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The charge recombination resulting from the numerous perovskite defects and the inferior buried interface remarkably deteriorates the performance of inorganic perovskite solar cells. Here, we introduce 4-aminobenzenesulfonic acid (ABSA) into the CsPbI perovskite precursor to simultaneously reduce perovskite defects through modulating CsPbI perovskite crystallization and heal the buried interface through in situ forming a ABSA dipolar interlayer. The interaction of the ABSA molecule with CsPbI precursor components hinders CsPbI perovskite crystallization, resulting in forming a compact and smooth CsPbI perovskite film with reduced defects and enhanced crystallinity. Meanwhile, ABSA molecules are excluded from the CsPbI perovskite crystal and pushed downward during the perovskite crystallization process. Consequently, ABSA molecules accumulate at the bottom surface of the CsPbI perovskite and in situ form an ABSA dipolar interlayer, which effectively heals the buried interface and promotes interfacial charge transfer. As a consequence, the planar carbon-based CsPbI cell with the ABSA additive demonstrates a largely improved performance with a power conversion efficiency up to 17.89%. In particular, the unencapsulated CsPbI cell maintains over 90% of the original efficiency in ambient air after 480 h of storage, indicating superior long-term stability.
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http://dx.doi.org/10.1021/acsami.5c12588 | DOI Listing |
J Phys Chem Lett
September 2025
State Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), School of Flexible Electronics (Future Technologies), Nanjing Tech University (NanjingTech), Nanjing 211816, Jiangsu, China.
Thermally evaporated perovskite light-emitting diodes (PeLEDs) hold great promise for high-quality display applications due to their exceptional large-area uniformity and ease of pixelation and integration. Beyond efficiency considerations, display technologies demanded exceptionally high luminance performance from LEDs. While the brightness of blue and green PeLEDs had progressed rapidly, the performance of red PeLEDs lagged significantly.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Longzihu New Energy Laboratory, Zhengzhou Institute of Emerging Industrial Technology, Henan University, Zhengzhou 450000, China.
We synthesized two linear dopant-free hole transport materials (HTMs), denoted as NT and iNT, by coupling methoxytriphenylamine donor unit with either naphtho[1,2-:5,6-']bis[1,2,5]thiadiazole or its isomeric counterparts naphtho[1,2-:5,6-']bis([1,2,3]thiadiazole) as acceptor units. The fused-ring isomerization structure of iNT endows it with a substantial dipole moment and well-aligned energy levels, which are highly favorable for efficient free-charge extraction. Compared to devices based on NT, CsPbI inorganic perovskite solar cells (IPSCs) employing iNT exhibited significantly enhanced performance, achieving a power conversion efficiency (PCE) of 18.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Electrical Engineering, Korea University, Seoul, 02841, Republic of Korea.
Neuromorphic computing addresses the von Neumann bottleneck by integrating memory and processing to emulate synaptic behavior. Artificial synapses enable this functionality through analog conductance modulation, low-power operation, and nanoscale integration. Halide perovskites with high ionic mobilities and solution processabilities have emerged as promising materials for such devices; however, inherent stochastic ion migration and thermal instability lead to asymmetric and nonlinear characteristics, ultimately impairing their learning and inference capabilities.
View Article and Find Full Text PDFLangmuir
September 2025
Jointly Constructed Key Laboratory of Power and Storage Batteries of Anhui Province, Anhui University of Science and Technology (AUST), Huainan, Anhui 232001, China.
Inorganic CsPbI perovskite solar cells (PSCs) hold notable promise but suffer from instability in maintaining the photoactive black phase under ambient and thermal conditions; this work systematically investigates the impacts of phenylenediamine dihydrochloride (PPD·2HCl, containing ammonium groups) and terephthalimidamide dihydrochloride (TPID·2HCl, featuring amidinium groups) ligands on device performance and stability, with a focus on dissecting TPID's thermal stabilization mechanisms. While both ligands enhance room-temperature phase stability via surface defect passivation, TPID·2HCl-treated devices exhibit superior thermal resilience: its amidinium group features delocalized electron density across the N-C-N skeleton, strengthening coordination with undercoordinated sites and mitigating lattice distortion under heat; thermogravimetric analysis (TGA) shows TPID·2HCl decomposes at ∼350 °C with gradual mass loss, surpassing PPD·2HCl's rapid degradation at ∼300 °C; density functional theory (DFT) calculations reveal TPID binds more strongly to the CsPbI surface (adsorption energy: -1.51 eV vs -1.
View Article and Find Full Text PDFSmall
August 2025
Department of Materials Science and Engineering, National Tsing Hua University, Hsinchu, 30013, Taiwan.
Chiral quantum emitters attract significant interest for their unique non-reciprocal photon-mediated properties and potential in quantum operations. Achieving chiral quantum emission has traditionally required sophisticated techniques like high magnetic fields or cryogenic temperatures, and room-temperature circularly polarized luminescence (CPL) from individual quantum emitters is rarely reported. Here, it is shown that certain CsPbI perovskite quantum dots (PQDs) exhibit both room-temperature quantum emission and intrinsic CPL.
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