Co-doped Carbon Dots Research Articles

One-pot fabrication of aluminium ion anchoring boric acid-carbon dots hybrid system and its highly selective fluorescence sensing for fluorine ion in water environment

Fluorine is one of the essential trace elements for human body, which is essential for calcification process in living organisms. In the paper, a “off–on” fluorescence sensor for fluorine ion based on aluminium ion and boric acid codoped carbon dots was synthesized and characterized. According to fluorescence analysis, the water-soluble sensor exhibited highly selective and sensitive for fluorine ion. In sensing process, F- could bind to Al3+ after the addition of fluorine ion, which resulted in the decomposition of Al-BA-CDs system, then intense yellow fluorescence signal appeared. Moreover, the fluorescence sensor exhibited low detecting limit (5.0 nanomolar level) by fluorescence titration spectrum. In addition, according to evaluate the fluorescence sensing properties of F- in HepG2 cell and zebra fish, this job greatly extended the use of F- sensor from aluminium ion and boric acid codoped carbon dots in organism. The work also provided an interesting idea for fabricating water-soluble fluorescence sensor for F-.

Gadolinium and Ytterbium-Doped carbon dots for Fluorescence/Magnetic Resonance/Computed tomography multimodal imaging

Multimodal imaging is a potent technique that integrates complementary information from various imaging modalities, offering comprehensive insights into disease diagnosis. However, the development of biocompatible multimodal probes remains a challenge. In this study, we present the synthesis, characterization, and application of gadolinium and ytterbium co-doped carbon dots (Yb/Gd-CDs) for triple-modal fluorescence (FL)/magnetic resonance (MR)/computed tomography (CT) imaging. Notably, Yb and Gd were successfully incorporated into the lattice of CDs using a facile one‐pot hydrothermal approach to obtain Yb/Gd-CDs. The Yb/Gd-CDs demonstrated an ultra-small size, excellent colloidal stability, and low toxicity, making them suitable for further in vivo applications. Moreover, the Yb/Gd-CDs exhibited excellent fluorescence, high X-ray attenuation (40.17 HU/g/L), and high T1 relaxivity (11.16 mM-1s−1) with an ultra-low r2/r1 ratio of 1.08, showcasing remarkable performance in in vivo fluorescence, T1-weighted MR, and CT imaging of mice. Yb/Gd-CDs show great promise for in vivo multimodal imaging, and this work provides a highly biocompatible CDs-based theranostic platform with multiple functions for disease diagnosis.

Investigating the effect of nitrogen and chlorine Co–doped carbon quantum dots in phenazine and quinoxaline sensitized solar cells

We investigated five dyes for dye-sensitized solar cells (DSSCs) relying upon derivatives of phenazine and quinoxaline and also studied their optical characteristics and the influence of functional groups such as (-CH3, -NO2, -C = O, -CN, and -OH) on these characteristics. When the prepared dyes are directly used at DSSCs, 9-Nitrobenzo[a]phenazin-5-ol (3b) dye device showed an improved Jsc (0.288 mA cm−2), Voc (0.437 V), FF (0.446), and η (0.056 %) than the sensitized solar cells by other dyes. In the following, nitrogen-doped carbon quantum dot and nitrogen, chlorine co-doped carbon quantum dot are used to improve the performance of DSSCs. The results showed that the device sensitized using the sensitizer (5-hydroxybenzo[α]phenazin-9-yl)(phenyl) methanone (3c)/NCQD has the highest photovoltaic efficiency with Jsc (0.979 mA cm−2), Voc (0.465 V), FF (0.370), and η (0.168 %). The N and Cl co-doped carbon dots were synthesized with a green approach to improve the performance of solar cells by the co-sensitization method. This approach is improving the efficiency of DCSSs with a simple, eco-friendly, and low-cost technique. Among the prepared sensitizers, (5-hydroxybenzo[α]phenazin-9-yl)(phenyl) methanone (3c)/N, Cl-CQD demonstrates the highest photovoltaic efficiency with Jsc (1.31 mA cm−2), Voc (0.495 V), FF (0.466), and η (0.303 %). FT-IR, XRD, 13C NMR, 1H NMR, TEM, EDS-Map, AFM, DLS, and PL studies were used to confirm the structure of the synthesized dyes and quantum dots.

