TY - CHAP
T1 - Stimuli-responsive Luminescent Polymers
AU - Gong, Weijie
AU - Shao, Aiwen
AU - Li, Jiangang
AU - Ma, Yun
AU - Wong, Wai Yeung
N1 - Publisher Copyright:
© The Royal Society of Chemistry 2024 Published by the Royal Society of Chemistry.
PY - 2024/10/2
Y1 - 2024/10/2
N2 - In summary, stimuli-responsive luminescent polymers that exhibit reversible modulations in optical properties in response to external triggers have attracted enormous interest. Mechanochromic polymers harness mechanical forces to induce chromic changes through alterations in molecular packing, geometry, and interactions. Thermochromic polymers exploit temperature-dependent conformational, aggregation, and phase transition effects to achieve thermal tunability. Photochromic systems use light to reversibly transform molecular structures and control properties. Electrochromic polymers utilize electrochemical redox reactions to switch between emissive and non-emissive states. Each approach offers unique advantages and has shown great potential for smart materials and devices. Looking forward, further elucidation of structure-property relationships and molecular engineering strategies will be crucial for improving the tunability, sensitivity, and stability of chromic polymers. Incorporating multi-stimuliresponsiveness and integrated sensing-display capabilities could yield intriguing multi-functional materials. Patternable processing and device integration must also be advanced for practical applications. Overall, stimuliresponsive polymeric systems hold promise as dynamic materials for sensors, memories, e-skins, anti-counterfeiting tags, camouflage, and encrypted optical communications.
AB - In summary, stimuli-responsive luminescent polymers that exhibit reversible modulations in optical properties in response to external triggers have attracted enormous interest. Mechanochromic polymers harness mechanical forces to induce chromic changes through alterations in molecular packing, geometry, and interactions. Thermochromic polymers exploit temperature-dependent conformational, aggregation, and phase transition effects to achieve thermal tunability. Photochromic systems use light to reversibly transform molecular structures and control properties. Electrochromic polymers utilize electrochemical redox reactions to switch between emissive and non-emissive states. Each approach offers unique advantages and has shown great potential for smart materials and devices. Looking forward, further elucidation of structure-property relationships and molecular engineering strategies will be crucial for improving the tunability, sensitivity, and stability of chromic polymers. Incorporating multi-stimuliresponsiveness and integrated sensing-display capabilities could yield intriguing multi-functional materials. Patternable processing and device integration must also be advanced for practical applications. Overall, stimuliresponsive polymeric systems hold promise as dynamic materials for sensors, memories, e-skins, anti-counterfeiting tags, camouflage, and encrypted optical communications.
UR - https://www.scopus.com/pages/publications/85211505843
U2 - 10.1039/BK9781837673551-00192
DO - 10.1039/BK9781837673551-00192
M3 - Chapter in an edited book (as author)
AN - SCOPUS:85211505843
T3 - RSC Polymer Chemistry Series
SP - 192
EP - 235
BT - RSC Polymer Chemistry Series
A2 - Wong, Wai-Yeung
A2 - Ma, Yun
PB - Royal Society of Chemistry
ER -