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The poly(3,4-ethylenedioxythiophene) polystyrenesulfonate (PEDOT/PSS) mixed polymer is characterized by high conductivity and a simple preparation process, making it an excellent hole transport material for inverted Sn-Pb perovskite solar cells (PSCs). However, the acidic substances produced by PEDOT/PSS upon exposure to moisture and quick crystallization of Sn-Pb perovskite films on its surface may decrease device performances. Herein, an effective bidirectional regulation strategy was developed by introducing 4-bromobenzylamine hydrochloride (4-BBAC) molecules into the interface between PEDOT/PSS and the perovskite, inducing efficient and stable inverted Sn-Pb PSCs. The 4-BBAC molecules modified the surface of PEDOT/PSS, improved the conductivity of PEDOT/PSS, and weakened the acidity caused by moisture absorption of PEDOT/PSS, thereby improving the stability of the resulting PSCs. Moreover, the crystallization process of the Sn-Pb perovskite can be controlled since 4-BBAC can react with SnI/PbI to form a two-dimensional phase, which can slow down the crystallization rate of Sn-Pb perovskite films for improved-quality perovskite films and prevent Sn from oxidation. The optimized (HC(NH))(CHNH)PbSnIBr devices exhibited a higher power conversion efficiency (PCE) of 18.36%, superior to that of the control PSCs (16.23%). Besides, the unencapsulated PSCs modified by 4-BBAC maintained 71% of their initial PCE after aging for 300 h under relative humidity conditions of 20 ∼ 30%, while the control PSCs showed almost no photovoltaic conversion efficiency under the same conditions. Overall, a new technical implementation scheme was provided to guide the future fabrication of efficient and stable Sn-Pb PSCs.
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http://dx.doi.org/10.1021/acsami.5c09034 | DOI Listing |
Light Sci Appl
September 2025
State Key Laboratory of Quantum Optics Technologies and Devices, Institute of Laser Spectroscopy, Shanxi University, 030006, Taiyuan, China.
The fast crystallization and facile oxidation of Sn of tin-lead (Sn-Pb) perovskites are the biggest challenges for their applications in high-performance near-infrared (NIR) photodetectors and imagers. Here, we introduce a multifunctional diphenyl sulfoxide (DPSO) molecule into perovskite precursor ink to response these issues by revealing its strong binding interactions with the precursor species. The regulated perovskite film exhibits a dense morphology, reduced defect density and prolonged carrier diffusion length.
View Article and Find Full Text PDFNat Commun
August 2025
School of Physics and Technology, Key Lab of Artificial Micro- and Nano-Structures of Ministry of Education, School of Microelectronics, Wuhan University, Wuhan, China.
All-perovskite tandem solar cells offer great promise for achieving low levelized cost of electricity, but their performance remains limited by insufficient near-infrared photon absorption in narrow bandgap tin-lead (Sn-Pb) subcells. Micron-thick Sn-Pb layers are essential for maximizing absorption, yet high-concentration precursor solutions often cause non-uniform crystallization, stoichiometric imbalance and limited carrier diffusion lengths. Here we identify the root cause of these limitations as the insufficient coordination of tin(II) iodide (SnI) in conventional dimethylformamide (DMF)/dimethyl sulfoxide (DMSO) binary solvent system at high precursor concentrations, resulting in Sn-rich colloids that nucleate detrimental Sn-rich phases in final films.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Electronic & Electrical Engineering, University College London, Roberts Building, London WC1E 7JE, U.K.
Mixed tin-lead (Sn-Pb) halide perovskites, with their tunable bandgaps (1.2-1.4 eV), show great promise for the development of highly efficient all-perovskite tandem solar cells.
View Article and Find Full Text PDFAdv Mater
August 2025
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, LIFM, School of Chemistry, IGCME, Sun Yat-Sen University, Guangzhou, 510275, P. R. China.
Narrow-bandgap (NBG) tin-lead (Sn-Pb) perovskites are vital for all-perovskite tandem solar modules (TSMs), yet their commercialization remains limited by challenges in balancing efficiency, stability, and sustainability. Here, we presented an oxidation-triggered blockchain molecular (BCM) interface engineering strategy, which modified the poly (3,4-ethylenedioxythiophene):poly (styrene sulfonate) (PEDOT:PSS) surface and constructed a dynamic functional layer at the buried PEDOT:PSS/Sn-Pb perovskite interface through synergistic effects of biocompatible rutin molecules and their oxidation derivatives. This approach enabled full-cycle optimization from film formation to operational longevity via sequential regulation of crystallization and carrier dynamics, along with persistent defect passivation through synergistic coordination and hydrogen bonding.
View Article and Find Full Text PDFNat Commun
August 2025
Zhejiang Provincial Engineering Research Center of Energy Optoelectronic Materials and Devices, Ningbo Institute of Materials Technology & Engineering, Chinese Academy of Sciences, Ningbo, China.
All-perovskite tandem solar cells (PTSCs) offer a promising approach to surpass the Shockley-Queisser (SQ) limit, driven by efficiently reducing thermalization and transmission losses. However, the efficiency and stability of the narrow-bandgap (NBG) subcells, which are essential for PTSC performance, remain severely constrained by challenges such as lattice instability, strain accumulation and halide migration under illumination. This study introduces a rigid sulfonate-based molecule, sodium naphthalene-1,3,6-trisulfonate (NTS), into tin-lead (Sn-Pb) perovskites, where it strengthens the Sn-I bond through Sn-trisulfonate coordination and reduces light-induced dynamic lattice distortions via the rigid NTS backbone.
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