Interfaces in Sb2S3 thin-film solar cells strongly affect their open-circuit voltage (V OC) and power conversion efficiency (PCE). Finding an effective method of reducing the defects is a promising approach for increasing the V OC and PCE. Herein, the use of an inorganic salt SbCl3 is reported for post-treatment on Sb2S3 films for surface passivation. It is found that a thin SbCl3 layer could form on the Sb2S3 surface and produce higher efficiency cells by reducing the defects and suppressing nonradiative recombination. Through density functional theory calculations, it is found that the passivation of the Sb2S3 surface by SbCl3 occurs via the interactions of Sb and Cl in SbCl3 molecules with S and Sb in Sb2S3, respectively. As a result, incorporating the SbCl3 layer highly improves the V OC from 0.58 to 0.72 V; an average PCE of 6.9 ± 0.1% and a highest PCE of 7.1% are obtained with an area of 0.1 cm2. The achieved PCE is the highest value in the Sb2S3 planar solar cells. In addition, the incorporated SbCl3 layer also leads to good stability of Sb2S3 devices, by which 90% of the initial performance is maintained for 1080 h of storage under ambient humidity (85 ± 5% relative humidity) at room temperature.

Metal halide perovskites have attracted rapid development and great attention mainly due to its excellent optoelectronic properties. Currently, the efficiency of inverted (p-i-n) PSCs are around 23%, which catch up...

The performance enhancement of inverted perovskite solar cells applying nickel oxide (NiOx) as the hole transport layer (HTL) has been limited by impurity ions (such as nitrate ions). Herein, we have proposed a strategy to obtain high‐quality NiOx nanoparticles via an ionic liquid‐assisted synthesis method (NiOx‐IL). Experimental and theoretical results illustrate that the cation of the ionic liquid can inhibit the adsorption of impurity ions on nickel hydroxide through a strong hydrogen bond and low adsorption energy, thereby obtaining NiOx‐IL HTL with high conductivity and strong hole‐extraction ability. Importantly, the removal of impurity ions can effectively suppress the redox reaction between the NiOx film and the perovskite film, thus slowing down the deterioration of device performance. Consequently, the modified inverted device shows a striking efficiency exceeding 22.62 %, and superior stability maintaining 92 % efficiency at a maximum power point tracking under one sun illumination for 1000 h.

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Although perovskite solar cells (PSCs) are on the road to industrialization, the operational stability under high efficiency still needs to be improved, and the water solubility of lead ions (Pb2+) will cause environmental pollution problems. Herein, it is successfully implanted an environment‐friendly (biodegradability) poly(butylene adipate‐coterephthalate) polymer (PBAT) into the perovskite film, which can passivate the uncoordinated Pb2+ and neutral iodine defects of the perovskite material because of the adequate carbonyl groups and benzene rings in PBAT polymer, thereby regulating the crystallization of perovskite film with lower trap density, inhibiting the nonradiative recombination and improving charge carrier transport. As a result, the polymer‐incorporated inverted PSCs achieve optimal conversion efficiencies of 22.07% (0.1 cm2) and 20.31% (1 cm2). Meanwhile, the incorporated device, after being encapsulated, exhibits a prominent improvement in operational stability of high‐efficiency device under maximum power point tracking and continuous one sunlight illumination, maintaining the initial efficiency of 80% for 3249 h. More importantly, the polymer network can protect Pb2+ from being dissolved by water and prevent nearly 98% of Pb2+ from leaking by directly immersing the polymer‐coated perovskite film in water. Environmental‐friendly molecules provide new hope for solving lead poisoning and improving device operational stability under high efficiency.