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Investigation of Polymer Chain Diffusion Behavior in Thin Slits Formed by Patch-Patterned Surfaces: Influence of Patch Properties
The diffusion dynamics of polymer chains within a narrow slit formed by two patch-patterned surfaces is investigated utilizing Langevin dynamics simulations. These surfaces feature periodically arranged attractive patches of size L and period d, with a staggered configuration of (0.5d, 0.5d) offsets...
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Published in: | Langmuir 2024-12, Vol.40 (52), p.27659-27666 |
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creator | Zhang, Hao-Nan Wang, Guo-Ao Qi, Hang-Kai Yang, Qing-Hui Luo, Meng-Bo |
description | The diffusion dynamics of polymer chains within a narrow slit formed by two patch-patterned surfaces is investigated utilizing Langevin dynamics simulations. These surfaces feature periodically arranged attractive patches of size L and period d, with a staggered configuration of (0.5d, 0.5d) offsets along the x and y axes. When d is fixed, the polymer chain exhibits normal diffusion over long time scales, with the translational diffusion coefficient D xy gradually decreasing to zero as L increases. Notably, our findings reveal four distinct diffusion modes: free-diffusion mode for L ≤ L 1, where the polymer chain is mainly in a desorption state; adsorption–desorption mode for L 1 < L ≤ L 2, involving transitions from a single-patch adsorption state to a desorption state; exchange-patch mode for L 2 < L ≤ L 3, where the polymer chain switches between a single-patch adsorption state and an upper-lower double-patch adsorption state by exchanging patches; and nondiffusion mode for L > L 3, where the polymer chain is primarily in a pinned state. Furthermore, as the patch attraction strength εps increases, D xy decreases due to an increase in the adsorption time of the polymer chain. Simultaneously, critical patch size thresholds L 1, L 2, and L 3, exhibit a decreasing trend. These observations highlight the significant influence of the confining slit and patch properties on the diffusion behavior of polymer chains. |
doi_str_mv | 10.1021/acs.langmuir.4c04264 |
format | article |
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These surfaces feature periodically arranged attractive patches of size L and period d, with a staggered configuration of (0.5d, 0.5d) offsets along the x and y axes. When d is fixed, the polymer chain exhibits normal diffusion over long time scales, with the translational diffusion coefficient D xy gradually decreasing to zero as L increases. Notably, our findings reveal four distinct diffusion modes: free-diffusion mode for L ≤ L 1, where the polymer chain is mainly in a desorption state; adsorption–desorption mode for L 1 < L ≤ L 2, involving transitions from a single-patch adsorption state to a desorption state; exchange-patch mode for L 2 < L ≤ L 3, where the polymer chain switches between a single-patch adsorption state and an upper-lower double-patch adsorption state by exchanging patches; and nondiffusion mode for L > L 3, where the polymer chain is primarily in a pinned state. Furthermore, as the patch attraction strength εps increases, D xy decreases due to an increase in the adsorption time of the polymer chain. Simultaneously, critical patch size thresholds L 1, L 2, and L 3, exhibit a decreasing trend. These observations highlight the significant influence of the confining slit and patch properties on the diffusion behavior of polymer chains.</description><identifier>ISSN: 0743-7463</identifier><identifier>ISSN: 1520-5827</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/acs.langmuir.4c04264</identifier><identifier>PMID: 39692868</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Langmuir, 2024-12, Vol.40 (52), p.27659-27666</ispartof><rights>2024 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a227t-5d1e5182b87116153be0a739385902ddd286df4af8b67a23da5c34f947439be3</cites><orcidid>0000-0002-0783-0352 ; 0000-0003-1433-9200</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39692868$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Hao-Nan</creatorcontrib><creatorcontrib>Wang, Guo-Ao</creatorcontrib><creatorcontrib>Qi, Hang-Kai</creatorcontrib><creatorcontrib>Yang, Qing-Hui</creatorcontrib><creatorcontrib>Luo, Meng-Bo</creatorcontrib><title>Investigation of Polymer Chain Diffusion Behavior in Thin Slits Formed by Patch-Patterned Surfaces: Influence of Patch Properties</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>The diffusion dynamics of polymer chains within a narrow slit formed by two patch-patterned surfaces is investigated utilizing Langevin dynamics simulations. These surfaces feature periodically arranged attractive patches of size L and period d, with a staggered configuration of (0.5d, 0.5d) offsets along the x and y axes. When d is fixed, the polymer chain exhibits normal diffusion over long time scales, with the translational diffusion coefficient D xy