Wavelength Of Exciting Light Research Articles

Photoluminescence studies of ZrO2:Tm3+/Yb3+ coatings formed by plasma electrolytic oxidation

Zirconia coatings doped with various contents of Tm3+ and Yb3+ were formed by the plasma electrolytic oxidation process of zirconium foils for 15 min in alkaline electrolyte containing Tm2O3 and Yb2O3 powders in different concentrations. The coatings were composed of monoclinic and tetragonal ZrO2 phases, but Tm and Yb incorporated into ZrO2 coatings induces phase transformation from monoclinic phase to tetragonal phase. The excitation photoluminescence (PL) spectra of ZrO2:Tm3+/Yb3+ coatings were featured by a broad band at around 280 nm related to zirconia host, and a peak at around 359 nm corresponding to the 3H6→1D2 transition of Tm3+. The coatings were excited by the 280 nm and 359 nm incident light, resulting in a strong zirconia PL band, and 1D2→3F4 down-conversion luminescence of Tm3+, respectively. With 980 nm excitation and subsequent absorption by Yb3+, an up-conversion PL was observed. Emission at 799 nm is attributed to the 3H4→3H6 transition of Tm3+. PL spectra of samples doped with 8 different combinations of Tm3+ and Yb3+, allow the analysis of the responsible mechanisms and their presentation in the Jablonski diagram. CIE chromaticity coordinates were calculated, revealing dependence of the PL color upon the Tm3+/Yb3+ doping concentration and excitation light wavelength. By 280 nm and 359 nm excitation, the samples emit cyan and purple light, respectively.

Real-time Volumetric Assessment of the Human Carotid Artery: Handheld Multispectral Optoacoustic Tomography

Background Multispectral optical imaging has the capability of resolving hemoglobin, lipid, and water. Volumetric multispectral optoacoustic tomography (MSOT) is a hybrid imaging technique that provides a unique combination of functional and molecular contrast with real-time handheld imaging. Purpose To investigate whether volumetric MSOT can provide real-time assessment of the anatomic and functional status of the human carotid artery bifurcation noninvasively. Materials and Methods Imaging of healthy volunteers (n = 16) was performed with a custom-designed handheld volumetric MSOT scanner capable of high-spatial-resolution (approximately 200 µm) and real-time (10 volumes/sec) three-dimensional imaging, while further providing spectroscopic capacity through fast tuning of the excitation light wavelength. For comparison and anatomic cross-validation, volunteers were also scanned with clinical B-mode US. Results Volumetric MSOT achieved real-time imaging and characterization of the entire carotid bifurcation area across three dimensions simultaneously captured in a single volumetric image frame. Analysis of the acquired data further showed that a higher contrast-to-noise ratio can be achieved for wavelengths corresponding to a high optical absorption of oxygenated hemoglobin. Conclusion The human carotid artery was visualized by using handheld volumetric multispectral optoacoustic tomography. This imaging approach is less prone to motion artifacts than are the conventional clinical imaging methods, holding promise for providing additional image-based biomarkers for noninvasive label-free assessment of carotid artery disease. © RSNA, 2019 Online supplemental material is available for this article. See also the editorial by Mezrich in this issue.

Analyzing the performance of the first-derivative fluorescence spectrum for estimating leaf nitrogen concentration.

Nitrogen (N) is an essential nutrient for crop growth. The rapid and non-destructive monitoring of N nutrition in crops through remote sensing is important for the accurate diagnosis and quality evaluation of crop growth status. Leaf nitrogen concentration (LNC), which has been widely utilized in remote sensing, serves as a crucial indicator for the monitoring of crops growth status. In this study, the first-derivative fluorescence spectrum (FDFS) based on laser-induced fluorescence (LIF) was proposed for LNC estimation in paddy rice. First, the correlation between the LNC and FDFS at each wavelength was analyzed in detail using different excitation light wavelengths (ELWs; 355, 420, and 556 nm). Then, FDFS was used as an input parameter to train a back-propagation neural networks (BPNN) model for LNC estimation. The coefficients of determination (R2) of the linear regression analysis between the measured and predicted LNC were 0.823, 0.743, and 0.837, corresponding to 355, 420, and 556 nm ELWs, respectively. Second, the principal components analysis was performed for the extraction of the main characteristics of FDFS, and the calculated variables were used for LNC inversion. The R2 values were 0.891, 0.815, and 0.907 for 355, 420, and 556 nm ELWs, respectively. In addition, the correlation between the ratio of FDFS and LNC was also analyzed, which can provide a reference for the selection of optimal wavelengths for LNC monitoring. The experimental results exhibited the promising potential of FDFS combined with multivariate analysis for LNC monitoring, which can allow additional fluorescence characteristics to improve the accuracy of LNC monitoring.

