Fluorescence Emission Research Articles

High-contrast multi-surface imaging of latent fingerprints using color-tunable YOF:Tb3+,Eu3+ ultrafine nanophosphors with high quantum yield.

Visualization of latent fingerprints (LFPs) using conventional powders has faced challenges on multicolor surfaces. However, these challenges are addressed by the advent of fluorescent powders in LFP detection, and they have redefined the effectiveness of the powder dusting method. In this study, color-tunable YOF:Tb3+,Eu3+ nanophosphors were examined for LFP recognition and were evaluated for their practicality on different types of surfaces. Under 254 nm UV irradiation, the LFPs developed using these nanophosphors showed clear and distinct ridge patterns with level 1, 2, and 3 details. The ultrafine particles of these nanophosphors adhered to the ridge patterns and replicated the minutiae of the LFPs. Meanwhile, the variation of the Tb3+/Eu3+ ratio demonstrated multicolor fluorescence emission from the nanophosphors, which provided better contrast between the ridge patterns on complex surfaces. Furthermore, the high luminescence quantum yield of the nanophosphors ensured high-resolution fluorescence images of the LFPs with a well-defined pattern that was recognizable even without any microscope or sophisticated instrumentation.

Highly Horizontal Oriented Tricomponent Exciplex Host with Multiple Reverse Intersystem Crossing Channels for High-Performance Narrowband Electroluminescence and Eye-Protection White Organic Light-Emitting Diodes.

Despite multiple-resonance thermally activated delayed fluorescence (MR-TADF) emitters with small full-width at half maximum are attractive for wide color-gamut display and eye-protection lighting applications, their inefficient reverse intersystem crossing (RISC) process and long exciton lifetime induce serious efficiency roll-off, which significantly limits their development. Herein, a novel device concept of building highly efficient tricomponent exciplex with multiple RISC channels is proposed to realize reduced exciton quenching and enhanced upconversion of nonradiative triplet excitons, and subsequently used as a host for high-performance MR-TADF organic light-emitting diodes (OLEDs). Compared with traditional binary exciplex, the tricomponent exciplex exhibits obviously improved photoluminescence quantum yield, emitting dipole orientation and RISC rate constant, and a record-breaking external quantum efficiency (EQE) of 30.4% is achieved for tricomponent exciplex p-PhBCzPh: PO-T2T: DspiroAc-TRZ (50: 20: 30) based OLED. Remarkably, maximum EQEs of 36.2% and 40.3% and ultralow efficiency roll-off with EQEs of 26.1% and 30.0% at 1000cd m-2 are respectively achieved for its sky-blue and pure-green MR-TADF doped OLEDs. Additionally, the blue emission unit hosted by tricomponent exciplex is combined with an orange-red TADF emission unit to achieve a double-emission-layer blue-hazard-free warm white OLED with an EQEmax of 30.3% and stable electroluminescence spectra over a wide brightness range.

Toxicogenetic, biochemical, and physiological effects of azoxystrobin and carbendazim fungicides over Lactuca sativa L. and Phaseolus vulgaris L.

Fungicides are pesticides that are frequently used in agriculture because of their action against fungal diseases. However, the widespread application of pesticides around the world raises environmental and public health concerns, since these compounds are toxic and can pose risks to ecosystems and human health. The aim of this study was to evaluate the phytotoxic, cytogenotoxic, and biochemical effects of azoxystrobin and carbendazim on Lactuca sativa L. and their physiological effects on Phaseolus vulgaris L. by analyzing the cell cycle and chromosomal and nuclear alterations in L. sativa; the biochemical effects of azoxystrobin and carbendazim on Phaseolus vulgaris L. and their physiological effects on Phaseolus vulgaris L. by analyzing the cell cycle and chromosomal and nuclear alterations in L. sativa; the biochemical effects by analyzing the activity of antioxidant enzymes in L. sativa; and the physiological effects by analyzing chlorophyll content and chlorophyll a fluorescence in P. vulgaris. It was observed that both fungicides were phytotoxic and cytotoxic, reducing root growth and the mitotic index, cytogenotoxic, increasing the occurrence of chromosomal alterations, as well as inducing oxidative stress and an increase in chlorophyll fluorescence emission and altered energy absorption in the plants used as a test system. In view of this, studies such as the one presented here indicate that the use of pesticides, even in small quantities, can lead to damage to the metabolism of plant organisms.

A Miniaturized and Highly Sensitive "Windmill" Three-Channel Fluorescence Detector for Simultaneous Detection of Various Mycotoxins.

