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Selective triplet exciton formation in a single molecule

激子 磷光 有机发光二极管 电致发光 单重态 自旋(空气动力学) 材料科学 比克西顿 光电子学 化学 化学物理 原子物理学 荧光 激发态 纳米技术 凝聚态物理 物理 光学 热力学 图层(电子)
作者
Kensuke Kimura,Kuniyuki Miwa,Hiroshi Imada,Miyabi Imai-Imada,Shota Kawahara,Jun Takeya,Maki Kawai,Michael Galperin,Yousoo Kim
出处
期刊:Nature [Nature Portfolio]
卷期号:570 (7760): 210-213 被引量:165
标识
DOI:10.1038/s41586-019-1284-2
摘要

The formation of excitons in organic molecules by charge injection is an essential process in organic light-emitting diodes (OLEDs)1–7. According to a simple model based on spin statistics, the injected charges form spin-singlet (S1) excitons and spin-triplet (T1) excitons in a 1:3 ratio2–4. After the first report of a highly efficient OLED2 based on phosphorescence, which is produced by the decay of T1 excitons, more effective use of these excitons has been the primary strategy for increasing the energy efficiency of OLEDs. Another route to improving OLED energy efficiency is reduction of the operating voltage2–6. Because T1 excitons have lower energy than S1 excitons (owing to the exchange interaction), use of the energy difference could—in principle—enable exclusive production of T1 excitons at low OLED operating voltages. However, a way to achieve such selective and direct formation of these excitons has not yet been established. Here we report a single-molecule investigation of electroluminescence using a scanning tunnelling microscope8–20 and demonstrate a simple method of selective formation of T1 excitons that utilizes a charged molecule. A 3,4,9,10-perylenetetracarboxylicdianhydride (PTCDA) molecule21–25 adsorbed on a three-monolayer NaCl film atop Ag(111) shows both phosphorescence and fluorescence signals at high applied voltage. In contrast, only phosphorescence occurs at low applied voltage, indicating selective formation of T1 excitons without creating their S1 counterparts. The bias voltage dependence of the phosphorescence, combined with differential conductance measurements, reveals that spin-selective electron removal from a negatively charged PTCDA molecule is the dominant formation mechanism of T1 excitons in this system, which can be explained by considering the exchange interaction in the charged molecule. Our findings show that the electron transport process accompanying exciton formation can be controlled by manipulating an electron spin inside a molecule. We anticipate that designing a device taking into account the exchange interaction could realize an OLED with a lower operating voltage. Recombination of excitons to produce molecular light emission is made more efficient by controlling electron spin within the molecule to produce spin-triplet excitons only, without the usual accompanying spin-singlet excitons.

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