Rational design of photocatalytic systems coupling the reduction of CO2 with water oxidation is vital for carbon-neutral technologies. Herein, we propose a strategy based on the synergistic assembly of polyoxometalates (POMs) within and on a porphyrinic metal–organic framework (MOF, PCN-222). Cross-scale integration of an S-scheme heterojunction and a molecular junction within a single POM@MOF-POM-TiO2 (TiO2@Ni4PCN-222) system is demonstrated. In this spatially compartmentalized platform, Ni4(H2O)2(PW9O34)210– (Ni4POM) confined in the MOF pores modulates the band structure and enhances the built-in electric field of the S-scheme heterojunction, promoting efficient bulk charge separation. Meanwhile, surface-exposed Ni4POM enables uniform TiO2 deposition, forming molecular-level W–O–Ti coordination contacts that act as electron-transport bridges. Benefiting from this dual mechanism, TiO2@Ni4PCN-222 achieves a CO evolution rate of 32.4 μmol g–1 h–1 with 98.0% selectivity in a gas–solid CO2 photoreduction system. In situ DRIFTS, illuminated KPFM, and QIS-XPS confirm the proposed mechanism.
Li et al. (Mon,) studied this question.