Molybdenum Disulfide Nanosheets Research Articles

The production of electrodes for microsupercapacitors based on MoS2-modified reduced graphene aerogels by 3D printing

Micro-supercapacitors (MSCs) are of interest because of their high power density and excellent cycling performance, offering a broad array of potential applications. However, preparing electrodes for the MSCs with an extremely high areal capacitance and energy density remains a challenge. We constructed MSC electrodes with an ultra-high area capacitance and a high energy density, using reduced graphene oxide aerogel (GA) and MoS2 as the active materials, combined with 3D printing and surface modification. Using 3D printing, we obtained electrodes with a stable macrostructure and a GA-crosslinked micropore structure. We also used a solution method to load the surface of the printed electrode with molybdenum disulfide nanosheets, further improving the electrochemical performance. The surface capacitance of the electrode reached 3.99 F cm−2, the power density was 194 W cm−2, and the energy density was 1 997 mWh cm−2, confirming its excellent electrochemical performance and cycling stability. This work provides a simple and efficient method for preparing MSC electrodes with a high areal capacitance and energy density, making them ideal for portable electronic devices.

Interactions of monolayer molybdenum disulfide sheets with metalloid antimony in aquatic environment: Adsorption, transformation, and joint toxicity

The tremendous application potentiality of transitional metal dichalcogenides (TMDs), such as molybdenum disulfide (MoS2) nanosheets, will unavoidably lead to increasing release into the environment, which could influence the fate and toxicity of co-existed contaminants. The present study discovered that 59.8 % of trivalent antimony [Sb(III)] was transformed by MoS2 to pentavalent Sb [Sb(V)] in aqueous solutions under light illumination, which was due to hole oxidation on the nanosheet surfaces. A synergistic toxicity between MoS2 and Sb(III, V) to algae (Chlorella vulgaris) was observed, as demonstrated by the lower median-effect concentrations of MoS2 + Sb(III)/Sb(V) (13.1 and 20.9 mg/L, respectively) than Sb(III)/Sb(V) (38.8 and 92.5 mg/L, respectively) alone. Particularly, MoS2 at noncytotoxic doses notably increased the bioaccumulation of Sb(III, V) in algae, causing aggravated oxidative damage, photosynthetic inhibition, and structural alterations. Metabolomics indicated that oxidative stress and membrane permeabilization were primarily associated with down-regulated amino acids involved in glutathione biosynthesis and unsaturated fatty acids. MoS2 co-exposure remarkably decreased the levels of thiol antidotes (glutathione and phytochelatins) and aggravated the inhibition on energy metabolism and ATP synthesis, compromising the Sb(III, V) detoxification and efflux. Additionally, extracellular P was captured by the nanosheets, also contributing to the uptake of Sb(V). Our findings emphasized the nonignorability of TMDs even at environmental levels in affecting the ecological hazard of metalloids, providing insight into comprehensive safety assessment of TMDs.

Electrodeposition of PdPt Nanoparticles on Edges and S-Vacancies in Exfoliated MoS2 Nanosheets for Enhanced Hydrogen Evolution Activity.

Deposition of metal nanoparticles onto the molybdenum disulfide (MoS2) nanosheets is an efficient method to tune the electronic structure of the MoS2 and maximize its catalytic performance towards the hydrogen evolution reaction (HER). Herein, we report the electrodeposition of Pd and Pt nanoparticles onto desulfurized MoS2 nanosheets (MoS2-x) to achieve an improved HER activity in an acidic electrolyte. The initial MoS2 powder was exfoliated and isolated through centrifugation, followed by electrochemical desulfurization to create defect sites. Subsequently, Pt and Pd nanoparticles were electrodeposited onto the S-vacancies of MoS2-x nanosheets. The resulting PdPt nanoparticles, with a diameter of 3.3 ±1.7 nm, were distributed across the surfaces of the nanosheets. A preferential deposition was evident at the edges of the nanosheets, particularly when Pd was deposited first followed by Pt. Owing to this preferential deposition of Pd and Pt and the synergistic interaction of MoS2-x with Pd and Pt, the prepared catalyst exhibited a low overpotential of 30 mV at 10 mA cm-2, which is 2.7× lower than the MoS2-x alone. The prepared catalyst exhibited a 1.7× increase in the mass activity at 20 mV overpotential, relative to that of a commercial Pt/C nanocatalyst, showcasing its promising potential as an alternative catalyst.