Meticulously designed red emission carbon dots as efficient and stable luminescent species for rapid latent fingerprint recognition and light emitting diodes

The preparation of carbon dots (CDs) emitting long wavelength has attracted more attentions due to their unique advantages in biological and optoelectronic fields, including the wide absorption, long PL lifetime and deep-tissue penetration. Herein, we prepare the nitrogen and sulfur co-doped red emission carbon dots (R-CDs) from the 2,4-diaminodiphenylamine (DDA) and thiourea via a solvothermal reaction, which exhibit reliable red emission at 613 nm and possess a high quantum yield (QY) of 34 %. Meanwhile, the structural analysis and theoretical calculation reveal that the sulfur doping from thiourea increases the nitrogen and oxygen content of CDs, leading to the red emission observed in R-CDs. Subsequently, we design an integrated fingerprints recognition system based on the R-CDs phosphors for the imaging of latent fingerprints (LFPs) and fast LFPs recognition, expanding the application of biometric identification and comparison technology based on fluorescence. Finally, we successfully apply the R-CDs into red and white light-emitting diodes, improving plant growth efficiency. As a result, this work provides a new in-depth insight of red emission CDs and expands the application in latent fingerprint recognition and light-emitting diodes.

Nitrogen and Chlorine Co-Doped Carbon Dots with Yellow-Green Emission as a Ratiometric Fluorescent and Colorimetric Dual-Signal Probe for Quercetin Detection and Cell Imaging

Despite the emergence of numerous carbon dots (CDs)-based sensors, most of them are fluorescent probes. To improve the reliability of the results, using ratiometric fluorescence/UV-vis absorption dual-signal probes is an effective method. Herein, nitrogen and chlorine co-doped carbon dots (N, Cl-CDs) with yellow-green fluorescence were prepared and used as a dual-function probe for ratiometric fluorescence/UV-vis. The detection range of the fluorescence method was 0.05–78[Formula: see text][Formula: see text]M, and the limit of detection (LOD) was 1.2[Formula: see text]nM (3[Formula: see text]/s). For the colorimetric method, the linear range was 0.05–186[Formula: see text][Formula: see text]M with LOD of 10.7[Formula: see text]nM. Importantly, the N, Cl-CDs were successfully used to detect Quercetin (QT) in actual water samples. Besides, due to their good biocompatibility, the N, Cl-CDs were applied to in vivo biological imaging of oocysts and shown the potential for environmental survey and biological assay.

An injectable chitosan-based hydrogel incorporating carbon dots with dual enzyme-mimic activities for synergistically treatment of bacteria infected wounds

Bacterial infections pose a serious threat to human health, and the emergence of superbugs and the growing antibiotic resistance phenomenon have made the development of novel antimicrobial products. In this paper, an ultrasmall Cu, N co-doped carbon dots (CDs-Cu-N) with excellent peroxidase mimic activity and enhanced catalase mimic activity was successfully prepared and anchored to an injectable chitosan (CS)-based hybrid hydrogel. As expected, the CDs-Cu-N-H2O2-CS hybrid hydrogel maintains the excellent enzyme-mimicking properties of CDs-Cu-N and shows superior antibacterial property, which has been proven to effectively promote the healing of S. aureus-infected wounds with good biocompatibility. Benefitting from the dual-enzyme-mimic activity of CDs-Cu-N, the hybrid hydrogel not only can catalyze the generation of highly toxic ROS from low concentration of H2O2 to inhibit the bacterial infections, but also can significantly promote the wound tissue repair and regeneration by improving the anoxic microenvironment and promoting neovascularization. In addition, this hybrid hydrogel also possessed excellent injectability and moldability. It can adapt to various the irregular shapes of acute wounds, maintaining a moist and safe microenvironment while prolonging the action time of nanozyme on wounds, thus promoting wound healing. This injectable hybrid hydrogel shows great potential applications in the field of wound infection management.

