Enhanced electron transfer mediated detection of hydrogen peroxide using a silver nanoparticle–reduced graphene oxide–polyaniline fabricated electrochemical sensor

The current study aims at the development of an electrochemical sensor based on a silver nanoparticle–reduced graphene oxide–polyaniline (AgNPs–rGO–PANI) nanocomposite for the sensitive and selective detection of hydrogen peroxide (H₂O₂). The nanocomposite was fabricated by simple in situ synthesis of PANI at the surface of rGO sheet which was followed by stirring with AEC biosynthesized AgNPs to form a nanocomposite. The AgNPs, GO, rGO, PANI, rGO–PANI, and AgNPs–rGO–PANI nanocomposite and their interaction were studied by UV-vis, FTIR, XRD, SEM, EDX and XPS analysis. AgNPs–rGO–PANI nanocomposite was loaded (0.5 mg cm⁻²) on a glassy carbon electrode (GCE) where the active surface area was maintained at 0.2 cm² for investigation of the electrochemical properties. It was found that AgNPs–rGO–PANI–GCE had high sensitivity towards the reduction of H₂O₂ than AgNPs–rGO which occurred at −0.4 V vs. SCE due to the presence of PANI (AgNPs have direct electronic interaction with N atom of the PANI backbone) which enhanced the rate of transfer of electron during the electrochemical reduction of H₂O₂. The calibration plots of H₂O₂ electrochemical detection was established in the range of 0.01 μM to 1000 μM (R² = 0.99) with a detection limit of 50 nM, the response time of about 5 s at a signal-to-noise ratio (S/N = 3). The sensitivity was calculated as 14.7 μA mM⁻¹ cm⁻² which indicated a significant potential as a non-enzymatic H₂O₂ sensor.

The current study aims at the development of an electrochemical sensor based on a silver nanoparticle–reduced graphene oxide–polyaniline (AgNPs–rGO–PANI) nanocomposite for the sensitive and selective detection of hydrogen peroxide (H₂O₂).     

Low-cost electrochemical detection of l-tyrosine using an rGO–Cu modified pencil graphite electrode and its surface orientation on a Ag electrode using an ex situ spectroelectrochemical method

A low cost reduced graphene oxide–copper hybrid nano thin-film modified Pencil Graphite Electrode has been employed to detect the l-tyrosine enantiomer. The free-standing rGO–Cu hybrid nano-thin film was prepared by a simple one-step liquid–liquid interface method. Electrochemical Cyclic Voltammetry, Differential Pulse Voltammetry, pH-dependent and scan rate dependent studies on bare PGE, Cu, rGO, and rGO–Cu for l-tyrosine have been explained in detail. The rGO–Cu modified PGE based biosensor exhibits good detection of l-tyrosine. The linear range detection limit was estimated to be 1 × 10⁻⁷ M. The calculated sensitivity is 0.4 μA ppm⁻¹ mm². This electroactive biosensor is easily fabricated and controlled and is cost-effective. The surface orientation of l-tyrosine on the Ag electrode at a particular potential and its comparison with vibrational DFT calculations have been studied for the first time.

A low cost reduced graphene oxide–copper hybrid nano thin-film modified pencil graphite electrode has been employed to detect the l-tyrosine enantiomer.     

Simultaneous electrochemical determination of levodopa and piroxicam using a glassy carbon electrode modified with a ZnO–Pd/CNT nanocomposite

