材料科学
阳极
石墨
非阻塞I/O
锂(药物)
纳米技术
化学工程
电池(电)
储能
导电体
阴极
电极
复合材料
医学
物理
工程类
内分泌学
物理化学
催化作用
功率(物理)
量子力学
化学
生物化学
作者
Qiaoyi Yan,Liqianyun Xu,Yi Zhao,Feng Wu,Renjie Chen,Li Li
标识
DOI:10.1021/acsami.3c02681
摘要
Although transition metal-based anodes for batteries are preferred owing to their higher energy density, the potential for structural collapse due to volume expansion has hindered their development. Herein, a simulated cellular structured anode composed of uniform nanoparticles and wrapped polydopamine is designed to direct the electronic/ionic diffusion channel and effectively address the volume expansion problem. The controlled-release effects of the polymer between the nano-interface protect the three-dimensional (3D) structures from collapsing during the electrochemical process. The constructed conductive networks along the NiO nanoparticle configurations effectively induce the transfer path and further accelerate the diffusion rate. Furthermore, interstitial filling unlocks the inactive component and triggers the deep delivery of electrons, which boosts battery performance. Therefore, the 3D structured PDA@NiO@G anode prepared from a recycled graphite conductive substrate exhibits excellent specific capacity (500 mAh g-1 at 0.1 A g-1) and significantly improved long-cycle performance (402 mAh g-1 after 500 cycles at 0.5 A g-1). The structure modulation strategy provides meaningful insight into transition metal anodes for the fabrication of high kinetics and prolonged life lithium-ion batteries, as well as the reuse of the spent graphite anode.
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