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      Nitrogen and Phosphorus Co-Doped Carbon Dots for Selective Detection of Nitro Explosives

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      ACS Omega
      American Chemical Society

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          Abstract

          In this work, a highly selective and sensitive method has been developed for the detection of trinitrophenol (TNP), which is a dangerous explosive. For this purpose, N and P co-doped carbon dots (NP-Cdots) have been used. Synthesis of N and P co-doped carbon dots has been carried out by a simple and quick method. X-ray photoelectron spectroscopy analysis was carried out to detect the doping of N and P. These carbon dots are insoluble in water (inNP-Cdots). These carbon dots were functionalized by treating them with conc. HNO 3 so that they become water-soluble (wsNP-Cdots). These dots were characterized by different analytical techniques such as IR, UV–vis, and fluorescence spectroscopy. The as-prepared wsNP-Cdots have good fluorescence properties. The average diameter of wsNP-Cdots is found to be 5.7 nm with an interlayer spacing ( d-spacing) of 0.16 nm. The as-prepared wsNP-Cdots are highly sensitive and selective toward TNP, as observed using a fluorescence quenching technique. The quenching constant for TNP is found to be very high (8.06 × 10 4 M –1), which indicates its high quenching ability. The limit of detection is found to be 23 μM.

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          Chemical sensors based on amplifying fluorescent conjugated polymers.

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              Tuning the acid/base properties of nanocarbons by functionalization via amination.

              The surface chemical properties and the electronic properties of vapor grown carbon nanofibers (VGCNFs) have been modified by treatment of the oxidized CNFs with NH(3). The effect of treatment temperature on the types of nitrogen functionalities introduced was evaluated by synchrotron based X-ray photoelectron spectroscopy (XPS), while the impact of the preparation methods on the surface acid-base properties was investigated by potentiometric titration, microcalorimetry, and zeta potential measurements. The impact of the N-functionalization on the electronic properties was measured by THz-Time Domain spectroscopy. The samples functionalized via amination are characterized by the coexistence of acidic and basic O and N sites. The population of O and N species is temperature dependent. In particular, at 873 K nitrogen is stabilized in substitutional positions within the graphitic structure, as heterocyclic-like moieties. The surface presents heterogeneously distributed and energetically different basic sites. A small amount of strong basic sites gives rise to a differential heat of CO(2) adsorption of 150 kJ mol(-1). However, when functionalization is carried out at 473 K, nitrogen moieties with basic character are introduced and the maximum heat of adsorption is significantly lower, at approximately 90 kJ mol(-1). In the latter sample, energetically different basic sites coexist with acidic oxygen groups introduced during the oxidative step. Under these conditions, a bifunctional acidic and basic surface is obtained with high hydrophilic character. N-functionalization carried out at higher temperature changes the electronic properties of the CNFs as evaluated by THz-TDS. The functionalization procedure presented in this work allows high versatility and flexibility in tailoring the surface chemistry of nanocarbon material to specific needs. This work shows the potential of the N-containing nanocarbon materials obtained via amination in catalysis as well as electronic device materials.
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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                04 February 2020
                18 February 2020
                : 5
                : 6
                : 2710-2717
                Affiliations
                Department of Chemistry, University of Mumbai , Vidyanagari, Santacruz (E), Mumbai 400 098, India
                Author notes
                [* ]E-mail: ssgarje@ 123456chem.mu.ac.in , ssgarje@ 123456yahoo.com . Phone: +91-22-2654 3368. Fax: +91-22-2652 8547.
                Article
                10.1021/acsomega.9b03234
                7033677
                32095694
                600b4df8-d67b-475c-994c-e658dba31acc
                Copyright © 2020 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 01 October 2019
                : 23 January 2020
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                ao9b03234

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