Polyaniline (PANI) layers are electrochemically obtained in the presence of four polysulfonic acids with different rigidities of the polymer backbone-iso-(and tere-)poly-(4,4'-(2,2'-disulfonic acid)-diphenylene-iso(tere)-phthalamide (i-PASA and t-PASA), polystyrenesulfonic acid (PSSA) and poly(2-acrylamido-2-methyl-1-propanesulfonic acid) (PAMPSA). Combined microgravimetric (EQCM) and electrochemical measurements are carried out in the course of polymerization and repetitive redox switching. It is found that after synthesis PASA-doped PANIs shows good stability with low exchange of mass in the course of voltammetric scans, while PAMPSA-doped PANI contains a large amount of water that gradually becomes expelled in the repetitive redox switching. PANI obtained in the presence of PSSA takes an intermediate position with respect to mass exchanged in the electrochemical redox process. XPS studies are used to obtain data for the extent of doping of the different PANI materials. The results show high doping level (about 0.5) for PASA- and PAMPSA- and lower level (0.32) for PSSA-doped PANI layers. Repeated electrochemical studies carried out with the specimens investigated by XPS after long-term storage in the dry state give evidence for structural rearrangement, perfect recuperation of the initial electrochemical activity and high stability of the electrochemical response.
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http://dx.doi.org/10.3390/polym12051050 | DOI Listing |
Analyst
January 2025
Guangdong Provincial Key Laboratory of Electronic Functional Materials and Devices, Huizhou University, Huizhou, 516007, China.
Disordered polymerization of polymers widens the polymerization degree distribution, which leads to uncontrollable thickness and significantly weakens their sensing performance. Herein, poly(sodium -styrenesulfonate)-functionalized reduced graphene oxide (PSS-rGO) with multichannel chain structures coated with thin polyaniline layer (PSS-rGO/PANI) nanocomposites was synthesized a facile interfacial polymerization route. The morphology and microstructure of the PSS-rGO/PANI nanocomposites were characterized using Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM).
View Article and Find Full Text PDFDalton Trans
January 2025
Department of Physics, RPS Degree College, Balana, Mahendergarh, Haryana 123029, India.
The present work reports a clear and improved hydrothermal methodology for the synthesis of MoSe nanoflowers (MNFs) at 210 °C. To observe the effect of temperature on the fascinating properties, the process temperature was modified by ±10 °C. The as-prepared MNFs were found to consist of 2D nanosheets, which assembled into a 3D flower-like hierarchical morphology van der Waals forces.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
School of Chemistry and Chemical Engineering, Central South University, Changsha 410083, Hunan, China. Electronic address:
Heterointerface engineering is an effective strategy to design and construct high-performance photocatalysts. Herein, polyaniline (PANI) nanoparticles and ZnTi layered double hydroxide (ZnTi-LDH) nanosheets were integrated to form organic-inorganic heterostructure (PANI/LDH) via d-π electronic coupling using in-situ polymerization for photocatalytic oxidation/reduction towards tetracycline (TC) and Cr(VI). The photocatalytic activity was closely related to feed amount of aniline (Ani) in the polymerization process, which the abundant PANI nanoparticles were evenly distributed on the surface of ZnTi-LDH nanosheets at the proper Ani feed amount, and thus reinforced d-π electronic coupling at the organic-inorganic interfaces more efficiently.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
Suzhou Research Institute of Shandong University, Suzhou, Jiangsu 215123, China.
As modification strategies are actively developed, the photothermal effect is expected to be a viable way to enhance the PEC water splitting performance. Herein, we demonstrate that the photothermal polyaniline (PANI) layer inserted between CoF cocatalyst and BiVO can enhance the photocurrent density of pure BiVO by 3.50 times.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Sauvage Laboratory for Smart Materials, School of Materials Science and Engineering, Harbin Institute of Technology (Shenzhen), Shenzhen, 518055, China.
Conventional solid-electrolyte interface (SEI) in aqueous Zn-ion batteries mainly acts as a physical barrier to prevent hydrogen evolution reaction (HER), while such SEI is prone to structural deterioration stemming from uneven Zn deposition at high current densities. Herein, we propose an in situ structural design of polymer-inorganic bilayer SEI with a proton holder feature by aniline-modulated electrolytes. The Zn(OTF) exhibits a lower LUMO energy level in comparison to aniline, resulting in the formation of a bilayer structure characterized by an inner ZnF layer and an outer polyaniline (PANI) layer.
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