Aucklandia lappa Decne carbon dots guided chemiluminescence: A sensitive detection strategy for salicylic acid

In this study, a novel chemiluminescent system was developed utilizing carbon dots (CDs) for the sensitive detection of salicylic acid. P,Cl co-doped carbon dots (P, Cl-CDs) was synthesized using discarded Aucklandia lappa Decne leaves as precursor materials through a one-step hydrothermal method. The morphology, structure, elemental composition, and properties of P, Cl-CDs were characterized by various methods including transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The synthesized P, Cl-CDs exhibited uniform particle size and excellent water solubility. It was observed that P, Cl-CDs could significantly enhance the chemiluminescence intensity of the acidic KMnO4 system by approximately 10 times. While salicylic acid could inhibit the acidic KMnO4 system sensitized by P, Cl-CDs. Based on this phenomenon, a new system for detecting salicylic acid was established. Under optimal experimental conditions, the concentration of salicylic acid displayed a linear relationship in the range of 1 to 100 μM, achieving a limit of detection (LOD) of 4.2 nM and a relative standard deviation (RSD) of 0.9 % (n = 11). The method was successfully applied to determine salicylic acid in aspirin tablets, yielding spike recoveries within the range of 96.9 %–104.3 %.

A Dual-Signal Sensing for the Visual and Luminescent Detection of p-Phenylenediamine Based on Cerium-Nitrogen-Co-Doped Carbon Dots.

Herein, a visual and luminescent dual-mode (colorimetric and fluorometric) method for the detection of P-phenylenediamine (PPD) in hair dye was successfully established based on cerium-nitrogen co-doped carbon dots (Ce, N-CDs) that displayed remarkable luminescence and peroxidase activity. Ce, N-CDs catalyzed H2O2 to produce superoxide anion, which then oxidized the colorless 3,3,5,5-tetramethylbenzidine (TMB) into blue oxidized TMB (oxTMB), capable of quenching the fluorescence through fluorescence resonance energy transfer (FRET) between Ce, N-CDs and oxTMB. The reducing properties of PPD could reduce oxTMB back to TMB, leading to a decrease in the absorption intensity of oxTMB and a fluorescence recovery of Ce, N-CDs. As a result, the quantitative detection of PPD could be achieved by measuring the absorption values of oxTMB and the fluorescence signal of Ce, N-CDs. The detection limits for PPD were calculated as 0.36 µM and 0.10 µM for colorimetry and fluorimetry, respectively. Furthermore, smartphone application (ColorPicker) capable of measuring the RGB value of the color was utilized in the detection system, facilitating on-site quantitative detection. This approach effectively shortens the detection time and simplifies the operation, offering a powerful and convenient tool for real-time monitoring of PPD.

Enhanced Corrosion Inhibition of Q235 Steel by N,S Co-Doped Carbon Dots: A Sustainable Approach for Industrial Pickling Corrosion Inhibitors.

A high yield of environmentally friendly N,S-codoped (N,S-CDs) and N-doping carbon points (N-CDs) carbon dots was achieved through a biochemical oxidation reaction at room temperature in this study. Acetaldehyde, sodium hydroxide, benzotriazole (BTA), and 2-mercaptobenzimidazole (MB) with a similar structure were used as raw materials. The microstructure and properties of the corrosion inhibitor for Q235 steel were evaluated by various experiments. The results demonstrated enhanced corrosion inhibition rates of the N,S-CDs compared to the N-CDs using electrochemical tests (93.83% vs 77.65%) and weight loss experiments (96.35% vs 91.65%) at 50 mg/L, respectively, compared to the blank material, indicating that N,S codoping can significantly improve the corrosion inhibition effect of carbon dots. The significant improvements were attributed to the formation of dense adsorption films and the hydrophobic properties of N and S-CDs nanoparticles on the steel surface, leading to an effective barrier against corrosion. The findings from this study provide important experimental data for potential industrial applications and hold important practical value in the field of pickling corrosion inhibitors.

The carbon dots with near-infrared electrochemiluminescence emission and low excitation potential for ultrasensitive analysis of microRNA-222

