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. 2019 Oct 16;9(57):32977–32983. doi: 10.1039/c9ra06113d

Gram-scale synthesis of nitrogen doped graphene quantum dots for sensitive detection of mercury ions and l-cysteine†

Yuang Mao 1,‡, Chang Zhao 1,‡, Shuyan Ge 2, Tao Luo 1, Jie Chen 1, Jiyang Liu 2, Fengna Xi 2,✉, Junjie Liu 1,✉
PMCID: PMC9073100  PMID: 35529120

Abstract

Sensitive and reliable detection of mercury ions (Hg2+) and l-cysteine (l-Cys) is of great significance for toxicology assessment, environmental protection, food analysis and human health. Herein, we present gram-scale synthesis of nitrogen doped graphene quantum dots (N-GQDs) for sensitive detection of Hg2+ and l-Cys. The N-GQDs are one-step synthesized using bottom-up molecular fusion in a hydrothermal process with gram-scale yield at a single run. N-GQDs exhibit good structural characteristics including uniform size (∼2.1 nm), high crystallinity, and single-layered graphene thickness. Successful doping of N atom enables bright blue fluorescence (absolute photoluminescence quantum yield of 24.8%) and provides unique selectivity towards Hg2+. Based on the fluorescence quenching by Hg2+ (turn-off mode), N-GQDs are able to serve as an effective fluorescent probe for sensitive detection of Hg2+ with low limit of detection (19 nM). As l-Cys could recover the fluorescence of N-GQDs quenched by Hg2+, fluorescent detection of l-Cys is also demonstrated using turn-off-on mode.

One-step and gram-scale synthesis of nitrogen doped graphene quantum dots is realized for their sensitive detection of Hg2+ and l-Cys.graphic file with name c9ra06113d-ga.jpg

1. Introduction

Metal ions and small biomarkers play crucial roles in various physiological and pathological processes.1,2 For instance, mercury ions (Hg2+) are one of the most toxic pollutants and are a great threat to the environment and human health. Even a small intake of Hg2+ (2 mg kg−1 body weight per day) can damage the nervous, endocrine and other systems, which further leads to many fatal diseases (e.g. headaches, renal failure, loss of intelligence quotient).3–5 On the other hand, as one of the essential amino acids and small biomarkers in human body, l-cysteine (l-Cys) possesses vital physiological functions in neuronal tissues, metabolism and detoxification.6–10 Abnormal levels of l-Cys can cause growth retardation, neurotoxic effect, Alzheimer's disease and coronary heart disease.8–10 Therefore, simple and sensitive detection of Hg2+ and l-Cys is of great importance.

Up to now, many methods including atomic absorption spectrometry (AAS), atomic fluorescence spectrometry (AFS), inductively-coupled plasma mass spectrometry (ICP-MS) and surface-enhanced Raman scattering (SERS) have been developed for the detection of Hg2+.1,11,12 However, these methods often require highly extensive instruments and sophisticated operation techniques. Several strategies including high performance liquid chromatography (HPLC) and capillary electrophoresis (CE) have been designed to detect l-Cys.7,10 Tedious and time-consuming procedures are usually required. Among various detection techniques, fluorescence detections have attracted considerable interests owing to the ease of operation, rapid detection, high sensitivity, and possibility for real-time monitoring and local observation.8,9,13,14 Until now, considerable efforts have been devoted to the development of fluorescent probes for monitoring Hg2+ or l-Cys.

Graphene quantum dots (GQDs) or 0D graphene are the newest addition to the nanocarbon family.15–17 Owing to its atomic thickness, nanometer scale (<10 nm) and quantum confinement effect, GQDs exhibit tunable photoluminescence, high photostability, low cytotoxicity, and superior water dispersibility.18,19 These unique properties promise a wide range of applications in biological imaging,15,20 catalysis,21–24 drug delivery,19 energy conversion and storage22,25 and especially sensing.21,26–32 In recent years, it has been proved that heteroatom doping can effectively regulate the property and selectivity of GQDs. Challenge remains in facile and gram-scale synthesis of heteroatom-doped GQDs with specific selectivity.

