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Citrate-hydrazine Hydrogen-Bonding Driven Single-Step Synthesis of Tunable near-IR Plasmonic, Anisotropic Silver Nanocrystals: Implications for SERS Spectroscopy of Inorganic Oxoanions

Satarupa Pattanayak, Abhishek Swarnkar, Amiya Priyam, Gopal M Bhalerao

Dalton Trans. 2014 Aug 21;43(31):11826-33.

PMID: 24957728

Abstract:

A simplified, single-step aqueous synthesis route to tunable anisotropic silver nanocrystals (NCs) has been developed by tailoring the hydrogen-bonding interactions between a mild stabilizer, sodium citrate, and a mild reductant, hydrazine hydrate. The structure directing ability of the H-bonding interaction was harnessed by keeping a stoichiometric excess of hydrazine under ambient conditions (pH 7, 25 °C). Decreasing the synthesis temperature to 5 °C imparts rigidity to the citrate-hydrazine H-bonding network, and the plasmon peak moves from 500 to 550 nm (using 40 mM hydrazine). On lowering the pH from 7 to 5, the H-bonding is further strengthened due to partial protonation of citrate and the plasmon peak is tuned to 790 nm. Further, we found that, at 5 °C and pH 5, there also exists a sub-stoichiometric regime in which maximum tunability of the plasmon peak (790→1010 nm) is achieved with 1 mM hydrazine. HR-TEM reveals that the near-IR plasmonic NCs are nanopyramids having a pentagonal base with edge length varying from 15 nm to 30 nm. Through second derivative FTIR analysis, a correlation between hydrogen-bonded molecular vibrations and the plasmon tunability has been established. The anisotropic NCs exhibit significant Raman enhancement on the citrate molecules. Further, a solution-phase, non-resonant SERS spectroscopic detection method for an inorganic contaminant of ground water, arsenite, has also been developed.

Chemicals Related in the Paper:

Catalog Number Product Name Structure CAS Number Price
AP206986905 Silver citrate hydrate Silver citrate hydrate 206986-90-5 Price
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