纳米晶
发光
镱
材料科学
化学物理
猝灭(荧光)
离子
分子
纳米材料
退火(玻璃)
兴奋剂
纳米技术
光化学
荧光
化学
光电子学
物理
复合材料
有机化学
量子力学
作者
Sheng Mei,Jiajia Zhou,Hong‐Tao Sun,Yangjian Cai,Ling‐Dong Sun,Dayong Jin,Chun‐Hua Yan
标识
DOI:10.1002/advs.202003325
摘要
Abstract At the organic–inorganic interface of nanocrystals, electron‐phonon coupling plays an important but intricate role in determining the diverse properties of nanomaterials. Here, it is reported that highly doping of Yb 3+ ions within the nanocrystal host can form an energy‐migration network. The networking state Yb 3+ shows both distinct Stark splitting peak ratios and lifetime dynamics, which allows quantitative investigations of quenching and thermal activation of luminescence, as the high‐dimensional spectroscopy signatures can be correlated to the attaching and de‐attaching status of surface molecules. By in‐situ surface characterizations, it is proved that the Yb‐O coordination associated with coordinated water molecules has significantly contributed to this reversible effect. Moreover, using this approach, the prime quencher OH can be switched to CH in the wet‐chemistry annealing process, resulting in the electron‐phonon coupling probability change. This study provides the molecular level insights and dynamics of the surface dark layer of luminescent nanocrystals.
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