Rational Design of Silicon Nanodots/Carbon Anodes by Partial Oxidization Strategy with High-Performance Lithium-Ion Storage

材料科学 阳极 纳米点 锂(药物) 碳纤维 化学工程 储能 纳米技术 阴极 复合数 电极 复合材料 光电子学 医学 功率(物理) 化学 物理 物理化学 量子力学 内分泌学 工程类
作者
Shanqiang Ou,Tao Meng,Zezhong Xie,Jin Feng,Qiushi Wang,Dong Zhou,Zhongfei Liu,Kun Wang,Changgong Meng,Yexiang Tong
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:14 (43): 48801-48811 被引量:12
标识
DOI:10.1021/acsami.2c11906
摘要

Silicon (Si) is considered a promising anode material for rechargeable lithium-ion batteries (LIBs) due to its high theoretical capacity, low working potential, and safety features. However, the practical use of Si-based anodes is hampered by their huge volume expansion during the process of lithiation/delithiation, and they have relatively low intrinsic electronic conductivity, therefore seriously restricting their application in energy storage. Here, we propose a facile approach to directly transform siliceous biomass (bamboo leaves) into a porous carbon skeleton-wrapped Si nanodot architecture through a partial oxidization strategy and magnesium thermal reaction to obtain a high Si nanodot component composite (denoted as Si/C-O). With the synergistic effect of the porous carbon skeleton structure and uniformly dispersed Si nanodots, the Si/C-O composite anode with a stable structure that can avoid pulverization and accommodate volume expansion during cycling is fabricated. As expected, the biomass-converted Si/C-O anode not only presents a high Si component (59.7 wt %) by TGA but also exhibits an excellent capacity of 1013 mAh g-1 at 0.5 A g-1 and robust cycling stability with a capacity retention of 526 mAh g-1 after 650 cycles. Moreover, the Si/C-O anode demonstrates considerable performance in practical LIBs when assembled with a commercial LiNi0.8Co0.1Mn0.1O2 cathode. This work provides an effective strategy and long-term insights into the utilization of porous Si-based materials converted by biomass to design and synthesize high-performance LIB materials.
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