Based on the double activation models of epoxides, the design and synthesis of ionic porous organic polymers (iPOPs) is considered to be very attractive and promising but has remained a great challenge in recent decades owing to electrostatic interactions between charged groups. In this contribution, we developed a two-in-one strategy to fabricate metalloporphyrin-based iPOPs with unique nanostructures (named AlPor-QP@POP), which are composed of aluminum porphyrin units and three-dimensional quaternary phosphonium salts that work synergistically in the cycloaddition of CO₂ with epoxides under mild conditions. The high symmetry of two monomers allows them to possess similar reactivity ratios and thus endows AlPor-QP@POP with densely located active sites, a large surface area and good CO₂ capture capacity. More importantly, bifunctional AlPor-QP@POP has enormous potential to produce cyclic carbonates with simulated flue gas under ambient conditions. Moreover, AlPor-QP@POP can be readily recycled and efficiently reused more than ten times without an obvious decrease in catalytic activity. Finally, kinetic investigations and a comparative study have been conducted to understand the possible mechanism of CO₂ catalytic cycloaddition.