147 results about "Luminophore" patented technology

The invention belongs to the technical field of immunoassay and biosensing detection, and particularly relates to a preparation method and application of an antibiotic electrochemical luminescence sensor based on a double-enhancement strategy. According to the invention, a bifunctional metal organic gel is used as a substrate, a graphite-phase carbon nitride quantum dot is used as a luminous body, and a self-assembly split aptamer walker is combined to construct the electrochemical luminescence sensor for sensitive detection of antibiotics. The sensor has the advantages of extremely high specificity and sensitivity, wide detection range, low detection limit and strong anti-interference performance, and has important scientific significance and application value in detection of antibiotic residues in the environment.

A long-persistent luminescence emitter containing a polymer that contains, relative to the total molar amount of an electron donor structural unit and an electron acceptor structural unit therein, 70 mol % or more of an electron donor structural unit and less than 30 mol % of an electron acceptor structural unit, or containing a polymer that contains, relative to the total molar amount of an electron donor structural unit and an electron acceptor structural unit therein. 70 mol % or more of an electron acceptor structural unit and less than 30 mol % of an electron donor structural unit. The emission decay after stopping light irradiation to the emitter is power law decay.

The invention discloses a construction method and application of an electrochemical luminescence (ECL) biosensor based on a cell membrane hydrogel antifouling interface, and belongs to the technical fields of photo / electrochemical analysis, interface antifouling and biosensing. According to the invention, the cell membrane hydrogel is used as an efficient antifouling interface, so that non-specific adsorption of interfering proteins in a sample to be detected is hindered, and the service life of the biosensor is prolonged. Meanwhile, a luminophor copper nanosheet and a quencher MnO2 nanosheet are both introduced into the cell membrane hydrogel, in the presence of alkaline phosphatase (ALP), L-ascorbic acid-2-trisodium phosphate is catalyzed and hydrolyzed into ascorbic acid, and then MnO2 is reduced to recover ECL emission of the copper nanosheet. Therefore, the ECL signal of the biosensor is in a rising trend along with the rising of the ALP concentration. Based on this, the constructed ECL biosensor realizes sensitive detection of ALP, the linear range is 10 <-5 >-10 < 4 > U / L, and the detection limit is as low as 3.4 * 10 <-6 > U / L, which indicates that the ECL biosensor has potential application in clinical diagnosis.

The invention relates to a lanthanide oxide electrochemiluminescence aptamer sensor with dual signal amplification for detecting acetamiprid as well as a preparation method and application of the lanthanide oxide electrochemiluminescence aptamer sensor. According to the sensor, terbium-doped europium oxide (Eu2O3: Tb < 3 + >) modified by gold nanoparticles (Au NPs) is used as a luminous body, and the electrochemical luminescence performance can be remarkably improved through multiple mechanisms: on one hand, the Au NPs can effectively promote generation of more sulfate free radicals; on the other hand, the surface defect passivation effect and the efficient synergistic effect of energy transfer jointly achieve effective amplification of signals. In addition, the wool ball-shaped Ag NPs is used as a plasma resonance signal amplification source, so that the ECL intensity of the sensor is further enhanced. The prepared electrochemical luminescence sensor with the dual signal amplification effect is used for detecting acetamiprid (ACE), has a wide linear range and a low detection limit, and has a wide application prospect in detection of acetamiprid residues in a water environment.

The utility model discloses a full-spectrum LED (light-emitting diode) lamp, which relates to the field of LED lamps and comprises a mounting plate, a luminous body fixedly mounted at the center of the bottom of the mounting plate, an annular groove formed in the bottom of the mounting plate, an outer cover movably inserted in the annular groove, a transparent cover fixedly mounted at the bottom of the outer cover, and the luminous body positioned in the outer cover and the transparent cover. Grooves are formed in the two sides of the inner ring wall of the annular groove, clamping blocks are movably inserted into the two grooves, springs are fixedly connected between the two clamping blocks and the corresponding grooves, clamping grooves are formed in the two sides of the inner wall of the outer cover, and the ends, extending out of the grooves, of the two clamping blocks can be clamped into the clamping grooves in the two sides of the inner wall of the outer cover correspondingly. Screw grooves are formed in the two sides of the outer wall of the outer cover, and second screw holes are formed in the two sides of the mounting plate. According to the LED lamp, the outer cover is clamped in the annular groove in a rotating mode, then the outer cover is fixed in the annular groove through the second bolts, installation of the outer cover is completed conveniently, operation is easy and convenient, and later maintenance of the lamp is facilitated.

