Excitation Spectra Research Articles

A dual-signal ECL-RET immunosensor based on VC-g-C3N4 and Ru-Zr-MOF for the detection of β2-MG

This work proposes a novel dual-signal electrochemiluminescence (ECL) immunosensor based on energy resonance transfer (RET) for the detection of β2-Microglobulin (β2-MG). Introducing carbon vacancy into g-C3N4 (VC-g-C3N4) can lead to the narrowing of the band gap and the reduction of LUMO, thereby significantly enhancing the ECL efficiency of the material. Meanwhile, Zr-MOF can effectively load Ru(bpy)32+ (Ru-Zr-MOF), enabling its stable existence on the electrode. The ECL emission spectrum of VC-g-C3N4 overlaps well with the fluorescence excitation spectrum of Ru-Zr-MOF, indicating an effective ECL-RET effect between them. As the concentration of β2-MG increases, the intensity of anodic ECL signal gradually increases, while the intensity of cathodic ECL signal gradually decreases. The difference between the cathodic and anodic ECL signals has a good linear relationship within the concentration range from 0.2 pg/mL to 200 ng/mL, with a detection limit of 27.73 fg/mL. The constructed immunosensor can be used for practical analysis in human serum. The proposed sensor has great potential in clinical detection of β2-MG, providing new insights for biomolecular detection and disease diagnosis.

Quantifying spin contamination in algebraic diagrammatic construction theory of electronic excitations.

Algebraic diagrammatic construction (ADC) is a computationally efficient approach for simulating excited electronic states, absorption spectra, and electron correlation. Due to their origin in perturbation theory, the single-reference ADC methods may be susceptible to spin contamination when applied to molecules with unpaired electrons. In this work, we develop an approach to quantify spin contamination in the ADC calculations of electronic excitations and apply it to a variety of open-shell molecules starting with either the unrestricted (UHF) or restricted open-shell (ROHF) Hartree-Fock reference wavefunctions. Our results show that the accuracy of low-order ADC approximations [ADC(2) and ADC(3)] significantly decreases when the UHF reference spin contamination exceeds 0.05a.u. Such strongly spin-contaminated molecules exhibit severe excited-state spin symmetry breaking that contributes to decreasing the quality of computed excitation energies and oscillator strengths. In a case study of phenyl radical, we demonstrate that spin contamination can significantly affect the simulated UV/Vis spectra, altering the relative energies, intensities, and order of electronic transitions. The results presented here motivate the development of spin-adapted ADC methods for open-shell molecules.

Crystal Growth and Spectroscopy of Yb2+-Doped CsI Single Crystal

The single crystals of CsI-Yb2+ were grown, and their spectroscopic studies were conducted. The observed luminescence in CsI-Yb2+ is due to 5d–4f transitions in Yb2+ ions. Using time-resolved spectroscopy, spin-allowed and spin-forbidden radiative transitions of ytterbium ions at room temperature were found. The excitation spectra of Yb2+ luminescence bands were obtained in the range of 3–45 eV. The mechanism of charge compensation of Yb2+ ions in a CsI crystal was also studied, the spectrum of the thermally stimulated depolarization current was measured, and the activation energies of the two observed peaks were calculated. These peaks belong to impurity–vacancy complexes in two different positions. The charge compensation of Yb2+ occurs via cation vacancies in the nearest-neighbor and next-nearest-neighbor positions.The Yb2+ ions are promising dopants for CsI scintillators and X-ray phosphors in combination with SiPM photodetectors.

Differentiating Nylon Samples with Visually Indistinguishable Fluorescence Using Principal Component Analysis and Common Dimension Partial Least Squares Linear Discriminant Analysis with Synchronous Fluorescence Spectroscopy.

