Au-Ag bimetallic nanodendrite synthesized viasimultaneous co-electrodeposition and its application as a SERS substrate
We presented a novel Au-Ag bimetallic nanodendrite constructed through simple one-step co-electrodeposition on a Pt surface in the presence of iodide ions as a co-reagent. Simultaneously, we maneuvered to generate hydrogen bubbles from the same surface by the reduction of proton to drive the growth...
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Published in | RSC advances Vol. 4; no. 8; pp. 3929 - 3933 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
01.12.2013
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Subjects | |
Online Access | Get full text |
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Summary: | We presented a novel Au-Ag bimetallic nanodendrite constructed through simple one-step co-electrodeposition on a Pt surface in the presence of iodide ions as a co-reagent. Simultaneously, we maneuvered to generate hydrogen bubbles from the same surface by the reduction of proton to drive the growth of deposition into the nanodendrite network structure. Au-Ag bimetallic nanodendrites composed of different atomic percentages of Au and Ag (0.00-5.12% Ag) were electrochemically synthesized by varying mole percentages of Au super(3+) and Ag super(+) in solutions. When atomic Ag concentration was from 0.39 to 3.84%, characteristic dendrite structure with high crystallinity was clearly observed; while, an imperfect nanodendrite structure became present when the atomic Ag concentration was over 3.84%. Further, the bimetallic nanodendrites with different Ag concentrations were used as a substrate for surface-enhanced Raman scattering (SERS) measurement. The SERS intensity of 2-naphthalenethiol was maximized when the nanodendrite containing 3.84% Ag was used. Incorporation of better plasmonic metal, Ag, into the nanodendrite structure was obviously advantages in enhancing SERS efficiency; while, maintaining a good bimetallic nanodendrite structure was a prerequisite for optimal SERS measurement. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-1 |
ISSN: | 2046-2069 |
DOI: | 10.1039/c3ra44916e |