Issue 41, 2025

Aqueous phase near-infrared emitters: water transfer of colloidal 2D PbS, PbSe and PbTe nanoplatelets

Abstract

Colloidal two-dimensional (2D) lead chalcogenide PbX (X = S, Se, Te) nanoplatelets (NPLs) are strongly confined narrow band gap semiconductors with tuneable efficent photoluminescence (PL) in the near-infrared (NIR). They hold high potential for the use as classical and quantum emitters in fiber-based photonics that operate at telecommunication wavelengths. Up to now, the insolubility of 2D PbX NCs in water and other polar solvents has been a challenge that complicates their post-synthesic processing, e.g. into future functional nanocomposites. Here, we describe a phase transfer protocol from hexane to water using 11-mercaptoundecanoic acid (MUA), which yields aqueous phase 2D PbS, PbSe, and PbTe NPLs with preserved shape, crystallinity and NIR PL (e.g. PbS: 724 nm, PbSe: 1023 nm and PbTe: 1184 nm). Water-soluble 2D PbSe shows efficient emission (up to 13% PL quantum yield at 1023 nm), thereby retaining 65% of the initial quantum yield and making it highly interesting as an aqueous NIR light source. By using X-ray photoelectron spectroscopy (XPS) and nuclear magnetic resonance (NMR), we follow the phase transfer on a molecular level and find two binding motifs of MUA to the 2D PbX surfaces: X-type bound thiolate and L-type bound thiol. Our results shine new light on mercaptocarboxylic acid based nanomaterial phase transfers and represent a crucial step for incorporating NIR-emissive 2D PbX into (fiber) optics.

Graphical abstract: Aqueous phase near-infrared emitters: water transfer of colloidal 2D PbS, PbSe and PbTe nanoplatelets

Supplementary files

Article information

Article type
Paper
Submitted
18 Aug 2025
Accepted
30 Sep 2025
First published
01 Oct 2025
This article is Open Access
Creative Commons BY license

Nanoscale, 2025,17, 24006-24016

Aqueous phase near-infrared emitters: water transfer of colloidal 2D PbS, PbSe and PbTe nanoplatelets

L. Biesterfeld, M. T. Vochezer, D. A. Rudolph and J. Lauth, Nanoscale, 2025, 17, 24006 DOI: 10.1039/D5NR03504J

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