Fluorescence spectroscopy is an attractive candidate for analyzing samples of nylon. Impurities within the polymers formed during the synthesis and processing of nylons give rise to the observed fluorescence, allowing for nylons to be analyzed based on their impurities. Nylons from the same source are expected to display similar fluorescence profiles, and nylons with different fluorescence are expected to be from different sources. This paper investigates an important case where different nylons displayed similar fluorescence, preventing easy discrimination. Samples of Nylon 6 and Nylon 6/12 had visually indistinguishable excitation-emission matrices (EEM), excitation spectra, fluorescence spectra, and synchronous fluorescence spectra at larger Δλ. By collecting synchronous fluorescence spectra at smaller Δλ, additional features in the fluorescence profiles were identified that allowed for some discrimination between the two nylons. Combining the EEM and synchronous fluorescence data with chemometric algorithms provided a clearer differentiation between the two nylons. parallel factor analysis, principal component analysis, and common dimension partial least squares (ComDim-PLS) showed two distinct clusters in the data, with ComDim-PLS providing the greatest distinction between the clusters. The loadings revealed the variables of interest to the ComDim-PLS were the 400 nm and 335 nm bands for all synchronous fluorescence spectra, the 460 nm and 310 nm bands for the Δλ = 20 nm and Δλ = 30 nm synchronous fluorescence spectra, and the 440 nm band for the Δλ = 20 nm synchronous fluorescence spectra. The linear discriminant analysis performed with the PLS data yielded a classification accuracy of 95% with the EEM data and 100% with the synchronous fluorescence data, displaying the power of this technique to differentiate two different nylons with visually indistinguishable fluorescence spectra.

Assessing the Determinants of Cavity Polariton Relaxation Using Angle-Resolved Photoluminescence Excitation Spectroscopy.

The strong coupling of light and matter within electromagnetic resonators leads to the formation of cavity polaritons whose hybrid nature may help certain ground and excited state chemical processes. To help enable the development of polariton chemistry, we have developed and applied a spectroscopic technique to leverage the relatively larger spatial coherence of polaritons to assess the determinants of relaxation in hybrid light-matter states. By exciting the lower polariton (LP) state in cavity samples filled with different metalloporphyrin chromophores, we measured and modeled angle-resolved photoluminescence excitation spectra. Our results suggest that the shortest lived constituent of the LP state characterized by specific Hopfield coefficients limits the light absorption of the intracavity molecules, which we equate with the effective polariton lifetime. Our results suggest that researchers need to consider the lifetimes of both photons and excitons participating in strong light-matter coupling when designing polaritonic systems and the methods they can use to assess the relaxation of polaritonic states.

Effect of different BaO contents on the photoluminescence properties of the Eu2+-doped high thermal stability Sr3−xBaxMgSi2O8 phosphors

In this study, 0.015 Eu[Formula: see text]-doped Sr[Formula: see text]BaxMgSi2O8 ([Formula: see text], 0.3, 0.6, 0.9) were used as compositions to find the effect of BaO content on their photoluminescence excitation (PLE) and photoluminescence emission (PL) properties. They were sintered at 1400°C in a reduction atmosphere of 95% N[Formula: see text]% H2 to form blue phosphors. X-ray diffraction pattern and SEM observation were used to analyze their crystal properties, and a fluorescence spectrophotometer was used to analyze their PLE and PL properties. After conducting a thorough analysis, our research primarily encompasses four significant research themes. First, SEM observations revealed that synthesized Eu[Formula: see text]-doped Sr[Formula: see text]BaxMgSi2O8 phosphors exhibit the formation of whisker-like structures. Therefore, the whisker-like structures in all the Eu[Formula: see text]-doped Sr[Formula: see text]BaxMgSi2O8 phosphors were analyzed using the HRTEM and its equipped EDS to find how BaO content influenced both the quantity and fineness of these whiskers. Second, we examined the impact of BaO content on the PLE and PL emission intensities of the Eu[Formula: see text]-doped Sr[Formula: see text]BaxMgSi2O8 phosphors across a temperature range from room temperature to 210°C. This investigation aimed to uncover the effects of BaO content and temperature on the thermal stability of the Eu[Formula: see text]-doped Sr[Formula: see text]BaxMgSi2O8 phosphors. Lastly, our fourth important investigation involved reorganizing the PLE spectra of the Eu[Formula: see text]-doped Sr[Formula: see text]BaxMgSi2O8 phosphors with the energy band as the x-axis. The Gaussian fitting function was applied to analyze the excitation spectra and discern the influence of BaO content on the value of the Stokes shift.

