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Magnetic fluids are the suspensions composed of magnetic nanoparticles, surfactants, and non-magnetic carrier liquids. Magnetic fluids are widely used in various fields, especially in sealing, because of their excellent features, including rapid magnetic response, flexible flow ability, tunable magneto-viscous effect, and reliable self-repairing capability. Here, we provide an in-depth, comprehensive insight into the theoretical analyses and diverse applications of magnetic fluids in sealing from three categories: static sealing, rotary sealing, and reciprocating sealing. We summarize the magnetic fluid sealing mechanisms and the development of magnetic fluid seals from 1960s to the present, particularly focusing on the recent progress of magnetic fluid seals. Although magnetic fluid sealing technology has been commercialized and industrialized, many difficulties still exist in its applications. At the end of the review, the present challenges and future prospects in the progress of magnetic fluid seals are also outlined. [ABSTRACT FROM AUTHOR]

Organic room-temperature phosphorescent (RTP) materials exhibiting reversible changes in optical properties upon exposure to external stimuli have shown great potential in diverse optoelectronic fields. Particularly, dynamic manipulation of response behaviors for such materials is of fundamental significance, but it remains a formidable challenge. Herein, a series of RTP polymers were prepared by incorporating phosphorescent rotors into polymer backbone, and these materials show color-tunable persistent luminescence upon excitation at different wavelengths. Experimental results and theoretical calculations revealed that the various molecular conformations of monomers are responsible for the excitation wavelength-dependent (Ex-De) RTP behavior. Impressively, after gaining insights into the underlying mechanism, dynamic control of Ex-De RTP behavior was achieved through thermal energy driven molecular rotations of monomers. Eventually, we demonstrate the practical applications of these amorphous polymers in anti-counterfeiting areas. These findings open new opportunities for the control of response behaviors of smart-responsive RTP materials through external stimuli rather than conventional covalent modification method. Organic room-temperature phosphorescent (RTP) materials exhibiting stimuli responsive reversible changes in optical properties show great potential in diverse optoelectronic fields but a lack of mechanistic understanding limits their development. Here, the authors prepare a series of RTP polymers by incorporating phosphorescent rotors into polymer backbones and demonstrate colortunable persistent luminescence upon excitation at different wavelengths [ABSTRACT FROM AUTHOR]

Organic room-temperature phosphorescent (RTP) materials exhibiting reversible changes in optical properties upon exposure to external stimuli have shown great potential in diverse optoelectronic fields. Particularly, dynamic manipulation of response behaviors for such materials is of fundamental significance, but it remains a formidable challenge. Herein, a series of RTP polymers were prepared by incorporating phosphorescent rotors into polymer backbone, and these materials show color-tunable persistent luminescence upon excitation at different wavelengths. Experimental results and theoretical calculations revealed that the various molecular conformations of monomers are responsible for the excitation wavelength-dependent (Ex-De) RTP behavior. Impressively, after gaining insights into the underlying mechanism, dynamic control of Ex-De RTP behavior was achieved through thermal energy driven molecular rotations of monomers. Eventually, we demonstrate the practical applications of these amorphous polymers in anti-counterfeiting areas. These findings open new opportunities for the control of response behaviors of smart-responsive RTP materials through external stimuli rather than conventional covalent modification method. Organic room-temperature phosphorescent (RTP) materials exhibiting stimuli responsive reversible changes in optical properties show great potential in diverse optoelectronic fields but a lack of mechanistic understanding limits their development. Here, the authors prepare a series of RTP polymers by incorporating phosphorescent rotors into polymer backbones and demonstrate colortunable persistent luminescence upon excitation at different wavelengths [ABSTRACT FROM AUTHOR]