This research work demonstrates an easy synthesis of Silver nanoparticles decorated Blue Carbon Dots-based Pectin films (AgNPs@BCDs/PN) and its use towards sensitive and selective detection of Tartrazine (TZ) in candy samples by spectrofluorimetry method. Blue Carbon Dots were prepared through hydrothermal treatment of Citric acid and Thiourea. AgNPs@BCDs were prepared using mechanical stirring. The particle sizes of AgNPs@BCDs were found to be in the range of 12.5 to 23.8 nm. Various techniques were deployed to explore the structural, morphological and photoluminescent behaviour of AgNPs@BCDs. The fluorescence method achieved a limit of detection (LOD) of 21.02 nM within the range of 0-32 μM. Combination of Photoinduced Electron Transfer (PET) and Surface state modulation was adopted for the sensing. The recoveries and relative standard deviations were 94.11-99.42 % and 1.61-1.91 % respectively. This work highlights the great application prospects of AgNPs@BCDs/PN for Tartrazine sensing in a rapid, simple and sensitive way.

Pursuing nanomaterials with high fluorescence quantum yields is of great significance in the fields of bioimaging, medical diagnosis, and food safety monitoring. This work reports on orange-emitting aggregation-induced emission (AIE) copper nanoclusters (Cu NCs) integrated with blue-emitting nitrogen-doped carbon dots (N-CDs), which enables highly sensitive detection of S2- and Zn2+ ions through an off-on ratiometric fluorescence method. The highly emissive Cu NCs was doped by Ce3+ with a high quantum yield of 51.30 % in aqueous solution. The S2- can induce fluorescence quenching of AIE Cu NCs/N-CDs from orange to blue, while Zn2+ can restore the orange fluorescence. The probe provided linear detection ranges of 0.5-170 μM for S2- and 0.05-200 μM for Zn2+, with detection limits of 0.17 μM and 0.02 μM, respectively. Moreover, a smartphone assistant ratiometric fluorescent test strips were developed for the rapid and visual detection of S2- and Zn2+. The AIE Cu NCs/N-CDs probe exhibited diverse fluorescence color responses, high fluorescence stability, and low cytotoxicity. The ratiometric system was successfully applied to the detection of S2- and Zn2+ in real water samples as well as in cellular and living imaging, demonstrating its potential in biochemical analysis and food safety monitoring.

Sensitive and reliable fluorescence chemosensors for the monitoring of Hg2+ levels are very important for the protection of environment and living systems. Herein, a simple thiourea-based irreversible fluorescence and colorimetric chemosensor L has been devised and characterised by various spectral analysis. Probe L selectively detects Hg2+ ion due to the binding site-signalling strategy, where the pyridine ring serves as the fluorophore unit and the thiourea moiety serves as the coordinating site. The incorporation of Hg2+ ions to a DMSO solution of L shows substantial alterations in the UV-Vis spectrum and fluorescence spectra. This alteration in absorption as well as fluorescence profile refers to the increase in the intra-molecular charge transfer (ICT) and chelation-induced enhanced fluorescence (CHEF) of L-Hg2+ complex. For the Hg2+ ion, the detection limit is reached up to 2.5 × 10-8 M, which is calculated from the IUPAC formula CDL = 3σ/slope. The Job's plot reveals a 1:1 binding stoichiometry between L and Hg2+. Applying Benesi-Hildebrand equation, the binding constant for the L-Hg2+ complex was estimated as 7.54 × 106 M-1. To validate the mechanism involved in the formation of L-Hg2+ complex, the DFT and TD-DFT calculations were performed in the gas phase. L has been used well to identify Hg2+ ions in soil samples over a wide pH range. The receptor L was also applied for cell imaging study.

The current synthetic strategies for carbon dots (CDs) are usually time-consuming, rely on complicated processes, and need high temperatures and energy. Recent studies have successfully synthesized CDs at room temperature. Unfortunately, most CDs synthesized at room temperature are obtained under harsh reaction conditions, prepared using aromatic precursors, or need a long time to generate. Therefore, an energy-free room-temperature rapid synthesis of CDs under mild conditions using aliphatic substrates is important. We aim to provide an innovative approach to synthesizing CDs to be used to develop the first fluorescence-based assay of the non-fluorescent anti-hyperlipidemic drug, fenofibrate.

