Shift Of Emission Wavelength Research Articles

Effect of varying threading dislocation densities on the optical properties of InGaN/GaN quantum wells with intentionally created V-shaped pits

The effect of varying threading dislocation densities on the internal quantum efficiencies (IQEs) of InGaN quantum wells (QWs), with and without intentionally created “V-pits,” is reported here. InGaN QW samples grown on GaN-on-sapphire templates with threading dislocation densities of <1 × 108 and <1 × 109 cm−2 are compared, with and without GaN/InGaN superlattice (SL) layers incorporated to intentionally open up the threading dislocation cores and form large-size “V-pits.” The formation of “V-pits” is confirmed by cross-sectional transmission electron microscopy to initiate from threading dislocations in the SL layers. The densities of the pits are confirmed by plan-view SEM to agree with the substrate threading dislocation densities. The experimental room temperature IQEs of the “V-pit” QW samples are enhanced to 15% ± 1% compared to 6% ± 2% for conventional QW samples. Both conventional and “V-pit” samples show insensitivity to the magnitude of the dislocation densities with respect to IQE performance, while the “V-pit” samples show shifts in the peak emission wavelengths compared to the conventional samples, attributed to strain modulation. This study provides additional understanding of the causes of the observed insensitivity of the IQEs to different threading dislocation densities.

Research on the influence of various factors on the fluorescence function of silver nanoclusters as biomarkers

This review focuses on the impact of numerous conditions on the fluorescence function of silver nanoclusters (AgNCs) as biomarkers. Factors such as particle size, structure and different ligand types are explored. First off, differential stability, sensitivity, cellular uptake, and biodistribution as well as red or blue shifts in absorption and emission wavelengths are caused by varied particle sizes. Furthermore, in the context of detecting microRNA using AgNC-based probes, the presence of a mismatched self-dimer structure is also crucial for achieving a significant red emission. In the final section, the considerable influence of ligandsdivided into primary and secondary ligandson the photoluminescence (PL) characteristics of atomically accurate AgNCs is examined with a focus on Ag29 nanoclusters.

Eosin-Y containing electrospun fibers for optical ammonia sensing based on wavelength shift

Sensors in recent days have been in great demand in industrial zones of simple, low-cost sensors for effectively sensing various gases. This research work develops electrospinning fibers for optical ammonia sensing based on the wavelength shift. The optical sensing fibers were produced approach by the electrospinning technique. The addition of cellulose acetate (CA) matrix with doped Eosin-Y is an NH3 fluorophore. The same light emitting diode (LED) light source was used to excite NH3-sensitive dyes at 380 nm peak wavelength. Display the eosin Y emission spectrum, with a maximum wavelength of 582 nanometers. The observed red emission wavelength shift and fluorescence intensity at 582 nm decreased with increasing concentrations of NH3. The emission spectrum of eosin-Y fluorescence at 582 nanometers is changed with increasing NH3 concentrations ranging from 0 to 500 parts per million. In this work, according to the experiment results, the sensitivity of NH3 sensors is 7.73. Finally, the electrospinning fibers for optical NH3 sensing developed as a result of this research enable effective sensing of NH3 concentrations in practical applications in a variety of fields, including medical and industrial.

A D-π-A-based near-infrared fluorescent probe with large Stokes shift for the detection of cysteine in vivo

