材料科学
费斯特共振能量转移
碳化
聚合物
能量转移
固态
纳米技术
化学工程
荧光
化学物理
物理化学
复合材料
光学
扫描电子显微镜
化学
物理
工程类
作者
Yu Wang,Yingxi Qin,Wenming Tian,Hongyu Zhang,Fengya Wang,Xianchang Yan,Shiqi Rong,Changxin Huangfu,Yushu Shi,Zhenming Wang,Lihua Yang,Hui Zhi,Aimiao Qin,Liang Feng
标识
DOI:10.1002/adfm.202402825
摘要
Abstract Carbonized polymer dots (CPDs) exhibiting tunable solid‐state emission (SSE) show great promise as rare‐earth‐free functional phosphors. Nevertheless, progress in this field has been hindered by the structural heterogeneity of CPDs and a lack of fundamental understanding of the underlying emission mechanisms. In this work, a universal approach is presented for the large‐scale, controlled synthesis of CPDs with tailored SSE properties. This strategy leverages intraparticle Förster resonance energy transfer (FRET) by incorporating selected fluorophores into self‐assembled CPDs nanostructures. The resulting CPDs exhibit exceptional SSE characteristics, such as high quantum yields, adjustable band structures, narrow emission linewidths, and excellent photostability in both solution and solid‐state. Moreover, the multifunctional capabilities of these CPDs are demonstrated, including efficient light harvesting, their potential as nanocarriers, and their application in light‐emitting diodes (LEDs). This findings establish self‐assembly‐mediated doping as a robust platform for engineering CPDs with unique SSE properties, underpinned by the principles of intraparticle FRET.
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