量子点
钙钛矿(结构)
激发
自旋(空气动力学)
电子
苯醌
接受者
材料科学
电荷(物理)
电子受体
载流子
凝聚态物理
光化学
化学
光电子学
物理
结晶学
量子力学
生物化学
热力学
作者
Lin Cheng,Rongrong Hu,Meizhen Jiang,Yumeng Men,Yang Wang,Jinlei Li,Tianqing Jia,Zhenrong Sun,Donghai Feng
出处
期刊:Nano Research
[Springer Nature]
日期:2024-01-24
卷期号:17 (12): 10649-10654
被引量:11
标识
DOI:10.1007/s12274-024-6466-z
摘要
The formation and evolution dynamics of charge separation (CS) in a complex of CsPbBr3 quantum dots (QDs) and 1,4-benzoquinone (BQ) molecules are measured with a high-sensitive pump-orientation-probe technique by which spin signals of the CS state are monitored. An extraordinarily long-lasting CS is observed, with a characteristic time being up to a dozen days under ambient conditions, due to electron transferring from QDs to BQ molecules. Upon the long-lived CS, spin coherences of both electrons and holes are detected at room temperature, with a spin dephasing time of 420 and 26 ps, respectively. The long-lived CS and spin coherence have important implications for applications of perovskite nanomaterials in photocatalysis, photovoltaics, and spintronics.
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