机械容积
荧光粉
材料科学
硼
光电子学
聚二甲基硅氧烷
光致发光
紫外线
纳米技术
摩擦电效应
发光
化学工程
热分解法
藻胆蛋白
紫外线
绿灯
强度(物理)
复合材料
作者
Yuhong Han,Junlu Sun,Jiajia Meng,Fuhang Jiao,Yuan Deng,Chong-Xin Shan,Ying Xiao,Lu Dong
出处
期刊:Rare Metals
[Springer Science+Business Media]
日期:2026-06-30
卷期号:45 (7)
摘要
ABSTRACT Mechanoluminescence (ML)—the emission of light in response to mechanical stimuli—offers a direct and visually intuitive route for transducing mechanical information into optical signals. Herein, we report a mixed‐anion strategy to prepare mixed‐anion borate Sr 2 B 5 O 9 Cl:Eu phosphors through a facile, low‐temperature, and ambient‐atmosphere solid‐state synthesis. Benefiting from the intrinsic self‐reducing nature of the borate host, the phosphors demonstrate distinct blue and red photoluminescence under different excitation wavelengths. When embedded in a polydimethylsiloxane (PDMS) matrix, Sr 2 B 5 O 9 Cl:Eu exhibits bright blue ML centered at 423 nm without pre‐irradiation. The ML intensity scales monotonically with the applied strain and decays under repeated mechanical stimulation. Interfacial triboelectric analyses reveal that the ML originates from a triboelectricity‐driven electron‐bombardment process at the phosphor–polymer interface. Leveraging this mechanism, a dual‐mode secure label is fabricated by blending Sr 2 B 5 O 9 Cl:Eu with a conventional green ML phosphor (ZnS:Cu) in PDMS, enabling reversible ultraviolet authentication and irreversible mechanochromic tamper indication. This work establishes mixed‐anion borates as a versatile platform for self‐reduced ML materials and highlights interfacial charge engineering as a powerful strategy for advanced information security in the emerging Internet of Things ecosystem.
科研通智能强力驱动
Strongly Powered by AbleSci AI