Metal–Organic Frameworks (MOFs) have emerged as advanced porous crystalline materials due to their highly ordered structures, ultra-high surface areas, fine-tunable pore sizes, and massive chemical diversity. These features, arising from the coordination between an almost unlimited number of metal ions/clusters and organic linkers, have resulted in significant interest in MOFs for applications in gas storage, catalysis, sensing, energy, and biomedicine. Beyond their stand-alone properties and applications, recent research has increasingly explored the integration of MOFs with other substrates, particularly electrodes, polymeric thin films, and glass surfaces, to create synergistic effects that enhance material performance and broaden application potential. Coating MOFs onto these substrates can yield significant benefits, including, but not limited to, improved sensitivity and selectivity in electrochemical sensors, enhanced mechanical and separation properties in membranes, and multifunctional coatings for optical and environmental applications. This review provides a comprehensive and up-to-date summary of recent advances (primarily from the past 3–5 years) in MOF coating techniques, including layer-by-layer assembly, in situ growth, and electrochemical deposition. This is followed by a discussion of the representative applications arising from MOF-substrate coating and an outline of key challenges and future directions in this rapidly evolving field. This article aims to serve as a focused reference point for researchers interested in both fundamental strategies and applied developments in MOF surface coatings.
This paper introduced a simple, efficient method to prepare mechanically strong lignin-based foams (lignofoams) with open-cell structures using a facile baking technique. The self-expansion of lignin occurred without any additional chemical blowing agents, foaming agents, plasticizers, or lubricants. During heating, kraft lignin softened, and the internal water, either initially adsorbed or generated in situ through the dehydration of hydroxyl groups, acted as a natural blowing agent for foaming a porous foam structure. Incorporating a small amount of polypropylene (PP) enhanced mechanical properties by coating the inner walls of open cells. The porous, softened composite was then cooled to room temperature and solidified into the self-expanded lignofoam. The resulting lignofoams exhibited tunable densities ranging from 0.21 to 0.49 g/cm3 and a maximum compressive strength of 3.6 MPa. The lignofoam also showed excellent thermal insulation properties with low thermal conductive coefficients (0.057–0.098 W/mK). These features highlight the great potential of lignofoam for a bio-based thermal insulation material for construction applications.