Carbon dioxide (CO2) emissions remain a pressing environmental challenge, underscoring the urgent need for innovative, energy-efficient solutions. In line with national and global commitments to climate action, advancing carbon capture and conversion technologies is mission-critical to sustainably reducing emissions and achieving a net-zero future. In this context, a recent study by Yuan-Biao Huang and co-workers has introduced a disruptive material—a prototypical covalent organic framework (COF)-based smart porous liquid (PL), COF-301-PL, that merges the benefits of solid COFs and liquid materials, enabling efficient CO2 capture and heterogeneous catalysis [1].

COF-301-PL is prepared in two steps: (1) surface grafting of a three-dimensional microporous COF, COF-301, with positively charged polyethylene glycol (PEG) and an organosilane co-functionalized imidazolium salt (PEG-Im-Si(OCH₃)₃); and (2) liquefaction via anchoring of a negatively charged PEG-tailed sulfonate (PEGS) canopy through ion exchange (Fig. 1). This ensures that COF-301-PL retains high microporosity (for gases such as CO2) while maintaining its fluidity. What makes COF-301-PL exceptional is its liquid-like properties and ‘breathing effect’, meaning its excellent mass transfer capability in the liquid phase, alongside the dynamic expansion and contraction of its pores in response to CO2 pressure. This feature enhances CO2 storage, accelerates mass transfer, and optimizes catalytic efficiency, making it superior to traditional solid adsorbents under identical conditions.

Schematic synthesis of the porous COF liquid COF-301-PL. NPs, nanoparticles.
Figure 1.

Schematic synthesis of the porous COF liquid COF-301-PL. NPs, nanoparticles.

Thanks to its strong CO2 capture ability, COF-301-PL serves as a gas reservoir for excellent CO2 conversion in the presence of the catalyst tetrabutylammonium bromide. It dramatically improves the transformation of CO2 and epoxide molecules into valuable cyclic carbonates, used in manufacturing plastics and pharmaceuticals. Compared to its solid COF counterpart and PEGS alone, COF-301-PL demonstrates 17-fold and 24-fold increases in catalytic efficiency, respectively. This advantage arises from COF-301-PL’s ability to store CO2 at high pressure and gradually release it, acting as a self-sustaining micro-reservoir for catalytic reactions. This eliminates the need for continuous CO2 supply, making industrial processes more efficient and energy-saving.

In essence, the development of COF-301-PL marks a milestone in porous liquid research. Its ability to reversibly adjust its pore structure to environmental conditions offers vast potential for improving industrial CO2 capture, chemical synthesis, and gas separation technologies. Future advances in this area could enable the porous liquids’ translation into large-scale commercial adoption. By combining structural flexibility with high adsorption and catalytic performance, COF-301-PL exemplifies how the disruptive material design of combining fluidity and porosity can profoundly impact the challenge of carbon capture and utilisation (CCU) [2].

FUNDING

S.M. thanks Research Ireland grant 21/PATH-S/9454, and SSPC Reward funding, AzAds.

Conflict of interest statement. None declared.

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