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The unprecedented development of perovskite solar cells (PSCs) makes them one of the most promising candidates for terawatt‐scale green energy production with low cost. However, the high boiling point solvents during the solution‐processed film deposition cause anisotropic crystal growth and toxic solvent vapor during high‐throughput manufacturing. Here, a dual‐component green solvent consisting of isopropyl acetate and acetonitrile is proposed to form a volatile perovskite precursor, which can realize the high‐quality perovskite thin film deposition by intermediate phase regulation. A room‐temperature stable perovskite intermediate phase is constructed with the engagement of isopropyl acetate as co‐solvent, which suppresses the exploding nucleation rate in volatile perovskite precursor, providing a fine grain growth rate and wide processing window in scalable film deposition. The corresponding PSCs fabricated by blade coating without anti‐solvents or gas quenching achieve power conversion efficiency (PCE) of 16.37 % and 15.29 % for the areas of 14.08 cm2 and 37.83 cm2, respectively. [ABSTRACT FROM AUTHOR]

In this work we have optimized the γ-radiation induced synthesis of Cu–Cu2O particles from aqueous CuSO4 solution by investigating the effect of pH. The obtained precipitate was analyzed by XRD and SEM techniques. The results indicated that at solution pH lower than 3.75, quasi-spherical Cu agglomerates can be formed while at pH higher than 4.40 only octahedron-shaped Cu2O particles are produced. At solution pH in the range from 3.75 to 4.40, a Cu–Cu2O mixture is produced. It was found that the relative amount of Cu2O in the Cu–Cu2O precipitate increases with pH in the studied range. The influence of solution pH on the Cu/Cu2O ratios in the product can be explained on the basis of pH-dependent competition kinetics between the reactions leading to either Cu or Cu2O formation. As a consequence, the composition and morphology of the Cu–Cu2O precipitate can be tuned by controlling pH of the aqueous CuSO4 solution during the γ-radiation induced synthesis. [ABSTRACT FROM AUTHOR]

Organic-inorganic halide perovskite solar cells (PSCs) have attracted significant attention in photovoltaic research, owing to their superior optoelectronic properties and cost-effective manufacturing techniques. However, the unbalanced charge carrier diffusion length in perovskite materials leads to the recombination of photogenerated electrons and holes. The inefficient charge carrier collecting process severely affects the power conversion efficiency (PCE) of the PSCs. Herein, a solution-processed SnO 2 array electron transport layer with precisely tunable micro-nanostructures is fabricated via a bubble-template-assisted approach, serving as both electron transport layers and scaffolds for the perovskite layer. Due to the optimized electron transporting pathway and enlarged perovskite grain size, the PSCs achieve a PCE of 25.35% (25.07% certificated PCE)., (© 2024 Wiley‐VCH GmbH.)

We demonstrate a new approach to pattern functional organic molecules with a template of foams, and achieve a resolution of sub 100 nm. The bubble-assisted assembly (BAA) process is consisted of two periods, including bubble evolution and molecular assembly, which are dominated by the Laplace pressure and molecular interactions, respectively. Using TPPS (meso-tetra(4-sulfonatophenyl) porphyrin), we systematically investigate the patterns and assembly behaviour in the bubble system with a series of characterizations, which show good uniformity in nanoscale resolution. Theoretical simulations reveal that TPPS's J-aggregates contribute to the ordered construction of molecular patterns. Finally, we propose an empirical rule for molecular patterning approach, that the surfactant and functional molecules should have the same type of charge in a two-component system. This approach exhibits promising feasibility to assemble molecular patterns at nanoscale resolution for micro/nano functional devices., (© 2021 Wiley-VCH GmbH.)

In this work we have optimized the γ-radiation induced synthesis of Cu-Cu2O particles from aqueous CuSO4 solution by investigating the effect of pH. The obtained precipitate was analyzed by XRD and SEM techniques. The results indicated that at solution pH lower than 3.75, quasi-spherical Cu agglomerates can be formed while at pH higher than 4.40 only octahedron-shaped Cu2O particles are produced. At solution pH in the range from 3.75 to 4.40, a Cu-Cu2O mixture is produced. It was found that the relative amount of Cu2O in the Cu-Cu2O precipitate increases with pH in the studied range. The influence of solution pH on the Cu/Cu2O ratios in the product can be explained on the basis of pH-dependent competition kinetics between the reactions leading to either Cu or Cu2O formation. As a consequence, the composition and morphology of the Cu-Cu2O precipitate can be tuned by controlling pH of the aqueous CuSO4 solution during the γ-radiation induced synthesis.