TY - JOUR
T1 - A Robust Mn-Based Metal–Organic Framework Cathode with Long-Cycle-Life Enabled by Metal Valence Stability and Hydrogen Bond Networks for High-Performance Sodium-Ion Batteries
AU - Wu, Yunling
AU - Bu, Yiming
AU - Li, Xinyang
AU - Dong, Xiangtao
AU - Zhou, Xuan
AU - Bu, Zipeng
AU - Fu, Lijun
AU - Wu, Yuping
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025
Y1 - 2025
N2 - Sodium-ion batteries (SIBs) hold significant potential for sustainable energy storage but face challenges in cathode material stability and capacity. Metal–organic frameworks (MOFs) are promising owing to their tunable structures and redox-active sites but often suffer structural degradation from metal ion valence changes during cycling. Here, a novel manganese-based MOF (Mn-PTO) is introduced, representing a new class of MOFs specifically engineered for enhanced stability and performance in SIBs. Mn-PTO addresses valence changes and structural degradation through two synergistic mechanisms. First, it ensures valence stability by confining redox activity to the ligand's carbonyl groups, stabilizing Mn ions in the divalent state, and preventing structural collapse. Second, its hydrogen bond network reinforces structural integrity and mitigates stresses from repeated ion insertion and extraction. These innovations enable Mn-PTO to deliver exceptional electrochemical performance, including remarkable cycling stability, maintaining a capacity of 118 mAh g−1 over 7,000 cycles at 5 A g−1. This performance surpasses most reported organic electrode materials. Additionally, Mn-PTO exhibits an impressive rate capability of 124 mAh g−1 at 20 A g−1. These results firmly establish Mn-PTO as a groundbreaking cathode material, offering a robust and durable solution to the limitations of traditional MOF-based systems.
AB - Sodium-ion batteries (SIBs) hold significant potential for sustainable energy storage but face challenges in cathode material stability and capacity. Metal–organic frameworks (MOFs) are promising owing to their tunable structures and redox-active sites but often suffer structural degradation from metal ion valence changes during cycling. Here, a novel manganese-based MOF (Mn-PTO) is introduced, representing a new class of MOFs specifically engineered for enhanced stability and performance in SIBs. Mn-PTO addresses valence changes and structural degradation through two synergistic mechanisms. First, it ensures valence stability by confining redox activity to the ligand's carbonyl groups, stabilizing Mn ions in the divalent state, and preventing structural collapse. Second, its hydrogen bond network reinforces structural integrity and mitigates stresses from repeated ion insertion and extraction. These innovations enable Mn-PTO to deliver exceptional electrochemical performance, including remarkable cycling stability, maintaining a capacity of 118 mAh g−1 over 7,000 cycles at 5 A g−1. This performance surpasses most reported organic electrode materials. Additionally, Mn-PTO exhibits an impressive rate capability of 124 mAh g−1 at 20 A g−1. These results firmly establish Mn-PTO as a groundbreaking cathode material, offering a robust and durable solution to the limitations of traditional MOF-based systems.
KW - hydrogen-bonding network
KW - metal-organic frameworks
KW - sodium-ion batteries
KW - structural degradation
KW - valence changes
UR - http://www.scopus.com/inward/record.url?scp=105000280406&partnerID=8YFLogxK
U2 - 10.1002/adfm.202500197
DO - 10.1002/adfm.202500197
M3 - 文章
AN - SCOPUS:105000280406
SN - 1616-301X
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -