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Developing multifunctional photocatalysts with efficient synergistic effects for selective photocatalytic CO2 reduction is sought-after yet challenging. Herein, a tandem photocatalytic strategy has been developed through sequential post-synthetic metalation (SPSM) of variable Ru/Co-sites into a trinuclear Cu-based COF, Cu3-BPY-COF, to construct a series of tri-metallized covalent-organic frameworks (COFs), Cu3-BPY-COF(Ru/Co)-X (X = 1, 2, or 3, corresponding to the Ru:Co molar ratios of 1/39.6, 1/19.6, or 1/12.7, respectively), for photocatalytic CO2 methanation in high selectivity. The introduction of a small fraction of Ru-sites confers the framework with enhanced visible-light response, while the Co-sites immobilized in the bipyridine units significantly boost the generation of CO to enrich its concentration around the active trinuclear Cu-sites, which enables dramatically improved photocatalytic CO2 reduction activity toward CH4. Significantly, the optimized Cu3-BPY-COF(Ru/Co)-2 showcases exceptional photocatalytic activity with a CH4 evolution rate of 31.5 µmol g-1 h-1 and selectivity of 95%, 15.0 times higher than that of Cu3-BPY-COF(Ru) merely introducing Ru-photosensitizer. The underlying photocatalytic mechanism has been studied to unveil how the ternary Ru/Co/Cu-sites collaborate to result in highly efficient and selective CO2-to-CH4 reduction, shedding light on the design of highly selective CO2 methanation photocatalysts by leveraging the synergistic effect of multiple active centers within heterometallic covalent-organic frameworks (HM-COFs).
Geng et al. (Fri,) studied this question.