Enabling Visible‐Light‐Charged Near‐Infrared Persistent Luminescence in Organics by Intermolecular Charge Transfer

Abstract

AbstractVisible light is a universal and user‐friendly excitation source; however, its use to generate persistent luminescence (PersL) in materials remains a huge challenge. Herein, the concept of intermolecular charge transfer (xCT) is applied in typical host–guest molecular systems, which allows for a much lower energy requirement for charge separation, thus enabling efficient charging of near‐infrared (NIR) PersL in organics by visible light (425–700 nm). Importantly, NIR PersL in organics occurs via the trapping of electrons from charge‐transfer aggregates (CTAs) into constructed trap states with trap depths of 0.63–1.17 eV, followed by the detrapping of these electrons by thermal stimulation, resulting in a unique light‐storage effect and long‐lasting emission up to 4.6 h at room temperature. The xCT absorption range is modulated by changing the electron‐donating ability of a series of acenaphtho[1,2‐b]pyrazine‐8,9‐dicarbonitrile‐based CTAs, and the organic PersL is tuned from 681 to 722 nm. This study on xCT interaction‐induced NIR PersL in organic materials provides a major step forward in understanding the underlying luminescence mechanism of organic semiconductors and these findings are expected to promote their applications in optoelectronics, energy storage, and medical diagnosis.