D-π-A dyes are an ideal strategy for building near-infrared fluorescent probes that have a large Stokes shift due to their excellent properties of adjustable emission wavelength and Stokes shift. Developing a near-infrared (NIR) fluorescent probe (JTPQ-Cys) capable of detecting cysteine (Cys) was the aim of this study. In JTPQ-Cys, julolidine served as the electron donor (D) and quinoline as the electron acceptor (A), with 3,4-ethylenedioxythiophene as the π-bridge. The π-conjugation and vibrational/rotational activity of the molecule were increased by the introduction of 3,4-ethylenedioxythiophene, causing the molecule to exhibit NIR emission and a large Stokes shift. When JTPQ-Cys was used to detect Cys, a clear fluorescence turn-on signal was observed at 741 nm, together with a Stokes shift of 268 nm. The limit of detection of JTPQ-Cys for Cys is 24 nM. Moreover, JTPQ-Cys has been utilized successfully for imaging studies of Cys in cells and zebrafish because it has good photostability, low cytotoxicity, and a high signal-to-noise ratio. Overall, our findings demonstrate the potential of JTPQ-Cys to be one of the best choices for detecting Cys in biological systems, and JTPQ is an ideal fluorophore to construct fluorescence dyes for bioimaging.

Development of a Ratiometric Fluorescent Cu(II) Indicator Based on Poly(N-isopropylacrylamide) Thermal Phase Transition and an Aminopyridyl Cu(II) Ligand.

An aqueous Cu2+ and Zn2+ indicator is reported based on copolymerizing aminopyridine ligands and the environment-sensitive dansyl fluorophore into the responsive polymer poly(N-isopropylacrylamide) (PNIPAm). The metal ion binding creates charge and solvation that triggers PNIPAm's thermal phase transition from hydrophobic globule to hydrophilic open coil. As a basis for sensing the metal-binding, the dansyl fluorescence emission spectra provide a signal at ca. 530 nm and a signal at 500 nm for the hydrophobic and hydrophilic environment, respectively, that are ratiometrically interpreted. The synthesis of the title pyridylethyl-pyridylmethyl-amine ligand (acronym PEPMA) with a 3-carbon linker to the copolymerizable group, aminopropylacrylamide (PEPMA-C3-acrylamide), is reported, along with a nonpolymerizable model ligand derivative. The response of the polymer is validated by increasing temperature from 25 °C to 49 °C, which causes a shift in maximum emission wavelength from 536 nm to 505 nm, along with an increase in the ratio of emission intensity of 505 nm/536 nm from 0.77 to 1.22 (λex = 330 nm) as the polymer releases water. The addition of divalent Cu or Zn to the indicator resulted in a dansyl emission shift of 10 nm to a longer wavelength, accompanied by fluorescence quenching in the case of Cu2+. The addition of EDTA to the Cu2+-loaded indicator reversed the fluorescence shift at 25 °C to 35 °C. The affinities of Cu2+ and Zn2+ for the PEPMA derivatives are log Kf = 11.85 and log Kf = 5.67, respectively, as determined by potentiometric titration. The single-crystal X-ray structure of the Cu2+-PEPMA derivative is five-coordinate, of-geometry intermediate between square-pyramidal and trigonal-bipyramidal, and is comparable to that of Cu2+ complexes with similar formation constants.

Synthesis of Carbon Dot Nanoparticles (C-Dot) from Seeds and Seedpods of Kesumba Keling (Bixa orellana) using Hydrothermal and Solvothermal Methods

C-dot is a 0-dimensional nanoparticle with photoluminescence properties and can be synthesized from plants, such as the Kesumba Keling plant. Kesumba Keling contains a red pigment sourced from the bixin and norbixin dyes containing functional groups like ‒COOH and ‒COO‒. These functional groups are anticipated to enhance the luminescence intensity produced by C-dot. This research focuses on synthesizing C-dots from Kesumba Keling seeds and seedpods using hydrothermal and solvothermal methods. It also involves an analysis of how different solvents and passivation agents affect the luminescence of C-dots, along with a comparison of the resulting fluorescent colors. The highest yield, at 73.26%, was achieved when using Kesumba Keling seedpods and ethanol as the solvent without adding urea. Furthermore, C-dots synthesized using ethanol as the solvent display a stronger luminescent glow compared to those produced using double-distilled water as the solvent. Additionally, all C-dots synthesized in this study emit a blue luminescence. Characterizing C-dots using a UV-Vis spectrophotometer reveals absorption peaks at two different wavelengths: 260‒280 nm and 320‒340 nm. These absorption peak results align with C-dot characteristics, as confirmed by Fourier transform infrared spectrophotometry. When comparing the intensity of C-dots, those derived from Kesumba Keling peel using the double-distilled water solvent with the addition of urea exhibit a higher intensity (measuring at 0.99) than C-dots obtained from Kesumba Keling peel using ethanol as a solvent with added urea. The solvothermal method is deemed the most effective for C-dot synthesis, as it yields the highest luminescence intensity, accompanied by an emission wavelength shift to 491.65 nm.

