材料科学
阳极
锂离子电池的纳米结构
阴极
化学工程
储能
纳米技术
电极
光电子学
电流(流体)
冶金
作者
Yajun Zhu,Tianli Han,Ting Zhou,Xiaofei Huang,Haojun Xu,Wentuan Bi,Jinyun Liu
标识
DOI:10.1021/acsami.5c25865
摘要
Silicon (Si) anodes exhibit remarkable theoretical capacity, enabling them to be attractive candidates for high-energy-density lithium-ion batteries. However, conventional surface-modification strategies on Si often fail due to insufficient adhesion between the coating and Si, thereby giving rise to interfacial degradation and poor ion/electron transport. Here, we develop a heterointerface-engineered Si@Co 0.85 Se/N-doped carbon (NC) anode. Porous Si is coated by metal–organic framework (MOF)-derived Co 0.85 Se, and Si@Co 0.85 Se is encapsulated in an NC matrix. This design establishes robust Co–Se–Si bonding at the heterointerface, enabling highly efficient ionic and electronic transport. The Si@Co 0.85 Se/NC anode delivers a large specific capacity of 1155.1 mA h g –1 after 100 cycles at 0.2 A g –1 and remains stable over 600 cycles at 1.0 A g –1 . As a pairing with a LiFePO 4 cathode, the full cell demonstrates exceptional cycling stability. In situ X-ray diffraction and in situ Raman spectroscopy confirm highly reversible electrochemical processes. These findings provide a heterointerface-designing strategy for Si-based anodes to achieve synergistic enhancement for high-performance energy storage.
科研通智能强力驱动
Strongly Powered by AbleSci AI