TY - JOUR
T1 - Effects of the Pd3Co nanoparticles-additive on the redox shuttle reaction in rechargeable Li-S batteries
AU - Yom, Jee Ho
AU - Cho, Sung Man
AU - Hwang, Sun Woo
AU - Yoon, Woo Young
N1 - Funding Information:
This work was supported by the Industrial Strategic Technology Development Program (10045221, Development of dendrite-free Limetal anode for high energy Li-metal secondary battery) funded by the Ministry of Knowledge Economy (MKE, Korea). This study was also supported by the National Research Foundation of Korea (NRF) and funded by a grant from the Korean government (MEST) (2011-0028757). The microstructures of the samples were observed by TEM at the Korea Basic Science Institute, Seoul Center.
Publisher Copyright:
© 2016 The Electrochemical Society.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2016
Y1 - 2016
N2 - A lithium-sulfur (Li-S) battery system with bimetallic electrode additive, which limit the dissolution of intermediate lithium polysulfides, is studied. Palladium-cobalt (Pd3Co) nanoparticles are successfully employed as redox promoters in Li-S cells. These cells show high capacity retention and excellent Coulombic efficiency, which are attributed to the fast charge transfer of Pd3Co. Characterization of the Pd3Co nanoparticles isperformed via high-resolution transmission electron microscopy, fast Fourier transform analysis, energy-dispersive X-ray, and X-ray diffraction. At 0.1 C-rate, the initial discharge and charge capacities of the Pd3Co-sulfur electrodes are 1.24 and 1.36 times higher than those of the bare sulfur electrodes. During the first discharge cycle, the overpotential of the Pd3Co electrode (100 mV) is much lower than that of the bare sulfur cell (190 mV). After 200 cycles at 1.0 C-rate, the Pd3Co-sulfur electrodes deliver a discharge capacity of 544 mAh g-1 a high Coulombic efficiency (99.6%). Moreover, the capacity retention of Pd3Co cells is 83.9%. The inductively coupled plasma-atomic emission spectroscopy and X-ray photoelectron spectroscopy data demonstrate that the Pd3Co nanoparticles can suppress the dissolution of lithium polysulfides and the shuttle effect. These results indicate that the reaction kinetics of the sulfur electrodes is enhanced by the Pd3Co nanoparticles.
AB - A lithium-sulfur (Li-S) battery system with bimetallic electrode additive, which limit the dissolution of intermediate lithium polysulfides, is studied. Palladium-cobalt (Pd3Co) nanoparticles are successfully employed as redox promoters in Li-S cells. These cells show high capacity retention and excellent Coulombic efficiency, which are attributed to the fast charge transfer of Pd3Co. Characterization of the Pd3Co nanoparticles isperformed via high-resolution transmission electron microscopy, fast Fourier transform analysis, energy-dispersive X-ray, and X-ray diffraction. At 0.1 C-rate, the initial discharge and charge capacities of the Pd3Co-sulfur electrodes are 1.24 and 1.36 times higher than those of the bare sulfur electrodes. During the first discharge cycle, the overpotential of the Pd3Co electrode (100 mV) is much lower than that of the bare sulfur cell (190 mV). After 200 cycles at 1.0 C-rate, the Pd3Co-sulfur electrodes deliver a discharge capacity of 544 mAh g-1 a high Coulombic efficiency (99.6%). Moreover, the capacity retention of Pd3Co cells is 83.9%. The inductively coupled plasma-atomic emission spectroscopy and X-ray photoelectron spectroscopy data demonstrate that the Pd3Co nanoparticles can suppress the dissolution of lithium polysulfides and the shuttle effect. These results indicate that the reaction kinetics of the sulfur electrodes is enhanced by the Pd3Co nanoparticles.
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U2 - 10.1149/2.0291610jes
DO - 10.1149/2.0291610jes
M3 - Article
AN - SCOPUS:84987732329
SN - 0013-4651
VL - 163
SP - A2179-A2184
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 10
ER -