Cherenkov excited short-wavelength infrared fluorescence imaging in vivo with external beam radiation.

.Cherenkov emission induced by external beam radiation therapy from a clinical linear accelerator (LINAC) can be used to excite phosphors deep in biological tissues. As with all luminescence imaging, there is a desire to minimize the spectral overlap between the excitation light and emission wavelengths, here between the Cherenkov and the phosphor. Cherenkov excited short-wavelength infrared (SWIR, 1000 to 1700 nm) fluorescence imaging has been demonstrated for the first time, using long Stokes-shift fluorophore PdSe quantum dots (QD) with nanosecond lifetime and an optimized SWIR detection. The intensity spectrum characteristic of Cherenkov emission leads to low overlap of this into the fluorescence spectrum of PdSe QDs in the SWIR range. Additionally, using a SWIR camera itself inherently ignores the stronger Cherenkov emission wavelengths dominant across the visible spectrum. The SWIR luminescence was shown to extend the depth sensitivity of Cherenkov imaging, which could be used for applications in radiotherapy sensing and imaging in human tissue with targeted molecular probes.

Analyzing the Effect of Fluorescence Characteristics on Leaf Nitrogen Concentration Estimation

Leaf nitrogen concentration (LNC) is a significant indicator of crops growth status, which is related to crop yield and photosynthetic efficiency. Laser-induced fluorescence is a promising technology for LNC estimation and has been widely used in remote sensing. The accuracy of LNC monitoring relies greatly on the selection of fluorescence characteristics and the number of fluorescence characteristics. It would be useful to analyze the performance of fluorescence intensity and ratio characteristics at different wavelengths for LNC estimation. In this study, the fluorescence spectra of paddy rice excited by different excitation light wavelengths (355 nm, 460 nm, and 556 nm) were acquired. The performance of the fluorescence intensity and fluorescence ratio of each band were analyzed in detail based on back-propagation neural network (BPNN) for LNC estimation. At 355 nm and 460 nm excitation wavelengths, the fluorescence characteristics related to LNC were mainly located in the far-red region, and at 556 nm excitation wavelength, the red region being an optimal band. Additionally, the effect of the number of fluorescence characteristics on the accuracy of LNC estimation was analyzed by using principal component analysis combined with BPNN. Results demonstrate that at least two fluorescence spectral features should be selected in the red and far-red regions to estimate LNC and efficiently improve the accuracy of LNC estimation.

DERS substrate based on NERS-SERS interaction in integrated microfluidic detection

The systematic simulation study of a structure with nanogap-enhanced Raman scattering and surface-enhanced Raman scattering (NERS-SERS) substrate is presented. This double-enhanced Raman scattering (DERS) substrate with coupling between the localized surface plasmons of noble metal nanosphere colloids and surface plasmon polaritons of a 1D sinusoidal noble metal nanograting is analyzed. With the excitation light wavelength at 785nm, the key structure parameters of noble metal nanospheres and sinusoidal noble metal nanogratings are deduced by FDTD. With the optimal DERS substrate, the SERS enhancement factor (EF) can be 9 orders of magnitude as possible. The DERS substrate was fabricated, and an extra SERS effect was demonstrated by experiments. This DERS substrate will be integrated with microfluidics in the next work, with the purpose of in situ, real-time, continuous detection of trace water soluble gas-phase or airborne agents, such as trace explosives in air.

(Invited) Biological Imaging Using up-Conversion Photoluminescence of Carbon Nanotubes