A device for luminescent imaging includes an array of imaging pixels, a photonic structure over the array of imaging pixels, and an array of features over the photonic structure. A first feature of the array of features is over a first pixel of the array of imaging pixels, and a second feature of the array of features is over the first pixel and spatially displaced from the first feature. A first luminophore is within or over the first feature, and a second luminophore is within or over the second feature. The device includes a radiation source to generate first photons having a first characteristic at a first time, and generate second photons having a second characteristic at a second time. The first pixel selectively receives luminescence emitted by the first and second luminophores responsive to the first photons at the first time and second photons at the second time, respectively.

The invention discloses a self-aggregation-induced emission type photosensitizer and a preparation method and application thereof. The photosensitizer has excellent AIE performance, and singlet oxygen can be efficiently generated after aggregation in a physiological environment; and the photosensitizer can effectively overcome the aggregation-induced quenching phenomenon, and has a synergistic effect with the lovir drugs, so that the anti-herpes virus activity is remarkably improved, and the dosage and side effects are reduced.

The invention discloses construction and application of a biosensor based on an efficient antifouling interface and dual signal amplification, and belongs to the technical fields of optical / electric analytical chemistry, biosensing and material science. According to the invention, the electrode interface is modified with polyaniline doped with polytannic acid as an antifouling film, so that non-specific adsorption of interfering biomolecules in a complex medium is resisted; euTb-MOF is prepared as an efficient luminous body, Tb < 3 + > can transfer energy of Tb < 3 + > and ligand to Eu < 3 + >, and effective signal self-enhancement is realized; according to the EuTb-MOF, the reduction of S2O8 < 2-> is promoted by utilizing the reversible conversion of valence states of Co < 2 + > / Co < 3 + > and Fe < 2 + > / Fe < 3 + > and the synergistic catalysis of Ag NPs, so that the electrochemical luminescence signal of the EuTb-MOF is further improved. Based on the above strategy, the constructed biosensor has high detection sensitivity and precision and long service life, the linear range is 10 fM to 100 nM, and the detection limit is as low as 3.62 fM.

The invention belongs to the technical field of chemiluminescence immunoassay, and particularly relates to application of a luminescence retarder in improving development quality of solid-phase membrane immunodetection. According to the invention, when the concentration of the delay agent is fixed, the time of luminescence starting delay and the concentration of the enzyme catalyst are in nonlinear negative correlation, that is, the delay time is obviously increased along with the reduction of the enzyme concentration. The nonlinear negative correlation is suitable for luminescent systems of different reinforcing agents. Benefited from the enzyme concentration dependent luminescence delay effect, the chemiluminescence liquid with the delay effect is used for improving the development quality of solid-phase membrane immunodetection for the first time, noise and background signals are suppressed, and the chemiluminescence liquid has wide application value in the aspect of solid-phase membrane immunodetection.

This invention belongs to the field of immunoassay and biosensing technology, and discloses a method for preparing a ratiometric ECL biosensor based on Eu / Tb-Lu MOGs. Using Eu / Tb-Lu MOGs as the luminescent material and H3-tctpy and luminol as ligands, a single-luminescent material with dual ECL emission is synthesized. Lanthanide ions provide the cathode ECL emission, enhanced by the antenna effect and Tb→Eu energy transfer; the anode emits light from luminol using dissolved oxygen in water, requiring only the addition of K2S2O8 as a single co-reactant, resulting in fewer side reactions and a stable signal. The dual-potential ratiometric sensing utilizes the dual ECL signal for self-calibration, improving anti-interference and reliability; the single-luminescent dual-potential system achieves synchronous anode / cathode luminescence, simplifying the system and improving detection accuracy. By detecting changes in the ECL signal of different concentrations of analytes, the detection of microRNA-126 is achieved.