Visualization Tools for Detecting Microcystin-LR in the Biological System via Near-Infrared Fluorescent Probes.

Numerous toxicological and epidemiological studies have shown that microcystin-LR (MC-LR) could cause a variety of toxicity to humans and animals. However, the absence of effective methods to trace MC-LR in biological systems has hindered the in-depth understanding of the mechanism of MC-LR toxicity. Near-infrared (NIR) fluorescent probes are crucial tools for accurate visualization and in-depth study of specific molecules in biological systems. Due to the lack of effective design strategies, NIR fluorescent probes for imaging MC-LR specifically in biological systems have not been reported yet. In order to address this pressing issue, herein, we have introduced a new and facile strategy to improve MC-LR detection and imaging in biological systems, and based on this design strategy, three NIR fluorescence probes (MC-RdTPA1, MC-RdTPA2, and MC-RdTPE1) have been constructed. These probes have several advantages: (i) have long emission wavelength and large Stokes shifts, which have great potential in vivo imaging applications; (ii) could selectively visualize MC-LR in cells; and (iii) showed stable fluorescence intensity in the pH range of 5.0-7.0. This work may provide a new avenue for the detection of MC-LR in biological systems and new tool to advance our knowledge of the mechanism of MC-LR toxicity.

Understanding Oligonucleotide Hybridization and the Role of Anchoring on the Single-Walled Carbon Nanotube Corona Phase for Viral Sensing Applications

Semiconducting single-walled carbon nanotubes (SWCNTs) with tailored corona phases (CPs), or surface adsorbed molecules, have emerged as a promising interface for sensing applications. The adsorption of an analyte can be specifically transduced as a modulation of their band gap near-infrared (nIR) photoluminescence (PL). One such CP ideal for this purpose is single-stranded DNA (ssDNA), where subsequent sequence dependent hybridization can result in PL emission wavelength shifts. Due to ssDNA adsorption to the SWCNT surface, the resultant non-canonical hybridization and its effect on SWCNT photophysical properties are not well understood. In this work, we study 20- and 21-mer DNA and RNA hybridization on the complementary ssDNA-SWCNT CP in the context of nucleic acid sensing for SARS-CoV-2 sequences as model analytes. We found that the van’t Hoff transition enthalpy of hybridization on SWCNT CP was -11.9 kJ mol-1, much lower than that of hybridization in solution (-707 kJ mol-1). We used SWCNT solvatochromism to calculate the solvent exposed surface area to indicate successful hybridization. We found that having a 30-mer anchor region in addition to the complementary region significantly improved PL response sensitivity and selectivity, with (GT)15 anchor preferred for RNA targets. Coincubation of ssDNA-SWCNT with analyte at 37°C resulted in faster hybridization kinetics without sacrificing specificity. Other methods aimed to improve CP rearrangement kinetics such as bath sonication and surfactant additions were ineffective. We also determined that target sequence choice is important as secondary structure formation in target is negatively correlated with hybridization. Best performing CPs showed detection limits of 11 nM and 13 nM for DNA and RNA targets respectively. Finally, we simulated sensing conditions using saliva environment, showing sensor compatibility in biofluids. In total, this work elucidates key design features and processing to enable sequence specific hybridization on ssDNA-SWCNT CP.

