TY - JOUR
T1 - High-Energy, High-Power Sodium-Ion Batteries from a Layered Organic Cathode
AU - Chen, Tianyang
AU - Wang, Jiande
AU - Tan, Bowen
AU - Zhang, Kimberly J.
AU - Banda, Harish
AU - Zhang, Yugang
AU - Kim, Dong Ha
AU - Dincă, Mircea
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/2/19
Y1 - 2025/2/19
N2 - Sodium-ion batteries (SIBs) attract significant attention due to their potential as an alternative energy storage solution, yet challenges persist due to the limited energy density of existing cathode materials. In principle, redox-active organic materials can tackle this challenge because of their high theoretical energy densities. However, electrode-level energy densities of organic electrodes are compromised due to their poor electron/ion transport and severe dissolution. Here, we report the use of a low-bandgap, conductive, and highly insoluble layered metal-free cathode material for SIBs. It exhibits a high theoretical capacity of 355 mAh g-1 per formula unit, enabled by a four-electron redox process, and achieves an electrode-level energy density of 606 Wh kg-1electrode (90 wt % active material) along with excellent cycling stability. It allows for facile two-dimensional Na+ diffusion, which enables a high intrinsic rate capability. Growth of the active cathode material in the presence of as little as 2 wt % carboxyl-functionalized carbon nanotubes improves charge transport and charge transfer kinetics and further enhances the power performance. Altogether, these allow the construction of SIB cells built from an affordable, sustainable organic small molecule, which provide a cathode energy density of 472 Wh kg-1electrode when charging/discharging in 90 s and a top specific power of 31.6
AB - Sodium-ion batteries (SIBs) attract significant attention due to their potential as an alternative energy storage solution, yet challenges persist due to the limited energy density of existing cathode materials. In principle, redox-active organic materials can tackle this challenge because of their high theoretical energy densities. However, electrode-level energy densities of organic electrodes are compromised due to their poor electron/ion transport and severe dissolution. Here, we report the use of a low-bandgap, conductive, and highly insoluble layered metal-free cathode material for SIBs. It exhibits a high theoretical capacity of 355 mAh g-1 per formula unit, enabled by a four-electron redox process, and achieves an electrode-level energy density of 606 Wh kg-1electrode (90 wt % active material) along with excellent cycling stability. It allows for facile two-dimensional Na+ diffusion, which enables a high intrinsic rate capability. Growth of the active cathode material in the presence of as little as 2 wt % carboxyl-functionalized carbon nanotubes improves charge transport and charge transfer kinetics and further enhances the power performance. Altogether, these allow the construction of SIB cells built from an affordable, sustainable organic small molecule, which provide a cathode energy density of 472 Wh kg-1electrode when charging/discharging in 90 s and a top specific power of 31.6
UR - http://www.scopus.com/inward/record.url?scp=85217101693&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85217101693&partnerID=8YFLogxK
U2 - 10.1021/jacs.4c17713
DO - 10.1021/jacs.4c17713
M3 - Article
C2 - 39904611
AN - SCOPUS:85217101693
SN - 0002-7863
VL - 147
SP - 6181
EP - 6192
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 7
ER -