纳米点
硅
材料科学
锂(药物)
空格(标点符号)
纳米技术
离子
无机化学
化学工程
碳纤维
光电子学
化学
有机化学
工程类
内分泌学
计算机科学
复合材料
操作系统
复合数
医学
作者
Bingjie Chen,Lianhai Zu,Yao Liu,Ruijing Meng,Yutong Feng,Chengxin Peng,Feng Zhu,Tian-Zi Hao,Jiajia Ru,Yonggang Wang,Jinhu Yang
标识
DOI:10.1002/anie.201915502
摘要
Abstract Incorporating nanoscale Si into a carbon matrix with high dispersity is desirable for the preparation of lithium‐ion batteries (LIBs) but remains challenging. A space‐confined catalytic strategy is proposed for direct superassembly of Si nanodots within a carbon (Si NDs⊂C) framework by copyrolysis of triphenyltin hydride (TPT) and diphenylsilane (DPS), where Sn atomic clusters created from TPT pyrolysis serve as the catalyst for DPS pyrolysis and Si catalytic growth. The use of Sn atomic cluster catalysts alters the reaction pathway to avoid SiC generation and enable formation of Si NDs with reduced dimensions. A typical Si NDs⊂C framework demonstrates a remarkable comprehensive performance comparable to other Si‐based high‐performance half LIBs, and higher energy densities compared to commercial full LIBs, as a consequence of the high dispersity of Si NDs with low lithiation stress. Supported by mechanic simulations, this study paves the way for construction of Si/C composites suitable for applications in future energy technologies.
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