Material-Selective Surface Chemistry for Nanoplasmonic Sensors: Optimizing Sensitivity and Controlling Binding to Local Hot Spots
2012 (English)In: Nano letters (Print), ISSN 1530-6984, E-ISSN 1530-6992, Vol. 12, no 2, 873-879 p.Article in journal (Refereed) Published
Optical sensors utilizing the principle of localized surface plasmon resonance (LSPR) offer the advantage of a simple label-free mode of operation, but the sensitivity is typically limited to a very thin region close to the surface. In bioanalytical sensing applications, this can be a significant drawback, in particular since the surface needs to be coated with a recognition layer in order to ensure specific detection of target molecules. We show that the signal upon protein binding decreases dramatically with increasing thickness of the recognition layer, highlighting the need for thin high quality recognition layers compatible with LSPR sensors. The effect is particularly strong for structures that provide local hot spots with highly confined fields, such as in the gap between pairs of gold disks. While our results show a significant improvement in sensor response for pairs over single gold disks upon binding directly to the gold surface, disk pairs did not provide larger signal upon binding of proteins to a recognition layer (already for around 3 nm thin layers) located on the gold. Local plasmonic hot spots are however shown advantageous in combination with directed binding to the hot spots. This was demonstrated using a structure consisting of three surface materials (gold, titanium dioxide, and silicon dioxide) and a new protocol for material-selective surface chemistry of these three materials, which allows for controlled binding only in the gap between pairs of disks. Such a design increased the signal obtained per bound molecule by a factor of around four compared to binding to single disks.
Place, publisher, year, edition, pages
American Chemical Society , 2012. Vol. 12, no 2, 873-879 p.
Localized surface plasmon resonance (LSPR); nanoplasmonics; biosensing; hot spot; chemical surface modification; nanofabrication
IdentifiersURN: urn:nbn:se:liu:diva-118822DOI: 10.1021/nl203917eISI: 000299967800058PubMedID: 22257106OAI: oai:DiVA.org:liu-118822DiVA: diva2:817148
Funding Agencies|SNSF (Swiss National Science Foundation) [PBEZA- 121238]; Swedish Foundation for Strategic Research; Wenner-Gren Foundations2015-06-042015-06-042015-06-18