Boosting photothermal conversion through array aggregation of metalloporphyrins in bismuth-based coordination frameworks

Materials capable of efficiently converting near-infrared (NIR) light into heat are highly sought after in biotechnology. In this study, two new three-dimensional (3D) porphyrin-based metal-organic frameworks (MOFs) with a sra-net, viz. CoTCPP-Bi/NiTCPP-Bi, were successfully synthesized. These MOFs feature bismuth carboxylate nodes interconnected by metalloporphyrinic spacers, forming one-dimensional (1D) arrays of closely spaced metalloporphyrins. Notably, the CoTCPP-Bi exhibits an approximate Co & ctdot;C distance of 3 & Aring;, leading to enhanced absorption of NIR light up to 1400 nm due to the presence of strong interlayer van der Waals forces. Furthermore, the spatial arrangement of the metalloporphyrins prevents axial coordination at the centers of porphyrin rings and stabilizes a CoII-based metalloradical. These characteristics promote NIR light absorption and non-radiative decay, thereby improving photothermal conversion efficiency. Consequently, CoTCPP-Bi can rapidly elevate the temperature from room temperature to 190 degrees C within 30 seconds under 0.7 W cm-2 energy power from 808 nm laser irradiation. Moreover, it enables solar-driven water evaporation with an efficiency of 98.5% and a rate of 1.43 kg m-2 h-1 under 1 sun irradiation. This research provides valuable insights into the strategic design of efficient photothermal materials for effective NIR light absorption, leveraging the principles of aggregation effect and metalloradical chemistry. A novel bismuth carboxyl metal-organic framework (MOF) with 1D metalloporphyrin aggregates and CoII-based metalloradicals demonstrates exceptional photothermal efficiency.