The dependence of electrocatalytic HER activity of decorated MoS2 with Cu nanoclusters

Molybdenum disulfide is a potential electrocatalytic material for water splitting with excellent stability and durability. Here, the electrocatalytic hydrogen evolution reaction performance of Molybdenum disulfide nanosheets decorated with copper nanoclusters was investigated. The Cu@MoS2–1:10 exhibited remarkable hydrogen evolution reaction activity, with an overpotential as low as 150 mV under acidic conditions. The First-principles calculations further confirmed the superior electrocatalytic performance of Cu@MoS2, with a minimum hydrogen adsorption free energy of -0.10 eV. The improved electrocatalytic activity of Cu@MoS2 arises from the accelerated charge migration at the interface. And the addition of Cu increases the number of active sites on the surface of MoS2. This work could offer insights into the advancement of additional non-precious metals and transition metal dichalcogenides.

Ultrahigh Polarization of Emitted Light by Quenched Emissive Material

AbstractThe emission of highly polarized light by organic light‐emitting diodes (OLEDs) is crucial for various applications; however, achieving such emission requires the use of polarizers, which reduce the device efficiency and durability. In this study, ultrahigh‐polarized light with a polarization ratio (PR) of 407:1 is achieved via the rapid thermal quenching (RTQ) of OLEDs. Poly(3,4‐ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) films, molybdenum disulfide (MoS2) nanosheets, and tungsten disulfide (WS2) nanosheets are applied as hole transport layers and surface‐alignment layers through surface treatment, including rubbing and/or ion‐beam exposure to align the molecules of the emissive materials, namely, {poly(9,9‐dioctylfluorene‐alt‐benzothiadiazole) (F8BT). Quenching is performed at 240 °C, at which F8BT has a nematic liquid crystal (NLC) phase with high molecular ordering. Upon quenching, the high molecular ordering of the NLC‐phased emissive layer instantaneously froze via RTQ, leading to the emission of highly polarized light. Consequently, the PEDOT:PSS‐, MoS2‐, and WS2‐based OLEDs exhibit ultrahigh PRs of 407:1, 349:1, and 328:1, respectively, for photoluminescence at a 540 nm peak wavelength. In contrast, for electroluminescence, the PEDOT:PSS‐based OLED exhibits a high PR of 395:1. This result is the best reported to date and is comparable to the PRs generated by polarizers, indicating that quenching can be utilized for the development of ultrahigh‐polarized light‐emitting devices.

Probing Polymorphic Stacking Domains in Mechanically Exfoliated Two-Dimensional Nanosheets Using Atomic Force Microscopy and Ultralow-Frequency Raman Spectroscopy.

As one of the key features of two-dimensional (2D) layered materials, stacking order has been found to play an important role in modulating the interlayer interactions of 2D materials, potentially affecting their electronic and other properties as a consequence. In this work, ultralow-frequency (ULF) Raman spectroscopy, electrostatic force microscopy (EFM), and high-resolution atomic force microscopy (HR-AFM) were used to systematically study the effect of stacking order on the interlayer interactions as well as electrostatic screening of few-layer polymorphic molybdenum disulfide (MoS2) and molybdenum diselenide (MoSe2) nanosheets. The stacking order difference was first confirmed by measuring the ULF Raman spectrum of the nanosheets with polymorphic stacking domains. The atomic lattice arrangement revealed using HR-AFM also clearly showed a stacking order difference. In addition, EFM phase imaging clearly presented the distribution of the stacking domains in the mechanically exfoliated nanosheets, which could have arisen from electrostatic screening. The results indicate that EFM in combination with ULF Raman spectroscopy could be a simple, fast, and high-resolution method for probing the distribution of polymorphic stacking domains in 2D transition metal dichalcogenide materials. Our work might be promising for correlating the interlayer interactions of TMDC nanosheets with stacking order, a topic of great interest with regard to modulating their optoelectronic properties.

