TY - JOUR
T1 - Deliberate introduction of mesopores into microporous activated carbon toward efficient Se cathode of Na−Se batteries
AU - Kim, Jin Koo
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).
Funding Information:
Ministry of Education, Grant/Award Number: NRF‐2019R1A2C2088047; National Research Foundation of Korea, Grant/Award Number: 2020R1A4A2002854 Funding information
Publisher Copyright:
© 2021 John Wiley & Sons Ltd.
PY - 2022/3/10
Y1 - 2022/3/10
N2 - Sodium-selenium (Na−Se) batteries are garnering increasing attention as promising energy storage systems because of the low cost of Na resources and the high volumetric capacity of Se. Nevertheless, their practical application is hindered by the low utilization rate of Se and the shuttle effect of polyselenide, which lead to unstable cycling performance. Therefore, extensive efforts are necessary to develop suitable carbon-based Se hosts. Here, we propose a simple method to introduce a controlled amount of mesopores into microporous carbon, which can remarkably improve the electrochemical performance of Na−Se batteries. The Se encapsulated in the optimized micro-mesoporous carbon exhibited a substantially improved cycling stability, with a capacity of 572 mA h g−1 at 0.5C after 150 cycles, which represents a 93% capacity retention from the second cycle. In addition, the Se could achieve a high reversible capacity of 214 mA h g−1, even at 20C. The results of this study provide guidance for distinguishing the roles of the micropores and mesopores of carbon in the Se host of Na−Se batteries: (a) Micropores are ideal reservoirs to confine Se in an amorphous form for stable electrochemical reactions with Na, and (b) mesopores provide pathways for Na+ ion diffusion and a buffer for the volume change of Se. The proposed method would be widely applicable to other types of microporous carbon with much higher specific surface areas, which can afford higher Se loading for more advanced alkali metal−Se batteries.
AB - Sodium-selenium (Na−Se) batteries are garnering increasing attention as promising energy storage systems because of the low cost of Na resources and the high volumetric capacity of Se. Nevertheless, their practical application is hindered by the low utilization rate of Se and the shuttle effect of polyselenide, which lead to unstable cycling performance. Therefore, extensive efforts are necessary to develop suitable carbon-based Se hosts. Here, we propose a simple method to introduce a controlled amount of mesopores into microporous carbon, which can remarkably improve the electrochemical performance of Na−Se batteries. The Se encapsulated in the optimized micro-mesoporous carbon exhibited a substantially improved cycling stability, with a capacity of 572 mA h g−1 at 0.5C after 150 cycles, which represents a 93% capacity retention from the second cycle. In addition, the Se could achieve a high reversible capacity of 214 mA h g−1, even at 20C. The results of this study provide guidance for distinguishing the roles of the micropores and mesopores of carbon in the Se host of Na−Se batteries: (a) Micropores are ideal reservoirs to confine Se in an amorphous form for stable electrochemical reactions with Na, and (b) mesopores provide pathways for Na+ ion diffusion and a buffer for the volume change of Se. The proposed method would be widely applicable to other types of microporous carbon with much higher specific surface areas, which can afford higher Se loading for more advanced alkali metal−Se batteries.
KW - hierarchically porous carbon
KW - mesopores
KW - micropores
KW - selenium cathode
KW - sodium−selenium batteries
UR - http://www.scopus.com/inward/record.url?scp=85117044299&partnerID=8YFLogxK
U2 - 10.1002/er.7389
DO - 10.1002/er.7389
M3 - Article
AN - SCOPUS:85117044299
SN - 0363-907X
VL - 46
SP - 3396
EP - 3408
JO - International Journal of Energy Research
JF - International Journal of Energy Research
IS - 3
ER -