In this work, we fabricate an oriented luminescent quantum dot (QD)-layered double hydroxide (LDH) nanocomposite material by the highly orderly and alternate assembly of trace CdTe QDs in dodecylbenzene sulfonate bilayer bunches on the organo-modified LDH exterior surfaces. Interestingly, the novel QD-LDH nanocomposites can remarkably amplify chemiluminescence (CL) of the luminol-H2O2 system, which is attributed to an inhibition of QD oxidation by H2O2, an increase in the radiative decay rate, and an inhibition in the nonradiative relaxation of QDs. In addition, a novel flow-through column-based CL resonance energy transfer is fabricated using luminol as energy donors and the solid luminescent QD-LDH nanocomposites as energy acceptors for signal amplification. The applicability of this flow-through column is evaluated by determining H2O2 using luminol-H2O2 CL system. The CL intensity exhibits a stable response to H2O2 over a concentration range from 0.5 to 60 μM with a detection limit as low as 0.3 μM. Finally, the proposed method has been successfully applied to detect H2O2 in snow samples, and the results agreed with those obtained by the standard spectrophotometric method. Our findings indicate that the new luminescent QD-LDH nanocomposite material would be used for high throughput screening of complex systems with different sized QDs.

So-called confinement effects at the interface of nanomaterials could spring up unique properties in catalytical activities and optical amplifiers. There is apparently no good reason to disregard confinement effect-amplified chemiluminescence (CL). In this work, confinement effects were first introduced into CL field using cetyltrimethylammonium bromide (CTAB) bilayer aggregates confined at the interface of the CTAB-carbon dots, which were prepared by one-step microwave irradiation using glycerol as carbon source in the presence of CTAB. Interestingly, it was found that the CTAB bilayer confined at the interface of carbon dots can amplify H2O2 induced ultraweak CL emissions, such as the Co(II)-triggered Fenton-like reaction, the peroxynitrous acid (ONOOH) system, and the peroxymonocarbonate (HCO4(-)) system. The study of fluorescent properties of the as-prepared CTAB-carbon dots and the comparison with the CL efficiency of their analogues indicated that the CTAB bilayer confined in carbon dots could act as a special micelle microenvironment, helping the access of reactive intermediates to the central carbon core. Our findings opened up new possibilities in confinement-enhanced CL emissions.

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