In this work, nitrogen and sulfur codoped near-infrared emission carbon dots (N,S-NIR-CDs) were used as neoteric electrochemiluminescence (ECL) emitters with high efficiency to construct a biosensor for ultrasensitive analysis of microRNA-222 (miRNA-222), which has been regarded as prospective biomarkers for early cancer diagnosis. Impressively, compared to conventional CDs with short ECL wavelength and large excitation voltage, N,S-NIR-CDs possessed wide sp2 domains and narrow band gap, leading to the near-infrared ECL emission at 680 nm and low excitation potential from −1.0 to 0 V, which not only decreased the photochemical damage for biomolecules but also reduced the side reaction. Moreover, an improved T7 Exonuclease induced cascade amplification (EICA) strategy was designed to transform trace miRNA-222 into plentiful output DNA in dual-cycle for greatly improving the target conversion efficiency. Therefore, by combining the N,S-NIR-CDs as neoteric ECL emitters and EICA strategy as signal amplifier, the constructed ECL biosensor could realize the ultrasensitive analysis of miRNA-222 with a identification limit of 5.65 aM and successfully employed in miRNA-222 analysis from liver cancer cell (HCCLM3 and MHCC-97L) lysate. This strategy developed a kind of neoteric CDs with NIR ECL emission and low excitation potential to establish a highly efficient biosensor for biomarker analysis, which prepared a road for early diseases diagnosis and lied a foundation for biological ECL imaging.

Platinum, palladium, and nitrogen co-doped carbon dots as efficient enhancers for acetonitrile-hydrogen peroxide chemiluminescence reaction and its application for sensitive determination of Fe(II) ions

In this work, we investigated the effect of platinum, palladium, and nitrogen co-doped carbon dots (Pt,Pd,N-CDs) on the acetonitrile-hydrogen peroxide (CH3CN–H2O2) chemiluminescence (CL) reaction. We found that Pt,Pd,N-CDs can remarkably amplify the CL intensity of this system (about 530-fold). Based on the gathered proofs, we deduced that the generated (1O2)2* molecules from the interaction between CH3CN and H2O2 under the alkaline medium can transfer their energy to Pt,Pd,N-CDs, which act as final emitting species in this CL reaction. Furthermore, we observed that the synthesized CDs function as catalysts, increasing the number of reactive oxygen species. In the presence of Fe(II), the CL signal of Pt,Pd,N-CD-based the system is greatly enhanced, which can be imputed to Fe(II)-catalyzed H2O2 dissociation. Utilizing this finding, an efficient CL assay was developed for the determination of Fe(II) in the range of 0.002–8.0 µM with a detection limit of 1.0 nM. Ultimately, the practicality and reliability of this method were tested by analyzing a certified reference material and spiked water samples.

Novel fluorescent probes based on sulfur and nitrogen co-doped carbon dots for determination of three N-substituted phenothiazine derivatives in dosage forms

In the current work, sulfur and nitrogen co-doped carbon dots (S,N-CDs) as simple, sensitive, and selective turn-off fluorescent nanosensors were utilized for analysis of three phenothiazine derivatives, including acetophenazine (APZ), chlorpromazine (CPH), and promethazine (PZH). S,N-CDs were synthesized through a green one-pot microwave-assisted technique using widely available precursors (thiourea and ascorbic acid). HRTEM, EDX, FTIR spectroscopy, UV–Vis absorption spectroscopy, and fluorescence spectroscopy were used to characterize the as-synthesized CDs. When excited at 330 nm, the carbon dots produced a maximum emission peak at 410 nm. The cited drugs statically quenched the S,N-CDs fluorescence as revealed by the Stern-Volmer equation. The current method represents the first spectrofluorimetric approach for the determination of the studied drugs without the need for chemical derivatization or harsh reaction conditions. The importance of the proposed work is magnified as the cited drugs do not have any fluorescent properties. The fluorescence of the developed sensor exhibited a linear response to APZ, CPH, and PZH in the concentration ranges of 5.0–100.0, 10.0–100.0, and 10.0–200.0 μM with detection limits of 1.53, 1.66, and 2.47 μM, respectively. The developed fluorescent probes have the advantages of rapidity and selectivity for APZ, CPH, and PZH analysis in tablets with acceptable % recoveries of (98.06–101.66 %). Evaluation of the method's greenness was performed using the Complementary Green Analytical Procedure Index (ComplexGAPI) and Analytical GREEnness metric (AGREE) metrics, indicating that the method is environmentally friendly. Validation of the proposed method was performed according to ICHQ2 (R1) guidelines.

Preparation of high quantum yield nitrogen and sulfur co-doped carbon dots for sensitive detection of Cu2+

Preparation of high quantum yield nitrogen and sulfur co-doped carbon dots for sensitive detection of Cu2+

Nitrogen and Sulfur co-doped Carbon dots as an "on-off-on" Fluorescent Sensor for the Detection of Hg2+ and Ampicillin.

