Mechanoluminescent (ML) materials featuring renewable mechanical‐to‐optical conversion have shown promising prospects in stress sensing, lighting, and display. However, the advancement in ML applications is being restrained by the obstacles in developing efficient ML materials and understanding the underlying ML mechanisms. Herein, a matrix evolution strategy to modulate the local microstructure and electronic environment around the luminescent activators is proposed, which not only supports the batch development of new ML materials but also provides a well‐connected platform for systematically revealing the mechanism of achieving efficient ML performance. The feasibility of the strategy is proved by constructing and evaluating a series of ML materials with matrix‐dependent luminescent properties in experimental‐theoretical collaboration. It is demonstrated that the construction of piezoluminescence is available in both non‐centrosymmetric and centrosymmetric matrices without being restricted by lattice symmetry. The inter‐electronic‐levels and shallow electron traps formed by activator doping enhance the electron recombination efficiency through tunneling and conduction band transfer pathways. The results are expected to accelerate the exploitation of ML material systems and to deepen the comprehensive apprehending of ML mechanisms, thereby guiding the rational design and widespread use of efficient ML materials.
Regulating fluorescence lifetime of lanthanide nanocomposites is highly desired for optical multiplexing applications, for instance, security printing, anticounterfeiting, and data storage. Herein, sensitive fluorescence lifetime tuning in nanocomposite fibers is reported which are composed of silica-coated gold nanorods assembled in Eu-polystyrene nanofibers. The prepared nanofibers possess unique properties of tunable fluorescence lifetime and distinct textured patterns together with superior flexibility and superhydrophobicity. In a single 612 nm emission channel, over ten different populations of fluorescence lifetime from the range of 322-551 µs are harvested. Thanks to the tunable fluorescence lifetime and different textured patterns, a security pattern to demonstrate optical multiplexing applications is designed. The security pattern hides the real information of "69" in a noticeable scene that shows fake information "8" under UV radiation or "13" by only watching their pattern structures.
A modified electrospinning setup with two-grounded-frame collector is proposed to fabricate aligned fiber arrays and fiber ropes. In this setup, two frames are placed under the spinneret, with the outer frame rotated with an electromotor and the inner frame hold still in a horizontal direction. Aligned nanofiber arrays can be collected rapidly on the inner frame. Influence of included angle and motor rotating speed on the arrays is discussed. In addition, through rotating one side of the inner frame, twisted fiber ropes with diameter 30~40 μm and length of 12 cm are obtained. Mechanical properties of the individual nanofiber ropes are also measured and discussed.
Ultrathin indium oxide (In2O3) microtubes were successfully fabricated by electrospinning, magnetron sputtering and followed calcination. The hollow In2O3tubes were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and UV-visible spectroscopy. Outer diameter of the microtubes was in the range of 700-900 nm, and inner diameter was about 400-600 nm. Optoelectronic properties of the In2O3tubes were investigated by irradiation of UV light with different wavelengths (254, 308 and 365 nm). It was found that the In2O3microtubes had a fast and strong response to UV irradiation.
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