The invention discloses construction and application of a biosensor for triggering controlled release based on adjacent induced DNA strand displacement, and belongs to the technical fields of electrochemical luminescence, biological analysis and nano science. According to the invention, by integrating adjacent induced DNA strand displacement and controlled release strategies, the ultra-sensitive self-closing dual-mode biosensor taking the Au-Ag nanocluster as a luminous body is developed, and the ultra-sensitive self-closing dual-mode biosensor is used for trace detection of neuron-specific enolase. Due to the synergistic characteristic between the double metals, the Au-Ag nanocluster has high electrochemical luminescence (ECL) efficiency. Meanwhile, the reduction of S2O8 < 2-> is catalyzed by cyclic conversion between Fe < 2 + > / Mn < 3 + > and Fe < 3 + > / Mn < 4 + >, and a large amount of SO4 <-> is generated for ECL emission. The specific binding between the target antigen and the antibody can drive DNA strand displacement to open a blocked hole, so that the electrochemical probe falls off and the probe is quenched to release, the self-closing of an electrochemical signal and an ECL signal is realized, the detection sensitivity and accuracy of the sensor are effectively improved, and the sensor is suitable for immunoassay of various biomarkers.

The invention belongs to the technical field of luminescence imaging detection, and particularly relates to an electrochemical luminescence imaging detection platform based on a closed bipolar electrode array and application. Comprising a sensor and a detection unit, a bipolar electrode array unit comprises an insulating substrate, an anode region and a cathode region, the anode region and the cathode region are isolated from each other and are of the same structure, and each anode region or each cathode region is provided with a plurality of independent holes which are arrayed in parallel; gold nanoparticles are loaded in a plurality of independent open pores of the parallel array in the anode region, and a Ru (bpy) 32 < + >-TPA system is constructed; au / g-C3N4 composite materials are loaded in a plurality of independent open pores of the parallel array in the cathode region, and an Au / g-C3N4-K2S2O8 system is constructed. According to the invention, based on the bipolar electrode array unit, the terpyridyl ruthenium and the gold / graphite phase carbon nitride are used as different illuminants to realize capture and quantitative analysis for synchronous detection of acetaminophen and rutin, and the detection accuracy and high-throughput analysis are ensured.

The present invention belongs to the technical field of core electronic industries and relates to a luminescent body competition ratio type double antibody sandwich immunosensor for the same co-reactant. It includes a sensing electrode, a second antibody bioconjugate, and a luminescent body; a first antibody and a first catalytic component are attached to the surface of the sensing electrode, and the second antibody bioconjugate is formed by covalently connecting a second catalytic component and a second antibody; both the first antibody and the second antibody can specifically bind to the antigen to be detected, so that the second antibody bioconjugate can be connected to the sensing electrode through the specific binding of the first antibody and the second antibody to the antigen to be detected; both the first catalytic component and the second catalytic component are composites of gold nanoparticles and reduced graphene oxide, the average particle size of the gold nanoparticles in the first catalytic component is 12-14 nm, and the average particle size of the gold nanoparticles in the second catalytic component is 3.3-3.5 nm; the luminescent body is Ru(bpy)3 2+ .

The invention discloses a method for detecting oxytetracycline (OTC) based on nitrogen-doped graphdiyne (2N-GY) electrochemical luminescence sensing. The prepared 2N-GY has an electrogenerated chemiluminescence signal, the surface of the electrode is modified with an aptamer (Apt I) of carboxylated 2N-GY and OTC, and then non-specific binding sites are closed by using BSA to obtain the modified electrode. The modified electrode is used as a working electrode, an electrochemiluminescence biosensor is constructed by continuously modifying OTC and quenching a probe (PDAs-Apt II), and quantitative analysis is carried out on the OTC by detecting the change of an electrochemiluminescence signal. According to the present invention, the two OTC aptamers (Apt I and Apt II) are adopted as the recognition molecules to construct the electrochemiluminescence biosensor so as to achieve the high-specificity and high-sensitivity detection of OTC, and can be used for the actual detection application of milk, and the novel carbon material is adopted to replace the toxic light-emitting reagent, such that the detection cost is reduced, and the safety problem existing in the traditional light-emitting system is reduced.

The invention belongs to the technical field of fluorescent probes, and particularly relates to a fluorescent probe for detecting pyrophosphoric acid or pyrophosphate based on ratiometric fluorescence, a preparation method and application. According to the fluorescent probe, cyclotriphosphazene is taken as a core platform, a naphthalimide-triphenylamine luminophore and a terpyridine recognition unit are introduced, a multi-arm fluorescent probe is integrally formed, coordination terpyridine interacts with metal ions Zn < 2 + >, fluorescence signals are induced to change, and therefore sensitive detection on PPi is achieved. The fluorescent probe has the advantages of quick response, high selectivity, interference resistance and low cost, and has important application value in the fields of environmental science, biological science and the like.

