Spectroscopy Research Articles

Estimating emission flux of H2S from fumarolic fields using vertical sensor array system

The emission flux of volatiles from each fumarolic field in volcanic and geothermal areas can be used to evaluate the current state of magmatic activity and predict its future trends. The emission flux of SO2 has been quantified in many fumarolic fields using remote sensing techniques, such as differential optical absorption spectroscopy (DOAS). However, most of these remote sensing techniques are inapplicable to fumarolic fields emitting volatiles depleted in SO2 to which most of the geothermal fields are classified. In this study, we developed a vertical sensor array system to quantify the emission flux of H2S from each fumarolic field by integrating the cross-sectional distributions of H2S concentrations in the volcanic plume using the vertical sensor array system. In Iwo-yama of the Kirishima volcanic complex, the cross-sectional distribution of H2S concentrations was determined using the walking traverse method by moving the vertical sensor array system in the plume perpendicular to the direction of plume transport. The emission flux of SO2 (2.2 ± 0.4 ton SO2/day) was estimated from that of H2S using the walking traverse method (2.6 ± 0.5 ton H2S/day) and the molar ratio of the plume (SO2/H2S=0.45) corresponds well with that estimated optically by JMA. We concluded that the emission flux quantified using the vertical sensor array system was reliable. In the Oyunuma pond in the Kuttara volcano, the emission flux of H2S was quantified as 2.0 ton H2S/day through the fixed point method, wherein the vertical sensor array system was fixed in one point, whereas the cross sectional distribution of H2S in the plume was estimated using the natural variation in wind direction. The topography is often irregular and wind direction is variable in most fumarolic fields; thus, in general, the fixed point method should be more suitable to determine the emission flux of H2S from fumarolic fields, wherein H2S occupies a major portion of the total sulfur emission.

Characterization of the interaction between the Sec61 translocon complex and ppαF using optical tweezers.

The Sec61 translocon allows the translocation of secretory preproteins from the cytosol to the endoplasmic reticulum lumen during polypeptide biosynthesis. These proteins possess an N-terminal signal peptide (SP) which docks at the translocon. SP mutations can abolish translocation and cause diseases, suggesting an essential role for this SP/Sec61 interaction. However, a detailed biophysical characterization of this binding is still missing. Here, optical tweezers force spectroscopy was used to characterize the kinetic parameters of the dissociation process between Sec61 and the SP of prepro-alpha-factor. The unbinding parameters including off-rate constant and distance to the transition state were obtained by fitting rupture force data to Dudko-Hummer-Szabo models. Interestingly, the translocation inhibitor mycolactone increases the off-rate and accelerates the SP/Sec61 dissociation, while also weakening the interaction. Whereas the translocation deficient mutant containing a single point mutation in the SP abolished the specificity of the SP/Sec61 binding, resulting in an unstable interaction. In conclusion, we characterize quantitatively the dissociation process between the signal peptide and the translocon, and how the unbinding parameters are modified by a translocation inhibitor.

Characterization of size-resolved charge distributions for triboelectrically charged microparticles via electrical mobility analysis coupled to optical particle spectrometry

In printing applications, microparticles are commonly triboelectrically charged with larger carrier particles. Here, we develop an impaction-differential mobility analyzer-optical particle spectrometer (DMA-OPS) system to examine the size-dependent charge distributions of toner particles in the 0.3 – 10 μm range resulting from triboelectric charging via acrylic-coated ferrite carrier. The toner-carrier blend is aerosolized, and toner particles are released from the carrier via inertial impaction of toner-carrier complexes. The toner particles are then classified by electrical mobility and their optical diameters are determined. We can produce toner particle size-dependent charge distributions, which can be converted to surface potentials, and charge-to-mass ratios.

