TY - JOUR
T1 - Water-Resistant Organic Room-Temperature Phosphorescence from Block Copolymers
AU - Chen, Huan
AU - Zhang, Yuanyuan
AU - Shan, Jingyi
AU - Dong, Mengyang
AU - Qian, Zhao
AU - Lv, Anqi
AU - Qian, Hu Jun
AU - Ma, Huili
AU - An, Zhongfu
AU - Gu, Long
AU - Huang, Wei
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/4/17
Y1 - 2025/4/17
N2 - Room-temperature phosphorescence (RTP) polymers have demonstrated significant potential for various applications due to their unique luminescent properties. However, most conventional RTP polymers are vulnerable to moisture and water, which can disrupt the hydrogen bonding network within the polymer and accelerate the non-radiative decay of triplet excitons of phosphors, leading to the quenching of RTP. Herein, we present a universal strategy to achieve water-resistant RTP polymers by designing amphiphilic block copolymers with microphase-separated structures. Specifically, the rigid hydrophilic phase, which is rich in carboxyl groups, forms hydrogen bonds that suppress non-radiative decay of the chromophores, resulting in RTP. Meanwhile, the hydrophobic phase effectively prevents water molecules from penetrating and disrupting the rigid polymer network. By combining the functions of both the hydrophilic and hydrophobic phases, the resulting RTP copolymers exhibit good water-resistant properties. Even after being immersed in water for one month, the copolymers maintain a green afterglow with a lifetime of 629 ms. Moreover, the water-resistant nature of these RTP polymers has also been demonstrated in potential applications of afterglow displays and anti-counterfeiting. This research offers valuable insights into the design of RTP materials with stability in aqueous environments and broadens the scope of their potential applications in diverse settings.
AB - Room-temperature phosphorescence (RTP) polymers have demonstrated significant potential for various applications due to their unique luminescent properties. However, most conventional RTP polymers are vulnerable to moisture and water, which can disrupt the hydrogen bonding network within the polymer and accelerate the non-radiative decay of triplet excitons of phosphors, leading to the quenching of RTP. Herein, we present a universal strategy to achieve water-resistant RTP polymers by designing amphiphilic block copolymers with microphase-separated structures. Specifically, the rigid hydrophilic phase, which is rich in carboxyl groups, forms hydrogen bonds that suppress non-radiative decay of the chromophores, resulting in RTP. Meanwhile, the hydrophobic phase effectively prevents water molecules from penetrating and disrupting the rigid polymer network. By combining the functions of both the hydrophilic and hydrophobic phases, the resulting RTP copolymers exhibit good water-resistant properties. Even after being immersed in water for one month, the copolymers maintain a green afterglow with a lifetime of 629 ms. Moreover, the water-resistant nature of these RTP polymers has also been demonstrated in potential applications of afterglow displays and anti-counterfeiting. This research offers valuable insights into the design of RTP materials with stability in aqueous environments and broadens the scope of their potential applications in diverse settings.
KW - Amphiphilic Block Copolymers
KW - Atom Transfer Radical Polymerization
KW - Room-Temperature Phosphorescence
KW - Water-Resistant Phosphorescence
UR - http://www.scopus.com/inward/record.url?scp=105003207013&partnerID=8YFLogxK
U2 - 10.1002/anie.202500610
DO - 10.1002/anie.202500610
M3 - 文章
AN - SCOPUS:105003207013
SN - 1433-7851
VL - 64
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 17
M1 - e202500610
ER -