The invention relates to the technical field of immunosensors, in particular to a double-ligand Cu-MOF composite material, an immunosensor, a preparation method and application. The preparation method of the double-ligand Cu-MOF composite material comprises the following steps: dissolving isoluminol and 2-aminoterephthalic acid in a first organic solvent, then adding glutaraldehyde, and stirring under a dark condition to obtain a solution A; dissolving polyether F127 in a mixed solvent, and then adding copper salt to obtain a solution B; and mixing the solution A and the solution B, and carrying out a first heating reaction to obtain Cu-ABEI. The invention also provides the double-ligand Cu-MOF composite material prepared by adopting the method, an antigen-combined illuminant, an immunosensor and a preparation method of the double-ligand Cu-MOF composite material. According to the invention, the problem that the ECL signal stability of isoluminol is poor is solved, and the problem that the sensitivity is low when an existing sensor is used for detecting DBP is also solved.

The invention discloses a chiral binaphthol-based fluorescent material as well as a preparation method and application thereof, and belongs to the technical field of organic photoelectric materials. The fluorescent material takes a chiral binaphthyl derivative as a skeleton, and a chiral binaphthyl group is introduced into a para-position position of tetrafluoroterephthalonitrile, so that a chiral space charge transfer luminescence system with a clear structure is formed. The preparation method comprises two steps of nucleophilic substitution reaction, the reaction condition is mild, the synthetic route is simple, and the yield is stable. The material has dual-state emission and aggregation enhanced luminescence characteristics, avoids aggregation quenching, has excellent circular polarization luminescence performance, has a luminescence asymmetry factor (Glum) of 3.6 * 10 <-3 >-5.9 * 10 <-3 >, and can still maintain stable chiral luminescence characteristics in a doped film. The material can be widely applied to the fields of commercial anti-counterfeiting, fluorescent ink, circular polarization luminescent devices, 3D display, information encryption, biological probes, LED light sources and the like, and has good industrial amplification potential and practical application value.

The invention provides a chemiluminescent composition and a dynamic coding device and method. The chemiluminescent composition comprises (i) a luminophor compound; (ii) a first metal ion selected from one or more of Mn < 2 + >, Co < 2 + >, Cr < 3 + >, Fe < 2 + >, Fe < 3 + >, Cu < 2 + >, Ni < 2 + >, Pb < 2 + >, Zn < 2 + >, Ru < 2 + >, Ce < 3 + >, Ag < + >, Pt < 2 + >, and any combination thereof; (iii) second metal ions selected from one or more of the group consisting of zirconium ions, molybdenum ions, titanium ions, vanadium ions, niobium ions, aluminum ions, and any combination thereof; (iv) an organic ligand; (v) a first co-reactant; (vi) a second co-reactant and (vii) a luminescence retarder. The chemiluminescent composition provided by the invention can be used for accurately controlling one or more of luminescence color / wavelength, luminescence starting time, luminescence duration and luminescence intensity, precise design can be carried out on the basis, and a novel chemiluminescent coding device and a novel chemiluminescent coding method which are high in sensitivity, high in information density, precise, anti-interference and anti-cracking are realized.

The utility model discloses a building detection lamp, which relates to the field of building detection, and comprises a hand-held handle, the top of the hand-held handle is connected with a luminous body through metal heads, the metal heads are connected at two ends of the luminous body in a sealing manner, a clamping mechanism for improving the replacement efficiency of a rubber block of the detection lamp is arranged in a movable block, and the clamping mechanism comprises a slot. The inserting grooves are symmetrically formed in the side face of the movable block up and down, and elastic pieces are symmetrically connected into the inserting grooves. According to the detection lamp for the building, when the movable block slides, the rubber block can be driven to move to the side face of a reinforcing steel bar for extrusion, the handle can be positioned on the reinforcing steel bar through extrusion of the rubber block, the detection lamp is placed at other positions of a reinforcing steel bar cage according to needs, the detection lamp cannot fall off, and therefore the structure of the reinforcing steel bar cage can be observed more conveniently; and the angle between the rubber block and the luminous body can be changed by rotating the rotating block, so that the detection lamp can adapt to the internal space of the reinforcement cage more easily.

