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Bioaerosols play a significant role in climate change and variation of ecological environment. To investigate characterization of atmospheric bioaerosols, we conducted lidar measurement for observing bioaerosols close to dust sources over northwest China in April, 2014. The developed lidar system can not only allowed us to measure the 32-channel fluorescent spectrum between 343â nm to 526â nm with a spectral resolution of 5.8â nm but also simultaneously detect polarisation measurements at 355â nm and 532â nm, as well as Raman scattering signals at 387â nm and 407â nm. According to the findings, the lidar system was able to pick up the robust fluorescence signal emitted by dust aerosols. Especially the polluted dust, the fluorescence efficiency could reach 0.17. In addition, the efficiency of single-band fluorescence typically rises as the wavelength goes up and the ratio of fluorescence efficiency of polluted dust, dust, air pollutant and background aerosols is about 4:3:8:2. Moreover, our results demonstrate that simultaneous measurements of depolarization at 532â nm and fluorescence could better distinguish fluorescent aerosols than those at 355â nm. This study enhances the ability of laser remote sensing for real-time detecting bioaerosol in the atmosphere.
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Polarization measurements have been widely used to detect aerosol properties by remote sensing in recent decades. To better understand the polarization characteristics of aerosols by lidar, the numerically exact T-matrix method was used to simulate the depolarization ratio (DR) of dust and smoke aerosols at typical laser wavelengths in this study. The results show that the DRs of dust and smoke aerosols have obviously different spectral dependences. Moreover, the ratio of DRs at two wavelengths has an obvious linear relationship with the microphysical properties of aerosols, including aspect ratio, effective radius and complex refractive index. At short wavelengths, we can use it to invert the absorption characteristics of particles, further improving the detection ability of lidar. Comparing the simulation results of different channels, DR, (color ratio) CR and (lidar ratio) LR have a good logarithmic fitting relationship at 532â nm and 1064â nm, which helps to classify the aerosol types. On this basis, a new inversion algorithm, "1ß+1α+2δ", was presented. By this algorithm, the backscattering coefficient (ß), extinction coefficient (α), DR (δ) at 532â nm and 1064â nm can be used to expand the range of inversion and compare lidar data with different configurations to obtain more extensive optical characteristics of aerosols. Our study enhances the application of laser remote sensing in aerosol observations more accurately.
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The application of a noble-metal-based plasmon-enhanced substrate to detect low-concentration analytes has attracted extensive attention. Most of the substrates used in recently reported researches are based on two-dimensional structures. Hence, we prepared a higher efficiency Raman activity substrate with a filter paper structure, which not only provides more plasmonic "hot spots," but also facilitates analyte extraction and detection due to the flexibility of the paper. The preparation of the plasmonic paper substrate adopted centrifugation to deposit the alloy nanoparticles onto the paper base. The optimal particle deposition condition was found by adjusting the centrifugal force and centrifugation time. Then, the surface-enhanced Raman spectroscopy (SERS) performance of the substrate was enhanced by altering the plasmon resonance peak on the surface of the nanoparticles. The enhancement factor of this paper-based substrate was 1.55×107, with high detection uniformity (10-6 M, rhodamine 6G) and a low detection limit (10-11 M, rhodamine 6G). Then, we applied the SERS substrate to pesticide detection; the detection limit of the thiram reached 10-6 M. As a result, the simple and cost-effective paper-based SERS substrate obtained in this way has high detection performance for pesticides and can be used for rapid detection in the field, which is beneficial to food safety and environmental safety.
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Chiral structures have a wide range of applications, such as biometric identification, chemical analysis, and chiral sensing. The simple fabrication process of chiral nanostructures that can produce a significant circular dichroism (CD) effect remains a challenge. Here, a three-dimensional (3D) cantilever-shaped nanostructure, which inherits the chiral advantages of 3D nanostructures and simplicity of 2D nanostructures, is proposed. The nanostructure can be prepared by the combination of one-time electron beam lithography and oblique-angle deposition and consists of a thin metal film with periodic holes such that two hanging arms were attached to the edges of holes. The length of the cantilever and the height difference between the two arms can be adjusted by controlling the tilt angle of beam current during the deposition processes. Numerical calculations showed that the enhancement of CD signal was achieved by plasmon distortion on the metal film by the lower hanging part of the cantilever structure. Furthermore, signals can be actively adjusted using a temperature-sensitive polydimethylsiloxane (PDMS) material. The angle between the lower cantilever and the top metal film was regulated by the change in PDMS volume with temperature. The results provide a new way to fabricating 3D nanostructures and a new mechanism to enhance the CD signal. The proposed nanostructure may have potential applications, such as in ultra-sensitive detection and remote temperature readout, and is expected to be an ultra-compact detection tool for nanoscale structural and functional information.