Morphological and Optical Characterization of Hydrothermally-Synthesized Two-Dimensional MoS2 Nanosheets

Transition metal dichalcogenides (TMDs) are extensively utilized in optoelectronics, sensors, and battery storage due to their versatile properties. Among the TMDs, Molybdenum disulfide (MoS2) nanosheets possess remarkable optical, electronic, and chemical properties. This study employed a cost-effective hydrothermal method to synthesize high-quality 2D MoS2 nanosheets. Different characterization techniques such as XRD, SEM, EDS, FTIR, Raman, UV–vis, and photoluminescence (PL) spectroscopy were utilized to evaluate the structural, morphological, chemical, and optical characteristics of the nanosheets. The XRD analysis revealed that the MoS2 nanosheets have a hexagonal crystal structure, with an average crystallite size of 27.76 nm. Furthermore, SEM images confirmed the formation of thin MoS2 nanosheets, with an estimated thickness ranging from 20–30 nm. The growth mechanism of the formation of MoS2 is discussed in detail. Different functional groups present in the material were analyzed using FTIR spectra. The difference in vibration modes analysed by Raman spectroscopy indicated the presence of layered nanosheets. The optical bandgap (2.20 eV) of the material was determined by analyzing its UV–vis spectroscopy data using the Tauc plot. PL analysis indicates a direct transition between the upper valence and lower conduction bands, suggesting that the nanosheets were synthesized with high quality. These findings have opened new possibilities for the use of MoS2 nanosheets in various applications such as optoelectronics and sensing devices.

Inkjet-printed thin-film transistors using surfactant-based transition-metal dichalcogenide nanocomposites suspended in polymeric semiconductors

Ink formulations containing a suspension of single-crystalline molybdenum disulfide (MoS2) nanosheets suspended in the polymeric semiconductor poly(3-hexylthiophene-2,5-diyl) (P3HT) were inkjet printed for the fabrication of thin-film transistors (TFT). The MoS2 nanosheets were treated with the surfactant trichloro(dodecyl)silane (DDTS) to functionalize the MoS2 surface and created a more stable suspension, reducing the agglomeration of MoS2 suspended in the P3HT solution. This ink formulation was inkjet printed onto the surface of thermal oxide coated, p+-Si wafers to form common-gate TFT device structures. The printed semiconductor formed the active region of a hybrid MoS2 suspension in P3HT of the TFTs. The field-effect mobility for the hybrid-ink TFTs was found to be three times (3×) higher compared to reference devices using pristine P3HT without the suspension. The functionalized MoS2 suspension was also found to form thinner nanosheet suspensions within the P3HT matrix that resulted in approximately 60% higher field-effect mobility compared to hybrid inks without the surfactant. The enhancement of the electrical properties of the TFTs was determined to be due to a structural change in the thin-film semiconductor. The observed current–voltage (I–V) changes were correlated to measurable structural alterations in the semiconductor thin film characterized by x-ray diffraction, atomic force microscopy, and UV–visible absorption spectroscopy.

Influence of Inorganic Anions on the Chemical Stability of Molybdenum Disulfide Nanosheets in the Aqueous Environment.

Chemical stability is closely associated with the transformations and bioavailabilities of engineered nanomaterials and is a key factor that governs broader and long-term application. With the growing utilization of molybdenum disulfide (MoS2) nanosheets in water treatment and purification processes, it is crucial to evaluate the stability of MoS2 nanosheets in aquatic environments. Nonetheless, the effects of anionic species on MoS2 remain largely unexplored. Herein, the stability of chemically exfoliated MoS2 nanosheets (ceMoS2) was assessed in the presence of inorganic anions. The results showed that the chemical stability of ceMoS2 was regulated by the nucleophilicities and the resultant charging effects of the anions in aquatic systems. The anions promote the dissolution of ceMoS2 by triggering a shift in the chemical potential of the ceMoS2 surface as a function of the anion nucleophilicity (i.e., charging effect). Fast charging with HCO3- and HPO42-/H2PO4- was validated by a phase transition from 1T to 2H and the emergence of MoV, and it promoted oxidative dissolution of the ceMoS2. Additionally, under sunlight, ceMoS2 dissolution was accelerated by NO3-. These findings provide insight into the ion-induced fate of ceMoS2 and the durability and risks of MoS2 nanosheets in environmental applications.

