Katie Sun, Ye Chan Kim, Russell J. Composto* and Karen I. Winey*,
{"title":"金纳米颗粒在共价键合弱聚电解质电刷中的吸附","authors":"Katie Sun, Ye Chan Kim, Russell J. Composto* and Karen I. Winey*, ","doi":"10.1021/acs.macromol.4c0233210.1021/acs.macromol.4c02332","DOIUrl":null,"url":null,"abstract":"<p >The adsorption of spherical citrate-coated gold nanoparticles (AuNPs) into poly(2-vinylpyridine) (P2VP) brushes was investigated using a quartz crystal microbalance with dissipation (QCM-D). This study examined the impacts of environmental pH and brush molecular weight (10 and 53 kg/mol) on AuNP adsorption kinetics and areal number densities. We synthesized and characterized the P2VP brushes, grafted onto a poly(glycidyl methacrylate) (PGMA) priming layer, on both silicon wafers and QCM-D sensors. Adsorption experiments explored the pH-dependent adsorption behavior of 10- and 20-nm diameter AuNPs. The QCM-D data show that higher molecular weight brushes enhanced AuNP uptake. At pH = 4.0, the swollen brushes promote greater adsorption compared with the collapsed brush state at pH = 6.2. This study highlights the advantages of the homopolymer brush architecture compared with the block copolymer brush architecture from our previous work. Additionally, it reaffirms the pH-mediated size selectivity observed in our prior study, where the smaller 10 nm AuNPs show preferential adsorption at higher pH. These findings provide insights into the impacts of brush molecular weight and environmental conditions on nanoparticle adsorption, with implications for designing smart surfaces for sensing and filtration applications.</p>","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"58 5","pages":"2412–2424 2412–2424"},"PeriodicalIF":5.2000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Gold Nanoparticle Adsorption in Covalently Bonded Weak Polyelectrolyte Brushes\",\"authors\":\"Katie Sun, Ye Chan Kim, Russell J. Composto* and Karen I. Winey*, \",\"doi\":\"10.1021/acs.macromol.4c0233210.1021/acs.macromol.4c02332\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The adsorption of spherical citrate-coated gold nanoparticles (AuNPs) into poly(2-vinylpyridine) (P2VP) brushes was investigated using a quartz crystal microbalance with dissipation (QCM-D). This study examined the impacts of environmental pH and brush molecular weight (10 and 53 kg/mol) on AuNP adsorption kinetics and areal number densities. We synthesized and characterized the P2VP brushes, grafted onto a poly(glycidyl methacrylate) (PGMA) priming layer, on both silicon wafers and QCM-D sensors. Adsorption experiments explored the pH-dependent adsorption behavior of 10- and 20-nm diameter AuNPs. The QCM-D data show that higher molecular weight brushes enhanced AuNP uptake. At pH = 4.0, the swollen brushes promote greater adsorption compared with the collapsed brush state at pH = 6.2. This study highlights the advantages of the homopolymer brush architecture compared with the block copolymer brush architecture from our previous work. Additionally, it reaffirms the pH-mediated size selectivity observed in our prior study, where the smaller 10 nm AuNPs show preferential adsorption at higher pH. These findings provide insights into the impacts of brush molecular weight and environmental conditions on nanoparticle adsorption, with implications for designing smart surfaces for sensing and filtration applications.</p>\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"58 5\",\"pages\":\"2412–2424 2412–2424\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.macromol.4c02332\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.macromol.4c02332","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Gold Nanoparticle Adsorption in Covalently Bonded Weak Polyelectrolyte Brushes
The adsorption of spherical citrate-coated gold nanoparticles (AuNPs) into poly(2-vinylpyridine) (P2VP) brushes was investigated using a quartz crystal microbalance with dissipation (QCM-D). This study examined the impacts of environmental pH and brush molecular weight (10 and 53 kg/mol) on AuNP adsorption kinetics and areal number densities. We synthesized and characterized the P2VP brushes, grafted onto a poly(glycidyl methacrylate) (PGMA) priming layer, on both silicon wafers and QCM-D sensors. Adsorption experiments explored the pH-dependent adsorption behavior of 10- and 20-nm diameter AuNPs. The QCM-D data show that higher molecular weight brushes enhanced AuNP uptake. At pH = 4.0, the swollen brushes promote greater adsorption compared with the collapsed brush state at pH = 6.2. This study highlights the advantages of the homopolymer brush architecture compared with the block copolymer brush architecture from our previous work. Additionally, it reaffirms the pH-mediated size selectivity observed in our prior study, where the smaller 10 nm AuNPs show preferential adsorption at higher pH. These findings provide insights into the impacts of brush molecular weight and environmental conditions on nanoparticle adsorption, with implications for designing smart surfaces for sensing and filtration applications.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.