We report an innovative, energy-free, and room-temperature preparation of fluorescent N-doped CDs utilizing aliphatic substrates in only 20 min. The synthesis was based on a self-exothermic Schiff base condensation reaction between methylglyoxal and ethylenediamine. The prepared CDs' antibacterial properties, biocompatibility, and cell-imaging ability were investigated. The fluorescence signal of the CDs was quantitively quenched upon adding increasing concentrations of fenofibrate in the range of 0.50-15.0 μg/mL. Therefore, the prepared CDs were applied as a nanosensor to develop the first fluorescence-based assay of fenofibrate. The reliability of the synthesized nanosensor was confirmed by the successful quantification of fenofibrate in pharmaceutical dosage forms, environmental water, weight loss herbal products, and dietary supplements. The obtained recovery ranged from 95.33 to 104.58 %. In addition, the minimal environmental impact of the developed fenofibrate sensing strategy was confirmed using the recently reported metrics.

The key advantage of this work is the use of an energy-free approach to synthesize CDs rapidly under mild conditions without aromatic substrates. This opens a new window for the eco-friendly synthesis of CDs that avoids the drawbacks of the traditional methods. Additionally, it is the first fluorescence nanosensor for sensing fenofibrate in various matrices, avoiding the limitations of the previous methods, such as high cost, poor selectivity, and low sensitivity.

2,4,6-Trinitrophenol (TNP) has high explosive risks and biological toxicity, and there has been considerable concern over the determination of TNP. In the present work, fluorescent carbon dots (CDs) stemmed from a green carbon source of pinecone by the facile hydrothermal approach. A novel environment- friendly fluorescent probe was developed to efficiently detect TNP by using the obtained CDs with remarkable fluorescence stability. The fluorescent CDs exhibited obvious excitation dependence with the highest peaks for excitation and emission occurring at 321 and 411 nm, respectively. The fluorescence intensity is significantly reduced by TNP owing to the inner filter effect with the CDs. The probe exhibited good linearity with TNP concentrations in the range of 0.025-20 μg mL-1, and the limit of detection was as low as 8.5 ng mL-1. Additionally, the probe proved successful in sensing TNP quantitatively in actual environmental samples with satisfied recoveries of 95.6-99.6%. The developed fluorescent probe offered an environment-friendly, efficient, rapid, and reliable platform for detecting trace TNP in the environmental field.Highlights Novel carbon dots were synthesised from green precursors of pineal powder.The highly effective quenching process was put down to the inner filter effect.The as-constructed fluorescent probe was successfully utilised for sensing 2,4,6-trinitrophenol in environmental samples.The proposed method was simple, rapid, efficient, economical, and eco-friendly.

In present work, blue carbon dots (b-CDs) were derived from ammonium citrate and guanidine hydrochloride, and red carbon dots (r-CDs) were stemmed from malonate, ethylenediamine and meso‑tetra (4-carboxyphenyl) porphin based on facile hydrothermal method. Eco-friendly ratiometric fluorescence probe was innovatively constructed to effectively measure Hg2+ utilizing b-CDs and r-CDs. The developed probe displayed two typical emission peaks at 450 nm from b-CDs and 650 nm from r-CDs under the excitation at 360 nm. Mercury ion has strong quenching effect on the fluorescence intensity at 450 nm due to the electron transfer process and the fluorescence change at 450 nm was used as the response signal, whereas the fluorescence intensity at 650 nm kept unchangeable which resulted from the chemical inertness between Hg2+ and r-CDs, serving as the reference signal in the sensing system. Under optimal circumstances, this probe exhibited an excellent linearity between the fluorescence response values of ΔF450/F650 and Hg2+ concentrations over range of 0.01-10 µmol/L, and the limit of detection was down to 5.3 nmol/L. Furthermore, this probe was successfully employed for sensing Hg2+ in practical environmental water samples with satisfied recoveries of 98.5%-105.0%. The constructed ratiometric fluorescent probe provided a rapid, environmental-friendly, reliable, and efficient platform for measuring trace Hg2+ in environmental field.

Contamination of ground water with pollutants released from various anthropogenic activities is a major concern due to its adverse effects on the environment and human health. Rapid and efficient detection of such pollutants is the first step toward remediation of the problem. Herein we report a two-point fluorescence turn OFF-ON detection method for Hg2+ ions using nitrogen doped carbon dots (NCDs). The NCDs obtained through solvothermal treatment of ammonium citrate tribasic in DMF at 190 °C for four hours exhibited a quantum yield of 9.67%. Hg2+ detection is demonstrated in two steps, first the quenching of the fluorescence of NCDs by Hg2+ and second the fluorescence recovery upon addition of ascorbic acid from different sources. A rapid filter paper-based detection device is demonstrated based on the principles developed.

