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In a mesoporous hybrid perovskite solar cell (PSC), the mesoporous scaffold plays key roles in controlling the crystallization of the perovskite material and in the charge carrier transport, and hence is critical for developing highly efficient PSCs. Here we report a study on blending micrometer-long TiO 2 nanorods (NRs) into the commonly used nanoparticles (NPs) to optimize the mesoporous structure, with the aim of enhancing the perovskite material loading and connectivity as well as light harvesting. It was found that with 5–10% of NR incorporation, a uniform scaffold can be spin-coated and the PSC performance was improved. In comparison to the pure NP-based device, the power conversion efficiency was increased by about 27% when 10% of the NRs were incorporated, due to enhanced light harvesting and charge collection. However, with more NR blending, a homogeneous scaffold cannot be formed, resulting in PSC performance degradation. These findings contribute to a better design of mesoporous scaffolds for high-performance PSCs. 

The chemical stabilities of hybrid perovskite materials demand further improvement toward long‐term and large‐scale photovoltaic applications. Herein, the enhanced chemical stability of CH₃NH₃PbI₃is reported by doping the divalent anion Se²⁻in the form of PbSe in precursor solutions to enhance the hydrogen‐bonding‐like interactions between the organic cations and the inorganic framework. As a result, in 100% humidity at 40 °C, the 10% w/w PbSe‐doped CH₃NH₃PbI₃films exhibited >140‐fold stability improvement over pristine CH₃NH₃PbI₃films. As the PbSe‐doped CH₃NH₃PbI₃films maintained the perovskite structure, a top efficiency of 10.4% with 70% retention after 700 h aging in ambient air is achieved with an unencapsulated 10% w/w PbSe:MAPbI₃‐based cell. As a bonus, the incorporated Se²⁻also effectively suppresses iodine diffusion, leading to enhanced chemical stability of the silver electrodes.

 

Formamidinium (FA)‐based lead iodide perovskites have emerged as the most promising light‐absorber materials in the prevailing perovskite solar cells (PSCs). However, they suffer from the phase‐instability issue in the ambient atmosphere, which is holding back the realization of the full potential of FA‐based PSCs in the context of high efficiency and stability. Herein, the tetraethylorthosilicate hydrolysis process is integrated with the solution crystallization of FA‐based perovskites, forming a new film structure with individual perovskite grains encapsulated by amorphous silica layers that are in situ formed at the nanoscale. The silica not only protects perovskite grains from the degradation but also enhances the charge‐carrier dynamics of perovskite films. The underlying mechanism is discussed using a joint experiment‐theory approach. Through this in situ grain encapsulation method, PSCs show an efficiency close to 20% with an impressive 97% retention after 1000‐h storage under ambient conditions.