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Analysis of optical injection on red and blue laser diodes for high bit-rate visible light communication
摘要： In this work, self-injection and external-injection in ～450 nm InGaN/GaN blue and ～650 nm InGaP/AlGaInP red diode lasers are investigated. A distinct locking characteristic is observed in the self-injection case with small 19 cm cavity length, demonstrating enhanced ～2.34 and ～2.07 GHz 3-dB bandwidths, corresponding to a factor of ～1.4 and ～1.1 improvement, and reduced ～60 and ～80 pm spectral linewidths, for the blue and the red lasers, respectively. Moreover, this short external cavity self-injection locked system exhibited superior performance by a factor of 1.1–1.3 compared to the long cavity (26 cm) configuration. Conversely, the external optical injection exhibited weak locking signature with improved linewidths by a factor of ～1.6–2.8 and reaching as small as ～70 and ～87 pm for the blue laser, respectively, while almost doubling in the peak powers. Later, on–off keying modulation technique based data transmission rates of up to 3.5 and 4.5 Gb/s are demonstrated on free-running blue and red laser diodes, respectively, employing an in-house laser diode mount based system. Moreover, owing to the bandwidth limitation of the optically injected systems, successful transmission of up to 2 Gb/s is demonstrated with better performance compared to the respective free-running cases, in particular, the external-optically injected system demonstrated more than double improvement in the bit-error-rate.
关键词： Visible light communication,Semiconductor laser diodes,External optical injection,Self-injection locking
更新于2025-11-28 14:23:57
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Modulating Protein-Protein Interactions with Visible-Light Responsive Peptide Backbone Photoswitches
摘要： Life relies on a myriad of carefully orchestrated processes, in which proteins and their direct interplay ultimately determine cellular function and disease. Modulation of these complex cross-talks has recently attracted attention, even as a novel therapeutic strategy. Here, we describe the synthesis and characterization of two visible-light responsive peptide backbone photoswitches based on azobenzene derivatives to exert optical control over protein-protein interactions (PPI). Our novel peptidomimetics undergo fast isomerization and reversibility with low photochemical fatigue under alternatively blue/green-light irradiation cycles. Both bind in the nanomolar rage to the protein of interest. Importantly, our best peptidomimetic displays a clear difference between isomers in its protein-binding capacity and, in turn, in its potential to inhibit enzymatic activity via PPI disruption. In addition, crystal structure determination, docking and MD calculations give a molecular interpretation and open new avenues in the design and synthesis of future photoswitchable PPI modulators.
关键词： protein-protein interactions,photopharmacology,visible-light irradiation,azobenzene,photoswitches
更新于2025-11-21 11:20:42
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Reusability and photocatalytic activity of bismuth-TiO2 nanocomposites for industrial wastewater treatment
摘要： In this study, bismuth-TiO2 nanotube (Bi-TNT) composites were used for the treatment of industrial wastewater. Bi-TNT were synthesized using two- and one-step anodization methods. The obtained composites were analyzed using X-ray diffraction, field emission scanning electron microscopy, UV–visible diffuse reflectance spectroscopy, Energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. For the two-step Bi-TNT composites, we investigated the effect of different Bi deposition times, Bi concentrations, and Bi deposition voltages on photodegradation efficiency. For the one-step Bi-TNT composites, we investigated the effect of different anodization voltages, anodization times, and Bi concentrations. Initially, the optimal synthesis conditions for two- and one-step Bi-TNT catalysts were identified and then these optimized conditions were used for industrial wastewater treatment that was collected from Banwol Sihwa Industrial Complex Republic of Korea. The Bi-TNT two- and one-step composites showed 2.0 and 2.5 times higher photocatalytic activity, respectively, for industrial wastewater treatment than that of TNT in visible-light. Recycling of Bi-TNT composites showed that the one-step composite method was more efficient and stable than the two-step method because Bi coupling and nanotube formation simultaneously occurred.
关键词： Recycling,Two- and one-step methods,Visible-light,Pollutant degradation,Bi-TiO2 composite
更新于2025-11-21 11:01:37
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Enhanced Charge Separation in g-C3N4 – BiOI Heterostructures for Visible Light Driven Photoelectrochemical Water Splitting
摘要： Heterojunctions of the low bandgap semiconductor bismuth oxyiodide (BiOI) with bulk multilayered graphitic carbon nitride (g-C3N4) and few layered graphitic carbon nitride sheets (g-C3N4-S) are synthesized and investigated as an active photoanode material for sunlight driven water splitting. HR-TEM and elemental mapping reveals formation of a unique heterostructure between BiOI platelets and the carbon nitride (g-C3N4 and g-C3N4-S) network that consisted of dendritic BiOI nanoplates surrounded by g-C3N4 sheets. The presence of BiOI in g-C3N4-S/BiOI and g-C3N4-S/BiOI nanocomposites extends the visible light absorption profile from 500 nm up to 650 nm. Due to excellent charge separation in g-C3N4/BiOI and g-C3N4-S/BiOI, evident from quenching of the carbon nitride photoluminescence (PL) and a decrease in the PL lifetime, a significant increase in photoelectrochemical performance is observed for both types of g-C3N4-BiOI heterojunctions. In comparison to heterojunctions of bulk g-C3N4 with BiOI, the nancomposite consisting of few layered sheets of g-C3N4 and BiOI exhibits higher photocurrent density due to lower recombination in few layered sheets. A synergistic trap passivation and charge separation is found to occur in the g-C3N4-S/BiOI nanocomposite heterostructure which results in a higher photocurrent and a lower charge transfer resistance.