Dy-Al-Ce codoped silica: a promising yellow laser glass with enhanced resistance to X-ray-induced photodarkening

To develop Dy doped silica glass with a higher irradiation resistance, which can be adapted to high power violet or blue LD pumped yellow laser fibers, the designed Dy-Al-Ce codoped silica glasses, 0.05Dy2O3-1.5Al2O3-xCe2O3-(98.45-x)SiO2 (x = 0, 0.05, 0.1, 0.25, 0.5), were prepared by the sol-gel method. Their excitation spectra, emission spectra and emission decay curves associated with the yellow emission from 4F9/2 to 6H13/2 of Dy were determined before and after the X-ray irradiation of 1000 Gy. The relation between these spectra and Ce-codoping concentrations is discussed, including the sensitization from Ce to Dy, the reverse energy transfer from Dy to Ce, and especially the X-ray-induced photodarkening, which is detrimental to the 576 nm yellow emission of Dy. The centers that cause the photodarkening are analyzed by electron paramagnetic resonance and radiation induced absorption spectra. It is found that Ce can effectively suppress the Al-oxygen hole center induced by the X-ray across the entire concentration range of Ce-codoping, but a new photodarkening center is generated at higher concentrations of Ce-codoping. Finally, the optimized Ce-codoping concentration of ∼0.1 mol% is used to achieve a promising yellow laser glass of Dy-Al-Ce codoped silica with enhanced irradiation resistance, resulting in its X-ray-induced photodarkening that is only 6% - 14% of that in the Ce-undoped.

References for Small Fluorescence Quantum Yields.

Three compounds with fluorescence quantum yields in the range of 10- 5 to 10- 4 and emission spectra covering the UV/Vis spectral range are suggested as new references for the determination of small fluorescence quantum yields. The compounds are thymidine (dT) in water, dibenzoylmethane (DBM) in ethanol, and malachite green chloride (MG) in water, representing the blue, green, and red regions of the spectrum, respectively. All compounds are easily handled, photostable, and commercially available. Furthermore, these compounds exhibit a mirror-image symmetry between their absorption and fluorescence spectra. This symmetry, along with closely aligned fluorescence excitation and absorption spectra, confirms that the observed emissions originate from the compounds themselves. The fluorescence quantum yields were determined via a relative approach as well as Strickler-Berg analysis in conjunction with time resolved fluorescence spectroscopy. Within the respective error margins, the two approaches yielded identical results.

Fano resonance in excitation spectroscopy and cooling of an optically trapped single atom

Electromagnetically induced transparency (EIT) can be used to cool an atom in a harmonic potential close to the ground state by addressing several vibrational modes simultaneously. Previous experimental efforts focus on trapped ions and neutral atoms in a standing wave trap. In this work, we demonstrate EIT cooling of an optically trapped single neutral atom, where the trap frequencies are an order of magnitude smaller than in an ion trap and a standing wave trap. We resolve the Fano resonance feature in fluorescence excitation spectra and the corresponding cooling profile in temperature measurements. A final temperature of around 6 µK is achieved with EIT cooling, a factor of 2 lower than the previous value obtained using polarization gradient cooling. Published by the American Physical Society 2024

Integrating K+ into Eu and Tb doped GdCa4O(BO3)3: A dual study on photoluminescence and structure

In this study, we investigate the structural and photoluminescence (PL) properties of rare-earth-doped GdCa4O(BO3)3 (GdCOB) phosphors, specifically focusing on the spectral behaviour induced by doping with Eu³⁺ and Tb³⁺ ions. The powder X-ray diffraction (XRD) spectra confirm the formation of a monoclinic phase. The XRD data were also refined by a Rietveld refinement method. The existence of B, O, Ca, Gd, Tb, Eu and K elements was verified by EDS spectra. We introduce a detailed examination of the charge compensation process using Kröger-Vink notation to clarify the mechanisms essential for tailoring the optical properties of the phosphors. The PL excitation spectrum of GdCOB:Eu3+, monitored at 611 nm, reveals sharp excitation peaks at 319, 361, 380, and 392 nm, corresponding to 7F0→5H3, 7F0→5D4, 7F0→7F0, and 7F0→5L6 transitions, respectively. The PL spectrum under excitation of 392 nm exhibits that phosphors doped with Eu3+ a significant red emission at 611 nm, which is attributed to the 5D₀→7F₂ transition. This emission intensity is particularly enhanced at non-centrosymmetric sites of the Eu³⁺ ions. Similarly, the PL excitation spectrum of GdCOB:Tb3+, monitored at 552 nm, displays distinct excitation peaks at 316, 341, 353, and 379 nm, which correspond to the transitions 7F₆→5D₀, 7 F₆→5L₇, 7F₆→5D₂, and 7F₆→5D₃, respectively. Tb³⁺-doped phosphors display a bright green emission, with a dominant peak at 552 nm, resulting from the 5D₄→7F₅ transition. Additionally, the introduction of K⁺ ions as co-dopants results in modifications to the local environments of Eu³⁺ and Tb³⁺ ions. These changes allow for fine-tuning of the emission peaks, significantly enhancing the luminescent output of the phosphors. Optimal doping concentrations of 5 mol% for Eu³⁺ and 1 mol% for Tb³⁺ enhance luminescent intensity and prevent concentration quenching. This phenomenon, often resulting in reduced PL intensity at higher dopant levels, is primarily due to dipole-dipole interactions, consistent with Dexter's theory of energy transfer. Strategic modulation of doping concentrations, coupled with a deep understanding of energy transfer mechanisms are critical for the development of advanced luminescent materials Our analysis of the Commission de l′Eclairage (CIE) chromaticity coordinates reveals enhanced energy transfer dynamics in rare-earth-doped borates, facilitating the tuning of luminescent properties. These results not only deepen our understanding of the fundamental physics governing such phosphors but also open pathways for the development of optoelectronic applications requiring consistent color output, such as LED technologies and solid-state lighting.