Study on the influence of chain extension and substituent position on charge transport properties and optoelectronic properties based on 2,5-di(pyrazine-2-yl)furan derivatives

In this paper, the basic structure of 2,5-di(pyrazine-2-yl)furan (DPF) was initially designed to tune the charge transport properties and photoelectric properties of organic materials by chain extension. Through the calculation of recombination energy, the structure with the introduction of anthracene group (DPF-A) is a stable P-type material with the smallest recombination energy in terms of adiabatic ionization potential, so the chain extended molecule DPF-A was selected as the base for the study of substituent positions. While thiophene, trifluorinated acyl, and methoxy groups were introduced to design DPF-A series derivatives. Density functional theory with high computational accuracy was applied to investigate geometric structure, orbital energy levels, ionization energy, electron affinity energy, and recombination energy. The results show that the increase (decrease) of the HOMO (LUMO) energy level leads to the red (blue)-shift of absorption wavelength and fluorescence emission wavelength; the vertical ionization potential decreases and the vertical electron affinity potential increases, thus the hole and electron injection barrier decreases; the decrease of the hole/electron recombination energy improves the charge transport ability of the molecule. Moreover, the adjustment of thiophene orientation and the position of the introduced group has the potential to transform the p-type material into an n-type material, resulting in the enhanced electron injection ability.

Near-infrared electrochemiluminescence of carbon nitride quantum dots for ultrasensitive microRNA assay

Herein, carbon nitride quantum dots (CNQDs) with efficient near-infrared electrochemiluminescence (NIR-ECL) and excellent biocompatibility were prepared as an emitter to construct an ultrasensitive regenerative biosensing platform for detection of microRNA-222 (miRNA-222). Impressively, the introduction of electron-rich pyrimidine effectively increased the conjugation effect of electrons on triazine ring in CNQDs to result in red shift of ECL emission wavelength from 483 nm to 690 nm with the increase of pyrimidine. Meanwhile, an improved circular DNA walker was assembled by the catalytic ligation of T4 DNA ligase instead of traditional base complementary pairing, which enhanced the stability of circular DNA walker to increase walking efficiency. Based on CNQDs as emitter and circular DNA walker as signal amplifier, a regenerative biosensor platform was prepared to achieve the ultrasensitive detection of miRNA-222 with the limit of detection of 2.39 aM and it was successfully applied for sensitive detection of miRNA-222 in the lysate of cancer cells. This work opened a promising road for synthesizing efficient NIR-ECL CNQDs to reduce damage to organisms and achieve deeper tissue penetration and provided a new method for biomarker detection and disease diagnosis.

Design of Polarity-Dependent Immunosensors Based on the Structural Analysis of Engineered Antibodies.

"Reagentless" immunosensors are emerging to address the challenge of practical and sensitive detection of important biomarkers in real biological samples without the need for multistep assays and user intervention, with applications ranging from research tools to point-of-care diagnostics. Selective target binding to an affinity reagent is detected and reported in one step without the need for washing or additional reporters. In this study, we used a structure-guided approach to identify a mutation site in an antibody fragment for the polarity-dependent fluorophore, Anap, such that upon binding of the protein target cardiac troponin I, the Anap-labeled antibody would produce a detectable and dose-dependent shift in emission wavelength. We observed a significant emission wavelength shift of the Anap-labeled anti-cTnI mutant, with a blue shift of up to 37 nm, upon binding to the cTnI protein. Key differences in the resulting emission spectra between target peptides in comparison to whole proteins were also found; however, the affinity and binding characteristics remained unaffected when compared to the wild-type antibody. We also highlighted the potential flexibility of the approach by incorporating a near-infrared dye, IRDye800CW, into the same mutation site, which also resulted in a dose-dependent wavelength shift upon target incubation. These reagents can be used in experiments and devices to create simpler and more efficient biosensors across a range of research, medical laboratory, and point-of-care platforms.