In this work, we demonstrate gram-scale synthesis of nitrogen doped graphene quantum dots (N-GQDs) for sensitive detection of Hg2+ and l-Cys. As illustrated in Fig. 1, N-GQDs were easily synthesized through one-step bottom-up strategy under hydrothermal condition. The as-prepared N-GQDs show bright and emission-independent fluorescence, uniform size, and good crystalline. Owing to specific electron transfer and aggregation, N-GQDs exhibit selective and sensitive fluorescence quenching towards Hg2+. In presence of l-Cys, the quenched fluorescence of N-GQDs/Hg2+ system could be recovered. Based on these fluorescence quenching (turn-off) and recovery (turn-off-on) processes, sensitive and simultaneous detection of Hg2+ and l-Cys are demonstrated.

Fig. 1. Schematic illustration for the preparation of N-GQDs and detection of Hg2+ and l-Cys.

Fig. 1

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2. Experimental

2.1. Materials and reagents

Pyrene, 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), NaOH, l-cysteine (l-Cys), l-histidine (His), d-methionine (Met), l-tryptophan, l-tyrosine (Tyr), l-leucine (Leu), l-threonine (Thr), l-alanine (Ala), l-glutamic acid (Glu), l-aspartic acid (Asp) and glycine (Gly) were obtained from Aladdin Chemistry Co. Ltd. (China). The standard solution of Hg2+ was purchased from National Standard Materials Center (China). Aqueous solutions of other cations were prepared from chloride salts (Ni2+, K+, Na+, Ca2+), nitrate salts (Zn2+, Cr3+, Ag+, Co2+, Cd2+, Pb2+, Fe3+), and sulfate salts (Mg2+, Cu2+, Al3+), respectively. All reagents are of analytical grade and used with further treatment. All aqueous solutions were prepared with ultrapure water (18.2 MΩ cm, Milli-Q, Millipore).

2.2. Characterizations

Transmission electron microscopic (TEM) images was taken on a JEM-2100 transmission electron microscope at operating voltage of 200 kV (JEOL Ltd., Japan). Atomic force microscopic (AFM) images were obtained using tapping mode by Bruker Multimode 8 (Bruker. Inc, USA). Elemental analysis of the N-GQDs was performed by X-ray photoelectron spectroscopy (XPS) with PHI5300 electron spectrometer (PE Ltd., USA) using Mg Kα radiation (250 W, 14 kV). Fluorescence spectra were recorded on RF-5301 PC spectrofluorometer (Shimadzu Corporation, Japan). Absolute photoluminescence quantum yield was measured using FL 3C-11 spectrofluorometer (Hariba Scientific, USA).

2.3. One-step preparation of N-GQDs

The precursor, 1,3,6-trinitropyrene, was synthesized according to the literature.17 N-GQDs were prepared using one-pot hydrothermal process. Briefly, 1,3,6-trinitropyrene (6 mM) and l-tryptophan (75 mM) were dissolved in NaOH (125 mM) with ultrasonic treatment for 0.5 h. The mixture was then transferred into 500 mL Teflon-lined autoclave and heated for 6 h at 200 °C. To optimize the preparation conditions, different concentrations of l-tryptophan (25–120 mM) and NaOH (5 mM to 0.5 M), reaction temperature (120–200 °C) and time (2–10 h) were used. After the reaction, the obtained solution was filtered through a 0.22 μm microporous membrane to remove insoluble carbon product. N-GQDs could be obtained by freeze-drying after dialysis (retained molecular weight of 1000 Da) for 24 h to remove unreacted small molecules. The synthesis yield for N-GQDs was calculated based on the precursor.