A highly conductive electrochemical sensor was constructed for the simultaneous electrochemical determination of levodopa and piroxicam by modification of a glassy carbon electrode with a ZnO–Pd/CNT nanocomposite (GCE/ZnO–Pd/CNTs). The ZnO–Pd/CNT nanocomposite was synthesized by the sol–gel procedure and was characterized by EDAX, MAP and SEM. The sensor was shown to improve the oxidation signal of levodopa and piroxicam by ∼70.2-fold and ∼41.5-fold, respectively. This marks the first time that the electrochemical behavior of levodopa and piroxicam have been investigated at the surface of GCE/ZnO–Pd/CNTs. The voltammogram showed a quasi-reversible signal and an irreversible redox signal for electro-oxidation of levodopa and piroxicam, respectively. The GCE/ZnO–Pd/CNTs showed a linear dynamic range of 0.6 to 100.0 μM (at a potential of ∼180 mV) and 0.1 to 90 μM (at a potential of ∼480 mV) with detection limits of 0.08 and 0.04 μM for the determination of levodopa and piroxicam, respectively. GCE/ZnO–Pd/CNTs were then applied for the determination of levodopa and piroxicam in real samples.

A highly conductive electrochemical sensor was constructed for the simultaneous electrochemical determination of levodopa and piroxicam by modification of a glassy carbon electrode with a ZnO–Pd/CNT nanocomposite (GCE/ZnO–Pd/CNTs).     

A dopamine electrochemical sensor based on a platinum–silver graphene nanocomposite modified electrode

A platinum–silver graphene (Pt–Ag/Gr) nanocomposite modified electrode was fabricated for the electrochemical detection of dopamine (DA). Electrochemical studies of the Pt–Ag/Gr nanocomposite towards DA detection were performed by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The CV analysis showed that Pt–Ag/Gr/GCE had enhanced electrocatalytic activity towards DA oxidation due to the synergistic effects between the platinum–silver nanoparticles and graphene. The DPV results showed that the modified sensor demonstrated a linear concentration range between 0.1 and 60 μM with a limit of detection of 0.012 μM. The Pt–Ag/Gr/GCE presented satisfactory results for reproducibility, stability and selectivity. The prepared sensor also showed acceptable recoveries for a real sample study.

A platinum–silver graphene nanocomposite was synthesized and characterized. A nanocomposite modified electrode was fabricated in order to investigate the electrochemical detection of dopamine.     

Simultaneous determination of hydroquinone and catechol by a reduced graphene oxide–polydopamine–carboxylated multi-walled carbon nanotube nanocomposite

A reduced graphene oxide–polydopamine–carboxylated multi-walled carbon nanotube (RGO–PDA–cMWCNT) nanocomposite was fabricated via a facile, one-pot procedure and was characterized by a variety of techniques. A novel electrochemical sensor based on RGO–PDA–cMWCNT was constructed to determine hydroquinone (HQ) and catechol (CT) simultaneously. This newly prepared nanocomposite shows excellent electrocatalytic efficacy in the electrode reaction of the two isomers. Specifically, the peak-to-peak potential difference between the two dihydroxybenzenes is 115 mV for oxidation, which is obviously larger than similar electrochemical sensors. The established method displays a wide linear range from 0.5 to 5000 μM with a detection limit (S/N = 3) of 0.066 μM for HQ and 0.073 μM for CT. In addition, this electrochemical approach has been tested to measure the two dihydroxybenzenes in real samples and satisfactory results were recorded.

A novel reduced graphene oxide–polydopamine–carboxylated multi-walled carbon nanotube nanocomposite (RGO–PDA–cMWCNT) was fabricated for the sensitive and simultaneous determination of hydroquinone (HQ) and catechol (CT).     

Simultaneous voltammetric detection of dopamine,ascorbic acid and uric acid using a poly(2-(N-morpholine)ethane sulfonic acid)/RGO modified electrode

A poly(2-(N-morpholine) ethane sulfonic acid)/reduced graphene oxide (RGO) modified glassy carbon electrode (GCE) was prepared using an electropolymerization method, and was characterized by scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). The electrochemical behaviors and simultaneous detection of ascorbic acid (AA), dopamine (DA) and uric acid (UA) at this electrode were studied by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Tests showed that this electrode exhibited excellent electrocatalytic activity towards the oxidation of AA, DA and UA. The oxidation peak currents of AA, DA and UA were proportional with their concentrations in the ranges 1.0 μM–30 μM (30 μM–100 μM), 0.05 μM–100 μM and 0.1 μM–100 μM, with detection limits of 0.43 μM, 0.0062 μM and 0.056 μM, respectively. In addition, this electrode exhibited an excellent selectivity, reproducibility and stability, and has been successfully used to determine real samples with satisfactory results.

