TY - JOUR
T1 - From molecular design to adaptive devices
T2 - Triazolopyridine-Thiophene donor-acceptor type conjugated polymers for flexible patterned electrochromics in displays and near-infrared camouflage
AU - Jian, Nannan
AU - Gong, Changchen
AU - Lin, Kaiwen
AU - Zhang, Kai
N1 - Publisher Copyright:
Copyright © 2026. Published by Elsevier B.V.
PY - 2026/10/15
Y1 - 2026/10/15
N2 - Donor–acceptor (D–A) type conjugated polymers are a prominent class of electrochromic materials, prized for their tunable colors, high optical contrast ( ΔT ), excellent coloration efficiency ( CE ), and good stability. However, the rational design of high-performance D–A type polymers and their integration into patterned flexible displays remain challenging. In this work, we reported a series of novel triazolopyridine-thiophene D–A type precursors based on alkyl substituted 2H-[1,2,3]triazolo[4,5- c ]pyridines (PTzs) acceptors and thiophenes (Ths) donors, synthesized via the Stille coupling and subsequently electropolymerized to obtain the corresponding polymers. The resulting polymers exhibit outstanding electrochromic performance, including an optical contrastof up to 88%, an ultrahigh coloration efficiency of 1481 cm2 C−1 in the near-infrared (NIR) region, and remarkable cycling stability (retaining >97% activity after 5000 cycles). Furthermore, flexible electrochromic devices (ECDs) fabricated based on the optimal material show stable, reversible color switching under bending and folding conditions. Finally, we demonstrate the practical potential of this materials system by constructing patterned flexible ECDs for smart displays and adaptive NIR camouflage applications.
AB - Donor–acceptor (D–A) type conjugated polymers are a prominent class of electrochromic materials, prized for their tunable colors, high optical contrast ( ΔT ), excellent coloration efficiency ( CE ), and good stability. However, the rational design of high-performance D–A type polymers and their integration into patterned flexible displays remain challenging. In this work, we reported a series of novel triazolopyridine-thiophene D–A type precursors based on alkyl substituted 2H-[1,2,3]triazolo[4,5- c ]pyridines (PTzs) acceptors and thiophenes (Ths) donors, synthesized via the Stille coupling and subsequently electropolymerized to obtain the corresponding polymers. The resulting polymers exhibit outstanding electrochromic performance, including an optical contrastof up to 88%, an ultrahigh coloration efficiency of 1481 cm2 C−1 in the near-infrared (NIR) region, and remarkable cycling stability (retaining >97% activity after 5000 cycles). Furthermore, flexible electrochromic devices (ECDs) fabricated based on the optimal material show stable, reversible color switching under bending and folding conditions. Finally, we demonstrate the practical potential of this materials system by constructing patterned flexible ECDs for smart displays and adaptive NIR camouflage applications.
KW - Coloration efficiency
KW - D-A type conjugated polymers
KW - Electrochromic
KW - Flexible devices
KW - Near-infrared camouflage
KW - Triazolopyridine-thiophene
UR - https://www.scopus.com/pages/publications/105043345951
U2 - 10.1016/j.solmat.2026.114529
DO - 10.1016/j.solmat.2026.114529
M3 - Article
AN - SCOPUS:105043345951
SN - 0927-0248
VL - 306
JO - Solar Energy Materials and Solar Cells
JF - Solar Energy Materials and Solar Cells
M1 - 114529
ER -