Epitaxial growth of rare-earth yttrium on nanosheets to form semicoherent interface in zinc implant

Molybdenum disulfide (MoS2) nanosheet as nano reinforcement exhibits great advantages in zinc (Zn) implant due to its coordinated crystal slip and grain boundary strain effect. Nevertheless, the poor interface bonding restrains the coordination effect of MoS2. In this work, rare earth yttrium (Y) was used to epitaxial grow on the vacancy nucleation sites of MoS2 plane through a gas phase reduction method, and then introduced into Zn to improve their interface bonding. On one hand, rare earth Y could form a semicoherent interface with Zn due to the similar atomic arrangement and small lattice misfit between (101)Y plane (0.272 nm) and (002)Zn plane (0.248 nm). On the other hand, it could be tightly integrated together with sulfur element of MoS2 via covalent bond. As a result, the plastic strain of composites was improved from 6.1 % to 10.45 %. Simultaneously, the fracture energy was also increased to 201 × 103 J/m2, since rare earth Y considerably promoted load transfer efficiency from Zn matrix to MoS2 and thereby significantly activated slip systems. Encouragingly, the mechanical strength of the Zn-based biocomposite simultaneously reached 273.3 ± 10.9 MPa due to load transfer strengthening and grain refinement.

Mechanisms and effects of amphiphilic lamellar nanofluid for enhanced oil recovery in low permeability reservoirs

Amphiphilic nanosheets have attracted more attention for enhanced oil recovery (EOR) owing to their unique properties. Here, the amphiphilic molybdenum disulfide (MoS2) nanosheets (AP-MDN) were prepared by functionalizing octadecyl amine (ODA) molecules onto the molybdenum disulfide nanosheets (MDN) surfaces. The dynamic stability and interfacial tension (IFT) measurements of AP-MDN nanofluid were evaluated. Besides, the mechanisms and effects of AP-MDN nanofluid for EOR were also systematically investigated and studied. Experimental results indicate that the dynamic stability of AP-MDN nanofluid is improved when MDN is successfully functionalized with ODA molecules. The IFT is decreased to 10-1 mN/m and micron-emulsions ranging from 1 µm ∼ 2 µm can be formed. In addition, the contraction rate of oil film exposed in ultra-low concentration AP-MDN nanofluid (50 mg/L) experiences two stages: a steep stage (8.5817 × 10-5 cm/s) and a gentle stage (0.6617 × 10-5 cm/s) owing to the generation of structuring disjoining pressure. Comprehensive mechanisms of AP-MDN nanofluid for EOR are also proposed and revealed. Moreover, oil washing efficiency of AP-MDN nanofluid is as high as 95.7 % when the soaking time is 6 hrs and temperature is 75 ℃. Core flooding experimental results demonstrate that the increase in shut-down time and the injection mode of multiple rounds with small slugs can better promote the interaction between AP-MDN nanofluid and crude oil in porous media. The highest oil recovery contributed by AP-MDN nanofluid is 19.1 %. These results are expected to promise AP-MDN nanofluid as an effective candidate for EOR.

Synergistic interaction between molybdenum disulfide nanosheet and metal organic framework for high performance supercapacitor

Zeolitic imidazolate framework-67 crystals (ZIF-67) anchored molybdenum disulfide nanosheets (MS) have been synthesized via a hydrothermal approach followed by a simple chemical method. The concentration of molybdenum disulfide was varied to investigate its impact on the electrochemical efficiency within the electrode nanocomposite. The shiny spot of this composite is the combination of two desirable properties, the conductive path created by MS, and the structural framework support provided by Zeolitic imidazolate framework-67 intercalated with nickel (Z67.Ni). The framework of Z67.Ni inhibits MS nanosheets from restacking over repeated charge and discharge cycles, which is why this specific nanocomposite was chosen. The superior synergistic impact of Z67.Ni crystals and MS nanosheets was established by the improved electrochemical behavior of Z67.Ni with 70 % weight percent of MS (Z67.Ni/MS7). This combination exhibited a specific capacitance of 308.5 F/ g at 1 A g−1 and a power density (Pd) of 2.78 kW kg−1 along with an exceptional energy density (Ed) of 83.98 W h kg−1. These impressive results highlight the high efficiency of this nanocomposite material for supercapacitor applications.

