Please use this identifier to cite or link to this item:
https://doi.org/10.1063/1.1800287
DC Field | Value | |
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dc.title | Formation of order molecular nanostructures on the Si(111)-(7×7) surface by patterned assembly | |
dc.contributor.author | Zhang, Y.P. | |
dc.contributor.author | Yong, K.S. | |
dc.contributor.author | Lai, Y.H. | |
dc.contributor.author | Xu, G.Q. | |
dc.contributor.author | Wang, X.S. | |
dc.date.accessioned | 2014-06-23T05:40:01Z | |
dc.date.available | 2014-06-23T05:40:01Z | |
dc.date.issued | 2004-10-04 | |
dc.identifier.citation | Zhang, Y.P., Yong, K.S., Lai, Y.H., Xu, G.Q., Wang, X.S. (2004-10-04). Formation of order molecular nanostructures on the Si(111)-(7×7) surface by patterned assembly. Applied Physics Letters 85 (14) : 2926-2928. ScholarBank@NUS Repository. https://doi.org/10.1063/1.1800287 | |
dc.identifier.issn | 00036951 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/76217 | |
dc.description.abstract | The use of copper clusters formed on the Si(111)-(7×7) surface was studied as a template for selective binding of molecules, forming ordered molecular nanostructures. It was shown that thiophene molecules preferentially bind to the copper clusters through the S-Cu interaction involving S lone-pair electrons. It was suggested that large-scale two-dimensional thiophene molecular nanostructures can be obtained using this patterned assembly technique. The feasibility for controllable growth of ordered molecular nanostructures on Si(111) surface was also demonstrated. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1063/1.1800287 | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.contributor.department | PHYSICS | |
dc.description.doi | 10.1063/1.1800287 | |
dc.description.sourcetitle | Applied Physics Letters | |
dc.description.volume | 85 | |
dc.description.issue | 14 | |
dc.description.page | 2926-2928 | |
dc.description.coden | APPLA | |
dc.identifier.isiut | 000224547300084 | |
Appears in Collections: | Staff Publications |
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