Single-walled carbon nanotubes (SWNTs) have been considered as nearly ideal luminescent probes for deep-tissue bioimaging because of their photoluminescence in near-infrared range known as the second optical window of biological tissues [1]. Moreover, efficient phonon-assisted up-conversion photoluminescence (UCPL) in SWNTs, for which the excitation light wavelength can be longer than the emission one, has recently been discovered [2, 3]. The UCPL phenomena enable SWNTs excited at wavelengths longer than ~1050-1200 nm to emit PL shorter than 1000 nm in which standard Si-based detectors have finite sensitivity. The availability of the UCPL thus potentially enhances the usefulness of SWNTs as luminescent probes in their bioimaging applications. We will report our recent progress in whole-body imaging of living mice with negligible autofluorescence using UCPL of SWNTs. We will also discuss application of the UCPL phenomena of SWNTs for near-infrared optical thermometry. [1] K. Welsher, Z. Liu, S. P. Sherlock, J. T. Robinson, Z. Chen, D. Daranciang, and H. Dai, Nat. Nanotechnol. 4, 773 (2009). [2] N. Akizuki, S. Aota, S. Mouri, K. Matsuda, and Y. Miyauchi, Nat. Commun. 6, 8920 (2015). [3] S. Aota, N. Akizuki, S. Mouri, K. Matsuda, and Y. Miyauchi, Appl. Phys. Express 9, 045103 (2016). Part of this study was supported by the Research Foundation for Opto-Science and Technology, the Nakatani Foundation, and by JSPS KAKENHI Grant Number JP15H05408.

Diarylethenes with a Narrow Singlet–Triplet Energy Gap Sensitizer: a Simple Strategy for Efficient Visible‐Light Photochromism

AbstractAll‐organic visible‐light photochromism is reported here via a novel strategy with narrow singlet–triplet energy gap (ΔEST) materials as a sensitizer. Taking advantage of the narrow ΔEST feature and the triplet–triplet energy transfer process, highly efficient photochromism of diarylethenes (DAEs) with both ring‐open and ring‐closure excitations shifted to visible light region is successfully achieved. Moreover, the wavelength of the visible excitation light can be easily modulated (e.g., from 405 to 470 nm) by elaborate selection of matched sensitized molecules. The “write‐and‐erase” application of this photochromic system in polymer films is further demonstrated. This strategy provides a simple and versatile selection of well‐matched DAE/sensitizer couples for visible‐light photochromism without complicated molecular design.

Wide-field autofluorescence-guided TUR-B for the detection of bladder cancer: a pilot study.

The aim of this pilot study was to assess the feasibility and value of wide-field autofluorescence imaging (AFI) for the detection of bladder cancer during transurethral resection of the bladder (TUR-B). For imaging, the D-Light/AF System (Karl Storz GmbH, Tuttlingen, Germany) and a customized band pass filter (≈480-780nm) at the eyepiece of the endoscope were used. The excitation light wavelength was 440nm. Representative spectral measurements of tissue autofluorescence (AF) were performed using a spectrometer attached behind the AF band pass filter in selected patients. During TUR-B, cystoscopy was performed in white light (WL) followed by wide-field AFI. Lesions were classified as suspicious or normal using either modality. Representative spectral measurements using excitation at a wavelength of 440nm resulted in significantly lower fluorescence intensity of malignant versus non-malignant tissue. Overall, 56 lesions (30 cancerous and 26 non-malignant) in 25 patients were assessed and classified by wide-field AFI. Papillary tumors as well as flat lesions lacked the green fluorescence seen in normal urothelium, thus emerging as "brown-reddish" areas. When compared with histopathological findings, the pooled per-lesion sensitivity and specificity for AF were 96.7 and 53.8%, respectively. For WL these values were 86.7 and 69.2%, respectively. Wide-field AFI imaging during TUR-B is simple and easy to use. Our preliminary data suggest that AFI has the potential to increase the detection rates of bladder tumors compared with WL without the need of intravesical instillation prior to the procedure.

Construction of Hierarchical Polymer Brushes on Upconversion Nanoparticles via NIR-Light-Initiated RAFT Polymerization

Photoinduced reversible addition-fragmentation chain transfer (RAFT) polymerization generally adopts high-energy ultraviolet (UV) or blue light. In combination with photoredox catalyst, the excitation light wavelength was extended to the visible and even near-infrared (NIR) region for photoinduced electron transfer RAFT polymerization. In this report, we introduce for the first time a surface NIR-light-initiated RAFT polymerization on upconversion nanoparticles (UCNPs) without adding any photocatalyst and construct a functional inorganic core/polymer shell nanohybrid for application in cancer theranostics. The multilayer core-shell UCNPs (NaYF4:Yb/Tm@NaYbF4:Gd@NaNdF4:Yb@NaYF4), with surface anchorings of chain transfer agents, can serve as efficient NIR-to-UV light transducers for initiating the RAFT polymerization. A hierarchical double block copolymer brush, consisting of poly(acrylic acid) (PAA) and poly(oligo(ethylene oxide)methacrylate-co-2-(2-methoxy-ethoxy)ethyl methacrylate) (PEG for short), was grafted from the surface in sequence. The targeting arginine-glycine-aspartic (RGD) peptide was modified at the end of the copolymer through the trithiolcarbonate end group. After loading of doxorubicin, the UCNPs@PAA-b-PEG-RGD exhibited an enhanced U87MG cancer cell uptake efficiency and cytotoxicity. Besides, the unique upconversion luminescence of the nanohybrids was used for the autofluoresence-free cell imaging and labeling. Therefore, our strategy verified that UCNPs could efficiently activate RAFT polymerization by NIR photoirradiation and construct the complex nanohybrids, exhibiting prospective biomedical applications due to the low phototoxicity and deep penetration of NIR light.

