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Combustion-driven synthesis route for bimetallic Ag-Bi nanoparticle-anchored carbon nanotube electrodes for high-performance supercapacitors

Authors
Cha, YoungsunKim, TaewonSeo, ByungseokChoi, Wonjoon
Issue Date
15-10월-2022
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Thermochemical synthesis; Bimetallic nanoparticle; Electrochemical electrode; Silver-bismuth hybrid; Combustion; Supercapacitor
Citation
CARBON, v.198, pp.11 - 21
Indexed
SCIE
SCOPUS
Journal Title
CARBON
Volume
198
Start Page
11
End Page
21
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/143718
DOI
10.1016/j.carbon.2022.07.003
ISSN
0008-6223
Abstract
Bimetallic nanostructures within carbon-based materials can overcome the fundamental limits of energy materials, which cannot be obtained using a single material. However, their synthesis involves time-consuming and complex processes that cause phase/interface segregation and non-uniformly distributed metal elements. Herein, we report a facile combustion-driven synthesis for bimetallic Ag-Bi nanoparticle (NP)-anchored carbon nanotube (CNT) electrodes. One-step combustion wave passing through freestanding films comprising Ag2O and Bi powders, nitrocellulose layers within CNTs enables high-density thermochemical reactions in seconds. The rapid heating-cooling rates induce the formation of liquefied Ag-Bi and trapping of metastable Ag-Bi phases at the carbon surfaces, thereby synthesizing homogeneously mixed bimetallic Ag-Bi NPs anchored on the CNTs, along with smaller diameters (similar to 20 nm) and high distribution density. A supercapacitor electrode employing them exhibits outstanding specific capacitance and retention (1372-1093 Fg(-1) at 2-5 mVs(-1), and 101.3% of the stabilized capacitance after 10,000 cycles at 100 mVs(-1)). This was attributed to the large active site surface area from the small diameters and high distribution density of the bimetallic Ag-Bi NPs by low surface energy, and highly stable adhesion to the CNTs. The synthesis strategy can be extended to a scalable fabrication method of various multi-metallic nanostructures for versatile electrochemical electrodes and catalysts.
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