材料科学
近红外光谱
纳米技术
红外线的
聚合物
碳化
高分子科学
光学
扫描电子显微镜
物理
复合材料
作者
Tianyang Han,Yajun Wang,Shengjie Ma,Mengfei Li,Ningning Zhu,Songyuan Tao,Jiajun Xu,Bin Sun,Yunlong Jia,Yuewei Zhang,Shoujun Zhu,Bai Yang
标识
DOI:10.1002/advs.202203474
摘要
Abstract Carbon dots (CDs) or carbonized polymer dots (CPDs) are an emerging class of optical materials that have exceptional applications in optoelectronic devices, catalysis, detection, and bioimaging. Although cell studies of CPDs have produced impressive results, in vivo imaging requires available CPDs to fluoresce in the near‐infrared‐II (NIR‐II) window (1000−1700 nm). Here, a two‐step bottom‐up strategy is developed to synthesize NIR‐CPDs that provide bright emissions in both NIR‐I and NIR‐II transparent imaging windows. The designed strategy includes a hydrothermal reaction to form a stable carbon core with aldehyde groups, followed by the Knoevenagel reaction to tether the molecular emission centers. This procedure is labor‐saving, cost‐efficient, and produces a high yield. The NIR‐CPDs enable high‐performance NIR‐II angiography and real‐time imaging of the disease degree of colitis noninvasively. This technology may therefore provide a next‐generation synthesis strategy for CPDs with rational molecular engineering that can accurately tune the absorption/emission properties of NIR‐emissive CPDs.
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