A comparative study on the spectral characteristics of nanosecond pulsed discharges in atmospheric He and a He+2.3%H2O mixture

Nanosecond pulsed discharges at atmospheric pressure in a pin-to-pin electrode configuration are well reproducible in time and space, which is beneficial to the fundamentals and applications of low-temperature plasmas. In this experiment, the discharges in helium (He) and He with 2.3% water vapor (H2O) are driven by a series of 10 ns overvoltage pulses (~13 kV). Special attention is paid to the spectral characteristics obtained in the center of discharges by time-resolved optical emission spectroscopy. It is found that in helium, the emission of atomic and molecular helium during the afterglow is more intense than that in the active discharge, while in the He+2.3%H2O mixture, helium emission is only observed during the discharge pulse and the molecular helium emission disappears. In addition, the emissions of OH(A-X) and Hα present similar behavior that increases sharply during the falling edge of the voltage pulse as the electrons cool down rapidly. The gas temperature is set to remain low at 540 K by fitting the OH(A-X) band. A comparative study on the emission of radiative species (He, He2, OH and H) is performed between these two discharge cases to derive their main production mechanisms. In both cases, the dominant primary ion is He+ at the onset of discharges, but their He+ charge transfer processes are quite different. Based on these experimental data and a qualitative discussion on the discharge kinetics, with regard to the present discharge conditions, it is shown that the electron-assisted three-body recombination processes appear to be the significant sources of radiative OH and H species in high-density plasmas.

Rapid Sample Pretreatment Facilitating SERS Detection of Trace Weak Organic Acids/Bases in Complex Matrices.

Fast and efficient sample pretreatment is the prerequisite for realizing surface-enhanced Raman spectroscopy (SERS) detection of trace targets in complex matrices, which is still a big issue for the practical application of SERS. Recently, we have proposed a highly performed liquid-liquid extraction (LLE)-back extraction (BE) for weak acids/bases extraction in drinking water and beverage samples. However, the performance efficiency decreased drastically on facing matrices like food and biological blood. Based on the total interaction energies among target, interferent, and extractant molecules, solid-phase extraction (SPE) with a higher selectivity was introduced in advance of LLE-BE, which enabled the sensitive (μg L-1 level) and rapid (within 10 min) SERS detection of both koumine (a weak base) and celastrol (a weak acid) in different food and biological samples. Further, the high SERS sensitivity was determined unmanned by Vis-CAD (a machine learning algorithm), instead of the highly demanded expert recognition. The generality of SPE-LLE-BE for various weak acids/bases (2 < pKa < 12), accompanied by the high efficiency, easy operation, and low cost, offers SERS as a powerful on-site and efficient inspection tool in food safety and forensics.

Silver nanopopcorns decorated on flexible membrane for SERS detection of nitrofurazone.

Thesynthesis of three-dimensional silver nanopopcorns (Ag NPCs) onto a flexible polycarbonate membrane (PCM) for the detection of nitrofurazone (NFZ) on the fish surface by surface-enhanced Raman spectroscopy (SERS)is presented. The proposed flexible Ag-NPCs/PCM SERS substrate exhibits significant Raman signal intensity enhancement with the measured enhancement factor of 2.36 × 106. This is primarily attributed to the hotspots created on Ag NPCs, including numerous nanoscale protrusions and internal crevices distributed across the surface of Ag NPCs. The detection of NFZ by this flexible SERS substrate demonstrates a low limit of detection (LOD) of 3.7 × 10-9M and uniform and reproducible Raman signal intensities with a relative standard deviation below 8.34%. It also exhibits excellent stability, retaining 70% of its efficacy even after 10days of storage. Notably, the practical detection of NFZ in tap water, honey water, and fish surfaces achieves LOD values of 1.35 × 10-8M, 5.76 × 10-7M, and 3.61 × 10-8M,respectively, which highlights its effectiveness across different sample types. The developed Ag-NPCs/PCM SERS substrate presents promising potential for sensitive SERS detection of toxic substances in real-world samples.