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Surface-enhanced Raman scattering (SERS) is recognized as one of the most favored techniques for enhancing Raman signals. The morphology of the SERS substrate profoundly affects molecular Raman spectra. This study aimed to construct a ring-mounted nanostructured substrate via liquid-liquid two-phase self-assembly incorporated with anodic aluminum oxide (AAO) membrane transfer techniques. High-density nanoparticles (NPs) assembled on AAO membranes were ascribed to reduce the diameters of the nanopores, with Au-Ag alloy NPs to regulate the dielectric constant so as to reveal the local surface plasmon resonance tunability. SERS engineered in this way allowed for the fabrication of a ring-mounted nanostructured substrate where the distribution density of NPs and dielectric constant could be independently fine-tuned. High SERS activity of the substrate was revealed by detecting the enhanced factor of crystal violet and rhodamine 6G molecules, which was up to 1.56 × 106. Moreover, SERS of thiram target molecules confirmed the supersensitivity and repeatability of the substrate as a practical application. The results of this study manifested a low-cost but high-efficiency ring-mounted nanostructured SERS substrate that might be suitable in many fields, including biosensing, medical research, environmental monitoring, and optoelectronics.
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Induced circular dichroism (ICD) is widely used in miniature polarizers, molecular detection, and negative refractive index media. However, enhancing and the dynamic regulation of ICD signals of achiral nanostructures in the visible and near-infrared range remain the current challenges. Here, monolayer borophene (MB) with anisotropic conductance was incorporated into achiral nanostructures, which consisted of achiral dielectric elliptical hole arrays (DENAs) placed on a silver substrate. Two narrowband ICD signals for DENAs/MB were achieved in the near-infrared range under different circularly polarized lights. The distributions of the magnetic field of DENAs/MB could explain the two narrowband ICD signals originating from the coupling of surface plasmon polariton resonances along the x- and y directions. Not only could the ICD signals be tuned by the structural parameters of DENAs/MB, but they could also be actively tuned by the incident angles of the excitation light and the carrier concentration of MB. In addition, the sensitivity and the figure of merit of DENAs/MB could reach 302/RIU and 61.0. These results provide a concise method for the design of dynamically adjustable chiral devices based on borophene and promote its application in molecular recognition and chiral catalysis.
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Lanthanide (Ln)-doped upconversion luminescence (UCL) materials have attracted worldwide attention due to their unique photophysical characteristics. However, how to effectively improve their UCL efficiency has always been an important scientific issue. Here, we design and fabricate ß-NaYF4 microtubes (MTs) with a natural hexagonal shape in the cross section and wedge shape on both top vertexes, which can be regarded as an optical waveguide. The UCL property of a single ß-NaYF4:Yb3+,Er3+(or Tm3+) MT is systematically investigated based on waveguide-excitation modes. It is found that the excitation light can be efficiently coupled in the ß-NaYF4:Yb3+,Er3+(or Tm3+) MT by modulating the angle between the wedge-shape end plane of MT and the microscope slide. In addition, it is clearly observed that the excitation light can be confined and propagate in the MT by introducing a 633 nm laser, which is mainly due to the natural waveguide structure with a stronger confinement and propagation effect of light, thereby enhancing light-to-MT interactions. The current work provides a powerful solution to build high-efficiency Ln-doped UCL materials, which may have potential applications in the optical communication and biomedical fields.
