二氧化锡
石墨烯
材料科学
阳极
量子点
锂(药物)
纳米技术
氧化锡
氧化石墨
石墨
石墨烯量子点
氧化物
电极
储能
复合数
化学工程
复合材料
化学
冶金
功率(物理)
医学
量子力学
物理化学
内分泌学
工程类
物理
作者
Bowen Li,Shouchun Bao,Qingke Tan,Rui Zhang,Liangjie Shan,Chao Wang,Guanglei Wu,Binghui Xu
标识
DOI:10.1016/j.jcis.2021.05.070
摘要
The spontaneous aggregation and poor electronic conductivity are widely recognized as the main challenges for practically applied nano-sized tin dioxide-based anode candidates in lithium-ion batteries. This work describes a hierarchical graphite and graphene oxide (GO) framework stabilized tin dioxide quantum dot composite (SnO2@C/GO), which is synthesized by a solid-state ball-milling treatment and a water-phase self-assembly process. Characterization results demonstrate the engineered inside nanostructured graphite and outside GO layers from the SnO2@C/GO composite jointly contribute to a good immobilization effect for the SnO2 quantum dots. The hierarchical carbonaceous matrix supported SnO2 quantum dots could maintain good structure stability over a long cycling life under high current densities. As an anodic electrochemically active material for lithium-ion batteries, the SnO2@C/GO composite shows a high reversible capacity of 1156 mAh·g−1 at the current density of 1000 mA·g−1 for 350 continual cycles as well as good rate performance. The large pseudocapacitive behavior in this electrode is favorable for promoting the lithium-ion storage capability under higher current densities. The whole synthetic route is simple and effective, which probably has good potential for further development to massively fabricate high-performance electrode active materials for energy storage.
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