http://www.cnr.it/ontology/cnr/individuo/prodotto/ID192407
Cysteamine-Based Functionalization of InAs Surfaces: Revealing the Critical Role of Oxide Interactions in Biasing Attachment (Articolo in rivista)
- Type
- Label
- Cysteamine-Based Functionalization of InAs Surfaces: Revealing the Critical Role of Oxide Interactions in Biasing Attachment (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/la203436r (literal)
- Alternative label
Maria Losurdo, P. C Wu, T.H. Kim, G. Bruno, A. S. Brown (2012)
Cysteamine-Based Functionalization of InAs Surfaces: Revealing the Critical Role of Oxide Interactions in Biasing Attachment
in Langmuir
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Maria Losurdo, P. C Wu, T.H. Kim, G. Bruno, A. S. Brown (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- IMIP CNR, Inst Inorgan Methodol & Plasmas, I-70126 Bari, Italy
Duke Univ, Dept Elect & Comp Engn, Durham, NC 27708 USA (literal)
- Titolo
- Cysteamine-Based Functionalization of InAs Surfaces: Revealing the Critical Role of Oxide Interactions in Biasing Attachment (literal)
- Abstract
- Attaching functional molecules such as thiols and proteins to semiconductor surfaces is increasingly exploited in functional devices such as sensors. Despite extensive research to understand this interface and demonstrate a robust protocol for attachment, the bonding chemistry of thiolates to III-V surfaces has been under great debate in the literature. This study provides a comprehensive chemical model for the attachment of thiols to InAs, an increasingly device-relevant III-V semiconductor, using cysteamine as a model molecule. We examine the attachment of cysteamine to InAs via the thiol group using X-ray photoelectron spectroscopy and spectroscopic ellipsometry and confirm that thiolate bonding to the substrate occurs preferentially to As sites over In sites as a limit These experiments explore the interplay of the native oxide chemical properties, the cysteamine concentration, and the evolving InAs surface chemistry with functionalization. The thiol-InAs interaction can be framed as a general acid-base reaction, where the nucleophilic and/or electrophilic attack of the surface (i.e., binding to In sites and/or As sites) depends on the acidity of the thiol. The roles of the initial oxide composition, the solvent of the functionalizing solution, and the cysteamine as a limiting reagent in fully displacing the oxide and creating In-S and As-S bonds are highlighted. (literal)
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- Autore CNR
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