are engineered by modulating functional groups (-NH2, -CH3, -OH, -NO2 and -F4) and metal nodes (Hf and Zr). This fine-tuning of MOF building blocks leads to an enhanced piezoelectric coefficient, gas capacity and light absorption to facilitate subsequent piezo-photocatalysis. Furthermore, the tunable band structure

SUBMITTER: Lan Y 

PROVIDER: S-EPMC12621135 | biostudies-literature | 2026 Jan

REPOSITORIES: biostudies-literature