A micrometric deflection fiber laser sensor controlled by polarized light pumping

This work presents a study of a deflection laser sensor using a pump light source with different polarization states and shows that controlling the polarization state of the pump source can achieve better control in the tuning of an erbium-doped fiber laser. Laser tuning uses a selective wavelength filter manufactured using a thin core fiber section between two single-mode fibers, while the deflection is applied using an angular mechanism. In addition, the sensor was analyzed according to the wavelength shift of the laser emission as a function of the angular micrometric deflection, and a sensitivity of −33.01 pm µrad−1 was obtained in a dynamic range from 0 to 89.3 µrad with an adjustment parameter R 2 = 0.993 61. We achieved dual-wavelength tuning with gradual shifting and single-wavelength tuning from 1531.5 nm to 1547.7 nm. This sensor exhibits potential applications in the bionic and robotic detection fields owing to its high sensitivity, good linearity, simple fabrication, and low cost.

Preparation of full-color carbon quantum dots with multiple emission centers

In recent years, carbon dots have attracted more and more attention due to their unique advantages, but there has been a great controversy about the study of their mechanism. A clear mechanism is of great importance for the structural design of carbon dots. To investigate the photoluminescence mechanism of carbon dots, full-color carbon dots with multiple emission centers were successfully prepared by using citric acid and water-soluble aniline blue. It is shown that the red shift of emission wavelength is attributed to the synergistic effect of N and O-related surface functional groups and quantum size. The successful preparation of cold white light diodes from mixed trichromatic carbon dots indicates that this type of carbon dot has important applications in light-emitting devices.

Stimuli-Responsive π-Conjugated Polymers Showing Solid-State Emission Based on Boron-Fused Azomethine Complexes with NNO-Tridentate Ligands.

We report stimuli-responsive luminescent π-conjugated polymers involving the boron-fused azomethine (BAm) structure with the NNO-tridentate ligands and demonstrate their application to film-type sensors. The acid-responsive properties of the polymers are provided by the free lone-pair electrons of the nitrogen atom on the BAm unit. The polymer films showed red shifts in emission wavelengths under acid vapor, and the responses were reversible and corresponded to deprotonation. Furthermore, owing to environmental sensitivity in the film state, unique luminescent color changes were observed. The bilayer films of the BAm polymer coated by poly(n-butyl methacrylate) exhibited vapochromic luminescence with gradual blue shifts (orange → yellow → green) by vapor annealing with chloroform depending on the exposure time. We demonstrated that these changes were applicable for evaluating solvent-vapor permeability of target membranes. This study shows that nitrogen substitution into existing organic compounds is effective for creating stimuli-responsive materials.

Control of Metal‐Rich Growth for GaN/AlN Superlattice Fabrication on Face‐to‐Face‐Annealed Sputter‐Deposited AlN Templates

GaN/AlN superlattices consisting of few‐monolayer GaN wells have attracted considerable attention for use in deep‐ultraviolet (DUV) light‐emitting devices. To avoid the formation of droplets and AlGaN interface layers, precise growth control is essential for fabricating superlattices with flat and abrupt interfaces. Herein, GaN/AlN superlattice structures are grown on face‐to‐face‐annealed sputter‐deposited AlN (FFA Sp‐AlN) template substrates using radio‐frequency plasma‐excited molecular beam epitaxy (RF‐MBE) utilizing in situ reflection high‐energy electron diffraction (RHEED) monitoring. Both AlN and GaN are grown under metal‐rich conditions, and subsequently, the droplets are eliminated by droplet elimination by radical beam irradiation (DERI) method for AlN and by growth interruption for GaN. Furthermore, the dependence of AlN thickness on the properties of superlattices is investigated. The AlN thickness changes linearly with the supply time of the Al metal; thus, the AlN thickness is easily controllable. A total of 20‐period GaN/AlN superlattices with flat and abrupt interfaces is fabricated, as confirmed using atomic force microscopy and X‐ray diffraction. Cathodoluminescence with a peak wavelength of 230–260 nm at room temperature is obtained from the fabricated superlattices. Moreover, the emission wavelength shifts with an increase in AlN thickness.