TWISP: A Transgenic Worm for Interrogating Signal Propagation in C. elegans.

Genetically encoded optical indicators and actuators of neural activity allow for all-optical investigations of signaling in the nervous system. But commonly used indicators, actuators and expression strategies are poorly suited for systematic measurements of signal propagation at brain scale and cellular resolution. Large scale measurements of the brain require indicators and actuators with compatible excitation spectra to avoid optical crosstalk. They must be highly expressed in every neuron but at the same time avoid lethality and permit the animal to reach adulthood. Their expression must also be compatible with additional fluorescent labels to locate and identify neurons, such as those in the NeuroPAL cell identification system. We present TWISP, a Transgenic Worm for Interrogating Signal Propagation, that addresses these needs and enables optical measurements of evoked calcium activity at brain scale and cellular resolution in the nervous system of the nematode Caenorhabditis elegans. We express in every neuron a non-conventional optical actuator, the gustatory receptor homolog GUR-3 + PRDX-2 under the control of a drug-inducible system QF + hGR, and calcium indicator GCAMP6 s, in a background with additional fluorophores of the NeuroPAL cell ID system. We show that this combination, but not others tested, avoids optical-crosstalk, creates strong expression in the adult, and generates stable transgenic lines for systematic measurements of signal propagation in the worm brain.

A (2+1)-dimensional domain wall at one-loop

We consider the domain wall in the (2+1)-dimensional ϕ4 double well model, created by extending the ϕ4 kink in an additional infinite direction. Classically, the tension is m3/3λ where λ is the coupling and m is the meson mass. At order O(λ0) all ultraviolet divergences can be removed by normal ordering, less trivial divergences arrive only at the next order. This allows us to easily quantize the domain wall, working at order O(λ0). We calculate the leading quantum correction to its tension as a two-dimensional integral over a function which is determined analytically. This integral is performed numerically, resulting in −0.0866m2. This correction has previously been computed twice in the literature, and the results of these two computations disagreed. Our result agrees with and so confirms that of Jaimunga, Semenoff and Zarembo. We also find, at this order, the excitation spectrum and a general expression for the one-loop tensions of domain walls in other scalar models.

Analysis of Properties and Macroscopic Defects of Metallic Bars, Pipes, and Strands through the Spectrum of Low-Frequency Excitations.

It is demonstrated that the application of piezoelectric sensors to metallic bars and strands can enable determining the status of the integrity of these elements through the spectrum of their acoustic excitations. The voltage output of the piezo, secured to metal bars or strands, is fed to the input of a Fast Fourier Transform analyzer, which allows displaying the spectrum of the excitations from which information on the length, overall quality of the metal, and the presence of defects can be obtained. We show that the analysis, performed on several materials and strands of different lengths, could be useful for cases in which visible inspection and/or direct access to the entire body of the metallic elements is not possible. Applications of our study for testing metallic structures embedded in concrete foundations are reported for construction sites.