Pretreatment-free SERS sensing of microplastics using a self-attention-based neural network on hierarchically porous Ag foams

Low-cost detection systems are needed for the identification of microplastics (MPs) in environmental samples. However, their rapid identification is hindered by the need for complex isolation and pre-treatment methods. This study describes a comprehensive sensing platform to identify MPs in environmental samples without requiring independent separation or pre-treatment protocols. It leverages the physicochemical properties of macroporous-mesoporous silver (Ag) substrates templated with self-assembled polymeric micelles to concurrently separate and analyze multiple MP targets using surface-enhanced Raman spectroscopy (SERS). The hydrophobic layer on Ag aids in stabilizing the nanostructures in the environment and mitigates biofouling. To monitor complex samples with multiple MPs and to demultiplex numerous overlapping patterns, we develop a neural network (NN) algorithm called SpecATNet that employs a self-attention mechanism to resolve the complex dependencies and patterns in SERS data to identify six common types of MPs: polystyrene, polyethylene, polymethylmethacrylate, polytetrafluoroethylene, nylon, and polyethylene terephthalate. SpecATNet uses multi-label classification to analyze multi-component mixtures even in the presence of various interference agents. The combination of macroporous-mesoporous Ag substrates and self-attention-based NN technology holds potential to enable field monitoring of MPs by generating rich datasets that machines can interpret and analyze.

Direct Determination of Carrier Parameters in Indium Tin Oxide Nanocrystals.

We develop here a comprehensive experimental approach to independently determine charge carrier parameters, namely, carrier density and mass, in plasmonic indium tin oxide nanocrystals. Typically, in plasmonic nanocrystals, only the ratio between these two parameters is accessible through optical absorption experiments. The multitechnique methodology proposed here combines single particle and ensemble optical and magneto-optical spectroscopies, also using 119Sn solid-state nuclear magnetic resonance spectroscopy to probe the surface depletion layer. Our methodology overcomes the limitations of standard fitting approaches based on absorption spectroscopy and ultimately gives access to carrier effective mass directly on the NCs, discarding the use of literature value based on bulk or thin film materials. We found that mass values depart appreciably from those measured on thin films; consequently, we found carrier density values that are different from reported literature values for similar systems. The effective mass was found to deviate from the parabolic approximation at a high carrier density. Finally, the dopant activation and defect diagram for ITO NCs for tin doping between 2.5 and 15% are determined. This approach can be generalized to other plasmonic heavily doped semiconductor nanostructures and represents, to the best of our knowledge, the only method to date to characterize the full Drude parameter space of 0-D nanosystems.

Effect of tin doping on the structural, optical, and dielectric properties of unintentionally β-Ga2O3 single crystal

Abstract This paper studied the structural, optical, electrical, and dielectric properties of the undoped and 0.05 mol% Sn-doped β-Ga2O3 single crystals through comprehensive characterizations by X-ray diffraction (XRD), Raman scattering, Optical transmittance spectroscopy, X-ray photoelectron spectroscopy (XPS), Ultraviolet photoelectron (UPS) spectroscopy, and dielectric measurements. The optical bandgap decreases as Sn content increases. The results of XPS showed that Sn atoms were successfully added to the host β-Ga2O3 crystal. The position of the Fermi level of 0.05 mol% Sn-doped β-Ga2O3 is calculated to be 2.56 eV above the valence band and 1.85 eV beneath the conduction band. Also, the computed value of the work function of 0.05% mole Sn-doped β-Ga2O3 is 4.53 eV. AC conductivity increases, while dielectric loss and dielectric constant decrease with increasing frequency.

