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Chain Conformation and Dynamics in Spin-Assisted Weak Polyelectrolyte Multilayers
We report on the effect of the deposition technique on film layering, stability, and chain mobility in weak polyelectrolyte layer-by-layer (LbL) films. Ellipsometry and neutron reflectometry (NR) showed that shear forces arising during spin-assisted assembly lead to smaller amounts of adsorbed polye...
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Published in: | Langmuir 2015-04, Vol.31 (13), p.3889-3896 |
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creator | Zhuk, Aliaksandr Selin, Victor Zhuk, Iryna Belov, Benjamin Ankner, John F Sukhishvili, Svetlana A |
description | We report on the effect of the deposition technique on film layering, stability, and chain mobility in weak polyelectrolyte layer-by-layer (LbL) films. Ellipsometry and neutron reflectometry (NR) showed that shear forces arising during spin-assisted assembly lead to smaller amounts of adsorbed polyelectrolytes within LbL films, result in a higher degree of internal film order, and dramatically improve stability of assemblies in salt solutions as compared to dip-assisted LbL assemblies. The underlying flattening of polyelectrolyte chains in spin-assisted LbL films was also revealed as an increase in ionization degree of the assembled weak polyelectrolytes. As demonstrated by fluorescence recovery after photobleaching (FRAP), strong binding between spin-deposited polyelectrolytes results in a significant slowdown of chain diffusion in salt solutions as compared to dip-deposited films. Moreover, salt-induced chain intermixing in the direction perpendicular to the substrate is largely inhibited in spin-deposited films, resulting in only subdiffusional ( |
doi_str_mv | 10.1021/acs.langmuir.5b00401 |
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Spallation Neutron Source (SNS)</creatorcontrib><description>We report on the effect of the deposition technique on film layering, stability, and chain mobility in weak polyelectrolyte layer-by-layer (LbL) films. Ellipsometry and neutron reflectometry (NR) showed that shear forces arising during spin-assisted assembly lead to smaller amounts of adsorbed polyelectrolytes within LbL films, result in a higher degree of internal film order, and dramatically improve stability of assemblies in salt solutions as compared to dip-assisted LbL assemblies. The underlying flattening of polyelectrolyte chains in spin-assisted LbL films was also revealed as an increase in ionization degree of the assembled weak polyelectrolytes. As demonstrated by fluorescence recovery after photobleaching (FRAP), strong binding between spin-deposited polyelectrolytes results in a significant slowdown of chain diffusion in salt solutions as compared to dip-deposited films. Moreover, salt-induced chain intermixing in the direction perpendicular to the substrate is largely inhibited in spin-deposited films, resulting in only subdiffusional (<2 Å) chain displacements even after 200 h exposure to 1 M NaCl solutions. 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Spallation Neutron Source (SNS)</creatorcontrib><title>Chain Conformation and Dynamics in Spin-Assisted Weak Polyelectrolyte Multilayers</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>We report on the effect of the deposition technique on film layering, stability, and chain mobility in weak polyelectrolyte layer-by-layer (LbL) films. Ellipsometry and neutron reflectometry (NR) showed that shear forces arising during spin-assisted assembly lead to smaller amounts of adsorbed polyelectrolytes within LbL films, result in a higher degree of internal film order, and dramatically improve stability of assemblies in salt solutions as compared to dip-assisted LbL assemblies. The underlying flattening of polyelectrolyte chains in spin-assisted LbL films was also revealed as an increase in ionization degree of the assembled weak polyelectrolytes. As demonstrated by fluorescence recovery after photobleaching (FRAP), strong binding between spin-deposited polyelectrolytes results in a significant slowdown of chain diffusion in salt solutions as compared to dip-deposited films. Moreover, salt-induced chain intermixing in the direction perpendicular to the substrate is largely inhibited in spin-deposited films, resulting in only subdiffusional (<2 Å) chain displacements even after 200 h exposure to 1 M NaCl solutions. 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Spallation Neutron Source (SNS)</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhuk, Aliaksandr</au><au>Selin, Victor</au><au>Zhuk, Iryna</au><au>Belov, Benjamin</au><au>Ankner, John F</au><au>Sukhishvili, Svetlana A</au><aucorp>Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States). Spallation Neutron Source (SNS)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chain Conformation and Dynamics in Spin-Assisted Weak Polyelectrolyte Multilayers</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2015-04-07</date><risdate>2015</risdate><volume>31</volume><issue>13</issue><spage>3889</spage><epage>3896</epage><pages>3889-3896</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><abstract>We report on the effect of the deposition technique on film layering, stability, and chain mobility in weak polyelectrolyte layer-by-layer (LbL) films. Ellipsometry and neutron reflectometry (NR) showed that shear forces arising during spin-assisted assembly lead to smaller amounts of adsorbed polyelectrolytes within LbL films, result in a higher degree of internal film order, and dramatically improve stability of assemblies in salt solutions as compared to dip-assisted LbL assemblies. The underlying flattening of polyelectrolyte chains in spin-assisted LbL films was also revealed as an increase in ionization degree of the assembled weak polyelectrolytes. As demonstrated by fluorescence recovery after photobleaching (FRAP), strong binding between spin-deposited polyelectrolytes results in a significant slowdown of chain diffusion in salt solutions as compared to dip-deposited films. Moreover, salt-induced chain intermixing in the direction perpendicular to the substrate is largely inhibited in spin-deposited films, resulting in only subdiffusional (<2 Å) chain displacements even after 200 h exposure to 1 M NaCl solutions. This persistence of polyelectrolyte layering has important ramifications for multistage drug delivery and optical applications of LbL assemblies.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>25768113</pmid><doi>10.1021/acs.langmuir.5b00401</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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title | Chain Conformation and Dynamics in Spin-Assisted Weak Polyelectrolyte Multilayers |
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