A sensitive electrochemical sensor for simultaneously detecting dopamine, ascorbic acid and uric acid.     

A reduced graphene oxide-β-cyclodextrin nanocomposite-based electrode for electrochemical detection of curcumin

Curcumin is a polyphenolic compound with anti-oxidative and anti-cancer properties that is obtained from turmeric plants. Several studies have demonstrated that cancer cells are not killed unless they are exposed to 5–50 mM of curcumin. Consequently, it is vital to control the concentration of curcumin in cancer therapy. In this study, a sensitive electrochemical sensor was fabricated based on a beta-cyclodextrin–reduced graphene oxide (β-CD–rGO) nanocomposite for measuring curcumin concentration. The effects of experimental factors were investigated and the optimum parametric conditions were determined using the Taguchi optimization method. The β-CD–rGO modified electrode exhibited good electrochemical properties for curcumin detection. The results of differential pulse voltammetry experiments unveiled that the sensor shows a linear response to curcumin concentration over the range of 0.05–10 mM with a detection limit of 33 nM and sensitivity of 4.813 μA μM⁻¹. The fabricated sensor exhibited selectivity in the presence of other electroactive species, e.g., propranolol, clomipramine and clonazepam.

In this study, a sensitive electrochemical sensor was fabricated based on a beta-cyclodextrin–reduced graphene oxide (β-CD–rGO) nanocomposite for measuring curcumin concentration.     

Single-atom niobium doped BCN nanotubes for highly sensitive electrochemical detection of nitrobenzene

Herein, single-atom niobium-doped boron–carbon–nitrogen nanotubes (SANb-BCN) were synthesized and utilized to fabricate an electrochemical sensor for the detection of nitrobenzene (NB), an environmental pollutant. SANb-BCN were characterized through scanning transmission electron microscopy, scanning electron microscopy, transmission electron microscopy, X-ray diffraction analysis, and Raman spectroscopy. The Nb-BNC material modified on a glassy carbon electrode (GCE) showed an excellent electrochemical response behavior toward NB. The SANb-BCN-modified GCE (SANb-BCN/GCE) gave rise to a prominent NB reduction peak at −0.6 V, which was positively shifted by 120 mV from the NB reduction peak of the bare GCE. Furthermore, the NB peak current (55.74 μA) obtained using SANb-BCN/GCE was nearly 42-fold higher than that using the bare GCE (1.32 μA), indicating that SANb-BCN/GCE is a highly sensitive electrochemical sensor for NB. An ultralow limit of detection (0.70 μM, S/N = 3) was also achieved. Furthermore, the SANb-BCN/GCE sensor was found to possess favorable anti-interference ability during NB detection; thus, the presence of various organic and inorganic coexisting species, including Mg²⁺, Cr⁶⁺, Cu²⁺, K⁺, Ca²⁺, NH⁴⁺, Cd²⁺, urea, 1-bromo-4-nitrobenzene, 3-hydroxybenzoic, terephthalic acid, 1-iodo-4-nitrobenzene, and toluene, minimally affected the NB detection signal. Notably, the SANb-BNC sensor material exhibited high sensitivity and specificity toward detection of NB in environmental samples. Thus, the use of the proposed sensor will serve as an effective alternative method for the identification and treatment of pollutants.

Herein, single-atom niobium-doped boron–carbon–nitrogen nanotubes (SANb-BCN) were synthesized and utilized to fabricate an electrochemical sensor for the detection of nitrobenzene (NB), an environmental pollutant.     