Yield estimation of North Korean underground nuclear tests using Lg-wave source spectra

In seismic nuclear monitoring, attenuation models are important prerequisites for reliably estimating the explosive yield in an uncalibrated region without the occurrence of standard events. The seismic moment obtained by fitting source spectra is related to the source energy. This approach is appropriate for estimating yield, as the attenuation effects on the propagation path can be accurately considered. In this study, we collected 2022 vertical component waveforms in and around the Korean Peninsula from May 2010 to May 2022 to construct a high-resolution broadband Lg-wave attenuation model and inverted the Lg-wave source excitation spectra of the nuclear explosion simultaneously with attenuation correction. We obtained the scalar seismic moments by fitting the theoretical source spectra based on the Brune (J. Geophys. Res., 1970, 75, 4997–5009) model. Under the given emplacement conditions and burial depths, the seismic moments can be used to estimate yields of the North Korean nuclear tests, which are 4.6, 8.5, 19.9, 20.9, 24.7, and 337.4 kt for six nuclear explosions that occurred between 2006 and 2017. Our results are consistent with those obtained from previous teleseismic observations.

ZN lattice gauge theories with matter fields

Motivated by the exotic phenomenology of certain quantum materials and recent advances in programmable quantum emulators, we here study fermions and bosons in ZN lattice gauge theories. We introduce a family of exactly soluble models, and characterize their orthogonal (semi)metallic ground states, the excitation spectrum, and the correlation functions. We further study integrability-breaking perturbations using an appropriately derived set of Feynman diagrammatic rules and borrowing physics associated to Anderson's orthogonality catastrophe. In the context of the ground states, we revisit Luttinger's theorem following Oshikawa's flux insertion argument and furthermore demonstrate the existence of a Luttinger surface of zeros in the fermionic Green's function. Upon inclusion of perturbations, we address the transition from the orthogonal metal to the normal state by condensation of certain excitations in the gauge sectors, so-called “e particles.” We furthermore discuss the effect of dynamics in the dual “m-particle” excitations, which ultimately leads to the formation of charge-neutral hadronic N-particle bound states. We present analytical arguments for the most important phases and estimates for phase boundaries of the model. Specifically, and in sharp distinction to quasi-one-dimensional ZN lattice gauge theories, renormalization group arguments imply that the phase diagram does not include an emergent deconfining U(1) phase in the limit of large number of fermion flavors. Therefore, in regards to lattice QED problems, ZN quantum emulators with N<∞ can at best be used for approximate solutions at intermediate length scales. Published by the American Physical Society 2024

Luminescence studies and Judd Ofelt parameterization of Dy3+ activated La2(WO4)3 yellow phosphor

The synthesis and detailed luminescence studies of a series of La2-xDyx(WO4)3 (x = 0.02, 0.1, 0.2, 0.4, 0.6, 0.8) phosphors synthesized via microwave-assisted co-precipitation technique is reported in this paper. The XRD analysis confirmed that the phosphors were crystalized in a monoclinic structure with space group C2/c and FTIR analysis identified the characteristic vibrational modes. Morphological studies were conducted using FESEM analysis, and the EDS technique substantiated the effective incorporation of Dy3+ ions in La2(WO4)3. The photoluminescence excitation and emission spectra of varying concentrations of Dy3+ ions were recorded and an optimum concentration of 10 % exhibited the highest intensity. The emission spectra of all phosphors were dominated by peaks at 484 nm and 574 nm. The radiative properties were evaluated using Judd-Ofelt analysis and the JO intensity parameters followed the trend Ω2 > Ω6 > Ω4. The gradual decrease in the decay lifetime value of 4F9/2 excited level with an increase in doping concentration elucidates concentration quenching phenomena due to dipole – quadrupole interaction. The emission data were also analyzed by calculating CIE coordinates and concluded that Dy3+ doped La2(WO4)3 phosphors have potential applications in yellow light generation.

PHire: A Novel Red Intracellular pH Sensor

Maintaining pH is critical for proper cellular and organ function. To measure intracellular pH, we made a novel genetically encoded protein, pHire, that increases red fluorescence with increasing pH. Thus, pHire allows for the coupling of multiple fluorescent tags without spectral overlap. We have expressed pHire in mammalian epithelial cells, Drosophila, and mice. In this study, our goal was to characterize pHire’s spectral properties by expression in human cells (HEK293) and in E.coli. To biophysically characterize pHire, we made a maltose binding protein (MBP)-pHire fusion protein to purify from E.coli. Pelleting individual colony growths revealed pink bacterial pellets which fluoresced with mCherry filters. Rather than purifying the MBP-pHire protein, equal volumes of bacteria were permeabilized with nigericin and high K+ solution for pH 5 to 9. These aliquots were then used to gather the fluorescence excitation and emission spectra of pHire, allowing us to determine the excitation and emission peaks of pHire as a function of pH. Our results showed peaks at Ex579 nm and Em611 nm, or roughly mCherry. Pelleted bacteria could also be fixed in perfusion chambers, revealing the same calibration curve as in mammalian cells and flies. Next, stable HEK293-pHire cells were selected to assay acid-base transport using NH4Cl or CO2/HCO3− in perfusion experiments. These HEK-pHire cells have less fluorescence than MBP-pHire bacteria but show the same Ex/Em peaks. However, an in-frame ATG 5’ to pHire in a mouse (adding 23 amino acids), removed pHire pH-dependence and decreased bacterial fluorescent output. Together these results indicate that pHire is biophysically similar in cells tested but that unstructured N-terminal additions block pH-responses. Funding: R25-DK101405, R21-DK129897. This is the full abstract presented at the American Physiology Summit 2024 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.

