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Fluorescence-based nanothermometers have potential to offer accuracy in the measurement of temperature using non-contact approaches. Herein, a C-dot/C-dot based dual-emission temperature sensing platform is fabricated through the electrostatic self-assembly of two kinds of fluorescent CDs with opposite charges. This dual-emission platform consists of several nearly-spherical CDs with two emission centers in blue (440 nm) and orange (590 nm) regions. The orange fluorescence exhibits discernible response to external temperatures in the range of ∼15 to 85 °C; on the other hand, the blue fluorescence remains nearly constant. A continuous fluorescence color change in response to temperature from orange to blue can be clearly observed by the naked eye. Thus, the as-prepared C-dot based dual-emission nanospheres can be used for optical thermometry with high reproducibility and sensitivity (0.93%/°C). Detailed characterization shows that temperature (in the 15-85 °C window) impacts the surface states of orange emissive CDs, leaving the blue emissive CDs unaffected. A model is proposed to explain the observations. Finally, by taking advantage of the excellent biocompatibility and stability, the CD based fluorescent nanothermometer is successfully used for the visual measurement of intracellular temperature variations.

Nitrogen doping can effectly adjust the compositions and structures of carbon dots and hence enhance their fluorescence. In this work, we report a fast and low-cost route for synthesis of nitrogen-doped carbon dots (N-CDs) by microwave pyrolysis of citric acid and ammonium within 7 min. The as-prepared N-CDs contain plentiful oxygen and nitrogen functional groups, and dispaly intense fluorescence with high quantum yield of ca. 44.3% and have an average size of 1.8 nm. The obtained N-CDs exhibit highly stable against photobleaching, ionic strengths, and can be used for selective and sensitive detection of Fe(III). It is postulated that the Fe 3+ -mediated fluorescence quenching is attributed to the charge transfer between N-CDs and Fe 3+ . In particular, the emission peaks from blue to red region can be tuned by interparticle distance of N-CDs, simply by increasing the concentration of N-CDs in aqueous solution, which indicates its potential applications as a promising optical image probe in multicolor cellular imaging., (Copyright © 2018 Elsevier Inc. All rights reserved.)

A series of dual-emission fluorescent probes was prepared from copper nanoclusters (Cu NCs) and carbon dots (CDs). They show two emission peaks (blue at 469 nm and red at 622 nm) when photoexcited at 365 nm. Upon exposure to sulfide, the Cu NCs will be deteriorated because they react with sulfide to form CuS. This results in the quenching of the red fluorescence of the Cu NCs, while the blue fluorescence of the CDs remains constant. Thus, the color of the nanocomposite changes from red to blue. The ratio of the fluorescences at the two wavelengths decreases linearly in the 2–10 ppb (26–128 nM) sulfide concentration range, and the limit of detection is 0.33 ppb (4.3 nM). The nanocomposite also was placed in an agar gel and then incorporated into a paper strip for fluorometric monitoring of gaseous hydrogen sulfide. Graphical abstract Schematic presentation of the synthesis of Cu NCs (copper nanoclusters)-CDs (carbon dots) dual-emission nano-assembly, Cu NCs-CDs-agar fluorescent film and their application for the detection of sulfide and H2S. [ABSTRACT FROM AUTHOR]