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Europium (Eu):Y 2 O 3 -nanoparticles/Mg:ZnO-nanowires/p-GaN and (Eu):chelate-based light-emitting diode (LED) structures have been fabricated, showing controlled mixed near-UV, violet, and red electroluminescence from trivalent europium. The magnesium (Mg)-doped ZnO (Mg:ZnO)-nanowires/p-GaN heterojunction were integrated into the LED structure and were covered on the top with the nanoparticle of yttrium oxide doped with trivalent europium ions (Eu 3+ :Y 2 O 3 ) or by Eu:chelate. Samples exhibit mixed UV/blue light at ∼384 nm coming from the Mg:ZnO structure and a sharp red emission at ∼611 nm related to the intra4f transition of Eu ions. It is found that with Mg doping of ZnO, the emission wavelength of LEDs in the near-ultraviolet region is shifted to a smaller wavelength, thus being better adapted to the trivalent europium excitation band. Radiative energy transfer is achieved through the strong overlap between the emission wavelength from n-(Mg:ZnO)/p-GaN heterojunction and 7 F 0 -5 L 6 absorption of Eu 3+ ions in the case of Eu:Y 2 O 3 or of the (Eu):chelate intensive absorption bands. Indeed, the (Eu):chelate/(Mg:ZnO)-nanowires/p-GaN structure appears to be more adapted to UV/blue and red dual emission than Eu:Y 2 O 3 , for which low absorption prevents efficient emission. Our results demonstrate that the designs of nano-LED structures and of the chelate ligands are crucial to enhance the performance of electroluminescence devices based on ZnO nanowire arrays and rare-earth metal complexes.

Reactive oxygen species (ROS), and notably hydrogen peroxide HO, are cellular second messengers that are known to control a variety of signaling processes. They can finely regulate the dynamics of signal transduction, cell response and ultimately tissue function. However, there are very few local, quantitative and time-resolved descriptions of their cellular organization at the scale of molecular reactions, due to the lack of efficient sensors. We thus developed a novel nanoprobe-based ROS detection system using the simultaneous imaging of single lanthanide nanoparticles (YAG:Ce and chemically reduced GdEuVO). We reveal that both particle luminescence signals are controlled by their HO local environment. By simultaneously tracking their luminescence, we devised a new approach providing a quantitative (0.5 μM accuracy in the 1-10 μM range) HO measurement with a 500 ms time resolution, surpassing all existing methods by two orders of magnitude, and revealing previously inaccessible molecular events controlling ROS concentration. We used this nanoprobe in living cells to track fast signaling pathways, by measuring the dynamics of HO intracellular concentrations, induced by endothelin-1 (ET-1) stimulation. We thus revealed the mechanisms controlling ROS production, notably the activity modulation of the ROS-producing enzyme NADPH oxidase by fast (<10 s) EGFR transactivation, and measured quantitatively their kinetic parameters through a minimal analytical model. Altogether, these results illustrate how lanthanide nanoparticle-based sensors are a powerful tool to dynamically probe molecular mechanisms shaping the oxidative cell response.