2.4. Fluorescent turn-off detection of Hg2+

The HEPES buffer solution (0.1 M, pH 6.0) containing tartaric acid (TA, 125 μM) was used for the detection of Hg2+. N-GQDs (0.07 mg mL−1) were mixed with Hg2+ at different concentrations (0.05–25 μM). After incubation at room temperature for 5 min, the fluorescence (FL) intensity in the absence (F0) and presence (F) of Hg2+ was measured with the excitation wavelength fixed at 370 nm. The relative fluorescence ratio (F/F0) and fluorescence quenching ratio (F0 − F)/F0 were used for calibration. Each detection was performed in triplicate.

For real sample analysis, the environmental sample was collected from Jinsha Lake (Hangzhou, China). Bacteria, algae and insoluble substances were removed by a 0.22 μm microporous membrane. The detection of Hg2+ was evaluated by standard addition method.

2.5. Fluorescence turn-off-on detection of l-Cys

As l-Cys can recover the fluorescence of N-GQDs quenched by Hg2+, fluorescence turn-off-on mode was applied to detect l-Cys. Briefly, N-GQDs (0.07 mg mL−1) was firstly mixed with Hg2+ (25 μM) and incubated for 5 min. Then, l-Cys was added at different concentrations (0.1–30.0 μM). After the mixed solution was incubated at room temperature for 5 min, the FL intensity was recorded (excited at 370 nm). The relative fluorescence recovery ratio (F1 − F)/F1 was used to evaluate the fluorescence recovery by l-Cys, where F and F1 represent the FL intensity in absence and presence of l-Cys, respectively.

3. Results and discussion

3.1. Gram-scale synthesis of N-GQDs

In present work, N-GQDs were synthesized using one-step hydrothermal fusion between trinitropyrene and tryptophan in NaOH medium (Fig. 1). Trinitropyrene was chosen as precursor because it has the same mother-nucleus structure as graphene and could be fused at alkaline medium. Tryptophan with N atoms and carboxyl groups was applied as dopant to introduce doped heteroatoms as well as functional groups on GQDs. As demonstrated in inset of Fig. 2A, GQDs with blue fluorescence are obtained. In order to obtain GQDs with excellent fluorescent properties, the conditions of hydrothermal reaction were optimized. The highest fluorescence (FL) intensity is obtained at a reaction of 6 h and 200 °C (Fig. S1A and S1B†). Obviously, high temperature can facilitate the efficiency of the bottom-up fusion. However, higher temperature was not investigated because it would have exceeded the tolerated range of the common Teflon-lined autoclave. Too short reaction time results in low concentration of GQDs due to incomplete molecule fusion, whereas too long time might result in GQDs stack. The FL intensity increases with the increase of tryptophan concentration and then reaches a plateau, presumably because the fusion between trinitropyrene and tryptophan is saturated (Fig. S1C†). The concentration of NaOH exhibits similar effects on the FL intensity of GQDs (Fig. S1D†). Thus, N-GQDs synthesized under the optimized conditions (75 mM l-tryptophan and 125 mM NaOH at 200 °C for 6 h) was applied for further investigation.

Fig. 2. (A) The FL excitation spectrum (EX, left) obtained at the emission wavelength of 445 nm and FL emission spectra (EM, right) of N-GQDs obtained with different excitation wavelength (340 to 410 nm, 10 nm increment). Insets are N-GQDs solution under daylight (left) and UV light (365 nm). (B) FL lifetime spectrum of N-GQDs. (C) TEM images of N-GQDs. Insets were the high-resolution TEM (HRTEM) image with indicated lattice parameter and size distribution of N-GQDs. (D) AFM image of the N-GQDs. Inset was the height profile along the red line.

Fig. 2

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The synthesis yield of obtained N-GQDs is as high as 91.2%, indicating high efficiency for the preparation of N-GQDs. It is worth noting that the volume of the autoclave in present work is 500 mL, which is significantly higher than that used in most GQDs synthesis (usually 25 mL or 50 mL volume). Even the reaction solution is only 40% of the volume of autoclave, more than 0.5 g of N-GQDs could be produced at a single run. Thus, gram-scale synthesis of N-GQDs could be realized using this green and one-step strategy.

