胶体金
PEG比率
聚乙二醇
纳米颗粒
吸附
纳米技术
化学工程
胶体
材料科学
表面电荷
聚合物
位阻效应
化学
有机化学
财务
物理化学
工程类
经济
作者
Yi He,M. Liu,Sheng Wang,Yiding Liu
出处
期刊:Small
[Wiley]
日期:2024-08-22
标识
DOI:10.1002/smll.202403216
摘要
Abstract The color‐changing self‐assembly and autonomous disassembly of colloidal gold nanoparticles (AuNPs) is reported by simply mixing negatively charged phosphine ligand‐capped AuNPs with partially oxidized polyethylene glycol (PEG). The assembly of AuNPs is initiated by PEG adsorption, which disrupts the hydration layer of AuNPs, leading to depletion attraction and reduction of hydration repulsion among the AuNPs. The oxidative species in PEG subsequently oxidize and remove the charged ligands from the AuNP surface, resulting in a decrease and reversal of the negative surface charge. This causes the PEG to adsorb on AuNPs in a tighter and more direct manner, providing strong steric shielding to the AuNPs, thereby triggering the disassembly of the AuNP assemblies. The self‐regulated assembly–disassembly process can be tuned widely by controlling chemical conditions of PEG, nanoparticle concentration, and the environmental conditions, suggesting potential applications as colorimetric time‐temperature indicators for food and medicine storage conditions. As a proof of concept, it is demonstrated that the lifetime of the color‐changing assembly–disassembly process can be extended from tens of minutes to weeks when subjected to a refrigerated environment, with tunability achievable through varying polymer conditions and storage atmospheres.
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