Matching the organic and inorganic counterparts during nucleation and growth of copper-based nanoparticles – in situ spectroscopic studies
Although syntheses in organic solvents provide access to a wide range of copper-based nanoparticles, the correlation between organic reactions in solution and nucleation and growth of nanoparticles with defined properties is not well understood. Here, we utilize the Multivariate Curve Resolution-Alt...
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Veröffentlicht in: | CrystEngComm 2015-01, Vol.17 (36), p.6962-6971 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Although syntheses in organic solvents provide access to a wide range of copper-based nanoparticles, the correlation between organic reactions in solution and nucleation and growth of nanoparticles with defined properties is not well understood. Here, we utilize the Multivariate Curve Resolution-Alternative Least Squares (MCR-ALS) methodology to examine spectroscopic data recorded
in situ
during the synthesis of copper-based nanoparticles. While earlier studies showed that depending on the temperature copper(
ii
) acetylacetonate reacts with benzyl alcohol and forms either copper oxides or copper nanoparticles, we link the inorganic reaction with their organic counterparts. From X-ray Absorption Near Edge Spectroscopy (XANES) and Ultraviolet-visible spectroscopy (UV-vis) data we learn that copper(
i
) oxide forms directly from the solution and is the final product at low temperature of 140 °C. We observe in Fourier Transformed Infrared (FTIR) spectra an increasing concentration of benzyl acetate that co-occurs with the formation of a copper enolate and evolution of benzaldehyde, which accompanies the reduction of copper ions. We also record the interaction of organic species at the Cu
2
O surface, which inhibits a further reduction to metallic copper. When we raise the synthesis temperature to 170 °C it turns out that the Cu
2
O is just an intermediate species. It subsequently transforms by solid-state reduction to metallic copper accompanied by oxidation of benzyl alcohol to benzaldehyde. |
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ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/C5CE00454C |