机械容积
材料科学
宽带
发光
渗透(战争)
光电子学
复合数
光学
激发
聚合物
穿透深度
生物医学工程
纳米技术
生物材料
持续发光
信号(编程语言)
近红外光谱
复合材料
双光子激发显微术
作者
Ziyi Niu,Pengfei Zhang,Wenbo Chen,Junyang Xia,Zhili Zhang,Jinwei Liu,Yanyan Li,BiTao Liu,Lei Zhao
标识
DOI:10.1002/lpor.202501948
摘要
ABSTRACT Near‐infrared (NIR) mechanoluminescence (ML) holds significant promise for in vivo biomechanical detection and imaging due to its self‐powered excitation and self‐recovery capabilities. However, its broader application remains constrained by the limited availability of suitable ML materials and the narrow spectral range of NIR emission. In this study, we report the Y 3 Ga 5 O 12 (YGO): Cr 3+ , Nd 3+ , Yb 3+ /polydimethylsiloxane (PDMS) NIR‐ML composite with broadband NIR emission tunable from 600 to 1100 nm, covering both the NIR‐I and NIR‐II windows. The ML of composite device is driven by an interfacial triboelectric effect arising from the mechanical interaction between the inorganic particles and the polymer matrix. Comparative studies on photon penetration through biological tissues reveal that co‐doping with Nd 3+ and Yb 3+ markedly enhances tissue penetration depth. Specifically, the luminescence decay rate in biological tissues is reduced by 20.8% relative to Cr 3+ single doping, indicating improved optical persistence and signal transmission. These findings demonstrate the potential of full‐spectrum NIR‐ML devices for high‐resolution, deep‐tissue biomechanical sensing and imaging. This work provides a generalizable design strategy for the development of broadband NIR‐ML materials tailored for in vivo mechanical diagnostics.
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