关键词： visible light driven photocatalysis,earth abundant semiconductor heterostructures,Graphenic semiconductors,photoelectrochemistry
更新于2025-11-21 11:01:37
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Photo-Sensitive Pb5S2I6 Crystal Incorporated Polydopamine Biointerface Coated on Nanoporous TiO2 as an Efficient Signal-on Photoelectrochemical Bioassay for Ultrasensitive Detection of Cr(VI) ions
摘要： An ultrasensitive Visible light-triggered photoelectrochemical (PEC) sensor was designed based on ideal photoactive lead sulfoiodide (Pb5S2I6) as low band gap crystal, which hydrothermally synthesized rapidly at low temperature (160°C) in hydrochloride acid media followed by its incorporation into polydopamine as reactive photo-biointerface, through a facile in situ electropolymerization method, coated on nanoporous TiO2 grown by anodization on Ti foil. The structure of as-prepared samples and their photoelectrochemical properties were fully characterized. This unique photo-sensitive Pb5S2I6 catalyst-based PEC bioassay was constructed for the detection of low-abundant Cr(VI) ion in real samples. Applying central composite design, individual and mutual interaction effects were evaluated to obtain optimized solution pH, applied potential and radiant light wavelength as operational factors influencing the PEC efficiency for Cr(VI) detection. At optimal condition, the proposed sensor due to effective suppress in electron–hole recombinations showed a very low detection limit of 3.0 nM, over a broad linear concentration range of 0.01 μM-80 μM in addition to high sensitivity versus 1.9 μA/μM Cr(VI). Proposed PEC sensor displayed high selectivity, reproducibility and stability as well as improved excitation conversion efficiency, which make it highly applicable using solar energy. The potential applicability of the designed sensor was evaluated in water, tomato juice and hair color.
关键词： Photoelectrochemical biosensor,Nanoporous TiO2,Cr(VI) ions,Visible light excitation.,Pb5S2I6 crystal
更新于2025-11-21 11:01:37
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G‐C3N4‐SiC‐Pt for Enhanced Photocatalytic H2 Production from Water under Visible Light Irradiation
摘要： The g-C3N4 and SiC has drawn increasing attention for application to visible light photocatalytic hydrogen evolution from water splitting due to their unique band structure and high physicochemical stability. In this study, g-C3N4-SiC heterojunction with loaded noble metal was constructed. The g-C3N4-SiC-Pt composite photocatalysts were successfully prepared by the combination method of a bio-reduction, sol-deposition and calcination. The layers of g-C3N4 were thinned and the SiC and Pt nanoparticles simultaneously were tightly bound to g-C3N4 by calcination in the process of preparing the g-C3N4-SiC-Pt. The heterojunction formed in the interface of SiC and g-C3N4 enhances the separation efficiency of the photogenerated electron-hole pairs. These composite photocatalysts achieve a high hydrogen evolution rate of 595.3 μmol·h-1·g-1 with a 1wt% of deposited Pt, 3.7- and 2.07-fold higher than g-C3N4-bulk and g-C3N4-SiC under visible-light irradiation with a quantum efficiency of 2.76% at 420 nm, respectively.
关键词： visible light,g-C3N4-SiC-Pt photocatalysts,hydrogen evolution,photocatalysis
更新于2025-11-21 11:01:37
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Preparation of Ag-AgVO3/g-C3N4 composite photo-catalyst and degradation characteristics of antibiotics
摘要： The degradation of tetracycline by silver vanadate (AgVO3), graphite-like carbon nitride (g-C3N4) and their composites was studied by visible light photocatalysis. Their structures and morphologies were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Their degradation intermediates were analyzed by GC-MS. Nanorod silver vanadate was synthesized by hydrothermal method. The results show that the gap between nanorods is reduced by adding spinning carbon nitride, and the photocatalytic performance of the composite is stronger than that of single material. The reaction rate constants of Ag-AgVO3/g-C3N4 composites were 0.0298 min-1, 2.4 and 2.0 times that of g-C3N4 (K=0.0125 min-1) and AgVO3 (K=0.0152 min-1), respectively. At 120 minutes, the degradation rate of the composites reached 83.6%. The degradation of tetracycline was confirmed by GC-MS, and a possible degradation process was proposed.
