TY - JOUR
T1 - An approach to flexible Na-ion batteries with exceptional rate capability and long lifespan using Na2FeP2O7 nanoparticles on porous carbon cloth
AU - Song, Hee Jo
AU - Kim, Da Sol
AU - Kim, Jae Chan
AU - Hong, Seong Hyeon
AU - Kim, Dong Wan
N1 - Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) Grant funded by the Ministry of Science, ICT, and Future Planning (No. 2016R1A2B2012728).
Publisher Copyright:
© The Royal Society of Chemistry.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017
Y1 - 2017
N2 - As post-Li-ion batteries (LIBs), rechargeable Na-ion batteries (NIBs) are considered as one of the potential candidates for large-scale energy storage systems because of the abundance and low cost of sodium resources, and similar electrochemical behavior of Na ions to Li ions for intercalation in cathodes. While there exist many challenges in the fabrication of cathodes, a polyanionic compound, Na2FeP2O7, has been in the spotlight as a potential cathode material for NIBs because of its rate capability, cyclability, and thermal stability. In this study, Na2FeP2O7 nanoparticles (NFP-NPs) embedded in carbon were prepared via a citric acid-assisted sol-gel method, followed by a post-heat treatment process. For the first time, NFP-NPs exhibited a reversible capacity close to the theoretical value (95 mA h g−1) over the voltage range of 2.0-4.0 V (vs. Na/Na+). Moreover, they displayed a superior rate capability of 77, 70, 66 and 65 mA h g−1 even at high rates of 10, 20, 30 and 60C, respectively. Equally notable is their exceptional long-term cyclability at high rates. At the rate of 10 and 60C, the capacity retention after 10 000 cycles is 83 and 84%, respectively. In addition, NFP-NPs uniformly loaded on the surface of flexible porous carbon cloth (NFP-NPs@PCC) electrodes without any conductive agents and polymeric binders also exhibit excellent rate capability and long-term cyclability at a high rate of 10C (56 mA h g−1 after 2000 cycles). We show high-performance free-standing NFP-NPs@PCC electrodes for possible application in flexible NIBs.
AB - As post-Li-ion batteries (LIBs), rechargeable Na-ion batteries (NIBs) are considered as one of the potential candidates for large-scale energy storage systems because of the abundance and low cost of sodium resources, and similar electrochemical behavior of Na ions to Li ions for intercalation in cathodes. While there exist many challenges in the fabrication of cathodes, a polyanionic compound, Na2FeP2O7, has been in the spotlight as a potential cathode material for NIBs because of its rate capability, cyclability, and thermal stability. In this study, Na2FeP2O7 nanoparticles (NFP-NPs) embedded in carbon were prepared via a citric acid-assisted sol-gel method, followed by a post-heat treatment process. For the first time, NFP-NPs exhibited a reversible capacity close to the theoretical value (95 mA h g−1) over the voltage range of 2.0-4.0 V (vs. Na/Na+). Moreover, they displayed a superior rate capability of 77, 70, 66 and 65 mA h g−1 even at high rates of 10, 20, 30 and 60C, respectively. Equally notable is their exceptional long-term cyclability at high rates. At the rate of 10 and 60C, the capacity retention after 10 000 cycles is 83 and 84%, respectively. In addition, NFP-NPs uniformly loaded on the surface of flexible porous carbon cloth (NFP-NPs@PCC) electrodes without any conductive agents and polymeric binders also exhibit excellent rate capability and long-term cyclability at a high rate of 10C (56 mA h g−1 after 2000 cycles). We show high-performance free-standing NFP-NPs@PCC electrodes for possible application in flexible NIBs.
UR - http://www.scopus.com/inward/record.url?scp=85015333031&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85015333031&partnerID=8YFLogxK
U2 - 10.1039/c7ta00727b
DO - 10.1039/c7ta00727b
M3 - Article
AN - SCOPUS:85015333031
SN - 2050-7488
VL - 5
SP - 5502
EP - 5510
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 11
ER -