Herein, a kind of N-doped fluorescent carbon dots (N-CDs) were prepared by using melamine and carboxymethyl cellulose (CMC) as precursors through a straightforward hydrothermal method. The designed sensor displayed a uniform nanoscale distribution, excellent hydrophilicity, and strong fluorescence emission with a fluorescence quantum yield of 37.98%. Moreover, the N-CDs could be utilized for Fe3+ detection by the fluorescence "On-Off" transition via the mechanism of internal filtration effect (IFE) and static quenching process. Two good linear relationships within the concentrations of Fe3+ from 10 to 100μM and 100 to 500 μM could be obtained, which indicated that the "On-Off" fluorescent sensor could quantitative analysis of Fe3+ and the calculated detection limit (LOD) was 0.510 μM (3σ/slope). Additionally, the N-CDs could be used for the detection of Fe3+ in the solid phase based on the fluorescence "On-Off" strategy, which is promising for anticounterfeiting application.

To fully utilize the wastes of the traditional Chinese herbs, a highly functionalized fluorescent carbon nano dots (CDs) based ferric ion sensor was prepared from forsythia residue via a one-step hydrothermal method. Under transmission electron microscope (TEM), the CDs were observed to be spherical with the diameter in the range of 5-20 nm. Comprehensive analyses documented the CDs' favorable morphology, diverse functional groups, high water solubility, remarkable optical properties, and exceptional stability under various environmental conditions. Moreover, the CDs exhibited good optical properties with vivid green photoluminescence (PL) when they were exposed to ultraviolet (UV) light. Furthermore, the prepared CDs demonstrated selective fluorescence quenching behavior towards ferric ions with satisfactory sensitivity and a low limit of detection (LOD) of 4.3 µM. Additionally, the CDs displayed good selectivity towards Fe3+ and the least interference with several other metal ions. Consequently, this strategy could be effectively applied to real water samples, demonstrating its potential for broader applications.

Pesticides in environmental samples pose significant risks to ecosystems and human health since they require precise and efficient detection methods. Imidacloprid (IMI), a widely used neonicotinoid insecticide, exemplifies these hazards due to its potential toxicity. This study addresses the urgent need for improved monitoring of such contaminants by introducing a novel fluorometric method for detecting IMI using nitrogen-doped graphite carbon dots (N-GCDs). The sensor operates by quenching fluorescence through the interaction of Cu2+ ions with N-GCDs. Subsequently, IMI binds to the imidazole group, chelates with Cu2+, and restores the fluorescence of N-GCDs. This alternating fluorescence behavior allows for the accurate identification of both Cu2+ and IMI. The sensor exhibits linear detection ranges of 20-100 nM for Cu2+ and 10-140 μg/L for IMI, with detection limits of 18 nM and 1.2 μg/L, respectively. The high sensitivity of this sensor enables the detection of real-world samples, which underscores its potential for practical use in environmental monitoring and agricultural safety.

The detection of anions using carbon dots (CDs) has received less attention compared to cations. Therefore, the present study aimed to develop a fluorescence sensor based on carbon dots (CDs) capable of detecting S2- in real water samples. The CDs were successfully prepared from the residues of a traditional Chinese herb, Gardenia, which emitted green photoluminescence (PL) under ultraviolet light irradiation. The as-prepared CDs were quasi-spherical in shape and ranged in size from 10 to 30 nm. Different detailed analyses proved that the CDs had good morphology, various functional groups, high water solubility, great optical features, and excellent stability under diverse environmental conditions. The ion detection showed that only Ag+ had the strongest fluorescence quenching effect on the CDs, however, the addition of S2- could recover their fluorescence. Based on these results, an "off-on" fluorescence sensor was achieved to selectively detect the concentration of S2- in real water samples with a limit of detection (LOD) of 39 μM, which further expanded the application of residues from traditional Chinese herbal medicine.

