Molecular engineering of narrow bandgap porphyrin derivatives for highly efficient photothermal conversion

摘要

Organic dyes based on porphyrin derivatives have been widely reported to show promising application in dyesensitized solar cells and organic solar cells due to their desired power conversion efficiency and extinction coefficient while their photothermal conversion performance is rarely reported, to date. Considering the design guideline of photothermal materials with wide near-infrared region absorption and large extinction coefficient, we designed and prepared a narrow bandgap donor-acceptor small molecule P(DPP)(4) based on porphyrin and diketopyrrolopyrrole, which showed a photothermal efficiency of 73.2% under irradiation of 808 nm laser, due to its aggregation-induced radical and distinct nonradiative decay. Furthermore, in an interfacial-heating water evaporation system, P(DPP)(4) exhibited an evaporation rate of 1.304 kg m(-2) h(-1) under 1 sun irradiation with a solar-energy-to-vapor efficiency of 90.6%, higher than most of the pure organic photothermal materials. This work provides a promising way for organic small molecules as solar absorbers with high solar-thermal conversion efficiency and reveals the great potential of organic semiconductors with aggregation-induced radical in photothermal materials.

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