TY - JOUR
T1 - Combustion-driven synthesis route for bimetallic Ag–Bi nanoparticle-anchored carbon nanotube electrodes for high-performance supercapacitors
AU - Cha, Youngsun
AU - Kim, Taewon
AU - Seo, Byungseok
AU - Choi, Wonjoon
N1 - Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government ( Ministry of Science and ICT ) (No. 2019R1A2C2085583 , No. 2020R1A5A1018153 ).
Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/10/15
Y1 - 2022/10/15
N2 - 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 (∼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.
AB - 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 (∼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.
KW - Bimetallic nanoparticle
KW - Combustion
KW - Electrochemical electrode
KW - Silver-bismuth hybrid
KW - Supercapacitor
KW - Thermochemical synthesis
UR - http://www.scopus.com/inward/record.url?scp=85133779712&partnerID=8YFLogxK
U2 - 10.1016/j.carbon.2022.07.003
DO - 10.1016/j.carbon.2022.07.003
M3 - Article
AN - SCOPUS:85133779712
SN - 0008-6223
VL - 198
SP - 11
EP - 21
JO - Carbon
JF - Carbon
ER -