Novel electrochemical/fluorescence dual-mode biosensor based on covalent organic framework for tetracycline detection

Excessive antibiotic residues increased the environmental damage and safety of animal products, leading to serious health threats. In this study, a dual-mode probe was developed and applied as an electrochemical/fluorescence sensor for tetracycline (TET) detection. The probe, comprising a fluorescent covalent organic framework, electroactive methylene blue, gold nanoparticles (AuNPs) and single-stranded DNA, was synthesized by self-assembly. A glassy carbon electrode was functionalized with molybdenum disulfide nanosheets, AuNPs, and aptamers. The probe exhibited fluorescent signals in solution and electrochemical signals after being specifically connected to the electrode via hybridization. In the presence of TET, the probe is be competitively expelled from the modified electrode, resulting in an increase in the fluorescent signal and a decrease in the electrochemical signal. The developed electrochemical/fluorescence dual-mode sensor enabled sensitive TET detection in the concentration range of 10 nM–10 mM, with minimum detection limits of 0.03 nM (electrochemical) and 0.05 nM (fluorescence). With its high selectivity, superior reproducibility, and excellent stability, the proposed dual-mode sensor demonstrates high reliability, and excellent application prospects for TET detection in milk and river water samples.

A new plant-esterase inhibition based electrochemical sensor with signal amplification by MoS2@N-CDs for chlorpyrifos detection.

Chlorpyrifos (CPF) is the most common pesticide entering the food chain and posing a threat to human health. This study presents a new electrochemical biosensor based on molybdenum disulfide nanosheets and nitrogen-doped carbon dot nanocomposite (MoS2@N-CDs) and kidney bean esterase (KdBE), and it is shown to achieve accurate detection of CPF. MoS2@N-CDs were prepared by a facile solvothermal method and characterized by electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. Electrochemical characterization confirmed that MoS2@N-CDs facilitated electron transfer and increased the electroactive surface area of the electrode, thereby improved the sensing performance of the electrode. The oxidation peak current of 1-naphthol, which was produced by the hydrolysis of 1-naphthyl acetate catalyzed by KdBE, was adopted as the signal of the sensor. CPF can suppress KdBE activity and consequently cause a decrease in the sensing signal. The experimental results show that the variation of sensing signal is a reliable index to evaluate the CPF level. Under the optimized conditions, the developed enzyme sensor showed superior CPF assay performance with a linear detection range as wide as 0.01-500 μg L-1 and LOD as low as 3.5 × 10-3 μg L-1 (S/N = 3). The inter- and intra-batch RSDs for electrode testing were 4.02% and 2.69%, respectively. Moreover, the developed biosensor also showed good stability and anti-interference. The spiked recoveries of CPF in oilseed rape and cabbage ranged from 98.09% to 106.01% with low relative standard deviation (RSD) (<5.23%), suggesting that the sensor is a promising tool to enable simple, low-cost but highly sensitive large-scale screening of CPF residues in food.

Biophysical and computational analyses of interaction of 2D MoS2 nanosheets with human haemoglobin coupled with NIR activated photothermal therapy

Molybdenum disulfide (MoS2) nanosheets can interact favourably with human haemoglobin and induce apoptosis in cancer cells via NIR-excited photothermal therapy.

Amplified detection of SARS-COV-2 B.1.1.529 (Omicron) gene oligonucleotides based on exonuclease III-aided MoS2 /AIE nanoprobes.

The coronavirus disease-2019 pandemic reflects the underdevelopment of point-of-care diagnostic technology. Nuclei acid (NA) detection is the "gold standard" method for the early diagnosis of the B.1.1.529 (Omicron) variant of severe acute respiratory syndrome-coronavirus disease-2. Polymerase chain reaction is the main method for NA detection but requires considerable manpower and sample processing taking ≥ 3h. To simplify the operation processes and reduce the detection time, exonuclease III (Exo III)-aided MoS2 /AIE nanoprobes were developed for rapid and sensitive detection of the oligonucleotides of Omicron. Molybdenum disulfide (MoS2 ) nanosheets with excellent optical absorbance and distinguishable affinity to single-strand and duplex DNAs were applied as quenchers, and aggregation-induced emission (AIE) molecules with high luminous efficiency were designed as donor in fluorescence resonance energy transfer-based nanoprobes. Exo III with catalytic capability was used for signal amplification to increase the sensitivity of detection. The composite nanoprobes detected the mutated nucleocapsid (N)-gene and spike (S)-gene oligonucleotides of Omicron within 40 min with a limit of detection of 4.7pM, and showed great potential for application in community medicine.

A point-of-care aptasensor based on the upconversion nanoparticles/MoS2 FRET system for the detection of Pseudomonas aeruginosa infection.