Potential application of mixed metal oxide nanoparticle-embedded glassy carbon electrode as a selective 1,4-dioxane chemical sensor probe by an electrochemical approach

Here, low-dimensional mixed metal oxide (ZnO/NiO/MnO₂) nanoparticles (NPs) were prepared to develop a selective, efficient and ultra-sensitive 1,4-dioxane sensor by using the wet-chemical method (co-precipitation) in alkaline medium at low temperature. Detailed characterization of the prepared calcined NPs was achieved via conventional methods, including X-ray diffraction, field emission scanning electron microscopy, and X-ray photoelectron, UV-vis, Fourier-transform infrared and energy dispersive X-ray spectroscopies. To develop a thin layer of nanomaterial on the fabricated electrode, a slurry of prepared NPs was used to coat the glassy carbon electrode (GCE) with conductive Nafion (5% in ethanol) binder. The fabricated electrochemical sensor showed good sensitivity (1.0417 μA μM⁻¹ cm⁻²), a wide linear dynamic range (0.12 nM to 1.2 mM), lower detection limit (9.14 ± 4.55 pM), short response time, good reproducibility, and long-term stability to selectively detect 1,4-dioxane in the optimized buffer system. Thus, this work presents a reliable alternative approach over existing methods to selectively detect hazardous chemicals in large scale for safety in the environmental and healthcare fields.

Low-dimensional ternary ZnO/NiO/MnO₂ nanoparticles were prepared by wet-chemical co-precipitation in alkaline medium and then used to develop a selective and ultra-sensitive 1,4-dioxane sensor using electrochemistry for the safety of healthcare and the environment.     

A sensitive electrochemical sensor based on ZIF-8–acetylene black–chitosan nanocomposites for rutin detection

Herein, we fabricated a sensitive rutin electrochemical sensor via modifying glassy carbon electrode (GCE) with zeolitic imidazolate framework-8 (ZIF-8) and acetylene black (AB) in the presence of chitosan (CS). The electrochemical activity and experimental parameters of the ZIF-8-AB-CS/GCE sensor were investigated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Under the optimal conditions, the sensor presented a reasonable linear response in the range of 0.1–10 μM with a limit of detection (LOD) as low as 0.004 μM (S/N = 3). The sensor possessed good reproducibility and high stability, and was successfully applied to detect rutin tablet samples with satisfactory results, which was attributed to the synergistic effect between ZIF-8 and AB. Meanwhile, the sensor displayed a potential application for detection of other analytes in real samples. Furthermore, a probable interaction mechanism was proposed to account for the interaction between rutin and the nanocomposite electrode, which was not discussed in previous reports.

A sensitive ZIF-8-AB-CS/GCE for rutin detection is constructed and the interaction between them is discussed for the first time.     

Simultaneous determination of methadone and morphine at a modified electrode with 3D β-MnO2 nanoflowers: application for pharmaceutical sample analysis

The present research synthesized manganese dioxide nano-flowers (β-MnO₂-NF) via a simplified technique for electro-catalytic utilization. Moreover, morphological characteristics and X-ray analyses showed Mn in the oxide form with β-type crystallographic structure. In addition, the research proposed a new efficient electro-chemical sensor to detect methadone at the modified glassy carbon electrode (β-MnO₂-NF/GCE). It has been found that oxidizing methadone is irreversible and shows a diffusion controlled procedure at the β-MnO₂-NF/GCE. Moreover, β-MnO₂-NF/GCE was considerably enhanced in the anodic peak current of methadone related to the separation of morphine and methadone overlapping voltammetric responses with probable difference of 510 mV. In addition, a linear increase has been observed between the catalytic peak currents gained by the differential pulse voltammetry (DPV) of morphine and methadone and their concentrations in the range between 0.1–200.0 μM and 0.1–250.0 μM, respectively. Furthermore, the limits of detection (LOD) for methadone and morphine were found to be 5.6 nM and 8.3 nM, respectively. It has been found that our electrode could have a successful application for detecting methadone and morphine in the drug dose form, urine, and saliva samples. Thus, this condition demonstrated that β-MnO₂-NF/GCE displays good analytical performances for the detection of methadone.