Iodine is essential for human growth and can enter the body through food, water, and air. Analyzing its presence in the environment is crucial for ensuring healthy human development. However, current large-scale instruments have limitations in the field analysis of iodine. Herein, a miniaturized purge and trap point discharge microplasma optical emission spectrometric (P&T-μPD-OES) device was developed for the field analysis of iodine in water. Volatile iodine molecules were produced from total inorganic iodine (TII) through a basic redox reaction under acidic conditions, then the purge and trap module effectively separated and preconcentrated iodine molecules. The iodine molecules were subsequently atomized and excited by the integrated point discharge microplasma and an iodine atomic emission line at 206.24 nm was monitored by the spectrometer. Under optimal conditions, this proposed method had a detection limit of 16.2 μg L-1 for iodine and a precision better than 4.8%. Besides, the accuracy of the portable device was validated by successful analysis of surface and groundwater samples and a comparison of the mass spectrometry method. This proposed portable, low-power device is expected to support rapid access to iodine levels and distribution in water.

A unique fluorescent molecule (ND-S) was obtained from Eosin Y in two simple yet high yielding steps (1). ND-S has special metal ion sensing ability, such that it can selectively detect toxic Hg2+ present in very low concentration in aqueous solutions in the presence of other competing metal ions. The host-guest complexation is ratiometric and is associated with significant increase in fluorescence during the process. Isothermal titration calorimetry (ITC) experiments provided thermodynamic parameters related to interaction between ND-S and Hg2+. Using inductively coupled plasma mass spectrometry (ICP-MS), the Hg2+(aq) removal efficiency of ND-S was estimated to be 99.88%. Appreciable limit of detection (LOD = 7.4 nM) was observed. Other competing ions did not interfere with the sensing of Hg2+ by ND-S. The effects of external stimuli (temperature and pH) were studied. Besides, the complex (ND-M), formed by 1:1 coordination of ND-S and Hg2+ was found to be effective against the survival of Gram-positive bacteria (S. aureus and B. subtilis) with a high selectivity index. Moreover, bacterial cell death mechanism was studied systematically. Overall, we have shown the transformation of a toxic species (Hg2+), extracted from polluted water by a biocompatible sensor (ND-S), into an effective and potent antibacterial agent (ND-M).

Mercury ion (Hg2+) is a highly toxic and ubiquitous pollutant, whose effective detection has aroused widespread concern. A novel ratiometric fluorescent sensor has been designed to rapidly and efficiently detect Hg2+ based on blue/red carbon dots (CDs) with environmental friendliness. This sensor was well characterized via TEM, FTIR, XPS, UV-vis, and zeta potential analysis and displayed excellent fluorescence properties and stability. The fluorescence of blue CDs at 447 nm was significantly quenched with the addition of Hg2+ resulted from the static quenching, whereas that of red CDs at 650 nm remained invariable. A sensitive method for Hg2+ determination was constructed in the range of 0.05-7.0 nmol mL-1 with optimal conditions, and the detection limit was down to 0.028 nmol mL-1. Meanwhile, compared to other 17 metal ions, the ratiometric fluorescent sensor exhibited high selectivity for Hg2+. Furthermore, satisfied recoveries had also been obtained for measuring trace Hg2+ in practical environmental samples. This developed ratiometric fluorescent sensor provided a reliable, environmental-friendly, rapid, and efficient platform for the detection of Hg2+ in environmental applications.

In this study, we designed and fabricated a spermine-responsive triple-emission ratiometric fluorescent probe using dual-emissive carbon nanoparticles and quantum dots, which improve the sensor's accuracy and reduce interfering environmental effects. The probe is advantageous for the proportionate detection of spermine because it has good emission resolution, and the maximum points of the two emission peaks differ by 95 nm. As a proof of concept, cuvettes and a 96-well plate were combined with a smartphone and YOLO series algorithms to accomplish real-time, visual, and high-throughput detection of seafood and meat freshness. In addition, the reaction mechanism was verified by density functional theory and fundamental characterizations. Upon exposure to different amounts of spermine, the intensity of the fluorescent probe changed linearly, and the fluorescent color shifted from yellow-green to red, with a limit of detection of 0.33 μM. To enable visual identification of food-originated spermine, a hydrogel-based visual sensing platform was successfully developed utilizing the triple-emission fluorescent probe. Consequently, spermine could be identified and quantified without complicated equipment.

