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Background: Photoluminescent materials have been used for diverse applications in thefields of science and engineering, such as optical storage, biological labeling, noninvasive imaging,solid-state lasers, light-emitting diodes, theranostics/theragnostics, up-conversion lasers, solar cells,spectrum modifiers, photodynamic therapy remote controllers, optical waveguide amplifiers andtemperature sensors. Nanosized luminescent materials could be ideal candidates in these applications.

Objective: This review is to present a brief overview of photoluminescent nanofibers obtainedthrough electrospinning and their emission characteristics.

Methods: To prepare bulk-scale nanosized materials efficiently and cost-effectively, electrospinningis a widely used technique. By the electrospinning method, a sufficiently high direct-current voltageis applied to a polymer solution or melt; and at a certain critical point when the electrostatic forceovercomes the surface tension, the droplet is stretched to form nanofibers. Polymer solutions or meltswith a high degree of molecular cohesion due to intermolecular interactions are the feedstock. Subsequentcalcination in air or specific gas may be required to remove the organic elements to obtainthe desired composition.

Results: The luminescent nanofibers are classified based on the composition, structure, and synthesismaterial. The photoluminescent emission characteristics of the nanofibers reveal intriguing featuressuch as polarized emission, energy transfer, fluorescent quenching, and sensing. An overview of theprocess, controlling parameters and techniques associated with electrospinning of organic, inorganicand composite nanofibers are discussed in detail. The scope and potential applications of these luminescentfibers also conversed.

Conclusion: The electrospinning process is a matured technique to produce nanofibers on a largescale. Organic nanofibers have exhibited superior fluorescent emissions for waveguides, LEDs andlasing devices, and inorganic nanofibers for high-end sensors, scintillators, and catalysts. Multifunctionalitiescan be achieved for photovoltaics, sensing, drug delivery, magnetism, catalysis, andso on. The potential of these nanofibers can be extended but not limited to smart clothing, tissueengineering, energy harvesting, energy storage, communication, safe data storage, etc. and it isanticipated that in the near future, luminescent nanofibers will find many more applications in diversescientific disciplines.

 

Fluorides are promising host materials for optical applications. This paper reports the photoluminescent (PL) and cathodoluminescent (CL) characteristics of barium hexafluorogermanate BaGeF 6 nanowires codoped with Ce 3+ , Tb 3+ and Sm 3+ rare earth ions, produced by a solvothermal route. The synthesized BaGeF 6 nanowires exhibit uniform morphology and size distribution. X-ray diffraction divulges the one-dimensional growth of crystalline BaGeF 6 structure, with the absence of any impurity phases. Visible luminescence is recorded from the nanowires in green and red regions, when the nanowires are codoped with Ce 3+ /Tb 3+ , and Ce 3+ /Tb 3+ /Sm 3+ , respectively, under a UV excitation source. The PL emission from the codoped BaGeF 6 nanowires, when excited by a 254 nm source, originates from the efficient energy transfer bridges between Ce 3+ , Tb 3+ and Sm 3+ ions. The decay time of the visible luminescent emission from the nanowires is in the order of subnanoseconds, being one of the shortest decay time records from inorganic scintillators. The CL emission from the BaGeF 6 nanowires in the tunable visible range reveals their potential use for the detection of high-energy radiation. The PL emissions are sensitive to H 2 O 2 at low concentrations, enabling their high-sensitivity detection of H 2 O 2 using BaGeF 6 nanowires. A comparison with BaSiF 6 nanowires is made in terms of decay time and its sensitivity towards H 2 O 2 . 

Inorganic materials with short radiative decay time are highly desirable for fast optical sensors. This paper reports fast photoluminescence (PL) from a series of barium hexafluorosilicate (BaSiF 6 ) superlong nanowires with high aspect ratios, codoped with Ce 3+ /Tb 3+ /Eu 3+ ions, with a subnanosecond decay time. Solvothermally synthesized BaSiF 6 nanowires exhibit a uniform morphology, with an average diameter less than 40 nm and aspect ratios of over several hundreds, grown in the c -axis direction with {110} surfaces. The PL emission from the codoped BaSiF 6 nanowires, when excited by a 254 nm source, is dependent on Tb 3+ concentration, and the energy transfer from Ce 3+ to Tb 3+ and to Eu 3+ ions allows efficient emissions in the visible spectra when excited by a near UV source. Annealing BaSiF 6 nanowires at 600 °C in a vacuum produced barium fluoride (BaF 2 ) nanowires composed of nanocrystals. Both BaSiF 6 and BaF 2 nanowires exhibit fast emissions in the visible spectra, with enhanced intensities compared with their codoped microparticle counterparts. The decay time of codoped BaSiF 6 nanowires is found to be shorter than that of codoped BaF 2 nanowires. The energy transfer is also observed in their cathodoluminescence spectra with high-energy irradiation.