A novel "windmill" three-channel light-emitting diode induced fluorescence detector (LED-IF) was proposed to maximize the excitation efficiency and fluorescence collection efficiency. Compared with the typical collinear arrangement, the fluorescence intensity of the three channels was increased by 7.85, 3.88, and 2.94 times, respectively. The compact shaping optical path was designed to obtain higher excitation efficiency and a lower background stray light effect caused by high divergence angle high-power ultraviolet (UV)-LEDs simultaneously, which increased the sensitivity of three channels by 4.6 to 5.7 times. It was found that using a photodiode (PD) with a flat window and a larger photosensitive surface can collect the Lambertian emission fluorescence in the flow cell more efficiently, increasing the signal-to-noise ratio of each channel 1.3 to 1.8 times. The limits of detection (LODs, 3 times peak-peak noise) of aflatoxin B2 (AFB2), ochratoxin (OTA), and zearalenone (ZEN) were 0.33, 1.80, and 28.2 ng/L, respectively. Finally, six mycotoxins were analyzed simultaneously by the detector coupling with HPLC. The results showed that the sensitivity of the detector was at the best level to date, which was better than that of the top commercial fluorescence detectors (FLDs). The developed detector has the advantages of having small volume, low cost, and long lifetime and being robust, which has wide application and market prospects.

Fabrication of a two-dimensional bi-lanthanide metal-organic framework as a ratiometric fluorescent sensor based on energy competition

Bimetallic lanthanide metal-organic frameworks (bi-Ln-MOFs) exhibit great appeal for ratiometric luminescent sensors due to their unique advantages. Specially, the low-lying energy of the empty 4f band of Ce4+ ions benefits Ce-MOFs with robust and broad fluorescent emission. Therefore, constructing ratiometric sensors based on Ce-MOFs is of significance but remains a challenge. Here, a two-dimensional (2D) bi-Ln-MOF is fabricated using Eu3+/Ce4+ and 5-boronoisophthalic acid (5-bop) via a crystal phase transformation strategy to construct a ratiometric luminescent Hg2+ sensor. Due to the lower energy gap of Ce4+ compared to Eu3+ and the corresponding stronger energy-absorption ability, the Ce4+ in bi-Ln-MOF shows a stronger and broader fluorescent emission than that of Eu3+. The substitution of the boric acid group in the bi-Ln-MOF by Hg2+ amplifies the difference between the two lanthanide ions. Therefore, the fluorescence intensity of Ce4+ increases whereas that of Eu3+ decreases accordingly, a behavior distinct from individual Eu-MOF or Ce-MOF performance. This novel bi-Ln-MOF sensor not only achieves a wide linear response range from 0.5 to 120 μM with a low detection limit of 167 nM for Hg2+, but also demonstrates exceptional selectivity and stability. The intriguing sensing mechanism of energy competition and the novel synthesis approach for 2D bi-Ln-MOF are anticipated to broaden the application possibilities of bi-Ln-MOFs for designing ratiometric sensors.

A Zn(II) Coordination Polymer for Fluorescent Turn-Off Selective Sensing of Heavy Metal Cation and Toxic Inorganic Anions.

A novel coordination polymer [Zn(atyha)2]n (1) (Hatyha = 2-(2-aminothiazole-4-yl)-2- hydroxyiminoacetic acid) was constructed by hydrothermal reaction of Zn2+ with Hatyha ligand. CP 1 exhibits a 2D (4,4)-connected topological framework with Schläfli symbol of {44·62}, where atyha- anions serve as tridentate ligands, bridging with Zn2+ through carboxylate, thiazole and oxime groups. CP 1 displays a strong ligand-based photoluminescence at 390 nm in the solid state, and remains significantly structurally stable in water. Interestingly, it can be utilized as a fluorescent probe for selective and sensitive sensing of Fe3+, Cr2O72- and MnO4- through the fluorescent turn-off effect with limit of detection (LOD) of 3.66 × 10-6, 2.38 × 10-5 and 2.94 × 10-6 M, respectively. Moreover, the efficient recyclability for detection of Fe3+ and Cr2O72- is better than that for MnO4-. The mechanisms of fluorescent quenching involve reversible overlap of UV-Vis absorption bands of the analytes (Fe3+, Cr2O72- and MnO4-) with fluorescence excitation and emission bands for CP 1, respectively.

Electrophysiological Analysis of Retinal Organoid Development Using 3D Microelectrodes of Liquid Metals.