Electrochemical sensor based on β-MnO₂ nanoflower-modified glassy carbon electrode for the simultaneous detection of methadone and morphine was fabricated.     

Ultrasensitive electrochemical detection of methyl parathion pesticide based on cationic water-soluble pillar[5]arene and reduced graphene nanocomposite

We report a rapid, sensitive and selective electrochemical sensor based on pillar[5]arene (CP5) reduced graphene (rGO) nanohybrid-modified glassy carbon electrode CP5-rGO/GCE for the trace detection of methyl parathion (MP) by differential pulse voltammetry (DPV) for the first time. Compared to beta-cyclodextrin (β-CD)-functionalized reduced graphene (rGO)-modified GCE β-CD-rGO/GCE, the proposed CP5-rGO/GCE sensor exhibits excellent electrochemical catalytic activity, rapid response, high sensitivity, good reproducibility and anti-interference ability towards MP. The recognition mechanism of β-CD/MP and CP5/MP was studied by ¹H NMR. The results indicate a higher supramolecular recognition capability between CP5 and MP compared to that between β-CD and MP. The β-CD-rGO and CP5-rGO nano-composites were prepared via a wet chemistry approach. The resulting nano-composites have been characterized by thermogravimetric analysis (TGA), fourier transform infrared spectrometry (FTIR), charge transfer resistance (R_ct) and zeta potential. The CP5-rGO/GCE combines the merits of CP5 and rGO, and is used for quantitative detection of MP. It has a low detection limit of 0.0003 μM (S/N = 3) and a linear response range of 0.001–150 μM for MP. This method has been used to detect MP in soil and waste water samples with satisfactory results. This study provides a promising electrochemical sensing platform and is a promising tool for the rapid, facile and sensitive analysis of MP.

A promising electrochemical sensing platform for the detection of methyl parathion based on cationic water-soluble pillar[5]arene reduced graphene nanocomposite.     

Hemin-doped metal–organic frameworks based nanozyme electrochemical sensor with high stability and sensitivity for dopamine detection

This study reports a new type of artificial nanozyme based on Hemin-doped-HKUST-1 (HKUST-1, also referred to as MOF-199; a face-centered-cubic MOF containing nanochannels) as a redox mediator for the detection of dopamine (DA). Hemin-doped-HKUST-1 was successfully synthesized by one-pot hydrothermal method, which was combined with reduced graphene oxide (rGO) modified on a glassy carbon electrode (GCE) to construct a sensor (Hemin-doped HKUST-1/rGO/GCE). The morphology and structure of Hemin-doped-HKUST-1 were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM) and infrared spectra (IR) techniques. The Hemin-doped HKUST-1/rGO nanozyme showed an excellent electrocatalytic activity for DA oxidation, which is due to the enhanced Hemin activity through the formation of a metal–organic framework (MOFs) and the synergy between the Hemin-doped HKUST-1 and rGO in nanozyme. The resulted sensor exhibited a high sensitivity of 1.224 μA μM⁻¹, with a lower detection limit of 3.27 × 10⁻⁸ M (S/N = 3) and a wide linear range of 0.03–10 μM for DA detection. In addition, due to the stabilizing effect of MOFs on heme, the sensor showed satisfactory stability and has been successfully applied to the detection of DA in serum samples, indicating that this work has potential value in clinical work.

Hemin-doped-HKUST-1 nanozyme has been successfully synthesized and used for dopamine detection with excellent reproducibility, stability and anti-interference.     

Simultaneous detection of acetaminophen and 4-aminophenol with an electrochemical sensor based on silver–palladium bimetal nanoparticles and reduced graphene oxide

In this paper, Ag–Pd bimetallic nanoparticles uniformly distributed on reduced graphene oxide (rGO) were synthesized by redox reaction between Pd²⁺, Ag⁺and GO, and were characterized by X-ray diffractometry, field emission scanning electron microscopy, electrochemical impedance spectroscopy and thermal gravimetric analyses. A novel electrochemical sensor was constructed based on these nanocomposites using glassy carbon as a substrate. Under optimal conditions, the linear ranges were 0.50–300.00 μM for PA and 1.00–300.00 μM for 4-AP, with the detection limits of 0.23 μM for PA and 0.013 μM for 4-AP, respectively. This sensor was successfully applied to the determination of PA in pharmaceutical formulations and gave satisfactory results with a lower detection limit, wider linear range and good reproducibility.

