RESUMO
Magneto-optical (MO) properties of the bilayed Au/BIG and trilayered Au/BIG/Au magneto-plasmonic crystals (MPCs) were analyzed by the finite-difference time-domain method. In contrast to the low deflection angle and transmission of the smooth thin film, all the heterostructures with perforated holes in the top Au film displayed a similar trend with two strong resonant bands in Faraday rotation and transmittance in the near infrared wavelength range. The bands and electric distribution relative to the component and hole structure were revealed. The MPC with plasmonic hexagonal holes was found to own superior Faraday effects with distinctive anisotropy. The evolution of the resonant bands with the size and period of hexagonal holes, the thickness of different layers, and the incident light polarization was illustrated. The Faraday rotation of the optimized bilayed and trilayered hexagonal MPCs was improved 15.3 and 17.5 times, and the transmittance was enhanced 12.1 and 11.1 folds respectively at the resonant wavelength in comparison to the continuous Au/BIG film, indicating that the systems might find potential application in MO devices.
RESUMO
Structure has been considered to play an important role in photocatalytic performance of the semiconductors, but the intrinsic factors were rarely revealed. Herein, ZnO nanomaterials in the structures of thin film, nanowire array and nanosheet array were synthesized, and their structural characteristics, optical properties, photocurrent response and photocatalytic efficiency were compared with each other for illustrating the issue. The photoluminescence intensity decreased in the order of nanosheets, thin film and nanowires for improved lifetime of the photoexcited charges. The absorption of the nanosheets and nanowires improved obviously in the visible range with a redshift of the absorption edge than that of the thin film. The nanowires possessed the highest response current of 82.65 µA at a response time of 2.0 ms in a sensitivity of 87.93 at the light frequency of 1 Hz, and gained the largest catalytic efficiency of 2.45 µg/cm2 h for the methylene blue degradation in UV light. Nevertheless, the improvement of catalytic efficiency of the nanosheets (up to 42.4%) was much larger than that of nanowires (5.7%) and thin film (2.6%) for the Au coating. The analysis revealed that the photocatalytic efficiency of the ZnO nanomaterials was modulated by the structure as it contained different surface area, roughness, defect and doping states, vacancies, polar and non-polar crystalline faces, which would provide structural design of semiconductor nanomaterials for the photoelectric and photocatalytic applications.
RESUMO
A ternary semiconductor ZnO/MoS2/Ag2S nanorod array in an intimate core-shell structure was synthesized on glass substrates. The physicochemical properties and photocatalytical performance of the specimen were characterized and compared with single ZnO and binary ZnO/Ag2S and ZnO/MoS2 nanorod arrays. It is found that the coating layers depressed the band edge emission of the ZnO core, improved light absorption in the visible range, reduced charge transfer resistance, and increased photocatalytic activity. The ternary heterojunction nanorod array possessed full solar absorption with an efficiency of 52.88% for the degradation of methylene blue under visible light in 30 min. The efficiency was higher than other arrays and was 7.6 times that of the ZnO array. Theory analysis revealed that the coating layer brought different band alignment in the heterojunctions for efficient charge separation and conduction, which was beneficial for the photocatalytic performance.
RESUMO
Phototreatment is at the leading edge of a research hot topic as a driving force for structural transformation, spectral and electromagnetism improvements, and the functional performance of nanomaterials. Light irradiation can excite surface plasmons in noble metal nanoparticles, create electron-hole pairs, and produce charge transfer in semiconductor substrates, which have led to it being widely used in surface-enhanced Raman spectroscopy (SERS) for life sciences, environmental protection, and biological analysis. Photo-induced enhanced Raman spectroscopy (PIERS) is a new technology developed on the basis of traditional SERS and has proven to be an efficient way to resolve several critical challenges thanks to its incomparable superiority for incontiguous operation, efficient charge separation and enrichment, and a large signal enhancement for a wide range of biomolecules at the trace level. This makes PIERS a powerful technique with very appealing and promising applications in various branches of analytical science. In this review, the enhancement mechanisms of PIERS are analyzed in comparison with SERS. Afterward, the parameters influencing the enhancement of PIERS, including the substrate, light irradiation, and relaxation are discussed in detail. Finally, some perspectives on further developments of PIERS are exemplified. The PIERS technique will continue to evolve and grow with new developments and its successful application in bioanalysis and life sciences.