Abstract
Understanding the thermal conductivity in MOF-polymer composites is crucial for optimizing their performance in applications involving heat transfer. In this work, several UiO66-polymer composites (where polymer is either PEG, PVDF, PS, PIM-1, PP or PMMA) are examined using molecular simulations. Our contribution highlights the interface's impact on thermal conductivity, observing an overall increasing trend attributable to the synergistic effect of MOF enhancing polymer thermal conductivity. Flexible polymers like PEG and PVDF exhibit increased compatibility with the MOF, facilitating their integration with the MOF lattice. However, this integration leads to a moderated enhancement in thermal conductivity compared to polymers that remain separate from the MOF structure, such as PS or PP. This effect can be attributed to alterations in phonon transport pathways and shifts in interfacial interactions between the polymer and MOF. Specifically, the infiltration of the polymer like PEG and PVDF into the MOF disrupted the MOF’s ordered network, introducing defects or barriers that hindered phonon propagation. In contrast, non-polar and rigid polymers like PP, PMMA, PS, and PIM-1 exhibited greater improvements in thermal conductivity when combined with MOFs compared to the flexible polymers PVDF and PEG. Most notably, our analysis identifies a critical interface region within approximately 30-50 Å that profoundly influences thermal conductivity. \textcolor{blue}{The interface region, as indicated by the density profile and radius of gyration, is notably shorter but plays a pivotal role in modulating thermal properties}. The sensitivity of the system to these interface characteristics underscores the crucial role of this particular interface area in dictating thermal conductivity. Our findings emphasize the sensitivity of thermal conductivity in polymer matrices to interface characteristics and highlight the critical role of a specific interface region in modulating thermal properties.