Despite of the substantial potential of human-derived retinal organoids, the degeneration of retinal ganglion cells (RGCs) during maturation limits their utility in assessing the functionality of later-born retinal cell subtypes. Additionally, conventional analyses primarily rely on fluorescent emissions, which limits the detection of actual cell functionality while risking damage to the 3D cytoarchitecture of organoids. Here, an electrophysiological analysis is presented to monitor RGC development in early to mid-stage retinal organoids, and compare distinct features with fully-mature mouse retina. This approach utilizes high-resolution 3D printing of liquid-metal microelectrodes, enabling precise targeting of specific inner retinal layers within organoids. The adaptable distribution and softness of these microelectrodes facilitate the spatiotemporal recording of inner retinal signals. This study not only demonstrates the functional properties of RGCs in retinal organoid development but also provides insights into their synaptic connectivity, reminiscent of fetal native retinas. Further comparison with fully-mature mouse retina in vivo verifies the organoid features, highlighting the potential of early-stage retinal organoids in biomedical research.

Effect of tert‐Butylation on the Photophysics of Thermally Activated Delayed Fluorescence Emitters

Thermally activated delayed fluorescence (TADF) emitters potentially can provide organic light‐emitting diodes with 100% internal quantum efficiency by harvesting triplet excitons. Generally, TADF emitters are small molecules that are not applicable for solution processability. The addition of tert‐butyl groups to the periphery of TADF emitters has proven to improve their solubility in various organic solvents, reduce aggregation‐induced quenching, and enhance the photoluminescence quantum yield (PLQY). This article studies the photophysical influence of the tert‐butyl group attached to an emitter with a carbazole acceptor and a triazine donor. The resulting t3CzTrz‐F is a blue–green TADF emitter, in which the addition of a tert‐butyl group increases the rate of reverse intersystem crossing (rISC), while simultaneously decreasing the nonradiative decay rate substantially. In addition, dilution of t3CzTrz‐F in a host matrix in film results in an enhanced PLQY, which is associated with a decrease in the nonradiative decay constant, while there is no change in the rISC rate. Through a solid‐state NMR study, the change in rISC and nonradiative rate upon tert‐butylation by enlarged intermolecular spacing and reduced vibrational and rotational freedom is rationalized, resulting in improved photophysical performance.

Achieving Dual Emission of Fluorescence and Phosphorescence from Anti-Kasha’s Metal–Organic Halides for Information Encryption

Achieving Dual Emission of Fluorescence and Phosphorescence from Anti-Kasha’s Metal–Organic Halides for Information Encryption

Coumarin-Phosphazenes: Enhanced Photophysical Properties from Hybrid Materials.

Phosphazenes have drawn a great deal of interest over the past 20 years as a potentially useful building block for the fabrication of fluorescent materials. The main objective of this work is to explore novel derivatives produced by coumarins, a class of chemicals well-known for their photophysical importance, and cyclophosphazenes. UV absorbance, fluorescence emission, quantum yield, and lifetime measurements were conducted to comprehend the optical properties. Furthermore, single-crystal X-ray analysis and theoretical calculations were carried out to confirm the structure of the molecule. The obtained findings collectively confirm the commendable optical properties exhibited by the studied compounds. Moreover, a detailed study of the crystal packing arrangement of DPP-Et-Kum-Et compound crystallized in the P21/n monoclinic space group revealed the presence of stacking interactions between the nonplanar conjugated benzene rings of the coumarins and the rigid diphenyl groups attached to the phosphazene ring. The crystal structure of the DPP-Kum-Me-Me compound is mainly based on classical C-H···O intermolecular hydrogen bonding interactions with an average distance of 2.52 Å. Importantly, the calculated absorption spectra of the compounds are in close agreement with the experimental data, further supporting their interesting electronic properties. Given that the DPP-Et-Kum-Et and DPP-Kum-Et compounds have the theoretically lowest band gaps (4.31 and 4.30 eV, respectively), the activation energies of these compounds were determined by an impedance analyzer using dc conductance values measured at different temperatures. The calculated activation energies for DPP-Et-Kum-Et and DPP-Kum-Et are 104.49 and 100.92 meV, respectively. The results demonstrate that both theoretical and experimental calculations are in agreement with each other and that the DPP-Kum-Et compound has the lowest conductivity.

Hexacarbazolylbenzene: An Excellent Host Molecule Causing Strong Guest Molecular Orientation and the High-Performance OLEDs.