关键词： Photo-catalysis,Carbon nitride,Antibiotics,Visible light,Silver vanadate
更新于2025-11-21 10:59:37
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Construction of novel Z-scheme Ag/ZnFe2O4/Ag/BiTa1-xVxO4 system with enhanced electron transfer capacity for visible light photocatalytic degradation of sulfanilamide
摘要： A novel Z-scheme system, Ag/ZnFe2O4/Ag/BiTa1-xVxO4 with enhanced electron transfer capacity was constructed for degrading sulfanilamide (SAM) using solar light. The photocatalytic activity of Ag/ZnFe2O4/Ag/BiTa1-xVxO4 was investigated. The effects of the mass ratio (ZnFe2O4:BiTaO4), doped V dose, Ag wt.% content, and irradiation time on the catalytic performance were evaluated. The reasonable mechanism of Ag/ZnFe2O4/Ag/BiTa1-xVxO4 solar photocatalytic degradation was also presented. These results reveal Ag/ZnFe2O4/Ag/BiTa1-xVxO4 possesses enhanced photocatalytic performance. The loaded Ag as electron mediator increases the electron transfer rate. Particularly, the doped V and the Fe ions from ZnFe2O4 form a powerful electron driving force, which enhances the electron transfer capacity. Ag/ZnFe2O4/Ag/BiTa1-xVxO4 shows optimal photocatalytic performance at 2.0 wt.% Ag and 0.5% doped V dose (ZnFe2O4:BiTaO4=1.0:0.5). Also, Ag/ZnFe2O4/Ag/BiTa1-xVxO4 exhibits high stability and repeatability in photocatalytic degradation. Several active species (?OH, ?O2?, and h+) are produced in the Z-scheme photodegradation of SAM. These results on the enhanced photocatalytic activity of Ag/ZnFe2O4/Ag/BiTa1-xVxO4 are ascribed to synergistic photocatalytic effects of ZnFe2O4 and BiTa1-xVxO4 mediated through Ag and driven by doped V and Fe ions. Therefore, the Z-scheme Ag/ZnFe2O4/Ag/BiTa1-xVxO4 photocatalytic technology proves to be promising for the solar photocatalytic treatment of antibiotics under solar light.
关键词： visible light,Electron transfer capacity,Ag/ZnFe2O4/Ag/BiTa1-xVxO4,photocatalytic,sulfanilamide
更新于2025-11-21 10:59:37
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Synthesis of MoS <sub/>2</sub> /TiO <sub/>2</sub> Nanophotocatalyst and Its Enhanced Visible Light Driven Photocatalytic Performance
摘要： Molybdenum disulfide (MoS2), as a typical layered transition metal sulfide, has been widely used in photocatalysis. Here, we report layered MoS2 nanosheet-coated TiO2 heterostructures that were prepared using a simple photo-assisted deposition method. The as-prepared samples were investigated in detail by using X-ray diffraction, Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. Results demonstrated that the MoS2 nanosheets uniformly covered the outer surface of TiO2. The visible light-sensitive photocatalytic activity was evaluated by the removal of methylene blue (MB) and 2-chlorophenol (2-CP) in aqueous solution. Thus, the MoS2/TiO2 heterostructures exhibited improved photocatalytic degradation activity under visible light compared with the pure TiO2. Under visible light irradiation for 90 min, the degradation efficiencies of MB and 2-CP over the MoS2/TiO2 sample (sunlight irradiation time: 30 min) are as high as 93.6% and 70.6%, respectively. Furthermore, the corresponding mechanism of enhanced photocatalytic activity is proposed on the basis of the comprehensively investigated results from the radical trapping experiments, photoluminescence spectroscopy, and electron spin resonance analysis. The hole oxidation, hydroxyl radicals, and superoxide anion radicals act as the active species simultaneously in the photodegradation of the dye molecules. However, of these species, hole oxidation played the most important roles in the photocatalytic reaction.
关键词： Photocatalytic,MoS2,Visible Light
更新于2025-11-20 15:33:11
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Visible-Light Plasmonic Enhancement of Catalytic Activity of Anisotropic Silver Nanoparticles
摘要： Synthesis of silver nanoparticles (AgNPs) in presence of copper salt (as the etchant) led to the formation of nanoparticle samples with different fractions of anisotropic particles. The proportion of anisotropic nanoparticles decreased with increase in ratio of precursor Cu salt in the preparation protocol. These AgNPs samples were found to catalyse p-nitrophenol reduction by glycerol and Fenton oxidation of methyl orange. The catalytic activity of these AgNPs samples for these reactions increased with the fraction of anisotropic nanoparticles in the catalyst samples. On conducting these reactions under cool white LED visible light, the catalytic activity of AgNPs catalyst samples increased by 2 to 3 times compared to that observed in dark. The photo-Fenton MO degradation catalytic activity obtained is among the best reported in literature. However, the order of the reaction did not change whether the reaction was conducted under visible light or in dark. Direct plasmonic catalytic mechanisms are proposed to explain the enhancement in reactivity under visible light.
关键词： Plasmonic Photocatalysis,Visible Light,Anisotropic Silver Nanoparticles
更新于2025-11-19 16:56:42