Single charge and exciton dynamics probed by molecular-scale-induced electroluminescence
arXiv:1803.10088 · doi:10.1021/acs.nanolett.8b01489
Abstract
Excitons and their constituent charge carriers play the central role in electroluminescence mechanisms determining the ultimate performance of organic optoelectronic devices. The involved processes and their dynamics are often studied with time-resolved techniques limited by spatial averaging that obscures the properties of individual electron-hole pairs. Here we overcome this limit and characterize single charge and exciton dynamics at the nanoscale by using time-resolved scanning tunnelling microscopy-induced luminescence (TR-STML) stimulated with nanosecond voltage pulses. We use isolated defects in C thin films as a model system into which we inject single charges and investigate the formation dynamics of a single exciton. Tuneable hole and electron injection rates are obtained from a kinetic model that reproduces the measured electroluminescent transients. These findings demonstrate that TR-STML can track dynamics at the quantum limit of single charge injection and can be extended to other systems and materials important for nanophotonic devices.
References in corpus (8)
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- Electrically-driven vibronic spectroscopy with sub-molecular resolution
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- Single Photon Emission from a Plasmonic Light Source Driven by a Local Field-Induced Coulomb Blockade
- A single hydrogen molecule as an intensity chopper in an electrically-driven plasmonic nanocavity
- Gigahertz frame rate imaging of charge-injection dynamics in a molecular light source
- Directly profiling the dark-state transition density via scanning tunneling microscope
- Measuring fine molecular structures with luminescence signal from an alternating current scanning tunneling microscope
- Orbitally resolved single-photon emission from an individual atomic vacancy center in a semiconductor