Owing to delocalized free electrons from mixed-valence MoV/MoVI sites, the resulting molybdenum-based polyoxometalates compounds exhibit broad-spectrum solar absorption and hold significant potential for solar energy utilization. However, in discrete molecular clusters, intervalence charge transfer remains confined within individual polyoxometalate units, restricting carrier mobility to intramolecular hopping. This study pioneers a three-dimensional Zn4MoV9MoVI4O40(mbim)2n polyoxometalate-based metal-organic framework (denoted as AHF-Zn4) that enables intercluster charge delocalization across the extended lattice, significantly enhancing photothermal conversion efficiency. Leveraging crystallographic insights, strategic substitution of 25% Zn2+ sites with magnetic metal ions (Co2+, Ni2+, Mn2+) further optimizes electron transport dynamics. X-ray absorption spectroscopy and density functional theory analyses revealed that the unfilled d orbitals of the heterometals provide more active electrons compared to Zn2+, facilitating the electron-vibration coupling effect, further increasing the nonradiative relaxation rate. Under 1 sun irradiation, the maximum temperature of AHF-CoZn3 based MOF can reach approximately 75 °C. Through integration with thermoelectric modules, the evaporator stably achieves an output power of 1088 mW m-2, enabling continuous power generation via the temperature gradient along the TE modules. This work provides a novel strategy for designing high-performance polyoxometalate-based MOF photothermal materials and demonstrates their potential applications in solar water purification, desalination, and solar thermoelectric power generation.
Li et al. (2026) studied this question.