Stimuli‐responsive photoluminescent copper(I) halides for scintillation, anticounterfeiting, and light‐emitting diode applications

AbstractHighly sensitive stimuli‐responsive luminescent materials are crucial for applications in optical sensing, security, and anticounterfeiting. Here, we report two zero‐dimensional (0D) copper(I) halides, (TEP)2Cu2Br4, (TEP)2Cu4Br6, and 1D (TEP)3Ag6Br9, which are comprised of isolated [Cu2Br4]2−, [Cu4Br6]2−, and [Ag6Br9]3− polyanions, respectively, separated by TEP+ (tetraethylphosphonium [TEP]) cations. (TEP)2Cu2Br4 and (TEP)2Cu4Br6 demonstrate greenish‐white and orange‐red emissions, respectively, with near unity photoluminescence quantum yields, while (TEP)3Ag6Br9 is a poor light emitter. Optical spectroscopy measurements and density‐functional theory calculations reveal that photoemissions of these compounds originate from self‐trapped excitons due to the excited‐state distortions in the copper(I) halide units. Crystals of Cu(I) halides are radioluminescence active at room temperature under both X‐ and γ‐rays exposure. The light yields up to 15,800 ph/MeV under 662 keV γ‐rays of 137Cs suggesting their potential for scintillation applications. Remarkably, (TEP)2Cu2Br4 and (TEP)2Cu4Br6 are interconvertible through chemical stimuli or reverse crystallization. In addition, both compounds demonstrate luminescence on‐off switching upon thermal stimuli. The sensitivity of (TEP)2Cu2Br4 and (TEP)2Cu4Br6 to the chemical and thermal stimuli coupled with their ultrabright emission allows their consideration for applications such as solid‐state lighting, sensing, information storage, and anticounterfeiting.

Effect of roasting process on the V (anti-tumor agent) recovery from the slag of the electric arc furnace (EAF)

Due to the lack of mineral sources of Vanadium (V) in many parts of the world and its recent applications in the field of medicine (as an anti-tumor agent), one of the biggest sources of V is the extraction of V as V2O5 from steel slag in melting process. In this study, the pyro-hydrometallurgical process has been investigated for the extraction of V from steel slag created in a convertor. To get an optimum process of salt roasting, the effect of roasting temperature, time, salt value, slag particle size, and cooling method have been investigated. For this purpose, slag samples were roasted with sodium carbonate and then dissolved in water. The amount of V2O5 obtained by optical spectrometry is the efficiency criterion of this process. Results showed that the optimum condition for the extraction of V2O5 from steel slag was 15 wt % of Na2CO3 as a salt roasting agent and hating for 60 min at 1100 °C.

Ultrasound-assisted Cu(II) Strecker-functionalized organocatalyst for green azide-alkyne cycloaddition and Ullmann reactions.

A new aminonitrile-functionalized Fe3O4 has been synthesized via the Strecker reaction, the designed aminonitrile ligand on the surface of the magnetic core coordinated to copper(II) to obtain the final new catalyst. The fabricated nanocatalyst was characterized by Fourier transform Infrared (FT-IR), Field Emission Scanning Electron Microscopy (FESEM), Energy-Dispersive X-ray spectroscopy (EDX), Transmission Electron Microscopy (TEM), Vibrating-Sample Magnetometer (VSM), Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), and Thermogravimetric Analysis (TGA). The high tendency of nitrogens in the aminonitrile functional group to make a complex with Cu(II) has caused the practical activity of this nucleus in this catalyst. This nanocatalyst performance was investigated in azide-alkyne Huisgen cycloaddition (3 + 2) reaction for achieving to 1,4-disubstituted 1,2,3-triazoles in water as a green media at room temperature. In another try, Classic Ullmann Reaction was investigated for the synthesis of biaryls at 85°C promoted by ultrasonic condition (37 kHz). The reaction scope was explored using different reactants and the results of using this developed catalytic system demonstrated its capacity to reduce the reaction time and enhance the reaction efficiency to provide good to excellent product yield. Conversely, the simple recycling and reusability of this catalyst for at least six times without any noticeable leaching of copper makes it a potential future catalyst for synthesizing such compounds.