Iodine is an essential element that is used to make thyroid hormones. However, people usually ignore their iodine nutrition level, thus leading to a series of thyroid diseases, particularly in areas where medical resources are scarce. Thus, development of a portable, economical, and simple method for the detection of urinary iodine is of significant importance. Herein, a solid-phase fluorescence filter effect (SPFFE) induced by iodine was used to develop an SPFFE-based point-of-care testing (POCT) platform for the detection of urinary iodine by coupling with headspace sample introduction. This method can not only alleviate the matrix interference that occurred in the conventional inner filter effect (IFE) but also achieve high sensitivity. Furthermore, the urinary iodine (UI) POCT platform was developed through the integration of a sample pretreatment and fluorescence readout. This whole system costs less than US $20 and provides accurate temperature control and a portable fluorescence reading within 15-20 min. Compared to the traditional IFE-based assay, the SPFFE-based POCT platform allows the selective detection of iodine as low as 10 nM and has a linear range of 0.05-4 μM. In addition, it provides notable visualization from blue-violet to orange-red in the presence of iodine, which tends to indicate the iodine nutritional status of the human body. Eventually, the clinical applicability and feasibility of the UIPOCT platform as an early diagnostic test kit were confirmed by determining the iodine in urine samples from children and pregnant women.

A ternary deep eutectic solvent (DES) consisting of choline chloride, lactic acid, and urea in a molar ratio of 1:2:2 was used to pretreat chamomile residue, followed by carbon dots (CDs) preparation using a one-pot solvothermal method. The CDs prepared under the suitable conditions had a high quantum yield of 47.34% and could be used as a bifunctional fluorescent probe for the detection of tartrazine and Fe(III). The concentration of tartrazine or Fe(III) had a good linear relationship with the fluorescence intensity of CDs that the determination coefficient (R²) was 0.9957 and 0.9943, and the limit of detection (LOD) was 40 nM and 119 nM, respectively. After verifying the different fluorescence quenching mechanisms of CDs by these two substances, a quantitative analysis was performed on real samples with recoveries of 90.70%∼104.29%. Overall, this study provided a promising technology for chemical conversion from low-cost chamomile residue to attractive bifunctional fluorescent probe.

In this study, we synthesized stable nitrogen-doped carbon dots by a simple and economical one-step hydrothermal method using l-cysteine and anhydrous ethylenediamine as precursors. The prepared carbon dots have bright and stable blue light emission near 383 nm and can be used as fluorescent probes to detect the concentration of Fe³⁺ in environmental waters. It was demonstrated that due to intermolecular electrostatic interaction, a non-fluorescent complex N-CDs/Fe³⁺ is formed by coordination of Fe³⁺ with amino and carboxyl functional groups on the surface of carbon dots. Therefore, in combination with internal filtration effect, the fluorescence of carbon dots can be quenched in the presence of Fe³⁺, and the degree of quenching is linearly related to the concentration of Fe³⁺. The limit of detection in deionized water was as low as 0.069 μM with R² of 0.998 and a linear range of 0.3 to 20 μM. In addition, satisfactory recoveries were achieved for the determination of Fe³⁺ in environmental water samples. The method is reliable, with highly sensitivity and selectivity, and has potential for practical applications in environmental metal analysis.

Bisphenol A (BPA) is an endocrine disrupting chemical and poses a grave threat to the human health. Herein, a fluorescent probe constructed with molecularly imprinted polymers decorated carbon dots (CDs@MIPs) was proposed for determination of BPA with high selectivity. The CDs@MIPs were constructed using BPA, 4-vinylpyridine and ethylene glycol dimethacrylate as template, functional monomer and cross linker, respectively. The obtained fluorescent probe not only owned a highly selective recognition function derived from MIPs but also displayed an excellent sensitivity for sensing BPA stemmed from CDs. The fluorescence intensity of CDs@MIPs was varied before and after the removal of BPA templates. The fluorescent decrease fraction of the fluorescent probe demonstrates a nice linearity in BPA concentration range of 10-2000 nM (r² = 0.9998) and the detection limit is as low as 1.5 nM. The fluorescent probe was triumphantly utilized to sense the level of BPA in real aqueous and plastic samples with good results. Moreover, the fluorescent probe offered a wonderful means for fast identification and sensitive detection of BPA from environmental aqueous samples.

