Polymer-engineered MXene composites have emerged as a versatile materials platform for electrochemical energy storage, offering a means to address key limitations associated with ion transport, structural instability, and interfacial reactivity. This review provides a unified perspective on how polymer integration modifies the structure–transport–stability relationships of MXene-based systems across Na-ion batteries, aqueous Zn-ion batteries, and supercapacitors. In Na-ion systems, polymer-mediated interlayer engineering and porosity control improve ion accessibility and mitigate diffusion limitations arising from the large ionic radius of Na+. In aqueous Zn-ion systems, polymer electrolytes and interfacial layers regulate Zn2+ solvation and deposition behavior, suppressing dendritic growth and parasitic reactions. In supercapacitors, polymer–MXene hybrids establish coupled ionic–electronic transport pathways and mechanically compliant architectures, enabling stable electrochemical performance under high-rate and deformable conditions. Particular emphasis is placed on the underlying mechanisms responsible for suppressing oxidation, preserving structural integrity, and extending cycle life, including interfacial passivation, desolvation regulation, and structural confinement. These coupled effects govern long-term electrochemical stability across different energy storage systems. Finally, recent advances in operando characterization, data-driven materials design, and scalable processing are discussed in the context of future development. By linking material design strategies to fundamental mechanisms, this review outlines a coherent framework for the rational development of polymer–MXene composites toward practical energy storage applications.
Beom et al. (Sun,) studied this question.