Fine Tuning of Multicolored Photoluminescence in Crystalline Magnetic Materials Constructed of Trimetallic EuxTb1-x[Co(CN)6] Cyanido-Bridged Chains.

Coordination compounds built of trivalent lanthanide ions have been demonstrated as promising solid-state materials for diverse photoluminescent applications and as attractive magnetic objects with the prospective application in information storage and spintronics. We present a synthetic methodology in which both luminescent and magnetic functionalities are induced within lanthanide-based coordination polymers by the application of hexacyanocobaltate(III) anions and 3-hydroxypyridine (3-OHpy), both coordinated to 4f-metal ions modulating the lanthanide-centered properties. We report a series of trimetallic cyanido-bridged chains {[EuIIIxTbIII1-x(3-OHpy)2(H2O)4][CoIII(CN)6]}·H2O (x = 1, 0.8, 0.5, 0.4, 0.3, 0.2, 0.1, 0; compounds 1, 2, ..., 7, 8). They reveal tunable visible photoluminescence ranging from green, through yellow and orange, to red color depending on the composition of material and the wavelength of UV excitation light. Such multicolored emission is realized by the adjusted ratio between red emissive Eu3+ and green emissive Tb3+ and by the selection of wavelengths of UV light controlling the intensities of Eu- and Tb-based components of visible luminescence. The photoluminescence is enhanced by the energy-transfer (ET) process from [CoIII(CN)6]3- and 3-OHpy to lanthanides, and the efficiencies of ET to Eu and Tb play an important role in the switchable emission. The whole family, 1-8, exhibits temperature-dependent paramagnetism due to the intrinsic property of lanthanide(3+) ions. Tb-containing 2-8 reveal the field-induced slow relaxation of magnetization due to the magnetic anisotropy of Tb3+. Moreover, the compounds built of large amounts of Tb reveal the double relaxation, the faster of a typical TbIII single-ion origin, and the slower originating from the magnetic dipole-magnetic dipole interactions between neighboring TbIII centers. Compound 2, which can be considered as a magnetically diluted sample, exhibits almost single relaxation process with the thermal energy barrier ΔE/kB of 35.8(6) K and τ0 = 1.1(2) × 10-8 s at Hdc = 1500 Oe, indicating a single-molecule magnet behavior.

Interference filter tilting to detect a polycyclic aromatic hydrocarbon at the second harmonic of wavelength modulation frequency.

We present a practical implementation of the wavelength-modulation spectroscopy technique with second-harmonic detection for selective detection and concentration measurements of polycyclic aromatic hydrocarbons (PAHs)-common fossil fuel pollutants. The method is based on excitation light wavelength modulation around the maximum of a narrow peak in the absorption spectrum of a PAH and lock-in detection of fluorescence at the second harmonic of the excitation wavelength modulation frequency. A violet LED is used as the excitation source and wavelength modulation is performed via narrowband interference filter tilting. Feasibility is demonstrated with a carcinogenic PAH, benzo(k)fluoranthene. Model computations are presented to estimate the influence of the background signal on the sensitivity of the method.

