Research Progress on Metal–Organic Framework Composites for Greenhouse Gas Adsorption and Separation

The excessive emission of greenhouse gases (CO2, CH4, SF6, and CF4.) is a primary driver of global climate change, making the development of efficient adsorption and separation technologies critically important for achieving carbon reduction goals. Metal–organic frameworks (MOFs) have attracted considerable attention in this field due to their crystalline porous structures, ultrahigh surface areas, and tunable pore architectures. However, pristine MOFs face significant bottlenecks including poor water stability, high bed pressure drops caused by their powdered form, and limited mass transfer, which severely hinder their industrial application. The integration of MOFs with functional materials such as carbon materials, polymers, metal oxides, and porous SiO2 offers a synergistic strategy to overcome these limitations. Carbon materials provide hydrophobic barriers and mesoporous transport channels, polymers enhance processability and mechanical strength, metal oxides introduce basic sites for enhanced chemisorption, and MOF-on-MOF heterostructures enable atomic-level interfacial integration and pore synergy. This review systematically summarizes recent advances in MOF composites for the separation of CO2, CH4, and fluorinated greenhouse gases (SF6, CF4.), with an emphasis on design strategies, structure–performance relationships, and synergistic mechanisms across different composite types. Finally, the current challenges including scalable synthesis, long-term stability, and separation performance under realistic conditions are discussed, and future directions toward rational design and functional synergy for industrial carbon capture and fluorinated gas emission reduction are envisioned.