

FOLLOWUS
School of materials science and engineering, Guangdong University of Petrochemical Technology, Maoming 525000, China
panlulu@163.com (L.L.P.)
shibosut@163.com (B.S.)
banjianfeng@gdupt.edu.cn (J.F.B.)
Received:23 May 2026,
Revised:2026-06-17,
Accepted:20 June 2026,
Online First:10 October 2026,
Published:2026-08
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Ren, C. Y.; Zhu, W. B.; Wu, D.; Yang, Z. L.; Li, S. Q.; Pan, L. L.; Shi, B.; Ban, J. F. Spatiotemporally programmable triple-responsive polyurethanes via dynamic-topology-coupling for rapid actuation and optical cryptography. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3791-6
Cai-Yun Ren, Wen-Bin Zhu, Di Wu, et al. Spatiotemporally Programmable Triple-responsive Polyurethanes
Ren, C. Y.; Zhu, W. B.; Wu, D.; Yang, Z. L.; Li, S. Q.; Pan, L. L.; Shi, B.; Ban, J. F. Spatiotemporally programmable triple-responsive polyurethanes via dynamic-topology-coupling for rapid actuation and optical cryptography. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3791-6 DOI:
Cai-Yun Ren, Wen-Bin Zhu, Di Wu, et al. Spatiotemporally Programmable Triple-responsive Polyurethanes
Although shape-memory polymers show significant potential in soft robotics and flexible electronics
their practical deployment is often limited by conventional bulk thermal triggering
which lacks spatiotemporal resolution and rapid response capabilities. To address this limitation
by engineered a class of triple-responsive (thermal/UV/NIR) shape-memory polyurethanes (H
n
-SPMUs)
via
a “dynamic-topology-coupling” strategy. Specifically
photo-reversible coumarin moieties were covalently tethered onto a stable epoxy-amine polyurethane skeleton. By systematically varying the alkyl spacer length
a critical structure-property correlation was elucidated: elongating the flexible spacer effectively alle
via
ted local steric hindrance
thereby accelerating the photochemical dimerization kinetics and increasing the topological crosslinking density. Consequently
the optimized H
n
-SPMUs decoupled network stability from dynamic responsiveness
achieving excellent multimodal actuation: rapid global thermal recovery at a mild 45 °C
rapid non-contact NIR actuation within 4 s driven by intrinsic photothermal conversion
and precise spatiotemporal 3D programming
via
localized 365 nm UV irradiation. Furthermore
by leveraging the catalyst-free
reversible [2+2
]
cycloaddition of coumarin units
the engineered network demonstrated on-demand photothermal self-healing and established a reliable platform for multi-cycle “write-store-erase” optical data encryption. This synergistic design paradigm provides a versatile material framework for untethered soft actuators and advanced anticounterfeiting technologies.
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