TY - JOUR
T1 - Effect of poly(N-vinyl-pyrrolidone) on electrochemical production of Cu nanoparticles
AU - Saito, Mikiko
AU - Ishii, Tomohiro
AU - Fujiwara, Hidemichi
AU - Homma, Takayuki
N1 - Funding Information:
A part of this study was supported by Nanotechnology Platform Project sponsored by MEXT, Japan, and by “Development of Systems and Technology for Advanced Measurement and Analysis,” JST, Japan.
Publisher Copyright:
© 2018 The Electrochemical Society.
PY - 2018
Y1 - 2018
N2 - Cu nanoparticles were synthesized via electrochemical deposition and the effect of the addition of poly(N-vinyl-pyrrolidone) (PVP) and pH on the properties of the nanoparticles was investigated. The Cu nanoparticles were prepared from an electrolyte containing copper acetate (pH 5.50) or copper sulfate (pH 4.14) by collecting the dispersed particles in the solution after electrochemical reduction. With the use of the acetate bath, formation of Cu2O at -0.2 and -1.5 V vs. Ag/AgCl was confirmed. On the other hand, Cu2O formation was not observed with the sulfate bath due to the lower pH, and the Cu nanoparticles could not be obtained at the potential of -1.5 V vs. Ag/AgCl. Surface enhanced Raman spectroscopy with plasmon sensors was used to investigate the transformations of PVP during electrolysis under the different conditions when Cu particles were and were not formed. For the dispersed nanoparticles in the electrolyte, it was observed that the C=O and C-N peaks of PVP also exhibited a red-shift. It was thus confirmed that PVP was coordinated to both the cathode electrode and dispersed nanoparticles in the electrolyte upon electrochemical reduction.
AB - Cu nanoparticles were synthesized via electrochemical deposition and the effect of the addition of poly(N-vinyl-pyrrolidone) (PVP) and pH on the properties of the nanoparticles was investigated. The Cu nanoparticles were prepared from an electrolyte containing copper acetate (pH 5.50) or copper sulfate (pH 4.14) by collecting the dispersed particles in the solution after electrochemical reduction. With the use of the acetate bath, formation of Cu2O at -0.2 and -1.5 V vs. Ag/AgCl was confirmed. On the other hand, Cu2O formation was not observed with the sulfate bath due to the lower pH, and the Cu nanoparticles could not be obtained at the potential of -1.5 V vs. Ag/AgCl. Surface enhanced Raman spectroscopy with plasmon sensors was used to investigate the transformations of PVP during electrolysis under the different conditions when Cu particles were and were not formed. For the dispersed nanoparticles in the electrolyte, it was observed that the C=O and C-N peaks of PVP also exhibited a red-shift. It was thus confirmed that PVP was coordinated to both the cathode electrode and dispersed nanoparticles in the electrolyte upon electrochemical reduction.
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U2 - 10.1149/2.0921802jes
DO - 10.1149/2.0921802jes
M3 - Article
AN - SCOPUS:85048416371
SN - 0013-4651
VL - 165
SP - E50-E57
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 2
ER -