材料科学
光致发光
发光
纳米技术
光电子学
热致变色
量子点
化学
有机化学
作者
Qi Chen,Liang Chen,Bing Zhu,Yilin Wu,Hao Jia,Chunyu Liu
出处
期刊:Small
[Wiley]
日期:2025-10-07
卷期号:21 (47): e08255-e08255
标识
DOI:10.1002/smll.202508255
摘要
Copper iodide clusters have emerged as a promising candidate for flexible optoelectronic devices due to their structural versatility and exceptional photoluminescence (PL) properties, yet their practical application is hindered by insufficient mechanical fragility and environmental stability. Herein, a scalable wet-spinning strategy is presented to fabricate ultrastable Cu4I4(L)4@CA fibers (L1 = 4-benzylpyridine; L2 = 4-tert-butylpyridine; CA = calcium alginate). The molecular encapsulation preserves high photoluminescence quantum yields (PLQYs >85%) at an ultralow 1 wt% doping while enabling fully reversible thermochromic switching: white to yellow (L1) and blue-purple to orange (L2) transitions across 80-300 K. The fibers demonstrate textile-grade flexibility and ultrahigh environmental stability (>98% PL retention under humidity/UV/solvents). Leveraging these properties, a dual-authentication encryption platform is pioneered featuring triple-state information switching (ambient, UV, and cryogenic states) and DNA-inspired binary photonic encoding using programmable Y-/cross-shaped spinnerets for data transcription. By harmonizing stimuli-responsive optoelectronics with textile processability, this work establishes a synergistic material platform for next-generation secure wearables, stealth luminescent textiles, and hierarchical anti-counterfeiting systems.
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