J

Jian Yu

Wuhan University

ORCID: 0000-0003-0591-0524

Publishes on biodegradable polymer synthesis and properties, Polymer crystallization and properties, Polymer Foaming and Composites. 311 papers and 9.4k citations.

311Publications
9.4kTotal Citations

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Top publicationsby citations

Controlling the Fiber Diameter during Electrospinning
Sergey V. Fridrikh, Jian Yu, Michael P. Brenner et al.|Physical Review Letters|2003
Cited by 937

We present a simple analytical model for the forces that determine jet diameter during electrospinning as a function of surface tension, flow rate, and electric current in the jet. The model predicts the existence of a terminal jet diameter, beyond which further thinning of the jet due to growth of the whipping instability does not occur. Experimental data for various electrospun fibers attest to the accuracy of the model.

Production of Submicrometer Diameter Fibers by Two‐Fluid Electrospinning
Cited by 424

Electrospinning of nanofibers of materials that are difficult to process using conventional techniques is reported. Two fluids are electrospun (see Figure) into fibers with core/shell morphology. The “electrospinnable” shell fluid serves as a process aid to electrospin the core fluid. Three examples are illustrated: production of fibers with diameters less than 100 nm, fibers formed of low-molecular-weight polyaniline, and non-blended electrospun silk fibers.

Phototunable Full‐Color Emission of Cellulose‐Based Dynamic Fluorescent Materials
Weiguo Tian, Jinming Zhang, Jian Yu et al.|Advanced Functional Materials|2017
Cited by 219

Abstract An iridescent chameleon‐like material that can change its colors under different circumstances is always desired in color‐on‐demand applications. Herein, a strategy based on trichromacy and the dynamically tunable fluorescence resonance energy transfer (FRET) process to design and prepare these chameleon‐like fluorescent materials is proposed. A set of trichromic (red, green, and blue), solid fluorescent materials are synthesized by covalently attaching spiropyran, fluorescein, and pyrene onto cellulose chains independently. After simply mixing them together, a full range of color is realized. The chameleon‐like nature of these materials is based on the dynamic tunable FRET process between donors (green and blue) and acceptors (red) in which the energy transfer efficiency can be finely tuned by irradiation. Ultimately, the reversible and nonlinear regulation of fluorescence properties, including color and intensity, is achieved on a timescale recognizable by the naked eye. Benefited by the excellent processability inherited from the cellulose derivatives, the as‐prepared materials are feasibly transformed into different forms. Particularly, a fluorescent ink with the complicated fluorescent input–output dependence suggests more than a proof‐of‐concept; indeed, it suggests a unique method of information encryption, security printing, and dynamic anticounterfeiting.