Hexacarbazolylbenzene (6CzPh), which is benzene substituted by six carbazole rings, is a simple and attractive compound. Despite the success of a wide variety of carbazole derivatives in organic light-emitting diodes (OLEDs), 6CzPh has not received attention so far. Here, excellent performances of 6CzPh are revealed as a host material in OLEDs regarding conventional host materials. Various strategies are implemented to improve the performance of OLEDs, e.g., triplet utilization by thermally activated delayed fluorescence (TADF) and phosphorescence emitters for maximizing internal quantum efficiency, and molecular orientation control for increasing outcoupling efficiency. The present host material is suited for both criteria. Robustness of the structure and sufficiently high triplet energy enables a high external quantum efficiency with a long device lifetime. Besides, the host material boosts the horizontal molecular orientations of several guest emitters. It is noteworthy that disk-shaped 4CzIPN marks the complete horizontal molecular orientations (Θh = 100%, S = -0.50). These results provide an effective way of improving efficiencies without sacrificing device durability for future OLEDs.

A Fluorescent Organic Probe for Naked-Eye Detection of Chloromethanes.

An organic fluorescent probe (OFP-TAR) with a propeller-like structure was designed and synthesized. The photoluminescence of OFP-TAR in solution exhibited a significant red shift with the increase of solvent polarity, enabling a transition of fluorescence emission from blue (445 nm) to yellow (540 nm). The organic thin-film materials based on OFP-TAR/PMMA exhibit significant color changes upon exposure to CH2Cl2, CHCl3, and CCl4, with their maximum fluorescence wavelengths measured at 445, 471, and 494 nm respectively. The device facilitates the visual detection of chloromethanes and is capable of enduring more than 7 cycles of testing. These materials can also be prepared as binary-coded microarray data storage devices or applied in the field of anti-counterfeiting. The quantum yields of guest-loaded crystals CH2Cl2@OFP-TAR, CHCl3@OFP-TAR and CCl4@OFP-TAR are observed as 19.13%, 8.79%, and 0.83% respectively, which are consistent with the tendency of OFP-TAR in CH2Cl2 (47.30%), CHCl3 (34.27%) and CCl4 (3.10%). The fluorescence properties of OFP-TAR, OFP-TAR/PMMA, guest-loaded and guest-free crystals provided insights into the special response mechanism of OFP-TAR towards different chloromethanes.

Energy transfer of Er3+-Nd3+ co-doped in tellurite glass via energy level match

Er3+/Nd3+ co-doped tellurate glass was prepared by melt quenching method. The relationship between the energy levels of two rare earth ions was studied by absorption spectra and excitation spectra. At 379/407/488 nm excitation, visible light, near-infrared (NIR) emission spectra, and fluorescence attenuation curves were measured. The NIR emission spectrum and fluorescence lifetime show that Er3+ can transfer energy to Nd3+, thus enhancing the NIR emission of Nd3+ in tellurate glass. In the co-doped sample, under excitation of 379/407/488 nm, the NIR emission of Nd3+ has a concentration quenching point related to Er3+, and the optimal co-doped concentration is 1mol% ErF3. At 365/451 nm excitation, NIR emission was not enhanced and no energy transfer occurred. In contrast to the energy transfer between conventional Er3+-Nd3+ co-doped glasses, this paper investigates the effect of matching the higher Er3+ energy levels with adjacent Nd3+ levels on the energy transfer. The energy transfer process of Er3+-Nd3+ co-doped glasses is studied in the energy level diagram.

Construction of Spin Crossover‐Fluorescent Bifunctional Cyclic Chain‐Like Fe(II) Compounds from Carbazole Ligands

AbstractThe incorporation of fluorescent properties into spin‐crossover (SCO) materials, aiming at controlling fluorescence via spin‐state transitions for applications in magneto‐optical switching and information processing, represents an appealing research direction. In this study, we prepared two examples of one‐dimensional cyclic chain‐like Fe(II) coordination polymers, denoted as [Fe(DPPC)2(NCS)2]⋅CH3OH⋅o‐C6H4Cl2 (1, DPPC=3,6‐di‐4‐pyridinyl‐9‐[4‐(4‐pyridinyl)phenyl]‐9H‐carbazole) and [Fe(PDPC)2(NCS)2] (2, PDPC=3,6‐di(pyridin‐4‐yl)‐9‐phenyl‐9H‐carbazole). Analyses through single‐crystal X‐ray studies and magnetic measurements validate the two‐step SCO behavior of 1 within the temperature range of 50~200 K. Additionally, when combined with temperature‐dependent fluorescence emission spectroscopy, the results demonstrate the coexistence of SCO and fluorescence in 1.