Nonvolatile Tunable Wavelength‐Selective Emitter with Phase‐Changing Material Ge2Sb2Te5 Designed by Bayesian Optimization Method

The ability to tune the emission wavelength of infrared emitter while maintaining wavelength‐selectivity remains a challenge. By incorporating the nonvolatile phase‐changing material Ge2Sb2Te5 (GST), a nonvolatile tunable wavelength‐selective emitter (gold (Au)‐GST‐Au structure) based on Fabry–Perot (FP) resonance theory is demonstrated. An algorithm based on Bayesian optimization (BO) and transfer matrix method (TMM) for optimal design is proposed. First, the influence of amorphous proportion on tunability is investigated. It is found that the peak emission wavelength shifts from 5.3 to 3.8 μm and peak emissivity increases from 0.75 to 0.98 with an increase of the amorphous proportion. Second, the influence of the thickness of the top and middle layer on the emission spectrum is studied. It is illustrated that the thickness of each layer has a significant impact on the emission spectrum. Finally, an objective function considering wavelength‐selectivity in atmospheric and nonatmospheric windows as well as tunability is proposed. The optimal structure can be realized within calculations for less than 0.027% of total candidate structures. When the weight w = 0, the optimal structural parameters are dAu = 0.0018 μm and dGST = 0.4318 μm; and the effect of the weight factor in objective function is also investigated.

Red-emitting Styryl-BODIPY dye with donor-π-acceptor architecture: Selective interaction with serum albumin via disaggregation-induced emission

Serum albumin (SA) is an abundant protein in mammalian blood plasma and a biomarker for various diseases, such as cirrhosis or hepatitis in the case of the liver. The research of fluorescent probes for SA based on host-guest interactions provides an opportunity to study the nature of intermolecular interactions and thus reveals the structure information of SA at the molecular level. However, some commercially available fluorescent probes, such as boron dipyrromethenes (BODIPYs) have a general tendency to form aggregates under an aqueous environment, which is a drawback for their use due to the strong quenching of the emission. Additionally, short emission wavelength and small Stokes shift are the other common shortcomings. In this work, we explore this unfavourable property and provide an effective method for developing an “off-on” type probe for SA. A new probe named BOD-Red with red-emitting aggregation/disaggregation characters was then designed, consisting of donor-π-acceptor (D-π-A) architecture where boron-dipyrromethene (BODIPY) core as electron acceptor and N-phenylpiperazine as electron donor. The extended π-conjugation system provides not only the increase of emission wavelength due to the enhancement of intramolecular charge transfer strength, but also forms a higher rigid coplanar backbone, which can modulate the photophysical properties and aggregation process. Furthermore, the incorporated N-(2-hydroxyethyl) piperazine group behaves as a SA-binding receptor. BOD-Red formed aggregates in an aqueous solution and was non-emissive. In the presence of SA, it exhibited a pronounced enhancement of emission intensity centred at 630 nm owing to the disaggregation-induce emission. Notably, this probe in solution was non-responsive to any other tested proteins and small molecules. The mechanism responsible for the binding of BOD-Red with BSA was analyzed by a combined experimental and computational approach. The practical utility of BOD-Red as a fluorescent turn-on sensor was validated by quantifying BSA in real samples with reasonable recovery percentages.