Aggregation-induced emission luminogens (AIEgens) are attracting extensive research attention in the biosensor fields. Herein, we report a new polyethyleneimine (PEI)-induced strategy for enhancing luminescence of TCBPE (an AIEgen) to promote its development in biosensor. The copolymer dots (TCBPE-PEI) with high quantum yield (39.7%) and outstanding stability were synthesized via a one-pot method. The fluorescence enhancement mechanism based on the PEI strategy originated from the restriction of intramolecular motions of TCBPEs and the form of donor-acceptor structures to decrease the inherent energy bandgap. Benefiting from chelating property of TCBPE-PEI by Cu²⁺, a fluorescence-quenching sensor for Cu²⁺ detection was developed based on the fluorescence quenching of the electron transfer effect. Especially, a good linear range of 10-250 nM with a low limit of detection 1.1 nM was achieved, and it was further applied in samples successfully. The current work provides a novel approach to fabricate AIEgen biosensors and shows great potential in Cu²⁺ detection.

Conventional Hg²⁺ visual sensors are unsustainable, hindering their practical application for improved water quality and health. In order to address this challenge, herein, N, S co-doped carbon nanodots (NS-CDs) were prepared and well characterized, presented the fluorescent monitoring for Hg²⁺ over other metal ions with the limit of detection (LOD) of 0.47 µM. Next, the CDs were successfully modified by thymine without any fluorescence labelling (referred to as T-NS-CDs). The sensitivity to Hg²⁺ cloud be noticeable enhanced due to the formation of T-Hg²⁺-T specific base pairs. Accordingly, the LOD was calculated with values as low as 1.56 nM. Furthermore, Hg²⁺ could be released and complexed with antidote (meso-2,3-dimercaptosuccinic acid) (DMSA-Hg²⁺), being the responsible for the reversible interconversion between T-Hg²⁺-T and DMSA-Hg²⁺. Interestingly, the proposed sensing system also applies to the fluorescent sensing for Hg²⁺ in tap water with satisfactory recoveries (96.97 %-101.38 %, RSD < 2 %). Thus, by simply combination of elemental doping and surface functionalization, the surface state and functionalities of CDs could be tailorable, endowing the fluorometric sensing towards Hg²⁺ in environmental system.

Optical biosensors are platforms that translate biological information into detectable optical signals, and have extensive applications in various fields due to their characteristics of high sensitivity, high specificity, dynamic sensing, etc. The development of optical sensing materials is an important part of optical sensors. In this review, we emphasize the role of microfluidic technology in the preparation of optical sensing materials and the application of the derived optical sensors in the biomedical field. We first present some common optical sensing mechanisms and the functional responsive materials involved. Then, we describe the preparation of these sensing materials by microfluidics. Afterward, we enumerate the biomedical applications of these optical materials as biosensors in disease diagnosis, drug evaluation, and organ-on-a-chip. Finally, we discuss the challenges and prospects in this field.

Establishment of a rapid, sensitive, visual, accurate and low-cost fluorescence detection system to detect multiple targets was of great significance in food safety evaluation, ecological environment monitoring and human health monitoring. In this work, a smartphone-assisted down/up-conversion dual-mode ratiometric fluorescence sensor was proposed based on metal-organic framework (NH₂-MIL-101(Fe)) and CdTe quantum dots (CdTe QDs) for visual detection of mercury ions (Hg²⁺) and L-penicillamine (L-PA), in which NH₂-MIL-101(Fe) was used as the reference signal and CdTe QDs was used as the response signal. The down-conversion fluorescence system at excitation wavelength of 300 nm (ex: 330 nm) was used to detect Hg²⁺ and L-PA, in which the detection limit of Hg²⁺ was 0.053 nM with the fluorescence color changed from green to blue, and the detection limit of L-PA was 1.10 nM with the fluorescence color changed from blue to green. Meanwhile, the up-conversion fluorescence system at excitation wavelength of 700 nm (ex: 700 nm) was used to detect Hg²⁺ and L-PA. The detection limits of Hg²⁺ and L-PA were 0.11 nM and 2.93 nM, respectively. The detection of Hg²⁺ and L-PA were also carried out based on the color extraction RGB values identified by the smartphone with a detection limit of 0.091 nM for Hg²⁺ and 8.97 nM for L-PA. In addition, the concentrations of Hg²⁺ and L-PA were evaluated by three-dimensional dynamic analysis in complex environments. The smartphone-assisted down/up-conversion dual-mode ratiometric fluorescence sensor system provides a new strategy for detection Hg²⁺ and L-PA in food safety evaluation, environmental monitoring and human health monitoring.