Assessment of trace elements in Iranian kefir samples by using ICP-OES technique

ABSTRACT In this research, levels of 12 trace elements (Al, Zn, Cd, Ni, Hg, Pb, Co, Cr, Se, Fe, As and Mn) were measured in Iranian kefir samples by using ICP-OES (Inductively Coupled Plasma Optical Emission Spectroscopy) method. Based on our findings, the maximum and minimum averages of essential elements were related to Fe (423 ± 146 µg/kg) and Se (not detected or ND), respectively, and the maximum and minimum averages of toxic elements were related to As (13.3 ± 4.68 µg/kg) and Hg (ND), respectively. Based on the amount of fat in the kefir samples, the highest mean values of toxic and essential elements was related to As (15.9 ± 5.25 µg/kg) and Fe (466 ± 177 µg/kg) in high-fat kefir samples, respectively. In addition, the correlation between the amount of fat and elements in the samples was shown with a multivariate principal component analysis (PCA). Based on the obtained results, the amount of trace elements in kefir samples was lower than the existing standards (Cd = 10, Pb = 20, Al = 500, Hg = 20, As = 140, Mn = 100 and Fe = 2700 µg/kg). Also, in reviewing the results by PCA analysis, the differences and similarities between the type and amount of toxic elements and essential elements in kefir samples have been shown. Finally, based on the obtained results, it can be concluded that the consumption of this food item can be safe due to the low level of elements below the acceptable limit.

Femtosecond laser-induced nanoparticle implantation into flexible substrate for sensitive and reusable microfluidics SERS detection

Surface-enhanced Raman spectroscopy (SERS) microfluidic system, which enables rapid detection of chemical and biological analytes, offers an effective platform to monitor various food contaminants and disease diagnoses. The efficacy of SERS microfluidic systems is greatly dependent on the sensitivity and reusability of SERS detection substrates to ensure repeated use for prolonged periods. This study proposed a novel process of femtosecond laser nanoparticle array (NPA) implantation to achieve homogeneous forward transfer of gold NPA on a flexible polymer film and accurately integrated it within microfluidic chips for SERS detection. The implanted Au-NPA strips show a remarkable electromagnetic field enhancement with the factor of 9 × 108 during SERS detection of malachite green (MG) solution, achieving a detection limit lower than 10 ppt, far better than most laser-prepared SERS substrates. Furthermore, Au-NPA strips show excellent reusability after several physical and chemical cleaning, because of the robust embedment of laser-implanted NPA in flexible substrates. To demonstrate the performance of Au-NPA, a SERS microfluidic system is built to monitor the online oxidation reaction between MG/NaClO reactants, which helps infer the reaction path. The proposed method of nanoparticle implantation is more effective than the direct laser structuring technique. It provides better performance for SERS detection, robustness of detection, and substrate flexibility and has a wider range of applications for microfluidic systems without any negative impact.

The Roles of Oil-Water Interfaces in Forming Ultrasmall CaSO4 Nanoparticles.

In natural and engineered environmental systems, calcium sulfate (CaSO4) nucleation commonly occurs at dynamic liquid-liquid interfaces. Although CaSO4 is one of the most common minerals in oil spills and oil-water separation, the mechanisms driving its nucleation at these liquid-liquid interfaces remain poorly understood. In this study, using in situ small-angle X-ray scattering (SAXS), we examined CaSO4 nucleation at oil-water interfaces and found that within 60 minutes of reaction, short rod-shaped nanoparticles (with a radius of gyration (Rg) of 17.2 ± 2.7 nm and a length of 38.2 ± 5.8 nm) had formed preferentially at the interfaces. Wide-angle X-ray scattering (WAXS) analysis identified these nanoparticles as gypsum (CaSO4·2H2O). In addition, spherial nanoparticles measuring 4.1 nm in diameter were observed at oil-water interfaces, where surface-enhanced Raman spectroscopy (SERS) revealed an elevated pH compared to the bulk solution. The negatively charged oil-water interfaces preferentially adsorb calcium ions, collectively promoting CaSO4 formation there. CaSO4 particle formation at the oil-water interface follows a nonclassical nucleation (N-CNT) pathway by forming ultrasmall amorphous spherical particles which then aggregate to form intermediate nanoparticles, subsequently growing into nanorod-shaped gypsum. These findings of this study provide insights into mineral scaling during membrane separation and can inform more efficient oil transport in energy recovery systems.

