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Green Synthesis of Flower‐Like BiVO <sub/>4</sub> Nanoparticles by Solution Combustion Method Using Lemon ( <i>Citrus Limon</i> ) Juice as a Fuel: Photocatalytic and Electrochemical Study
摘要： BiVO4 have been proven to be one of the most promising photocatalyst for degradation of organic dyes and also exhibit good electrochemical performances in heavy metal detection. Herein, we have developed a simple, economic and low-cost combustion synthesis of BiVO4 nanoparticles using bismuth nitrate as an oxidiser, lemon (Citrus Limon) juice as fuel. The prepared nanoparticles were characterized by Powder X-ray diffractometer (PXRD), Fourier Transform-Infrared spectroscopy (FTIR), Diffused Reflectance Spectroscopy (DRS), Photoluminescence Spectroscopy (PL), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) analytical techniques. Flower-like morphology BiVO4 nanoparticles were observed for higher ratio of fuel (Citrus Limon). BiVO4 nanoparticles showed an excellent photocatalytic activity towards degradation of Indigo Carmine dye in solution. Further, BiVO4 modified electrode was examined for the detection of Hg (II) using electrochemical techniques.
关键词： BiVO4,Nanoparticles,Electrochemical performance,Photocatalytic activity,Photoluminescence
更新于2025-09-23 15:23:52
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Free Exciton Absorptions and Quasi-reversible Redox Actions in Polypyrrole–Polyaniline–Zinc Oxide Nanocomposites as Electron Transporting Layer for Organic Light Emitting Diode and Electrode Material for Supercapacitors
摘要： The ternary nanocomposite comprised of PPY–PANI (polypyrrole–polyaniline) copolymer and zinc oxide (ZnO), synthesized by implying chemical oxidative polymerization of pyrrole monomer in presence of ammonium persulfate as oxidant with varying ZnO concentrations. The shifting of bands and their corresponding change in nano-strain of as-prepared PPY–PANI–ZnO nanocomposite of varying concentration was confirmed by the Fourier transform inferred spectroscopy (FTIR). The surface morphological images of PPY–PANI–ZnO nanocomposites revealed the nano-flake like structure attributed to the embodiment of ZnO and increase in agglomeration was detected with the increasing concentration of ZnO. The optimized reduction in band gap up to ~ 1.02 eV and red-shift of absorption edge of ZnO in visible region side was detected for 10% PPY–PANI–ZnO nanocomposite. The relatively slow decay component and higher non radiative electron–hole recombination rate showed the better electron transport properties with chromaticity in ideal blue region for 10% PPY–PANI–ZnO nanocomposite. The higher current density ~ 7.95 A/cm2, high dielectric constant ~ 1960 at 373 K, high reduction potential ~ + 0.687 V with high specific capacitance (~ 436.14 F/g) at 10 mV s?1 and better thermal firmness was observed for 10% PPY–PANI–ZnO nanocomposite. The relatively high discharge time ~ 2600 s and high power density with meagre loss in energy density at high current density was also observed for 10% PPY–PANI–ZnO nanocomposite. These robust properties confirmed that the proposed 10% PPY–PANI–ZnO nanocomposite could be employed as electron transporting material for OLEDs as well as for high performance and efficient supercapacitors.
关键词： PPY–PANI–ZnO nanocomposites,Electrochemical performance,Chemical oxidative polymerization,PL,Electron transport layer
更新于2025-09-23 15:23:52
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Electrochemical properties of PEDOT: PSS /V2O5 hybrid fiber based supercapacitors
摘要： Binary conducting polymer (CP)/transition metal oxides (TMOs) fiber-based supercapacitors (FSCs) are considered to possess good electrochemical performance and cyclic stability compared with unitary ones since TMOs within FSCs can prevent the structure damage of CP during charge/discharge cycles to some extent. In this study, the CP/TMOs hybrid fibers are made by directly injecting the solution into capillary. Poly(3,4-ethylenedioxythiophene): polystyrene sulfonate /30 wt% vanadium pentoxide (PEDOT: PSS/30 wt% V2O5) fiber-based electrode has good electrochemical performance and cyclic stability (cycle retention: 94.02% after 4000 cycles at 0.1 mA/cm2). The energy density of the PEDOT: PSS/30 wt% V2O5 fiber in gel electrolyte is 1.37 μWh/cm2 at power density of 20 μW/cm2, which is much lower than the one in organic electrolyte (21.46 μWh/cm2 at power densities of 162.5 μW/cm2). Therefore, the method developed in this work induces good electrochemical performance for hybrid FSCs and promotes scalable fabrication of FSCs.
