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      Ultratrace Detection of Nickel(II) Ions in Water Samples Using Dimethylglyoxime-Doped GQDs as the Induced Metal Complex Nanoparticles by a Resonance Light Scattering Sensor

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          Abstract

          This study aimed to synthesize dimethylglyoxime (DMG) (N-source)-doped graphene quantum dots (N-GQDs) via simultaneous pyrolysis of citric acid and 1.0% (w/v) DMG. The maximum excitation wavelength (λ max, ex = 380 nm) of the N-GQD solution (49% quantum yield (QY)) was a red shift with respect to that of bare GQDs (λ max, ex = 365 nm) (46% QY); at the same maximum emission wavelength (λ max, em = 460 nm), their resonance light scattering (RLS) intensity peak was observed at λ max, ex/em = 530/533 nm. FTIR, X-ray photoelectron spectroscopy, XRD, energy-dispersive X-ray spectroscopy, and transmission electron microscopy analyses were performed to examine the synthesized materials. The selective and sensitive detection of Ni 2+ using the RLS intensity was performed at 533 nm under the optimum conditions consisting of both 25 mg L –1 N-GQDs and 2.5 mg L –1 DMG in the ammonium buffer solution of pH 9.0. The linearity of Ni 2+ was 50.0–200.0 μg L –1 with a regression line, y = 5.031 x – 190.4 ( r 2 = 0.9948). The limit of detection (LOD) and the limit of quantitation (LOQ) were determined to be 20.0 and 60.0 μg L –1, respectively. The method precision expressed as % RSDs was 4.90 for intraday ( n = 3 × 3) and 7.65 for interday ( n = 5 × 3). This developed method afforded good recoveries of Ni 2+ in a range of 85–108% when spiked with real water samples. Overall, this innovative method illustrated the identification and detection of Ni 2+ as a DMG complex with N-GQDs, and the detection was highly sensitive and selective.

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          Nitrogen-doped graphene quantum dots with oxygen-rich functional groups.

          Graphene quantum dots (GQDs) represent a new class of quantum dots with unique properties. Doping GQDs with heteroatoms provides an attractive means of effectively tuning their intrinsic properties and exploiting new phenomena for advanced device applications. Herein we report a simple electrochemical approach to luminescent and electrocatalytically active nitrogen-doped GQDs (N-GQDs) with oxygen-rich functional groups. Unlike their N-free counterparts, the newly produced N-GQDs with a N/C atomic ratio of ca. 4.3% emit blue luminescence and possess an electrocatalytic activity comparable to that of a commercially available Pt/C catalyst for the oxygen reduction reaction (ORR) in an alkaline medium. In addition to their use as metal-free ORR catalysts in fuel cells, the superior luminescence characteristic of N-GQDs allows them to be used for biomedical imaging and other optoelectronic applications. © 2011 American Chemical Society
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            Strongly green-photoluminescent graphene quantum dots for bioimaging applications.

            Strongly fluorescent graphene quantum dots (GQDs) have been prepared by one-step solvothermal method with PL quantum yield as high as 11.4%. The GQDs have high stability and can be dissolved in most polar solvents. Because of fine biocompatibility and low toxicity, GQDs are demonstrated to be excellent bioimaging agents.
              • Record: found
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              Influence of nitrogen doping on oxygen reduction electrocatalysis at carbon nanofiber electrodes.

              Nondoped and nitrogen-doped (N-doped) carbon nanofiber (CNF) electrodes were prepared via a floating catalyst chemical vapor deposition (CVD) method using precursors consisting of ferrocene and either xylene or pyridine to control the nitrogen content. Structural and compositional differences between the nondoped and N-doped varieties were assessed using TEM, BET, Raman, TGA, and XPS. Electrochemical methods were used to study the influence of nitrogen doping on the oxygen reduction reaction (ORR). The N-doped CNF electrodes demonstrate significant catalytic activity toward oxygen reduction in aqueous KNO(3) solutions at neutral to basic pH. Electrochemical data are presented which indicate that the ORR proceeds by the peroxide pathway via two successive two-electron reductions. However, for N-doped CNF electrodes, the reduction process can be treated as a catalytic regenerative process where the intermediate hydroperoxide (HO(2)(-)) is chemically decomposed to regenerate oxygen, 2HO(2)(-) O(2) + 2OH(-). The proposed electrocatalysis mechanisms for ORR at both nondoped and N-doped varieties are supported by electrochemical simulations and by measured difference in hydroperoxide decomposition rate constants. Remarkably, approximately 100 fold enhancement for hydroperoxide decomposition is observed for N-doped CNFs, with rates comparable to the best known peroxide decomposition catalysts. Collectively the data indicate that exposed edge plane defects and nitrogen doping are important factors for influencing adsorption of reactive intermediates (i.e., superoxide, hydroperoxide) and for enhancing electrocatalysis for the ORR at nanostructured carbon electrodes.

                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                02 June 2021
                15 June 2021
                : 6
                : 23
                : 14796-14805
                Affiliations
                []Materials Chemistry Research Center, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University , Khon Kaen 40002, Thailand
                []Nuclear Technology Research and Development Center, Thailand Institute of Nuclear Technology (Public Organization) , Nakhon Nayok 26120, Thailand
                [§ ]Nanomaterials Chemistry Research Unit, Department of Chemistry, Faculty of Science and Technology, Nakhon Si Thammarat Rajabhat University , Nakhon Si Thammarat 80280, Thailand
                []Department of Advanced Materials Science and Engineering, Hanseo University , Seosan, Chungnam 31962, Republic of Korea
                []Department of Industrial Engineering, Faculty of Engineering, King Mongkut’s Institute of Technology Ladkrabang , Bangkok 10520, Thailand
                [# ]Department of Chemistry, Faculty of Science, Srinakharinwirot University , Bangkok 10110, Thailand
                Author notes
                [* ]Email: sakcha2@ 123456kku.ac.th . Phone: +66-815-455-388.
                [* ]Email: nuntichoo@ 123456gmail.com . Phone: +66-832-826-932.
                Author information
                https://orcid.org/0000-0002-0154-7388
                https://orcid.org/0000-0002-2891-1135
                Article
                10.1021/acsomega.1c00190
                8209797
                34151061
                fe9e11cd-8fa8-4024-bd96-de1765968f5c
                © 2021 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 12 January 2021
                : 25 May 2021
                Funding
                Funded by: Khon Kaen University, doi 10.13039/501100004071;
                Award ID: NA
                Funded by: Thailand Institute of Nuclear Technology, doi NA;
                Award ID: NA
                Funded by: Department of Chemistry, Srinakharinwirot University, doi NA;
                Award ID: NA
                Funded by: Center of Excellence for Innovation in Chemistry, doi NA;
                Award ID: NA
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                Article
                Custom metadata
                ao1c00190
                ao1c00190

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