纳米晶
化学
量子点
俄歇效应
激子
超快激光光谱学
半导体
电子转移
光诱导电子转移
电子
光谱学
螺旋钻
光化学
化学物理
原子物理学
纳米技术
光电子学
材料科学
物理
凝聚态物理
量子力学
作者
Haixin Lei,Liulin Lv,Xionglin Zhou,Shaojie Liu,Meiyi Zhu,Huifeng Wang,Haiyan Qin,Qun Fang,Xiaogang Peng
摘要
Single-molecule spectroscopy offers state-resolved measurements on charge-transfer reactions of single semiconductor nanocrystals, leading to the discovery of up to six single-charge transfer reactions with seven transient states for single CdSe/CdS core/shell nanocrystals with water (or oxygen) as the hole (or electron) acceptors. Kinetic rates of three photoinduced single-hole transfer reactions decrease significantly upon increasing the number of excess electrons in a nanocrystal, mainly due to efficient Auger nonradiative recombination of the charged single excitons. Conversely, the kinetic rates of three single-electron transfer reactions of an unexcited nanocrystal increase proportionally to the number of excess electrons in it. Results here reveal that charge-transfer reactions of nanocrystals, at the center of nearly all their functions, could only be deciphered at a state-resolved level on a single nanocrystal. Size-dependent studies validate the weakly confined semiconductor nanocrystals, instead of strongly confined ones (quantum dots), as optimal candidates for photochemical and optoelectronic applications.
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