TY - JOUR
T1 - Self-Supporting Fiber-Anchor-Encapsulated MnCN2@Cyclized-PAN Anode for High-Performance Flexible Li-Ion Batteries
AU - Guo, Penghui
AU - Wu, Chongteng
AU - Shen, Xing
AU - Li, Hanlou
AU - Li, Yongjian
AU - Zhang, Yiming
AU - Wang, Jing
AU - Chen, Lai
AU - Su, Yuefeng
AU - Yang, Weiyou
AU - Wu, Feng
AU - Tan, Guoqiang
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025
Y1 - 2025
N2 - MnCN2 has rich and wide interlayer channels, making it a potentially high-capacity fast-charging anode material for Li-ion batteries. However, intrinsic metastability causes severe chemical and structural deterioration, suppressing capacity output and cycle reversibility. Here, an anchor-encapsulation strategy is proposed for stabilizing surface chemistry and bulk structure and developing an in situ synthesis process for constructing a fiber-encapsulated composite anode. Electrospinning is adopted to realize large-area fabrication of self-supporting electrode and uses the polyacrylonitrile cyclization to achieve chemical anchoring design. The obtained structure features highly oriented MnCN2 nano-crystallines embedded within cyclized-polyacrylonitrile frameworks, forming a fiber-anchor-encapsulated MnCN2@cPAN. Systematic studies disclose synergistic physical and chemical interactions between cPAN and MnCN2. Chemical anchoring facilitates fast electron and ion transport and also stable interface, and compact encapsulation alleviates volume change and electrolyte's erosion. Because of the improvement on electrical, chemical, and volumetric properties, the composite design enables promising electrochemical performance, including a large initial capacity of 825 mAh g−1 at 0.1 C, a high-rate capability of 335 mAh g−1 at 10 C, and a remarkable capacity retention of 80% after 800 cycles at 1 C. It demonstrates a great potential for Li-ion batteries, where LiNi0.8Mn0.1Co0.1O2//MnCN2@cPAN pouch-cell exhibits an excellent cycle performance of 86% capacity retention after 100 cycles.
AB - MnCN2 has rich and wide interlayer channels, making it a potentially high-capacity fast-charging anode material for Li-ion batteries. However, intrinsic metastability causes severe chemical and structural deterioration, suppressing capacity output and cycle reversibility. Here, an anchor-encapsulation strategy is proposed for stabilizing surface chemistry and bulk structure and developing an in situ synthesis process for constructing a fiber-encapsulated composite anode. Electrospinning is adopted to realize large-area fabrication of self-supporting electrode and uses the polyacrylonitrile cyclization to achieve chemical anchoring design. The obtained structure features highly oriented MnCN2 nano-crystallines embedded within cyclized-polyacrylonitrile frameworks, forming a fiber-anchor-encapsulated MnCN2@cPAN. Systematic studies disclose synergistic physical and chemical interactions between cPAN and MnCN2. Chemical anchoring facilitates fast electron and ion transport and also stable interface, and compact encapsulation alleviates volume change and electrolyte's erosion. Because of the improvement on electrical, chemical, and volumetric properties, the composite design enables promising electrochemical performance, including a large initial capacity of 825 mAh g−1 at 0.1 C, a high-rate capability of 335 mAh g−1 at 10 C, and a remarkable capacity retention of 80% after 800 cycles at 1 C. It demonstrates a great potential for Li-ion batteries, where LiNi0.8Mn0.1Co0.1O2//MnCN2@cPAN pouch-cell exhibits an excellent cycle performance of 86% capacity retention after 100 cycles.
KW - anchor-encapsulation
KW - cyclized-PAN
KW - Li-ion batteries
KW - MnCN
KW - self-supporting
UR - https://www.scopus.com/pages/publications/105021501857
U2 - 10.1002/adfm.202524597
DO - 10.1002/adfm.202524597
M3 - Article
AN - SCOPUS:105021501857
SN - 1616-301X
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -