2016
DOI: 10.1039/c6tc03027k
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Synthesis of amphiphilic carbon quantum dots with phosphorescence properties and their multifunctional applications

Abstract: Amphiphilic quantum dots with phosphorescence properties have been synthesized and applied for ion detection and two-photon cell imaging.

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Cited by 107 publications
(73 citation statements)
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“…The PVA is found to be an ideal candidate for preparing composite film. CDs@PVA composite film can be easily fabricated by homogeneous dispersion of as‐prepared CDs into a PVA aqueous solution, followed by coating and drying/annealing . Such a method is very simple, in contrast to the abovementioned chemical methods for CDs‐based composites.…”
Section: Synthesis Of Cds‐based Composite Materialsmentioning
confidence: 99%
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“…The PVA is found to be an ideal candidate for preparing composite film. CDs@PVA composite film can be easily fabricated by homogeneous dispersion of as‐prepared CDs into a PVA aqueous solution, followed by coating and drying/annealing . Such a method is very simple, in contrast to the abovementioned chemical methods for CDs‐based composites.…”
Section: Synthesis Of Cds‐based Composite Materialsmentioning
confidence: 99%
“…The CDs dispersed in water or in PVA film showed emissions at 400 nm when excited under 325 nm, but the CDs in a PVA matrix displayed an extra phosphorescence at 500 nm with a lifetime of 350 ms after UV light was turned off ( Figure a–c). Later, two RTP composites with lifetimes of 450 and 8.7 ms were prepared by doping CDs and CDs in PVA and PU matrices, respectively . More recently, thermal‐treatment controlled RTP composites were discovered in which the green phosphorescence appeared in different CDs@PVA films after different thermal annealings (150 or 200 °C) .…”
Section: Photoluminescence Of Cds‐based Composite Materialsmentioning
confidence: 99%
“…[15,19,34] According to these considerations,w ehave found ao nepot method for the facile and quick preparation of ultralong RTP( URTP) CDs.A ss hown in Figure 1a,b,g ram-scale URTP CDs can be obtained in afew minutes via microwaveassisted heating of an ethanolamine and phosphoric acid aqueous solution, and subsequent dialysis purification and freeze-drying (more details in Supporting Information). [26][27][28][29][30][31][32] Note that the as-developed method features facile,quick and scalable merits,t he obtained product possesses URTP life-time and could potentially be employed as security ink in anti-counterfeiting and information protection. Importantly,t he CDs present the longest RTPlifetime to be 1.46 s(more than 10 s to naked eye,F igure 1c and Video 1i nS upporting Information) among the reported CDs-based materials to date.…”
mentioning
confidence: 99%
“…[26,47] Thec haracteristic absorption peaks located at 1689, 1280, 1421, and 937 cm À1 originate from the stretching vibrations of C=Oa nd CÀOb onds,a nd the in-plane and out-of-plane bending vibration of ÀOH on aromatic carboxyl groups (ÀCOOH), respectively. [26,[47][48][49] These FTIR results can be further confirmed by the XPS analysis.Asshown in Figure 2f, the TA-CDs mainly contain Ca nd Oe lements with corresponding contents to be 63.32 %a nd 36.68 %, respectively. TheH RX PS C1ss pectrum can be deconvoluted into four peaks at 284.6, 285.6, 288.8, and 290.5 eV (Figure 2g), contributing to C=Ca nd CÀOb onds, ÀCOOH group,a nd p!p*s hake-up of aromatic network, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…[48][49][50] The HR XPS O1ss pectrum is fitted by two peaks at 531.8 and 533 eV that can be assigned to O=Ca nd CÀOb onds, respectively ( Figure 2h). [26,47,48] Moreover,t he 1 Ha nd 13 CNMR spectra exhibit that the TA-CDs only contain aromatic H(7.62-8.48 ppm) and carboxyl H(13.28 ppm), and sp 2 C( 129.58-134.89 ppm) and carboxyl C( 167.12 and 167.05 ppm), respectively (Supporting Information, Figures S1 and S2). [51,52] To further clarify the formation and chemical structure of TA-CDs,F TIR and NMR spectra of the precursor TA were also measured and compared with that of the TA-CDs.I n detail, the obviously reduced absorption at 3427 cm À1 ( À OH stretching vibration from carboxyl groups) and increased absorptions at 1610, 1578, 1510, and 1421 cm À1 (C=Cstretching vibrations) in FTIR spectra from TA to TA-CDs imply the loss of carboxyl groups and production of more sp 2 structures in the TA-CDs (Figure 2e).…”
Section: Resultsmentioning
confidence: 99%