Emission peak shifted incoherent random laser through the combined effects of coupling of surface plasmons in a triangular shaped silver nanostructure, microbubbles, and the waveguiding mechanism

The random laser (RL) is now becoming an essential tool for various photonics applications, and a plethora of research advancements in RL coupled with developments in the field of techniques of syntheses of various nanostructured materials is taking place. But the realization of tuning the peak emission wavelength of RL is still very challenging. However, in this report we have demonstrated an emission peak shifted tunable low threshold incoherent RL in the visible region in a gain medium of a commercially available dye laser material and by employing the rarely used scatterer materials of triangular silver nanoparticles (TSN), microbubbles, and the waveguiding mechanism. The scattering properties of trapped microbubbles, along with the localized surface plasmon resonance property of TSN of appropriate concentration within waveguided thin films composed of glass substrates, have been methodically investigated to demonstrate the reduction in lasing threshold and tunability in the peak emission wavelength. A two-fold reduction in RL threshold by addition of TSN in the disordered system, along with a considerable narrowing down of the emission spectra to a few nanometers, are obtained. Furthermore, the peak emission wavelength shift of 6 nm is reported by suitably changing the system configuration by the addition of an optimum concentration of TSN along with trapped microbubbles. The as-developed system shows high-quality laser performance with the maximum value of η=0.64, a quantity describing the ratio of the number of stimulated radiative photons within RL and the total number of emissive photons. We propose that the total internal reflections from the microbubble surface, along with plasmonic enhancement and scattering from the TSN, mediate the waveguided RL to achieve the low threshold. Therefore, this report is an early step towards demonstrating efficient RL in a ternary scattering system. Many more avenues for investigating this developing research issue may be helpful for the future development of affordable and robust optoelectronic devices.

CuInS2 Nanocrystals Embedded PMMA Composite Films: Adjustment of Polymer Molecule Weights and Application in Remote-Type White LEDs.

The commercial application of colloidal semiconductor nanocrystals has been realized owing to the development of composite film technology. Here, we demonstrated the fabrication of green and red emissive CuInS2 nanocrystals embedded polymer composite films of equal thickness by using a precise solution casting method. The impacts of polymer molecular weight on the dispersibility of CuInS2 nanocrystals were then systematically studied through evaluating the decrease in transmittance and red shift of emission wavelength. The composite films made from PMMA of small molecular weights exhibited higher transmittance. Applications of these green and red emissive composite films as color converters in remote-type light-emitting devices were further demonstrated.

Detection and Bioimaging of Glutathione in Cells via a Turn-On Near-Infrared Fluorescent Nanoprobe Composed of Ag2S Quantum Dots and CoOOH Nanosheets

The variations of the microenvironment in cells are always associated with changes in the concentrations of some active species. However, visual detection of these species is still a challenge. In this work, near-infrared (NIR)-emitting fluorescent Ag2S quantum dots (Ag2S QDs) were synthesized via a rapid microwave reaction under normoxic conditions, which were utilized as sensitive fluorescent nanoprobes in sensing and bioimaging of glutathione (GSH) combined with CoOOH nanosheets (CoOOH NSs). The negatively charged Ag2S QDs can easily and effectively attach to the surface of CoOOH NSs to form the Ag2S QD/CoOOH nanoprobe through electrostatic interactions, accompanied by the quenching of the fluorescence of Ag2S QDs at 685 nm via the inner-filter effect (IFE). However, upon the addition of GSH, the fluorescence of Ag2S QDs was recovered due to the reduction of CoOOH NSs into Co2+ by GSH. Meanwhile, the fluorescent emission wavelength shifts slightly, which may result from the ligand exchange reaction between GSH and d-penicillamine (DPA) to form comodified Ag2S QDs. Based on the low toxicity and high tissue penetration depth of the NIR fluorescence of the Ag2S QDs and the good biocompatibility of CoOOH NSs, the nanoprobe composed of Ag2S QDs and CoOOH NSs was successfully applied in bioimaging, which can distinguish the normal cells and cancer cells, the semiquantitative content of endogenous and exogenous GSH. The as-developed strategy not only provides a simple, convenient, cost-effective, and rapid platform for the diagnosis of clinical diseases related to GSH but shows great prospects in fluorescence-assisted surgery.