A smart insulation material achieving self-reporting and autonomous repairing against electrical and mechanical damages based on targeted controllable microcapsules

Under the long-term action of electrical and mechanical stresses, irreversible micro-damages, such as electrical trees and cracks tend to occur inside solid insulation materials, leading to insulation failures, which have no effective countermeasures. This study develops a multi-responsive, target-controlled microcapsule to endow the epoxy resin with dual functions of self-reporting and autonomous repair against internal damage even under strong electric fields without human intervention. A turn-on mechanism for self-reporting signals is designed, to be applicable to electrical tree damage inside an epoxy matrix. In situ UV emissions generated by the partial discharge during electrical treeing are employed to automatically cure the microcapsule core material released into the damaged channel. This triggers aggregation-induced emission (AIE) signals and simultaneously repairs the damaged matrix. The polyurethane hybrid shell filled with magnetic particles endows the microcapsules with magnetic response characteristics. Under the control of a directional magnetic field, the microcapsule is concentrated around the vulnerable areas, obtaining high fluorescence emission intensity under low doping content without affecting the matrix performance. This method enables the autonomous inspection and maintenance of electric equipment and electronic devices under live working and provides new insight into the bionic intelligence of electrical and electronic insulation materials.

Synthesis, structure, fluorescence, and magnetic studies of a series of transition metal complexes with oxygen-bridged phenylene tricarboxylic acid ligand

In this work, 4-(2-carboxyphenoxy)phthalic acid ligand (H3bppa), 4,4′-dipyridyl (4,4′-dipy), 1,10-phenanthroline (phen), 2,2′-dipyridyl (2,2′-dipy) and transition metal ions Zn2+, Cu2+, Mn2+, Ni2+, Co2+ were used to synthesize metal complexes by solvothermal reaction. Ten complexes were synthesized, namely, [Zn(H2bppa)2(H2O)4]·4H2O (1), [Mn(H2bppa)2(H2O)4]·4H2O (2), [Co(H2bppa)2(H2O)4]·4H2O (3), [Mn(H2bppa)2 (2,2′-dipy) (H2O)]n (4), [Cu(H2bppa)2 (2,2′-dipy) (H2O)]n (5), [Mn3(bppa)2(4,4′-dipy)2 (H2O)6]n (6), [Co(Hbppa) (phen)2 (H2O)] (7) and [Ni(Hbppa) (phen)2 (H2O)] (8), [Mn(Hbppa) (phen) (H2O)]n (9), [Cu(Hbppa) (phen) (H2O)]n (10). Structural datas were collected by X-ray single crystal diffractometer, the results show that complexes 1, 2, 3, 7 and 8 are zero-dimensional mononuclear structure, 4, 5, 9 and 10 are one-dimensional chain structure, 6 is three-dimensional network structure. Furthermore, solid state fluorescence properties were performed on complexes H3bppa and 1–8, magnetic properties were performed on complexes 2–8. The fluorescence experiment results show that the fluorescence intensity of complexes 1–8 is weaker than that of H3bppa, and the fluorescence emission spectrum of complex 1 undergoes a blue shift relative to the H3bppa. Magnetic testing data analysis shows that complexes 2, 3 and 8 have antiferromagentic properties and complexes 4, 5, 6 and 7 have ferromagentic properties.

Dual-targeted fluorescent probe for tracking polarity and phase transition processes during lipophagy.

Eukaryotic cells regulate various cellular processes through membrane-bound and membrane-less organelles, enabling active signal communication and material exchange. Lysosomes and lipid droplets are representative organelles, contributing to cell lipophagy when their interaction and metabolism are disrupted. Our limited understanding of the interacting behaviours and physicochemical properties of different organelles during lipophagy hinders accurate diagnosis and treatment of related diseases. In this contribution, we report a fluorescent probe, PTZ, engineered for dual-targeting of lipid droplets and lysosomes. PTZ can track liquid-liquid phase separation and respond to polarity shifts through ratiometric fluorescence emission, elucidating the lipophagy process from the perspective of organelle behavior and physicochemical properties. Leveraging on the multifunctionality of PTZ, we have successfully tracked the polarity and dynamic changes of lysosomes and lipid droplets during lipophagy. Furthermore, an unknown homogeneous transition of lipid droplets and lysosomes was discovered, which provided a new perspective for understanding lipophagy processes. And this work is expected to serve as a reference for diagnosis and treatment of lipophagy-related diseases.

