2022
DOI: 10.1007/s00216-022-03901-2
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Green-emitting carbon quantum dots as a dual-mode fluorescent and colorimetric sensor for hypochlorite

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Cited by 20 publications
(11 citation statements)
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“…It seems that hypochlorite and luminol exhibit direct chemiluminescence (CL) under alkaline conditions without any catalyst. 32,33 This argument was confirmed by a blue luminescence seen on the surface of the BDD electrode directly after the addition of 10 mM NaClO without any potential applied (ESI; S2 †). Accordingly, it is concluded that the ECL signal was generated by the remaining luminol that did not react with hypochlorite through the CL reaction.…”
Section: Resultsmentioning
confidence: 70%
See 1 more Smart Citation
“…It seems that hypochlorite and luminol exhibit direct chemiluminescence (CL) under alkaline conditions without any catalyst. 32,33 This argument was confirmed by a blue luminescence seen on the surface of the BDD electrode directly after the addition of 10 mM NaClO without any potential applied (ESI; S2 †). Accordingly, it is concluded that the ECL signal was generated by the remaining luminol that did not react with hypochlorite through the CL reaction.…”
Section: Resultsmentioning
confidence: 70%
“…Having the same characteristic with H 2 O 2 as reactive oxygen species (ROS), 32,33 hypochlorite was expected to act as a coreactant in the ECL system; indeed it quenches the ECL signals. It seems that hypochlorite and luminol exhibit direct chemiluminescence (CL) under alkaline conditions without any catalyst.…”
Section: Resultsmentioning
confidence: 99%
“…A sharp amido peak (C=O) at 1650 cm −1 was observed in the spectrum of B‐CNDs, indicating that the formamide used as a reaction solvent may have become incorporated into the carbon structure of the CNDs. [ 48 ] G‐CNDs showed a different spectrum pattern from B‐CNDs: hydrophilic functional groups from phenolic –OH (1320 cm −1 ) and –NH 2 (1619 cm −1 ) were dominantly observed, [ 49,50 ] in addition to aromatic vibration peaks (880, 954, and 1036 cm −1 ), and conjugated C=C (1435 and 1619 cm −1 ). These hydrophilic functional groups imparted the G‐CNDs with high dispersibility in water.…”
Section: Resultsmentioning
confidence: 99%
“…A sharp amido peak (C=O) at 1650 cm À1 was observed in the spectrum of B-CNDs, indicating that the formamide used as a reaction solvent may have become incorporated into the carbon structure of the CNDs. [48] G-CNDs showed a different spectrum pattern from B-CNDs: hydrophilic functional groups from phenolic -OH (1320 cm À1 ) and -NH 2 (1619 cm À1 ) were dominantly observed, [49,50] CNDs at +4.6 mV and +20 mV, respectively. The significantly higher positive value of G-CNDs reflects the rich amino groups of G-CNDs, [51] which is consistent with the result of the corresponding FTIR spectrum.…”
Section: Optical Characterization Cndsmentioning
confidence: 94%
“…CDs can be synthesized by many methods including hydrothermal reactions, 15 microwave-assisted technique, 16 laser ablation, 17 chemical oxidation 18 and solid-state reaction. 19 Compared with other methods, microwave-assisted technology has many advantages, such as simplicity, environmental protection, economy, short reaction time, low energy consumption and high reaction yield. The synthesis of CDs can use the microwave oven.…”
Section: Introductionmentioning
confidence: 99%