A solar concentrator device is provided. The solar concentrator device includes a waveguide having a luminophore and a first refractive index; a photovoltaic component operably coupled to the waveguide; and a film disposed onto a surface of the waveguide, the film having a second refractive index. The second refractive index of the film is lower than the first refractive index of the waveguide. The waveguide and the film are visibly transparent.

A method is provided to simultaneously identify and quantify critical structure attributes (CSAs) in proteoforms or proteoform families that includes the steps of:1. injecting a sample into a reagent stream of one or more detection enhanced molecular recognition reagents;2. incubating the combined sample:reagent(s) during migration through an analytical platform the causes molecular recognition reagent(s) to be sequestered by a specific critical structure attribute (CSA) in the analyte to form a luminon (An:*Sas) complex;3. using a sequestron selector in the reagent stream to overtake the luminon complex in a down-stream size exclusion chromatography (SEC) column to achieve mixing and formation of an Nc˜Pas:An:*Sas, Pas:An:*Sas, or *Pas:An:*Sas sequestome complex;4. resolving this sequestome complex from any unbound affinity selector(s) such as *Sas or *Pas, and non-analytes in the SEC column;5. transporting the resolved sequestome complex into a flow-through detection means that detects and quantifies CSAs in fluorescent labeled *Sas or *Pas bearing luminon or sequestome complex to generate data for the construction of critical structure attribute ratio plots as a function of elapsed fermentation time.

The present invention provides a transparent luminescent solar concentrator (TLSC), the TLSC comprising a luminophore and a waveguide for guiding light emitted from the luminophore. The TLSC has a light utilization efficiency (LUE) greater than or equal to about 1.

The invention relates to Eu-Dy MOF gel, a preparation method thereof, an eye pad type fluorescence sensor and application, and the Eu-Dy MOF gel is obtained by compounding Eu < 3 + > and Dy < 3 + > as metal sources and 3, 5-dicarboxyphenylboronic acid as a ligand. On the basis of a covalent binding reaction principle, boric acid functionalized MOFs are used as a luminous body, some organic ligands with specific recognition target objects are introduced through specific functional groups such as boric acid groups, and the organic ligand 3, 4, 5, 6, 7, 8-tetracarboxylic acid containing lysozyme reaction sites (boric acid groups,-B (OH) 2-) is added into the luminous body. The functionalized MOF gel probe prepared and synthesized by connecting 2, 5-dicarboxyphenylboronic acid with lanthanide metal ions (Eu < 3 + > and Dy < 3 + >) in the luminous MOFs gel has the characteristic of specifically recognizing a lysozyme target object.

The invention discloses a preparation method of a colorful and white-light long-afterglow luminescent material and full-color display application thereof.The preparation method of the long-afterglow luminescent material comprises the steps that a luminous body solution is dropwise added to a polymer matrix, hot pressing is conducted at the temperature of 190-210 DEG C for at least 5 minutes, cooling is conducted to the room temperature, and the long-afterglow luminescent material is obtained, the luminous body solution comprises luminous small molecules and a solvent, the luminous small molecules are one or a mixture of more of sarranine, coumarin and acridone, the polymer matrix comprises a polymer, and the polymer is a styrene-acrylonitrile copolymer. The white light afterglow luminescent material with chromaticity coordinates closer to standard white light can be obtained only by taking sarranine, coumarin and acridone as luminescent micromolecules without complicated energy transfer while colorful afterglow luminescence is induced.

A luminophore has the general formula EA2−xRExSi5−x−yAlx+yN8−yOy:A, where0<x≤2 and 0≤y≤2, EA is an element or a combination of elements from the group of alkaline earth elements, RE is an element or a combination of elements from the group of rare earth elements, and A is an activator element. A method for the production of a luminophore and a radiation-emitting component are further disclosed.

The invention discloses a method for obtaining circularly polarized luminescence by covalently anchoring a chiral liquid crystal through light-induced anthraquinone molecules. The method comprises the following steps: S1, adding a solution of a chiral dopant into nematic liquid crystals, stirring until the solution is transparent, and obtaining a binary assembly after a solvent is volatilized; s2, adding a solution of an achiral object into the binary assembly, and volatilizing the solvent to obtain a ternary cholesteric liquid crystal assembly; the achiral guest is a polycyclic conjugated quinone derivative. Under the induction of 365nm ultraviolet light, a diaryl acetylene part and anthraquinone molecules in the ternary cholesteric liquid crystal assembly are covalently bound, so that a new luminous body with a green emission color is formed, and the luminous body generated in situ is well arranged in an original liquid crystal and is beneficial to generating nearly pure circularly polarized light; more importantly, a new method is provided for construction of the circular polarization luminescent material through the non-covalent doping-covalent anchoring mode.

