Efficient Red/Near‐Infrared‐Emissive Carbon Nanodots with Multiphoton Excited Upconversion Fluorescence
Red/near‐infrared (NIR) emissive carbon nanodots (CNDs) with photoluminescence (PL) quantum yield (QY) of 57% are prepared via an in situ solvent‐free carbonization strategy for the first time. 1‐Photon and 2‐photon cellular imaging is demonstrated by using the CNDs as red/NIR fluorescence agent due...
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Published in | Advanced science Vol. 6; no. 17; pp. 1900766 - n/a |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
John Wiley & Sons, Inc
01.09.2019
John Wiley and Sons Inc Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2198-3844 2198-3844 |
DOI | 10.1002/advs.201900766 |
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Summary: | Red/near‐infrared (NIR) emissive carbon nanodots (CNDs) with photoluminescence (PL) quantum yield (QY) of 57% are prepared via an in situ solvent‐free carbonization strategy for the first time. 1‐Photon and 2‐photon cellular imaging is demonstrated by using the CNDs as red/NIR fluorescence agent due to the high PL QY and low biotoxicity. Further study shows that the red/NIR CNDs exhibit multiphoton excited (MPE) upconversion fluorescence under excitation of 800–2000 nm, which involves three NIR windows (NIR‐I, 650–950 nm; NIR‐II, 1100–1350; NIR‐III, 1600–1870 nm). 2‐Photon, 3‐photon, and 4‐photon excited fluorescence of the CNDs under excitation of different wavelengths is achieved. This study develops an in situ solvent‐free carbonization method for efficient red/NIR emissive CNDs with MPE upconversion fluorescence, which may push forward the application of the CNDs in bioimaging.
Red/near‐infrared (NIR) emissive carbon nanodots (CNDs) with photoluminescence quantum yield of 57% are demonstrated via an in situ solvent‐free strategy. 1‐Photon and 2‐photon cellular imaging is demonstrated. Furthermore, multiphoton excited red/NIR fluorescence of the CNDs is achieved. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2198-3844 2198-3844 |
DOI: | 10.1002/advs.201900766 |