Solvent-Solute Coordination Engineering for Efficient Perovskite Luminescent Solar Concentrators

Luminescent solar concentrators (LSCs) enable large-area collection of sunlight relevant to building-integrated photovoltaics. Reduced-dimensional metal halide perovskite nanoplatelets (PNPLs) have recently emerged as candidates for low-loss large-area LSCs due to the optoelectronic properties of perovskites combined with the large Stokes shift attainable using the multiple quantum well (MQW) structure. LSCs using bromine-based PNPLs have been demonstrated; however, the band gaps of bromine-based perovskites limit the absorption range. Iodine-based PNPLs allow broader absorption, but emission can be achieved only if the chemistry of PbIx2-x precursor complexes is engineered to provide the appropriate MQW distribution. Here, by controlling the polarity and Lewis basicity of the precursor solution, we modify the solvent-Pb2+ coordination and synthesize PNPLs having a uniform MQW distribution. This improves energy funneling, enabling a film PLQY (photoluminescence quantum yield) of 56% and 10 x 10 cm LSCs with an optical conversion efficiency of 2.0%, a 1.3-fold enhancement compared to the best previously reported room-temperature-fabricated perovskite LSCs.