Choosing a camera and optimizing system parameters for speckle contrast optical spectroscopy

Speckle contrast optical spectroscopy (SCOS) is an emerging camera-based technique that can measure human cerebral blood flow (CBF) with high signal-to-noise ratio (SNR). At low photon flux levels typically encountered in human CBF measurements, camera noise and nonidealities could significantly impact SCOS measurement SNR and accuracy. Thus, a guide for characterizing, selecting, and optimizing a camera for SCOS measurements is crucial for the development of next-generation optical devices for monitoring human CBF and brain function. Here, we provide such a guide and illustrate it by evaluating three commercially available complementary metal–oxide–semiconductor cameras, considering a variety of factors including linearity, read noise, and quantization distortion. We show that some cameras that are well-suited for general intensity imaging could be challenged in accurately quantifying spatial contrast for SCOS. We then determine the optimal operating parameters for the preferred camera among the three and demonstrate measurement of human CBF with this selected low-cost camera. This work establishes a guideline for characterizing and selecting cameras as well as for determining optimal parameters for SCOS systems.

Spectroscopic Survey of Faint Planetary-nebula Nuclei. IV. The A35-type Central Star of Pa 27* *Based on observations obtained with the Hobby–Eberly Telescope (HET), which is a joint project of the University of Texas at Austin, the Pennsylvania State University, Ludwig-Maximillians-Universität München, and Georg-August Universität Göttingen. The HET is named in honor of its principal benefactors, William P. Hobby and Robert

We present optical spectroscopy of the 12th-magnitude central star of the planetary nebula (PN) Patchick 27 (Pa 27), obtained during a survey of faint PN nuclei (PNNs) with the Low-Resolution Spectrograph of the Hobby–Eberly Telescope. The optical spectrum of Pa 27 is that of a K0 III red giant with rotationally broadened lines. However, the star is detected in the near-ultraviolet (near-UV) with GALEX, showing that a hot binary component is also present. The spectral-energy distribution from the near-UV to the mid-infrared can be fitted with a combination of the K0 III giant and a hot PNN with an effective temperature of about 50,000 K. Photometric observations of Pa 27, both ground-based and from TESS, show a low-amplitude sinusoidal variation with a period of 7.36 days, probably due to starspots on a rotating and magnetically active cool giant. Pa 27 is a new member of the rare class of “A35-type central stars,” which are binary PNNs consisting of a spotted late-type star and a hot pre–white dwarf. They are likely the result of a situation where an asymptotic-giant-branch (AGB) star ejects its outer layers in a dense wind, part of which is captured by a distant companion, spinning up its rotation by accretion of material and angular momentum. We suggest several useful follow-up observations.

In Situ Surface-Enhanced Raman Spectroscopy on Organic Mixed Ionic-Electronic Conductors: Tracking Dynamic Doping in Light-Emitting Electrochemical Cells.

