Maximum flux: using time-resolved neutron reflectometry to improve our understanding of surface-initiated polymerisation

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dc.contributor.authorGresham, IJen_AU
dc.contributor.authorPrescott, SWen_AU
dc.contributor.authorNelson, Aen_AU
dc.contributor.authorRobertson, Hen_AU
dc.contributor.authorJohnson, ECen_AU
dc.contributor.authorWebber, GBen_AU
dc.contributor.authorWanless, EJen_AU
dc.date.accessioned2023-06-16T00:10:37Zen_AU
dc.date.available2023-06-16T00:10:37Zen_AU
dc.date.issued2021-11-24en_AU
dc.date.statistics2023-04-24en_AU
dc.description.abstractPolymer brushes are dense arrays of surface-tethered polymers that possess desirable qualities, such as lubricity and fouling resistance, provided that their structure and chemistry are correctly tuned [1]. Surface-initiated polymerisation (SIP) is the primary method for synthesising these brushes with the physicochemical properties required to imbue surfaces with the aforementioned qualities. However, previous work [2,3] indicates that polymers synthesised by SIP deviate from polymers produced via solution polymerisation, likely due to the proximity of initiators in the tethered case. This deviation is not well understood, which impedes the structural characterisation of the resulting brushes. As structure dictates behaviour [1], understanding the nature of the brushes produced by SIP facilitates the rational design of functional brush coatings. Here we present a study of brushes synthesised via SIP of the well-characterised polymer poly(N-isopropyl acrylamide) (PNIPAM) using time-resolved neutron reflectometry (NR). First, we demonstrate that we can control the polymer initiator density and examine the relationship between molecular weight and grafting density. We then observe a series of SIP reactions from surfaces with different initiator densities in situ using time-resolved NR. To our knowledge, this is the first time that the structure of a growing polymer brush has been directly observed. The results confirm that a high initiator density leads to poor control early in the reaction, and explain several phenomena observed by previous NR experiments [4,5]. This experiment paves the way for further kinetic experiments on Platypus and will be of interest to anyone interested in the dynamic assembly of interfaces over timescales of 10 minutes to several hours. © 2021 The Authorsen_AU
dc.identifier.citationGresham, I., Prescott, S., Nelson, A., Robertson, H., Johnson, E., Weber, G., & Wanless, E., (2021). Maximum flux: using time-resolved neutron reflectometry to improve our understanding of surface-initiated polymerisation. Presentation to the ANSTO User Meeting, 24-26 November 2021, Online. Retrieved from: https://events01.synchrotron.org.au/event/146/contributions/4294/contribution.pdfen_AU
dc.identifier.conferenceenddate26 November 2021en_AU
dc.identifier.conferencenameANSTO User Meeting 2021en_AU
dc.identifier.conferenceplaceOnlineen_AU
dc.identifier.conferencestartdate24 November 2021en_AU
dc.identifier.urihttps://events01.synchrotron.org.au/event/146/contributions/4294/contribution.pdfen_AU
dc.identifier.urihttps://apo.ansto.gov.au/handle/10238/15058en_AU
dc.language.isoenen_AU
dc.publisherAustralian Nuclear Science and Technology Organisationen_AU
dc.subjectFlux densityen_AU
dc.subjectNeutron reflectorsen_AU
dc.subjectPolymerizationen_AU
dc.subjectFoulingen_AU
dc.subjectChemistryen_AU
dc.subjectArray processorsen_AU
dc.titleMaximum flux: using time-resolved neutron reflectometry to improve our understanding of surface-initiated polymerisationen_AU
dc.typeConference Presentationen_AU
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