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In situ synthesis and electronic transport of the carbon-coated Ag@C/MWCNT nanocomposite

A nanocomposite of Ag@C nanocapsules dispersed in a multi-walled carbon nanotube (MWCNT) matrix was fabricated in situ by a facile arc-discharge plasma approach, using bulk Ag as the raw target and methane gas as the carbon source. It was found that the Ag@C nanocapsules were ∼10 nm in mean diameter...

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Detalles Bibliográficos
Autores principales: Wang, Dongxing, Li, Da, Muhammad, Javid, Zhou, Yuanliang, Wang, Ziming, Lu, Sansan, Dong, Xinglong, Zhang, Zhidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078491/
https://www.ncbi.nlm.nih.gov/pubmed/35539142
http://dx.doi.org/10.1039/c8ra00078f
Descripción
Sumario:A nanocomposite of Ag@C nanocapsules dispersed in a multi-walled carbon nanotube (MWCNT) matrix was fabricated in situ by a facile arc-discharge plasma approach, using bulk Ag as the raw target and methane gas as the carbon source. It was found that the Ag@C nanocapsules were ∼10 nm in mean diameter, and the MWCNTs had 17–32 graphite layers in the wall with a thickness of 7–10 nm, while a small quantity of spherical carbon cages (giant fullerenes) were also involved with approximately 20–30 layers of the graphite shell. Typical dielectric behavior was dominant in the electronic transport of Ag@C/MWCNT nanocomposites; however, this was greatly modified by metallic Ag cores with respect to pure MWCNTs. A temperature-dependent resistance and I–V relationship provided evidence of a transition from Mott–David variable range hopping [ln ρ(T) ∼ T(−1/4)] to Shklovskii–Efros variable range hopping [ln ρ(T) ∼ T(−1/2)] at 5.4 K. A Coulomb gap, Δ(C) ≈ 0.05 meV, was obtained for the Ag@C/MWCNT nanocomposite system.