gradually decreasing to zero as L increases. Notably, our findings reveal four distinct diffusion modes: free-diffusion mode for L ≤ L 1, where the polymer chain is mainly in a desorption state; adsorption–desorption mode for L 1 < L ≤ L 2, involving transitions from a single-patch adsorption state to a desorption state; exchange-patch mode for L 2 < L ≤ L 3, where the polymer chain switches between a single-patch adsorption state and an upper-lower double-patch adsorption state by exchanging patches; and nondiffusion mode for L > L 3, where the polymer chain is primarily in a pinned state. Furthermore, as the patch attraction strength εps increases, D xy decreases due to an increase in the adsorption time of the polymer chain. Simultaneously, critical patch size thresholds L 1, L 2, and L 3, exhibit a decreasing trend. These observations highlight the significant influence of the confining slit and patch properties on the diffusion behavior of polymer chains.</description><issn>0743-7463</issn><issn>1520-5827</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kEtPwzAQhC0EgvL4Bwj5yCXFzyTmBuVVCYlK7T1yknVrlMTFTpB65J_j0sKRy1paz8xqPoQuKRlTwuiNrsK40d2yHawfi4oIlooDNKKSkUTmLDtEI5IJnmQi5SfoNIR3QojiQh2jE65SxfI0H6GvafcJobdL3VvXYWfwzDWbFjyerLTt8IM1Zgjbr3tY6U_rPI7bxSqOeWP7gJ-cb6HG5QbPdF-tkjh78F1czQdvdAXhFk870wzQVfCTv5XhmXdr8L2FcI6OjG4CXOzfM7R4elxMXpLXt-fp5O410YxlfSJrCpLmrMwzSlMqeQlEZ1zxXCrC6rqOfWojtMnLNNOM11pWXBglIgNVAj9D17vYtXcfQ6xctDZU0ESE4IZQcCpSJbkkWZSKnbTyLgQPplh722q_KSgptuyLyL74ZV_s2Ufb1f7CUEYkf6Zf2FFAdoKt_d0Nvot9_8_8BksjlQs</recordid><startdate>20241231</startdate><enddate>20241231</enddate><creator>Zhang, Hao-Nan</creator><creator>Wang, Guo-Ao</creator><creator>Qi, Hang-Kai</creator><creator>Yang, Qing-Hui</creator><creator>Luo, Meng-Bo</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0783-0352</orcidid><orcidid>https://orcid.org/0000-0003-1433-9200</orcidid></search><sort><creationdate>20241231</creationdate><title>Investigation of Polymer Chain Diffusion Behavior in Thin Slits Formed by Patch-Patterned Surfaces: Influence of Patch Properties</title><author>Zhang, Hao-Nan ; Wang, Guo-Ao ; Qi, Hang-Kai ; Yang, Qing-Hui ; Luo, Meng-Bo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a227t-5d1e5182b87116153be0a739385902ddd286df4af8b67a23da5c34f947439be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Hao-Nan</creatorcontrib><creatorcontrib>Wang, Guo-Ao</creatorcontrib><creatorcontrib>Qi, Hang-Kai</creatorcontrib><creatorcontrib>Yang, Qing-Hui</creatorcontrib><creatorcontrib>Luo, Meng-Bo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Hao-Nan</au><au>Wang, Guo-Ao</au><au>Qi, Hang-Kai</au><au>Yang, Qing-Hui</au><au>Luo, Meng-Bo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of Polymer Chain Diffusion Behavior in Thin Slits Formed by Patch-Patterned Surfaces: Influence of Patch Properties</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2024-12-31</date><risdate>2024</risdate><volume>40</volume><issue>52</issue><spage>27659</spage><epage>27666</epage><pages>27659-27666</pages><issn>0743-7463</issn><issn>1520-5827</issn><eissn>1520-5827</eissn><abstract>The diffusion dynamics of polymer chains within a narrow slit formed by two patch-patterned surfaces is investigated utilizing Langevin dynamics simulations. These surfaces feature periodically arranged attractive patches of size L and period d, with a staggered configuration of (0.5d, 0.5d) offsets along the x and y axes. When d is fixed, the polymer chain exhibits normal diffusion over long time scales, with the translational diffusion coefficient D xy gradually decreasing to zero as L increases. Notably, our findings reveal four distinct diffusion modes: free-diffusion mode for L ≤ L 1, where the polymer chain is mainly in a desorption state; adsorption–desorption mode for L 1 < L ≤ L 2, involving transitions from a single-patch adsorption state to a desorption state; exchange-patch mode for L 2 < L ≤ L 3, where the polymer chain switches between a single-patch adsorption state and an upper-lower double-patch adsorption state by exchanging patches; and nondiffusion mode for L > L 3, where the polymer chain is primarily in a pinned state. Furthermore, as the patch attraction strength εps increases, D xy decreases due to an increase in the adsorption time of the polymer chain. Simultaneously, critical patch size thresholds L 1, L 2, and L 3, exhibit a decreasing trend. These observations highlight the significant influence of the confining slit and patch properties on the diffusion behavior of polymer chains.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>39692868</pmid><doi>10.1021/acs.langmuir.4c04264</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-0783-0352</orcidid><orcidid>https://orcid.org/0000-0003-1433-9200</orcidid></addata></record> |
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title | Investigation of Polymer Chain Diffusion Behavior in Thin Slits Formed by Patch-Patterned Surfaces: Influence of Patch Properties |
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