Organic–Inorganic Copassivation Enables Environmentally Benign Water-Soluble InP Quantum Dots for Pb 2+ Ion Detection
Source abstract
Abstract
Heavy-metal pollution, particularly from lead ions, threatens environmental and human health, necessitating sensitive detection methods. Fluorescent probes based on colloidal quantum dots (QDs) offer a promising solution, yet toxicity concerns of the state-of-the-art Cd/Pb-based QDs and achieving high-quality water-soluble eco-friendly QDs remain challenging due to ineffective surface passivation during phase transfer. Here, we demonstrate an organic–inorganic surface copassivation strategy to obtain eco-friendly water-soluble InP-based QDs with excellent optical properties. By employing organic mercaptopropionic acid together with inorganic zinc salts during ligand exchange, both surface cationic and anionic sites are effectively passivated, yielding water-soluble InP/ZnSe/ZnS QDs with a high photoluminescence quantum yield of up to 91%, monoexponential decay dynamics, and outstanding stability. Utilizing these bright QDs as fluorescent probes, ultrasensitive and selective detection of Pb 2+ ions with a 0.3 nM detection limit is achieved, comparable to conventional probes. This work establishes a general design principle for high-quality water-soluble QDs and highlights the potential use of eco-friendly QDs for aqueous-based applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Carbon and Quantum Dots Applications · Nanocluster Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Physics and Optoelectronic Engineering, Hangzhou Institute for Advanced Study
University of Chinese Academy of Sciences
State Key Laboratory of Infrared Physics
Shanghai Institute of Technical Physics, Chinese Academy of Sciences
Funding
Natural Science Foundation of Zhejiang Province · Hangzhou Institute for Advanced Study, UCAS
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