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https://doi.org/10.1002/adfm.201700523
Title: | Distinct Bimodal Roles of Aromatic Molecules in Controlling Gold Nanorod Growth for Biosensing | Authors: | Soh, J.H Lin, Y Thomas, M.R Todorova, N Kallepitis, C Yarovsky, I Ying, J.Y Stevens, M.M |
Keywords: | Alkalinity Aromatic compounds Aromatization Aspect ratio Binding energy Bins Medical applications Molecules Nanorods Phosphatases Plasmons Redox reactions Surface plasmon resonance Synthesis (chemical) ALkaline phosphatase Anisotropic growth Aromatic additives Gold nanorod Plasmonic sensing Gold |
Issue Date: | 2017 | Citation: | Soh, J.H, Lin, Y, Thomas, M.R, Todorova, N, Kallepitis, C, Yarovsky, I, Ying, J.Y, Stevens, M.M (2017). Distinct Bimodal Roles of Aromatic Molecules in Controlling Gold Nanorod Growth for Biosensing. Advanced Functional Materials 27 (29) : 1700523. ScholarBank@NUS Repository. https://doi.org/10.1002/adfm.201700523 | Rights: | Attribution 4.0 International | Abstract: | New aromatic molecule–seed particle interactions are examined and exploited to control and guide seed-mediated gold nanorod (Au NR) growth. This new approach enables better understanding of how small molecules impact the synthesis of metallic nanostructures, catalyzing their use in various biomedical applications, such as plasmonic biosensing. Experimental studies and theoretical molecular simulations using a library of aromatic molecules, making use of the chemical versatility of the molecules with varied spatial arrangements of electron-donating/withdrawing groups, charge, and Au-binding propensity, are performed. Au NR growth is regulated by two principal mechanisms, producing either a red or blue shift in the longitudinal localized surface plasmon resonance (LLSPR) peaks. Aromatic molecules with high redox potentials produce an increase in NR aspect ratio and red shift of LLSPR peaks. In contrast, molecules that strongly bind gold surfaces result in blue shifts, demonstrating a strong correlation between their binding energy and blue shifts produced. Through enzymatic conversion of selected molecules, 4-aminophenylphosphate to 4-aminophenol, opposing growth mechanisms at opposite extremes of target concentration are obtained, and a chemical pathway for performing plasmonic enzyme-linked immunosorbent assays is established. This unlocks new strategies for tailoring substrate design and enzymatic mechanisms for controlling plasmonic response to target molecules in biosensing applications. © 2017 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim | Source Title: | Advanced Functional Materials | URI: | https://scholarbank.nus.edu.sg/handle/10635/181257 | ISSN: | 1616301X | DOI: | 10.1002/adfm.201700523 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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