TY - JOUR
T1 - Rational synthesis of uniform yolk–shell Ni–Fe bimetallic sulfide nanoflakes@porous carbon nanospheres as advanced anodes for high-performance potassium-/sodium-ion batteries
AU - Yang, Su Hyun
AU - Park, Seung Keun
AU - Park, Gi Dae
AU - Kim, Ju Hyeong
AU - Kang, Yun Chan
N1 - Funding Information:
This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (NRF-2019R1A2C2088047 and 2020R1A4A2002854).
Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2021/8/1
Y1 - 2021/8/1
N2 - The identification of electrode materials suitable for hosting both K+ and Na+ is more challenging than that for Li+ due to the larger ionic radii of K+ and Na+. Thus, the design and fabrication of advanced electrode materials with excellent electrochemical properties for both potassium-ion batteries (KIBs) and sodium-ion batteries (SIBs) is extremely challenging. Herein, a unique yolk–shell-structured Ni–Fe bimetallic sulfide nanoflake@carbon nanosphere (NFS@C) is designed as a high-performance anode for both KIBs and SIBs via a combination of the infiltration method and sulfidation process. During the first infiltration process under vacuum, Ni and Fe precursors can easily penetrate though the shell into the central void of HMCSs with the help of capillary force. The subsequent sulfidation can transform these precursors into their corresponding sulfides, resulting in the formation of NFS@C yolk–shell nanospheres. These rationally engineered architectures provide enough space to buffer the huge volume expansion of Ni–Fe sulfides upon cycling and supply ample channels for the diffusion of ions, thus providing a well-defined conductive network in the entire electrode. Therefore, NFS@C yolk–shell nanospheres exhibit excellent cycling stability (297 mA h g−1 at 0.1 A g−1 after 250 cycles) and rate capability (52 mA h g−1 at 7.0 A g−1) for potassium storage. Furthermore, NFS@C nanospheres as anodes for SIBs exhibited high discharge capacity (417 mA h g−1 at 0.2 A g−1 after 250 cycles) and stable capacity (140 mA h g−1) even at a high current density (10.0 A g−1).
AB - The identification of electrode materials suitable for hosting both K+ and Na+ is more challenging than that for Li+ due to the larger ionic radii of K+ and Na+. Thus, the design and fabrication of advanced electrode materials with excellent electrochemical properties for both potassium-ion batteries (KIBs) and sodium-ion batteries (SIBs) is extremely challenging. Herein, a unique yolk–shell-structured Ni–Fe bimetallic sulfide nanoflake@carbon nanosphere (NFS@C) is designed as a high-performance anode for both KIBs and SIBs via a combination of the infiltration method and sulfidation process. During the first infiltration process under vacuum, Ni and Fe precursors can easily penetrate though the shell into the central void of HMCSs with the help of capillary force. The subsequent sulfidation can transform these precursors into their corresponding sulfides, resulting in the formation of NFS@C yolk–shell nanospheres. These rationally engineered architectures provide enough space to buffer the huge volume expansion of Ni–Fe sulfides upon cycling and supply ample channels for the diffusion of ions, thus providing a well-defined conductive network in the entire electrode. Therefore, NFS@C yolk–shell nanospheres exhibit excellent cycling stability (297 mA h g−1 at 0.1 A g−1 after 250 cycles) and rate capability (52 mA h g−1 at 7.0 A g−1) for potassium storage. Furthermore, NFS@C nanospheres as anodes for SIBs exhibited high discharge capacity (417 mA h g−1 at 0.2 A g−1 after 250 cycles) and stable capacity (140 mA h g−1) even at a high current density (10.0 A g−1).
KW - Bimetallic sulfides
KW - Hollow carbon nanosphere
KW - Potassium-ion batteries
KW - Sodium-ion batteries
KW - Yolk–shell structure
UR - http://www.scopus.com/inward/record.url?scp=85097662383&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2020.127963
DO - 10.1016/j.cej.2020.127963
M3 - Article
AN - SCOPUS:85097662383
SN - 1385-8947
VL - 417
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 127963
ER -