A facile method has been developed to extract oxidized carbon quantum dots (QDs) directly from activated carbon (AC) by chemical oxidation. The method has several advantages including low cost, high yield of QDs (>10%), and large-scale production. The as-prepared oxidized carbon QDs are mainly graphitic structure nanocrystals of 3-4 nm in diameter, have abundant carboxyl groups at their surfaces, and exhibit strong electrochemiluminescent (ECL) activity, suggesting promising applications in ECL biosensing and imaging. The ECL properities, including ECL activities in the absence and presence of coreactants, effects of the size and surface passivation on the oxidized carbon QDs ECL were investigated and discussed in detail.

Free chlorine was found to be able to destroy the passivated surface of the graphene quantum dots (GQDs) obtained by pyrolyzing citric acid, resulting in significant quenching of their fluorescence (FL) signal. After optimizing some experimental conditions (including response time, concentration of GQDs, and pH value of solution), a green and facile sensing system has been developed for the detection of free residual chlorine in water based on FL quenching of GQDs. The sensing system exhibits many advantages, such as short response time, excellent selectivity, wide linear response range, and high sensitivity. The linear response range of free chlorine (R(2) = 0.992) was from 0.05 to 10 μM. The detection limit (S/N = 3) was as low as 0.05 μM, which is much lower than that of the most widely used N-N-diethyl-p-phenylenediamine (DPD) colorimetric method. This sensing system was finally used to detect free residual chlorine in local tap water samples. The result agreed well with that by the DPD colorimetric method, suggesting the potential application of this new, green, sensitive, and facile sensing system in drinking water quality monitoring.

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A dinitrophenyl hydrazone colorimetric anion sensor (receptor 1) was synthesized and its recognition properties towards various anions were investigated by naked eye observation and spectroscopic methods, namely UV‐vis and 1H NMR titrations in DMSO. The addition of AcO−, F− and H2PO4− to receptor 1 resulted in marked red shift of the charge‐transfer absorbance band (Δλ=91 nm, 407 nm to 498 nm) concomitant with a 'naked‐eye' detectable colour change from yellow to pink. However, both the colour and spectral changes were reversible by the addition of cations (MII) of 3d5‐10 as well as CdII, HgII, MgII and CaII. Subsequently, complementary IMP/INH logic functions based on colour and spectral switching (ON/OFF) were affirmed. The sensor can, thus be utilized as a colorimetric molecular switch modulated by F−/MII.

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