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The concentration conditions for the deposition of lead sulfide and hydroxide in a citrate-ammonia reaction system by varying the pH value and the concentration of the ammonium iodide dopant are calculated. Kinetic studies of the process of conversion of lead salt into sulfide by varying the concentration of NHI in solution within the range of 0.0-0.4 M show an inhibitory effect of ammonium iodide, which reduces the constant of the effective rate of the conversion process by almost 20 times. Thin films of lead sulfide with a thickness of 100 to 650 nm are synthesized by chemical bath deposition in the presence of NHI on sitall and glass substrates. The introduction of NHI into the reaction mixture decreases the size of crystallites forming the films and increases the fraction of nanoparticles to 17%. The films deposited during 90 min contain 48.5-51.7 at% of lead, 47.4-47.9 at% of sulfur, and up to 3.7 at% of iodine; the content of iodine can reach 17.1 at% in the initial period of deposition (after 20 min of deposition). The calculated fractal dimension of the surface of the iodine-doped PbS(I) films ( = 2.04-2.14) corresponds to the process of film formation by the cluster-cluster aggregation mechanism with small sticking probability (reaction-limited cluster aggregation model (RLCA)). According to the X-ray diffraction data, the PbS(I) films have a cubic structure of the NaCl (1) type; an increase in the concentration of NHI in the solution results in an increase in the lattice parameter from 0.59315(1) to 0.59442(3) nm, which is probably due to the substitution of sulfur ions for iodine ones. According to optical studies, the introduction of ammonium iodide into the reaction mixture leads to a shift of the absorption edge to the high-energy region and the appearance of an additional (impurity) band. The PbS films deposited in the presence of NHI do not require additional photosensitization operations and show a relatively high volt-watt sensitivity to IR radiation at anomalously small values of the time constant.
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http://dx.doi.org/10.1039/d2cp01815b | DOI Listing |
Org Lett
September 2025
National Key Laboratory of Advanced Drug Delivery and Release Systems, School of Pharmaceutical Sciences & Institute of Materia Medica, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250117, P. R. China.
A method for the conversion of isoxazoles into thiazoles by skeleton rearrangement has been achieved by an ammonium iodide-catalyzed cycloaddition protocol under mild conditions with a broad substrate scope and good functional group tolerance. Most appealingly, the reaction can proceed smoothly without the addition of any transition metal catalyst. Detailed mechanistic studies, including control experiments and key reaction intermediate characterization, reveal an intermolecular [3+2] cycloaddition reaction pathway.
View Article and Find Full Text PDFOrg Lett
September 2025
Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
A palladium-catalyzed difunctional fluoroalkylative carbonylation of 1,3-enynes with fluoroalkyl halides and ammonium iodide has been developed, providing rapid access to fluoroalkylated allenyl primary amides with a broad substrate scope, high chemo- and regioselectivity, and good functional group tolerance.
View Article and Find Full Text PDFOrg Biomol Chem
August 2025
Department of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok, 10330 Thailand.
An efficient electrochemical synthesis of -ureidobenzonitrile derivatives from 2-aminobenzamides and isothiocyanates was developed using ammonium iodide as the electrolyte and mediator (0.5 equivalent). This iodide-mediated desulfurization-cyclization process proceeds under mild conditions in an undivided cell with graphite electrodes, delivering a broad range of products in good to excellent yields (44 examples, up to 98%).
View Article and Find Full Text PDFPolymers (Basel)
July 2025
Centre of Excellence in Solar Cells & Renewable Energy, Department of Physics and Environmental Science, SSES, Sharda University, Greater Noida 201310, India.
The increasing demand for high-performance energy storage devices has stimulated interest in advanced electrolyte materials. Among them, ionic liquids (ILs) stand out for their thermal stability, wide electrochemical windows, and good ionic conductivity. When doped into polymeric matrices, these ionic liquids form hybrid polymeric electrolytes that synergize the benefits of both liquid and solid electrolytes.
View Article and Find Full Text PDFAdv Sci (Weinh)
July 2025
Department of Solution-Processing of Hybrid Materials and Devices, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Kekuléstraße 5, 12489, Berlin, Germany.
Halide perovskites (HaP), with their exceptional optoelectronic properties and high-power conversion efficiencies in photovoltaic devices, hold promise for photoelectrochemical (PEC) applications in green fuel and chemical production. However, their stability in aqueous environments remains a challenge. This study investigates the stability and degradation mechanisms of the 2D Ruddlesden-Popper phase phenylethyl ammonium lead iodide (PEA PbI) thin films in aqueous electrolytes under dark and illuminated conditions.
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