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Versatile species have been increasingly recognized as important components and possible fluorescence origins in carbon dots synthesized via a bottom-up route. Herein, we use 2,7-naphthalenediol an...

Lead halide perovskite quantum dots (PQDs) have recently been proposed as scalable and color-tunable single emitters, but their slow spontaneous emission (1–10 ns) creates a mismatch with high-spee...

Herein, we report an ethanothermal synthesis of multicolor fluorescent carbon dots (CDs) by using a series of phenols and oxidants as the precursors. The emission colors of CDs are well-controlled at blue, green, yellow or red wavelengths by adjusting the combination of a phenol and an oxidant. And the naphthalenediol with highly reactivity and the oxidant with heavy halogen atom result in CDs exhibiting long wavelength emission. The resulting nanodots are characterized as amorphous aggregates with abundant oxygen species. The phenol-derived CDs can be used as highly processible fillers to fabricate epoxy composites, and a white light-emitting diode (LED) employing the multicolor CDs/epoxy composite as the light converter is also demonstrated.

Fluorophores and hydrogen bonding interactions play key roles in the fluorescence properties of bottom-up carbon dots. In this work, an excited-state intramolecular proton-transfer (ESIPT) active fluorophore, 5-chloro-6-ethoxy-4,7-dihydroxyisoindoline-1,3-dione (CEDD) and a non-ESIPT 7-cyano-5,8-dihydroxyquinoxaline-6-carboxamide (CDQC) are extracted from 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) based carbon dots. The enol form of CEDD shows a weak blue, small Stokes shift and short lifetime emission under the aprotic or alkali conditions, but the keto form exhibits a strong green, large Stokes shift and long lifetime emission in a protic or an acidic environment. Due to the lack of the ESIPT process, CDQC has no dual emission characteristics, but shows efficient solid-state emission. By virtue of the ESIPT ability of CEDD, multiple anti-counterfeiting methods are achieved by using hydrogen chloride, ammonia, and fluorescence lifetime imaging, as well as dimethyl sulfoxide as the encryption/decryption tools.

Lead halide perovskite quantum dots (PQDs) have recently been proposed as a scalable and color-tunable quantum source, but their slow spontaneous emission creates a mismatch with high-speed nanophotonic devices. Here, we demonstrate fast and bright emission in PQD films coupled to silver nanowire networks (NWKs), in which polyvinyl alcohol (PVA) is used as a spacer to regulate the lossy characteristics of the plasmonic cavity. Compared with bare quartz, the PVA substrate shows a considerable enhancement effect on the apparent emission intensity, but a reduction in the emission rate of PQD excitons. The efficient NWK-PQD coupling generates an increase in the emission intensity of a factor of 6.0 (average 3.4) and simultaneously a 2.4-fold (average 1.9) enhancement in the emission rate. However, an opposite PVA spacer thickness dependence for Purcell factor and quantum yield is observed, indicating that the fast and bright emission would be a trade-off between the Purcell-enhanced radiative rate and large metal loss. These results are believed to provide fundamental guidance on plasmonic cavity design for perovskite-based nanophotonic devices.

Hybrid nanostructures comprising conjugated polymers (CPs) and plasmonic metals show excellent performance in light harvesting. However, the energy transfer mechanism of the CP film to nearby metal nanoparticles, especially knowledge of the characteristic distance, is still unclear. Here, quenching of the emission of a CP film in proximity to a monolayer of graphene-nanodot-supported silver nanoparticles (GND-Ag NPs) is investigated. Uniform Ag NPs with D = 3.2 nm were grown on GNDs in situ under mild light irradiation, and a series of bilayer structures of GND-Ag NPs/CPs were constructed by spin-coating blue, green and red light-emitting poly(9,9-dioctylfluorene) (PFO), poly(9,9-dioctylfluorene-alt-benzothiadiazole) (F8BT) and poly[2-methoxy-5-(2′-ethylhexyloxy)-p-phenylene vinylene] (MEH-PPV),respectively, on top of the GND-Ag NP plane. The spacer distance was controlled by the layers of assembled polyelectrolytes. Both steady and transient photoluminescence (PL) spectra showed emission quenching of the bilayer structures, providing the maximum efficiency of 99% for the F8BT films. The surface density of GND-Ag NPs and the spacer distance-dependent PL quenching data were analyzed within the plasmonic resonant energy transfer model, and the extracted characteristic distances are 6 nm, 3 nm and 10 nm for the PFO, F8BT and MEH-PPV systems, respectively. Current-sensing atomic force microscopy shows that the GND-Ag NPs/F8BT film exhibits enhanced electrical conductivity. These results are believed to be important for the development of plasmonic enhanced polymer photovoltaics and photocatalysis.

The plasmonic enhancement of conjugated polymer (CP) based light-emitting device calls for large scale and high quality plasmonic crystals (PlCs). Herein, silver nanocubes with diameters of 55 nm and 100 nm have been respectively assembled into closely packed PlC-55 and PlC-100 through oil-water interfacial assembly method. By coupling with the PlCs, the photoluminescence (PL) of polyfluorene copolymer can be enhanced in a broad range of excitation and emission wavelengths, exhibiting over 10-fold enhancement in PL intensity as the PlC-CP separation is controlled at 11 nm by using polyvinylalcohol as a spacer. The Purcell factors of CPs show both particle size and emission wavelength dependence, where the maximum value of 4.5 are found in CPs that are placed on PlC-100 at wavelengths near the CP emission peak.