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Elementos da Série dos Lantanídeos , Nanopartículas , Elementos da Série dos Lantanídeos/química , Lasers , Luminescência , Nanopartículas/químicaRESUMO
All-Inorganic perovskite CsPbX3 (X = Cl, Br, I) quantum dots (QDs) have attracted tremendous attention in the past few years for their appealing performance in optoelectronic applications. Major properties of CsPbX3 QDs include the positive photoconductivity (PPC) and the defect tolerance of the in-band trap states. Here it is reported that when hybridizing CsPbX3 QDs with indium tin oxide (ITO) nanocrystals to form CsPbX3 -ITO nano-heterojunctions (NHJs), a voltage tuned photoresponse-from PPC to negative photoconductivity (NPC) transform-is achieved in lateral drain-source structured ITO/CsPbX3 -ITO-NHJs/ITO devices. A model combining exciton, charge separation, transport, and most critical the voltage driven electron filling of the in-band trap states with drain-source voltage (VDS ) above a threshold, is proposed to understand this unusual PPC-NPC transform mechanism, which is different from that of any known nanomaterial system. This finding exhibits potentials for developing devices such as photodetectors, optoelectronic switches, and memories.
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Pontos Quânticos , Compostos de EstanhoRESUMO
It is great challenge and interesting for researchers to fabricate substrates for enhanced Raman and sensor, and assemble some easy-to-synthesize metallic nanomaterials into controllable nanostructures with special morphologies and arrangements, via alternating current (AC) electric field. The Au-Ag alloy nanoparticles (Au-Ag alloy NPs) colloidal suspension with excellent dispersibility synthesized by wet chemical method, and the morphology of the assembly can be well controlled by regulating the frequency of the AC electric field. Au-Ag alloy nanochains array (Au-Ag ANCs) with dense plasmonic "hot spots" is formed when the AC electric field of 4Vpp-30kHz is applied, which is supported by the result of finite element method (FEM) numerical simulation. Experimental results demonstrate that Au-Ag ANCs show excellent SERS activity: Au-Ag ANCs can detect both Rhodamine 6G (Rh6G) and crystal violet (CV) in the magnitude order of 10-10 M, and the Raman peaks intensity and analyte concentration has a strong linear correlation (R2 is 0.99339 and 0.95916, respectively). Besides, the introduction of Au-Ag ANCs makes the Raman spectra intensity of thiram (a pesticide) with a concentration of 30â ppm on the surface of the blank ITO glass significantly enhanced, and it can detect thiram with a concentration as low as 0.03â ppm. In addition, Au-Ag ANCs substrate exhibits great uniformity and stability, so they have considerable application potential in the field of quantitative detection of trace substances.
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Induced circular dichroism (ICD) has been used to detect biomolecular conformations through the coupling between chiral molecules and achiral metal nanostructures with the localized surface plasmon (LSP). However, this ICD is always weak and cannot be dynamically adjusted. Here, we put dielectric and graphene nanostructures on a metal-substrate for restricting more light energies and obtaining dynamic adjustable performance. A composite nanostructure array composed of achiral silicon-nanorods on a metal-substrate and graphene-ribbons (ASMG) is theoretically investigated. Two strong ICD signals appear in the THz region. Near-field magnetic distributions of ASMG reveal that the two strong ICD signals are mainly due to the surface plasmon resonances (SPPs) on the metal-substrate and LSP in the graphene nanostructures, respectively. The ICD signals strongly depend on the geometric parameters of ASMG and are dynamically adjusted by just changing the Fermi levels of graphene-ribbons. In addition, left-handed ASMG and right-handed ASMG can be used to identify the chiral molecular solutions with different chiralities. The maximum enhancement factor of the chiral molecular solutions could reach up to 3500 times in the THz region. These results can help to design dynamically adjustable THz chiral sensors and promote their application in biological monitoring and asymmetric catalysis.
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Técnicas Biossensoriais/instrumentação , Dicroísmo Circular/instrumentação , Nanocompostos/química , Óptica e Fotônica , Grafite , Campos Magnéticos , Nanopartículas Metálicas , Nanotubos de Carbono , Silício , Estereoisomerismo , Ressonância de Plasmônio de SuperfícieRESUMO
A novel method to control the parameters of a chiral fiber grating structure is proposed. Mode couplings are controlled in real time during the twisting fabrication process. This chiral grating structure can satisfy the phase-matching condition for generating high-quality orbital angular momentum (OAM) beams, with an order mode of conversion efficiency over 99.9%. Both theoretical analysis and experimental results of this OAM mode conversion have been investigated, with good agreement. The results demonstrate a dual-OAM beam converter with a charge of ±1 for the right- and left-handed CLPGs, respectively. The high-quality OAM beam generated in this twisted single-mode fiber process may find excellent applications in optical communications.