Simultaneous detection of acetaminophen and 4-aminophenol with a highly sensitive electrochemical sensor based on silver–palladium bimetal nanoparticles and reduced graphene oxide.     

Cytidine-stabilized copper nanoclusters as a fluorescent probe for sensing of copper ions and hemin

We reported a sensitive and selective fluorescence “turn on–off” strategy for detection of Cu²⁺ and hemin, respectively. The fluorescence “turn on” sensor for Cu²⁺ detection had a wide linear range of 0.05–2.0 μM with a limit of detection (LOD) of 0.032 μM, and the fluorescence “turn off” sensor for hemin detection possessed a wide linear range of 0.05–4.0 μM with an LOD of 0.045 μM. The sensor for Cu²⁺ or hemin exhibited high selectivity over other possible substances. In addition, it was demonstrated by using various analytical characterization techniques that the fluorescence “turn on” sensor for Cu²⁺ was constructed on the basis of the formation of water-soluble fluorescent copper nanoclusters (CuNCs), and the fabrication of the fluorescence “turn off” sensor for hemin was predominately based on the inner filter effect of hemin on the fluorescence of the CuNCs. Finally, the proposed fluorescence “turn on–off” sensor system was successfully applied for detection of Cu²⁺ in lake water samples and hemin in duck blood samples.

A sensitive and selective fluorescence “turn on–off” strategy for simultaneous detection of Cu²⁺ and hemin was proposed on the basis of the formation of fluorescent CuNCs and the inner filter effect of hemin on the fluorescence of the CuNCs.     

Facile one-pot method of AuNPs/PEDOT/CNT composites for simultaneous detection of dopamine with a high concentration of ascorbic acid and uric acid

In this research, a facile one-pot method was used to synthesize gold/poly-3,4-ethylene-dioxythiophene/carbon nanotube (AuNPs/PEDOT/CNTs) composite material. The composite material was investigated by Fourier Transform Infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM). Then the synthesized nanocomposite material was dropped on a bare glassy carbon electrode (GCE) to improve the detection performance of dopamine with a high concentration of ascorbic acid and uric acid. The electrochemical behavior of AuNPs/PEDOT/CNTs/GCE was studied by Cyclic Voltammetry (CV), Differential Pulse Voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). Under optimum conditions, AuNPs/PEDOT/CNTs/GCE showed a good linear response in the concentration range from 9.14 to 29.704 μM with a detection limit (LOD) and sensitivity of 0.283 μM and 1.557 μA μM⁻¹, respectively. This sensor was applied to detect practical samples with good average recovery. It also exhibited good reproducibility and stability.

A facile one-pot method was used to synthesize ternary composite material. This modified electrode exhibited good ability of detecting dopamine. It also exhibited excellent anti-interference ability and stability.      

A simple electrochemical sensor based on rGO/MoS2/CS modified GCE for highly sensitive detection of Pb(ii) in tobacco leaves

High-performance electrode modification materials play a crucial role in improving the sensitivity of sensor detection in electrochemical determination of heavy metals. In this study, a rGO/MoS₂/CS nanocomposite modified glassy carbon electrode (GCE) was used to construct a sensitive sensor for detecting lead ions in tobacco leaves. The reduced graphene oxide (rGO) was used to increase the conductivity of the sensor, and the nano-flowered MoS₂ could provide a large reaction specific surface area and a certain active site for heavy metal reaction. Chitosan (CS) was used to improve the enrichment ability of heavy metals and increase the electrocatalytic activity of electrode. Thus, an electrochemical sensor with excellent performance in reproducibility, stability and anti-interference ability was established. The stripping behavior of Pb(ii) and the application conditions of the sensor were studied by square wave anodic stripping voltammetry (SWASV). The investigation indicated that the sensor exhibited high detection sensitivity in the range of 0.005–0.05–2.0 μM, and the limit of detection (LOD) was 0.0016 μM. This work can provide a fast and effective method for determination of Pb(ii) in samples with low content, such as tobacco leaves.