A GSH-Responsive Prodrug with Simultaneous Triple-Activation Capacity for Photodynamic/Sonodynamic Combination Therapy with Inhibited Skin Phototoxicity.

Herein, a dual-sensitizer prodrug, named pro-THPC, has been designed to function as both a photosensitizer and a sonosensitizer prodrug for precise antitumor combination therapy with minimized skin phototoxicity. Pro-THPC could be activated by glutathione (GSH) to release the dual-sensitizer, THPC, which simultaneously switches on fluorescence emission and combined capabilities of photodynamic therapy (PDT) and sonodynamic therapy (SDT). Pro-THPC is further formulated into nanoparticles (NPs) for water dispersity to enable in vivo applications. In vivo fluorescence imaging shows that the pro-THPC NPs group exhibits a significantly higher tumor-to-normal tissue ratio (T/N) (T/N = 5.2 ± 0.55) compared to the "always on" THPC NPs group (T/N = 2.9 ± 0.47) and the pro-THPC NPs group co-administrated with GSH synthesis inhibitor (buthionine sulfoximine, BSO) (T/N = 3.2 ± 0.63). In addition, the generation of the designed dual-sensitizer's reactive oxygen species (ROS) is effectively confined within the tumor tissues due to the relatively strong correlation between ROS generation and fluorescence emission. In vivo studies further demonstrate the remarkable efficacy of the designed pro-THPC NPs to eradicate tumors through the combination of PDT and SDT while significantly reducing skin phototoxicity.

Multiple resonance delayed fluorescence emitter with C3 symmetry for high-performance solution-processed OLEDs

Solution-processed organic materials that exhibit both high emission efficiency and narrowband emission characteristics are rare, and the performance of corresponding solution-processed organic light-emitting diodes (sOLEDs) remains inadequate for practical applications. This study proposes a proof-of-concept design aimed at enhancing both solution processing capability and emission efficiency in multiple-resonance induced thermally activated delayed fluorescence (MR-TADF) materials through the integration of multiple emitting units. A unique emitter named TriBNCz is synthesized and characterized, incorporating three MR-building blocks onto a single phenyl ring, resulting in sky-blue emission with a peak at 490 nm and a small full width at half maximum (FWHM) of 25 nm. Significant improvements in solution processing attributes, including solubility and film-forming properties, are achieved. Moreover, except for the MR effect of the excited states, long-range charge transfer properties of excited states are also obtained. The multiple charge transfer channels contribute to higher rate of reverse intersystem crossing (kRISC). The optimized sOLED device exhibits a maximum external quantum efficiency (EQEmax) of 17.8 %. Furthermore, by employing 5TCzBN as a sensitizer, the sensitized sOLED achieves an EQEmax of 28.8 % and a high-level EQE of 26.1 % at 1000 cd m−2, with an FWHM of 30 nm and Commission Internationale de I’Éclairage (CIE) coordinates of (0.103, 0.497), representing one of the best results among narrowband emission sOLEDs. This research opens a new avenue to develop high-performance solution-processed organic materials and sOLED devices.

Green synthesis of carbon dots from mangosteen peel for fluorescent cancer cells

Recently, carbon dots (CDs) have received significant attention owing to their outstanding optical properties, good solubility, and low toxicity. In this research, CDs were synthesized by a hydrothermal method based on an environmentally friendly and straightforward strategy, using only mangosteen peel and deionized water. The synthesized CDs had an average size of 3.09 ± 0.38 nm. The absorbance spectrum peak for the CDs was seen at 282 nm, and the central wavelength of fluorescence emission was observed at 433 nm under an excitation wavelength of 355 nm. An aqueous solution of CDs exhibited bright green fluorescence when observed with the naked eye under UV irradiation. Both Fourier transform infrared and X-ray photoelectron spectroscope measurements were taken to determine the elemental compositions of the organic substance functional groups on the surface of the CD, such as hydroxyl, carboxyl, and carbonyl groups. These functional groups originate the different emission centers leading to multicolor fluorescent emissions. Furthermore, the synthesized CDs were found to have good biocompatibility with organic and biological materials. The remarkable properties of CDs, including their nanoscale dimensions, strong multicolor fluorescent emissions, non-toxicity, and excellent cell compatibility, could effectively permeate the cell membrane, cytoplasm, and nucleus and provide fluorescence emission. This suggests a significant potential for CDs in fluorescent cell staining applications. Finally, the CDs were used as a fluorescent dye for human colon cancer cells, as they exhibited excellent fluorescence for cell staining.