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In printable mesoporous perovskite solar cells (p-MPSCs), the perovskite films deposited from room-temperature solvents can effectively optimize the interface between the perovskite films and the electrodes. However, the low crystallization rate of perovskite thin films at room temperature often leads to the formation of nonphotoactive phases and an increase in the density of defect states. To accelerate the crystallization of perovskite films at room temperature, acetonitrile (ACN) is introduced as a cosolvent in the binary solvent system of 2-methoxyethanol/-methyl-2-pyrrolidone (2 ME/NMP). The high volatility and excellent wettability of ACN improve the crystallization rate of perovskite films and optimize their crystallinity. Furthermore, the introduction of the multifunctional additive Phenformin hydrochloride in the perovskite precursor solution further optimizes the crystallization process of the perovskite films, passivating deep defects in the perovskite films and forming high-quality perovskite films in the mesopores. The optimized p-MPSCs achieve a power conversion efficiency (PCE) of 18.30%, which is the highest PCE for room temperature perovskite film p-MPSCs. Moreover, the optimized p-MPSCs exhibit negligible hysteresis and excellent reproducibility, showing no significant PCE degradation after being stored in air for over 3000 h.
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http://dx.doi.org/10.1021/acsami.5c04888 | DOI Listing |
Adv Mater
September 2025
Key Lab of Artificial Micro- and Nano-Structures of Ministry of Education of China, School of Physics and Technology, Wuhan University, Wuhan, 430072, China.
Sequential deposition technique is widely used to fabricate perovskite films with large grain size in perovskite solar cells (PSCs). Residual lead halide (PbI) in the perovskite film tends to be decomposed into metallic lead (Pb) under long-term heating or light soaking. Here, a chiral levetiracetam (LEV) dopant containing α-amide and pyrrolidone groups is introduced into the PbI precursor solution.
View Article and Find Full Text PDFACS Omega
September 2025
Institut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé (ICPEES), UMR-7515 CNRS-Université de Strasbourg, 25 rue Becquerel, 67087 Strasbourg, France.
For photodetection applications using 3D hybrid perovskites (HPs), dense and thick films or compacted powders in wafer form are needed and generally require large amounts of HPs. HPs are also often combined with a graphene/carbon layer to improve their conductivity. Among HP synthesis methods, mechanosynthesis, a green synthesis method, provides a large amount of powders, which are furthermore easily densified in compact wafers due to their mechanical activation.
View Article and Find Full Text PDFAtomic layer deposition (ALD) enables an excellent surface coverage and uniformity in the preparation of large-area metal-oxide thin films. In particular, ALD-processed SnO has demonstrated great potential as an electron transport layer in flexible perovskite solar cells (PSCs) and tandem modules. However, the poor electrical conductivities and surface wettabilities of amorphous SnO remain critical challenges for commercialization.
View Article and Find Full Text PDFThe functionalization of thin, flexible glass with piezoelectric oxides is a pathway toward transparent electromechanical devices. The crystallization of lead zirconate titanate thin films on thick, rigid glass is previously demonstrated using flash lamp annealing to selectively anneal the films, without damaging the substrates. In this work, a 2-step process suitable for Schott AF 32 eco glass and Corning Willow glass is developed, both 100 μm thick, the latter of which is compatible with roll-to-roll processes.
View Article and Find Full Text PDFThe formation of heterostructure interfaces from quantum dots (or nanocrystals) and lower-dimensional (2D or quasi-2D) materials enables interfacial and optoelectronic property tuning. However, this strategy has not been sufficiently characterized, for example, the application of cesium halide nanocrystals to quasi-2D perovskite structures is underexplored, and the mechanisms of the resulting structural modifications and specific nanocrystal roles are not fully understood. Herein, the effects of postsynthetically surface-modifying quasi-2D perovskite films with CsX ( = Cl, Br, I) nanocrystals are examined to bridge this gap.
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