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Photoelectrochemical biosensor for microRNA detection based on a MoS2/g-C3N4/black TiO2 heterojunction with Histostar@AuNPs for signal amplification
摘要： Herein, a novel photoelectrochemical (PEC) biosensor was developed for the ultrasensitive detection of microRNA-396a based on a MoS2/g-C3N4/black TiO2 heterojunction as the photoactive material and gold nanoparticles carrying Histostar antibodies (Histostar@AuNPs) for signal amplification. Briefly, MoS2/g-C3N4/black TiO2 was deposited on an indium tin oxide (ITO) electrode surface, after which gold nanoparticles (AuNPs) and probe DNA were assembled on the modified electrode. Hybridization with miRNA-396a resulted in a rigid DNA:RNA hybrid being formed, which was recognized by the S9.6 antibody. The captured antibody can further conjugate with the secondary IgG antibodies of Histostar@AuNPs, thereby leading to the immobilization of horse radish peroxidase (HRP). In the presence of HRP, the oxidation of 4-chloro-1-naphthol (4-CN) by H2O2 was accelerated, producing the insoluble product benzo-4-chlorohexadienone on the electrode surface and causing a significant decrease in the photocurrent. The developed biosensor could detect miRNA-396a at concentrations from 0.5 fM to 5000 fM, with a detection limit of 0.13 fM. Further, the proposed method can also be used to investigate the effect of heavy metal ions on the expression level of miRNAs. Results suggest that the biosensor developed herein offers a promising platform for the ultrasensitive detection of miRNA.
关键词： S9.6 antibody,Histostar@AuNPs,MicroRNA detection,MoS2/g-C3N4/black TiO2 heterojunction,Photoelectrochemical biosensor
更新于2025-11-14 17:04:02
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Rapid gas-liquid detonation synthesis of core-shell structural graphite coated TiO2 nanoparticles
摘要： Here we demonstrate a simple, rapid for the controlled synthesis of core-shell structural graphite coated TiO2 nanoparticle (TiO2@G), which are directly prepared by detonation chemical decomposition of the gas-liquid mixture of CH4, O2, C6H6 and TiCl4 in milliseconds. Various techniques, including XPS, TEM, XRD and Raman were employed to investigate the products. It is found that the sphere, good disperse mixed crystal TiO2 nanoparticles with crystal size of 10–30 nm were coated with thick graphite layers. Based on Zeldovich Neuman-Doring (ZND) model, the detonation synthesis mechanism of core-shell structure TiO2@G is discussed. This rapid synthesis method can be extended to the preparation of other core-shell materials.
关键词： Gas-liquid detonation,Graphite coated TiO2,Core-shell structure,Composite materials,Formation mechanism
更新于2025-11-14 17:04:02
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Hierarchical TiO <sub/>2</sub> microspheres composed with nanoparticle-decorated nanorods for the enhanced photovoltaic performance in dye-sensitized solar cells
摘要： Hierarchical TiO2 microspheres composed of nanoparticle-decorated nanorods (NP-MS) were successfully prepared with a two-step solvothermal method. There were three benefits associated with the use of NP-MS as a photoanode material. The decoration of nanoparticles improved the specific surface area and directly enhanced the dye loading ability. Rutile nanorods serving as electron transport paths resulted in fast electron transport and inhibited the charge recombination process. The three-dimensional hierarchical NP-MS structure supplied a strong light scattering capability and good connectivity. Thus, the hierarchical NP-MS combined the beneficial properties of improved scattering capability, dye loading ability, electron transport and inhibited charge recombination. Attributed to these advantages, a photoelectric conversion efficiency of up to 7.32% was obtained with the NP-MS film-based photoanode, resulting in a 43.5% enhancement compared to the efficiency of the P25 film-based photoanode (5.10%) at a similar thickness. Compared to traditional photoanodes with scattering layers or scattering centers, the fabrication process for single layered photoanodes with enhanced scattering capability was very simple. We believe the strategy would be beneficial for the easy fabrication of efficient dye-sensitized solar cells.
关键词： electron transport,dye-sensitized solar cells,solvothermal method,Hierarchical TiO2 microspheres,photovoltaic performance
更新于2025-11-14 17:04:02
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NiSe as an effective co-catalyst coupled with TiO2 for enhanced photocatalytic hydrogen evolution
摘要： Construction of semiconductor heterojunctions can effectively accelerate the separation of photo-induced charge carriers and thereby enhance photocatalytic activity. Here, NiSe was used as an effective co-catalyst to construct an active NiSe/TiO2 heterojunction for improving the photocatalytic H2 production of TiO2. The resultant 10%NiSe/TiO2 heterojunction exhibited 11 times higher photocatalytic H2-production activity than that of bare TiO2. The NiSe/TiO2 heterojunction and the photo-reduction of partial Ni2t to Ni0 notably accelerated the separation and transfer of photo-excited electron-hole pairs, and thus resulted in obvious improvement of H2-evolution activity. This work holds promise for the application of NiSe in photocatalysis as a high-efficiency photocatalytic cocatalyst.
