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A molten salt (MS) method is designed for the preparation of carbon dot-based room temperature phosphorescent (RTP) materials. Carbon dots (CDs) are in situ formed and confined in inorganic salts during the recrystallization process. The composite materials CDs@MS and their RTP were characterized by scanning electron microscopy (SEM), powder X-ray diffraction (PXRD) and low temperature (77 K) fluorescence and phosphorescence spectroscopy. The as-prepared CDs@MS exhibits long lifetime RTP (up to 886 ms) and excitation dependent phosphorescence, i.e., the emission can be facilely tuned from 510 nm to 573 nm (green to yellow color) by changing the excitation wavelength. The RTP phenomenon is ascribed to the fact that the crystallization of molten salts forms a rigid structure, which preserves the triplet state of CDs and suppresses the nonradiative transition. It was found that the high charge density of metal ions plays a critical role in reducing the energy gap for realizing effective intersystem crossing. CD-based RTP materials with yellow phosphorescent emission are achieved from a variety of carbon sources and a gram-scale synthetic method. The excitation dependent RTP feature of CDs@MS nanocomposites could provide a novel dual security protection strategy in high-level information anticounterfeiting.

White-light-emitting devices (WLEDs) are considered to be a promising illumination source; especially, the WLEDs based on carbon dots (CDs) with white fluorescence have attracted extensive research interest. Herein, we report the design and implementation of solid white-light-emitting phosphors (WCDs@PS), which combine blue and orange emissive CDs (BCDs and OCDs) assisted by polystyrene (PS) through a self-assembly technique. Based on these phosphors (OCDs/BCDs = 1.2:1), the obtained WLEDs display a warm white light with International Commission on Illumination (CIE) coordinates of (0.35, 0.36), a high color rendering index of 93.2, a low correlated color temperature of 4075 K, and a luminous efficiency of up to 14.8 lm·W -1 . Interestingly, these WLEDs exhibit temperature-dependent emission performance, whose light-emission spectrum can be adjusted in situ from white (λ ∼ 400-730 nm) to blue (λ ∼ 440 nm) in the range of 20-80 °C. A change in CIE coordinates from (0.35, 0.36) to (0.32, 0.23) was also observed. The temperature-driven tunable LEDs as a thermochromism device could broaden the application of CDs-based lighting systems in special displays.

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 H 2 S.

The development of full-color/white carbon-dot-based light-emitting diodes (LEDs) has been achieved, which show promising applications in full-color and flexible displays, backlights, and novel lighting sources. The gram-level synthesis of these full-color carbon dots (CDs) from citric acid by controlling the temperature has been achieved. By increasing the temperature from 120 to 180 °C, two, four, and six light-emitting CDs can be obtained, for which the emission wavelength shifts from 440 to 585 nm. This result reveals that temperature has a huge impact on the evolution of surface states, that is, increasing the temperature brings about enhanced surface functionalization and passivation, resulting in a red shift of the emission wavelength and enhancement of quantum yield. Then, full-color CDs/polymer composite phosphors are fabricated for efficient phosphor-based LED devices with quench-resistant solid-state fluorescence. By regulating the proportion of various CDs/polymer phosphors, white LEDs are realized with Commission Internationale de L'Eclairage coordinates of (0.32, 0.33) and a color rendering index of 82.7. The as-prepared CD-based full/white color LEDs can prove to be promising candidates for alternative light sources., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

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.)