3.2. Fluorescence property, morphology and composition of N-GQDs

Fig. 2A demonstrates the fluorescent excitation and emission spectra of N-GQDs. As shown, the maximum excitation at 370 nm gives the maximum emission at 445 nm. It is worth noting that the maximum FL emission of N-GQDs remains unchanged when the excitation wavelength changes. In addition, a narrow emission is revealed with the half-peak width of about 55 nm (excited at 370 nm). These emission-independent and narrow emission suggest that N-GQDs have uniform structure and luminescent states. The absolute quantum yield is 24.8% with a lifetime of 6.9 ns (Fig. 2B).

As revealed by transmission electron microscopy (TEM), the size of N-GQDs is uniform with average size of ∼2.1 nm. The crystallinity of N-GQDs was confirmed by high resolution TEM (HRTEM). The lattice spacing of 0.25 nm corresponds to the graphene (100) planes (Fig. 2C). Good crystallinity of N-GQDs might be attributed to the trinitropyrene precursor (Fig. 1), which has the mother-nucleus structure as graphene. The atomic force microscopic (AFM) image shows that the thickness of N-GQDs is about 1.0 nm. Considering the doped heteroatoms and surface groups, the as-prepared N-GQDs are mostly single-layered (Fig. 2D). The uniform size, good crystalline and homogeneous thickness suggest excellent structure characteristics of N-GQDs, which also support the narrow and emission-independent fluorescence.

The composition of N-GQDs was investigated by X-ray photoelectron spectroscopy (XPS). XPS survey spectrum reveals the presence of C, O, and N with atomic percentages of 78.7%, 17.3% and 4.0%, respectively (Fig. 3A), indicating successful introduction of N atoms on GQDs. The high resolution C 1s spectrum clearly evidences the presence of C–C Created by potrace 1.16, written by Peter Selinger 2001-2019 C (sp2 C, 284.6 eV), C–O/C–N (285.5 eV) and O–C Created by potrace 1.16, written by Peter Selinger 2001-2019 O (288.0 eV), respectively (Fig. 3B).17 According to the high resolution O 1s spectrum, N-GQDs contains carboxyl group (532.8 eV) and hydroxyl group (531.4 eV) (Fig. 3C).33 The pyrrole N (C–N–C, 398.7 eV) and graphite N (N–(C)3, 399.2 eV) in high resolution N 1s spectrum indicate that N atoms have successfully doped into the carbon skeleton of GQDs.34 In addition, N-GQDs also contain some primary amino groups (C–N–H, 400.1 eV) (Fig. 3D).

Fig. 3. XPS survey spectrum (A) and high resolution C 1s (B), O 1s (C), and N 1s (D) spectra of N-GQDs.

Fig. 3

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3.3. Selective fluorescence quenching of N-GQDs towards Hg2+

The selectivity of N-GQDs towards different metal ions was investigated. As demonstrated in Fig. 4A, K+, Na+, Ca2+, Mg2+, Zn2+, Al3+, Ni2+, Co2+, Cr3+, Pb2+, Cd2+, and Ag+ hardly affect the fluorescence of N-GQDs. On the contrary, Hg2+, Fe3+ and Cu2+ could quench the fluorescence of N-GQDs. However, the quenching efficiency of Hg2+ is significantly higher than that of Fe3+ and Cu2+, indicating the potential for sensitive detection of Hg2+. In contrast to most reported GQDs-based fluorescent sensors, which usually applied to detect Fe3+ or Cu2+, GQDs with Hg2+ sensitivity is rarely reported. Tartaric acid (TA) is chosen as masking agent to eliminate the interference of Fe3+ and Cu2+. As shown in Fig. S2,† the addition of TA has no effect on the fluorescence of N-GQDs. In the presence of TA (125 μM), the fluorescence of N-GQDs quenched by Hg2+ is similar with that obtained in mixture of Hg2+ and all other ions in Fig. 4A (Fig. 4B). Hence, selective fluorescence response of N-GQDs towards Hg2+ could be achieved.