The rapid detection of Pseudomonas aeruginosa (P. aeruginosa) is of great significance for the diagnosis of medical infection. In view of the above, a novel aptasensor based on fluorescence resonance energy transfer (FRET) was developed. It contained aptamer-coupled upconversion nanoparticles (UCNPs-apt) as a donor (excitation 980nm) and molybdenum disulfide (MoS2) nanosheets as an acceptor. The upconversion fluorescence aptamer system was investigated to obtain the optimal parameters of MoS2 concentration, the incubation time of UCNPs-apt/MoS2 and P. aeruginosa, and pH. Based on the optimal parameters, a linear calibrationequation (emission 654nm) with a wide detection range 8.7 × 10 ~ 8.7 × 107cfu/mL, a high coefficient of determination R2 0.9941, and a low limit of determination (LOD) 15.5cfu/mL were established. The method was validated with P. aeruginosa infected foci of mouse wound. The advantage of this aptasensor isthat analysisresults can be obtained within 1.5h, which was much faster than that ofthe standard method (18-24h). Furthermore, combined with a portable instrument, it can be used as a point-of-care testing for the early detection of P. aeruginosa infection, which is useful for selecting the correct antibiotics to achieve good therapeutic effects. Additionally, it also has a broad application prospect in food and environmental areas.

Unveiling Xanthine Presence in Rohu Fish Using Ag+-Doped MoS2 Nanosheets Through Electrochemical Analysis.

Here, we envisage the development of the rapid, reliable, and facile electrochemical sensor for the primary detection of xanthine (Xn) which is significant for the food quality measurement, based on the silver-doped molybdenum disulfide (Ag@MoS2) nanosheets. The structural and compositional properties of the prepared samples were tested through X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, and X-ray photon spectroscopy (XPS). The two-dimensional (2D) MoS2 nanosheets provide the large surface area for the sensing applications and the silver ions help in the enhanced electrochemical response. The fabricated enzymatic biosensor exhibits magnificent cyclic stability with a limit of detection of 27nM. Also, the sensor was tested for rapid, reproducible, specific, and regenerable up to 10 cycles and has a shelf life of 2weeks. The outcomes of this study suggest that the proposed matrix could be employed for the fabrication of devices for early detection of xanthine.

Design of a Novel Electrochemical Aptasensor Based on Molybdenum Disulfide Nanosheets for Lysozyme Detection

Design of a Novel Electrochemical Aptasensor Based on Molybdenum Disulfide Nanosheets for Lysozyme Detection

Aptamer-based flares hybridized with single-stranded DNA-conjugated MoS2 nanosheets for ratiometric fluorescence sensing and imaging of potassium ions and adenosine triphosphate in human fluids and living cells

Addressing the limitations observed in previous studies, where the quantitative range of nanoprobes for detecting K+ and adenosine triphosphate (ATP) did not cover concentrations found within living cells, the present study aimed to develop ratiometric nanoprobes that can accurately sense changes in K+ and ATP levels in living cells and quantify them in human fluids. The proposed nanoprobes consisted of recognition flares modified with 6-carboxyfluorescein (FAM) and 5-carboxytetramethylrhodamine (TAMRA), along with thiolate single-stranded DNA (ssDNA) and molybdenum disulfide nanosheets (MoS2 NSs). The thiolate ssDNA acts as a linker between the flares and the MoS2 NSs, directly forming a functional nanostructure at room temperature. The direct conjugation of labeled flares to the MoS2 NSs simplifies the fabrication process. In the absence of K+ and ATP, the hybridization of flares and thiolate ssDNA caused FAM to move away from TAMRA, suppressing the fluorescence resonance energy transfer (FRET) process. However, upon the introduction of K+ and ATP, the flares undergo a structural transformation via the formation of G-quadruplex formation and the generation of hairpin-shaped structures, respectively. This structural change leads to the release of the flares from the ssDNA-conjugated nanosheet surface. The release of the flares brings FAM and TAMRA into close proximity, allowing FRET to occur, leading to FRET and static quenching. By monitoring the ratio between the fluorescence intensities of FAM and TAMRA, the concentration of K+ (5–100 mM) and ATP (0.3–5 mM) can be accurately determined by the proposed nanoprobes. The advantages of these nanoprobes lie in their ability to provide ratiometric measurements, which enhance the accuracy and reliability of the quantification process. The proposed nanoprobes offer potential applications as ratiometric imaging probes for monitoring K+ and ATP-related reactions in living cells, providing valuable insights into cellular processes. Additionally, they can be employed for determining the levels of K+ and ATP in human fluids, offering potential diagnostic applications in various clinical settings.