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Colloidal indium phosphide (InP) quantum dots (QDs) have emerged as promising cadmium-free alternatives due to their tunable emission and compliance with environmental regulations. This study presents a strategy in synthesizing aminophosphine-based high-efficiency green-emissive InP QDs through precisely controlled in-situ etching and interfacial engineering. By employing ZnF2 as an etchant during both nucleation and shelling stages, atomic-level defect passivation is achieved in magic-sized InP clusters while preserving crystallographic integrity. The synergistic integration of tri-n-octylphosphine ligands during nucleation and ZnSe interfacial layers in ZnSeS/ZnS shell growth effectively suppressed the occurrence of excessive etching, yielding green-emission QDs with exceptional photoluminescence quantum yield (93%) and narrow emission linewidth (36 nm). Advanced surface modification using carboxylic acid–thiol bifunctional ligands further enhanced charge transport properties. Prototype quantum dot light-emitting diodes fabricated from these optimized QDs demonstrated performance in InP-based devices, achieving the maximum external quantum efficiency of 4.6% and a peak maximum luminance exceeding 13,000 cd/m2. The etching–optical properties–surface passivation interdependence in InP QDs was investigated by femtosecond transient absorption spectra. This work establishes a universal framework for balancing oxide removal efficiency and core dissolution in InP QDs. The developed approach offers practical solutions to long-standing challenges in controlling defects during InP QD synthesis.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).
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