Fig. 4. (A) The relative FL ratio of the N-GQDs in the presence of different metal ions (25 μM). (B) The relative FL ratio of the N-GQDs in the presence of Hg2+ or Hg2+ + mixed ions (all other ions in A) with tartaric acid (TA, 125 μM). (C) FL lifetime spectrum of N-GQDs in the presence of Hg2+. (D) The dynamic light scattering of N-GQDs in the presence of Hg2+.

Fig. 4

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The mechanism for the fluorescence quenching of N-GQDs by Hg2+ was investigated. Firstly, we measured the fluorescence lifetime of N-GQDs after interaction with Hg2+. The lifetime of N-GQDs in presence of Hg2+ is 0.6 ns (Fig. 4C), which is remarkably shorter than that of N-GQDs itself (6.9 ns). This indicates fluorescence quenching by electron transfer between N-GQDs and Hg2+, presumably because of the electron-donating moieties on GQDs formed by doped N atoms (Fig. 1). In addition, the remarkable change of particle size was also investigated by the dynamic light scattering (DLS). The average size of particles in N-GQDs-Hg2+ mixture is 1038.7 nm, indicating Hg2+-induced aggregation of N-GQDs. (Fig. 4D). Thus, aggregation-induced-quenching also occurs (Fig. 1).

3.4. Fluorescent turn-off detection of Hg2+ using N-GQDs as fluorescent probes

Owning to selective fluorescence quenching by Hg2+, fluorescent sensor (turn-off mode) was developed for the detection of Hg2+ using N-GQDs as fluorescent probe. To achieve the highest sensitivity, the detection conditions including pH and incubation time were optimized. As shown in Fig. 5A, the highest fluorescence quenching exists at pH 6. Too low a pH value (pH 3–5) might weaken the interaction between N-GQDs and metal ions through protonation of N atoms on GQDs whereas too high a pH value (pH 7) possibly converts metal ions into hydroxide. At the same time, fast kinetics is observed and a plateau of fluorescence intensity appeared within 3 min (Fig. 5B), indicating the strong interaction between N-GQDs and Hg2+. Under the optimized conditions, remarkable decrease in FL intensity towards different concentration of N-GQDs is observed (Fig. 5C). Good linearity existed between fluorescent quenching ratio (F0 − F)/F0 and Hg2+ concentration from 50 nM to 15 μM (Fig. 5D). The limit of detection (LOD) is 19 nM at a signal-to-noise ratio of 3. As shown in Table S1 (ESI†), the detection limit obtained with the present method was lower than those obtained by carbon dots (CDs),35 F doped CDs (F-CDs),36 N doped CDs (N-CDs),37 N and S co-doped CDs (N, S-CDs),38,39 N doped GQDs (N-GCDs),34 sulfur and nitrogen co-doped GQDs (S,N-GQDs),40 and N-GQDs,41 but higher than that obtained using Rhodamine B assisted GQDs (RhB-GQDs)42 and N and S co-doped GQDs (N, S-GQDs).43

Fig. 5. (A) The relative FL ratio of N-GQDs with Hg2+ at different pH. (B) The effect of incubation time on fluorescent quenching ratio of N-GQDs caused by Hg2+ (25 μM). (C) FL emission spectra of N-GQDs in the presence of different concentrations of Hg2+. (D) The linear dependence of (F0 − F)/F0 on concentration of Hg2+.

Fig. 5

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The application of the as-prepared fluorescent sensor for detection of Hg2+ in environmental samples (lake water) was investigated (Table 1). As the original Hg2+ is not detected, the standard addition method was applied to evaluate the detection reliability. Good recoveries ranged from 96.4% to 98.6% were obtained, indicating the potential application of N-GQDs in real analysis.

