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dc.contributor.authorYang, Y.
dc.contributor.authorCiampi, Simone
dc.contributor.authorZhu, Y.
dc.contributor.authorGooding, J.
dc.date.accessioned2017-01-30T13:36:19Z
dc.date.available2017-01-30T13:36:19Z
dc.date.created2016-07-24T19:30:44Z
dc.date.issued2016
dc.identifier.citationYang, Y. and Ciampi, S. and Zhu, Y. and Gooding, J. 2016. Light-Activated Electrochemistry for the Two-Dimensional Interrogation of Electroactive Regions on a Monolithic Surface with Dramatically Improved Spatial Resolution. Journal of Physical Chemistry C. 120 (24): pp. 13032-13038.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/33314
dc.identifier.doi10.1021/acs.jpcc.6b02289
dc.description.abstract

The concept of light-activated electrochemistry (LAE) was recently presented where faradaic electrochemistry could be spatially resolved on a monolithic silicon electrode by illuminating the specific region with light. A major implication from the previous study using illumination from the nonsolution side, or backside, is that the spatial resolution is limited by the finite thickness of silicon wafer. To overcome this restriction, and enable the further application of LAE, in combination with optical imaging for example, herein the spatial resolution of LAE using topside illumination (illumination from the solution side) is explored. The applied potential and irradiated light intensity are found to have significant effects on the spatial resolution. A spatial resolution of ~30 µm was achieved with optimal parameters, which is a 20 times improvement compared with the previously reported backside illumination design, demonstrating the potential application of the strategy including microarray patterning of silicon or for single cell analysis.

dc.publisherAmerican Chemical Society
dc.titleLight-Activated Electrochemistry for the Two-Dimensional Interrogation of Electroactive Regions on a Monolithic Surface with Dramatically Improved Spatial Resolution
dc.typeJournal Article
dcterms.source.volume120
dcterms.source.number24
dcterms.source.startPage13032
dcterms.source.endPage13038
dcterms.source.issn1932-7447
dcterms.source.titleJournal of Physical Chemistry C
curtin.note

This open access article is distributed under the Creative Commons license http://creativecommons.org/licenses/by-nc/4.0/

curtin.departmentNanochemistry Research Institute
curtin.accessStatusOpen access


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