{"title":"溶剂质量和三价离子对聚电解质电刷构象的协同调节","authors":"Minglun Li , Marina Ruths , Bilin Zhuang , Jing Yu","doi":"10.1016/j.giant.2025.100363","DOIUrl":null,"url":null,"abstract":"<div><div>Surface polyelectrolyte brush materials responsive to solvent quality and added ions have widespread applications in interfacial materials. The interplay between solvent quality and ion valency plays a pivotal role in determining the conformation of polyelectrolyte brushes, yet its mechanisms remain underexplored. In this study, we systematically investigate these coupling effects on sodium poly(styrene sulfonate) (PSS) brushes through a combination of theoretical modeling, all-atom molecular dynamics (MD) simulations, and atomic force microscopy (AFM) experiments. By tuning the water-to-isopropyl alcohol (IPA) ratio in binary solvents, we reveal that solvent quality drives a gradual decrease in brush height, culminating in a rapid collapse at higher IPA volume fractions (<span><math><mrow><msub><mi>ϕ</mi><mtext>IPA</mtext></msub><mo>≈</mo><mn>0.8</mn></mrow></math></span>). Theoretically, we extend our unified framework for ion-valency effects to incorporate Flory–Huggins interaction parameters derived from solvent solubility parameters, yielding predictions consistent with experimental and simulation results. Our findings highlight that the solvent-polymer interactions govern brush height more significantly than dielectric constants in mixed solvents. Solvent-induced brush collapse occurs uniformly, whereas multivalent ions induce localized adsorption, leading to chain aggregation and non-homogeneous collapse. The constructed brush height landscape further demonstrates that solvent quality predominates for short chains, while both solvent quality and ion valency exhibit synergistic and nonlinear effects on longer chains, with pronounced collapse transitions observed under specific conditions. This study provides a comprehensive understanding of the coupled effects of solvent quality and ion valency on polyelectrolyte brushes, offering valuable insights for designing stimuli-responsive surfaces. These findings are particularly relevant for applications in vapor sensing, gas separation, and advanced surface engineering technologies, where precise control over brush height and morphology is crucial.</div></div>","PeriodicalId":34151,"journal":{"name":"GIANT","volume":"24 ","pages":"Article 100363"},"PeriodicalIF":4.9000,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic regulation of polyelectrolyte brush conformations by solvent quality and trivalent ions\",\"authors\":\"Minglun Li , Marina Ruths , Bilin Zhuang , Jing Yu\",\"doi\":\"10.1016/j.giant.2025.100363\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Surface polyelectrolyte brush materials responsive to solvent quality and added ions have widespread applications in interfacial materials. The interplay between solvent quality and ion valency plays a pivotal role in determining the conformation of polyelectrolyte brushes, yet its mechanisms remain underexplored. In this study, we systematically investigate these coupling effects on sodium poly(styrene sulfonate) (PSS) brushes through a combination of theoretical modeling, all-atom molecular dynamics (MD) simulations, and atomic force microscopy (AFM) experiments. By tuning the water-to-isopropyl alcohol (IPA) ratio in binary solvents, we reveal that solvent quality drives a gradual decrease in brush height, culminating in a rapid collapse at higher IPA volume fractions (<span><math><mrow><msub><mi>ϕ</mi><mtext>IPA</mtext></msub><mo>≈</mo><mn>0.8</mn></mrow></math></span>). Theoretically, we extend our unified framework for ion-valency effects to incorporate Flory–Huggins interaction parameters derived from solvent solubility parameters, yielding predictions consistent with experimental and simulation results. Our findings highlight that the solvent-polymer interactions govern brush height more significantly than dielectric constants in mixed solvents. Solvent-induced brush collapse occurs uniformly, whereas multivalent ions induce localized adsorption, leading to chain aggregation and non-homogeneous collapse. The constructed brush height landscape further demonstrates that solvent quality predominates for short chains, while both solvent quality and ion valency exhibit synergistic and nonlinear effects on longer chains, with pronounced collapse transitions observed under specific conditions. This study provides a comprehensive understanding of the coupled effects of solvent quality and ion valency on polyelectrolyte brushes, offering valuable insights for designing stimuli-responsive surfaces. These findings are particularly relevant for applications in vapor sensing, gas separation, and advanced surface engineering technologies, where precise control over brush height and morphology is crucial.</div></div>\",\"PeriodicalId\":34151,\"journal\":{\"name\":\"GIANT\",\"volume\":\"24 \",\"pages\":\"Article 100363\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-07-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"GIANT\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666542525000128\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"GIANT","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666542525000128","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Synergistic regulation of polyelectrolyte brush conformations by solvent quality and trivalent ions
Surface polyelectrolyte brush materials responsive to solvent quality and added ions have widespread applications in interfacial materials. The interplay between solvent quality and ion valency plays a pivotal role in determining the conformation of polyelectrolyte brushes, yet its mechanisms remain underexplored. In this study, we systematically investigate these coupling effects on sodium poly(styrene sulfonate) (PSS) brushes through a combination of theoretical modeling, all-atom molecular dynamics (MD) simulations, and atomic force microscopy (AFM) experiments. By tuning the water-to-isopropyl alcohol (IPA) ratio in binary solvents, we reveal that solvent quality drives a gradual decrease in brush height, culminating in a rapid collapse at higher IPA volume fractions (). Theoretically, we extend our unified framework for ion-valency effects to incorporate Flory–Huggins interaction parameters derived from solvent solubility parameters, yielding predictions consistent with experimental and simulation results. Our findings highlight that the solvent-polymer interactions govern brush height more significantly than dielectric constants in mixed solvents. Solvent-induced brush collapse occurs uniformly, whereas multivalent ions induce localized adsorption, leading to chain aggregation and non-homogeneous collapse. The constructed brush height landscape further demonstrates that solvent quality predominates for short chains, while both solvent quality and ion valency exhibit synergistic and nonlinear effects on longer chains, with pronounced collapse transitions observed under specific conditions. This study provides a comprehensive understanding of the coupled effects of solvent quality and ion valency on polyelectrolyte brushes, offering valuable insights for designing stimuli-responsive surfaces. These findings are particularly relevant for applications in vapor sensing, gas separation, and advanced surface engineering technologies, where precise control over brush height and morphology is crucial.
期刊介绍:
Giant is an interdisciplinary title focusing on fundamental and applied macromolecular science spanning all chemistry, physics, biology, and materials aspects of the field in the broadest sense. Key areas covered include macromolecular chemistry, supramolecular assembly, multiscale and multifunctional materials, organic-inorganic hybrid materials, biophysics, biomimetics and surface science. Core topics range from developments in synthesis, characterisation and assembly towards creating uniformly sized precision macromolecules with tailored properties, to the design and assembly of nanostructured materials in multiple dimensions, and further to the study of smart or living designer materials with tuneable multiscale properties.