Detection of Hg2+ in environmental water samples.

Sample Concentration of (μM) RSD (n = 3, %) Recovery (%)
Added Hg2+ Found by N-GQDs
1 3.00 2.91, 2.83, 2.96 2.2 96.7
2 7.00 6.72, 6.65, 6.88 1.8 96.4
3 12.0 11.6, 11.9, 12.0 1.7 98.6
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3.5. Detection of l-Cys based on fluorescent off-on mode

As illustrated in Fig. 6A, the fluorescence of N-GQDs quenched by Hg2+ could be recovered after addition of l-Cys to the N-GQDs-Hg2+ system. As shown in Fig. 6B, l-Cys itself has no effect on the fluorescence intensity of N-GQDs. The possible interference of other nine common amino acids on the detection of l-Cys was investigated. As shown in Fig. 6A, these amino acids could not significantly restore the fluorescence of N-GQDs quenched by Hg2+, indicating good selectivity of l-Cys. We speculate that the fluorescence recovery by l-Cys is due to the specific binding between –SH and Hg2+. In support of this notion, glutathione (GSH, tripeptide composed of Cys, glycine, and glutamic acid) and homocysteine (Hcy, only include an additional –CH2– before –SH in comparison with Cys) also recover the fluorescence to some extent because of the similar structure as Cys (Fig. S3†). Fluorescence turn-off-on sensing mode could be developed for individual detection of l-Cys as a proof-of-demonstration. As shown in Fig. 6C, the fluorescence of N-GQDs gradually restores with increasing the concentration of l-Cys. Good linear relationship is found between fluorescence recovery rate and the concentration of l-Cys from 100 nM to 50 μM (DL of 29 nM) (Fig. 6D). As shown in Table S2,† the detection limit obtained with the present method was lower than those obtained by N,S-CDs-Fe3+,44 N-CDs-Hg2+,47 Eu-GQDs-Cu2+,48 and N-GQDs-Hg2+,49 but higher than that obtained using CDs-Hg2+,45 N-CDs@V2O5,46 and N-GQDs-Hg2+.49 The application of the N-GQDs-Hg2+ system for detection of l-Cys in environmental samples (lake water) was investigated using standard addition method (Table S3†). Good recoveries ranged from 94.1% to 97.8% were obtained.

Fig. 6. (A) The relative FL ratio of N-GQDs with Hg2+ in the presence of different amino acid. (B) FL emission spectra of N-GQDs in the absence and presence of l-Cys (50 μM). (C) FL emission spectra of N-GQDs with Hg2+ (25 μM) in the presence of different concentrations of l-Cys. (D) The linear dependence of (F1 – F)/F1 on concentration of l-Cys.

Fig. 6

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4. Conclusions

Gram-scale synthesis of nitrogen doped graphene quantum dots (N-GQDs) with Hg2+ sensitivity was readily achieved using one-step hydrothermal process. Such blue N-GQDs exhibit good characteristics including uniform size, good crystalline, bright and emission-independent fluorescence and single-layered graphene thickness. The ability to interact with Hg2+ results in selective and sensitive fluorescence quenching through electron transfer and aggregation. With N-GQDs being fluorescent probes, turn-off sensing of Hg2+ and turn-off-on detection of l-cysteine were demonstrated. The easy preparation and good characteristics of N-GQDs promise a large variety of applications, including optical sensing, photocatalysis and bioimaging.

Conflicts of interest

There are no conflicts to declare.

Supplementary Material

RA-009-C9RA06113D-s001

Acknowledgments

The authors gratefully acknowledge the financial support from the National Natural Science Foundation of China (No. 81860512), Guangxi Natural Science Foundation (2016GXNSFBA380194), and the Zhejiang Provincial Natural Science Foundation of China (LY19B050008).

†

Electronic supplementary information (ESI) available. See DOI: 10.1039/c9ra06113d

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