Herein, a fluorescent "on-off-on" nanosensor based on N,S-CDs was developed for highly precise and sensitive recognition of Hg2+ and ampicillin (AMP). Nitrogen and sulfur co-doped carbon dots with blue fluorescence were synthesized by one-pot hydrothermal method using ammonium citrate and DL-methionine as precursors. N,S-CDs exhibited a surface abundant in -OH, -COOH, and -NH2 groups, aiding in creating non-fluorescent ground state complexes when combined with Hg2+, leading to the suppression of N,S-CDs' fluorescence. Subsequent to additional AMP application, the mixed system's fluorescence was restored. Based on this N,S-CDs sensing system, the thresholds for detection for AMP and Hg2+ were discovered to be 0.121 µM and 0.493 µM, respectively. Furthermore, this methodology proved effective in identifying AMP in real samples of tap and lake water, yielding satisfactory results. Consequently, in the area of bioanalysis in intricate environmental sample work, the sensing system showed tremendous promise.

N, S co-doped carbon dots for fluorescent and colorimetric dual-mode detection of Co(II) in actual water

This study focuses on the synthesis of nitrogen and sulfur co-doped carbon dots (N, S-CDs) using a hydrothermal method, and its application as a fluorescence and colorimetric dual-mode probe for simple and rapid detection of Co(II). When Co(II) reacts with N, S-CDs, metallic bonds are formed, leading to a static quenching effect (SQE). The electrostatic interaction between positive-charged cobalt complexes and negative-charged N, S-CDs induces the aggregation of metal complexes, increasing the particle size from 5.44 nm to 258.72 nm and resulting in a noticeable visual color change ultimately. N, S-CDs exhibited excellent potential for application in actual water samples, with the low detection limit (LOD) of 2.64 µM and 1.57 µM via fluorescence and colorimetric methods, respectively, and the recovery rate ranged from 94 % to 103 %. As far as we consider, the cross-referenced dual-mode platform proposed here may be an attractive strategy for the construction of high-performance sensors available for metal ion detection in actual aquatic environments.

Improved mercury ions (Hg2+) detection by composite silver nanoparticles (AgNPs) and nitrogen - Sulfur co-doped carbon dots (N, S-CDs)

Heteroatom doping has been demonstrated as an efficient method to increase the fluorescence quantum yield efficiency of carbon dots. Co-doping with heteroatoms leads to additional active sites on carbon dots, both extending their use in sensing systems and improving the sensitivity of detection. In this study, the synthesis of nitrogen and sulfur co-doped carbon dots (N, S-CDs) through a single step hydrothermal process was reported, utilizing citric acid and thiourea as sources of carbon, nitrogen, respectively. This N, S-CDs was composited with silver nanoparticles (AgNPs) to detect mercury ions (Hg2+) with reabsorption principle. The fluorescence intensity of the carbon dots was vanished by AgNPs due to the reabsorption effect due to overlap between emission spectrum of N, S-CDs and absorption spectrum of AgNPs, and it is recovered by the addition of Hg2+ due to formation Ag/Hg amalgam. As a result, composite of N, S-CDs-AgNPs can be used as a fluorescence "turn-on" probe for rapid and highly sensitive detection of Hg2+. The lowest limit of detection (LOD) of Hg2+ is 10 nM with linear detection in the range of 1 nM - 1.0 μM. This LOD is improved three-order of magnitude as compared to the N, S-CDs only with detection limit in 10 μM. This result proves that the composite of N, S–CDs-AgNPs is a very sensitive fluorescence probe for mercury ions detection. This work will also provide ideas for creating and building novel fluorescence probes for similar applications.

Efficient electrochemical synthesis of green fluorescent carbon dots for curcumin detection in common foods

Curcumin (Cur) is commonly employed as a food additive in the pharmaceutical and food industries. However, improper use of curcumin can lead to adverse effects on human health. In this research, we developed an electrochemical approach for the synthesis of green fluorescence nitrogen and sulfur co-doped carbon dots (G-CDs) specifically designed for curcumin detection. The prepared G-CDs displayed strong fluorescent emissions at 540 nm, along with notable attributes such as excellent fluorescence stability against photobleaching, and resilience to changes in ionic strength. The G-CDs demonstrated selective recognition of curcumin, resulting in fluorescence quenching in a linear range of 0–140 μmol/L, with an impressive detection limit of 46.4nmol/L. Five distinct food samples were effectively detected for curcumin using the developed G-CDs nanoprobe, yielding satisfactory outcomes. This newly proposed approach offers simplicity, outstanding sensitivity, and selectivity, showcasing its promising capabilities as an alternative method for Cur detection without the need for specialized instruments.

