Novel approaches for digital data storage are imperative, as storage capacities are drastically being outpaced by the exponential growth in data generation. Optical data storage represents the most promising alternative to traditional magnetic and solid-state data storage. In this paper, a novel and energy efficient approach to optical data storage using rare-earth ion doped inorganic insulators is demonstrated. In particular, the nanocrystalline alkaline earth halide BaFCl:Sm is shown to provide great potential for multilevel optical data storage. Proof-of-concept demonstrations reveal for the first time that these phosphors could be used for rewritable, multilevel optical data storage on the physical dimensions of a single nanocrystal. Multilevel information storage is based on the very efficient and reversible conversion of Sm to Sm ions upon exposure to UV-C light. The stored information is then read-out using confocal optics by employing the photoluminescence of the Sm ions in the nanocrystals, with the signal strength depending on the UV-C fluence used during the write step. The latter serves as the mechanism for multilevel data storage in the individual nanocrystals, as demonstrated in this paper. This data storage platform has the potential to be extended to 2D and 3D memory for storage densities that could potentially approach petabyte/cm levels.

Structural design of photocatalysts is of great technological importance for practical applications. A rational design of architecture can not only promote the synthetic performance of photocatalysts but also bring convenience in their application procedure. Nanofibers have been established as one of the most ideal architectures of photocatalysts. However, simultaneous optimization of the photocatalytic efficiency, mechanical strength, and thermal/chemical tolerance of nanofibrous photocatalysts remains a big challenge. Here, we demonstrate a novel design of TiO2-SiO2 composite fiber as an efficient photocatalyst with excellent synthetic performance. Core-shell mesoporous SiO2 fiber with high flexibility was employed as the backbone for supporting ultrasmall TiO2 nanowhiskers of the anatase phase, constructing core@double-shell fiber with luffa-sponge-like appearance. Benefitting from their continuously long fibrous morphology, highly porous structure, and completely inorganic nature, the TiO2-SiO2 composite fibers simultaneously possess high photocatalytic reactivity, good flexibility, and excellent thermal and chemical stability. This novel architecture of TiO2-SiO2 glass composite fiber may find extensive use in the environment remediation applications.

Structural design is of great importance to the performance of photocatalysts in environmental remediation. Therefore, micro/nanofibrous morphology and nanoporous local structures have been found to be beneficial to improve the photocatalytic activity. In this investigation, we report the design and fabrication of flexible and thermal stable nanoporous SiO2–TiO2 composite fibers as efficient photocatalysts. Combining electrospinning and modified Stöber techniques, core‐shell and mesoporous SiO2 fibers with high flexibility were fabricated and employed as the scaffold for supporting TiO2 nanoparticles. A nanoporous shell of TiO2 nanoparticles was then muffled over the SiO2 fibers to form core@dual‐shell SiO2–TiO2 composite fibers with hierarchically porous structure, which were conveniently patterned into a nonwoven, recyclable film. This nonwoven film exhibits better photocatalytic activity for Rhodamine B degradation under UV irradiation compared with some other TiO2‐based materials reported in recent years.

No abstract

This work develops a high-transparency amorphous film with a wide transmission window and high refractive index, which can potentially meet the strong demand of integrating functional nanoparticles for the next-generation hybrid optoelectronic films.