关键词： transition metal oxides,supercapacitor,Conducting polymers,electrochemical performance,hybrid fiber
更新于2025-09-23 15:23:52
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Ultrathin two-dimensional conjugated metala??organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis
摘要： Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) have recently emerged for potential applications in (opto-)electronics, chemiresistive sensing, and energy storage and conversion, due to their excellent electrical conductivity, abundant active sites, and intrinsic porous structures. However, developing ultrathin 2D c-MOF nanosheets (NSs) for facile solution-processing and integration into devices remains a great challenge, mostly due to unscalable synthesis, low yield, limited lateral size and low crystallinity. Here, we report a surfactant-assisted solution synthesis toward ultrathin 2D c-MOF NSs, including HHB-Cu (HHB=hexahydroxybenzene), HHB-Ni and HHTP-Cu (HHTP=2,3,6,7,10,11-hexahydroxytriphenylene). For the first time, we achieve single-crystalline HHB-Cu(Ni) NSs featured with a thickness of 4-5 nm (~8-10 layers) and a lateral size of 0.25-0.65 μm2, as well as single-crystalline HHTP-Cu NSs with a thickness of ~5.1±2.6 nm (~10 layers) and a lateral size of 0.002-0.02 μm2. Benefiting from the ultrathin feature, the synthetic NSs allow fast ion diffusion and high utilization of active sites. As a proof of concept, when serving as a cathode material for Li-ion storage, HHB-Cu NSs deliver a remarkable rate capability (charge within 3 min) and long-term cycling stability (90% capacity retention after 1000 cycles), superior to the corresponding bulk materials and other reported MOF cathodes.
关键词： Li-ion batteries,Two-dimensional conjugated metal-organic frameworks,electrochemical performance,surfactant-assisted synthesis,ultrathin nanosheets
更新于2025-09-23 15:19:57
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Sonochemical synthesis of a 2D–2D MoSe <sub/>2</sub> /graphene nanohybrid electrode material for asymmetric supercapacitors
摘要： Molybdenum selenide (MoSe2) nanosheets are prepared by a simple and facile sonochemical route. To optimize the synthesis process, the sonication is tested at three different time durations (15, 30 and 45 min) with a constant power of 500 W. In order to improve the electrochemical performance of the exfoliated MoSe2 nanosheets, we report the hybridization of 2D-MoSe2 with 2D-graphene by a simple solvothermal method. The exfoliated MoSe2 nanosheets are perpendicularly oriented on the surface of the graphene nanosheets. These MoSe2 nanosheet edges have a large number of electrochemically active sites, and the graphene sheets provide effective mass transportation of ions at the electrode–electrolyte interface. Cyclic voltammetry reveals the pseudocapacitive behaviour of a MoSe2/graphene nanohybrid based electrode. From galvanostatic charge–discharge studies, the specific capacitance is found to be 945 F g?1 at a current density of 1 A g?1. An asymmetric supercapacitor (ASC) device is fabricated, which delivers a specific capacitance of 75 F g?1 (@1 A g?1) with an energy density of 26.6 W h kg?1 and a power density of 0.8 kW kg?1, and it retains 88% of its capacitance even after 3000 cycles.
关键词： MoSe2,asymmetric supercapacitor,sonochemical synthesis,graphene,nanohybrid,electrochemical performance
更新于2025-09-19 17:15:36
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Nanoforest of 3C–SiC/graphene by laser chemical vapor deposition with high electrochemical performance
摘要： Nanoforests of 3C–SiC/graphene films are prepared by laser chemical vapor deposition (LCVD). The effectiveness of nanoforest-like 3C–SiC/graphene film as electrode materials for supercapacitors has been investigated by cyclic voltammetry and galvanostatic charge-discharge tests in 0.5 M H2SO4 solution. The specific capacitance is 8.533 mF/cm2 at a current density of 20 μA/cm2, which is 15 times higher than of previous reports of composited 3C–SiC/graphene films. The electrode exhibits good rate capability and cycling stability with 90.5% capacitance retention after 10000 cycles. The nanoforest-like 3C–SiC/graphene thick film shows a 3D porous structure with exposed graphene conductive network contributing to the greatly enhanced electrochemical performance in an environmentally aqueous electrolyte. These nanoforest-like 3C–SiC/graphene films can be promising for electrochemical energy storage applications.
关键词： Nanoforest,LCVD,3C–SiC films,Graphene,Electrochemical performance
更新于2025-09-11 14:15:04
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End-pump high efficiency 355 nm laser with a convex–concave cavity and optically-uncoated Brewster angle-cut LiB <sub/>3</sub> O <sub/>5</sub> crystal
摘要： Porous organic polymers (POPs), with features of permanent nanopores and designable frameworks, show great promise as sulfur host materials to restrain the shuttling of polysulfides, one of the main obstacles in the development of lithium–sulfur batteries. However, the simple physical entrapment from weak intermolecular interactions via a typical melt-diffusion method results in the diffusive loss of polysulfides that has thus far restricted their potential. Herein, a facile strategy for introducing chemical covalent interactions between POPs and sulfur via the regulation of sulfur infiltration temperature is reported. The results show that increasing the temperature to a suitable value, e.g., 400 °C, for a fluorinated triazine-based framework (FCTF), enables chemical bonding between the sulfur and aromatic FCTF backbone. Benefitting from the synergetic chemical and physical confinement effect, the shuttling of polysulfides can be efficiently restrained. As a result, the sample features superior sulfur utilization, high-rate performances, and good cycle stability, as compared with the sample with only physical confinement. The proposed strategy can also be extended to other POPs, such as the boroxine-linked covalent organic framework, by judiciously tailoring the infiltration temperatures. The findings disclose the important role of infiltration temperatures in developing efficient cathode host materials for lithium–sulfur batteries.
关键词： porous organic polymers,electrochemical performance,covalent chemical interactions,lithium–sulfur batteries,elevated sulfur infiltration temperature
更新于2025-09-11 14:15:04