Deep-red emission of Mn4+ and Cr3+ in (Li1−xAx)2MgTiO4 (A=Na and K) phosphor: Potential application as W-LED and compact spectrometer

Mn4+ doped and Mn4+/Cr3+ co-doped alkali metal titanate phosphors have been prepared by solid state reaction method. A part of Li+ ions in the Li2MgTiO4: Mn4+ are substituted with Na+ and K+ ions and consequently the intensity of Mn4+ emission at 678nm is enhanced by 1.7 and 2.5 times, respectively. In the Mn4+/Cr3+ co-doped (Li0.95K0.05)2MgTi0.999O4, both emission of Cr3+at 726nm and emission of Mn4+ at 678nm of Mn4+ are observed. It is interesting to find that the intensity ratio of 726–678nm emissions in the Mn4+/Cr3+ phosphor continually increases with excitation wavelength increasing from 290nm to 455nm, which means that the intensity ratio in turn can be used to identify the excitation light wavelength. This refers a possible approach to design novel compact light-wavelength detector or spectrometer based on the phosphor. The mechanism of Na+ or K+ substitution induced luminescence enhancement in the Mn4+ phosphor and the competition between the Cr3+ and Mn4+ emissions in the Mn4+/Cr3+ co-doped has been discussed.

Research on the Interaction between Biomaterials of Human Serum and Dibazol by Fluorescence Spectroscopy

The interaction of dibazol to serum was investigated by fluorescence and UV-vis spectroscopy. The fluorescence experiment results show that the fluorescence of human serum can be effectively induced by light wave. The maximum fluorescence intensity of serum is excited at 280 nm and the peak wavelength is about 334 nm. It can also be concluded that the fluorescence intensity gradually increase with the increasing excitation light wavelength. The range of the fluorescence spectroscopy of serum-dibazol system induced by excited at different wavelength is about 290 - 450 nm. The fluorescence intensity of the interaction system of dibazol-serum is significantly reduced, indicating that the fluorescence quenching of serum occurred strongly caused by dibazol and there is a new compound formed between dibazol and serum. The absorption spectra show that there is a large blue in the system of dibazol and serum, which reveal that there is a kind of new complex between dibazol and serum. It is very significance to study the interaction between dibazol and serum for understanding of drug’s toxicity and its distribution in the organism.

Light emitting mechanisms dependent on stoichiometry of Si-rich-SiNx films grown by PECVD

Light emission and morphology of silicon-rich silicon nitride films grown by plasma-enhanced chemical vapor deposition were investigated versus film’s stoichiometry. The excess silicon content in the films was controlled varying the NH3/SiH4 gas flow ratio from 0.45 up to 1.0. High-temperature annealing was employed to form the silicon quantum dots (QDs) and to enhance the photoluminescence (PL) in visible spectral range. The PL spectrum was found to be complex. The competition of five PL bands leads to the non-monotonous variation of total PL peak position in the range of 1.55–2.95 eV when the Si excess content increases. The shape of PL spectra depends also on an excitation light wavelength. It is shown that for the films fabricated with R ≤ 0.56 and R ≥ 0.67 the dominant contribution into PL spectra is given by native SiNx defects, whereas in the films obtained with R = 0.59–0.67 the Si-QDs form the main radiative channel. The highest PL intensity is detected in Si-rich SiNx films grown at R = 0.59–0.67 as well. PL mechanisms are discussed in terms of the contribution of different radiative channels in the light emission process that can show the ways for the optimization of SiNx light-emitting properties.

Functional 2D nanomaterials for optoelectronics based on langmuir bacteriorhodopsin films

We have tested the possibility of using monomolecular layers of bacteriorhodopsin (BR) for the synthesis of highly sensitive and highly selective sensors based on second harmonic generation and surface plasma waves. We have used various methods to study the optical and nonlinear optical properties of Langmuir-Blodgett films of BR in order to clarify the extent to which specific properties of BR molecules are retained during their transfer from the surface of water to a solid substrate. We show that the second harmonic generation method is efficient for analyzing the molecular orientation and quality of Langmuir-Blodgett films. The experimental nonlinear optical susceptibility of second order BR molecules is 3.4·10−11m/V. The relative change in the resonant wave vector is (3.6±0.1)·10−2 at an excitation light wavelength of 630nm. We have obtained a BR spectrum with the effective excitation by incident radiation of surface plasma waves. On the basis of these studies, we have proposed new schemes of biosensors operating on the basis of second harmonic generation and surface plasma resonance caused by fundamental frequency reflection from BR monomolecular layers. This scheme was tested for a model device and demonstrated the possibility of obtaining sensitivities of the order of 1011 molecules/cm3.