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Chiral plasmonic nanostructures have become a promising platform for polarization converters and molecular analysis. However, the circular dichroism (CD) of planar chiral plasmonic nanostructures is always weak and difficult for dynamic adjustment. In this work, graphene sheets (GSs) are introduced in planar metal chiral split rings (MCSRs) to enhance and dynamically adjust their CD effect. The chiral split rings consist of rotated big and small split rings. Simulation results show that the plasmonic coupling between MCSRs and GSs can enhance the absorption and CD spectra of MCSRs at two resonant wavelengths. The surface current distributions reveal that the CD signals are due to the localized surface plasmon resonances on the big and small split rings, respectively. The loss distributions illustrate that the increased loss mainly locates in GSs. In addition, the CD spectra of MCSRs/GSs can be dynamically adjusted and influenced by the Fermi energy of GSs, the geometric parameters of MCSRs and, the mediums in the environment. It can be used to detect the environmental temperature and concentration. The results help to design dynamically adjustable chiral nanostructures and promote their applications in environment detection.
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Perovskite and chalcogenide quantum dots (QDs) are important nano semiconductors. It has been a challenge to synthesize heterostructural QDs combining perovskite and chalcogenide with tailorable photoelectronic properties. In this report, heterostructural CsPbX3-PbS (X = Cl, Br, I) QDs were successfully synthesized via a room temperature in situ transformation route. The CsPbX3-PbS QDs show a tunable dual emission feature with the visible and near-infrared (NIR) photoluminescence (PL) corresponding to CsPbX3 and PbS, respectively. Typically, the formation and evolution of the heterostructural CsPbBr3-PbS QDs with reaction time was investigated. Femtosecond transient absorption spectroscopy (TAS) was applied to illuminate the exciton dynamics in CsPbBr3-PbS QDs. The mild synthetic method and TAS proved perovskite to PbS energy transfer may pave the way toward highly efficient QD photovoltaic and optoelectronic devices.
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The monolayer graphene-noble metallic nanostructure hybrid system with excellent optical characteristic, which is deserved pay attentions in the study of surface-enhanced Raman scattering spectroscopy. In this work, a hybrid sandwich structure is designed to transfer single-layer graphene to the surface of discs substrate covered by silver film and assembly of the dense Au nanoparticles (AuNPs). Blu-ray disc has a cycle density of approximately 5.7 times that of DVD-R due to the different storage capacities of these optical discs. In the research, enhancement effects have been explored for two different periodic grating structures. Compared to spectra of Si/G structure, Graphene Raman spectra from Blu-grating/AuNPs/G structure and Blu-grating/G/AuNPs enhancement multiples at the 2D peak position possesses different Raman responses of 1.09 and 2.51 times, respectively. The sandwich hybrid structure of Ag grating/graphene/AuNPs obtains a Raman enhancement factor (EF) of 6.2×108 for Rhodamine 6G and surface-enhanced Raman Scattering(SERS) detection limit of 0.1 nM. These findings can be attributed to the electric field enhancement of the hybrid structure and the chemical enhancement of graphene. This study provides a new approach for SERS detection and offers a new technique for designing SERS sensors with grapheme-plasmon hybrid structures.
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Circular dichroism (CD) is useful in polarization conversion, negative refraction chemical analysis, and bio-sensing. To achieve strong CD signals, researchers constantly break the symmetry of nanostructures. However, how to further enhance the CD based on a new mechanism has become a new challenge in this field. In this work, a hybrid plasmonic chiral system composed of an array of graphene ribbons (GRs) over h-shaped sliver chiral nanostructures (HSCNs) is theoretically investigated. Results demonstrate that the plasmonic coupling between HSCNs and GRs results in different enhanced absorptions for different circularly polarized lights. The absorbance of right circularly polarized light is enhanced to perfect absorption; the absorption of left circularly polarized light is enhanced weakly. It leads to the CD effect of HSCNs@GRs approaching 88%. The loss distributions of HSCNs and HSCNs@GRs reveal that the absorption is enhanced and transferred from HSCNs to GRs. Moreover, the current distributions of HSCNs@GRs are simplified to equivalent LC resonant circuits, which can qualitatively explain the change of CD signals by tuning geometrical parameters of HSCNs@GRs. The findings of this work provide a new method of enhancing chirality and benefit the design of graphene-based chiral optoelectronic devices.
