TY - JOUR
T1 - Bifunctional Conducting Polymer Coated CoP Core–Shell Nanowires on Carbon Paper as a Free-Standing Anode for Sodium Ion Batteries
AU - Zhang, Jing
AU - Zhang, Kai
AU - Yang, Junghoon
AU - Lee, Gi Hyeok
AU - Shin, Jeongyim
AU - Wing-hei Lau, Vincent
AU - Kang, Yong Mook
N1 - Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (NRF-2017R1A2B3004383), the energy efficiency and resources of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) grant funded by the Ministry of Knowledge Economy, Korean government (No. 20152020105420), Creative Materials Discovery Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (NRF-2017M3D1A1039553). K.Z. would like to acknowledge Korea Research Fellowship Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT (No. 2016H1D3A1906790).
Publisher Copyright:
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/7/16
Y1 - 2018/7/16
N2 - This study proposes a conformal surface coating of conducting polymer for protecting 1D nanostructured electrode material, thereby enabling a free-standing electrode without binder for sodium ion batteries. Here, polypyrrole (PPy), which is one of the representative conducting polymers, encapsulated cobalt phosphide (CoP) nanowires (NWs) grown on carbon paper (CP), finally realizes 1D core–shell CoP@PPy NWs/CP. The CoP core is connected to the PPy shell via strong chemical bonding, which can maintain a Co–PPy framework during charge/discharge. It also possesses bifunctional features that enhances the charge transfer and buffers the volume expansion. Consequently, 1D core–shell CoP@PPy NWs/CP demonstrates superb electrochemical performance, delivering a high areal capacity of 0.521 mA h cm−2 at 0.15 mA cm−2 after 100 cycles, and 0.443 mA h cm−2 at 1.5 mA cm−2 even after 1000 cycles. Even at a high current density of 3 mA cm−2, a significant areal discharge capacity reaching 0.285 mA h cm−2 is still maintained. The outstanding performance of the CoP@PPy NWs/CP free-standing anode provides not only a novel insight into the modulated volume expansion of anode materials but also one of the most effective strategies for binder-free and free-standing electrodes with decent mechanical endurance for future secondary batteries.
AB - This study proposes a conformal surface coating of conducting polymer for protecting 1D nanostructured electrode material, thereby enabling a free-standing electrode without binder for sodium ion batteries. Here, polypyrrole (PPy), which is one of the representative conducting polymers, encapsulated cobalt phosphide (CoP) nanowires (NWs) grown on carbon paper (CP), finally realizes 1D core–shell CoP@PPy NWs/CP. The CoP core is connected to the PPy shell via strong chemical bonding, which can maintain a Co–PPy framework during charge/discharge. It also possesses bifunctional features that enhances the charge transfer and buffers the volume expansion. Consequently, 1D core–shell CoP@PPy NWs/CP demonstrates superb electrochemical performance, delivering a high areal capacity of 0.521 mA h cm−2 at 0.15 mA cm−2 after 100 cycles, and 0.443 mA h cm−2 at 1.5 mA cm−2 even after 1000 cycles. Even at a high current density of 3 mA cm−2, a significant areal discharge capacity reaching 0.285 mA h cm−2 is still maintained. The outstanding performance of the CoP@PPy NWs/CP free-standing anode provides not only a novel insight into the modulated volume expansion of anode materials but also one of the most effective strategies for binder-free and free-standing electrodes with decent mechanical endurance for future secondary batteries.
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U2 - 10.1002/aenm.201800283
DO - 10.1002/aenm.201800283
M3 - Article
AN - SCOPUS:85045223465
SN - 1614-6832
VL - 8
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 20
M1 - 1800283
ER -