Liquid bidentate ligand for full ligand coverage towards efficient near-infrared perovskite quantum dot LEDs

58Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Perovskite quantum dots (PQDs) show promise in light-emitting diodes (LEDs). However, near-infrared (NIR) LEDs employing PQDs exhibit inferior external quantum efficiency related to the PQD emitting in the visible range. One fundamental issue arises from the PQDs dynamic surface: the ligand loss and ions migration to the interfacial sites serve as quenching centers, resulting in trap-assisted recombination and carrier loss. In this work, we developed a chemical treatment strategy to eliminate the interface quenching sites and achieve high carrier utilization. We employ a bidentate and liquid agent (Formamidine thiocyanate, FASCN) with tight binding to suppress the ligand loss and the formation of interfacial quenching sites: the FASCN-treated films exhibit fourfold higher binding energy than the original oleate ligands. Furthermore, the short ligands (carbon chain <3) enable the treated films to show eightfold higher conductivity; and the liquid characteristics of FASCN avoid the use of high polar solvents and guarantee better passivation. The high conductivity ensures efficient charge transportation, enabling PQD-based NIR-LEDs to have a record-low voltage of 1.6 V at 776 nm. Furthermore, the champion EQE of the treated LEDs is ~23%: this is twofold higher than the control, and represents the highest among reported PQD-based NIR-LEDs.

Cite

CITATION STYLE

APA

Liu, Z. S., Wang, Y., Zhao, F., Li, H. H., Liu, W. Z., Shen, W. S., … Liao, L. S. (2025). Liquid bidentate ligand for full ligand coverage towards efficient near-infrared perovskite quantum dot LEDs. Light: Science and Applications, 14(1). https://doi.org/10.1038/s41377-024-01704-x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free