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A chiral nanostructure array is designed, which is composed of a bilayer rotational F4-shaped nanoarray configuration. The surface plasmon resonance and circular dichroism are studied by changing the parameters of the structure. The results show that the structure has strong multiband circular dichroism, which is attributed to the coupling of the layers. In theory, based on the Born-Kuhn model, the upper and lower nanostructures are equivalent to electric dipoles. By analyzing the coupling mode of electric dipoles in the upper and lower layer, the mechanism of circular dichroism and the shift of the circular dichroism resonance are revealed. Besides, there are several specific modes that are fault tolerant of fabrication issues. This feature unveils the bright prospect of spectral anti-interference. So, the suggested chiral nanostructure can be used in biologically targeted molecular detection and spectral sensing.
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Asymmetric transmission (AT) holds significant applications in controlling polarization and propagation directions of electromagnetic waves. In this paper, tilted rectangular nanohole (TRNH) arrays in a square lattice are proposed to realize an AT effect. Numerical results show two AT modes in the transmission spectrum, and they are ascribed to the localized surface plasmon resonances around the two ends of TRNH and surface plasmon polaritons on the golden film. AT properties of the TRNH strongly depend on structural parameters, such as width, length, thickness, and tilted angle of TRNH. Results provide a novel mechanism for generating AT effect and offer potential plasmonic device applications, such as asymmetric wave splitters and optical isolators.
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Gold bilayered slit arrays with rectangular holes embedded into the metal surface are designed to enhance the circular dichroism (CD) effect of gold bilayered slit arrays. The rectangular holes in these arrays block electric currents and generate localized surface plasmons around these holes, thereby strengthening the CD effect. The CD enhancement factor depends strongly on the rotational angle and the structural parameters of the rectangular holes; this factor can be enhanced further by drilling two additional rectangular holes into the metal surfaces of the arrays. These results help facilitate the design of chiral structures to produce a strong CD effect and large electric fields.
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Asymmetric transmission (AT) has significant applications in optical polarization control. In this paper, we propose a kind of periodic nanoslit rather than the protruding planar structures, such as G-shaped structure and coupled split-ring resonators, to realize the AT effect. The planar periodic obliquely intersecting nanoslits (OINs) in the gold film, composed of gratings with an infinite length and tilted nanoslits with a finite length, are proposed to realize the AT effect by performing the finite element method. Obvious dips in the AT spectra result from the circular localized surface plasmon resonance around the two terminals of the tilted nanoslits and from the surface plasmon polariton resonances on the film and in the gratings or tilted nanoslits. In addition, the AT effect strongly depends on the geometric parameters of the OINs. The film can be straightly powered on as an in-plane electrical conductor, which broadens its applications in optoelectronic devices. Overall, these results are beneficial in designing devices to achieve AT for polarization transformation.
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A concise method is proposed to fabricate L-shaped Ag nanostructures (LSANs) for generating chirality. Prepared by glancing angle deposition, the LSAN composed of two slices with different thickness is stacked on self-assembled monolayer polystyrene nanosphere arrays by controlling substrate azimuth and deposition time. The strong optical chirality of LSANs is achieved in visible and near-IR regions by measurement. For the circular dichroism spectrum of LSANs, the intensity is enlarged, and its peaks red-shift with increasing thickness difference. When LSANs are stacked on polystyrene spheres of different diameters, enlargement and red-shift are also observed in their circular dichroism spectra with increasing thickness difference. The numerical calculations of finite element method show that the two slices composing LSAN provide cross-electric dipoles and their thickness difference provides phase difference for generating optical chirality. This study not only provides a concise and scalable method for fabricating chiral plasmonic nanostructures but also contributes to understand the knowledge of the mechanism of circular dichroism.