High-performance electrode modification materials play a crucial role in improving the sensitivity of sensor detection in electrochemical determination of heavy metals.     

An ‘‘off–on–off’’ sensor for sequential detection of Cu2+ and hydrogen sulfide based on a naphthalimide–rhodamine B derivative and its application in dual-channel cell imaging

A novel colorimetric and fluorometric sensor with unique dual-channel emission to sequentially detect Cu²⁺ and hydrogen sulfide (H₂S) was synthesized from naphthalimide–rhodamine B through the PET and FRET mechanism. The sensor showed a selective “off–on” fluorescence response with a 120-fold increase toward Cu²⁺, and its limits of detection were 0.26 μM and 0.17 μM for UV-vis and fluorescence measurements, respectively. In addition, 1–Cu²⁺ was an efficient “on–off” sensor to detect H₂S with detection limits of 0.40 μM (UV-vis measurement) and 0.23 μM (fluorescence measurement), respectively. Furthermore, the sensor can also be used for biological imaging of intracellular staining in living cells. Therefore, the sensor should be highly promising for the detection of low level Cu²⁺ and H₂S with great potential in many practical applications.

A novel colorimetric and fluorometric sensor with unique dual-channel emission to sequentially detect Cu²⁺ and hydrogen sulfide (H₂S) was synthesized from naphthalimide–rhodamine B through the PET and FRET mechanism.     

Highly sensitive and selective detection of naproxen via molecularly imprinted carbon dots as a fluorescent sensor

The overuse and inappropriate discharge of naproxen, a common anti-inflammatory medication and an emerging contaminant in water, is detrimental to human health and bodies of water. Here, we design a fluorescent sensor based on molecularly imprinted carbon dots (CDs) for highly selective detection of trace amounts of naproxen. The CDs were encapsulated into the pores of silica through a sol–gel based method and provide fluorescent signal. After removal of the template molecules, a molecularly imprinted polymer layer was formed and the fluorescence of the CDs sensor was selectively quenched by naproxen. A detection limit of as low as 0.03 μM and a linear range of 0.05–4 μM for detecting naproxen in aqueous solution were obtained. High recoveries of naproxen levels in waste water and urine samples for practical application were also achieved. In addition, the accurate detection performance of sensor was maintained during the UV degradation of naproxen.

A highly selective fluorescent sensor for naproxen utilizes carbon dots as the fluorophore and molecularly imprinted polymer to provide the recognition sites. The fluorescence of carbon dots can be selectively quenched by naproxen.     

Co2+ detection,cell imaging,and temperature sensing based on excitation-independent green-fluorescent N-doped carbon dots

Green-fluorescent N-doped carbon dots (N-CDs) have been successfully fabricated using hydrothermal treatment of tyrosine and urea. The N-CDs obtained showed excitation-independent emission, superior stability and strong photoluminescence with a quantum yield of ca. 9.8%. Based on these striking behaviors, the as-prepared N-CDs have been utilized in Co²⁺ detection and temperature sensing. Due to an inner filter effect, the N-CDs obtained were dramatically quenched by Co²⁺ with linear ranges of 0.1 μM–10 μM, 25 μM–275 μM and 300 μM–400 μM, and they had a detection limit of 0.15 μM. The use of the as-prepared N-CDs has been extended to visualize Co²⁺ fluctuations in living cells. Additionally, the N-CDs obtained have also been applied for use as a temperature sensor with a linear range of 25–80 °C.

Green-fluorescent N-doped carbon dots (N-CDs) have been successfully fabricated using hydrothermal treatment of tyrosine and urea.