4.7 Article

Nitrogen/sulfur-doped dual-emission carbon dots with tunable fluorescence for ratiometric sensing of ferric ions and cell membrane imaging

Journal

APPLIED SURFACE SCIENCE
Volume 572, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2021.151447

Keywords

Dual-emission CDs; Long wavelength; Tunable fluorescence; Nitrogen/sulfur doped; Ratiometric Fe3+ sensing; Cell membrane imaging

Funding

  1. GDAS' Project of Science and Technology Development [2019GDASYL-0103013, 2017GDASCX-0102, 2018GDASCX-0102]
  2. Third Batch of Xijiang Innovation and Entrepreurship Team Projects in Zhaoqing

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This study successfully synthesized nitrogen/sulfur-doped dual-emission CDs through solvothermal treatment of sodium alginate and glutathione in formamide, presenting excellent photostability, high nitrogen level, tunable fluorescence, and low detection limit for Fe3+ sensing. The fluorescence-tunable dual-emission CDs exhibited great potential in environmental monitoring and specific cell membrane imaging due to their unique properties.
Intrinsic dual-emission carbon dots (CDs) with long wavelength and self-calibration attributes are critical in fluorescence sensing and imaging, but their synthesis remains a great challenge. Here, nitrogen/sulfur-doped dual-emission CDs (NS-CDs) of different sizes were controllably synthesized by solvothermally treatment of sodium alginate (SA) and glutathione (GSH) in formamide. Interestingly, these as-prepared NS-CDs exhibit enchanting dual-emission behavior at 480 and 650 nm, tunable fluorescence, superior photostability, and high nitrogen level up to 19.57%. The decreasing mass ratio of SA/GSH for the synthesis can lead to larger size and lower graphitic nitrogen for NS-CDs, ultimately giving the enhanced photoluminescence (PL) and tunable fluorescence changing from cyan to white-blue. The selected dual-emission NS-CDs showed superior selectivity and sensitivity for ratiometric Fe3+ sensing with a detection limit as low as 0.56 mu M because of the aggregation of NS-CDs induced by Fe3+, and achieved the Fe3+ detection in environment water. Moreover, the fluorescence-tunable NS-CDs possessing plenteous hydrophilic groups exhibit excellent biocompatibility and unprecedented localized capability for specific cell membrane imaging. This study designs a facile and economical strategy to prepare dual-emission CDs with long wavlength, tunable fluorescence and high nitrogen level, which present bright prospects in environmental monitoring and cell imaging.

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