Design of coherent wideband radiation process in a Nd3+-doped high entropy glass system.

We discover that the spatially coherent radiation within a certain frequency range can be obtained without a common nonlinear optical process. Conventionally, the emission spectra were obtained by de-exciting excited centers from real excited energy levels to the ground state. Our findings are achieved by deploying a high-entropy glass system (HEGS) doped with neodymium ions. The HEGS exhibits a much broader infrared absorption than common glass systems, which can be attributed to be high-frequency optical branch phonons or allowable multi-phonon processes caused by phonon broadening in the system. A broadened phonon-assisted wideband radiation (BPAWR) is induced if the pump laser is absorbed by the system. The subsequent low-threshold self-absorption coherence modulation (SACM) can be controlled by changing excitation wavelengths, sample size, and doping concentrations. The SACM can be red-shifted through the emission of phonons of the excited species and be blue-shifted by absorbing phonons before they are de-excited. There is a time delay up to 1.66 ns between the pump pulse and the BPAWR when measured after traveling through a 35 mm long sample, which is much longer than the Raman process. The BPAWR-SACM can amplify the centered non-absorption band with a gain up to 26.02 dB. These results reveal that the shift of the novel radiation is determined by the frequency of the non-absorption band near the absorption region, and therefore the emission shifts can be modulated by changing the absorption spectrum. When used in fiber lasers, the BPAWR-SACM process may help to achieve tunability.

Magnetic tuning of upconversion luminescence in Au/NaGdF4:Yb3+/Er3+ nanocomposite.

Lanthanide-doped upconversion nanoparticles (UCNPs) NaGdF4:Yb3+/Er3+ have received increasing attention due to their unique optical-magnetic bifunctional properties. Here, we show that the luminescent intensity from NaGdF4:Yb3+/Er3+ nanoparticles decreases monotonously with increasing the applied magnetic field from 0 to 37.1 T, while plasmon-enhanced upconversion luminescence in Au/NaGdF4:Yb3+/Er3+ nanocomposite is independent of a magnetic field lower than 6 T. The surface plasmon resonances could compensate for the energetic mismatching between the excitation light and the energy-level gaps induced by magnetic field and enhance the radiative efficiency, which is the main factor for achieving this stable upconversion emission in this nanocomposite under a magnetic field not higher than 6 T. These findings provide a novel route for exploring the magnetic control of upconversion luminescence in lanthanide-doped bifunctional nanoparticles.

Enhanced upconversion luminescence through core/shell structures and its application for detecting organic dyes in opaque fishes.

Here, we report the enhanced upconversion luminescence of NaLuF4:18%Yb(3+),2%Er(3+) through core/shell structures. Among NaYF4, NaGdF4, and NaLuF4 shells, the first one presents the highest efficiency. These upconversion fluorescent nanoprobes with an oleic acid/PEG hybrid ligand can efficiently capture Rhodamine B (RB) and sodium fluorescein (SF) in opaque fishes to present their residues in vivo through luminescence resonant energy transfer (LRET) processes. It can be confirmed based on LRET technology that no RB is absorbed by opaque fishes after incubating in the aqueous solution of 1 µg ml(-1) RB for one day, while SF residue can be obviously detected after incubating in the aqueous solution of 1 µg ml(-1) SF for one day. The merit of this LRET technology with the upconversion nanoparticle (UCNP) donor is ascribed to the deep penetration depth of the infrared pumping laser and high signal to noise ratio.