In the domain of organic mixed ionic-electronic conductors (OMIECs), simultaneous transport and coupling of ionic and electronic charges are crucial for the function of electrochemical devices in organic electronics. Understanding conduction mechanisms and chemical reactions in operational devices is pivotal for performance enhancement and is necessary for the informed and systematic development of more promising materials. Surface-enhanced Raman spectroscopy (SERS) is a potent tool for monitoring electrochemical evolution and dynamic doping in operational devices, offering enhanced sensitivity to subtle spectral changes. We demonstrate the utility of SERS for in situ tracking of doping in OMIECs in an organic light-emitting electrochemical cell (LEC) containing a conjugated polymer (poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene]; MEH-PPV), a molecular anion (lithium triflate), and an electrolyte network (poly(ethylene oxide); PEO). SERS enhancement is achieved via an interleaved layer of gold particles formed by spontaneous breakup of a deposited thin gold film. The results successfully highlight the ability of SERS to unveil time-resolved MEH-PPV doping and polaron formation, elucidating the effects of triflate ion transfer in the operating device and validating the electrochemical doping model in LECs.

A Wettability Contrast SERS Droplet Assay for Multiplexed Analyte Detection.

Droplet assay platforms have emerged as a significant methodology, providing distinct advantages such as sample compartmentalization, high throughput, and minimal analyte consumption. However, inherent complexities, especially in multiplexed detection, remain a challenge. We demonstrate a novel strategy to fabricate a plasmonic droplet assay platform (PDAP) for multiplexed analyte detection, enabling surface-enhanced Raman spectroscopy (SERS). PDAP efficiently splits a microliter droplet into submicroliter to nanoliter droplets under gravity-driven flow by wettability contrast between two distinct regions. The desired hydrophobicity and adhesive contrast between the silicone oil-grafted nonadhesive hydrophilic zone with gold nanoparticles is attained through (3-aminopropyl) triethoxysilane (APTES) functionalization of gold nanoparticles (AuNPs) using a scotch-tape mask. The wettability contrast surface facilitates the splitting of aqueous droplets with various surface tensions (ranging from 39.08 to 72 mN/m) into ultralow volumes of nanoliters. The developed PDAP was used for the multiplexed detection of Rhodamine 6G (Rh6G) and Crystal Violet (CV) dyes. The limit of detection for 120 nL droplet using PDAP was found to be 134 pM and 10.1 nM for Rh6G and CV, respectively. These results align with those from previously reported platforms, highlighting the comparable sensitivity of the developed PDAP. We have also demonstrated the competence of PDAP by testing adulterant spiked milk and obtained very good sensitivity. Thus, PDAP has the potential to be used for the multiplexed screening of food adulterants.

Surface-Enhanced Raman Spectroscopy-Based Detection of EMT-Related Targets in Endometrial Cancer: Potential for Diagnosis and Prognostic Prediction.

Epithelial-mesenchymal transformation (EMT) is one of the important mechanisms of malignancy in endometrial cancer, and detection of EMT targets is a key challenge to explore the mechanism of endometrial carcinoma (EC) malignancy and discover novel therapeutic targets. This study attempts to use surface-enhanced Raman spectroscopy (SERS), a highly sensitive, ultrafast, and highly specific analytical technology, to rapidly detect microRNA-200a-3p and ZEB1 in endometrial cancer cell lines. The silver nanoparticles were decorated with iodine and calcium ions, can capture the SERS fingerprints of microRNA-200a-3p and ZEB1 protein, and effectively avoid the interference of impurity signals. At the same time, the method has high sensitivity for the detection of the above EMT targets, and the lowest detection limits for microRNA-200a-3p and ZEB1 are 4.5 pmol/mL and 10 ng/mL, respectively. At the lowest detection concentration, the method still has high stability. In addition, principal component analysis can not only identify microRNA-200a-3p and ZEB1 protein from a variety of EMT-associated microRNA and proteins but also identify them in the total RNA and total protein of endometrial cancer cell lines and normal endometrial epithelial cell lines. This study modified silver nanoparticles with iodine and calcium ions and for the first time captured the fingerprints of EMT-related targets microRNA-200a-3p and ZEB1 at the same time without label, and the method has high sensitivity and stability. This SERS-based method has immense potential for elucidating the molecular mechanisms of EMT-related EC, as well as identifying biomarkers for malignant degree and prognosis prediction.