Orange luminescence of α-Al2O3 related to clusters consisting of F centers and divalent cations.

The orange luminescence of α-Al2O3 under UV excitation is characterized by a 2.07-eV orange broadband emission that has not yet been elucidated. This emission is present in natural and synthetic crystals and powders, as well as in Be-treated samples. All orange-luminescent materials have low Fe concentration (mostly <1000 ppm) with traces of divalent cations, mostly Mg, or Be in Be-diffused material (dozens of ppm). Mg2+, Mn2+, and Be2+ cations substitute for trivalent Al. To accommodate the charge deficit, several defects are created, including oxygen vacancies also called F centers. Indeed, our excitation spectra revealed the presence of several different F centers (F, F+, and clustered F2, F2 +, F2 2+) in those samples. However, the thermal stability and the measured luminescence lifetimes do not match with previously reported characteristics of isolated F centers. Based on our experiments, we suggest that a complex aggregate of two F centers (F2 2+) trapped at divalent cations is a major cause of this uncommon microsecond lifetime emission, even if a variety of other defects, including Cr3+, V3+, or interstitial Al3+, are present.

Luminescent properties and dosimetric behavior of Eu-ion-doped ASO4 (A = Ca, Sr, and Ba)

We investigated the luminescence properties and dosimetric behavior of Eu-ion-doped ASO4 (A = Ca, Sr, or Ba) phosphors synthesized using the coprecipitation method. Structural analysis of the phosphors was performed using X-ray diffraction patterns, which revealed that the prepared samples exhibited a pure phase with diffraction peaks matching those of undoped orthorhombic structures. The luminescence properties of the phosphors were examined by measuring photoluminescence and photoluminescence excitation spectra. We found that both Eu2+ and Eu3+ emissions were detected for A = Ba and Ca, whereas only Eu2+ emission was observed for A = Sr. Further, time-resolved photoluminescence decay curves indicate the presence of Eu2+ and Eu3+ luminescence with different lifetimes. The optically stimulated luminescence (OSL) and thermoluminescence (TL) responses of the samples were investigated. The OSL and TL responses were found to vary linearly with the irradiation dose. This study sheds light on the potential applications of Eu-ion-doped ASO4 phosphors in radiation dosimetry and optoelectronic devices.

Synergistic effect of inner filtering effect and host-guest interaction based on β-cyclodextrin fluorophore for promoted 4-nitrophenol detection

Efficient detection of 4- nitrophenol (4-NP) organic pollutant is always a very important issue due to the rapid development of chemical industry and the abuse of pesticides and so on. Here, we designed and synthesized a novel supramolecular fluorescent probe, 4-[4-(acetylamino)styryl]-1-cyclodextrin pyridinium p-toluenesulfonate (ASPT-β-CD), for the selective and sensitive detection of 4-NP. The introduction of β-CD not only improves the water solubility of probe and can also be used as a host to encapsulate 4-NP. In alkaline aqueous solution, the absorption spectrum of 4-NP overlaps the excitation spectrum of ASPT-β-CD and suggests that an internal filtration effect occurs between them. We explored the possible response mechanism and speculated that the high selectivity and high sensitivity were derived from the synergistic effect of inner filtering effect and host-guest interaction. Benefiting from the synergistic effect, the proposed sensor ASPT-β-CD displayed significant "turn-off" after adding 4-NP, while showing a fast response to 4-NP within 2min and low LOD about 0.01μM. In addition, this method has been successfully applied to the determination of 4-NP in lake water samples, indicating that the obtained ASPT-β-CD has great practical application potential in the environmental field.