This invention discloses the construction and application of a biosensor based on autocatalytic induced emission amplification and a bifunctional peptide, belonging to the fields of electrochemiluminescence, sensing analysis, and nanomaterials technology. In this invention, by integrating recognition (HWRGWV), charge neutralization (DE), antifouling (DKDKDKDKDK), and anchoring (C) fragments, a bifunctional peptide with antibody-targeted immobilization and interfacial anti-adsorption properties was designed, improving the target capture efficiency and antifouling capability at the interface. Simultaneously, AuAgTb-MOF with a synergistic amplification effect was developed as the luminescent agent. Specifically, 3,5-dicarboxyphenylboronic acid is used to enhance the Tb... 3+ Antenna effect and Ag NPs on S2O8 2‑ The catalysis significantly promoted the luminescence of AuAgTb-MOF. The intramolecular self-enhanced design of AuAgTb-MOF not only reduced energy transfer loss but also simplified the construction of the biosensor. Based on this, the constructed biosensor exhibited a fluorescence intensity of 3.38 × 10⁻⁶. ‑5 The low detection limit of U / mL enables sensitive and accurate detection of the biomarker carbohydrate antigen 242, providing a positive reference for the clinical diagnosis of pancreatic cancer.

The application belongs to the technical field of organic luminescent materials, and discloses a near-infrared organic scintillator material and a preparation method thereof. Based on the phosphorescence resonance energy transfer mechanism, the application uses an organic phosphorescence scintillator o-ITC crystal as an energy donor, and a near-infrared fluorescent luminophore RB or BBT-TPA as an energy acceptor. The near-infrared fluorescent luminophore material is dissolved in an organic solvent, and then the organic phosphorescence scintillator is added. The solvent is removed under specific conditions using a vacuum rotary evaporator, and finally the near-infrared organic scintillator material RB@o-ITC and BBT-TPA@o-ITC is obtained. The material effectively prolongs the luminescence wavelength of the organic scintillator. The maximum radiation luminescence wavelength of the BBT-TPA@o-ITC material reaches 920 nm, and the material has a wide application prospect in the fields of X-ray imaging, organic light-emitting diodes, biological imaging, advanced encryption and anti-counterfeiting, information storage and the like.

The invention discloses an electrochemical luminescence biosensor based on a functionalized nuclear track membrane. According to the electrochemical luminescence biosensor, a nuclear track membrane is used as a substrate, and terpyridyl ruthenium functionalized silver nanoparticles are modified in nanometer pore channels of the nuclear track membrane and are used as ECL illuminants; a gold nano layer is loaded on the outer surface of the nuclear track membrane through a spin-coating method, and a trialkali matrix consisting of a dopamine aptamer and an auxiliary chain containing a hydrophobic group is fixed. When the dopamine is combined with the main chain of the aptamer, the structure of the trialkali matrix is unwound to release an auxiliary chain, the hydrophobic barrier is eliminated, so that the nano pore channel is converted into an open state from a closed state, and the material in the pore channel is in contact with a co-reactant tripropylamine (TPrA) in the electrolyte to generate a remarkably enhanced ECL signal. The dopamine concentration is in a good linear relationship with the ECL strength in a range of 0.1 nM to 10 mu M (R2 is equal to 0.995). According to the sensor, the interface stability is enhanced through the gold nanolayer, the recognition precision is improved through the aptamer, the pore permeability is dynamically regulated and controlled through the hydrophobic group, and high-selectivity detection of dopamine is achieved.

The present invention discloses a fluorescent probe for detecting H2O2. The probe is constructed with silicon rhodamine as the parent body and phenylborate structure as the recognition group. In the presence of H2O2, H2O2 first coordinates with the boron atom, and then oxidizes the B-C bond to form borate, which can be rapidly hydrolyzed in water, simultaneously releasing the silicon rhodamine luminophore. The free silicon rhodamine dye emits red fluorescence through excitation, thereby achieving the purpose of detecting H2O2. The fluorescent probe for detecting H2O2 in the present invention has the structure shown in Formula I: #imgabs0#