Hybrid perovskites are promising materials for new sustainable photovoltaic applications to operate under low lighting conditions, such as the reuse of residual photons that are wasted during indoor lighting. The requirements for a perovskite solar cell (PSC) to offer maximum power conversion efficiency (PCE) under low illumination conditions are not totally clear in the literature. In this work, the PCE of the commonly used SnO2 electron transport layer (ETL) is improved by a facile method, doping the precursor nanoparticles with small concentrations of a Pb source. Under low illumination conditions (i.e., 0.1 mW cm−2) the PCE is enhanced from 18.8% to 34.2%. From a complete analysis of the ETLs and devices using several structural and electrical techniques it is observed that the parameter that improves the most is the shunt resistance of the device which avoids the parallel leakage of the photogenerated current. The present work clearly shows that the shunt resistance is a very important parameter that needs to be optimized in PSCs for low illumination conditions.

Perovskite nanomaterials have been fascinating for commercial applications and fundamental research owing to their excellent optical properties and satisfactory processability. They are expected to be alternative downconversion materials in phosphor-converted LEDs for lighting or display technology. However, owing to their low formation energy and large specific surface area, perovskite nanomaterials are sensitive to environmental stress like humidity, heat, etc. In this paper, cubic CsPbI 3 quantum dots (QDs) with improved stability are synthesized using (3-aminopropyl)triethoxysilane (APTES). These luminescent CsPbI 3 QDs passivated by APTES not only show excellent stability when stored in hexane but also possess outstanding steadiness for lattice structure when prepared as a thin film in open air. They do not decompose immediately in the water. Such excellent stability is attributed to the hindrance from hydrolysis of APTES, which forms an analogous core−shell structure to protect the "core" CsPbI 3 QDs. Furthermore, an additional iodine source is added to enhance their emissionm and CsPbI 3 QDs with a PLQY of 84% are synthesized.

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