关键词： NiSe/TiO2,Photoreduction,Heterojunction,Metal Ni0,Photocatalytic H2 evolution
更新于2025-11-14 17:04:02
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Improving Photovoltaic and Enzymatic-Sensing Performance by Coupling Core-Shell Au Nanorod@TiO2 Heterostructure with Bioinspired L-DOPA Polymer
摘要： The photoelectrochemistry (PEC) performance of TiO2 is somewhat limited by its wide band gap and low quantum efficiency, and the innovation of its composite materials provides a promising solution for an improved performance. Herein, a composite of an Au nanorod@TiO2 core-shell nanostructure (AuNR@TiO2) and a melanin-like L-DOPA polymer (PD) is designed and prepared, where the outer-layer PD tethered by the TiO2-hydroxyl complexation and the AuNR core can intensify the long-wavelength light harvesting, and the AuNR@TiO2 core-shell structure can strengthen the hot-electron transfer to TiO2. The photocurrent of the PD/AuNR@TiO2 is 8.4-fold improved versus that of commercial TiO2, and the maximum incident photon-to-electron conversion efficiency reaches 65% in the UV-visible-near-infrared region. In addition, the novel PD/AuNR@TiO2 photocatalyst possesses the advantages of good biocompatibility and stability, which can act as a versatile PEC biosensing platform for providing biocompatible environment and improving detection sensitivity. Herein, a PEC enzymatic biosensor of glucose is developed on the basis of the immobilization of dual enzyme (glucose oxidase (GOx) and horseradish peroxidase (HRP)) in PD and the signalling strategy of biocatalytic precipitation. In phosphate buffer containing glucose and 4-chloro-1-naphthol, the HRP-catalyzed oxidation of 4-chloro-1-naphthol by GOx-generated H2O2 can form a precipitate on the electrode, by which the decrement of photocurrent intensity is proportional to the common logarithm of glucose concentration. The linear detection range is from 0.05 μM to 10.0 mM glucose, with a limit of detection of 0.01 μM (S/N=3). Glucose in some human serum samples is analyzed with satisfactory results.
关键词： Au nanorod@TiO2 core-shell heterostructure,biocatalytic precipitation,bioinspired L-DOPA polymer,photoelectrochemistry,enzymatic sensing of glucose
更新于2025-11-14 17:04:02
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Charge transport and electron recombination suppression in dye-sensitized solar cells using graphene quantum dots
摘要： In this study, TiO2 photoelectrodes were sensitized in different concentration of Graphene Quantum Dots (GQDs) solution to enhance photovoltaic performance and charge transport of DSSC. The performance of pristine TiO2 and TiO2-GQDs photoelectrodes were compared to investigate the effect of GQDs incorporation in DSSC. It was found GQDs increased light absorption of TiO2 photoelectrode at visible spectrum in the range of λ = 375 nm to λ = 600 nm, resulting highest current–density, Jsc and photon-to-current conversion efficiency, ?c. Solar cell sensitized in 7.5 mg/ml concentration of GQDs known as (PG 7.5) cell shown the highest reading by 15.49 mA cm?2 and 6.97%, which indicated an improvement by 28.07% and 70.83% for Jsc and ? compare to pristine TiO2 DSSC at 12.10 mA cm?2 and 4.08%. Photoluminescence property own by GQDs may enhance photon emission to visible region when uv-ray excited on solar cell. Thus, generate more electron-hole pairs in the photoelectrode and enhance the photovoltaic parameters of DSSC. PG 7.5 cell also exhibited lowest series resistance (Rs) of 36.60 Ω, highest charge transfer resistance (Rct2) of 41.98 Ω and electron lifetime of 6.33 ms among other DSSC. These possibly due to suppression of recombination between TiO2/dye/electrolyte interfaces. Hence, resulting highest charge collection efficiency (CCE) of 53.42%. The EIS analysis confirmed the PV performance of the best cell of PG 7.5 since the same cell also generated the best photon-current conversion efficiency (PCE). This study revealed GQDs can enhanced photovoltaic parameter and charge collection efficiency of DSSC.
关键词： Charge collection efficiency,GQDs-DSSC,TiO2-GQDs,Charge transport
更新于2025-11-14 17:04:02
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Plasmonic Au nanoparticles supported on both sides of TiO2 hollow spheres for maximising photocatalytic activity under visible light
摘要： A strategy of intensifying the visible light harvesting ability of anatase TiO2 hollow spheres (HSs) was developed, in which both sides of TiO2 HSs were utilised for stabilising Au nanoparticles (NPs) through the sacrificial templating method and convex surface-induced confinement. The composite structure of single Au NP yolk-TiO2 shell-Au NPs, denoted as Au@Au(TiO2, was rendered and confirmed by the transmission electron microscopy analysis. Au@Au(TiO2 showed enhanced photocatalytic activity in the degradation of methylene blue and phenol in aqueous phase under visible light reference materials such as surpassing that of other Au(TiO2 by 77% and Au@P25 by 52%, respectively, in phenol degradation.
