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Molecular mechanism of monodisperse colloidal tin-doped indium oxide nanocrystals by a hot-injection approach.


ABSTRACT: Molecular mechanisms and precursor conversion pathways associated with the reactions that generate colloidal nanocrystals are crucial for the development of rational synthetic protocols. In this study, Fourier transform infrared spectroscopy technique was employed to explore the molecular mechanism associated with the formation of tin-doped indium oxide (ITO) nanocrystals. We found that the reaction pathways of the indium precursor were not consistent with simple ligand replacements proposed in the literature. The resulting understanding inspired us to design a hot-injection approach to separate the ligand replacements of indium acetate and the aminolysis processes, generating quality ITO nanocrystals with decent size distributions. The hot-injection approach was readily applied to the synthesis of ITO nanocrystals with a broad range of tin doping. Structural, chemical, and optical analyses revealed effective doping of Sn4+ ions into the host lattices, leading to characteristic and tunable near-infrared surface plasmon resonance peaks. The size control of ITO nanocrystals by multiple hot-injections of metal precursors was also demonstrated.

SUBMITTER: Jin Y 

PROVIDER: S-EPMC3626570 | biostudies-literature | 2013 Apr

REPOSITORIES: biostudies-literature

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Molecular mechanism of monodisperse colloidal tin-doped indium oxide nanocrystals by a hot-injection approach.

Jin Yizheng Y   Yi Qing Q   Ren Yuping Y   Wang Xin X   Ye Zhizhen Z  

Nanoscale research letters 20130402 1


Molecular mechanisms and precursor conversion pathways associated with the reactions that generate colloidal nanocrystals are crucial for the development of rational synthetic protocols. In this study, Fourier transform infrared spectroscopy technique was employed to explore the molecular mechanism associated with the formation of tin-doped indium oxide (ITO) nanocrystals. We found that the reaction pathways of the indium precursor were not consistent with simple ligand replacements proposed in  ...[more]

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