Photoluminescence of (ZnO)X-Z(SiO2)Y:(MnO)Z green phosphors prepared by direct thermal synthesis: The effect of ZnO/SiO2 ratio and Mn2+ concentration on luminescence

Green light emitting Zn2SiO4:Mn2+ phosphors have been synthetised by the solid-state reaction in ambient atmosphere at 1300°C for 2h, with ZnO, SiO2 and MnO2 as the reagents. The ZnO/SiO2 molar ratio varied from 2 to 0.5. The doping level was in a lower concentration range (0.01≤x≤0.05). The effect of both the Mn2+ concentration and ZnO/SiO2 molar ratio on luminescence intensity and decay was investigated in detail. The microstructure and phase composition of prepared phosphors were characterised by scanning electron microscopy (SEM) and X-ray powder diffraction (XRD). XRD results indicate that the pure α-Zn2SiO4 phase with rhombohedral structure was obtained after heat treatment. The prepared phosphors exhibit a strong green emission centred at 525nm from the 4T1→6A1 forbidden transition. The highest emission intensity was observed for phosphors with ZnO/SiO2 molar ratio equal to 1.0, and the Mn2+ concentration x=0.03 (ZSMn3). The emission intensity of the ZSMn3 phosphor is comparable with the commercial Zn2SiO4:Mn2+ phosphor. The decay curves can be characterised by double exponential function. After fitting a fast component τ1∼2ms and a slow component τ2∼10ms were obtained. The decay times decrease significantly with increasing Mn2+ concentration. The decay time and luminescence mechanism depend on the excitation light wavelength. Temperature dependent luminescence of the ZSMn3 phosphor in the temperature range of 25–200°C was studied.

Kinetics of photochemical reactions of a new biphotochromic compound upon photolysis with light of different wavelengths

Using the method of microsecond flash photolysis with UV and visible light, the spectral and kinetic characteristics of intermediate products of photolysis in toluene and methanol solutions of a new biphotochromic compound have been studied, in which two photochromic moieties, spironaphthoxazine and azomethine, are linked to each other in such a way that there is conjugation between π-electronic systems of the moieties in the ground state of the molecule. Two intermediate products have detected, whose relative efficiency of formation substantially depends on the solvent and the wavelength of excitation light.

Functional 2D nanomaterials for optoelectronic equipment on the basis of langmuir–blodgett bacteriorhodopsin films

We have tested the possibility of using monomolecular layers of bacteriorhodopsin (BR) for the synthesis of highly sensitive and highly selective sensors based on second harmonic generation and surface plasma waves. We have used various methods to study the optical and nonlinear optical properties of Langmuir-Blodgett films of BR in order to clarify the extent to which specific properties of BR molecules are retained during their transfer from the surface of water to a solid substrate. We show that the second harmonic generation method is efficient for analyzing the molecular orientation and quality of Langmuir-Blodgett films. The experimental nonlinear optical susceptibility of second order BR molecules is 3.4 · 10-11m/V. The relative change in the resonant wave vector is (3.6 ± 0.1)·10-2at an excitation light wavelength of 630 nm. We have obtained a BR spectrum with the effective excitation by incident radiation of surface plasma waves. On the basis of these studies, we have proposed new schemes of biosensors operating on the basis of second harmonic generation and surface plasma resonance caused by fundamental frequency reflection from BR monomolecular layers. This scheme was tested for a model device and demonstrated the possibility of obtaining sensitivities of the order of 1011molecules/cm3.

Sensitivity Enhancement of Transition Metal Dichalcogenides/Silicon Nanostructure-based Surface Plasmon Resonance Biosensor.

In this work, we designed a sensitivity-enhanced surface plasmon resonance biosensor structure based on silicon nanosheet and two-dimensional transition metal dichalcogenides. This configuration contains six components: SF10 triangular prism, gold thin film, silicon nanosheet, two-dimensional MoS2/MoSe2/WS2/WSe2 (defined as MX2) layers, biomolecular analyte layer and sensing medium. The minimum reflectivity, sensitivity as well as the Full Width at Half Maximum of SPR curve are systematically examined by using Fresnel equations and the transfer matrix method in the visible and near infrared wavelength range (600 nm to 1024 nm). The variation of the minimum reflectivity and the change in resonance angle as the function of the number of MX2 layers are presented respectively. The results show that silicon nanosheet and MX2 layers can be served as effective light absorption medium. Under resonance conditions, the electrons in these additional dielectric layers can be transferred to the surface of gold thin film. All silicon-MX2 enhanced sensing models show much better performance than that of the conventional sensing scheme where pure Au thin film is used, the highest sensitivity can be achieved by employing 600 nm excitation light wavelength with 35 nm gold thin film and 7 nm thickness silicon nanosheet coated with monolayer WS2.