Carbon Dots with Spatially-Mediated-N/S-Co-Doping Enabling One-Year Stable Lubricant with Oil Leakage Detection Capability.

The dispersion stability of nano-lubricating additives is crucial for the shelf life of lubricant and its practical applications. Nitrogen-sulfur co-doped carbon dots (N,S@CDs) via a one-step hydrothermal method with nitropyrene and thiourea as raw materials are hereby presented. The N and S elements are selectively distributed throughout the entire carbon skeleton with a doping amount of 22.6 at%. The as-synthesized N,S@CDs exhibit excellent dispersion stability in PEG200 and maintain stability for over one year. The experiment results indicate that N,S@CDs significantly improve the anti-wear and friction reduction properties of PEG200, while the friction coefficientis reduced from 0.25 to 0.09 with 1.5 wt% N,S@CDs addition, and the wear volume, depth, and width are reduced by 68%, 52%, and 57%, respectively. The good lubrication performance is attributed to N,S@CDs excellent dispersion stability, enhanced filling and polishing effects, and complex tribochemical reactions caused by heteroatom doping to form a stable protective film on the worn surface. Furthermore, the as-prepared N,S@CDs exhibit intrinsic fluorescence intensity in PEG200 with the photoluminescence quantum yield (PLQY) of 12.5% and remain fluorescent stable during the long-term friction process, therefore the N,S@CDs have a potential application prospect in non-destructive detection of oil leakage via fluorescence labeling method.

Investigation of the Application and Mechanism of Nitrogen and Phosphorus Co-doped Carbon Dots for Mercury Ion Detection.

In this paper, we obtained nitrogen and phosphorus co-doped carbon dots through a hydrothermal method using o-phenylenediamine and citric acid in a 40% phosphoric acid environment. The carbon dots emitted fluorescence at 476nm under excitation at 408nm and exhibited good selectivity and high sensitivity towards mercury ions. These carbon dots showed excellent dispersibility in water and maintained stable fluorescence even in high concentration salt environments. The interaction between mercury ions and functional groups on the carbon dots surface through electrostatic interaction resulted in static quenching. Simultaneously, by detecting the lifetime and transient absorption spectra of the carbon dots, we observed that the coordination of mercury ions with the carbon dots broadened the band structure of the carbon dots, and the existing photoinduced electron transfer process increased the non-radiative transition channel. The combined effect of dynamic quenching and static quenching significantly reduced the fluorescence intensity of the carbon dots at 476nm. The carbon dots exhibited linear detection of mercury ions in the range of 0.01-1 µM, with a detection limit as low as 0.0245 µM. In terms of practical water environmental detection applications, these carbon dots were able to effectively detect mercury ions in tap water and lake water, demonstrating their broad application prospects in the field of environmental metal analysis.

Cobalt-nitrogen co-doped carbon dots for the colorimetric and fluorometric dual-mode detection of gallic acid

Gallic acid (GA), widely used in food and medicine production industries. Herein, a kind of newly synthesized cobalt-nitrogen co-doped carbon dots (Co,N-CDs) with dual functional properties of oxidase-like activity and photoluminescence property could oxidize the 3,3′,5,5′-tetramethylbenzidine (TMB) to oxTMB with a new absorption peak at 653 nm. In addition, it was found that oxTMB performed a fluorescence-quenching effect on Co,N-CDs at 440 nm attributed to FRET (Fluorescence resonance energy transfer). Reductive GA could reduce oxTMB to TMB, weaken the blue color, and restore the fluorescence of Co,N-CDs. Thus, a colorimetric and fluorometric method for dual-mode detection of GA was established. The synthesis of the dual-signal probe was completed with a single and environmental precursor in just one step. Simultaneously, the dual-mode detection reduced detection limits, broadened the linear range and improved anti-interference ability. This method exhibited a satisfactory application prospect in the actual detection of GA in tea beverages.