关键词： confinement,photocatalytic degradation,visible light,TiO2 hollow spheres,plasmonic Au nanoparticles
更新于2025-11-14 17:04:02
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Effective synthesis of nanoscale anatase TiO <sub/>2</sub> single crystals using activated carbon template to enhance the photodegradation of crystal violet
摘要： Nanoscale anatase TiO2 single crystals were successfully synthesized using three kinds of activated carbon (AC) templates through a simple sol–gel method. The optimal photocatalyst (T‐WOAC) was obtained using wood‐based AC template. X‐ray diffraction, transmission electron microscopy and Brunauer–Emmett–Teller analyses revealed that T‐WOAC possessed a small crystallite size of 8.7 nm and a clear mesoporous structure. The photocatalytic properties of samples were then evaluated through photodegradation of crystal violet (CV). Results implied that the photocatalysts prepared using the AC templates exhibited superior photocatalytic activity to that of the original TiO2. This enhancement may be due to the small crystallite size, large specific surface area and pore volume of the catalysts prepared with ACs. T‐WOAC showed high photocatalytic activity, CV degradation of 99.01% after 120 min of irradiation and k = 0.03914 min?1, which is 3.9 times higher than that of the original TiO2 (k = 0.00994 min?1). This result can be mainly attributed to the application of WOAC with moderate specific surface area and pore volume to produce T‐WOAC. Alkaline conditions benefitted the photodegradation of CV over photocatalysts. This work proposes a possible degradation mechanism of CV and indicates that the fabricated photocatalysts can be used to effectively remove CV from aqueous solutions.
关键词： photocatalyst,anatase TiO2 single crystals,sol–gel,crystal violet,activated carbon
更新于2025-11-14 17:04:02
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Mechanical analysis of the interface bonding state of a TiO2 film/Si substrate
摘要： TiO2 film is prepared on the surface of a natural oxide layer of a monocrystalline silicon substrate via RF magnetron sputtering. HRTEM (High Resolution Transmission Electron Microscope) imaging and EDX spectroscopy are performed on the sample interface, demonstrating that the film sample has a two-layer structure. Combined with XRD, the analysis shows that the upper film is a crystalline TiO2 film with a thickness of approximately 30 nm and that the lower film is a natural amorphous SiO2 oxide film with a thickness of approximately 22 nm. A geometric phase analysis (GPA) and Hooke's law are used to analyse the stress and bonding state at the interfaces between the monocrystalline silicon substrate and the natural oxide layer, between rutile TiO2 and the natural oxide layer, and between anatase TiO2 and the natural oxide layer. It is concluded that the interface bonding state of the monocrystalline silicon/natural oxide layer is good and that the interface bonding state at the interface between rutile and the natural oxide layer is better than that between anatase and the natural oxide layer.
关键词： geometric phase analysis,Hooke's law,natural oxidation,interface bonding states,TiO2
更新于2025-11-14 17:04:02
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Mesoporous TiO2-BiOBr Microspheres with Tailorable Adsorption Capacities for Photodegradation of Organic Water Pollutants: Probing Adsorption-Photocatalysis Synergy by Combining Experiments and Kinetic Modeling
摘要： Understanding adsorption-photocatalysis synergy helps advance solar-driven photodegradation of organic wastewater pollutants. To evaluate the synergy, mesoporous TiO2(amorphous)-BiOBr microspheres were facilely synthesized as model photocatalysts and characterized by XRD, SEM, TEM/HRTEM, XPS, nitrogen adsorption-desorption, UV-vis DRS, photoluminescence, and FTIR. The characterizations and photodegradation tests suggested that the composites had both adsorption sites and photocatalysis sites on BiOBr phase, while homogeneously distributed TiO2 in BiOBr microplates tailored the size of BiOBr crystallites. Accordingly, surface areas of the composites spanned from 22 to 155 m2/g and adsorption capacities for methyl orange (MO) ranged from 16 to 54 mg/g, controlled by the TiO2 content. In addition to experiments, kinetic modeling that combined adsorption with photocatalysis was developed and aided elucidating the synergy and quantitatively evaluating the composites with extracted rate constants from experimental data. The rate constant of the composite (Ti/Bi = 0.6) was calculated to be 3 times that of the pure BiOBr. Though adsorption promoted MO photodegradation, the capacity of the composite for MO adsorption and photodegradation decreased dramatically during the cycling tests. Nevertheless, this problem did not happen during photodegradation of rhodamine B and phenol on the composite and photodegradation of MO on pure BiOBr. This was explained by possible accumulation of degradation intermediates on the composite surface. This study provides a useful approach to investigate the adsorption-photocatalysis synergy from the perspectives of experiments and kinetic modeling and implies the necessity of scrutinizing the adverse effects of high levels of adsorption on recyclability of the photocatalysts.
关键词： Organic pollutants photodegradation,Kinetic modeling,TiO2-BiOBr microspheres,Tailorable adsorption capacities,Adsorption-photocatalysis synergy
更新于2025-11-14 17:03:37